Rodney Scott

Visiting Fellow
Adjunct Senior Lecturer

Associate Professor Rodney Scott is a Visiting Fellow in the School of Business at UNSW, Canberra.

His substantive role is as the Chief Policy Advisor for New Zealand’s State Services Commission, where he leads advice on the design and direction of New Zealand’s public services. He has previously worked at senior and executives levels; in management and advisory roles; in the public, private, and not-for-profit sectors; in Australia and New Zealand. Rodney holds an adjunct affiliation to the Australia and New Zealand School of Government where he is a member of the research committee, and is the Chair of the Victoria University of Wellington School of Government Trust.

Rodney was a 2018 Fellow In Practice at Oxford University’s Blavatnik School of Government, and a 2017 Innovations Fellow at Harvard University’s Kennedy School of Government. He has lectured in graduate programmes and executive training across four continents. Rodney completed PhD studies in system dynamics and public management at the University of Queensland, including the dissertation “Group model building and mental model change” which was awarded “best doctoral thesis” by the Australia and New Zealand Academy of Management. He is widely published in system dynamics, operations research, group decision, public policy, and public administration. His current research interests include interagency collaboration, governance, performance management, institutional memory, social identity, public service motivation, and public service ethics. Rodney particularly welcomes contact from Australian researchers looking to understand New Zealand public management in a comparative context.

PUBLICATIONS

Books
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Scott R, 2018, Group Model Building Using Systems Dynamics to Achieve Enduring Agreement, Springer
2018
Scott RJ; Boyd R, 2017, Interagency Performance Targets: A Case Study of New Zealand’s Results Programme, Business of Government, IBM, New York, http://www.businessofgovernment.org/sites/default/files/Interagency%20Performance%20Targets.pdf
2017
Preprints
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Wyss AB; Sofer T; Lee MK; Terzikhan N; Nguyen JN; Lahousse L; Latourelle JC; Smith AV; Bartz TM; Feitosa MF; Gao W; Ahluwalia TS; Tang W; Oldmeadow C; Duan Q; Jong KD; Wojczynski MK; Wang X-Q; Noordam R; Hartwig FP; Jackson VE; Wang T; Obeidat M; Hobbs BD; Huan T; Kichaev G; Jin J; Graff M; Harris TB; Kalhan R; Heckbert SR; Paternoster L; Burkart KM; Liu Y; Holliday EG; Wilson JG; Vonk JM; Sanders J; Barr RG; Mutsert RD; Menezes AMB; Adams HHH; Berge MVD; Joehanes R; Launer LJ; Morrison AC; Sitlani CM; Celedón JC; Kritchevsky SB; Scott RJ; Christensen K; Rotter JI; Bonten TN; César Wehrmeister F; Bossé Y; Franceschini N; Brody JA; Kaplan RC; Lohman K; McEvoy M; Province MA; Rosendaal FR; Taylor KD; Nickle DC; North KE; Fornage M; Psaty BM; Myers RH; O’Connor G; Hansen T; Laurie CC; Cassano P; Sung J; Kim WJ; Attia JR; Lange L; Boezen HM; Thyagarajan B; Rich SS; Mook-Kanamori DO; Horta BL; Uitterlinden AG; Sin DD; Im HK; Cho MH; Brusselle GG; Gharib SA; Dupuis J; Manichaikul A; London SJ, Multiethnic meta-analysis identifies new loci for pulmonary function, http://dx.doi.org/10.1101/196048
Wain LV; Vaez A; Jansen R; Joehanes R; van der Most PJ; Erzurumluoglu AM; O'Reilly P; Cabrera CP; Warren HR; Rose LM; Verwoert GC; Hottenga J-J; Strawbridge RJ; Esko T; Arking DE; Hwang S-J; Guo X; Kutalik Z; Trompet S; Shrine N; Teumer A; Ried JS; Bis JC; Smith AV; Amin N; Nolte IM; Lyytikäinen L-P; Mahajan A; Wareham NJ; Hofer E; Joshi PK; Kristiansson K; Traglia M; Havulinna AS; Goel A; Nalls MA; Sõber S; Vuckovic D; Luan J; Del Greco M. F; Ayers KL; Marrugat J; Ruggiero D; Lopez LM; Niiranen T; Enroth S; Jackson AU; Nelson CP; Huffman JE; Zhang W; Marten J; Gandin I; Harris SE; Zemonik T; Lu Y; Evangelou E; Shah N; de Borst MH; Mangino M; Prins BP; Campbell A; Li-Gao R; Chauhan G; Oldmeadow C; Abecasis G; Abedi M; Barbieri CM; Barnes MR; Batini C; Beilby J; Blake T; Boehnke M; Bottinger EP; Braund PS; Brown M; Brumat M; Campbell H; Chambers JC; Cocca M; Collins F; Connell J; Cordell HJ; Damman JJ; Davies G; de Geus EJ; de Mutsert R; Deelen J; Demirkale Y; Doney ASF; Dörr M; Farrall M; Ferreira T; Frånberg M; Gao H; Giedraitis V; Gieger C; Giulianini F; Gow AJ; Hamsten A; Harris TB; Hofman A; Holliday EG; Hui J; Jarvelin M-R; Johansson Å; Johnson AD; Jousilahti P; Jula A; Kähönen M; Kathiresan S; Khaw K-T; Kolcic I; Koskinen S; Langenberg C; Larson M; Launer LJ; Lehne B; Liewald DCM; Lin L; Lind L; Mach F; Mamasoula C; Menni C; Mifsud B; Milaneschi Y; Morgan A; Morris AD; Morrison AC; Munson PJ; Nandakumar P; Tri Nguyen Q; Nutile T; Oldehinkel AJ; Oostra BA; Org E; Padmanabhan S; Palotie A; Paré G; Pattie A; Penninx BWJH; Poulter N; Pramstaller PP; Raitakari OT; Ren M; Rice K; Ridker PM; Riese H; Ripatti S; Robino A; Rotter JI; Rudan I; Saba Y; Pierre AS; Sala CF; Sarin A-P; Schmidt R; Scott R; Seelen MA; Shields DC; Siscovick D; Sorice R; Stanton A; Stott DJ; Sundström J; Swertz M; Taylor KD; Thom S; Tzoulaki I; Tzourio C; Uitterlinden AG; Vöker U; Vollenweider P; Wild S; Willemsen G; Wright AF; Yao J; Thériault S; Conen D; John A; Sever P; Debette S; Mook-Kanamori DO; Zeggini E; Spector TD; Harst PVD; Palmer CNA; Vergnaud A-C; Loos RJF; Polasek O; Starr JM; Girotto G; Hayward C; Kooner JS; Lindgren CM; Vitart V; Samani NJ; Tuomilehto J; Gyllensten U; Knekt P; Deary IJ; Ciullo M; Elosua R; Keavney BD; Hicks AA; Scott RA; Gasparini P; Laan M; Liu Y; Watkins H; Hartman CA; Salomaa V; Toniolo D; Perola M; Wilson JF; Schmidt H; Zhao JH; Lehtimäki T; van Duijn CM; Gudnason V; Psaty BM; Peters A; Rettig R; James A; Jukema JW; Strachan DP; Palmas W; Metspalu A; Ingelsson E; Boomsma DI; Franco OH; Bochud M; Newton-Cheh C; Munroe PB; Elliott P; Chasman DI; Chakravarti A; Knight J; Morris AP; Levy D; Tobin MD; Snieder H; Caulfield MJ; Ehret GB, Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney, http://dx.doi.org/10.1101/110833
Reay WR; Shair SIE; Geaghan MP; Riveros C; Holliday EG; McEvoy MA; Hancock S; Peel R; Scott RJ; Attia JR; Cairns MJ, Genetically informed precision drug repurposing for lung function and implications for respiratory infection, http://dx.doi.org/10.1101/2020.06.25.20139816
Ruderfer DM; Ripke S; McQuillin A; Boocock J; Stahl EA; Pavlides JMW; Mullins N; Charney AW; Ori APS; Loohuis LMO; Domenici E; Di Florio A; Papiol S; Kalman JL; Adolfsson R; Agartz I; Agerbo E; Akil H; Albani D; Albus M; Alda M; Alexander M; Allardyce J; Alliey-Rodriguez N; Als TD; Amin F; Anjorin A; Arranz MJ; Awasthi S; Bacanu SA; Badner JA; Baekvad-Hansen M; Bakker S; Band G; Barchas JD; Barroso I; Bass N; Bauer M; Baune BT; Begemann M; Bellenguez C; Belliveau RA; Bellivier F; Bender S; Bene J; Bergen SE; Berrettini WH; Bevilacqua E; Biernacka JM; Bigdeli TB; Black DW; Blackburn H; Blackwell JM; Blackwood DHR; Pedersen CB; Boehnke M; Boks M; Borglum AD; Bramon E; Breen G; Brown MA; Bruggeman R; Buccola NG; Buckner RL; Budde M; Bulik-Sullivan B; Bumpstead SJ; Bunney W; Burmeister M; Buxbaum JD; Bybjerg-Grauholm J; Byerley W; Cahn W; Cai G; Cairns MJ; Campion D; Cantor RM; Carr VJ; Carrera N; Casas JP; Casas M; Catts SV; Cervantes P; Chambert KD; Chan RCK; Chen EYH; Chen RYL; Cheng W; Cheung EFC; Chong SA; Clarke T-K; Cloninger CR; Cohen D; Cohen N; Coleman JRI; Collier DA; Cormican P; Coryell W; Craddock N; Craig DW; Crespo-Facorro B; Crowley JJ; Cruceanu C; Curtis D; Czerski PM; Dale AM; Daly MJ; Dannlowski U; Darvasi A; Davidson M; Davis KL; de Leeuw CA; Degenhardt F; Favero JD; DeLisi LE; Deloukas P; Demontis D; DePaulo JR; di Forti M; Dikeos D; Dinan T; Djurovic S; Dobbyn AL; Donnelly P; Donohoe G; Drapeau E; Dronov S; Duan J; Dudbridge F; Duncanson A; Edenberg H; Edkins S; Ehrenreich H; Eichhammer P; Elvsashagen T; Eriksson J; Escott-Price V; Esko T; Essioux L; Etain B; Fan CC; Farh K-H; Farrell MS; Flickinger M; Foroud TM; Forty L; Frank J; Franke L; Fraser C; Freedman R; Freeman C; Freimer NB; Friedman JI; Fromer M; Frye MA; Fullerton JM; Gade K; Garnham J; Gaspar HA; Gejman PV; Genovese G; Georgieva L; Giambartolomei C; Giannoulatou E; Giegling I; Gill M; Gillman M; Pedersen MG; Giusti-Rodriguez P; Godard S; Goes F; Goldstein JI; Gopal S; Gordon SD; Gordon-Smith K; Gratten J; Gray E; Green EK; Green MJ; Greenwood TA; Grigoroiu-Serbanescu M; Grove J; Guan W; Gurling H; Parra JG; Gwilliam R; de Haan L; Hall J; Hall M-H; Hammer C; Hammond N; Hamshere ML; Hansen M; Hansen T; Haroutunian V; Hartmann AM; Hauser J; Hautzinger M; Heilbronner U; Hellenthal G; Henskens FA; Herms S; Hipolito M; Hirschhorn JN; Hoffmann P; Hollegaard MV; Hougaard DM; Huang H; Huckins L; Hultman CM; Hunt SE; Ikeda M; Iwata N; Iyegbe C; Jablensky AV; Jamain S; Jankowski J; Jayakumar A; Joa I; Jones I; Jones LA; Jonsson EG; Julia A; Jureus A; Kahler AK; Kahn RS; Kalaydjieva L; Kandaswamy R; Karachanak-Yankova S; Karjalainen J; Karlsson R; Kavanagh D; Keller MC; Kelly BJ; Kelsoe J; Kennedy JL; Khrunin A; Kim Y; Kirov G; Kittel-Schneider S; Klovins J; Knight J; Knott SV; Knowles JA; Kogevinas M; Konte B; Kravariti E; Kucinskas V; Kucinskiene ZA; Kupka R; Kuzelova-Ptackova H; Landen M; Langford C; Laurent C; Lawrence J; Lawrie S; Lawson WB; Leber M; Leboyer M; Lee PH; Keong JLC; Legge SE; Lencz T; Lerer B; Levinson DF; Levy SE; Lewis CM; Li JZ; Li M; Li QS; Li T; Liang K-Y; Liddle J; Lieberman J; Limborska S; Lin K; Linszen DH; Lissowska J; Liu C; Liu J; Lonnqvist J; Loughland CM; Lubinski J; Lucae S; Macek M; MacIntyre DJ; Magnusson PKE; Maher BS; Mahon PB; Maier W; Malhotra AK; Mallet J; Malt UF; Markus HS; Marsal S; Martin NG; Mata I; Mathew CG; Mattheisen M; Mattingsdal M; Mayoral F; McCann OT; McCarley RW; McCarroll SA; McCarthy MI; McDonald C; McElroy SL; McGuffin P; Mclnnis MG; McIntosh AM; McKay JD; McMahon FJ; Medeiros H; Medland SE; Meier S; Meijer CJ; Melegh B; Melle I; Meng F; Mesholam-Gately RI; Metspalu A; Michie PT; Milani L; Milanova V; Mitchell PB; Mokrab Y; Montgomery GW; Moran JL; Morken G; Morris DW; Mors O; Mortensen PB; Mowry BJ; Mühleisen TW; Müller-Myhsok B; Murphy KC; Murray RM; Myers RM; Myin-Germeys I; Neale BM; Nelis M; Nenadic I; Nertney DA; Nestadt G; Nicodemus KK; Nievergelt CM; Nikitina-Zake L; Nimgaonkar V; Nisenbaum L; Nordentoft M; Nordin A; Nöthen MM; Nwulia EA; O’Callaghan E; O’Donovan C; Colm O; O’Neill FA; Oedegaard KJ; Oh S-Y; Olincy A; Olsen L; Oruc L; Os JV; Owen MJ; Paciga SA; Palmer CNA; Palotie A; Pantelis C; Papadimitriou GN; Parkhomenko E; Pato C; Pato MT; Paunio T; Pearson R; Perkins DO; Perlis RH; Perry A; Pers TH; Petryshen TL; Pfennig A; Picchioni M; Pietilainen O; Pimm J; Pirinen M; Plomin R; Pocklington AJ; Posthuma D; Potash JB; Potter SC; Powell J; Price A; Pulver AE; Purcell SM; Quested D; Ramos-Quiroga JA; Rasmussen HB; Rautanen A; Ravindrarajah R; Regeer EJ; Reichenberg A; Reif A; Reimers MA; Ribases M; Rice JP; Richards AL; Ricketts M; Riley BP; Rivas F; Rivera M; Roffman JL; Rouleau GA; Roussos P; Rujescu D; Salomaa V; Sanchez-Mora C; Sanders AR; Sawcer SJ; Schall U; Schatzberg AF; Scheftner WA; Schofield PR; Schork NJ; Schwab SG; Scolnick EM; Scott LJ; Scott RJ; Seidman LJ; Serretti A; Sham PC; Weickert CS; Shehktman T; Shi J; Shilling PD; Sigurdsson E; Silverman JM; Sim K; Slaney C; Slominsky P; Smeland OB; Smoller JW; So H-C; Sobell JL; Soderman E; Hansen CS; Spencer CCA; Spijker AT; Clair DS; Stefansson H; Stefansson K; Steinberg S; Stogmann E; Stordal E; Strange A; Straub RE; Strauss JS; Streit F; Strengman E; Strohmaier J; Stroup TS; Su Z; Subramaniam M; Suvisaari J; Svrakic DM; Szatkiewicz JP; Szelinger S; Tashakkori-Ghanbaria A; Thirumalai S; Thompson RC; Thorgeirsson TE; Toncheva D; Tooney PA; Tosato S; Toulopoulou T; Trembath RC; Treutlein J; Trubetskoy V; Turecki G; Vaaler AE; Vedder H; Vieta E; Vincent J; Visscher PM; Viswanathan AC; Vukcevic D; Waddington J; Waller M; Walsh D; Walshe M; Walters JTR; Wang D; Wang Q; Wang W; Wang Y; Watson SJ; Webb BT; Weickert TW; Weinberger DR; Weisbrod M; Weiser M; Werge T; Weston P; Whittaker P; Widaa S; Wiersma D; Wildenauer DB; Williams NM; Williams S; Witt SH; Wolen AR; Wong EHM; Wood NW; Wormley BK; Wu JQ; Xi S; Xu W; Young AH; Zai CC; Zandi P; Zhang P; Zheng X; Zimprich F; Zollner S; Corvin A; Fanous AH; Cichon S; Rietschel M; Gershon ES; Schulze TG; Cuellar-Barboza AB; Forstner AJ; Holmans PA; Nurnberger JI; Andreassen OA; Lee SH; O’Donovan MC; Sullivan PF; Ophoff RA; Wray NR; Sklar P; Kendler KS, Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes, http://dx.doi.org/10.1101/173435
Marshall C; Howrigan D; Merico D; Thiruvahindrapuram B; Wu W; Greer D; Antaki D; Shetty A; Holmans P; Pinto D; Gujral M; Brandler W; Malholtra D; Wang Z; Fuentes Fajarado K; Ripke S; Agartz I; Agerbo E; Albus M; Alexander M; Amin F; Atkins J; Bacanu S; Belliveau R; Bergen S; Bertalan M; Bevilacqua E; Bigdeli T; Black D; Bruggeman R; Buccola N; Buckner R; Bulik-Sullivan B; Byerley W; Cahn W; Cai G; Cairns M; Campion D; Cantor R; Carr V; Carrera N; Catts S; Chambert K; Cheng W; Cloninger C; Cohen D; Cormican P; Craddock N; Crespo-Facorro B; Crowley J; Curtis D; Davidson M; Davis K; Degenhardt F; Del Favero J; DeLisi L; Demontis D; Dikeos D; Dinan T; Djurovic S; Donohoe G; Drapeau E; Duan J; Dudbridge F; Eichhammer P; Eriksson J; Escott-Price V; Essioux L; Fanous A; Farh K-H; Farrell M; Frank J; Franke L; Freedman R; Freimer N; Friedman J; Forstner A; Fromer M; Genovese G; Georgieva L; Gershon E; Giegling I; Giusti-Rodriguez P; Godard S; Goldstein J; Gratten J; Haan L; Hamshere M; Hansen M; Hansen T; Haroutunian V; Hartmann A; Henskens F; Herms S; Hirschhorn J; Hoffmann P; Hofman A; Hollegaard M; Hougaard D; Huang H; Ikeda M; Joa I; Kahler A; Kahn R; Kalaydjieva L; Karjalainen J; Kavanagh D; Keller M; Kelly B; Kennedy J; Kim Y; Knowles J; Konte B; Laurent C; Lee P; Lee S; Legge S; Lerer B; Levy D; Liang K-Y; Lieberman J; Lonnqvist J; Loughland C; Magnusson P; Maher B; Maier W; Mallet J; Mattheisen M; Mattingsdal M; McCarley R; McDonald C; McIntosh A; Meier S; Meijer C; Melle I; Mesholam-Gately R; Metspalu A; Michie P; Milani L; Milanova V; Mokrab Y; Morris D; Mors O; Muller-Myhsok B; Murphy K; Murray R; Myin-Germeys I; Nenadic I; Nertney D; Nestadt G; Nicodemus K; Nisenbaum L; Nordin A; O'Callaghan E; O'Dushlaine C; Oh S-Y; Olincy A; Olsen L; O'Neill F; Os J; Pantelis C; Papadimitriou G; Parkhomenko E; Pato M; Paunio T; Perkins D; Pers T; PIetilainen O; Pimm J; Pocklington A; Powell J; Price A; Pulver A; Purcell S; Quested D; Rasmussen H; Reichenberg A; Reimers M; Richards A; Roffman J; Roussos P; Ruderfer D; Salomaa V; Sanders A; Savitz A; Schall U; Schulze T; Schwab S; Scolnick E; Scott R; Seidman L; Shi J; Silverman J; Smoller J; Soderman E; Spencer C; Stahl E; Strengman E; Strohmaier J; Stroup TS; Suvisaari J; Svrakic D; Szatkiewicz J; Thirumalai S; Tooney P; Veijola J; Visscher P; Waddington J; Walsh D; Webb B; Weiser M; Wildenauer D; Williams N; Williams S; Witt S; Wolen A; Wormley B; Wray N; Wu J; Zai C; Adolfsson R; Andreassen O; Blackwood D; Borglum A; Bramon E; Buxbaum J; Cichon S; Collier D; Corvin A; Daly M; Darvasi A; Domenici E; Esko T; Gejman P; Gill M; Gurling H; Hultman C; Iwata N; Jablensky A; Jonsson E; Kendler K; Kirov G; Knight J; Levinson D; Li Q; McCarroll S; McQuillin A; Moran J; Mortensen P; Mowry B; Nothen M; Ophoff R; Owen M; Palotie A; Pato C; Petryshen T; Posthuma D; Rietschel M; Riley B; Rujescu D; Sklar P; St Clair D; Walters J; Werge T; Sullivan P; O'Donovan M; Scherer S; Neale B; Sebat J, A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects, http://dx.doi.org/10.1101/040493
Wang X; Kho PF; Ramachandran D; Bafligil C; Amant F; Goode EL; Scott RJ; Tomlinson I; Evans DG; Crosbie EJ; Dörk T; Spurdle AB; Glubb DM; O’Mara TA, Multi-trait genome-wide association study identifies novel endometrial cancer risk loci that are associated with obesity or female testosterone levels, http://dx.doi.org/10.1101/2021.08.01.21261455
Kho P-F; Partida GC; Dörk T; Goode EL; Lambrechts D; Scott RJ; Spurdle AB; O’Mara TA; Glubb DM, Multi-tissue transcriptome-wide association study identifies genetic mechanisms underlying endometrial cancer susceptibility, http://dx.doi.org/10.1101/2020.12.03.20243758
Kar SP; Lindström S; Hung RJ; Lawrenson K; Schmidt MK; O’Mara TA; Glubb DM; Tyrer JP; Schildkraut JM; Chang-Claude J; Alsulimani AGM; Antón FM; Beeghly-Fadiel A; Bjørge L; Bodelon C; Brauch H; Burghaus S; Campa D; Carney M; Chen C; Chen Z; Daly MB; Bois AD; Ekici AB; Ewing A; Fasching P; Flanagan JM; Gawelko J; Giles GG; Hamilton RJ; Harris HR; Heitz F; Hildebrandt M; Hillemanns P; Huang R-Y; Imaz L; Irmejs A; Jakubowska A; Jensen A; John EM; Kannisto P; Karlan BY; Khusnutdinova E; Kiemeney LA; Kjaer SK; Klapdor R; Kleiblova P; Köbel M; Konopka B; Krakstad C; Lessel D; Lophatananon A; May T; Mieszkowska AD; Monteiro AN; Moysich K; Muir K; Nielsen SF; Odunsi K; Olsson H; Park-Simon T-W; Permuth JB; Peterlongo P; Podgorski A; Prentice R; Radice P; Risch HA; Runnebaum IB; Rzepecka IK; Scott RJ; Setiawan VW; Siddiqui N; Sieh W; Śpiewankiewicz B; Szafron LM; Thompson CL; Titus LJ; Turnbull C; Usmani N; van Altena AM; Vega-Gliemmo A; Vergote I; Vierkant RA; Vijai J; Winham SJ; Winqvist R; Yu H; Lambrechts D; Thompson DJ; Goode EL; Zheng W; Tomlinson IPM; Berchuck A; Ramus SJ; Chanock SJ; Easton DF; Chenevix-Trench G; Gayther SA; Spurdle AB; Eeles RA; Kraft P; Pharoah PDP, Combining genome-wide studies of breast, prostate, ovarian and endometrial cancers maps cross-cancer susceptibility loci and identifies new genetic associations, http://dx.doi.org/10.1101/2020.06.16.146803
Glubb DM; Thompson DJ; Aben KKH; Alsulimani A; Amant F; Annibali D; Attia J; Barricarte A; Beckmann MW; Berchuck A; Bermisheva M; Bernardini MQ; Bischof K; Bjorge L; Bodelon C; Brand AH; Brenton JD; Brinton L; Bruinsma F; Buchanan DD; Burghaus S; Butzow R; Cai H; Carney ME; Chanock SJ; Chen C; Chen XQ; Chen Z; Cook LS; Cunningham JM; Vivo ID; deFazio A; Doherty JA; Dörk T; Bois AD; Dunning AM; Dürst M; Edwards T; Edwards RP; Ekici AB; Ewing A; Fasching PA; Ferguson S; Flanagan JM; Fostira F; Fountzilas G; Friedenreich CM; Gao B; Gaudet MM; Gawełko J; Gentry-Maharaj A; Giles GG; Glasspool R; Goodman MT; Gronwald J; Harris HR; Harter P; Hein A; Heitz F; Hildebrandt MAT; Hillemanns P; Høgdall E; Høgdall CK; Holliday EG; Huntsman DG; Huzarski T; Jakubowska A; Jensen A; Jones ME; Karlan BY; Karnezis A; Kelley JL; Khusnutdinova E; Killeen JL; Kjaer SK; Klapdor R; Köbel M; Konopka B; Konstantopoulou I; Kopperud RK; Koti M; Kraft P; Kupryjanczyk J; Lambrechts D; Larson MC; Marchand LL; Lele SB; Lester J; Li AJ; Liang D; Liebrich C; Lipworth L; Lissowska J; Lu L; Lu KH; Macciotta A; Mattiello A; May T; McAlpine J; McGuire V; McNeish IA; Menon U; Modugno F; Moysich KB; Nevanlinna H; Odunsi K; Olsson H; Orsulic S; Osorio A; Palli D; Park-Simon T-W; Pearce CL; Pejovic T; Permuth JB; Podgorska A; Ramus SJ; Rebbeck TR; Riggan MJ; Risch HA; Rothstein JH; Runnebaum I; Scott RJ; Sellers TA; Senz J; Setiawan VW; Siddiqui N; Sieh W; Spiewankiewicz B; Sutphen R; Swerdlow AJ; Szafron L; Teo SH; Thompson PJ; Thomsen LCV; Titus L; Tone A; Tumino R; Turman C; Vanderstichele A; Edwards DV; Vergote I; Vierkant RA; Wang Z; Wang-Gohrke S; Webb PM; White E; Whittemore AS; Winham SJ; Wu X; Wu AH; Yannoukakos D; Spurdle AB; O’Mara TA, Cross-cancer genome-wide association study of endometrial cancer and epithelial ovarian cancer identifies genetic risk regions associated with risk of both cancers, http://dx.doi.org/10.1101/2020.04.29.20084095
Schmidt AF; Holmes MV; Preiss D; Swerdlow D; Denaxas S; Fatemifar G; Faraway R; Finan C; Lumbers T; Henry A; Valentine D; Fairhurst-Hunter Z; Hartwig FP; Horta BL; Hypponen E; Power C; Moldovan M; van Iperen E; Hovingh K; Demuth I; Norman K; Steinhagen-Thiessen E; Demuth J; Bertram L; Lill CM; Coassin S; Willeit J; Kiechl S; Willeit K; Mason D; Wright J; Morris R; Wanamethee G; Whincup P; Ben-Shlomo Y; McLachlan S; Price JF; Kivimaki M; Welch C; Sanchez-Galvez A; Marques-Vidal P; Nicolaides A; Panayiotou AG; Onland-Moret NC; van der Schouw YT; Matullo G; Fiorito G; Guarrera S; Sacerdote C; Wareham NJ; Langenberg C; Scott RA; Luan J; Bobak M; Malyutina S; Pajak A; Kubinova R; Tamosiunas A; Pikhart H; Grarup N; Pedersen O; Hansen T; Linneberg A; Jess T; Cooper J; Humphries SE; Brilliant M; Kitchner T; Hakonarson H; Carrell DS; McCarty CA; Lester KH; Larson EB; Crosslin DR; Andrade MD; Roden DM; Denny JC; Carty C; Hancock S; Attia J; Holliday E; Scott R; Schofield P; O’Donnell M; Yusuf S; Chong M; Pare G; van der Harst P; Said MA; Eppinga RN; Verweij N; Snieder H; Christen T; Mook-Kanamori DO; Gustafsson S; Lind L; Ingelsson E; Pazoki R; Franco O; Hofman A; Uitterlinden A; Dehghan A; Teumer A; Baumeister S; Dörr M; Lerch MM; Völker U; Völzke H; Ward J; Pell JP; Meade T; Christophersen IE; Maitland-van der Zee AH; Baranova EV; Young R; Ford I; Campbell A; Padmanabhan S; Bots ML; Grobbee DE; Froguel P; Thuillier D; Roussel R; Bonnefond A; Cariou B; Smart M; Bao Y; Kumari M; Mahajan A; Hopewell JC; Seshadri S; Dale C; Costa RPE; Ridker PM; Chasman DI; Reiner AP; Ritchie MD; Lange LA; Cornish AJ; Dobbins SE; Hemminki K; Kinnersley B; Sanson M; Labreche K; Simon M; Bondy M; Law P; Speedy H; Allan J; Li N; Went M; Weinhold N; Morgan G; Sonneveld P; Nilsson B; Goldschmidt H; Hemminki K; Sud A; Engert A; Hansson M; Hemingway H; Asselbergs FW; Patel RS; Keating BJ; Sattar N; Houlston R; Casas JP; Hingorani AD, Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9, http://dx.doi.org/10.1101/329052
Evangelou E; Warren HR; Mosen-Ansorena D; Mifsud B; Pazoki R; Gao H; Ntritsos G; Dimou N; Cabrera CP; Karaman I; Ng FL; Evangelou M; Witkowska K; Tzanis E; Hellwege JN; Giri A; Velez Edwards DR; Sun YV; Cho K; Gaziano JM; Wilson PWF; Tsao PS; Kovesdy CP; Esko T; Mägi R; Milani L; Almgren P; Boutin T; Debette S; Ding J; Giulianini F; Holliday EG; Jackson AU; Li-Gao R; Lin W-Y; Luan J; Mangino M; Oldmeadow C; Prins B; Qian Y; Sargurupremraj M; Shah N; Surendran P; Thériault S; Verweij N; Willems SM; Zhao J-H; Amouyel P; Connell J; de Mutsert R; Doney ASF; Farrall M; Menni C; Morris AD; Noordam R; Paré G; Poulter NR; Shields DC; Stanton A; Thom S; Abecasis G; Amin N; Arking DE; Ayers KL; Barbieri CM; Batini C; Bis JC; Blake T; Bochud M; Boehnke M; Boerwinkle E; Boomsma DI; Bottinger EP; Braund PS; Brumat M; Campbell A; Campbell H; Chakravarti A; Chambers JC; Chauhan G; Ciullo M; Cocca M; Collins F; Cordell HJ; Davies G; de Borst MH; de Geus EJ; Deary IJ; Deelen J; Del Greco FM; Demirkale CY; Dörr M; Ehret GB; Elosua R; Enroth S; Erzurumluoglu AM; Ferreira T; Frånberg M; Franco OH; Gandin I; Gasparini P; Giedraitis V; Gieger C; Girotto G; Goel A; Gow AJ; Gudnason V; Guo X; Gyllensten U; Hamsten A; Harris TB; Harris SE; Hartman CA; Havulinna AS; Hicks AA; Hofer E; Hofman A; Hottenga J-J; Huffman JE; Hwang S-J; Ingelsson E; James A; Jansen R; Jarvelin M-R; Joehanes R; Johansson Å; Johnson AD; Joshi PK; Jousilahti P; Jukema JW; Jula A; Kähönen M; Kathiresan S; Keavney BD; Khaw K-T; Knekt P; Knight J; Kolcic I; Kooner JS; Koskinen S; Kristiansson K; Kutalik Z; Laan M; Larson M; Launer LJ; Lehne BC; Lehtimäki T; Levy D; Liewald DCM; Lin L; Lind L; Lindgren CM; Liu Y; Loos RJF; Lopez LM; Lu L; Lyytikäinen L-P; Mahajan A; Mamasoula C; Marrugat J; Marten J; Milaneschi Y; Morgan A; Morris AP; Morrison AC; Munson PJ; Nalls MA; Nandakumar P; Nelson CP; Newton-Cheh C; Niiranen T; Nolte IM; Nutile T; Oldehinkel AJ; Oostra BA; O'Reilly PF; Org E; Padmanabhan S; Palmas W; Palotie A; Pattie A; Penninx BWJH; Perola M; Peters A; Polasek O; Pramstaller PP; Quang Tri N; Raitakari OT; Ren M; Rettig R; Rice K; Ridker PM; Reid JS; Riese H; Ripatti S; Robino A; Rose LM; Rotter JI; Rudan I; Ruggiero D; Saba Y; Sala CF; Salomaa V; Samani NJ; Sarin A-P; Schmidt R; Schmidt H; Shrine N; Siscovick D; Smith AV; Schneider H; Sõber S; Sorice R; Starr JM; Stott DJ; Strachan DP; Strawbridge RJ; Sundström J; Swertz MA; Taylor KD; Teumer A; Tobin MD; Toniolo D; Traglia M; Trompet S; Tuomilehto J; Tzourio C; Uitterlinden AG; Vaez A; van der Most PJ; van Duijn CM; Vergnaud A-C; Verwoert GC; Vitart V; Völker U; Vollenweider P; Vuckovic D; Watkins H; Wild SH; Willemsen G; Wilson JF; Wright AF; Yao J; Zemunik T; Zhang W; Attia JR; Butterworth AS; Chasman D; Conen D; Cucca F; Danesh J; Hayward C; Howson JMM; Laakso M; Lakatta EG; Langenberg C; Melander O; Mook-Kanamori DO; Munroe PB; Palmer CNA; Risch L; Scott RA; Scott RJ; Sever P; Spector TD; van der Harst P; Wareham NJ; Zeggini E; Brown MJ; Metspalu A; Hung AM; O'Donnell CJ; Edwards TL; Psaty BM; Tzoulaki I; Barnes MR; Wain LV; Elliott P; Caulfield MJ, Genetic analysis of over one million people identifies 535 novel loci for blood pressure, http://dx.doi.org/10.1101/198234
Okbay A; Baselmans BML; De Neve J-E; Turley P; Nivard MG; Fontana MA; Meddens FSW; Linnér RK; Rietveld CA; Derringer J; Gratten J; Lee JJ; Liu JZ; de Vlaming R; Conley DC; Smith GD; Hofman A; Johannesson M; Laibson DI; Medland SE; Meyer MN; Pickrell JK; Esko T; Krueger RF; Beauchamp JP; Koellinger PD; Benjamin DJ; Bartels M; Cesarini D, Genetic Associations with Subjective Well-Being Also Implicate Depression and Neuroticism, http://dx.doi.org/10.1101/032789
Fachal L; Aschard H; Beesley J; Barnes DR; Allen J; Kar S; Pooley KA; Dennis J; Michailidou K; Turman C; Soucy P; Lemaçon A; Lush M; Tyrer JP; Ghoussaini M; Marjaneh MM; Jiang X; Agata S; Aittomäki K; Alonso MR; Andrulis IL; Anton-Culver H; Antonenkova NN; Arason A; Arndt V; Aronson KJ; Arun BK; Auber B; Auer PL; Azzollini J; Balmaña J; Barkardottir RB; Barrowdale D; Beeghly-Fadiel A; Benitez J; Bermisheva M; Bialkowska K; Blanco AM; Blomqvist C; Blot W; Bogdanova NV; Bojesen SE; Bolla MK; Bonanni B; Borg A; Bosse K; Brauch H; Brenner H; Briceno I; Brock IW; Brooks-Wilson A; Brüning T; Burwinkel B; Buys SS; Cai Q; Caldés T; Caligo MA; Camp NJ; Campbell I; Canzian F; Carroll JS; Carter BD; Castelao JE; Chiquette J; Christiansen H; Chung WK; Claes KBM; Clarke CL; Collaborators GEMOS; Collaborators EMBRACE; Collée JM; Cornelissen S; Couch FJ; Cox A; Cross SS; Cybulski C; Czene K; Daly MB; la Hoya MD; Devilee P; Diez O; Ding YC; Dite GS; Domchek SM; Dörk T; dos-Santos-Silva I; Droit A; Dubois S; Dumont M; Duran M; Durcan L; Dwek M; Eccles DM; Engel C; Eriksson M; Evans DG; Fasching PA; Fletcher O; Floris G; Flyger H; Foretova L; Foulkes WD; Friedman E; Fritschi L; Frost D; Gabrielson M; Gago-Dominguez M; Gambino G; Ganz PA; Gapstur SM; Garber J; García-Sáenz JA; Gaudet MM; Georgoulias V; Giles GG; Glendon G; Godwin AK; Goldberg MS; Goldgar DE; González-Neira A; Greene MH; Grip M; Gronwald J; Grundy A; Guénel P; Hahnen E; Haiman CA; Håkansson N; Hall P; Hamann U; Harrington PA; Hartikainen JM; Hartman M; He W; Healey CS; Heemskerk-Gerritsen BAM; Heyworth J; Hillemanns P; Hogervorst FBL; Hollestelle A; Hooning MJ; Hopper JL; Howell A; Huang G; Hulick PJ; Imyanitov EN; Isaacs C; Iwasaki M; Jager A; Jakimovska M; Jakubowska A; James P; Janavicius R; Jankowitz RC; John EM; Johnson N; Jones ME; Jukkola-Vuorinen A; Jung A; Kaaks R; Kang D; Karlan BY; Keeman R; Kerin MJ; Khusnutdinova E; Kiiski JI; Kirk J; Kitahara CM; Ko Y-D; Konstantopoulou I; Kosma V-M; Koutros S; Kubelka-Sabit K; Kwong A; Kyriacou K; Laitman Y; Lambrechts D; Lee E; Leslie G; Lester J; Lesueur F; Lindblom A; Lo W-Y; Long J; Lophatananon A; Loud JT; Lubinski J; MacInnis RJ; Maishman T; Makalic E; Mannermaa A; Manoochehri M; Manoukian S; Margolin S; Martinez ME; Matsuo K; Maurer T; Mavroudis D; Mayes R; McGuffog L; McLean C; Mebirouk N; Meindl A; Middha P; Miller N; Miller A; Montagna M; Moreno F; Mulligan AM; Muñoz-Garzon VM; Muranen TA; Narod SA; Nassir R; Nathanson KL; Neuhausen SL; Nevanlinna H; Neven P; Nielsen FC; Nikitina-Zake L; Norman A; Offit K; Olah E; Olopade OI; Olsson H; Orr N; Osorio A; Pankratz VS; Papp J; Park SK; Park-Simon T-W; Parsons MT; Paul J; Pedersen IS; Peissel B; Peshkin B; Peterlongo P; Peto J; Plaseska-Karanfilska D; Prajzendanz K; Prentice R; Presneau N; Prokofyeva D; Pujana MA; Pylkäs K; Radice P; Ramus SJ; Rantala J; Rau-Murthy R; Rennert G; Risch HA; Robson M; Romero A; Rossing CM; Saloustros E; Sánchez-Herrero E; Sandler DP; Santamariña M; Saunders C; Sawyer EJ; Scheuner MT; Schmidt DF; Schmutzler RK; Schneeweiss A; Schoemaker MJ; Schöttker B; Schürmann P; Scott C; Scott RJ; Senter L; Seynaeve CMD; Shah M; Sharma P; Shen C-Y; Shu X-O; Singer CF; Slavin TP; Smichkoska S; Southey MC; Spinelli JJ; Spurdle AB; Stone J; Stoppa-Lyonnet D; Sutter C; Swerdlow AJ; Tamimi RM; Tan YY; Tapper WJ; Taylor JA; Teixeira MR; Tengström M; Teo SH; Terry MB; Teulé A; Thomassen M; Thull DL; Tibiletti MG; Tischkowitz M; Toland AE; Tollenaar RAEM; Tomlinson I; Torres D; Torres-Mejía G; Troester MA; Tung N; Tzardi M; Ulmer H-U; Vachon CM; van Asperen CJ; der Kolk LEV; van Rensburg EJ; Vega A; Viel A; Vijai J; Vogel MJ; Wang Q; Wappenschmidt B; Weinberg CR; Weitzel JN; Wendt C; Wildiers H; Winqvist R; Wolk A; Wu AH; Yannoukakos D; Zhang Y; Zheng W; Pharoah PDP; Chang-Claude J; García-Closas M; Schmidt MK; Milne RL; Kristensen VN; French JD; Edwards SL; Antoniou AC; Chenevix-Trench G; Simard J; Easton DF; Kraft P; Dunning AM, Fine-mapping of 150 breast cancer risk regions identifies 178 high confidence target genes, http://dx.doi.org/10.1101/521054
Book Chapters
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Gould T; Fairuz B. Jamaluddin M; Petit J; J. King S; Nixon B; Scott R; Pockney P; D. Dun M, 2019, 'Finding Needles in Haystacks: The Use of Quantitative Proteomics for the Early Detection of Colorectal Cancer', in Advances in the Molecular Understanding of Colorectal Cancer, IntechOpen, http://dx.doi.org/10.5772/intechopen.80942
2019
Scott R, 2018, 'Desired Outcomes of Group Model Building', in Group Model Building Using Systems Dynamics to Achieve Enduring Agreement, Springer, pp. 5 - 18
2018
Scott R, 2018, 'Introduction', in Group Model Building Using Systems Dynamics to Achieve Enduring Agreement, Springer, pp. 1 - 4
2018
Scott R, 2018, 'Basic Elements of Group Model Building', in Group Model Building Using Systems Dynamics to Achieve Enduring Agreement, Springer, pp. 19 - 28
2018
Scott R, 2018, 'Outcomes of Group Model Building', in Group Model Building Using Systems Dynamics to Achieve Enduring Agreement, Springer, pp. 29 - 44
2018
Scott R, 2018, 'Communication Quality, Insight, Consensus and Commitment to Conclusions', in Group Model Building Using Systems Dynamics to Achieve Enduring Agreement, Springer, pp. 45 - 54
2018
Scott R, 2018, 'Mental Model Alignment', in Group Model Building Using Systems Dynamics to Achieve Enduring Agreement, Springer, pp. 55 - 68
2018
Scott R, 2018, 'Explanatory Mechanisms for Group Model Building', in Group Model Building Using Systems Dynamics to Achieve Enduring Agreement, Springer, pp. 69 - 86
2018
Scott R, 2018, 'Comparing Participant Support for Different Explanatory Mechanisms', in Group Model Building Using Systems Dynamics to Achieve Enduring Agreement, Springer, pp. 87 - 98
2018
Scott R, 2018, 'Building Integrated Theory', in Group Model Building Using Systems Dynamics to Achieve Enduring Agreement, Springer, pp. 99 - 113
2018
Scott R, 2018, 'Discussion', in Group Model Building Using Systems Dynamics to Achieve Enduring Agreement, Springer, pp. 115 - 119
2018
Win AK; Scott RJ, 2018, 'Genetic and Environmental Modifiers of Cancer Risk in Lynch Syndrome', in Hereditary Colorectal Cancer, Springer International Publishing, pp. 67 - 89, http://dx.doi.org/10.1007/978-3-319-74259-5_5
2018
Scott R; Cavana RY; Cameron D, 2017, 'Interpersonal Success Factors for Strategy Implementation: A Case Study Using Group Model Building', in System Dynamics Soft and Hard Operational Research, Springer, pp. 133 - 162
2017
Scott RJ; Boyd R, 2016, 'Results, Targets and Measures to Drive Collaboration: Lessons from the New Zealand Better Public Services reforms', in The Three Sector Solution Delivering public policy in collaboration with not-for-profits and business, ANU Press, pp. 235 - 257
2016
Riveros C; Vimieiro R; Holliday EG; Oldmeadow C; Wang JJ; Mitchell P; Attia J; Scott RJ; Moscato PA, 2015, 'Identification of genome-wide SNP-SNP and SNP-clinical Boolean interactions in age-related macular degeneration.', in , pp. 217 - 255, http://dx.doi.org/10.1007/978-1-4939-2155-3_12
2015
Jaworska-Bieniek K; Lener M; Muszynska M; Serrano-Fernández P; Sukiennicki G; Durda K; Gromowski T; Gupta S; Kladny J; Wiechowska-Kozlowska A; Grodzki T; Jaworowska E; Lubinski J; Górecka-Szyld B; Wilk G; Huzarski T; Byrski T; Cybulski C; Gronwald J; Debniak T; Ashuryk O; Toloczko-Grabarek A; Morawski A; Scott RJ; Jakubowska A; Lubinski J, 2015, 'CHAPTER 22. Selenium and Cancer', in Food and Nutritional Components in Focus, Royal Society of Chemistry, pp. 377 - 390, http://dx.doi.org/10.1039/9781782622215-00377
2015
Wong‐Brown MW; Scott RJ, 2014, 'Genetic Susceptibility to Triple‐Negative Breast Cancers', in , Wiley, http://dx.doi.org/10.1002/9780470015902.a0025352
2014
J. R; Reeves S; Talseth-Palmer B, 2012, 'The Role of Modifier Genes in Lynch Syndrome', in Colorectal Cancer Biology - From Genes to Tumor, InTech, http://dx.doi.org/10.5772/28021
2012
Scott RJ; Lubinski J, 2009, 'Genetic epidemiology studies in hereditary non-polyposis colorectal cancer.', in , pp. 89 - 102, http://dx.doi.org/10.1007/978-1-60327-492-0_4
2009
Mendes A; Scott RJ; Moscato P, 2008, 'Microarrays--identifying molecular portraits for prostate tumors with different Gleason patterns.', in , pp. 131 - 151, http://dx.doi.org/10.1007/978-1-60327-148-6_8
2008
Scott RJ; Sobol HH, 1999, 'Prognostic implications of cancer susceptibility genes: any news?', in , pp. 71 - 84, http://dx.doi.org/10.1007/978-3-642-59945-3_5
1999
Scott RJ; Spycher M; Weber W; Müller H, 1992, 'Familial Adenomatous Polyposis: Current Status in Switzerland', in Familial Cancer Control, Springer Berlin Heidelberg, pp. 13 - 15, http://dx.doi.org/10.1007/978-3-642-77582-6_4
1992
Conference Abstracts
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Scott RJ; Wong-Brown M; McPhillips M; Dooley S; Spigelman A; Gleeson M; Meldrum C, 2015, 'The curious case of a woman with two BRCA1 mutations in trans', in Hereditary Cancer in Clinical Practice, Springer Science and Business Media LLC, Vol. 13, http://dx.doi.org/10.1186/1897-4287-13-s2-a11
2015
Mather KA; Thalamuthu A; Oldmeadow C; Song F; Armstrong NJ; Poljak A; Holliday L; McEvoy M; Kwok J; Assareh A; Reppermund S; Ames D; Wright M; Trollor JN; Schofield PW; Brodaty H; Scott RJ; Schofield PR; Attia JR; Sachdev PS, 2014, 'Genome-wide significant results identified for plasma apolipoprotein H levels [Abstract P4-012]', in Alzheimer's & Dementia, Alzheimer's Association International Conference (AAIC) 2014, Copenhagen, Denmark, Vol. 10, pp. P788 - P788, presented at Alzheimer's Association International Conference (AAIC) 2014, Copenhagen, Denmark, 12 July 2014 - 17 July 2014, http://dx.doi.org/10.1016/j.jalz.2014.05.1526
2014
Chouraki VA; Jakobsdottir J; Mather K; Adams H; Mollon J; Oldmeadow C; Thalamuthu A; Tanaka T; Scott R; Levy D; Holliday L; Song F; Thambisetty M; Poljak A; Eiriksdottir G; Sachdev PS; Gupta VB; Martins R; Launer L; Dobson R; Brodaty H; Attia J; Lovestone S; Gudnason V; Ikram M; Seshadri S, 2014, 'A genome-wide meta-analysis of plasma clusterin levels in the CHARGE consortium [Abstract P3-071]', in Alzheimer's & Dementia, Alzheimer’s Association International Conference (AAIC) 2014, Copenhagen, Denmark, Vol. 10, pp. P652 - P653, presented at Alzheimer’s Association International Conference (AAIC) 2014, Copenhagen, Denmark, 12 July 2014 - 17 July 2014, http://dx.doi.org/10.1016/j.jalz.2014.05.1159
2014
Conference Papers
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Pariyar M; Mathe A; Scott R; Avery-Kiejda K, 2020, 'Abstract P6-10-26: Identification of copy number variation associated with lymph node metastasis in triple negative breast cancer', in Poster Session Abstracts, American Association for Cancer Research, presented at Abstracts: 2019 San Antonio Breast Cancer Symposium; December 10-14, 2019; San Antonio, Texas, http://dx.doi.org/10.1158/1538-7445.sabcs19-p6-10-26
2020
O'Mara TA; Glubb DM; Buchanan DD; Lambrechts D; Hall P; Tham E; Trovik J; Goode EL; Fasching P; Dörk T; Scott RJ; Auer PL; Milne RL; Giles GG; Perry J; Vivo ID; Tomlinson I; Easton DF; Thompson DJ; Spurdle AB, 2018, 'Abstract 230: Joint genome-wide association study of endometrial cancer and ovarian cancer identifies a novel genetic risk region at 14q23.3', in Epidemiology, American Association for Cancer Research, presented at Proceedings: AACR Annual Meeting 2018; April 14-18, 2018; Chicago, IL, http://dx.doi.org/10.1158/1538-7445.am2018-230
2018
Berry N; Scott RJ; Sutton R; Trahair TN; Rowlings P; Enjeti AK, 2018, '16. Australian AIEOP-BFM 2009 acute lymphoblastic leukaemia high-risk findings – Enrichment of IKZF1 deletions and other curious findings', in Cancer Genetics, Elsevier BV, pp. 41 - 42, http://dx.doi.org/10.1016/j.cancergen.2018.04.077
2018
Campbell IG; Li N; Rowley S; Goode D; Devereux L; McInerny S; Grewal N; Lee A; Trainer A; Wong-Brown M; Scott R; Gorringe K; James P, 2018, 'Abstract PD1-04: The contribution of rare variants, polygenic risk, and novel candidate genes to the hereditary risk of breast cancer in a large cohort of breast cancer families', in Poster Discussion Abstracts, American Association for Cancer Research, presented at Abstracts: 2017 San Antonio Breast Cancer Symposium; December 5-9, 2017; San Antonio, Texas, http://dx.doi.org/10.1158/1538-7445.sabcs17-pd1-04
2018
Berry N; Scott R; Sutton R; Trahair T; Rowlings P; Enjeti A, 2017, 'HD-SNP Microarray Analysis of the Study 9 High Risk ALL Patients—Increased Yield of Important Prognostic Information', in Cancer Genetics, Elsevier BV, pp. 42 - 43, http://dx.doi.org/10.1016/j.cancergen.2017.04.034
2017
Scott RJ, 2016, 'Do capability reviews improve agency performance? A quantitative summative assessment of the New Zealand Performance Improvement Framework', in Public Management Research Conference, Public Management Research Conference, Aarhus, presented at Public Management Research Conference, Aarhus, 22 June 2016 - 24 June 2016
2016
Scott RJ; Boyd R, 2016, 'Collaborating for results in New Zealand: Evaluation using mixed methods and triangulation.', in Collaborating for results in New Zealand: Evaluation using mixed methods and triangulation., International Public Management Network, St Gallen Switzerland, presented at International Public Management Network, St Gallen Switzerland, 01 June 2016 - 03 June 2016
2016
Campbell IG; Thompson ER; Rowely SM; Li N; McInerny S; Devereux L; Wong-Brown MW; Trainer AH; Mitchell G; Scott RJ; James PA, 2016, 'Abstract P2-09-02: Panel testing for familial breast cancer: Tension at the boundary of research and clinical care', in Poster Session Abstracts, American Association for Cancer Research, presented at Abstracts: Thirty-Eighth Annual CTRC-AACR San Antonio Breast Cancer Symposium; December 8-12, 2015; San Antonio, TX, http://dx.doi.org/10.1158/1538-7445.sabcs15-p2-09-02
2016
Vitalis H; Scott RJ, 2015, 'Joint ventures in the public sector: Translating lessons from the private sector to New Zealand government departments', in Joint ventures in the public sector: Translating lessons from the private sector to New Zealand government departments, Australia and New Zealand Academy of Management, Queenstown, New Zealand, presented at Australia and New Zealand Academy of Management, Queenstown, New Zealand, 01 December 2015 - 04 December 2015, http://dx.doi.org/10.13140/RG.2.1.3836.2645
2015
Scott RJ; Boyd R, 2015, 'The New Zealand Better Public Services Results: a comparative analysis linking inter-agency collaboration with outcome performance', in The New Zealand Better Public Services Results: a comparative analysis linking inter-agency collaboration with outcome performance, Australia and New Zealand Academy of Management, Queenstown, New Zealand, presented at Australia and New Zealand Academy of Management, Queenstown, New Zealand, 01 December 2015 - 04 December 2015, http://dx.doi.org/10.13140/RG.2.1.4884.8401
2015
Scott RJ; Cavana RY; Cameron D, 2014, 'Group model building - do clients value reported outcomes?', in Group model building - do clients value reported outcomes?, International System Dynamics Society, Delft, Netherlands, presented at International System Dynamics Society, Delft, Netherlands, 16 July 2014 - 19 July 2014, http://www.systemdynamics.org/conferences/2014/proceed/papers/P1017.pdf
2014
Cavana RY; Smith T; Scott RJ; O'Connor S, 2014, 'Causal mapping of the New Zealand natural resources sector: a group model building approach.', in Causal mapping of the New Zealand natural resources sector: a group model building approach., International System Dynamics Society, Delft, Netherlands, presented at International System Dynamics Society, Delft, Netherlands, 16 July 2014 - 19 July 2014, http://www.systemdynamics.org/conferences/2014/proceed/papers/P1412.pdf
2014
Scott RJ, 2013, 'Evaluating long-term impact of qualitative system dynamics workshops on participant mental models', in Evaluating long-term impact of qualitative system dynamics workshops on participant mental models, International System Dynamics Society, Boston, USA, presented at International System Dynamics Society, Boston, USA, 17 July 2013 - 21 July 2013, http://www.systemdynamics.org/conferences/2013/proceed/papers/P1084.pdf
2013
Scott RJ; Cavana RY; Cameron D, 2013, 'Mechanisms for understanding mental model change in group model building', in 57th Annual Meeting of the International Society for the Systems Sciences, ISSS 2013: Curating the Conditions for a Thrivable Planet, Hai Phong Vietnam, pp. 301 - 319, presented at International Society for Systems Sciences, Hai Phong Vietnam, 16 July 2013 - 20 July 2013, http://journals.isss.org/index.php/proceedings57th/article/viewFile/2056/711
2013
Grice DM; Bauer DC; Duesing K; Li D; Greenfield P; Nielsen S; Draganic B; Smith S; Pockney P; Scott R; Hannan GN, 2013, 'Abstract LB-237: Human and microbial transcriptomics from lean and obese individuals with colorectal cancer: A comparison of Total and Poly A RNA sequencing from clinical samples.', in Molecular and Cellular Biology, American Association for Cancer Research, presented at Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC, http://dx.doi.org/10.1158/1538-7445.am2013-lb-237
2013
Scott RJ; Wong-Brown M; Meldrum CJ; Avery-Kiejda K, 2013, 'Abstract P2-07-05: Prevalence of germline BRCA1 and BRCA2 mutations in triple-negative breast cancer patients unselected for family history', in Poster Session Abstracts, American Association for Cancer Research, presented at Abstracts: Thirty-Sixth Annual CTRC-AACR San Antonio Breast Cancer Symposium - Dec 10-14, 2013; San Antonio, TX, http://dx.doi.org/10.1158/0008-5472.sabcs13-p2-07-05
2013
Scott RJ; Cavana RY; Cameron D, 2012, 'Improving consensus and commitment to strategy implementation: evaluating systems thinking workshops', in Improving consensus and commitment to strategy implementation: evaluating systems thinking workshops, Australia and New Zealand Academy of Management, Perth, Australia, presented at Australia and New Zealand Academy of Management, Perth, Australia, 01 December 2012 - 04 December 2012, http://www.anzam.org/wp-content/uploads/pdf-manager/289_ANZAM-2012-205.PDF
2012
Scott RJ; Cavana RY; Cameron D; Maani KE, 2012, 'Evaluation of group model building in a strategy implementation context: a New Zealand government case study', in Evaluation of group model building in a strategy implementation context: a New Zealand government case study, International System Dynamics Conference., St Gallen, Switzerland, presented at International System Dynamics Conference., St Gallen, Switzerland, 17 July 2012 - 21 July 2012, http://www.systemdynamics.org/conferences/2012/proceed/papers/P1464.pdf
2012
Scott RJ; Cavana RY; Cameron D, 2012, 'Evaluating the impact of systems thinking workshops on strategy implementation in a government department', in Evaluating the impact of systems thinking workshops on strategy implementation in a government department, Operational Research Society New Zealand, Wellington, New Zealand, pp. 337 - 337, presented at 46th ORSNZ Annual Conference, Wellington, New Zealand, 10 December 2012 - 11 December 2012
2012
Baines KJ; Simpson JL; Scott RJ; Wood LG; Gibson P, 2010, 'Molecular Phenotypes Of Asthma Defined By Gene Expression Profiling', in C93. MOLECULAR AND CLINICAL PHENOTYPING OF ASTHMA, American Thoracic Society, presented at American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans, http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a5097
2010
Henskens F; Carr V; Catts S; Jablensky A; Michie P; Loughland C; McCabe K; Mowry B; Nasir A; Pantelis C; Rasser P; Paul D; Richards J; Schall U; Scott R, 2010, 'THE AUSTRALIAN SCHIZOPHRENIA RESEARCH BANK (ASRB): AN EXAMPLE OF ERESEARCH', in SCHIZOPHRENIA RESEARCH, ELSEVIER SCIENCE BV, Florence, ITALY, pp. 427 - 428, presented at 2nd Conference of the Schizophrenia-International-Research-Society (SIRS), Florence, ITALY, 10 April 2010 - 14 April 2010, http://dx.doi.org/10.1016/j.schres.2010.02.788
2010
Ashton KA; Bowden NA; Kairupan CF; Avery-Kiejda KA; Zhang XD; Hersey P; Scott RJ, 2010, 'Abstract 3944: Base excision repair and gene expression profiling in malignant melanoma', in Cellular and Molecular Biology, American Association for Cancer Research, presented at Proceedings: AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010; Washington, DC, http://dx.doi.org/10.1158/1538-7445.am10-3944
2010
Bowden NA; Ashton KA; Avery-Kiejda KA; Zhang XD; Hersey P; Scott RJ, 2010, 'Abstract 3938: Altered nucleotide excision repair gene expression after cisplatin treatment in melanoma', in Cellular and Molecular Biology, American Association for Cancer Research, presented at Proceedings: AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010; Washington, DC, http://dx.doi.org/10.1158/1538-7445.am10-3938
2010
Talseth-Palmer BA; Brenne IS; Ashton K; Evans TJ; McPhillips M; Groombridge C; Kurzawski G; Spigelman A; Lubinski J; Scott RJ, 2010, 'Colorectal cancer susceptibility loci on chr 8q23.3 and 11q23.1 as modifiers for disease expression in Lynch syndrome', in EJC SUPPLEMENTS, PERGAMON-ELSEVIER SCIENCE LTD, Oslo, NORWAY, pp. 22 - 22, presented at 21st Meeting of the European-Association-for-Cancer-Research, Oslo, NORWAY, 26 June 2010 - 29 June 2010, http://dx.doi.org/10.1016/S1359-6349(10)70892-2
2010
Conference Presentations
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Scott RJ; Boyd R, 2016, 'Case studies in collaborating for better public services', presented at Australia Political Science Association, Sydney, 26 September 2016 - 28 September 2016
2016
Grube D; Scott RJ; Corbett J; Lovell H; Butler T, 2016, 'Institutional Memory and Collaborative Governance – Is it Possible to Have Both?', presented at Australian Political Science Association, Sydney, 26 September 2016 - 28 September 2016
2016
Scott RJ, 2016, 'Assessing the performance of agency chief executives', presented at Australian Political Science Association, Sydney, 26 September 2016 - 28 September 2016
2016
Journal articles
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Ip E; McNeil C; Grimison P; Scheinberg T; Tudini E; Ho G; Scott RJ; Brown C; Sandroussi C; Guitera P; Spurdle AB; Goodwin A, 2021, 'Catastrophic chemotherapy toxicity leading to diagnosis of Fanconi anaemia due to FANCD1/BRCA2 during adulthood: description of an emerging phenotype.', J Med Genet, http://dx.doi.org/10.1136/jmedgenet-2021-108072
2021
Ni G; Zeng J; Revez JA; Wang Y; Zheng Z; Ge T; Restuadi R; Kiewa J; Nyholt DR; Coleman JRI; Smoller JW; Schizophrenia Working Group of the Psychiatric Genomics Consortium ; Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium ; Yang J; Visscher PM; Wray NR, 2021, 'A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts.', Biol Psychiatry, vol. 90, pp. 611 - 620, http://dx.doi.org/10.1016/j.biopsych.2021.04.018
2021
Griffin C; Vilain R; King S; Nixon S; Gooley A; Bray S; Lynam J; Walker MM; Scott RJ; Paul C, 2021, 'Mind Over Matter: Confronting Challenges in Post-Mortem Brain Biobanking for Glioblastoma Multiforme', Biomarker Insights, vol. 16, pp. 117727192110133 - 117727192110133, http://dx.doi.org/10.1177/11772719211013359
2021
Kho PF; Wang X; Cuéllar-Partida G; Dörk T; Goode EL; Lambrechts D; Scott RJ; Spurdle AB; O'Mara TA; Glubb DM, 2021, 'Multi-tissue transcriptome-wide association study identifies eight candidate genes and tissue-specific gene expression underlying endometrial cancer susceptibility.', Commun Biol, vol. 4, pp. 1211, http://dx.doi.org/10.1038/s42003-021-02745-3
2021
Connor T; McPhillips M; Hipwell M; Ziolkowski A; Oldmeadow C; Clapham M; Pockney PG; Lis E; Banasiewicz T; Pławski A; Scott RJ, 2021, 'CD36 polymorphisms and the age of disease onset in patients with pathogenic variants within the mutation cluster region of APC.', Hered Cancer Clin Pract, vol. 19, pp. 25, http://dx.doi.org/10.1186/s13053-021-00183-0
2021
Scott RJ; Mehta A; Macedo GS; Borisov PS; Kanesvaran R; El Metnawy W, 2021, 'Genetic testing for homologous recombination repair (HRR) in metastatic castration-resistant prostate cancer (mCRPC): challenges and solutions.', Oncotarget, vol. 12, pp. 1600 - 1614, http://dx.doi.org/10.18632/oncotarget.28015
2021
Lubiński J; Jaworowska E; Derkacz R; Marciniak W; Białkowska K; Baszuk P; Scott RJ; Lubiński JA, 2021, 'Survival of Laryngeal Cancer Patients Depending on Zinc Serum Level and Oxidative Stress Genotypes.', Biomolecules, vol. 11, pp. 865 - 865, http://dx.doi.org/10.3390/biom11060865
2021
Reay WR; El Shair SI; Geaghan MP; Riveros C; Holliday EG; McEvoy MA; Hancock S; Peel R; Scott RJ; Attia JR; Cairns MJ, 2021, 'Genetic association and causal inference converge on hyperglycaemia as a modifiable factor to improve lung function.', Elife, vol. 10, http://dx.doi.org/10.7554/eLife.63115
2021
Li N; Zethoven M; McInerny S; Devereux L; Huang Y-K; Thio N; Cheasley D; Gutiérrez-Enríquez S; Moles-Fernández A; Diez O; Nguyen-Dumont T; Southey MC; Hopper JL; Simard J; Dumont M; Soucy P; Meindl A; Schmutzler R; Schmidt MK; Adank MA; Andrulis IL; Hahnen E; Engel C; Lesueur F; Girard E; Neuhausen SL; Ziv E; Allen J; Easton DF; Scott RJ; Gorringe KL; James PA; Campbell IG, 2021, 'Evaluation of the association of heterozygous germline variants in NTHL1 with breast cancer predisposition: an international multi-center study of 47,180 subjects.', NPJ Breast Cancer, vol. 7, pp. 52, http://dx.doi.org/10.1038/s41523-021-00255-3
2021
Wiik MU; Evans T-J; Belhadj S; Bolton KA; Dymerska D; Jagmohan-Changur S; Capellá G; Kurzawski G; Wijnen JT; Valle L; Vasen HFA; Lubinski J; Scott RJ; Talseth-Palmer BA, 2021, 'A genetic variant in telomerase reverse transcriptase (TERT) modifies cancer risk in Lynch syndrome patients harbouring pathogenic MSH2 variants.', Sci Rep, vol. 11, pp. 11401, http://dx.doi.org/10.1038/s41598-021-90501-2
2021
Li N; Lim BWX; Thompson ER; McInerny S; Zethoven M; Cheasley D; Rowley SM; Wong-Brown MW; Devereux L; Gorringe KL; Sloan EK; Trainer A; Scott RJ; James PA; Campbell IG, 2021, 'Investigation of monogenic causes of familial breast cancer: data from the BEACCON case-control study.', NPJ Breast Cancer, vol. 7, pp. 76, http://dx.doi.org/10.1038/s41523-021-00279-9
2021
Lener MR; Reszka E; Marciniak W; Lesicka M; Baszuk P; Jabłońska E; Białkowska K; Muszyńska M; Pietrzak S; Derkacz R; Grodzki T; Wójcik J; Wojtyś M; Dębniak T; Cybulski C; Gronwald J; Kubisa B; Pieróg J; Waloszczyk P; Scott RJ; Jakubowska A; Narod SA; Lubiński J, 2021, 'Blood cadmium levels as a marker for early lung cancer detection.', J Trace Elem Med Biol, vol. 64, pp. 126682, http://dx.doi.org/10.1016/j.jtemb.2020.126682
2021
Billings R; Ashton KA; Tucker K; Ziolkowski A; McPhillips M; Hipwell M; Scott RJ, 2021, 'CTNNB1 exon 3 mutations in desmoid and other tumours', Pathology, vol. 53, pp. S41 - S41, http://dx.doi.org/10.1016/j.pathol.2021.06.080
2021
Mullins N; Forstner AJ; O’Connell KS; Coombes B; Coleman JRI; Qiao Z; Als TD; Bigdeli TB; Børte S; Bryois J; Charney AW; Drange OK; Gandal MJ; Hagenaars SP; Ikeda M; Kamitaki N; Kim M; Krebs K; Panagiotaropoulou G; Schilder BM; Sloofman LG; Steinberg S; Trubetskoy V; Winsvold BS; Won HH; Abramova L; Adorjan K; Agerbo E; Al Eissa M; Albani D; Alliey-Rodriguez N; Anjorin A; Antilla V; Antoniou A; Awasthi S; Baek JH; Bækvad-Hansen M; Bass N; Bauer M; Beins EC; Bergen SE; Birner A; Bøcker Pedersen C; Bøen E; Boks MP; Bosch R; Brum M; Brumpton BM; Brunkhorst-Kanaan N; Budde M; Bybjerg-Grauholm J; Byerley W; Cairns M; Casas M; Cervantes P; Clarke TK; Cruceanu C; Cuellar-Barboza A; Cunningham J; Curtis D; Czerski PM; Dale AM; Dalkner N; David FS; Degenhardt F; Djurovic S; Dobbyn AL; Douzenis A; Elvsåshagen T; Escott-Price V; Ferrier IN; Fiorentino A; Foroud TM; Forty L; Frank J; Frei O; Freimer NB; Frisén L; Gade K; Garnham J; Gelernter J; Giørtz Pedersen M; Gizer IR; Gordon SD; Gordon-Smith K; Greenwood TA; Grove J; Guzman-Parra J; Ha K; Haraldsson M; Hautzinger M; Heilbronner U; Hellgren D; Herms S; Hoffmann P; Holmans PA; Huckins L; Jamain S; Johnson JS; Kalman JL, 2021, 'Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology', Nature Genetics, vol. 53, pp. 817 - 829, http://dx.doi.org/10.1038/s41588-021-00857-4
2021
Rogoża-Janiszewska E; Malińska K; Górski B; Scott RJ; Cybulski C; Kluźniak W; Lener M; Jakubowska A; Gronwald J; Huzarski T; Lubiński J; Dębniak T, 2021, 'Prevalence of germline TP53 variants among early-onset breast cancer patients from Polish population.', Breast Cancer, vol. 28, pp. 226 - 235, http://dx.doi.org/10.1007/s12282-020-01151-7
2021
Złowocka-Perłowska E; Dębniak T; Słojewski M; van de Wetering T; Tołoczko-Grabarek A; Cybulski C; Scott RJ; Lubiński J, 2021, 'Survival of bladder or renal cancer in patients with CHEK2 mutations.', PLoS One, vol. 16, pp. e0257132, http://dx.doi.org/10.1371/journal.pone.0257132
2021
Pariyar M; Johns A; Thorne RF; Scott RJ; Avery-Kiejda KA, 2021, 'Copy number variation in triple negative breast cancer samples associated with lymph node metastasis.', Neoplasia, vol. 23, pp. 743 - 753, http://dx.doi.org/10.1016/j.neo.2021.05.016
2021
Ahadova A; Seppälä TT; Engel C; Gallon R; Burn J; Holinski-Feder E; Steinke-Lange V; Möslein G; Nielsen M; Ten Broeke SW; Laghi L; Dominguez-Valentin M; Capella G; Macrae F; Scott R; Hüneburg R; Nattermann J; Hoffmeister M; Brenner H; Bläker H; von Knebel Doeberitz M; Sampson JR; Vasen H; Mecklin J-P; Møller P; Kloor M, 2021, 'The "unnatural" history of colorectal cancer in Lynch syndrome: Lessons from colonoscopy surveillance.', Int J Cancer, vol. 148, pp. 800 - 811, http://dx.doi.org/10.1002/ijc.33224
2021
Ngo TTD; Lea RA; Maksemous N; Eccles DA; Smith RA; Dunn PJ; Thao VC; Ha TMT; Bùi CB; Haupt LM; Scott R; Griffiths LR, 2021, 'The MinION as a cost-effective technology for diagnostic screening of the SCN1A gene in epilepsy patients.', Epilepsy Res, vol. 172, pp. 106593, http://dx.doi.org/10.1016/j.eplepsyres.2021.106593
2021
Skerrett-Byrne DA; Bromfield EG; Murray HC; Jamaluddin MFB; Jarnicki AG; Fricker M; Essilfie AT; Jones B; Haw TJ; Hampsey D; Anderson AL; Nixon B; Scott RJ; Wark PAB; Dun MD; Hansbro PM, 2021, 'Time-resolved proteomic profiling of cigarette smoke-induced experimental chronic obstructive pulmonary disease.', Respirology, vol. 26, pp. 960 - 973, http://dx.doi.org/10.1111/resp.14111
2021
Kho P-F; Amant F; Annibali D; Ashton K; Attia J; Auer PL; Beckmann MW; Black A; Brinton L; Buchanan DD; Chanock SJ; Chen C; Chen MM; Cheng THT; Cook LS; Crous-Bous M; Czene K; De Vivo I; Dennis J; Dörk T; Dowdy SC; Dunning AM; Dürst M; Easton DF; Ekici AB; Fasching PA; Fridley BL; Friedenreich CM; García-Closas M; Gaudet MM; Giles GG; Goode EL; Gorman M; Haiman CA; Hall P; Hankinson SE; Hein A; Hillemanns P; Hodgson S; Hoivik EA; Holliday EG; Hunter DJ; Jones A; Kraft P; Krakstad C; Lambrechts D; Le Marchand L; Liang X; Lindblom A; Lissowska J; Long J; Lu L; Magliocco AM; Martin L; McEvoy M; Milne RL; Mints M; Nassir R; Otton G; Palles C; Pooler L; Proietto T; Rebbeck TR; Renner SP; Risch HA; Rübner M; Runnebaum I; Sacerdote C; Sarto GE; Schumacher F; Scott RJ; Setiawan VW; Shah M; Sheng X; Shu X-O; Southey MC; Tham E; Tomlinson I; Trovik J; Turman C; Tyrer JP; Van Den Berg D; Wang Z; Wentzensen N; Xia L; Xiang Y-B; Yang HP; Yu H; Zheng W; Webb PM; Thompson DJ; Spurdle AB; Glubb DM; O'Mara TA, 2021, 'Mendelian randomization analyses suggest a role for cholesterol in the development of endometrial cancer.', Int J Cancer, vol. 148, pp. 307 - 319, http://dx.doi.org/10.1002/ijc.33206
2021
Xavier A; Scott RJ; Talseth-Palmer B, 2021, 'Exome sequencing of familial adenomatous polyposis-like individuals identifies both known and novel causative genes.', Clin Genet, vol. 100, pp. 478 - 483, http://dx.doi.org/10.1111/cge.14029
2021
Baszuk P; Janasik B; Pietrzak S; Marciniak W; Reszka E; Białkowska K; Jabłońska E; Muszyńska M; Lesicka M; Derkacz R; Grodzki T; Wójcik J; Wojtyś M; Dębniak T; Cybulski C; Gronwald J; Kubisa B; Wójcik N; Pieróg J; Gajić D; Waloszczyk P; Scott RJ; Wąsowicz W; Jakubowska A; Lubiński J; Lener MR, 2021, 'Lung Cancer Occurrence-Correlation with Serum Chromium Levels and Genotypes.', Biol Trace Elem Res, vol. 199, pp. 1228 - 1236, http://dx.doi.org/10.1007/s12011-020-02240-6
2021
Pietrzak S; Wójcik J; Baszuk P; Marciniak W; Wojtyś M; Dębniak T; Cybulski C; Gronwald J; Alchimowicz J; Masojć B; Waloszczyk P; Gajić D; Grodzki T; Jakubowska A; Scott RJ; Lubiński J; Lener MR, 2021, 'Influence of the Levels of Arsenic, Cadmium, Mercury and Lead on Overall Survival in Lung Cancer.', Biomolecules, vol. 11, pp. 1160 - 1160, http://dx.doi.org/10.3390/biom11081160
2021
Baszuk P; Stadnik P; Marciniak W; Derkacz R; Jakubowska A; Cybulski C; Huzarski T; Gronwald J; Dębniak T; Białkowska K; Pietrzak S; Kładny J; Scott RJ; Lubiński J; Lener MR, 2021, 'Low Blood-As Levels and Selected Genotypes Appears to Be Promising Biomarkers for Occurrence of Colorectal Cancer in Women.', Biomedicines, vol. 9, pp. 1105 - 1105, http://dx.doi.org/10.3390/biomedicines9091105
2021
Glubb DM; Thompson DJ; Aben KKH; Alsulimani A; Amant F; Annibali D; Attia J; Barricarte A; Beckmann MW; Berchuck A; Bermisheva M; Bernardini MQ; Bischof K; Bjorge L; Bodelon C; Brand AH; Brenton JD; Brinton LA; Bruinsma F; Buchanan DD; Burghaus S; Butzow R; Cai H; Carney ME; Chanock SJ; Chen C; Chen XQ; Chen Z; Cook LS; Cunningham JM; De Vivo I; DeFazio A; Doherty JA; Dork T; du Bois A; Dunning AM; Durst M; Edwards T; Edwards RP; Ekici AB; Ewing A; Fasching PA; Ferguson S; Flanagan JM; Fostira F; Fountzilas G; Friedenreich CM; Gao B; Gaudet MM; Gawelko J; Gentry-Maharaj A; Giles GG; Glasspool R; Goodman MT; Gronwald J; Harris HR; Harter P; Hein A; Heitz F; Hildebrandt MAT; Hillemanns P; Hogdall E; Hogdall CK; Holliday EG; Huntsman DG; Huzarski T; Jakubowska A; Jensen A; Jones ME; Karlan BY; Karnezis A; Kelley JL; Khusnutdinova E; Killeen JL; Kjaer SK; Klapdor R; Kobel M; Konopka B; Konstantopoulou I; Kopperud RK; Koti M; Kraft P; Kupryjanczyk J; Lambrechts D; Larson MC; Le Marchand L; Lele S; Lester J; Li AJ; Liang D; Liebrich C; Lipworth L; Lissowska J; Lu L; Lu KH; Macciotta A; Mattiello A; May T; McAlpine JN; McGuire V; McNeish IA; Menon U; Modugno F; Moysich KB; Nevanlinna H; Odunsi K; Olsson H; Orsulic S; Osorio A; Palli D; Park-Simon T-W; Pearce CL; Pejovic T; Permuth JB; Podgorska A; Ramus SJ; Rebbeck TR; Riggan MJ; Risch HA; Rothstein JH; Runnebaum IB; Scott RJ; Sellers TA; Senz J; Setiawan VW; Siddiqui N; Sieh W; Spiewankiewicz B; Sutphen R; Swerdlow AJ; Szafron LM; Teo SH; Thompson PJ; Thomsen LCV; Titus L; Tone A; Tumino R; Turman C; Vanderstichele A; Edwards DV; Vergote I; Vierkant RA; Wang Z; Wang-Gohrke S; Webb PM; White E; Whittemore AS; Winham SJ; Wu X; Wu AH; Yannoukakos D; Spurdle AB; O'Mara TA, 2021, 'Cross-Cancer Genome-Wide Association Study of Endometrial Cancer and Epithelial Ovarian Cancer Identifies Genetic Risk Regions Associated with Risk of Both Cancers', CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, vol. 30, pp. 217 - 228, http://dx.doi.org/10.1158/1055-9965.EPI-20-0739
2021
Kapoor PM; Mavaddat N; Choudhury PP; Wilcox AN; Lindström S; Behrens S; Michailidou K; Dennis J; Bolla MK; Wang Q; Jung A; Abu-Ful Z; Ahearn T; Andrulis IL; Anton-Culver H; Arndt V; Aronson KJ; Auer PL; Freeman LEB; Becher H; Beckmann MW; Beeghly-Fadiel A; Benitez J; Bernstein L; Bojesen SE; Brauch H; Brenner H; Brüning T; Cai Q; Campa D; Canzian F; Carracedo A; Carter BD; Castelao JE; Chanock SJ; Chatterjee N; Chenevix-Trench G; Clarke CL; Couch FJ; Cox A; Cross SS; Czene K; Dai JY; Earp HS; Ekici AB; Eliassen AH; Eriksson M; Evans DG; Fasching PA; Figueroa J; Fritschi L; Gabrielson M; Gago-Dominguez M; Gao C; Gapstur SM; Gaudet MM; Giles GG; González-Neira A; Guénel P; Haeberle L; Haiman CA; Håkansson N; Hall P; Hamann U; Hatse S; Heyworth J; Holleczek B; Hoover RN; Hopper JL; Howell A; Hunter DJ; John EM; Jones ME; Kaaks R; Keeman R; Kitahara CM; Ko YD; Koutros S; Kurian AW; Lambrechts D; Le Marchand L; Lee E; Lejbkowicz F; Linet M; Lissowska J; Llaneza A; Macinnis RJ; Martinez ME; Maurer T; Mclean C; Neuhausen SL; Newman WG; Norman A; O'brien KM; Olshan AF; Olson JE; Olsson H; Orr N; Perou CM; Pita G, 2021, 'Combined Associations of a Polygenic Risk Score and Classical Risk Factors with Breast Cancer Risk', Journal of the National Cancer Institute, vol. 113, pp. 329 - 337, http://dx.doi.org/10.1093/jnci/djaa056
2021
Scott RJ; Merton ERK, 2021, 'When the going gets tough, the goal-committed get going: overcoming the transaction costs of inter-agency collaborative governance', Public Management Review, vol. 23, pp. 1640 - 1663, http://dx.doi.org/10.1080/14719037.2021.1879916
2021
Butler T; Schofield PW; Knight L; Ton B; Greenberg D; Scott RJ; Grant L; Keech AC; Gebski V; Jones J; Ellis A; Weatherburn D; Wilhelm K; Jones A; Churchill A; Allnutt S; Mitchell PB; Chappell D; Deste C; Villa D; Carr V, 2021, 'Sertraline hydrochloride for reducing impulsive behaviour in male, repeat-violent offenders (ReINVEST): Protocol for a phase IV, double-blind, placebo-controlled, randomised clinical trial', BMJ Open, vol. 11, pp. e044656, http://dx.doi.org/10.1136/bmjopen-2020-044656
2021
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Feng H; Gusev A; Pasaniuc B; Wu L; Long J; Abu-full Z; Aittomäki K; Andrulis IL; Anton-Culver H; Antoniou AC; Arason A; Arndt V; Aronson KJ; Arun BK; Asseryanis E; Auer PL; Azzollini J; Balmaña J; Barkardottir RB; Barnes DR; Barrowdale D; Beckmann MW; Behrens S; Benitez J; Bermisheva M; Białkowska K; Blanco A; Blomqvist C; Boeckx B; Bogdanova NV; Bojesen SE; Bolla MK; Bonanni B; Borg A; Brauch H; Brenner H; Briceno I; Broeks A; Brüning T; Burwinkel B; Cai Q; Caldés T; Caligo MA; Campbell I; Canisius S; Campa D; Carter BD; Carter J; Castelao JE; Chang-Claude J; Chanock SJ; Christiansen H; Chung WK; Claes KBM; Clarke CL; Couch FJ; Cox A; Cross SS; Cybulski C; Czene K; Daly MB; de la Hoya M; De Leeneer K; Dennis J; Devilee P; Diez O; Domchek SM; Dörk T; dos-Santos-Silva I; Dunning AM; Dwek M; Eccles DM; Ejlertsen B; Ellberg C; Engel C; Eriksson M; Fasching PA; Fletcher O; Flyger H; Fostira F; Friedman E; Fritschi L; Frost D; Gabrielson M; Ganz PA; Gapstur SM; Garber J; García-Closas M; García-Sáenz JA; Gaudet MM; Giles GG; Glendon G; Godwin AK; Goldberg MS; Goldgar DE; González-Neira A; Greene MH; Gronwald J; Guénel P; Haiman CA, 2020, 'Transcriptome-wide association study of breast cancer risk by estrogen-receptor status', Genetic Epidemiology, vol. 44, pp. 442 - 468, http://dx.doi.org/10.1002/gepi.22288
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Maltby VE; Lea RA; Burnard S; Xavier A; Van Cao T; White N; Kennedy D; Groen K; Sanders KA; Seeto R; Bray S; Gresle M; Laverick L; Butzkueven H; Scott RJ; Lechner-Scott J, 2020, 'Epigenetic differences at the HTR2A locus in progressive multiple sclerosis patients.', Sci Rep, vol. 10, pp. 22217, http://dx.doi.org/10.1038/s41598-020-78809-x
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Kapoor PM; Lindström S; Behrens S; Wang X; Michailidou K; Bolla MK; Wang Q; Dennis J; Dunning AM; Pharoah PDP; Schmidt MK; Kraft P; García-Closas M; Easton DF; Milne RL; Chang-Claude J; Breast Cancer Association Consortium , 2020, 'Assessment of interactions between 205 breast cancer susceptibility loci and 13 established risk factors in relation to breast cancer risk, in the Breast Cancer Association Consortium.', Int J Epidemiol, vol. 49, pp. 216 - 232, http://dx.doi.org/10.1093/ije/dyz193
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Malińska K; Deptuła J; Rogoża-Janiszewska E; Górski B; Scott R; Rudnicka H; Kashyap A; Domagała P; Hybiak J; Masojć B; Cybulski C; Kram A; Boer M; Kiedrowicz M; Lubiński J; Dębniak T, 2020, 'Constitutional variants in POT1, TERF2IP, and ACD genes in patients with melanoma in the Polish population.', Eur J Cancer Prev, vol. 29, pp. 511 - 519, http://dx.doi.org/10.1097/CEJ.0000000000000633
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Kamitaki N; Sekar A; Handsaker RE; de Rivera H; Tooley K; Morris DL; Taylor KE; Whelan CW; Tombleson P; Loohuis LMO; Ripke S; Neale BM; Corvin A; Walters JTR; Farh KH; Holmans PA; Lee P; Bulik-Sullivan B; Collier DA; Huang H; Pers TH; Agartz I; Agerbo E; Albus M; Alexander M; Amin F; Bacanu SA; Begemann M; Belliveau RA; Bene J; Bergen SE; Bevilacqua E; Bigdeli TB; Black DW; Bruggeman R; Buccola NG; Buckner RL; Byerley W; Cahn W; Cai G; Cairns MJ; Campion D; Cantor RM; Carr VJ; Carrera N; Catts SV; Chambert KD; Chan RCK; Chen RYL; Chen EYH; Cheng W; Cheung EFC; Chong SA; Cloninger CR; Cohen D; Cohen N; Cormican P; Craddock N; Crespo-Facorro B; Crowley JJ; Curtis D; Davidson M; Davis KL; Degenhardt F; Del Favero J; DeLisi LE; Demontis D; Dikeos D; Dinan T; Djurovic S; Donohoe G; Drapeau E; Duan J; Dudbridge F; Durmishi N; Eichhammer P; Eriksson J; Escott-Price V; Essioux L; Fanous AH; Farrell MS; Frank J; Franke L; Freedman R; Freimer NB; Friedl M; Friedman JI; Fromer M; Genovese G; Georgieva L; Gershon ES; Giegling I; Giusti-Rodríguez P; Godard S; Goldstein JI; Golimbet V; Gopal S; Gratten J; de Haan L; Mitjans M, 2020, 'Complement genes contribute sex-biased vulnerability in diverse disorders', Nature, vol. 582, pp. 577 - 581, http://dx.doi.org/10.1038/s41586-020-2277-x
2020
Groen K; Maltby VE; Scott RJ; Tajouri L; Lechner-Scott J, 2020, 'Concentrations of plasma-borne extracellular particles differ between multiple sclerosis disease courses and compared to healthy controls.', Mult Scler Relat Disord, vol. 45, pp. 102446, http://dx.doi.org/10.1016/j.msard.2020.102446
2020
Shu X; Bao J; Wu L; Long J; Shu X-O; Guo X; Yang Y; Michailidou K; Bolla MK; Wang Q; Dennis J; Andrulis IL; Castelao JE; Dörk T; Gago-Dominguez M; García-Closas M; Giles GG; Lophatananon A; Muir K; Olsson H; Rennert G; Saloustros E; Scott RJ; Southey MC; Pharoah PDP; Milne RL; Kraft P; Simard J; Easton DF; Zheng W, 2020, 'Evaluation of associations between genetically predicted circulating protein biomarkers and breast cancer risk.', Int J Cancer, vol. 146, pp. 2130 - 2138, http://dx.doi.org/10.1002/ijc.32542
2020
Scott RJ; Macaulay M, 2020, 'Making sense of New Zealand’s ‘spirit of service’: social identity and the civil service', Public Money and Management, vol. 40, pp. 579 - 588, http://dx.doi.org/10.1080/09540962.2020.1735109
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Burn J; Sheth H; Elliott F; Reed L; Macrae F; Mecklin J-P; Möslein G; McRonald FE; Bertario L; Evans DG; Gerdes A-M; Ho JWC; Lindblom A; Morrison PJ; Rashbass J; Ramesar R; Seppälä T; Thomas HJW; Pylvänäinen K; Borthwick GM; Mathers JC; Bishop DT; CAPP2 Investigators , 2020, 'Cancer prevention with aspirin in hereditary colorectal cancer (Lynch syndrome), 10-year follow-up and registry-based 20-year data in the CAPP2 study: a double-blind, randomised, placebo-controlled trial.', Lancet, vol. 395, pp. 1855 - 1863, http://dx.doi.org/10.1016/S0140-6736(20)30366-4
2020
Scott RJ; Boyd R, 2020, 'Determined to succeed: Can goal commitment sustain interagency collaboration?', PUBLIC POLICY AND ADMINISTRATION, http://dx.doi.org/10.1177/0952076720905002
2020
Groen K; Maltby VE; Scott RJ; Tajouri L; Lechner-Scott J, 2020, 'Erythrocyte microRNAs show biomarker potential and implicate multiple sclerosis susceptibility genes.', Clin Transl Med, vol. 10, pp. 74 - 90, http://dx.doi.org/10.1002/ctm2.22
2020
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2019
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Xavier A; Scott RJ; Talseth-Palmer BA, 2019, 'TAPES: A tool for assessment and prioritisation in exome studies.', PLoS Comput Biol, vol. 15, pp. e1007453, http://dx.doi.org/10.1371/journal.pcbi.1007453
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Dominguez-Valentin M; Seppälä TT; Sampson JR; Macrae F; Winship I; Evans DG; Scott RJ; Burn J; Möslein G; Bernstein I; Pylvänäinen K; Renkonen-Sinisalo L; Lepistö A; Lindblom A; Plazzer J-P; Tjandra D; Thomas H; Green K; Lalloo F; Crosbie EJ; Hill J; Capella G; Pineda M; Navarro M; Vidal JB; Rønlund K; Nielsen RT; Yilmaz M; Elvang LL; Katz L; Nielsen M; Ten Broeke SW; Nakken S; Hovig E; Sunde L; Kloor M; Knebel Doeberitz MV; Ahadova A; Lindor N; Steinke-Lange V; Holinski-Feder E; Mecklin J-P; Møller P, 2019, 'Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report.', Hered Cancer Clin Pract, vol. 17, pp. 28, http://dx.doi.org/10.1186/s13053-019-0127-3
2019
Figlioli G; Bogliolo M; Catucci I; Caleca L; Lasheras SV; Pujol R; Kiiski JI; Muranen TA; Barnes DR; Dennis J; Michailidou K; Bolla MK; Leslie G; Aalfs CM; Balleine R; Baxter R; Braye S; Carpenter J; Dahlstrom J; Forbes J; Lee CS; Marsh D; Morey A; Pathmanathan N; Scott R; Simpson P; Spigelman A; Wilcken N; Yip D; Zeps N; Adank MA; Adlard J; Agata S; Cadoo K; Agnarsson BA; Ahearn T; Aittomäki K; Ambrosone CB; Andrews L; Anton-Culver H; Antonenkova NN; Arndt V; Arnold N; Aronson KJ; Arun BK; Asseryanis E; Auber B; Auvinen P; Azzollini J; Balmaña J; Barkardottir RB; Barrowdale D; Barwell J; Beane Freeman LE; Beauparlant CJ; Beckmann MW; Behrens S; Benitez J; Berger R; Bermisheva M; Blanco AM; Blomqvist C; Bogdanova NV; Bojesen A; Bojesen SE; Bonanni B; Borg A; Brady AF; Brauch H; Brenner H; Brüning T; Burwinkel B; Buys SS; Caldés T; Caliebe A; Caligo MA; Campa D; Campbell IG; Canzian F; Castelao JE; Chang-Claude J; Chanock SJ; Claes KBM; Clarke CL; Collavoli A; Conner TA; Cox DG; Cybulski C; Czene K; Daly MB; de la Hoya M; Devilee P; Diez O; Ding YC; Dite GS; Ditsch N; Domchek SM; Dorfling CM; dos-Santos-Silva I; Durda K, 2019, 'The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer', npj Breast Cancer, vol. 5, http://dx.doi.org/10.1038/s41523-019-0127-5
2019
Petit J; Carroll G; Gould T; Pockney P; Dun M; Scott RJ, 2019, 'Cell-Free DNA as a Diagnostic Blood-Based Biomarker for Colorectal Cancer: A Systematic Review.', J Surg Res, vol. 236, pp. 184 - 197, http://dx.doi.org/10.1016/j.jss.2018.11.029
2019
Mavaddat N; Michailidou K; Dennis J; Lush M; Fachal L; Lee A; Tyrer JP; Chen TH; Wang Q; Bolla MK; Yang X; Adank MA; Ahearn T; Aittomäki K; Allen J; Andrulis IL; Anton-Culver H; Antonenkova NN; Arndt V; Aronson KJ; Auer PL; Auvinen P; Barrdahl M; Beane Freeman LE; Beckmann MW; Behrens S; Benitez J; Bermisheva M; Bernstein L; Blomqvist C; Bogdanova NV; Bojesen SE; Bonanni B; Børresen-Dale AL; Brauch H; Bremer M; Brenner H; Brentnall A; Brock IW; Brooks-Wilson A; Brucker SY; Brüning T; Burwinkel B; Campa D; Carter BD; Castelao JE; Chanock SJ; Chlebowski R; Christiansen H; Clarke CL; Collée JM; Cordina-Duverger E; Cornelissen S; Couch FJ; Cox A; Cross SS; Czene K; Daly MB; Devilee P; Dörk T; dos-Santos-Silva I; Dumont M; Durcan L; Dwek M; Eccles DM; Ekici AB; Eliassen AH; Ellberg C; Engel C; Eriksson M; Evans DG; Fasching PA; Figueroa J; Fletcher O; Flyger H; Försti A; Fritschi L; Gabrielson M; Gago-Dominguez M; Gapstur SM; García-Sáenz JA; Gaudet MM; Georgoulias V; Giles GG; Gilyazova IR; Glendon G; Goldberg MS; Goldgar DE; González-Neira A; Grenaker Alnæs GI; Grip M; Gronwald J; Grundy A; Guénel P; Haeberle L; Hahnen E; Haiman CA; Håkansson N; Hamann U; Hankinson SE, 2019, 'Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes', American Journal of Human Genetics, vol. 104, pp. 21 - 34, http://dx.doi.org/10.1016/j.ajhg.2018.11.002
2019
Berry NK; Scott RJ; Rowlings P; Enjeti AK, 2019, 'Clinical use of SNP-microarrays for the detection of genome-wide changes in haematological malignancies.', Crit Rev Oncol Hematol, vol. 142, pp. 58 - 67, http://dx.doi.org/10.1016/j.critrevonc.2019.07.016
2019
Pietrzak S; Wójcik J; Scott RJ; Kashyap A; Grodzki T; Baszuk P; Bielewicz M; Marciniak W; Wójcik N; Dębniak T; Masojć B; Pieróg J; Cybulski C; Gronwald J; Wojtyś M; Kubisa B; Sukiennicki G; Deptuła J; Waloszczyk P; Jakubowska A; Lubiński J; Lener MR, 2019, 'Influence of the selenium level on overall survival in lung cancer.', J Trace Elem Med Biol, vol. 56, pp. 46 - 51, http://dx.doi.org/10.1016/j.jtemb.2019.07.010
2019
Morten BC; Chiu S; Oldmeadow C; Lubinski J; Scott RJ; Avery-Kiejda KA, 2019, 'The intron 3 16 bp duplication polymorphism of p53 (rs17878362) is not associated with increased risk of developing triple-negative breast cancer.', Breast Cancer Res Treat, vol. 173, pp. 727 - 733, http://dx.doi.org/10.1007/s10549-018-5039-9
2019
Xavier MJ; Nixon B; Roman SD; Scott RJ; Drevet JR; Aitken RJ, 2019, 'Paternal impacts on development: identification of genomic regions vulnerable to oxidative DNA damage in human spermatozoa.', Hum Reprod, vol. 34, pp. 1876 - 1890, http://dx.doi.org/10.1093/humrep/dez153
2019
Iglesias AI; Mishra A; Vitart V; Bykhovskaya Y; Höhn R; Springelkamp H; Cuellar-Partida G; Gharahkhani P; Bailey JNC; Willoughby CE; Li X; Yazar S; Nag A; Khawaja AP; Polašek O; Siscovick D; Mitchell P; Tham YC; Haines JL; Kearns LS; Hayward C; Shi Y; van Leeuwen EM; Taylor KD; Wang JJ; Rochtchina E; Attia J; Scott R; Holliday EG; Wong TY; Baird PN; Xie J; Inouye M; Viswanathan A; Sim X; Bonnemaijer P; Rotter JI; Martin NG; Zeller T; Mills RA; Souzeau E; Staffieri SE; Jonas JB; Schmidtmann I; Boutin T; Kang JH; Lucas SEM; Beutel ME; Wilson JF; Donnelly P; Barroso I; Blackwell JM; Bramon E; Brown MA; Casas JP; Corvin A; Deloukas P; Duncanson A; Jankowski J; Markus HS; Mathew CG; Palmer CNA; Plomin R; Rautanen A; Sawcer SJ; Trembath RC; Wood NW; Spencer CCA; Band G; Bellenguez C; Freeman C; Hellenthal G; Giannoulatou E; Pirinen M; Pearson R; Strange A; Su Z; Vukcevic D; Langford C; Hunt SE; Edkins S; Gwilliam R; Blackburn H; Bumpstead SJ; Dronov S; Gillman M; Gray E; Hammond N; Jayakumar A; McCann OT; Liddle J; Potter SC; Ravindrarajah R; Ricketts M; Waller M; Weston P; Widaa S; Whittaker P; Allingham RR; Brilliant MH, 2019, 'Erratum to: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases (Nature Communications, (2018), 9, 1, (1864), 10.1038/s41467-018-03646-6)', Nature Communications, vol. 10, http://dx.doi.org/10.1038/s41467-018-07819-1
2019
Söderholm M; Pedersen A; Lorentzen E; Stanne TM; Bevan S; Olsson M; Cole JW; Fernandez-Cadenas I; Hankey GJ; Jimenez-Conde J; Jood K; Lee JM; Lemmens R; Levi C; Mitchell BD; Norrving B; Rannikmäe K; Rost NS; Rosand J; Rothwell PM; Scott R; Strbian D; Sturm JW; Sudlow C; Traylor M; Thijs V; Tatlisumak T; Woo D; Worrall BB; Maguire JM; Lindgren A; Jern C, 2019, 'Genome-wide association meta-analysis of functional outcome after ischemic stroke', Neurology, vol. 92, pp. E1271 - E1283, http://dx.doi.org/10.1212/WNL.0000000000007138
2019
Hnatyszyn A; Hryhorowicz S; Kaczmarek-Ryś M; Lis E; Słomski R; Scott RJ; Pławski A, 2019, 'Colorectal carcinoma in the course of inflammatory bowel diseases.', Hered Cancer Clin Pract, vol. 17, pp. 18, http://dx.doi.org/10.1186/s13053-019-0118-4
2019
Dębniak T; Scott RJ; Lea RA; Górski B; Masojć B; Cybulski C; Kram A; Maleszka R; Gromowski T; Paszkowska-Szczur K; Kashyap A; Lener MR; Malińska K; Rogoża E; Murawa D; Rudnicka H; Deptuła J; Lubiński J, 2019, 'Founder Mutations for Early Onset Melanoma as Revealed by Whole Exome Sequencing Suggests That This is Not Associated with the Increasing Incidence of Melanoma in Poland.', Cancer Res Treat, vol. 51, pp. 337 - 344, http://dx.doi.org/10.4143/crt.2018.157
2019
Xavier A; Olsen MF; Lavik LA; Johansen J; Singh AK; Sjursen W; Scott RJ; Talseth-Palmer BA, 2019, 'Comprehensive mismatch repair gene panel identifies variants in patients with Lynch-like syndrome.', Mol Genet Genomic Med, vol. 7, pp. e850, http://dx.doi.org/10.1002/mgg3.850
2019
Tan AG; Kifley A; Flood VM; Holliday EG; Scott RJ; Cumming RG; Mitchell P; Wang JJ, 2019, 'Evaluating the associations between obesity and age-related cataract: A Mendelian randomization study', American Journal of Clinical Nutrition, vol. 110, pp. 969 - 976, http://dx.doi.org/10.1093/ajcn/nqz167
2019
Gill D; James NE; Monori G; Lorentzen E; Fernandez-Cadenas I; Lemmens R; Thijs V; Rost NS; Scott R; Hankey GJ; Lindgren A; Jern C; Maguire JM, 2019, 'Genetically Determined Risk of Depression and Functional Outcome after Ischemic Stroke: Mendelian Randomization Study', Stroke, vol. 50, pp. 2219 - 2222, http://dx.doi.org/10.1161/STROKEAHA.119.026089
2019
Harold D; Connolly S; Riley BP; Kendler KS; McCarthy SE; McCombie WR; Richards A; Owen MJ; O'Donovan MC; Walters JTR; Donnelly P; Bates L; Barroso I; Blackwell JM; Bramon E; Brown MA; Casas JP; Corvin A; Deloukas P; Duncanson A; Jankowski J; Markus HS; Mathew CG; Palmer CNA; Plomin R; Rautanen A; Sawcer SJ; Trembath RC; Viswanathan AC; Wood NW; Spencer CCA; Band G; Bellenguez C; Freeman C; Hellenthal G; Giannoulatou E; Hopkins L; Pirinen M; Pearson R; Strange A; Su Z; Vukcevic D; Langford C; Hunt SE; Edkins S; Gwilliam R; Blackburn H; Bumpstead SJ; Dronov S; Gillman M; Gray E; Hammond N; Jayakumar A; McCann OT; Liddle J; Potter SC; Ravindrarajah R; Ricketts M; Waller M; Weston P; Widaa S; Whittaker P; Ripke S; Neale BM; Farh KH; Holmans PA; Lee P; Bulik-Sullivan B; Collier DA; Huang H; Pers TH; Agartz I; Agerbo E; Albus M; Alexander M; Amin F; Bacanu SA; Begemann M; Belliveau RA; Bene J; Bergen SE; Bevilacqua E; Bigdeli TB; Black DW; Bruggeman R; Buccola NG; Buckner RL; Byerley W; Cahn W; Cai G; Campion D; Cantor RM; Carr VJ; Carrera N; Catts SV; Chambert KD; Chan RCK; Chan RYL; Chen EYH; Cheng W, 2019, 'Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia', American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, vol. 180, pp. 223 - 231, http://dx.doi.org/10.1002/ajmg.b.32716
2019
Lee PH; Anttila V; Won H; Feng YCA; Rosenthal J; Zhu Z; Tucker-Drob EM; Nivard MG; Grotzinger AD; Posthuma D; Wang MMJ; Yu D; Stahl EA; Walters RK; Anney RJL; Duncan LE; Ge T; Adolfsson R; Banaschewski T; Belangero S; Cook EH; Coppola G; Derks EM; Hoekstra PJ; Kaprio J; Keski-Rahkonen A; Kirov G; Kranzler HR; Luykx JJ; Rohde LA; Zai CC; Agerbo E; Arranz MJ; Asherson P; Bækvad-Hansen M; Baldursson G; Bellgrove M; Belliveau RA; Buitelaar J; Burton CL; Bybjerg-Grauholm J; Casas M; Cerrato F; Chambert K; Churchhouse C; Cormand B; Crosbie J; Dalsgaard S; Demontis D; Doyle AE; Dumont A; Elia J; Grove J; Gudmundsson OO; Haavik J; Hakonarson H; Hansen CS; Hartman CA; Hawi Z; Hervás A; Hougaard DM; Howrigan DP; Huang H; Kuntsi J; Langley K; Lesch KP; Leung PWL; Loo SK; Martin J; Martin AR; McGough JJ; Medland SE; Moran JL; Mors O; Mortensen PB; Oades RD; Palmer DS; Pedersen CB; Pedersen MG; Peters T; Poterba T; Poulsen JB; Ramos-Quiroga JA; Reif A; Ribasés M; Rothenberger A; Rovira P; Sánchez-Mora C; Satterstrom FK; Schachar R; Artigas MS; Steinberg S; Stefansson H; Turley P; Walters GB; Werge T; Zayats T; Arking DE; Bettella F; Buxbaum JD, 2019, 'Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders', Cell, vol. 179, pp. 1469 - 1482.e11, http://dx.doi.org/10.1016/j.cell.2019.11.020
2019
Seppälä TT; Ahadova A; Dominguez-Valentin M; Macrae F; Evans DG; Therkildsen C; Sampson J; Scott R; Burn J; Möslein G; Bernstein I; Holinski-Feder E; Pylvänäinen K; Renkonen-Sinisalo L; Lepistö A; Lautrup CK; Lindblom A; Plazzer J-P; Winship I; Tjandra D; Katz LH; Aretz S; Hüneburg R; Holzapfel S; Heinimann K; Valle AD; Neffa F; Gluck N; de Vos Tot Nederveen Cappel WH; Vasen H; Morak M; Steinke-Lange V; Engel C; Rahner N; Schmiegel W; Vangala D; Thomas H; Green K; Lalloo F; Crosbie EJ; Hill J; Capella G; Pineda M; Navarro M; Blanco I; Ten Broeke S; Nielsen M; Ljungmann K; Nakken S; Lindor N; Frayling I; Hovig E; Sunde L; Kloor M; Mecklin J-P; Kalager M; Møller P, 2019, 'Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report.', Hered Cancer Clin Pract, vol. 17, pp. 8, http://dx.doi.org/10.1186/s13053-019-0106-8
2019
Escala-Garcia M; Guo Q; Dörk T; Canisius S; Keeman R; Dennis J; Beesley J; Lecarpentier J; Bolla MK; Wang Q; Abraham J; Andrulis IL; Anton-Culver H; Arndt V; Auer PL; Beckmann MW; Behrens S; Benitez J; Bermisheva M; Bernstein L; Blomqvist C; Boeckx B; Bojesen SE; Bonanni B; Børresen-Dale AL; Brauch H; Brenner H; Brentnall A; Brinton L; Broberg P; Brock IW; Brucker SY; Burwinkel B; Caldas C; Caldés T; Campa D; Canzian F; Carracedo A; Carter BD; Castelao JE; Chang-Claude J; Chanock SJ; Chenevix-Trench G; Cheng TYD; Chin SF; Clarke CL; Cordina-Duverger E; Couch FJ; Cox DG; Cox A; Cross SS; Czene K; Daly MB; Devilee P; Dunn JA; Dunning AM; Durcan L; Dwek M; Earl HM; Ekici AB; Eliassen AH; Ellberg C; Engel C; Eriksson M; Evans DG; Figueroa J; Flesch-Janys D; Flyger H; Gabrielson M; Gago-Dominguez M; Galle E; Gapstur SM; García-Closas M; García-Sáenz JA; Gaudet MM; George A; Georgoulias V; Giles GG; Glendon G; Goldgar DE; González-Neira A; Alnæs GIG; Grip M; Guénel P; Haeberle L; Hahnen E; Haiman CA; Håkansson N; Hall P; Hamann U; Hankinson S; Harkness EF; Harrington PA; Hart SN; Hartikainen JM; Hein A; Hillemanns P; Hiller L; Holleczek B; Hollestelle A, 2019, 'Genome-wide association study of germline variants and breast cancer-specific mortality', British Journal of Cancer, vol. 120, pp. 647 - 657, http://dx.doi.org/10.1038/s41416-019-0393-x
2019
Zhang X; Morten BC; Scott RJ; Avery-Kiejda KA, 2019, 'A Simple Migration/Invasion Workflow Using an Automated Live-cell Imager.', J Vis Exp, http://dx.doi.org/10.3791/59042
2019
Biswas M; Dias TH; Holliday E; Hancock S; Attia J; Scott R; Newby D; Kerr KP; Milward L, 2018, 'Preliminary Studies of the Prevalence and Possible Clinical Consequences of Potential Simple and Multifactorial Drug and Gene Interactions of Anti-depressants in Older Australians', Frontiers in Pharmacology, vol. 9, http://dx.doi.org/10.3389/conf.fphar.2018.63.00021
2018
Ten Broeke SW; van der Klift HM; Tops CMJ; Aretz S; Bernstein I; Buchanan DD; de la Chapelle A; Capella G; Clendenning M; Engel C; Gallinger S; Gomez Garcia E; Figueiredo JC; Haile R; Hampel HL; Hopper JL; Hoogerbrugge N; von Knebel Doeberitz M; Le Marchand L; Letteboer TGW; Jenkins MA; Lindblom A; Lindor NM; Mensenkamp AR; Møller P; Newcomb PA; van Os TAM; Pearlman R; Pineda M; Rahner N; Redeker EJW; Olderode-Berends MJW; Rosty C; Schackert HK; Scott R; Senter L; Spruijt L; Steinke-Lange V; Suerink M; Thibodeau S; Vos YJ; Wagner A; Winship I; Hes FJ; Vasen HFA; Wijnen JT; Nielsen M; Win AK, 2018, 'Cancer Risks for PMS2-Associated Lynch Syndrome.', J Clin Oncol, vol. 36, pp. 2961 - 2968, http://dx.doi.org/10.1200/JCO.2018.78.4777
2018
Dias T; Biswas M; Daneshi N; Holliday E; Hancock S; Kerr K; Munro I; Attia J; Scott R; Milward L, 2018, 'Potential Clinically Significant Drug and Gene Interactions Involving Cytochrome P450 Family 2 Subfamily D Member 6 (CYP2D6) Relevant to Opioids Used for Chronic Pain in Community-dwelling Older Australians', Frontiers in Pharmacology, vol. 9, http://dx.doi.org/10.3389/conf.fphar.2018.63.00002
2018
Maltby VE; Lea RA; Graves MC; Sanders KA; Benton MC; Tajouri L; Scott RJ; Lechner-Scott J, 2018, 'Genome-wide DNA methylation changes in CD19+ B cells from relapsing-remitting multiple sclerosis patients.', Sci Rep, vol. 8, pp. 17418, http://dx.doi.org/10.1038/s41598-018-35603-0
2018
O’Mara TA; Glubb DM; Amant F; Annibali D; Ashton K; Attia J; Auer PL; Beckmann MW; Black A; Bolla MK; Brauch H; Brenner H; Brinton L; Buchanan DD; Burwinkel B; Chang-Claude J; Chanock SJ; Chen C; Chen MM; Cheng THT; Clarke CL; Clendenning M; Cook LS; Couch FJ; Cox A; Crous-Bous M; Czene K; Day F; Dennis J; Depreeuw J; Doherty JA; Dörk T; Dowdy SC; Dürst M; Ekici AB; Fasching PA; Fridley BL; Friedenreich CM; Fritschi L; Fung J; García-Closas M; Gaudet MM; Giles GG; Goode EL; Gorman M; Haiman CA; Hall P; Hankison SE; Healey CS; Hein A; Hillemanns P; Hodgson S; Hoivik EA; Holliday EG; Hopper JL; Hunter DJ; Jones A; Krakstad C; Kristensen VN; Lambrechts D; Marchand LL; Liang X; Lindblom A; Lissowska J; Long J; Lu L; Magliocco AM; Martin L; McEvoy M; Meindl A; Michailidou K; Milne RL; Mints M; Montgomery GW; Nassir R; Olsson H; Orlow I; Otton G; Palles C; Perry JRB; Peto J; Pooler L; Prescott J; Proietto T; Rebbeck TR; Risch HA; Rogers PAW; Rübner M; Runnebaum I; Sacerdote C; Sarto GE; Schumacher F; Scott RJ; Setiawan VW; Shah M; Sheng X; Shu XO; Southey MC; Swerdlow AJ; Tham E, 2018, 'Identification of nine new susceptibility loci for endometrial cancer', Nature Communications, vol. 9, pp. 3166, http://dx.doi.org/10.1038/s41467-018-05427-7
2018
Anttila V; Bulik-Sullivan B; Finucane HK; Walters RK; Bras J; Duncan L; Escott-Price V; Falcone GJ; Gormley P; Malik R; Patsopoulos NA; Ripke S; Wei Z; Yu D; Lee PH; Turley P; Grenier-Boley B; Chouraki V; Kamatani Y; Berr C; Letenneur L; Hannequin D; Amouyel P; Boland A; Deleuze JF; Duron E; Vardarajan BN; Reitz C; Goate AM; Huentelman MJ; Ilyas Kamboh M; Larson EB; Rogaeva E; George-Hyslop PS; Hakonarson H; Kukull WA; Farrer LA; Barnes LL; Beach TG; Yesim Demirci F; Head E; Hulette CM; Jicha GA; Kauwe JSK; Kaye JA; Leverenz JB; Levey AI; Lieberman AP; Pankratz VS; Poon WW; Quinn JF; Saykin AJ; Schneider LS; Smith AG; Sonnen JA; Stern RA; Van Deerlin VM; Van Eldik LJ; Harold D; Russo G; Rubinsztein DC; Bayer A; Tsolaki M; Proitsi P; Fox NC; Hampel H; Owen MJ; Mead S; Passmore P; Morgan K; Nöthen MM; Rossor M; Lupton MK; Hoffmann P; Kornhuber J; Lawlor B; McQuillin A; Al-Chalabi A; Bis JC; Ruiz A; Boada M; Seshadri S; Beiser A; Rice K; Van Der Lee SJ; De Jager PL; Geschwind DH; Riemenschneider M; Riedel-Heller S; Rotter JI; Ransmayr G; Hyman BT; Cruchaga C; Alegret M; Winsvold B; Palta P; Farh KH; Cuenca-Leon E; Furlotte N; Kurth T, 2018, 'Analysis of shared heritability in common disorders of the brain', Science, vol. 360, http://dx.doi.org/10.1126/science.aap8757
2018
Chatterjee G; Pai T; Hardiman T; Avery-Kiejda K; Scott RJ; Spencer J; Pinder SE; Grigoriadis A, 2018, 'Molecular patterns of cancer colonisation in lymph nodes of breast cancer patients.', Breast Cancer Res, vol. 20, pp. 143, http://dx.doi.org/10.1186/s13058-018-1070-3
2018
Groen K; Lea RA; Maltby VE; Scott RJ; Lechner-Scott J, 2018, 'Letter to the editor: blood processing and sample storage have negligible effects on methylation.', Clin Epigenetics, vol. 10, pp. 22, http://dx.doi.org/10.1186/s13148-018-0455-6
2018
Kennedy DW; White NM; Benton MC; Fox A; Scott RJ; Griffiths LR; Mengersen K; Lea RA, 2018, 'Critical evaluation of linear regression models for cell-subtype specific methylation signal from mixed blood cell DNA.', PLoS One, vol. 13, pp. e0208915, http://dx.doi.org/10.1371/journal.pone.0208915
2018
Maltby VE; Lea RA; Ribbons KA; Sanders KA; Kennedy D; Min M; Scott RJ; Lechner-Scott J, 2018, 'DNA methylation changes in CD4+ T cells isolated from multiple sclerosis patients on dimethyl fumarate.', Mult Scler J Exp Transl Clin, vol. 4, pp. 2055217318787826, http://dx.doi.org/10.1177/2055217318787826
2018
Ni G; Moser G; Ripke S; Neale BM; Corvin A; Walters JTR; Farh KH; Holmans PA; Lee P; Bulik-Sullivan B; Collier DA; Huang H; Pers TH; Agartz I; Agerbo E; Albus M; Alexander M; Amin F; Bacanu SA; Begemann M; Belliveau RA; Bene J; Bergen SE; Bevilacqua E; Bigdeli TB; Black DW; Bruggeman R; Buccola NG; Buckner RL; Byerley W; Cahn W; Cai G; Campion D; Cantor RM; Carr VJ; Carrera N; Catts SV; Chambert KD; Chan RCK; Chen RYL; Chen EYH; Cheng W; Cheung EFC; Chong SA; Cloninger CR; Cohen D; Cohen N; Cormican P; Craddock N; Crowley JJ; Curtis D; Davidson M; Davis KL; Degenhardt F; Del Favero J; Demontis D; Dikeos D; Dinan T; Djurovic S; Donohoe G; Drapeau E; Duan J; Dudbridge F; Durmishi N; Eichhammer P; Eriksson J; Escott-Price V; Essioux L; Fanous AH; Farrell MS; Frank J; Franke L; Freedman R; Freimer NB; Friedl M; Friedman JI; Fromer M; Genovese G; Georgieva L; Giegling I; Giusti-Rodríguez P; Godard S; Goldstein JI; Golimbet V; Gopal S; Gratten J; de Haan L; Hammer C; Hamshere ML; Hansen M; Hansen T; Haroutunian V; Hartmann AM; Henskens FA; Herms S; Hirschhorn JN; Hoffmann P; Hofman A; Hollegaard MV; Hougaard DM, 2018, 'Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood', American Journal of Human Genetics, vol. 102, pp. 1185 - 1194, http://dx.doi.org/10.1016/j.ajhg.2018.03.021
2018
Iglesias AI; Mishra A; Vitart V; Bykhovskaya Y; Höhn R; Springelkamp H; Cuellar-Partida G; Gharahkhani P; Bailey JNC; Willoughby CE; Li X; Yazar S; Nag A; Khawaja AP; Polašek O; Siscovick D; Mitchell P; Tham YC; Haines JL; Kearns LS; Hayward C; Shi Y; Van Leeuwen EM; Taylor KD; Wang JJ; Rochtchina E; Attia J; Scott R; Holliday EG; Baird PN; Xie J; Inouye M; Viswanathan A; Sim X; Bonnemaijer P; Rotter JI; Martin NG; Zeller T; Mills RA; Staffieri SE; Jonas JB; Schmidtmann I; Boutin T; Kang JH; Lucas SEM; Wong TY; Beutel ME; Wilson JF; Allingham RR; Brilliant MH; Budenz DL; Christen WG; Fingert J; Friedman DS; Gaasterland D; Gaasterland T; Hauser MA; Kraft P; Lee RK; Lichter PR; Liu Y; Loomis SJ; Moroi SE; Pericak-Vance MA; Realini A; Richards JE; Schuman JS; Scott WK; Singh K; Sit AJ; Vollrath D; Weinreb RN; Wollstein G; Zack DJ; Zhang K; Donnelly P; Barroso I; Blackwell JM; Bramon E; Brown MA; Casas JP; Corvin A; Deloukas P; Duncanson A; Jankowski J; Markus HS; Mathew CG; Palmer CNA; Plomin R; Rautanen A; Sawcer SJ; Trembath RC; Wood NW; Spencer CCA; Band G; Bellenguez C; Freeman C; Hellenthal G; Giannoulatou E; Pirinen M, 2018, 'Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases', Nature Communications, vol. 9, http://dx.doi.org/10.1038/s41467-018-03646-6
2018
Sina AAI; Carrascosa LG; Liang Z; Grewal YS; Wardiana A; Shiddiky MJA; Gardiner RA; Samaratunga H; Gandhi MK; Scott RJ; Korbie D; Trau M, 2018, 'Epigenetically reprogrammed methylation landscape drives the DNA self-assembly and serves as a universal cancer biomarker.', Nat Commun, vol. 9, pp. 4915, http://dx.doi.org/10.1038/s41467-018-07214-w
2018
Kamien B; Ronan A; Poke G; Sinnerbrink I; Baynam G; Ward M; Gibson WT; Dudding-Byth T; Scott RJ, 2018, 'A Clinical Review of Generalized Overgrowth Syndromes in the Era of Massively Parallel Sequencing.', Mol Syndromol, vol. 9, pp. 70 - 82, http://dx.doi.org/10.1159/000484532
2018
Jamaluddin MFB; Ko Y-A; Kumar M; Brown Y; Bajwa P; Nagendra PB; Skerrett-Byrne DA; Hondermarck H; Baker MA; Dun MD; Scott RJ; Nahar P; Tanwar PS, 2018, 'Proteomic Profiling of Human Uterine Fibroids Reveals Upregulation of the Extracellular Matrix Protein Periostin.', Endocrinology, vol. 159, pp. 1106 - 1118, http://dx.doi.org/10.1210/en.2017-03018
2018
Morten B; Scott R; Avery-Kiejda K, 2018, 'PO-107 A potential role for DELTA40P53 in the regulation of breast cancer stem cells', ESMO Open, vol. 3, pp. A62 - A62, http://dx.doi.org/10.1136/esmoopen-2018-eacr25.148
2018
Ruderfer DM; Ripke S; McQuillin A; Boocock J; Stahl EA; Pavlides JMW; Mullins N; Charney AW; Ori APS; Loohuis LMO; Domenici E; Di Florio A; Papiol S; Kalman JL; Trubetskoy V; Adolfsson R; Agartz I; Agerbo E; Akil H; Albani D; Albus M; Alda M; Alexander M; Alliey-Rodriguez N; Als TD; Amin F; Anjorin A; Arranz MJ; Awasthi S; Bacanu SA; Badner JA; Baekvad-Hansen M; Bakker S; Band G; Barchas JD; Barroso I; Bass N; Bauer M; Baune BT; Begemann M; Bellenguez C; Belliveau RA; Bellivier F; Bender S; Bene J; Bergen SE; Berrettini WH; Bevilacqua E; Biernacka JM; Bigdeli TB; Black DW; Blackburn H; Blackwell JM; Blackwood DHR; Pedersen CB; Boehnke M; Boks M; Borglum AD; Bramon E; Breen G; Brown MA; Bruggeman R; Buccola NG; Buckner RL; Budde M; Bulik-Sullivan B; Bumpstead SJ; Bunney W; Burmeister M; Buxbaum JD; Bybjerg-Grauholm J; Byerley W; Cahn W; Cai G; Cairns MJ; Campion D; Cantor RM; Carr VJ; Carrera N; Casas JP; Casas M; Catts SV; Cervantes P; Chambert KD; Chan RCK; Chen EYH; Chen RYL; Cheng W; Cheung EFC; Chong SA; Clarke TK; Cloninger CR; Cohen D; Cohen N; Coleman JRI; Collier DA; Cormican P; Coryell W; Craddock N; Craig DW, 2018, 'Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes', Cell, vol. 173, pp. 1705 - 1715.e16, http://dx.doi.org/10.1016/j.cell.2018.05.046
2018
Joo JE; Dowty JG; Milne RL; Wong EM; Dugué PA; English D; Hopper JL; Goldgar DE; Giles GG; Southey MC; Sexton A; Christian A; Trainer A; Spigelman A; Fellows A; Shelling A; De Fazio A; Blackburn A; Crook A; Meiser B; Patterson B; Clarke C; Saunders C; Hunt C; Scott C; Amor D; Marsh D; Edkins E; Salisbury E; Haan E; Neidermayr E; Macrae F; Farshid G; Lindeman G; Chenevix-Trench G; Mann G; Gill G; Thorne H; Campbell I; Hickie I; Winship I; Goldblatt J; Flanagan J; Kollias J; Visvader J; Stone J; Taylor J; Burke J; Saunus J; Forbes J; Beesley J; Kirk J; French J; Tucker K; Wu K; Phillips K; Lipton L; Andrews L; Lobb E; Walker L; Kentwell M; Spurdle A; Cummings M; Gleeson M; Harris M; Jenkins M; Young MA; Delatycki M; Wallis M; Burgess M; Price M; Brown M; Bogwitz M; Field M; Friedlander M; Gattas M; Saleh M; Hayward N; Pachter N; Cohen P; Duijf P; James P; Simpson P; Fong P; Butow P; Williams R; Kefford R; Scott R; Balleine R; Dawson SJ; Lok S; O'Connell S; Greening S; Nightingale S; Edwards S; Fox S; McLachlan SA; Lakhani S; Thomas S; Antill Y, 2018, 'Heritable DNA methylation marks associated with susceptibility to breast cancer /631/67/69 /631/337/176/1988 /692/699/67/1347 /692/308/2056 /45 /45/61 article', Nature Communications, vol. 9, http://dx.doi.org/10.1038/s41467-018-03058-6
2018
Evangelou E; Warren HR; Mosen-Ansorena D; Mifsud B; Pazoki R; Gao H; Ntritsos G; Dimou N; Cabrera CP; Karaman I; Ng FL; Evangelou M; Witkowska K; Tzanis E; Hellwege JN; Giri A; Velez Edwards DR; Sun YV; Cho K; Gaziano JM; Wilson PWF; Tsao PS; Kovesdy CP; Esko T; Mägi R; Milani L; Almgren P; Boutin T; Debette S; Ding J; Giulianini F; Holliday EG; Jackson AU; Li-Gao R; Lin WY; Luan J; Mangino M; Oldmeadow C; Prins BP; Qian Y; Sargurupremraj M; Shah N; Surendran P; Thériault S; Verweij N; Willems SM; Zhao JH; Amouyel P; Connell J; de Mutsert R; Doney ASF; Farrall M; Menni C; Morris AD; Noordam R; Paré G; Poulter NR; Shields DC; Stanton A; Thom S; Abecasis G; Amin N; Arking DE; Ayers KL; Barbieri CM; Batini C; Bis JC; Blake T; Bochud M; Boehnke M; Boerwinkle E; Boomsma DI; Bottinger EP; Braund PS; Brumat M; Campbell A; Campbell H; Chakravarti A; Chambers JC; Chauhan G; Ciullo M; Cocca M; Collins F; Cordell HJ; Davies G; de Borst MH; de Geus EJ; Deary IJ; Deelen J; Del Greco M F; Demirkale CY; Dörr M; Ehret GB; Elosua R; Enroth S; Erzurumluoglu AM; Ferreira T; Frånberg M; Franco OH; Gandin I, 2018, 'Erratum to: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (Nature Genetics, (2018), 50, 10, (1412-1425), 10.1038/s41588-018-0205-x)', Nature Genetics, vol. 50, pp. 1755, http://dx.doi.org/10.1038/s41588-018-0297-3
2018
Abdullah N; Murad NAA; Attia J; Oldmeadow C; Kamaruddin MA; Jalal NA; Ismail N; Jamal R; Scott RJ; Holliday EG, 2018, 'Differing Contributions of Classical Risk Factors to Type 2 Diabetes in Multi-Ethnic Malaysian Populations.', Int J Environ Res Public Health, vol. 15, http://dx.doi.org/10.3390/ijerph15122813
2018
Xavier MJ; Mitchell LA; McEwan KE; Scott RJ; Aitken RJ, 2018, 'Genomic integrity in the male germ line: evidence in support of the disposable soma hypothesis.', Reproduction, vol. 156, pp. 269 - 282, http://dx.doi.org/10.1530/REP-18-0202
2018
Ko Y-A; Jamaluddin MFB; Adebayo M; Bajwa P; Scott RJ; Dharmarajan AM; Nahar P; Tanwar PS, 2018, 'Extracellular matrix (ECM) activates β-catenin signaling in uterine fibroids.', Reproduction, vol. 155, pp. 61 - 71, http://dx.doi.org/10.1530/REP-17-0339
2018
Wu L; Shi W; Long J; Guo X; Michailidou K; Beesley J; Bolla MK; Shu XO; Lu Y; Cai Q; Al-Ejeh F; Rozali E; Wang Q; Dennis J; Li B; Zeng C; Feng H; Gusev A; Barfield RT; Andrulis IL; Anton-Culver H; Arndt V; Aronson KJ; Auer PL; Barrdahl M; Baynes C; Beckmann MW; Benitez J; Bermisheva M; Blomqvist C; Bogdanova NV; Bojesen SE; Brauch H; Brenner H; Brinton L; Broberg P; Brucker SY; Burwinkel B; Caldés T; Canzian F; Carter BD; Castelao JE; Chang-Claude J; Chen X; Cheng TYD; Christiansen H; Clarke CL; Collée M; Cornelissen S; Couch FJ; Cox D; Cox A; Cross SS; Cunningham JM; Czene K; Daly MB; Devilee P; Doheny KF; Dörk T; Dos-Santos-Silva I; Dumont M; Dwek M; Eccles DM; Eilber U; Eliassen AH; Engel C; Eriksson M; Fachal L; Fasching PA; Figueroa J; Flesch-Janys D; Fletcher O; Flyger H; Fritschi L; Gabrielson M; Gago-Dominguez M; Gapstur SM; García-Closas M; Gaudet MM; Ghoussaini M; Giles GG; Goldberg MS; Goldgar DE; González-Neira A; Guénel P; Hahnen E; Haiman CA; Håkansson N; Hall P; Hallberg E; Hamann U; Harrington P; Hein A; Hicks B; Hillemanns P; Hollestelle A; Hoover RN; Hopper JL; Huang G; Humphreys K, 2018, 'A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer', Nature Genetics, vol. 50, pp. 968 - 978, http://dx.doi.org/10.1038/s41588-018-0132-x
2018
Rhead B; Brorson IS; Berge T; Adams C; Quach H; Moen SM; Berg-Hansen P; Celius EG; Sangurdekar DP; Bronson PG; Lea RA; Burnard S; Maltby VE; Scott RJ; Lechner-Scott J; Harbo HF; Bos SD; Barcellos LF, 2018, 'Increased DNA methylation of SLFN12 in CD4+ and CD8+ T cells from multiple sclerosis patients.', PLoS One, vol. 13, pp. e0206511, http://dx.doi.org/10.1371/journal.pone.0206511
2018
Groen K; Maltby VE; Lea RA; Sanders KA; Fink JL; Scott RJ; Tajouri L; Lechner-Scott J, 2018, 'Erythrocyte microRNA sequencing reveals differential expression in relapsing-remitting multiple sclerosis.', BMC Med Genomics, vol. 11, pp. 48, http://dx.doi.org/10.1186/s12920-018-0365-7
2018
Ligthart S; Vaez A; Võsa U; Stathopoulou MG; de Vries PS; Prins BP; Van der Most PJ; Tanaka T; Naderi E; Rose LM; Wu Y; Karlsson R; Barbalic M; Lin H; Pool R; Zhu G; Macé A; Sidore C; Trompet S; Mangino M; Sabater-Lleal M; Kemp JP; Abbasi A; Kacprowski T; Verweij N; Smith AV; Huang T; Marzi C; Feitosa MF; Lohman KK; Kleber ME; Milaneschi Y; Mueller C; Huq M; Vlachopoulou E; Lyytikäinen L-P; Oldmeadow C; Deelen J; Perola M; Zhao JH; Feenstra B; LifeLines Cohort Study ; Amini M; CHARGE Inflammation Working Group ; Lahti J; Schraut KE; Fornage M; Suktitipat B; Chen W-M; Li X; Nutile T; Malerba G; Luan J; Bak T; Schork N; Del Greco M F; Thiering E; Mahajan A; Marioni RE; Mihailov E; Eriksson J; Ozel AB; Zhang W; Nethander M; Cheng Y-C; Aslibekyan S; Ang W; Gandin I; Yengo L; Portas L; Kooperberg C; Hofer E; Rajan KB; Schurmann C; den Hollander W; Ahluwalia TS; Zhao J; Draisma HHM; Ford I; Timpson N; Teumer A; Huang H; Wahl S; Liu Y; Huang J; Uh H-W; Geller F; Joshi PK; Yanek LR; Trabetti E; Lehne B; Vozzi D; Verbanck M; Biino G; Saba Y; Meulenbelt I; O'Connell JR; Laakso M; Giulianini F; Magnusson PKE; Ballantyne CM; Hottenga JJ; Montgomery GW; Rivadineira F; Rueedi R; Steri M; Herzig K-H; Stott DJ; Menni C; Frånberg M; St Pourcain B; Felix SB; Pers TH; Bakker SJL; Kraft P; Peters A; Vaidya D; Delgado G; Smit JH; Großmann V; Sinisalo J; Seppälä I; Williams SR; Holliday EG; Moed M; Langenberg C; Räikkönen K; Ding J; Campbell H; Sale MM; Chen Y-DI; James AL; Ruggiero D; Soranzo N; Hartman CA; Smith EN; Berenson GS; Fuchsberger C; Hernandez D; Tiesler CMT; Giedraitis V; Liewald D; Fischer K; Mellström D; Larsson A; Wang Y; Scott WR; Lorentzon M; Beilby J; Ryan KA; Pennell CE; Vuckovic D; Balkau B; Concas MP; Schmidt R; Mendes de Leon CF; Bottinger EP; Kloppenburg M; Paternoster L; Boehnke M; Musk AW; Willemsen G; Evans DM; Madden PAF; Kähönen M; Kutalik Z; Zoledziewska M; Karhunen V; Kritchevsky SB; Sattar N; Lachance G; Clarke R; Harris TB; Raitakari OT; Attia JR; van Heemst D; Kajantie E; Sorice R; Gambaro G; Scott RA; Hicks AA; Ferrucci L; Standl M; Lindgren CM; Starr JM; Karlsson M; Lind L; Li JZ; Chambers JC; Mori TA; de Geus EJCN; Heath AC; Martin NG; Auvinen J; Buckley BM; de Craen AJM; Waldenberger M; Strauch K; Meitinger T; Scott RJ; McEvoy M; Beekman M; Bombieri C; Ridker PM; Mohlke KL; Pedersen NL; Morrison AC; Boomsma DI; Whitfield JB; Strachan DP; Hofman A; Vollenweider P; Cucca F; Jarvelin M-R; Jukema JW; Spector TD; Hamsten A; Zeller T; Uitterlinden AG; Nauck M; Gudnason V; Qi L; Grallert H; Borecki IB; Rotter JI; März W; Wild PS; Lokki M-L; Boyle M; Salomaa V; Melbye M; Eriksson JG; Wilson JF; Penninx BWJH; Becker DM; Worrall BB; Gibson G; Krauss RM; Ciullo M; Zaza G; Wareham NJ; Oldehinkel AJ; Palmer LJ; Murray SS; Pramstaller PP; Bandinelli S; Heinrich J; Ingelsson E; Deary IJ; Mägi R; Vandenput L; van der Harst P; Desch KC; Kooner JS; Ohlsson C; Hayward C; Lehtimäki T; Shuldiner AR; Arnett DK; Beilin LJ; Robino A; Froguel P; Pirastu M; Jess T; Koenig W; Loos RJF; Evans DA; Schmidt H; Smith GD; Slagboom PE; Eiriksdottir G; Morris AP; Psaty BM; Tracy RP; Nolte IM; Boerwinkle E; Visvikis-Siest S; Reiner AP; Gross M; Bis JC; Franke L; Franco OH; Benjamin EJ; Chasman DI; Dupuis J; Snieder H; Dehghan A; Alizadeh BZ, 2018, 'Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders.', Am J Hum Genet, vol. 103, pp. 691 - 706, http://dx.doi.org/10.1016/j.ajhg.2018.09.009
2018
Fullerton JM; Klauser P; Lenroot RK; Shaw AD; Overs B; Heath A; Cairns MJ; Atkins J; Scott R; Schofield PR; Weickert CS; Pantelis C; Fornito A; Whitford TJ; Weickert TW; Zalesky A, 2018, 'Differential effect of disease-associated ST8SIA2 haplotype on cerebral white matter diffusion properties in schizophrenia and healthy controls', Translational Psychiatry, vol. 8, http://dx.doi.org/10.1038/s41398-017-0052-z
2018
Dębniak T; Scott RJ; Górski B; Masojć B; Kram A; Maleszka R; Cybulski C; Paszkowska-Szczur K; Kashyap A; Murawa D; Malińska K; Kiedrowicz M; Rogoża-Janiszewska E; Rudnicka H; Deptuła J; Domagała P; Kluźniak W; Lener MR; Lubiński J, 2018, 'BRCA1/2 mutations are not a common cause of malignant melanoma in the Polish population.', PLoS One, vol. 13, pp. e0204768, http://dx.doi.org/10.1371/journal.pone.0204768
2018
Scott RJ; Willink PW; Norton BM, 2018, 'Biogeography and Distribution of the Cryptic Species Rosyface ShinerNotropis rubellusand Carmine ShinerNotropis percobromusin Illinois', Copeia, vol. 106, pp. 524 - 531, http://dx.doi.org/10.1643/ci-17-668
2018
Holmes M; Connor T; Oldmeadow C; Pockney PG; Scott RJ; Talseth-Palmer BA, 2018, 'CD36 - a plausible modifier of disease phenotype in familial adenomatous polyposis.', Hered Cancer Clin Pract, vol. 16, pp. 14, http://dx.doi.org/10.1186/s13053-018-0096-y
2018
Cox AJ; Zhang P; Evans TJ; Scott RJ; Cripps AW; West NP, 2018, 'Gene expression profiles in whole blood and associations with metabolic dysregulation in obesity.', Obes Res Clin Pract, vol. 12, pp. 204 - 213, http://dx.doi.org/10.1016/j.orcp.2017.07.001
2018
Painter JN; O'Mara TA; Morris AP; Cheng THT; Gorman M; Martin L; Hodson S; Jones A; Martin NG; Gordon S; Henders AK; Attia J; McEvoy M; Holliday EG; Scott RJ; Webb PM; Fasching PA; Beckmann MW; Ekici AB; Hein A; Rübner M; Hall P; Czene K; Dörk T; Dürst M; Hillemanns P; Runnebaum I; Lambrechts D; Amant F; Annibali D; Depreeuw J; Vanderstichele A; Goode EL; Cunningham JM; Dowdy SC; Winham SJ; Trovik J; Hoivik E; Werner HMJ; Krakstad C; Ashton K; Otton G; Proietto T; Tham E; Mints M; Ahmed S; Healey CS; Shah M; Pharoah PDP; Dunning AM; Dennis J; Bolla MK; Michailidou K; Wang Q; Tyrer JP; Hopper JL; Peto J; Swerdlow AJ; Burwinkel B; Brenner H; Meindl A; Brauch H; Lindblom A; Chang-Claude J; Couch FJ; Giles GG; Kristensen VN; Cox A; Zondervan KT; Nyholt DR; MacGregor S; Montgomery GW; Tomlinson I; Easton DF; Thompson DJ; Spurdle AB, 2018, 'Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses.', Cancer Med, vol. 7, pp. 1978 - 1987, http://dx.doi.org/10.1002/cam4.1445
2018
Scott R; Bardach E, 2018, 'A comparison of management adaptations for joined‐up government: Lessons from New Zealand', Australian Journal of Public Administration, http://dx.doi.org/10.1111/1467-8500.12348
2018
Wyss AB; Sofer T; Lee MK; Terzikhan N; Nguyen JN; Lahousse L; Latourelle JC; Smith AV; Bartz TM; Feitosa MF; Gao W; Ahluwalia TS; Tang W; Oldmeadow C; Duan Q; de Jong K; Wojczynski MK; Wang X-Q; Noordam R; Hartwig FP; Jackson VE; Wang T; Obeidat M; Hobbs BD; Huan T; Gui H; Parker MM; Hu D; Mogil LS; Kichaev G; Jin J; Graff M; Harris TB; Kalhan R; Heckbert SR; Paternoster L; Burkart KM; Liu Y; Holliday EG; Wilson JG; Vonk JM; Sanders JL; Barr RG; de Mutsert R; Menezes AMB; Adams HHH; van den Berge M; Joehanes R; Levin AM; Liberto J; Launer LJ; Morrison AC; Sitlani CM; Celedón JC; Kritchevsky SB; Scott RJ; Christensen K; Rotter JI; Bonten TN; Wehrmeister FC; Bossé Y; Xiao S; Oh S; Franceschini N; Brody JA; Kaplan RC; Lohman K; McEvoy M; Province MA; Rosendaal FR; Taylor KD; Nickle DC; Williams LK; Burchard EG; Wheeler HE; Sin DD; Gudnason V; North KE; Fornage M; Psaty BM; Myers RH; O'Connor G; Hansen T; Laurie CC; Cassano PA; Sung J; Kim WJ; Attia JR; Lange L; Boezen HM; Thyagarajan B; Rich SS; Mook-Kanamori DO; Horta BL; Uitterlinden AG; Im HK; Cho MH; Brusselle GG; Gharib SA; Dupuis J; Manichaikul A; London SJ, 2018, 'Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function.', Nat Commun, vol. 9, pp. 2976, http://dx.doi.org/10.1038/s41467-018-05369-0
2018
Białkowska K; Marciniak W; Muszyńska M; Baszuk P; Gupta S; Jaworska-Bieniek K; Sukiennicki G; Durda K; Gromowski T; Prajzendanc K; Cybulski C; Huzarski T; Gronwald J; Dębniak T; Scott RJ; Lubiński J; Jakubowska A, 2018, 'Association of zinc level and polymorphism in MMP-7 gene with prostate cancer in Polish population.', PLoS One, vol. 13, pp. e0201065, http://dx.doi.org/10.1371/journal.pone.0201065
2018
Evangelou E; Warren HR; Mosen-Ansorena D; Mifsud B; Pazoki R; Gao H; Ntritsos G; Dimou N; Cabrera CP; Karaman I; Ng FL; Evangelou M; Witkowska K; Tzanis E; Hellwege JN; Giri A; Velez Edwards DR; Sun YV; Cho K; Gaziano JM; Wilson PWF; Tsao PS; Kovesdy CP; Esko T; Mägi R; Milani L; Almgren P; Boutin T; Debette S; Ding J; Giulianini F; Holliday EG; Jackson AU; Li-Gao R; Lin WY; Luan J; Mangino M; Oldmeadow C; Prins BP; Qian Y; Sargurupremraj M; Shah N; Surendran P; Thériault S; Verweij N; Willems SM; Zhao JH; Amouyel P; Connell J; de Mutsert R; Doney ASF; Farrall M; Menni C; Morris AD; Noordam R; Paré G; Poulter NR; Shields DC; Stanton A; Thom S; Abecasis G; Amin N; Arking DE; Ayers KL; Barbieri CM; Batini C; Bis JC; Blake T; Bochud M; Boehnke M; Boerwinkle E; Boomsma DI; Bottinger EP; Braund PS; Brumat M; Campbell A; Campbell H; Chakravarti A; Chambers JC; Chauhan G; Ciullo M; Cocca M; Collins F; Cordell HJ; Davies G; Borst MHD; Geus EJD; Deary IJ; Deelen J; Del Greco M F; Demirkale CY; Dörr M; Ehret GB; Elosua R; Enroth S; Erzurumluoglu AM; Ferreira T; Frånberg M; Franco OH; Gandin I, 2018, 'Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits', Nature Genetics, vol. 50, pp. 1412 - 1425, http://dx.doi.org/10.1038/s41588-018-0205-x
2018
Li N; Rowley SM; Goode DL; Amarasinghe KC; McInerny S; Devereux L; LifePool Investigators ; Wong-Brown MW; Lupat R; Lee JEA; Hughes S; Thompson ER; Zethoven M; Li J; Trainer AH; Gorringe KL; Scott RJ; James PA; Campbell IG, 2018, 'Mutations in RECQL are not associated with breast cancer risk in an Australian population.', Nat Genet, vol. 50, pp. 1346 - 1348, http://dx.doi.org/10.1038/s41588-018-0206-9
2018
Grasby K; Jahanshad N; Painter J; Colodro-Conde L; Bralten J; Hibar D; Lind P; Pizzagalli F; Ching CRK; McMahon MA; Shatokhina N; Zsembik LCP; Agartz I; Alhusaini S; Almeida MAA; Alnæs D; Amlien I; Andersson M; Ard T; Armstrong N; Ashley-Koch A; Atkins J; Bernard M; Brouwer R; Buimer EEL; Bülow R; Bürger C; Cannon D; Chakravarty M; Chen Q; Cheung J; Couvy-Duchesne B; Dale A; Dalvie S; de Araujo T; de Zubicaray G; de Zwarte SMC; den Braber A; Doan NT; Dohm K; Ehrlich S; Engelbrecht H-R; Erk S; Fan CC; Fedko I; Foley S; Ford J; Fukunaga M; Garrett M; Ge T; Giddaluru S; Goldman A; Green M; Groenewold N; Grotegerd D; Gurholt T; Gutman B; Hansell N; Harris M; Harrison M; Haswell C; Hauser M; Herms S; Heslenfeld D; Ho NF; Hoehn D; Hoffmann P; Holleran L; Hoogman M; Hottenga J-J; Ikeda M; Janowitz D; Jansen I; Jia T; Jockwitz C; Kanai R; Karama S; Kasperaviciute D; Kaufmann T; Kelly S; Kikuchi M; Klein M; Knapp M; Knodt A; Krämer B; Lam M; Lancaster T; Lee P; Lett T; Lewis L; Lopes-Cendes I; Luciano M; Macciardi F; Marquand A; Mathias S; Melzer T; Milaneschi Y; Mirza-Schreiber N; Moreira JCV; Mühleisen T; Müller-Myhsok B; Najt P; Nakahara S; Nho K; Olde Loohuis L; Orfanos DP; Pearson J; Pitcher T; Pütz B; Quidé Y; Ragothaman A; Rashid F; Reay W; Redlich R; Reinbold C; Repple J; Richard G; Riedel B; Risacher S; Rocha C; Mota NR; Salminen L; Saremi A; Saykin A; Schlag F; Schmaal L; Schofield P; Secolin R; Shapland CY; Shen L; Shin J; Shumskaya E; Sønderby I; Sprooten E; Strike L; Tansey K; Teumer A; Thalamuthu A; Thomopoulos S; Tordesillas-Gutiérrez D; Turner J; Uhlmann A; Vallerga CL; van der Meer D; van Donkelaar MMJ; van Eijk L; van Erp TGM; van Haren NEM; van Rooij D; van Tol M-J; Veldink J; Verhoef E; Walton E; Wang M; Wang Y; Wardlaw J; Wen W; Westlye L; Whelan C; Witt S; Wittfeld K; Wolf C; Wolfers T; Wu JQ; Yasuda C; Zaremba D; Zhang Z; Zhu A; Zwiers M; Artiges E; Assareh A; Ayesa-Arriola R; Belger A; Brandt C; Brown G; Cichon S; Curran J; Davies G; Degenhardt F; Dennis M; Dietsche B; Djurovic S; Doherty C; Espiritu R; Garijo D; Gil Y; Gowland P; Green R; Häusler A; Heindel W; Ho B-C; Hoffmann W; Holsboer F; Homuth G; Hosten N; Jack C; Jang M; Jansen A; Kimbrel N; Kolskår K; Koops S; Krug A; Lim K; Luykx J; Mathalon D; Mather K; Mattay V; Matthews S; Van Son JM; McEwen S; Melle I; Morris D; Mueller B; Nauck M; Nordvik J; Nöthen M; O’Leary D; Opel N; Paillère Martinot ML; Pike B; Preda A; Quinlan E; Rasser P; Ratnakar V; Reppermund S; Steen V; Tooney P; To F, 2018, 'The genetic architecture of the human cerebral cortex', , http://dx.doi.org/10.1101/399402
2018
Corbett J; Grube DC; Lovell H; Scott R, 2018, 'Singular memory or institutional memories? Toward a dynamic approach', Governance, vol. 31, pp. 555 - 573, http://dx.doi.org/10.1111/gove.12340
2018
Burnard S; Lechner-Scott J; Scott RJ, 2017, 'EBV and MS: Major cause, minor contribution or red-herring?', Mult Scler Relat Disord, vol. 16, pp. 24 - 30, http://dx.doi.org/10.1016/j.msard.2017.06.002
2017
Schmiegel W; Scott RJ; Dooley S; Lewis W; Meldrum CJ; Pockney P; Draganic B; Smith S; Hewitt C; Philimore H; Lucas A; Shi E; Namdarian K; Chan T; Acosta D; Ping-Chang S; Tannapfel A; Reinacher-Schick A; Uhl W; Teschendorf C; Wolters H; Stern J; Viebahn R; Friess H; Janssen K-P; Nitsche U; Slotta-Huspenina J; Pohl M; Vangala D; Baraniskin A; Dockhorn-Dworniczak B; Hegewisch-Becker S; Ronga P; Edelstein DL; Jones FS; Hahn S; Fox SB, 2017, 'Blood-based detection of RAS mutations to guide anti-EGFR therapy in colorectal cancer patients: concordance of results from circulating tumor DNA and tissue-based RAS testing.', Mol Oncol, vol. 11, pp. 208 - 219, http://dx.doi.org/10.1002/1878-0261.12023
2017
Berry N; Dixon-McIver A; Scott R; Ziolkowski A; Enjeti A, 2017, 'Evaluation of Integrating HD-SNP Microarray Into the Workflow for CLL and MM: Challenges and Culture Changes', Cancer Genetics, vol. 214-215, pp. 44 - 44, http://dx.doi.org/10.1016/j.cancergen.2017.04.040
2017
Davies G; Lam M; Harris S; Trampush J; Luciano M; Hill D; Hagenaars S; Ritchie S; Marioni R; Fawns-Ritchie C; Liewald DCM; Okely J; Ahola-Olli A; Barnes CLK; Bertram L; Bis J; Burdick K; Christoforou A; DeRosse P; Djurovic S; Espeseth T; Giakoumaki S; Giddaluru S; Gustavson D; Hayward C; Hofer E; Ikram A; Karlsson R; Knowles E; Lahti J; Leber M; Li S; Mather K; Melle I; Morris D; Oldmeadow C; Palviainen T; Payton A; Pazoki R; Petrovic K; Reynolds C; Sargurupremraj M; Scholz M; Smith J; Smith A; Terzikhan N; Thalamuthu A; Trompet S; Lee SVD; Ware E; Windham G; Wright M; Yang J; Yu J; Ames D; Amin N; Amouyel P; Andreassen O; Armstrong N; Assareh A; Attia J; Attix D; Avramopoulos D; Bennett D; Böhmer A; Boyle P; Brodaty H; Campbell H; Cannon T; Cirulli E; Congdon E; Conley ED; Corley J; Cox S; Dale A; Dehghan A; Dick D; Dickinson D; Eriksson J; Evangelou E; Faul J; Ford I; Freimer N; Gao H; Giegling I; Gillespie N; Gordon S; Gottesman R; Griswold M; Gudnason V; Harris T; Hartmann A; Hatzimanolis A; Heiss G; Holliday E; Joshi P; Kähönen M; Kardia SLR; Karlsson I; Kleineidam L; Knopman D; Kochan N; Konte B; Kwok J; Hellard SL; Lee T; Lehtimäki T; Li S-C; Liu T; Koini M; London E; Longstreth W; Lopez O; Loukola A; Luck T; Lundervold A; Lundquist A; Lyytikäinen L-P; Martin N; Montgomery G; Murray A; Need A; Noordam R; Nyberg L; Ollier W; Papenberg G; Pattie A; Polasek O; Poldrack R; Psaty B; Reppermund S; Riedel-Heller S; Rose R; Rotter J; Roussos P; Rovio S; Saba Y; Sabb F; Sachdev P; Satizabal C; Schmid M; Scott R; Scult M; Simino J; Slagboom E; Smyrnis N; Soumaré A; Stefanis N; Stott D; Straub R; Sundet K; Taylor A; Taylor K; Tzoulaki I; Tzourio C; Uitterlinden A; Vitart V; Voineskos A; Kaprio J; Wagner M; Wagner H; Weinhold L; Wen H; Widen E; Yang Q; Zhao W; Adams HHH; Arking D; Bilder R; Bitsios P; Boerwinkle E; Chiba-Falek O; Corvin A; Jager PD; Debette S; Donohoe G; Elliott P; Fitzpatrick A; Gill M; Glahn D; Hägg S; Hansell N; Hariri A; Ikram K; Jukema W; Vuoksimaa E; Keller M; Kremen W; Launer L; Lindenberger U; Palotie A; Pedersen N; Pendleton N; Porteous D; Räikkönen K; Raitakari O; Ramirez A; Reinvang I; Rudan I; Rujescu D; Schmidt R; Schmidt H; Schofield P; Schofield P; Starr J; Steen V; Trollor J; Turner S; Duijn CV; Villringer A; Weinberger D; Weir D; Wilson J; Malhotra A; McIntosh A; Gale C; Seshadri S; Mosley T; Bressler J; Lencz T; Deary I, 2017, 'Ninety-nine independent genetic loci influencing general cognitive function include genes associated with brain health and structure (N = 280,360)', , http://dx.doi.org/10.1101/176511
2017
Gorski M; Most PJVD; Teumer A; Chu AY; Li M; Mijatovic V; Nolte IM; Cocca M; Taliun D; Gomez F; Li Y; Tayo B; Tin A; Feitosa MF; Aspelund T; Attia J; Biffar R; Bochud M; Boerwinkle E; Borecki I; Bottinger EP; Chen M-H; Chouraki V; Ciullo M; Coresh J; Cornelis MC; Curhan GC; Adamo APD; Dehghan A; Dengler L; Ding J; Eiriksdottir G; Endlich K; Enroth S; Esko T; Franco OH; Gasparini P; Gieger C; Girotto G; Gottesman O; Gudnason V; Gyllensten U; Hancock SJ; Harris TB; Helmer C; Höllerer S; Hofer E; Hofman A; Holliday EG; Homuth G; Hu FB; Huth C; Hutri-Kähönen N; Hwang S-J; Imboden M; Johansson Å; Kähönen M; König W; Kramer H; Krämer BK; Kumar A; Kutalik Z; Lambert J-C; Launer LJ; Lehtimäki T; de Borst MH; Navis G; Swertz M; Liu Y; Lohman K; Loos RJF; Lu Y; Lyytikäinen L-P; McEvoy MA; Meisinger C; Meitinger T; Metspalu A; Metzger M; Mihailov E; Mitchell P; Nauck M; Oldehinkel AJ; Olden M; Wjh Penninx B; Pistis G; Pramstaller PP; Probst-Hensch N; Raitakari OT; Rettig R; Ridker PM; Rivadeneira F; Robino A; Rosas SE; Ruderfer D; Ruggiero D; Saba Y; Sala C; Schmidt H; Schmidt R; Scott RJ; Sedaghat S; Smith AV; Sorice R; Stengel B; Stracke S; Strauch K; Toniolo D; Uitterlinden AG; Ulivi S; Viikari JS; Völker U; Vollenweider P; Völzke H; Vuckovic D; Waldenberger M; Wang JJ; Yang Q; Chasman DI; Tromp G; Snieder H; Heid IM; Fox CS; Köttgen A; Pattaro C; Böger CA; Fuchsberger C, 2017, 'Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.', Sci Rep, vol. 7, pp. 46835, http://dx.doi.org/10.1038/srep46835
2017
Abdullah N; Abdul Murad NA; Mohd Haniff EA; Syafruddin SE; Attia J; Oldmeadow C; Kamaruddin MA; Abd Jalal N; Ismail N; Ishak M; Jamal R; Scott RJ; Holliday EG, 2017, 'Predicting type 2 diabetes using genetic and environmental risk factors in a multi-ethnic Malaysian cohort.', Public Health, vol. 149, pp. 31 - 38, http://dx.doi.org/10.1016/j.puhe.2017.04.003
2017
Gorski M; Van Der Most PJ; Teumer A; Chu AY; Li M; Mijatovic V; Nolte IM; Cocca M; Taliun D; Gomez F; Li Y; Tayo B; Tin A; Feitosa MF; Aspelund T; Attia J; Biffar R; Bochud M; Boerwinkle E; Borecki I; Bottinger EP; Chen MH; Chouraki V; Ciullo M; Coresh J; Cornelis MC; Curhan GC; D'Adamo AP; Dehghan A; Dengler L; Ding J; Eiriksdottir G; Endlich K; Enroth S; Esko T; Franco OH; Gasparini P; Gieger C; Girotto G; Gottesman O; Gudnason V; Gyllensten U; Hancock SJ; Harris TB; Helmer C; Höllerer S; Hofer E; Hofman A; Holliday EG; Homuth G; Hu FB; Huth C; Hutri-Kähönen N; Hwang SJ; Imboden M; Johansson A; Kähönen M; König W; Kramer H; Krämer BK; Kumar A; Kutalik Z; Lambert JC; Launer LJ; Lehtimäki T; De Borst MH; Navis G; Swertz M; Liu Y; Lohman K; Loos RJF; Lu Y; Lyytikäinen LP; McEvoy MA; Meisinger C; Meitinger T; Metspalu A; Metzger M; Mihailov E; Mitchell P; Nauck M; Oldehinkel AJ; Olden M; Penninx BWJH; Pistis G; Pramstaller PP; Probst-Hensch N; Raitakari OT; Rettig R; Ridker PM; Rivadeneira F; Robino A; Rosas SE; Ruderfer D; Ruggiero D; Saba Y; Sala C; Schmidt H; Schmidt R; Scott RJ, 2017, '1000 Genomes-based metaanalysis identifies 10 novel loci for kidney function', Scientific Reports, vol. 7, http://dx.doi.org/10.1038/srep45040
2017
Smith-Anttila CJA; Bensing S; Alimohammadi M; Dalin F; Oscarson M; Zhang MD; Perheentupa J; Husebye ES; Gustafsson J; Björklund P; Fransson A; Nordmark G; Rönnblom L; Meloni A; Scott RJ; Hökfelt T; Crock PA; Kämpe O, 2017, 'Identification of endothelin-converting enzyme-2 as an autoantigen in autoimmune polyendocrine syndrome type 1', Autoimmunity, vol. 50, pp. 223 - 231, http://dx.doi.org/10.1080/08916934.2017.1332183
2017
Gromowski T; Gapska P; Scott RJ; Kąklewski K; Marciniak W; Durda K; Lener M; Górski B; Cybulski C; Sukiennicki G; Kaczmarek K; Jaworska-Bieniek K; Paszkowska-Szczur K; Waloszczyk P; Lubiński J; Dębniak T, 2017, 'Serum 25(OH)D concentration, common variants of the VDR gene and lung cancer occurrence.', Int J Cancer, vol. 141, pp. 336 - 341, http://dx.doi.org/10.1002/ijc.30740
2017
Naudin C; Smith B; Bond DR; Dun MD; Scott RJ; Ashman LK; Weidenhofer J; Roselli S, 2017, 'Characterization of the early molecular changes in the glomeruli of Cd151 -/- mice highlights induction of mindin and MMP-10.', Sci Rep, vol. 7, pp. 15987, http://dx.doi.org/10.1038/s41598-017-15993-3
2017
Dymerska D; Gołębiewska K; Kuświk M; Rudnicka H; Scott RJ; Billings R; Pławski A; Boruń P; Siołek M; Kozak-Klonowska B; Szwiec M; Kilar E; Huzarski T; Byrski T; Lubiński J; Kurzawski G, 2017, 'New EPCAM founder deletion in Polish population.', Clin Genet, vol. 92, pp. 649 - 653, http://dx.doi.org/10.1111/cge.13026
2017
Cybulski C; Kluźniak W; Huzarski T; Wokołorczyk D; Kashyap A; Jakubowska A; Szwiec M; Byrski T; Dębniak T; Górski B; Sopik V; Akbari MR; Sun P; Gronwald J; Narod SA; Lubiński J; Dębniak T; Dymerska D; Kurzawski G; Lubiński J; Dymerska D; Tutlewska K; Kuswik M; Rudnicka H; Scott RJ; Billings R; Pławski A; Lubinski J; Kurzawski G; Gromowski T; Kąklewski K; Marciniak W; Durda K; Lener M; Sukiennicki G; Kaczmarek K; Jaworska-Bieniek K; Paszkowska-Szczur K; Waloszczyk P; Lubiński J; Dębniak T; Gronwald J; Hemminki K; Försti A; Huzarski T; Gronwald J; Cybulski C; Oszurek O; Szwiec M; Gugała K; Stawicka M; Morawiec Z; Mierzwa T; Falco M; Janiszewska H; Kilar E; Marczyk E; Kozak-Klonowska B; Siołek M; Surdyka D; Wiśniowski R; Posmyk M; Domagała P; Byrski T; Sun P; Lubiński J; Narod SA; Imyanitov EN; Kaczmarek K; Muszyńska M; Marciniak W; Sukiennicki G; Lener M; Durda K; Jaworska-Bieniek K; Gromowski T; Prajzendanc K; Peruga N; Huzarski T; Byrski T; Gronwald J; Cybulski C; Dębniak T; Morawski A; Jakubowska A; Lubiński J; Lener MR; Scott RJ; Kluźniak W; Gronwald J; Baszuk P; Cybulski C; Wiechowska-Kozłowska A; Huzarski T; Kładny J; Pietrzak S; Soluch A; Jakubowska A; Lubiński J; Plawski A; Prajzendanc K; Jakubowska A; Lubiński J; Rashid UR; Naeemi H; Muhammad N; Lubiński J; Jakubowska A; Loya A; Yusuf MA; Savanevich A; Aszurek O; Gronwald J; Lubiński J; Mathe A; Wong-Brown M; Locke W; Stirzaker C; Braye SG; Forbes JF; Clark S; Avery-Kiejda K; Scott RJ; Tomiczek-Szwiec J; Huzarski T; Szwiec M; Gronwald J; Cybulski C; Marczyk E; Jakubowicz J; Kilar E; Sibilski R; Stawicka M; Morawiec Z; Mierzwa T; Falco M; Janiszewska H; Kozak-Klonowska B; Siołek M; Surdyka D; Wiśniowski R; Posmyk R; Domagała P; Lubiński J; Szwiec M; Tomiczek-Szwiec J; Huzarski T; Cybulski C; Lubiński J, 2017, 'Meeting abstracts from the Annual Conference on Hereditary Cancers 2016', Hereditary Cancer in Clinical Practice, vol. 15, http://dx.doi.org/10.1186/s13053-017-0081-x
2017
Hansen MF; Johansen J; Sylvander AE; Bjørnevoll I; Talseth-Palmer BA; Lavik LAS; Xavier A; Engebretsen LF; Scott RJ; Drabløs F; Sjursen W, 2017, 'Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome.', Clin Genet, vol. 92, pp. 405 - 414, http://dx.doi.org/10.1111/cge.12994
2017
Thompson ER; Wong-Brown M; Rowley SM; Dooley S; Lil N; Hipwell M; McInerny S; Meldrum C; Devereux L; Mossman D; Trainer AH; Millar B-R; Mitchell G; Smith C; James PA; Campbell IG; Scott RJ; Klonowska K; Jakubowska A; Maksimenko J; Irmejs A; Nakazawa-Miklasevica M; Melbarde-Gorkusa I; Trofimovics G; Gardovskis J; Miklasevics E; Tęcza K; Pamuła-Piłat J; Łanuszewska J; Grzybowska E; Miklasevics E; Szwiec M; Tomiczek-Szwiec J; Gełej M; Cybulski C; Huzarski T; Kilar E; Oczko-Wojciechowska M; Świerniak M; Krajewska J; Kowalska M; Tyszkiewicz T; Pawlaczek A; Jarząb M; Kowal M; Rusinek D; Zebracka-Gala J; Czarniecka A; Jarzab B; Plawski A; Borun P; Szczepinska J; Siolek M; Kozak-Klonowska B; Kaczmarek K; Muszyńska M; Marciniak W; Sukiennicki G; Lener M; Durda K; Jaworska-Bieniek K; Gromowski T; Huzarski T; Byrski T; Gronwald J; Oszurek O; Cybulski C; Dębniak T; Morawski A; Jakubowska A; Lubiński J; Sukiennicki G; Muszyńska M; Marciniak W; Kaczmarek K; Lener M; Durda K; Jaworska-Bieniek K; Gromowski T; Huzarski T; Byrski T; Gronwald J; Oszurek O; Cybulski C; Dębniak T; Morawski A; Jakubowska A; Lubiński J; Post M, 2017, 'Meeting abstracts from the Annual Conference on Hereditary Cancers 2015', Hereditary Cancer in Clinical Practice, vol. 15, http://dx.doi.org/10.1186/s13053-017-0074-9
2017
Pan X; Bowman M; Scott RJ; Fitter J; Smith R; Zakar T, 2017, 'Promoter Methylation Pattern Controls Corticotropin Releasing Hormone Gene Activity in Human Trophoblasts.', PLoS One, vol. 12, pp. e0170671, http://dx.doi.org/10.1371/journal.pone.0170671
2017
Strumidło A; Skiba S; Scott RJ; Lubiński J, 2017, 'The potential role of miRNAs in therapy of breast and ovarian cancers associated with BRCA1 mutation.', Hered Cancer Clin Pract, vol. 15, pp. 15, http://dx.doi.org/10.1186/s13053-017-0076-7
2017
Daneshi N; Holliday E; Hancock S; Schneider JJ; Scott RJ; Attia J; Milward EA, 2017, 'Prevalence of clinically actionable genotypes and medication exposure of older adults in the community.', Pharmgenomics Pers Med, vol. 10, pp. 17 - 27, http://dx.doi.org/10.2147/PGPM.S123719
2017
Scott RJ; Boyd R, 2017, 'Joined-Up for What? Response to Carey and Harris on Adaptive Collaboration', Australian Journal of Public Administration, vol. 76, pp. 138 - 144, http://dx.doi.org/10.1111/1467-8500.12233
2017
Maguire JM; Bevan S; Stanne TM; Lorenzen E; Fernandez-Cadenas I; Hankey GJ; Jimenez-Conde J; Jood K; Lee JM; Lemmens R; Levi C; Norrving B; Rannikmae K; Rost N; Rosand J; Rothwell PM; Scott R; Strbian D; Sturm J; Sudlow C; Traylor M; Thijs V; Tatlisumak T; Wieloch T; Woo D; Worrall BB; Jern C; Lindgren A, 2017, 'GISCOME – Genetics of Ischaemic Stroke Functional Outcome network: A protocol for an international multicentre genetic association study', European Stroke Journal, vol. 2, pp. 229 - 237, http://dx.doi.org/10.1177/2396987317704547
2017
Scott RJ, 2017, 'The PerformanceStat Potential: A Leadership Strategy for Producing Results Robert D.Behn (Brookings Institution Press, Washington DC, 2014, ISBN 978-0-8157-2527-5 (paperback), 413 pp.)', Australian Journal of Public Administration, vol. 76, pp. 268 - 270, http://dx.doi.org/10.1111/1467-8500.12226
2017
Berry NK; Dixon-McIver A; Scott RJ; Rowlings P; Enjeti AK, 2017, 'Detection of complex genomic signatures associated with risk in plasma cell disorders.', Cancer Genet, vol. 218-219, pp. 1 - 9, http://dx.doi.org/10.1016/j.cancergen.2017.08.004
2017
Scott RJ, 2017, 'Explaining how group model building supports enduring agreement', Journal of Management and Organization, pp. 1 - 24, http://dx.doi.org/10.1017/jmo.2017.12
2017
Michailidou K; Lindström S; Dennis J; Beesley J; Hui S; Kar S; Lemaçon A; Soucy P; Glubb D; Rostamianfar A; Bolla MK; Wang Q; Tyrer J; Dicks E; Lee A; Wang Z; Allen J; Keeman R; Eilber U; French JD; Chen XQ; Fachal L; McCue K; Reed AEMC; Ghoussaini M; Carroll JS; Jiang X; Finucane H; Adams M; Adank MA; Ahsan H; Aittomäki K; Anton-Culver H; Antonenkova NN; Arndt V; Aronson KJ; Arun B; Auer PL; Bacot F; Barrdahl M; Baynes C; Beckmann MW; Behrens S; Benitez J; Bermisheva M; Bernstein L; Blomqvist C; Bogdanova NV; Bojesen SE; Bonanni B; Børresen-Dale AL; Brand JS; Brauch H; Brennan P; Brenner H; Brinton L; Broberg P; Brock IW; Broeks A; Brooks-Wilson A; Brucker SY; Brüning T; Burwinkel B; Butterbach K; Cai Q; Cai H; Caldés T; Canzian F; Carracedo A; Carter BD; Castelao JE; Chan TL; Cheng TYD; Chia KS; Choi JY; Christiansen H; Clarke CL; Collée M; Conroy DM; Cordina-Duverger E; Cornelissen S; Cox DG; Cox A; Cross SS; Cunningham JM; Czene K; Daly MB; Devilee P; Doheny KF; Dörk T; Dos-Santos-Silva I; Dumont M; Durcan L; Dwek M; Eccles DM; Ekici AB; Eliassen AH; Ellberg C; Elvira M; Engel C, 2017, 'Association analysis identifies 65 new breast cancer risk loci', Nature, vol. 551, pp. 92 - 94, http://dx.doi.org/10.1038/nature24284
2017
De Vries PS; Sabater-Lleal M; Chasman DI; Trompet S; Ahluwalia TS; Teumer A; Kleber ME; Chen MH; Wang JJ; Attia JR; Marioni RE; Steri M; Weng LC; Pool R; Grossmann V; Brody JA; Venturini C; Tanaka T; Rose LM; Oldmeadow C; Mazur J; Basu S; Frånberg M; Yang Q; Ligthart S; Hottenga JJ; Rumley A; Mulas A; De Craen AJM; Grotevendt A; Taylor KD; Delgado GE; Kifley A; Lopez LM; Berentzen TL; Mangino M; Bandinelli S; Morrison AC; Hamsten A; Tofler G; De Maat MPM; Draisma HHM; Lowe GD; Zoledziewska M; Sattar N; Lackner KJ; Völker U; McKnight B; Huang J; Holliday EG; McEvoy MA; Starr JM; Hysi PG; Hernandez DG; Guan W; Rivadeneira F; McArdle WL; Slagboom PE; Zeller T; Psaty BM; Uitterlinden AG; De Geus EJC; Stott DJ; Binder H; Hofman A; Franco OH; Rotter JI; Ferrucci L; Spector TD; Deary IJ; März W; Greinacher A; Wild PS; Cucca F; Boomsma DI; Watkins H; Tang W; Ridker PM; Jukema JW; Scott RJ; Mitchell P; Hansen T; O'Donnell CJ; Smith NL; Strachan DP; Dehghan A, 2017, 'Comparison of HapMap and 1000 genomes reference panels in a large-scale genome-wide association study', PLoS ONE, vol. 12, pp. e0167742, http://dx.doi.org/10.1371/journal.pone.0167742
2017
Wain LV; Vaez A; Jansen R; Joehanes R; Van Der Most PJ; Erzurumluoglu AM; O'Reilly PF; Cabrera CP; Warren HR; Rose LM; Verwoert GC; Hottenga JJ; Strawbridge RJ; Esko T; Arking DE; Hwang SJ; Guo X; Kutalik Z; Trompet S; Shrine N; Teumer A; Ried JS; Bis JC; Smith AV; Amin N; Nolte IM; Lyytikäinen LP; Mahajan A; Wareham NJ; Hofer E; Joshi PK; Kristiansson K; Traglia M; Havulinna AS; Goel A; Nalls MA; Sõber S; Vuckovic D; Luan J; Del Greco FM; Ayers KL; Marrugat J; Ruggiero D; Lopez LM; Niiranen T; Enroth S; Jackson AU; Nelson CP; Huffman JE; Zhang W; Marten J; Gandin I; Harris SE; Zemunik T; Lu Y; Evangelou E; Shah N; De Borst MH; Mangino M; Prins BP; Campbell A; Li-Gao R; Chauhan G; Oldmeadow C; Abecasis G; Abedi M; Barbieri CM; Barnes MR; Batini C; Beilby J; Blake T; Boehnke M; Bottinger EP; Braund PS; Brown M; Brumat M; Campbell H; Chambers JC; Cocca M; Collins F; Connell J; Cordell HJ; Damman JJ; Davies G; De Geus EJ; De Mutsert R; Deelen J; Demirkale Y; Doney ASF; Dörr M; Farrall M; Ferreira T; Frånberg M; Gao H; Giedraitis V; Gieger C; Giulianini F; Gow AJ; Hamsten A; Harris TB, 2017, 'Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets from Blood and the Kidney', Hypertension, vol. 70, pp. e4 - e19, http://dx.doi.org/10.1161/HYPERTENSIONAHA.117.09438
2017
Milne RL; Kuchenbaecker KB; Michailidou K; Beesley J; Kar S; Lindström S; Hui S; Lemaçon A; Soucy P; Dennis J; Jiang X; Rostamianfar A; Finucane H; Bolla MK; McGuffog L; Wang Q; Aalfs CM; Abctctb I; Adams M; Adlard J; Agata S; Ahmed S; Ahsan H; Aittom KÄ; Fares AE; Allen J; Ambrosone CB; Amos CI; Andrulis IL; Anton-Culver H; Antonenkova NN; Arndt V; Arnold N; Aronson KJ; Auber B; Auer PL; Ausems MGM; Azzollini J; François B; Balma JN; Barile M; Barjhoux L; Barkardottir RB; Barrdahl M; Barnes D; Barrowdale D; Baynes C; Beckmann MW; Benitez J; Bermisheva M; Bernstein L; Bignon YJ; Blazer KR; Blok MJ; Blomqvist C; Blot W; Bobolis K; Boeckx B; Bogdanova NV; Bojesen A; Bojesen SE; Bonanni B; Anne-Lise BD; Bozsik A; Bradbury AR; Brand JS; Brauch H; Brenner H; Brigitte BDP; Brewer C; Brinton L; Broberg P; Angela BW; Brunet J; Brüning T; Burwinkel B; Buys SS; Byun J; Cai Q; Cald TÉ; Caligo MA; Campbell I; Canzian F; Caron O; Carracedo A; Carter BD; Esteban C; Castera L; Virginie CM; Chan SB; Jenny CC; Chanock SJ; Chen X; Cheng TYD; Chiquette J; Christiansen H; Claes KB; Clarke CL; Conner T; Conroy DM, 2017, 'Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer', Nature Genetics, vol. 49, pp. 1767 - 1778, http://dx.doi.org/10.1038/ng.3785
2017
Maltby VE; Lea RA; Sanders KA; White N; Benton MC; Scott RJ; Lechner-Scott J, 2017, 'Differential methylation at MHC in CD4+ T cells is associated with multiple sclerosis independently of HLA-DRB1.', Clin Epigenetics, vol. 9, pp. 71, http://dx.doi.org/10.1186/s13148-017-0371-1
2017
Delforce SJ; Lumbers ER; de Meaultsart CC; Wang Y; Proietto A; Otton G; Scurry J; Verrills NM; Scott RJ; Pringle KG, 2017, 'Expression of renin–angiotensin system (RAS) components in endometrial cancer', Endocrine Connections, vol. 6, pp. 9 - 19, http://dx.doi.org/10.1530/EC-16-0082
2017
Avery-Kiejda KA; Mathe A; Scott RJ, 2017, 'Genome-wide miRNA, gene and methylation analysis of triple negative breast cancer to identify changes associated with lymph node metastases.', Genom Data, vol. 14, pp. 1 - 4, http://dx.doi.org/10.1016/j.gdata.2017.07.004
2017
Najdawi F; Crook A; Maidens J; McEvoy C; Fellowes A; Pickett J; Ho M; Nevell D; McIlroy K; Sheen A; Sioson L; Ahadi M; Turchini J; Clarkson A; Hogg R; Valmadre S; Gard G; Dooley SJ; Scott RJ; Fox SB; Field M; Gill AJ, 2017, 'Lessons learnt from implementation of a Lynch syndrome screening program for patients with gynaecological malignancy', Pathology, vol. 49, pp. 457 - 464, http://dx.doi.org/10.1016/j.pathol.2017.05.004
2017
Hungate EA; Vora SR; Gamazon ER; Moriyama T; Best T; Hulur I; Lee Y; Evans T-J; Ellinghaus E; Stanulla M; Rudant J; Orsi L; Clavel J; Milne E; Scott RJ; Pui C-H; Cox NJ; Loh ML; Yang JJ; Skol AD; Onel K, 2016, 'A variant at 9p21.3 functionally implicates CDKN2B in paediatric B-cell precursor acute lymphoblastic leukaemia aetiology.', Nat Commun, vol. 7, pp. 10635, http://dx.doi.org/10.1038/ncomms10635
2016
Easton DF; Lesueur F; Decker B; Michailidou K; Li J; Allen J; Luccarini C; Pooley KA; Shah M; Bolla MK; Wang Q; Dennis J; Ahmad J; Thompson ER; Damiola F; Pertesi M; Voegele C; Mebirouk N; Robinot N; Durand G; Forey N; Luben RN; Ahmed S; Aittomäki K; Anton-Culver H; Arndt V; Australian Ovarian Cancer Study Group ; Baynes C; Beckman MW; Benitez J; Van Den Berg D; Blot WJ; Bogdanova NV; Bojesen SE; Brenner H; Chang-Claude J; Chia KS; Choi J-Y; Conroy DM; Cox A; Cross SS; Czene K; Darabi H; Devilee P; Eriksson M; Fasching PA; Figueroa J; Flyger H; Fostira F; García-Closas M; Giles GG; Glendon G; González-Neira A; Guénel P; Haiman CA; Hall P; Hart SN; Hartman M; Hooning MJ; Hsiung C-N; Ito H; Jakubowska A; James PA; John EM; Johnson N; Jones M; Kabisch M; Kang D; kConFab Investigators ; Kosma V-M; Kristensen V; Lambrechts D; Li N; Lifepool Investigators ; Lindblom A; Long J; Lophatananon A; Lubinski J; Mannermaa A; Manoukian S; Margolin S; Matsuo K; Meindl A; Mitchell G; Muir K; NBCS Investigators ; Nevelsteen I; van den Ouweland A; Peterlongo P; Phuah SY; Pylkäs K; Rowley SM; Sangrajrang S; Schmutzler RK; Shen C-Y; Shu X-O; Southey MC; Surowy H; Swerdlow A; Teo SH; Tollenaar RAEM; Tomlinson I; Torres D; Truong T; Vachon C; Verhoef S; Wong-Brown M; Zheng W; Zheng Y; Nevanlinna H; Scott RJ; Andrulis IL; Wu AH; Hopper JL; Couch FJ; Winqvist R; Burwinkel B; Sawyer EJ; Schmidt MK; Rudolph A; Dörk T; Brauch H; Hamann U; Neuhausen SL; Milne RL; Fletcher O; Pharoah PDP; Campbell IG; Dunning AM; Le Calvez-Kelm F; Goldgar DE; Tavtigian SV; Chenevix-Trench G, 2016, 'No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing.', J Med Genet, vol. 53, pp. 298 - 309, http://dx.doi.org/10.1136/jmedgenet-2015-103529
2016
Chen MM; O'Mara TA; Thompson DJ; Painter JN; Australian National Endometrial Cancer Study Group (ANECS) ; Attia J; Black A; Brinton L; Chanock S; Chen C; Cheng TH; Cook LS; Crous-Bou M; Doherty J; Friedenreich CM; Garcia-Closas M; Gaudet MM; Gorman M; Haiman C; Hankinson SE; Hartge P; Henderson BE; Hodgson S; Holliday EG; Horn-Ross PL; Hunter DJ; Le Marchand L; Liang X; Lissowska J; Long J; Lu L; Magliocco AM; Martin L; McEvoy M; National Study Of Endometrial Cancer Genetics Group (NSECG) ; Olson SH; Orlow I; Pooler L; Prescott J; Rastogi R; Rebbeck TR; Risch H; Sacerdote C; Schumacher F; Wendy Setiawan V; Scott RJ; Sheng X; Shu X-O; Turman C; Van Den Berg D; Wang Z; Weiss NS; Wentzensen N; Xia L; Xiang Y-B; Yang HP; Yu H; Zheng W; Pharoah PDP; Dunning AM; Tomlinson I; Easton DF; Kraft P; Spurdle AB; De Vivo I, 2016, 'GWAS meta-analysis of 16 852 women identifies new susceptibility locus for endometrial cancer.', Hum Mol Genet, vol. 25, pp. 2612 - 2620, http://dx.doi.org/10.1093/hmg/ddw092
2016
Walker MM; Keely SJ; Scott RJ; Talley NJ, 2016, 'Genetics, Mucosal Inflammation and the Environment in Post-Infectious Chronic Gut Syndromes', The American Journal of Gastroenterology Supplements, vol. 3, pp. 46 - 51, http://dx.doi.org/10.1038/ajgsup.2016.14
2016
Masson AL; Talseth-Palmer BA; Evans TJ; McElduff P; Spigelman AD; Hannan GN; Scott RJ, 2016, 'Copy number variants associated with 18p11.32, DCC and the promoter 1B region of APC in colorectal polyposis patients', Meta Gene, vol. 7, pp. 95 - 104, http://dx.doi.org/10.1016/j.mgene.2015.12.005
2016
De Vries PS; Chasman DI; Sabater-Lleal M; Chen MH; Huffman JE; Steri M; Tang W; Teumer A; Marioni RE; Grossmann V; Hottenga JJ; Trompet S; Müller-Nurasyid M; Zhao JH; Brody JA; Kleber ME; Guo X; Wang JJ; Auer PL; Attia JR; Yanek LR; Ahluwalia TS; Lahti J; Venturini C; Tanaka T; Bielak LF; Joshi PK; Rocanin-Arjo A; Kolcic I; Navarro P; Rose LM; Oldmeadow C; Riess H; Mazur J; Basu S; Goel A; Yang Q; Ghanbari M; Gonnekewillemsen ; Rumley A; Fiorillo E; De Craen AJM; Grotevendt A; Scott R; Taylor KD; Delgado GE; Yao J; Kifley A; Kooperberg C; Qayyum R; Lopez L; Berentzen TL; Räikkönen K; Massimomangino ; Bandinelli S; Peyser PA; Wild S; Trégouët DA; Wright AF; Marten J; Zemunik T; Morrison AC; Sennblad B; Tofler G; De Maat MPM; De Geus EJC; Lowe GD; Zoledziewska M; Sattar N; Binder H; Völker U; Waldenberger M; Khaw KT; Mcknight B; Huang J; Jenny NS; Holliday EG; Qi L; Mcevoy MG; Becker DM; Starr JM; Sarin AP; Hysi PG; Hernandez DG; Jhun MA; Campbell H; Hamsten A; Sarin F; Mcardle WL; Eline Slagboom P; Zeller T; Koenig W; Psaty B; Haritunians T; Liu J; Palotie A; Uitterlinden AG; Stott DJ; Hofman A; Franco OH, 2016, 'A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration', Human Molecular Genetics, vol. 25, pp. 358 - 370, http://dx.doi.org/10.1093/hmg/ddv454
2016
Talseth-Palmer BA; Bauer DC; Sjursen W; Evans TJ; Mcphillips M; Proietto A; Otton G; Spigelman AD; Scott RJ, 2016, 'Targeted next-generation sequencing of 22 mismatch repair genes identifies Lynch syndrome families', Cancer Medicine, vol. 5, pp. 929 - 941, http://dx.doi.org/10.1002/cam4.628
2016
Southey MC; Goldgar DE; Winqvist R; Pylkäs K; Couch F; Tischkowitz M; Foulkes WD; Dennis J; Michailidou K; van Rensburg EJ; Heikkinen T; Nevanlinna H; Hopper JL; Dörk T; Claes KBM; Reis-Filho J; Teo ZL; Radice P; Catucci I; Peterlongo P; Tsimiklis H; Odefrey FA; Dowty JG; Schmidt MK; Broeks A; Hogervorst FB; Verhoef S; Carpenter J; Clarke C; Scott RJ; Fasching PA; Haeberle L; Ekici AB; Beckmann MW; Peto J; dos-Santos-Silva I; Fletcher O; Johnson N; Bolla MK; Sawyer EJ; Tomlinson I; Kerin MJ; Miller N; Marme F; Burwinkel B; Yang R; Guénel P; Truong T; Menegaux F; Sanchez M; Bojesen S; Nielsen SF; Flyger H; Benitez J; Zamora MP; Perez JIA; Menéndez P; Anton-Culver H; Neuhausen S; Ziogas A; Clarke CA; Brenner H; Arndt V; Stegmaier C; Brauch H; Brüning T; Ko YD; Muranen TA; Aittomäki K; Blomqvist C; Bogdanova NV; Antonenkova NN; Lindblom A; Margolin S; Mannermaa A; Kataja V; Kosma VM; Hartikainen JM; Spurdle AB; Wauters E; Smeets D; Beuselinck B; Floris G; Chang-Claude J; Rudolph A; Seibold P; Flesch-Janys D; Olson JE; Vachon C; Pankratz VS; McLean C; Haiman CA; Henderson BE; Schumacher F; Marchand LL; Kristensen V; Alnæs GG; Zheng W; Hunter DJ; Lindstrom S, 2016, 'PALB2, CHEK2 and ATM rare variants and cancer risk: Data from COGS', Journal of Medical Genetics, vol. 53, pp. 800 - 811, http://dx.doi.org/10.1136/jmedgenet-2016-103839
2016
Lener MR; Scott RJ; Wiechowska-Kozłowska A; Serrano-Fernández P; Baszuk P; Jaworska-Bieniek K; Sukiennicki G; Marciniak W; Muszyńska M; Kładny J; Gromowski T; Kaczmarek K; Jakubowska A; Lubiński J, 2016, 'Serum Concentrations of Selenium and Copper in Patients Diagnosed with Pancreatic Cancer.', Cancer Res Treat, vol. 48, pp. 1056 - 1064, http://dx.doi.org/10.4143/crt.2015.282
2016
Guo ST; Chi MN; Yang RH; Guo XY; Zan LK; Wang CY; Xi YF; Jin L; Croft A; Tseng HY; Yan XG; Farrelly M; Wang FH; Lai F; Wang JF; Li YP; Ackland S; Scott R; Agoulnik IU; Hondermarck H; Thorne RF; Liu T; Zhang XD; Jiang CC, 2016, 'INPP4B is an oncogenic regulator in human colon cancer', Oncogene, vol. 35, pp. 3049 - 3061, http://dx.doi.org/10.1038/onc.2015.361
2016
Kamien B; Dadd T; Buckman M; Ronan A; Dudding T; Meldrum C; Scott R; Mina K, 2016, 'Somatic-gonadal mosaicism causing Sotos syndrome.', Am J Med Genet A, vol. 170, pp. 3360 - 3362, http://dx.doi.org/10.1002/ajmg.a.37867
2016
Morten BC; Wong-Brown MW; Scott RJ; Avery-Kiejda KA, 2016, 'The presence of the intron 3 16 bp duplication polymorphism of p53 (rs17878362) in breast cancer is associated with a low Δ40p53:p53 ratio and better outcome.', Carcinogenesis, vol. 37, pp. 81 - 86, http://dx.doi.org/10.1093/carcin/bgv164
2016
Wong SQ; Scott R; Fox SB, 2016, 'KRAS mutation testing in colorectal cancer: the model for molecular pathology testing in the future', Colorectal Cancer, vol. 5, pp. 73 - 80, http://dx.doi.org/10.2217/crc-2015-0009
2016
McKenzie R; Scott RJ; Otton G; Scurry J, 2016, 'Early changes of endometrial neoplasia revealed by loss of mismatch repair gene protein expression in a patient diagnosed with Lynch syndrome.', Pathology, vol. 48, pp. 78 - 80, http://dx.doi.org/10.1016/j.pathol.2015.11.003
2016
Morten BC; Scott RJ; Avery-Kiejda KA, 2016, 'Comparison of Three Different Methods for Determining Cell Proliferation in Breast Cancer Cell Lines.', J Vis Exp, http://dx.doi.org/10.3791/54350
2016
Cheng TH; Thompson DJ; O'Mara TA; Painter JN; Glubb DM; Flach S; Lewis A; French JD; Freeman-Mills L; Church D; Gorman M; Martin L; National Study of Endometrial Cancer Genetics Group (NSECG) ; Hodgson S; Webb PM; Australian National Endometrial Cancer Study Group (ANECS) ; Attia J; Holliday EG; McEvoy M; Scott RJ; Henders AK; Martin NG; Montgomery GW; Nyholt DR; Ahmed S; Healey CS; Shah M; Dennis J; Fasching PA; Beckmann MW; Hein A; Ekici AB; Hall P; Czene K; Darabi H; Li J; Dörk T; Dürst M; Hillemanns P; Runnebaum I; Amant F; Schrauwen S; Zhao H; Lambrechts D; Depreeuw J; Dowdy SC; Goode EL; Fridley BL; Winham SJ; Njølstad TS; Salvesen HB; Trovik J; Werner HM; Ashton K; Otton G; Proietto T; Liu T; Mints M; Tham E; RENDOCAS ; Consortium C; Jun Li M; Yip SH; Wang J; Bolla MK; Michailidou K; Wang Q; Tyrer JP; Dunlop M; Houlston R; Palles C; Hopper JL; AOCS Group ; Peto J; Swerdlow AJ; Burwinkel B; Brenner H; Meindl A; Brauch H; Lindblom A; Chang-Claude J; Couch FJ; Giles GG; Kristensen VN; Cox A; Cunningham JM; Pharoah PDP; Dunning AM; Edwards SL; Easton DF; Tomlinson I; Spurdle AB, 2016, 'Five endometrial cancer risk loci identified through genome-wide association analysis.', Nat Genet, vol. 48, pp. 667 - 674, http://dx.doi.org/10.1038/ng.3562
2016
Pattaro C; Teumer A; Gorski M; Chu AY; Li M; Mijatovic V; Garnaas M; Tin A; Sorice R; Li Y; Taliun D; Olden M; Foster M; Yang Q; Chen MH; Pers TH; Johnson AD; Ko YA; Fuchsberger C; Tayo B; Nalls M; Feitosa MF; Isaacs A; Dehghan A; D'Adamo P; Adeyemo A; Dieffenbach AK; Zonderman AB; Nolte IM; Van Der Most PJ; Wright AF; Shuldiner AR; Morrison AC; Hofman A; Smith AV; Dreisbach AW; Franke A; Uitterlinden AG; Metspalu A; Tonjes A; Lupo A; Robino A; Johansson Å; Demirkan A; Kollerits B; Freedman BI; Ponte B; Oostra BA; Paulweber B; Krämer BK; Mitchell BD; Buckley BM; Peralta CA; Hayward C; Helmer C; Rotimi CN; Shaffer CM; Müller C; Sala C; Van Duijn CM; Saint-Pierre A; Ackermann D; Shriner D; Ruggiero D; Toniolo D; Lu Y; Cusi D; Czamara D; Ellinghaus D; Siscovick DS; Ruderfer D; Gieger C; Grallert H; Rochtchina E; Atkinson EJ; Holliday EG; Boerwinkle E; Salvi E; Bottinger EP; Murgia F; Rivadeneira F; Ernst F; Kronenberg F; Hu FB; Navis GJ; Curhan GC; Ehret GB; Homuth G; Coassin S; Thun GA; Pistis G; Gambaro G; Malerba G; Montgomery GW; Eiriksdottir G; Jacobs G; Li G; Wichmann HE; Campbell H; Schmidt H, 2016, 'Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function', Nature Communications, vol. 7, http://dx.doi.org/10.1038/ncomms10023
2016
Bolton KA; Avery-Kiejda KA; Holliday EG; Attia J; Bowden NA; Scott RJ, 2016, 'A polymorphic repeat in the IGF1 promoter influences the risk of endometrial cancer.', Endocr Connect, vol. 5, pp. 115 - 122, http://dx.doi.org/10.1530/EC-16-0003
2016
Scott RJ; Cavana RY; Cameron D, 2016, 'Client Perceptions of Reported Outcomes of Group Model Building in the New Zealand Public Sector', Group Decision and Negotiation, vol. 25, pp. 77 - 101, http://dx.doi.org/10.1007/s10726-015-9433-y
2016
Rosand J; Mitchell BD; Ay H; de Bakker PIW; Gwinn K; Kittner SJ; Lindgren A; Meschia JF; Pulit SL; Sudlow CLM; Thijs V; Woo D; Worrall BB; Arnett DK; Benavente O; Cole JW; Dichgans M; Grewal RP; Jern C; Conde JJ; Johnson JA; Lee JM; Levi C; Markus HS; Melander O; Rexrode K; Rothwell PM; Rundek T; Sacco RL; Schmidt R; Sharma P; Slowik A; Wasssertheil-Smoller S, 2016, 'Loci associated with ischaemic stroke and its subtypes (SiGN): A genome-wide association study', The Lancet Neurology, vol. 15, pp. 174 - 184, http://dx.doi.org/10.1016/S1474-4422(15)00338-5
2016
Bolton KA; Holliday EG; Attia J; Bowden NA; Avery-Kiejda KA; Scott RJ, 2016, 'A novel polymorphic repeat in the upstream regulatory region of the estrogen-induced gene EIG121 is not associated with the risk of developing breast or endometrial cancer.', BMC Res Notes, vol. 9, pp. 287, http://dx.doi.org/10.1186/s13104-016-2086-3
2016
Okbay A; Baselmans BML; De Neve J-E; Turley P; Nivard MG; Fontana MA; Meddens SFW; Linnér RK; Rietveld CA; Derringer J; Gratten J; Lee JJ; Liu JZ; de Vlaming R; Ahluwalia TS; Buchwald J; Cavadino A; Frazier-Wood AC; Furlotte NA; Garfield V; Geisel MH; Gonzalez JR; Haitjema S; Karlsson R; van der Laan SW; Ladwig K-H; Lahti J; van der Lee SJ; Lind PA; Liu T; Matteson L; Mihailov E; Miller MB; Minica CC; Nolte IM; Mook-Kanamori D; van der Most PJ; Oldmeadow C; Qian Y; Raitakari O; Rawal R; Realo A; Rueedi R; Schmidt B; Smith AV; Stergiakouli E; Tanaka T; Taylor K; Thorleifsson G; Wedenoja J; Wellmann J; Westra H-J; Willems SM; Zhao W; LifeLines Cohort Study ; Amin N; Bakshi A; Bergmann S; Bjornsdottir G; Boyle PA; Cherney S; Cox SR; Davies G; Davis OSP; Ding J; Direk N; Eibich P; Emeny RT; Fatemifar G; Faul JD; Ferrucci L; Forstner AJ; Gieger C; Gupta R; Harris TB; Harris JM; Holliday EG; Hottenga J-J; De Jager PL; Kaakinen MA; Kajantie E; Karhunen V; Kolcic I; Kumari M; Launer LJ; Franke L; Li-Gao R; Liewald DC; Koini M; Loukola A; Marques-Vidal P; Montgomery GW; Mosing MA; Paternoster L; Pattie A; Petrovic KE; Pulkki-Råback L; Quaye L; Räikkönen K; Rudan I; Scott RJ; Smith JA; Sutin AR; Trzaskowski M; Vinkhuyzen AE; Yu L; Zabaneh D; Attia JR; Bennett DA; Berger K; Bertram L; Boomsma DI; Snieder H; Chang S-C; Cucca F; Deary IJ; van Duijn CM; Eriksson JG; Bültmann U; de Geus EJC; Groenen PJF; Gudnason V; Hansen T; Hartman CA; Haworth CMA; Hayward C; Heath AC; Hinds DA; Hyppönen E; William WG; Järvelin M-R; Jöckel K-H; Kaprio J; Kardia SLR; Keltikangas-Järvinen L; Kraft P; Kubzansky LD; Lehtimäki T; Magnusson PKE; Martin NG; McGue M; Metspalu A; Mills M; de Mutsert R; Oldehinkel AJ; Pasterkamp G; Pedersen NL; Plomin R; Polasek O; Power C; Rich SS; Rosendaal FR; den Ruijter HM; Schlessinger D; Schmidt H; Svento R; Schmidt R; Alizadeh BZ; Sørensen TIA; Spector TD; Starr JM; Stefansson K; Steptoe A; Terracciano A; Thorsteinsdottir U; Thurik AR; Timpson NJ; Tiemeier H; Uitterlinden AG; Vollenweider P; Wagner GG; Weir DR; Yang J; Conley DC; Smith GD; Hofman A; Johannesson M; Laibson DI; Medland SE; Meyer MN; Pickrell JK; Esko T; Krueger RF; Beauchamp JP; Koellinger PD; Benjamin DJ; Bartels M; Cesarini D, 2016, 'Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.', Nat Genet, vol. 48, pp. 1591, http://dx.doi.org/10.1038/ng1216-1587b
2016
Thompson ER; Rowley SM; Li N; McInerny S; Devereux L; Wong-Brown MW; Trainer AH; Mitchell G; Scott RJ; James PA; Campbell IG, 2016, 'Panel Testing for Familial Breast Cancer: Calibrating the Tension Between Research and Clinical Care.', J Clin Oncol, vol. 34, pp. 1455 - 1459, http://dx.doi.org/10.1200/JCO.2015.63.7454
2016
Groen K; Maltby VE; Sanders KA; Scott RJ; Tajouri L; Lechner-Scott J, 2016, 'Erythrocytes in multiple sclerosis - forgotten contributors to the pathophysiology?', Mult Scler J Exp Transl Clin, vol. 2, pp. 2055217316649981, http://dx.doi.org/10.1177/2055217316649981
2016
Sjursen W; McPhillips M; Scott RJ; Talseth-Palmer BA, 2016, 'Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations.', Mol Genet Genomic Med, vol. 4, pp. 223 - 231, http://dx.doi.org/10.1002/mgg3.198
2016
Johnson NA; Kypri K; Latter J; Attia J; McEvoy M; Dunlop A; Scott R, 2016, 'Genetic feedback to reduce alcohol consumption in hospital outpatients with risky drinking: Feasibility and acceptability', Public Health Research and Practice, vol. 26, http://dx.doi.org/10.17061/phrp2641645
2016
Okbay A; Beauchamp JP; Fontana MA; Lee JJ; Pers TH; Rietveld CA; Turley P; Chen GB; Emilsson V; Meddens SFW; Oskarsson S; Pickrell JK; Thom K; Timshel P; De Vlaming R; Abdellaoui A; Ahluwalia TS; Bacelis J; Baumbach C; Bjornsdottir G; Brandsma JH; Pina Concas M; Derringer J; Furlotte NA; Galesloot TE; Girotto G; Gupta R; Hall LM; Harris SE; Hofer E; Horikoshi M; Huffman JE; Kaasik K; Kalafati IP; Karlsson R; Kong A; Lahti J; Van Der Lee SJ; Deleeuw C; Lind PA; Lindgren KO; Liu T; Mangino M; Marten J; Mihailov E; Miller MB; Van Der Most PJ; Oldmeadow C; Payton A; Pervjakova N; Peyrot WJ; Qian Y; Raitakari O; Rueedi R; Salvi E; Schmidt B; Schraut KE; Shi J; Smith AV; Poot RA; St Pourcain B; Teumer A; Thorleifsson G; Verweij N; Vuckovic D; Wellmann J; Westra HJ; Yang J; Zhao W; Zhu Z; Alizadeh BZ; Amin N; Bakshi A; Baumeister SE; Biino G; Bønnelykke K; Boyle PA; Campbell H; Cappuccio FP; Davies G; De Neve JE; Deloukas P; Demuth I; Ding J; Eibich P; Eisele L; Eklund N; Evans DM; Faul JD; Feitosa MF; Forstner AJ; Gandin I; Gunnarsson B; Halldórsson BV; Harris TB; Holliday EG; Heath AC; Hocking LJ; Homuth G; Horan MA, 2016, 'Genome-wide association study identifies 74 loci associated with educational attainment', Nature, vol. 533, pp. 539 - 542, http://dx.doi.org/10.1038/nature17671
2016
Purrington KS; Visscher DW; Wang C; Yannoukakos D; Hamann U; Nevanlinna H; Cox A; Giles GG; Eckel-Passow JE; Lakis S; Kotoula V; Fountzilas G; Kabisch M; Rüdiger T; Heikkilä P; Blomqvist C; Cross SS; Southey MC; Olson JE; Gilbert J; Deming-Halverson S; Kosma VM; Clarke C; Scott R; Jones JL; Zheng W; Mannermaa A; Jane Carpenter for ABCTC Investigators ; Eccles DM; Vachon CM; Couch FJ, 2016, 'Genes associated with histopathologic features of triple negative breast tumors predict molecular subtypes', Breast Cancer Research and Treatment, vol. 157, pp. 117 - 131, http://dx.doi.org/10.1007/s10549-016-3775-2
2016
Tan AG; Kifley A; Mitchell P; Rochtchina E; Flood VM; Cumming RG; Jun G; Holliday EG; Scott RJ; Teo YY; Klein BEK; Cheng CY; Iyengar SK; JinWang J, 2016, 'Associations between methylenetetrahydrofolate reductase polymorphisms, serum homocysteine levels, and incident cortical cataract', JAMA Ophthalmology, vol. 134, pp. 522 - 528, http://dx.doi.org/10.1001/jamaophthalmol.2016.0167
2016
Sanders KA; Benton MC; Lea RA; Maltby VE; Agland S; Griffin N; Scott RJ; Tajouri L; Lechner-Scott J, 2016, 'Next-generation sequencing reveals broad down-regulation of microRNAs in secondary progressive multiple sclerosis CD4+ T cells.', Clin Epigenetics, vol. 8, pp. 87, http://dx.doi.org/10.1186/s13148-016-0253-y
2016
Lubinski J; Scott RJ; Sijmons R; Theissen SM, 2016, 'Thank you to all our manuscript reviewers in 2015', Hereditary Cancer in Clinical Practice, vol. 14, http://dx.doi.org/10.1186/s13053-016-0047-4
2016
Okbay A; Baselmans BML; De Neve JE; Turley P; Nivard MG; Fontana MA; Meddens SFW; Linnér RK; Rietveld CA; Derringer J; Gratten J; Lee JJ; Liu JZ; De Vlaming R; SAhluwalia T; Buchwald J; Cavadino A; Frazier-Wood AC; Furlotte NA; Garfield V; Geisel MH; Gonzalez JR; Haitjema S; Karlsson R; Der Laan SW; Ladwig KH; Lahti J; Van Der Lee SJ; Lind PA; Liu T; Matteson L; Mihailov E; Miller MB; CMinica C; MNolte I; Mook-Kanamori D; Van Der Most PJ; Oldmeadow C; Qian Y; Raitakari O; Rawal R; Realo A; Rueedi R; Schmidt B; Smith AV; Stergiakouli E; Tanaka T; Taylor K; Wedenoja J; Wellmann J; Westra HJ; MWillems S; Zhao W; Study LLC; Amin N; Bakshi A; Boyle PA; Cherney S; Cox SR; Davies G; Davis OSP; Ding J; Direk N; Eibich P; Emeny RT; Fatemifar G; Faul JD; Ferrucci L; Forstner A; Gieger C; Gupta R; Harris TB; Harris JM; Holliday EG; Hottenga JJ; De Jager PL; Kaakinen MA; Kajantie E; Karhunen V; Kolcic I; Kumari M; Launer LJ; Franke L; Li-Gao R; Koini M; Loukola A; Marques-Vidal P; Montgomery GW; Mosing MA; Paternoster L; Pattie A; Petrovic KE; Pulkki-R'back L; Quaye L; R'ikkönen K; Rudan I; Scott RJ; Smith JA; Sutin AR; Trzaskowski M, 2016, 'Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses', Nature Genetics, vol. 48, pp. 624 - 633, http://dx.doi.org/10.1038/ng.3552
2016
Thompson DJ; O'Mara TA; Glubb DM; Painter JN; Cheng T; Folkerd E; Doody D; Dennis J; Webb PM; Australian National Endometrial Cancer Study Group (ANECS) ; Gorman M; Martin L; Hodgson S; National Study of Endometrial Cancer Genetics Group (NSECG) ; Michailidou K; Tyrer JP; Maranian MJ; Hall P; Czene K; Darabi H; Li J; Fasching PA; Hein A; Beckmann MW; Ekici AB; Dörk T; Hillemanns P; Dürst M; Runnebaum I; Zhao H; Depreeuw J; Schrauwen S; Amant F; Goode EL; Fridley BL; Dowdy SC; Winham SJ; Salvesen HB; Trovik J; Njolstad TS; Werner HMJ; Ashton K; Proietto T; Otton G; Carvajal-Carmona L; Tham E; Liu T; Mints M; for RENDOCAS ; Scott RJ; McEvoy M; Attia J; Holliday EG; Montgomery GW; Martin NG; Nyholt DR; Henders AK; Hopper JL; Traficante N; AOCS Group ; Ruebner M; Swerdlow AJ; Burwinkel B; Brenner H; Meindl A; Brauch H; Lindblom A; Lambrechts D; Chang-Claude J; Couch FJ; Giles GG; Kristensen VN; Cox A; Bolla MK; Wang Q; Bojesen SE; Shah M; Luben R; Khaw K-T; Pharoah PDP; Dunning AM; Tomlinson I; Dowsett M; Easton DF; Spurdle AB, 2016, 'CYP19A1 fine-mapping and Mendelian randomization: estradiol is causal for endometrial cancer.', Endocr Relat Cancer, vol. 23, pp. 77 - 91, http://dx.doi.org/10.1530/ERC-15-0386
2016
Morten BC; Scott RJ; Avery-Kiejda KA, 2016, 'Comparison of the QuantiGene 2.0 Assay and Real-Time RT-PCR in the Detection of p53 Isoform mRNA Expression in Formalin-Fixed Paraffin-Embedded Tissues- A Preliminary Study.', PLoS One, vol. 11, pp. e0165930, http://dx.doi.org/10.1371/journal.pone.0165930
2016
Painter JN; Kaufmann S; O'Mara TA; Hillman KM; Sivakumaran H; Darabi H; Cheng THT; Pearson J; Kazakoff S; Waddell N; Hoivik EA; Goode EL; Scott RJ; Tomlinson I; Dunning AM; Easton DF; French JD; Salvesen HB; Pollock PM; Thompson DJ; Spurdle AB; Edwards SL, 2016, 'A Common Variant at the 14q32 Endometrial Cancer Risk Locus Activates AKT1 through YY1 Binding.', Am J Hum Genet, vol. 98, pp. 1159 - 1169, http://dx.doi.org/10.1016/j.ajhg.2016.04.012
2016
Pringle KG; Delforce SJ; Wang Y; Ashton KA; Proietto A; Otton G; Caroline Blackwell C; Scott RJ; Lumbers ER, 2016, 'Renin–angiotensin system gene polymorphisms and endometrial cancer', Endocrine Connections, vol. 5, pp. 128 - 135, http://dx.doi.org/10.1530/EC-15-0112
2016
Scott RJ; Cavana RY; Cameron D, 2016, 'Recent evidence on the effectiveness of group model building', European Journal of Operational Research, vol. 249, pp. 908 - 918, http://dx.doi.org/10.1016/j.ejor.2015.06.078
2016
Mehta D; Tropf FC; Gratten J; Bakshi A; Zhu Z; Bacanu S-A; Hemani G; Magnusson PKE; Barban N; Esko T; Metspalu A; Snieder H; Mowry BJ; Kendler KS; Yang J; Visscher PM; McGrath JJ; Mills MC; Wray NR; Lee SH; Schizophrenia Working Group of the Psychiatric Genomics Consortium, LifeLines Cohort Study, and TwinsUK ; Andreassen OA; Bramon E; Bruggeman R; Buxbaum JD; Cairns MJ; Cantor RM; Cloninger CR; Cohen D; Crespo-Facorro B; Darvasi A; DeLisi LE; Dinan T; Djurovic S; Donohoe G; Drapeau E; Escott-Price V; Freimer NB; Georgieva L; de Haan L; Henskens FA; Joa I; Julià A; Khrunin A; Lerer B; Limborska S; Loughland CM; Macek M; Magnusson PKE; Marsal S; McCarley RW; McIntosh AM; McQuillin A; Melegh B; Michie PT; Morris DW; Murphy KC; Myin-Germeys I; Olincy A; Van Os J; Pantelis C; Posthuma D; Quested D; Schall U; Scott RJ; Seidman LJ; Toncheva D; Tooney PA; Waddington J; Weinberger DR; Weiser M; Wu JQ, 2016, 'Evidence for Genetic Overlap Between Schizophrenia and Age at First Birth in Women.', JAMA Psychiatry, vol. 73, pp. 497 - 505, http://dx.doi.org/10.1001/jamapsychiatry.2016.0129
2016
Lener MR; Scott RJ; Kluźniak W; Baszuk P; Cybulski C; Wiechowska-Kozłowska A; Huzarski T; Byrski T; Kładny J; Pietrzak S; Soluch A; Jakubowska A; Lubiński J, 2016, 'Do founder mutations characteristic of some cancer sites also predispose to pancreatic cancer?', Int J Cancer, vol. 139, pp. 601 - 606, http://dx.doi.org/10.1002/ijc.30116
2016
Marioni RE; Ritchie SJ; Joshi PK; Hagenaars SP; Okbay A; Fischer K; Adams MJ; Hill WD; Davies G; Nagy R; Amador C; Läll K; Metspalu A; Liewald DC; Campbell A; Wilson JF; Hayward C; Esko T; Porteous DJ; Gale CR; Deary IJ; Beauchamp JP; Fontana MA; Lee JJ; Pers TH; Rietveld CA; Turley P; Chen GB; Emilsson V; Meddens SF; Oskarsson S; Pickrell JK; Thom K; Timshel P; de Vlaming R; Abdellaoui A; Ahluwalia TS; Bacelis J; Baumbach C; Bjornsdottir G; Brandsma JH; Concas MP; Derringer J; Furlotte NA; Galesloot TE; Girotto G; Gupta R; Hall LM; Harris SE; Hofer E; Horikoshi M; Huffman JE; Kaasik K; Kalafati IP; Karlsson R; Kong A; Lahti J; van der Lee SJ; de Leeuw C; Lind PA; Lindgren KO; Liu T; Mangino M; Marten J; Mihailov E; Miller MB; van der Most PJ; Oldmeadow C; Payton A; Pervjakova N; Peyrot WJ; Qian Y; Raitakari O; Rueedi R; Salvi E; Schmidt B; Schraut KE; Shi J; Smith AV; Poot RA; St Pourcain B; Teumer A; Thorleifsson G; Verweij N; Vuckovic D; Wellmann J; Westra HJ; Yang J; Zhao W; Zhu Z; Alizadeh BZ; Amin N; Bakshi A; Baumeister SE; Biino G; Bønnelykke K; Boyle PA; Campbell H; Cappuccio FP, 2016, 'Genetic variants linked to education predict longevity', Proceedings of the National Academy of Sciences of the United States of America, vol. 113, pp. 13366 - 13371, http://dx.doi.org/10.1073/pnas.1605334113
2016
Li N; Thompson ER; Rowley SM; McInerny S; Devereux L; Goode D; LifePool Investigators ; Wong-Brown MW; Scott RJ; Trainer AH; Gorringe KL; James PA; Campbell IG, 2016, 'Reevaluation of RINT1 as a breast cancer predisposition gene.', Breast Cancer Res Treat, vol. 159, pp. 385 - 392, http://dx.doi.org/10.1007/s10549-016-3944-3
2016
Grimson S; Cox AJ; Pringle KG; Burns C; Lumbers ER; Blackwell CC; Scott RJ, 2016, 'The prevalence of unique SNPs in the renin-angiotensin system highlights the need for pharmacogenetics in Indigenous Australians', Clinical and Experimental Pharmacology and Physiology, vol. 43, pp. 157 - 160, http://dx.doi.org/10.1111/1440-1681.12525
2016
Couch FJ; Kuchenbaecker KB; Michailidou K; Mendoza-Fandino GA; Nord S; Lilyquist J; Olswold C; Hallberg E; Agata S; Ahsan H; Aittomäki K; Ambrosone C; Andrulis IL; Anton-Culver H; Arndt V; Arun BK; Arver B; Barile M; Barkardottir RB; Barrowdale D; Beckmann L; Beckmann MW; Benitez J; Blank SV; Blomqvist C; Bogdanova NV; Bojesen SE; Bolla MK; Bonanni B; Brauch H; Brenner H; Burwinkel B; Buys SS; Caldes T; Caligo MA; Canzian F; Carpenter J; Chang-Claude J; Chanock SJ; Chung WK; Claes KBM; Cox A; Cross SS; Cunningham JM; Czene K; Daly MB; Damiola F; Darabi H; De La Hoya M; Devilee P; Diez O; Ding YC; Dolcetti R; Domchek SM; Dorfling CM; Dos-Santos-Silva I; Dumont M; Dunning AM; Eccles DM; Ehrencrona H; Ekici AB; Eliassen H; Ellis S; Fasching PA; Figueroa J; Flesch-Janys D; Försti A; Fostira F; Foulkes WD; Friebel T; Friedman E; Frost D; Gabrielson M; Gammon MD; Ganz PA; Gapstur SM; Garber J; Gaudet MM; Gayther SA; Gerdes AM; Ghoussaini M; Giles GG; Glendon G; Godwin AK; Goldberg MS; Goldgar DE; González-Neira A; Greene MH; Gronwald J; Guénel P; Gunter M; Haeberle L; Haiman CA; Hamann U; Hansen TVO; Hart S; Healey S; Heikkinen T; Henderson BE; Herzog J, 2016, 'Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer', Nature Communications, vol. 7, http://dx.doi.org/10.1038/ncomms11375
2016
Painter JN; O'Mara TA; Marquart L; Webb PM; Attia J; Medland SE; Cheng T; Dennis J; Holliday EG; McEvoy M; Scott RJ; Ahmed S; Healey CS; Shah M; Gorman M; Martin L; Hodgson SV; Beckmann MW; Ekici AB; Fasching PA; Hein A; Rübner M; Czene K; Darabi H; Hall P; Li J; Dörk T; Dürst M; Hillemanns P; Runnebaum IB; Amant F; Annibali D; Depreeuw J; Lambrechts D; Neven P; Cunningham JM; Dowdy SC; Goode EL; Fridley BL; Winham SJ; Njølstad TS; Salvesen HB; Trovik J; Werner HMJ; Ashton KA; Otton G; Proietto A; Mints M; Tham E; Bolla MK; Michailidou K; Wang Q; Tyrer JP; Hopper JL; Peto J; Swerdlow AJ; Burwinkel B; Brenner H; Meindl A; Brauch H; Lindblom A; Chang-Claude J; Couch FJ; Giles GG; Kristensen VN; Cox A; Pharoah PDP; Tomlinson I; Dunning AM; Easton DF; Thompson DJ; Spurdle AB, 2016, 'Genetic risk score mendelian randomization shows that obesity measured as body mass index, but not waist:hip ratio, is causal for endometrial cancer', Cancer Epidemiology Biomarkers and Prevention, vol. 25, pp. 1503 - 1510, http://dx.doi.org/10.1158/1055-9965.EPI-16-0147
2016
Okbay A; Baselmans BML; Neve J-ED; Turley P; Nivard MG; Fontana MA; Meddens SFW; Linnér RK; Rietveld CA; Derringer J; Gratten J; Lee JJ; Liu JZ; de Vlaming R; Ahluwalia TS; Buchwald J; Cavadino A; Frazier-Wood AC; Furlotte NA; Garfield V; Geisel MH; Gonzalez JR; Haitjema S; Karlsson R; van der Laan SW; Ladwig K-H; Lahti J; van der Lee SJ; Lind PA; Liu T; Matteson L; Mihailov E; Miller MB; Minica CC; Nolte IM; Mook-Kanamori D; van der Most PJ; Oldmeadow C; Qian Y; Raitakari O; Rawal R; Realo A; Rueedi R; Schmidt B; Smith AV; Stergiakouli E; Tanaka T; Taylor K; Thorleifsson G; Wedenoja J; Wellmann J; Westra H-J; Willems SM; Zhao W; LifeLines Cohort Study ; Amin N; Bakshi A; Bergmann S; Bjornsdottir G; Boyle PA; Cherney S; Cox SR; Davies G; Davis OSP; Ding J; Direk N; Eibich P; Emeny RT; Fatemifar G; Faul JD; Ferrucci L; Forstner AJ; Gieger C; Gupta R; Harris TB; Harris JM; Holliday EG; Hottenga J-J; Jager PLD; Kaakinen MA; Kajantie E; Karhunen V; Kolcic I; Kumari M; Launer LJ; Franke L; Li-Gao R; Liewald DC; Koini M; Loukola A; Marques-Vidal P; Montgomery GW; Mosing MA; Paternoster L; Pattie A; Petrovic KE; Pulkki-Råback L; Quaye L; Räikkönen K; Rudan I; Scott RJ; Smith JA; Sutin AR; Trzaskowski M; Vinkhuyzen AE; Yu L; Zabaneh D; Attia JR; Bennett DA; Berger K; Bertram L; Boomsma DI; Snieder H; Chang S-C; Cucca F; Deary IJ; van Duijn CM; Eriksson JG; Bültmann U; de Geus EJC; Groenen PJF; Gudnason V; Hansen T; Hartman CA; Haworth CMA; Hayward C; Heath AC; Hinds DA; Hyppönen E; Iacono WG; Järvelin M-R; Jöckel K-H; Kaprio J; Kardia SLR; Keltikangas-Järvinen L; Kraft P; Kubzansky LD; Lehtimäki T; Magnusson PKE; Martin NG; McGue M; Metspalu A; Mills M; de Mutsert R; Oldehinkel AJ; Pasterkamp G; Pedersen NL; Plomin R; Polasek O; Power C; Rich SS; Rosendaal FR; den Ruijter HM; Schlessinger D; Schmidt H; Svento R; Schmidt R; Alizadeh BZ; Sørensen TIA; Spector TD; Starr JM; Stefansson K; Steptoe A; Terracciano A; Thorsteinsdottir U; Thurik AR; Timpson NJ; Tiemeier H; Uitterlinden AG; Vollenweider P; Wagner GG; Weir DR; Yang J; Conley DC; Smith GD; Hofman A; Johannesson M; Laibson DI; Medland SE; Meyer MN; Pickrell JK; Esko T; Krueger RF; Beauchamp JP; Koellinger PD; Benjamin DJ; Bartels M; Cesarini D, 2016, 'Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.', Nat Genet, vol. 48, pp. 970, http://dx.doi.org/10.1038/ng0816-970c
2016
Kamien B; Digilio MC; Novelli A; O'Donnell S; Bain N; Meldrum C; Dudding-Byth T; Scott RJ; Goel H, 2015, 'Narrowing the critical region for overgrowth within 13q14.2-q14.3 microdeletions.', Eur J Med Genet, vol. 58, pp. 629 - 633, http://dx.doi.org/10.1016/j.ejmg.2015.10.006
2015
Rush A; Christiansen JH; Farrell JP; Goode SM; Scott RJ; Spring KJ; Byrne JA, 2015, 'Biobank classification in an australian setting', Biopreservation and Biobanking, vol. 13, pp. 212 - 218, http://dx.doi.org/10.1089/bio.2015.0007
2015
Mavaddat N; Pharoah PDP; Michailidou K; Tyrer J; Brook MN; Bolla MK; Wang Q; Dennis J; Dunning AM; Shah M; Luben R; Brown J; Bojesen SE; Nordestgaard BG; Nielsen SF; Flyger H; Czene K; Darabi H; Eriksson M; Peto J; Dos-Santos-Silva I; Dudbridge F; Johnson N; Schmidt MK; Broeks A; Verhoef S; Rutgers EJ; Swerdlow A; Ashworth A; Orr N; Schoemaker MJ; Figueroa J; Chanock SJ; Brinton L; Lissowska J; Couch FJ; Olson JE; Vachon C; Pankratz VS; Lambrechts D; Wildiers H; Van Ongeval C; Van Limbergen E; Kristensen V; Grenaker Alnæs G; Nord S; Borresen-Dale AL; Nevanlinna H; Muranen TA; Aittomäki K; Blomqvist C; Chang-Claude J; Rudolph A; Seibold P; Flesch-Janys D; Fasching PA; Haeberle L; Ekici AB; Beckmann MW; Burwinkel B; Marme F; Schneeweiss A; Sohn C; Trentham-Dietz A; Newcomb P; Titus L; Egan KM; Hunter DJ; Lindstrom S; Tamimi RM; Kraft P; Rahman N; Turnbull C; Renwick A; Seal S; Li J; Liu J; Humphreys K; Benitez J; Pilar Zamora M; Arias Perez JI; Menéndez P; Jakubowska A; Lubinski J; Jaworska-Bieniek K; Durda K; Bogdanova NV; Antonenkova NN; Dörk T; Anton-Culver H; Neuhausen SL; Ziogas A; Bernstein L; Devilee P; Tollenaar RAEM; Seynaeve C; Van Asperen CJ; Cox A; Cross SS; Reed MWR, 2015, 'Prediction of breast cancer risk based on profiling with common genetic variants', Journal of the National Cancer Institute, vol. 107, http://dx.doi.org/10.1093/jnci/djv036
2015
Dun MD; Chalkley RJ; Faulkner S; Keene S; Avery-Kiejda KA; Scott RJ; Falkenby LG; Cairns MJ; Larsen MR; Bradshaw RA; Hondermarck H, 2015, 'Proteotranscriptomic Profiling of 231-BR Breast Cancer Cells: Identification of Potential Biomarkers and Therapeutic Targets for Brain Metastasis.', Mol Cell Proteomics, vol. 14, pp. 2316 - 2330, http://dx.doi.org/10.1074/mcp.M114.046110
2015
Stirzaker C; Zotenko E; Song JZ; Qu W; Nair SS; Locke WJ; Stone A; Armstong NJ; Robinson MD; Dobrovic A; Avery-Kiejda KA; Peters KM; French JD; Stein S; Korbie DJ; Trau M; Forbes JF; Scott RJ; Brown MA; Francis GD; Clark SJ, 2015, 'Methylome sequencing in triple-negative breast cancer reveals distinct methylation clusters with prognostic value', Nature Communications, vol. 6, pp. 5899 - 5899, http://dx.doi.org/10.1038/ncomms6899
2015
Mathe A; Wong-Brown M; Morten B; Forbes JF; Braye SG; Avery-Kiejda KA; Scott RJ, 2015, 'Novel genes associated with lymph node metastasis in triple negative breast cancer.', Sci Rep, vol. 5, pp. 15832, http://dx.doi.org/10.1038/srep15832
2015
Pundavela J; Roselli S; Faulkner S; Attia J; Scott RJ; Thorne RF; Forbes JF; Bradshaw RA; Walker MM; Jobling P; Hondermarck H, 2015, 'Nerve fibers infiltrate the tumor microenvironment and are associated with nerve growth factor production and lymph node invasion in breast cancer.', Mol Oncol, vol. 9, pp. 1626 - 1635, http://dx.doi.org/10.1016/j.molonc.2015.05.001
2015
Carvajal-Carmona LG; O'Mara TA; Painter JN; Lose FA; Dennis J; Michailidou K; Tyrer JP; Ahmed S; Ferguson K; Healey CS; Pooley K; Beesley J; Cheng T; Jones A; Howarth K; Martin L; Gorman M; Hodgson S; National Study of Endometrial Cancer Genetics Group (NSECG) ; Australian National Endometrial Cancer Study Group (ANECS) ; Wentzensen N; Fasching PA; Hein A; Beckmann MW; Renner SP; Dörk T; Hillemanns P; Dürst M; Runnebaum I; Lambrechts D; Coenegrachts L; Schrauwen S; Amant F; Winterhoff B; Dowdy SC; Goode EL; Teoman A; Salvesen HB; Trovik J; Njolstad TS; Werner HMJ; Scott RJ; Ashton K; Proietto T; Otton G; Wersäll O; Mints M; Tham E; RENDOCAS ; Hall P; Czene K; Liu J; Li J; Hopper JL; Southey MC; Australian Ovarian Cancer Study (AOCS) ; Ekici AB; Ruebner M; Johnson N; Peto J; Burwinkel B; Marme F; Brenner H; Dieffenbach AK; Meindl A; Brauch H; GENICA Network ; Lindblom A; Depreeuw J; Moisse M; Chang-Claude J; Rudolph A; Couch FJ; Olson JE; Giles GG; Bruinsma F; Cunningham JM; Fridley BL; Børresen-Dale A-L; Kristensen VN; Cox A; Swerdlow AJ; Orr N; Bolla MK; Wang Q; Weber RP; Chen Z; Shah M; Pharoah PDP; Dunning AM; Tomlinson I; Easton DF; Spurdle AB; Thompson DJ, 2015, 'Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk.', Hum Genet, vol. 134, pp. 231 - 245, http://dx.doi.org/10.1007/s00439-014-1515-4
2015
Nead KT; Sharp SJ; Thompson DJ; Painter JN; Savage DB; Semple RK; Barker A; Australian National Endometrial Cancer Study Group (ANECS) ; Perry JRB; Attia J; Dunning AM; Easton DF; Holliday E; Lotta LA; O'Mara T; McEvoy M; Pharoah PDP; Scott RJ; Spurdle AB; Langenberg C; Wareham NJ; Scott RA, 2015, 'Evidence of a Causal Association Between Insulinemia and Endometrial Cancer: A Mendelian Randomization Analysis.', J Natl Cancer Inst, vol. 107, http://dx.doi.org/10.1093/jnci/djv178
2015
Movahedi M; Bishop DT; Macrae F; Mecklin JP; Moeslein G; Olschwang S; Eccles D; Evans DG; Maher ER; Bertario L; Bisgaard ML; Dunlop MG; Ho JWC; Hodgson SV; Lindblom A; Lubinski J; Morrison PJ; Murday V; Ramesar RS; Side L; Scott RJ; Thomas HJW; Vasen HF; Burn J; Mathers JC, 2015, 'Obesity, aspirin, and risk of colorectal cancer in carriers of hereditary colorectal cancer: A prospective investigation in the CAPP2 study', Journal of Clinical Oncology, vol. 33, pp. 3591 - 3597, http://dx.doi.org/10.1200/JCO.2014.58.9952
2015
Lener M; Muszyńska M; Jakubowska A; Jaworska-Bieniek K; Sukiennicki G; Kaczmarek K; Durda K; Gromowski T; Serrano-Fernández P; Kładny J; Wiechowska-Kozłowska A; Grodzki T; Jaworowska E; Lubiński J; Górecka-Szyld B; Wilk G; Huzarski T; Byrski T; Cybulski C; Gronwald J; Dębniak T; Ashuryk O; Tołoczko-Grabarek A; Morawski A; Scott RJ; Lubiński J, 2015, 'Selenium as a marker of cancer risk and of selection for control examinations in surveillance.', Contemp Oncol (Pozn), vol. 19, pp. A60 - A61, http://dx.doi.org/10.5114/wo.2014.47131
2015
Scott R; Dooley S; Lewis W; Meldrum C; Pockney P; Draganic B; Smith S; Jones F; Hewitt C; Phillimore H; Lucas A; Shi E; Namdarian K; Chan T; Acosta D; Chan S-P; Fox S, 2015, 'P-273 Concordance of RAS mutation status in CRC patients by comparison of results from circulating tumour DNA and tissue-based testing', Annals of Oncology, vol. 26, pp. iv80 - iv80, http://dx.doi.org/10.1093/annonc/mdv233.270
2015
Kurlapska A; Serrano-Fernandez P; Baszuk P; Gupta S; Starzynska T; Malecka-Panas E; Dabrowski A; Debniak T; Kurzawski G; Suchy J; Rogoza-Mateja W; Scott RJ; Lubinski J, 2015, 'Cumulative effects of genetic markers and the detection of advanced colorectal neoplasias by population screening', CLINICAL GENETICS, vol. 88, pp. 234 - 240, http://dx.doi.org/10.1111/cge.12481
2015
Moscovis SM; Gordon AE; Al Madani OM; Gleeson M; Scott RJ; Hall ST; Burns C; Blackwell C, 2015, 'Virus Infections and Sudden Death in Infancy: The Role of Interferon-γ.', Front Immunol, vol. 6, pp. 107, http://dx.doi.org/10.3389/fimmu.2015.00107
2015
Gu BJ; Field J; Dutertre S; Ou A; Kilpatrick TJ; Lechner-Scott J; Scott R; Lea R; Taylor BV; Stankovich J; Butzkueven H; Gresle M; Laws SM; Petrou S; Hoffjan S; Akkad DA; Graham CA; Hawkins S; Glaser A; Bedri SK; Hillert J; Matute C; Antiguedad A; ANZgene Consortium ; Wiley JS, 2015, 'A rare P2X7 variant Arg307Gln with absent pore formation function protects against neuroinflammation in multiple sclerosis.', Hum Mol Genet, vol. 24, pp. 5644 - 5654, http://dx.doi.org/10.1093/hmg/ddv278
2015
Mathe A; Scott RJ; Avery-Kiejda KA, 2015, 'MiRNAs and Other Epigenetic Changes as Biomarkers in Triple Negative Breast Cancer.', Int J Mol Sci, vol. 16, pp. 28347 - 28376, http://dx.doi.org/10.3390/ijms161226090
2015
Maltby VE; Graves MC; Lea RA; Benton MC; Sanders KA; Tajouri L; Scott RJ; Lechner-Scott J, 2015, 'Genome-wide DNA methylation profiling of CD8+ T cells shows a distinct epigenetic signature to CD4+ T cells in multiple sclerosis patients.', Clin Epigenetics, vol. 7, pp. 118, http://dx.doi.org/10.1186/s13148-015-0152-7
2015
Serrano-Fernandez P; Dymerska D; Kurzawski G; Derkacz R; Sobieszczańska T; Banaszkiewicz Z; Roomere H; Oitmaa E; Metspalu A; Janavičius R; Elsakov P; Razumas M; Petrulis K; Irmejs A; Miklaševičs E; Scott RJ; Lubiński J, 2015, 'Cumulative Small Effect Genetic Markers and the Risk of Colorectal Cancer in Poland, Estonia, Lithuania, and Latvia.', Gastroenterol Res Pract, vol. 2015, pp. 204089, http://dx.doi.org/10.1155/2015/204089
2015
Holliday EG; Traylor M; Malik R; Bevan S; Falcone G; Hopewell JC; Cheng YC; Cotlarciuc I; Bis JC; Boerwinkle E; Boncoraglio GB; Clarke R; Cole JW; Fornage M; Furie KL; Ikram MA; Jannes J; Kittner SJ; Lincz LF; Maguire JM; Meschia JF; Mosley TH; Nalls MA; Oldmeadow C; Parati EA; Psaty BM; Rothwell PM; Seshadri S; Scott RJ; Sharma P; Sudlow C; Wiggins KL; Worrall BB; Rosand J; Mitchell BD; Dichgans M; Markus HS; Levi C; Attia J; Wray NR, 2015, 'Genetic overlap between diagnostic subtypes of ischemic stroke', Stroke, vol. 46, pp. 615 - 619, http://dx.doi.org/10.1161/STROKEAHA.114.007930
2015
Abdullah N; Abdul Murad NA; Attia J; Oldmeadow C; Mohd Haniff EA; Syafruddin SE; Abd Jalal N; Ismail N; Ishak M; Jamal R; Scott RJ; Holliday EG, 2015, 'Characterizing the genetic risk for Type 2 diabetes in a Malaysian multi-ethnic cohort.', Diabet Med, vol. 32, pp. 1377 - 1384, http://dx.doi.org/10.1111/dme.12735
2015
Sapkota Y; Low S-K; Attia J; Gordon SD; Henders AK; Holliday EG; MacGregor S; Martin NG; McEvoy M; Morris AP; Takahashi A; Scott RJ; Kubo M; Zondervan KT; Montgomery GW; Nyholt DR, 2015, 'Association between endometriosis and the interleukin 1A (IL1A) locus.', Hum Reprod, vol. 30, pp. 239 - 248, http://dx.doi.org/10.1093/humrep/deu267
2015
Vilhjálmsson BJ; Yang J; Finucane HK; Gusev A; Lindström S; Ripke S; Genovese G; Loh PR; Bhatia G; Do R; Hayeck T; Won HH; Neale BM; Corvin A; Walters JTR; Farh KH; Holmans PA; Lee P; Bulik-Sullivan B; Collier DA; Huang H; Pers TH; Agartz I; Agerbo E; Albus M; Alexander M; Amin F; Bacanu SA; Begemann M; Belliveau RA; Bene J; Bergen SE; Bevilacqua E; Bigdeli TB; Black DW; Bruggeman R; Buccola NG; Buckner RL; Byerley W; Cahn W; Cai G; Campion D; Cantor RM; Carr VJ; Carrera N; Catts SV; Chambert KD; Chan RCK; Chen RYL; Chen EYH; Cheng W; Cheung EFC; Chong SA; Cloninger CR; Cohen D; Cohen N; Cormican P; Craddock N; Crowley JJ; Curtis D; Davidson M; Davis KL; Degenhardt F; Del Favero J; Delisi LE; Demontis D; Dikeos D; Dinan T; Djurovic S; Donohoe G; Drapeau E; Duan J; Dudbridge F; Durmishi N; Eichhammer P; Eriksson J; Escott-Price V; Essioux L; Fanous AH; Farrell MS; Frank J; Franke L; Freedman R; Freimer NB; Friedl M; Friedman JI; Fromer M; Georgieva L; Gershon ES; Giegling I; Giusti-Rodrguez P; Godard S; Goldstein JI; Golimbet V; Gopal S; Gratten J; Grove J; De Haan L; Hammer C; Hamshere ML, 2015, 'Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores', American Journal of Human Genetics, vol. 97, pp. 576 - 592, http://dx.doi.org/10.1016/j.ajhg.2015.09.001
2015
Moir-Meyer GL; Pearson JF; Lose F; Australian National Endometrial Cancer Study Group ; Scott RJ; McEvoy M; Attia J; Holliday EG; Hunter Community Study ; Studies of Epidemiology and Risk Factors in Cancer Heredity ; Pharoah PD; Dunning AM; Thompson DJ; Easton DF; Spurdle AB; Walker LC, 2015, 'Rare germline copy number deletions of likely functional importance are implicated in endometrial cancer predisposition.', Hum Genet, vol. 134, pp. 269 - 278, http://dx.doi.org/10.1007/s00439-014-1507-4
2015
Thompson ER; Gorringe KL; Rowley SM; Li N; McInerny S; Wong-Brown MW; Devereux L; Li J; Lifepool Investigators ; Trainer AH; Mitchell G; Scott RJ; James PA; Campbell IG, 2015, 'Reevaluation of the BRCA2 truncating allele c.9976A > T (p.Lys3326Ter) in a familial breast cancer context.', Sci Rep, vol. 5, pp. 14800, http://dx.doi.org/10.1038/srep14800
2015
Sapkota Y; Attia J; Gordon SD; Henders AK; Holliday EG; Rahmioglu N; MacGregor S; Martin NG; McEvoy M; Morris AP; Scott RJ; Zondervan KT; Montgomery GW; Nyholt DR, 2015, 'Genetic burden associated with varying degrees of disease severity in endometriosis.', Mol Hum Reprod, vol. 21, pp. 594 - 602, http://dx.doi.org/10.1093/molehr/gav021
2015
Cheng THT; Thompson D; Painter J; O'Mara T; Gorman M; Martin L; Palles C; Jones A; Buchanan DD; Win AK; Hopper J; Jenkins M; Lindor NM; Newcomb PA; Gallinger S; Conti D; Schumacher F; Casey G; Giles GG; Pharoah P; Peto J; Cox A; Swerdlow A; Couch F; Cunningham JM; Goode EL; Winham SJ; Lambrechts D; Fasching P; Burwinkel B; Brenner H; Brauch H; Chang-Claude J; Salvesen HB; Kristensen V; Darabi H; Li J; Liu T; Lindblom A; Hall P; de Polanco ME; Sans M; Carracedo A; Castellvi-Bel S; Rojas-Martinez A; Aguiar Jnr S; Teixeira MR; Dunning AM; Dennis J; Otton G; Proietto T; Holliday E; Attia J; Ashton K; Scott RJ; McEvoy M; Dowdy SC; Fridley BL; Werner HMJ; Trovik J; Njolstad TS; Tham E; Mints M; Runnebaum I; Hillemanns P; Dörk T; Amant F; Schrauwen S; Hein A; Beckmann MW; Ekici A; Czene K; Meindl A; Bolla MK; Michailidou K; Tyrer JP; Wang Q; Ahmed S; Healey CS; Shah M; Annibali D; Depreeuw J; Al-Tassan NA; Harris R; Meyer BF; Whiffin N; Hosking FJ; Kinnersley B; Farrington SM; Timofeeva M; Tenesa A; Campbell H; Haile RW; Hodgson S; Carvajal-Carmona L; Cheadle JP; Easton D; Dunlop M; Houlston R; Spurdle A; Tomlinson I, 2015, 'Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1.', Sci Rep, vol. 5, pp. 17369, http://dx.doi.org/10.1038/srep17369
2015
Darabi H; McCue K; Beesley J; Michailidou K; Nord S; Kar S; Humphreys K; Thompson D; Ghoussaini M; Bolla MK; Dennis J; Wang Q; Canisius S; Scott CG; Apicella C; Hopper JL; Southey MC; Stone J; Broeks A; Schmidt MK; Scott RJ; Lophatananon A; Muir K; Beckmann MW; Ekici AB; Fasching PA; Heusinger K; Dos-Santos-Silva I; Peto J; Tomlinson I; Sawyer EJ; Burwinkel B; Marme F; Guénel P; Truong T; Bojesen SE; Flyger H; Benitez J; González-Neira A; Anton-Culver H; Neuhausen SL; Arndt V; Brenner H; Engel C; Meindl A; Schmutzler RK; Arnold N; Brauch H; Hamann U; Chang-Claude J; Khan S; Nevanlinna H; Ito H; Matsuo K; Bogdanova NV; Dörk T; Lindblom A; Margolin S; Kosma VM; Mannermaa A; Tseng CC; Wu AH; Floris G; Lambrechts D; Rudolph A; Peterlongo P; Radice P; Couch FJ; Vachon C; Giles GG; McLean C; Milne RL; Dugué PA; Haiman CA; Maskarinec G; Woolcott C; Henderson BE; Goldberg MS; Simard J; Teo SH; Mariapun S; Helland Å; Haakensen V; Zheng W; Beeghly-Fadiel A; Tamimi R; Jukkola-Vuorinen A; Winqvist R; Andrulis IL; Knight JA; Devilee P; Tollenaar RAEM; Figueroa J; García-Closas M; Czene K; Hooning MJ; Tilanus-Linthorst M; Li J; Gao YT; Shu XO, 2015, 'Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression', American Journal of Human Genetics, vol. 97, pp. 22 - 34, http://dx.doi.org/10.1016/j.ajhg.2015.05.002
2015
Lubinski J; Scott RJ; Sijmons R; Bayliss K, 2015, 'Thank you to all our manuscript reviewers in 2014', Hereditary Cancer in Clinical Practice, vol. 13, http://dx.doi.org/10.1186/s13053-015-0029-y
2015
Wong-Brown MW; Meldrum CJ; Carpenter JE; Clarke CL; Narod SA; Jakubowska A; Rudnicka H; Lubinski J; Scott RJ, 2015, 'Prevalence of BRCA1 and BRCA2 germline mutations in patients with triple-negative breast cancer', Breast Cancer Research and Treatment, vol. 150, pp. 71 - 80, http://dx.doi.org/10.1007/s10549-015-3293-7
2015
Wong-Brown M; Avery-Kiejda K; Scott RJ, 2015, 'Genetic insights into breast cancer risk', Hereditary Cancer in Clinical Practice, vol. 13, http://dx.doi.org/10.1186/1897-4287-13-s1-a1
2015
Thompson ER; Gorringe KL; Rowley SM; Wong-Brown MW; McInerny S; Li N; Trainer AH; Devereux L; Doyle MA; Li J; Lupat R; Delatycki MB; LifePool Investigators ; Mitchell G; James PA; Scott RJ; Campbell IG, 2015, 'Prevalence of PALB2 mutations in Australian familial breast cancer cases and controls.', Breast Cancer Res, vol. 17, pp. 111, http://dx.doi.org/10.1186/s13058-015-0627-7
2015
Painter JN; O'Mara TA; Batra J; Cheng T; Lose FA; Dennis J; Michailidou K; Tyrer JP; Ahmed S; Ferguson K; Healey CS; Kaufmann S; Hillman KM; Walpole C; Moya L; Pollock P; Jones A; Howarth K; Martin L; Gorman M; Hodgson S; National Study of Endometrial Cancer Genetics Group (NSECG) ; CHIBCHA Consortium ; De Polanco MME; Sans M; Carracedo A; Castellvi-Bel S; Rojas-Martinez A; Santos E; Teixeira MR; Carvajal-Carmona L; Shu X-O; Long J; Zheng W; Xiang Y-B; Australian National Endometrial Cancer Study Group (ANECS) ; Montgomery GW; Webb PM; Scott RJ; McEvoy M; Attia J; Holliday E; Martin NG; Nyholt DR; Henders AK; Fasching PA; Hein A; Beckmann MW; Renner SP; Dörk T; Hillemanns P; Dürst M; Runnebaum I; Lambrechts D; Coenegrachts L; Schrauwen S; Amant F; Winterhoff B; Dowdy SC; Goode EL; Teoman A; Salvesen HB; Trovik J; Njolstad TS; Werner HMJ; Ashton K; Proietto T; Otton G; Tzortzatos G; Mints M; Tham E; RENDOCAS ; Hall P; Czene K; Liu J; Li J; Hopper JL; Southey MC; Australian Ovarian Cancer Study (AOCS) ; Ekici AB; Ruebner M; Johnson N; Peto J; Burwinkel B; Marme F; Brenner H; Dieffenbach AK; Meindl A; Brauch H; GENICA Network ; Lindblom A; Depreeuw J; Moisse M; Chang-Claude J; Rudolph A; Couch FJ; Olson JE; Giles GG; Bruinsma F; Cunningham JM; Fridley BL; Børresen-Dale A-L; Kristensen VN; Cox A; Swerdlow AJ; Orr N; Bolla MK; Wang Q; Weber RP; Chen Z; Shah M; French JD; Pharoah PDP; Dunning AM; Tomlinson I; Easton DF; Edwards SL; Thompson DJ; Spurdle AB, 2015, 'Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk.', Hum Mol Genet, vol. 24, pp. 1478 - 1492, http://dx.doi.org/10.1093/hmg/ddu552
2015
Dębniak T; Gromowski T; Scott RJ; Gronwald J; Huzarski T; Byrski T; Kurzawski G; Dymerska D; Górski B; Paszkowska-Szczur K; Cybulski C; Serrano-Fernandez P; Lubiński J, 2015, 'Management of ovarian and endometrial cancers in women belonging to HNPCC carrier families: review of the literature and results of cancer risk assessment in Polish HNPCC families.', Hered Cancer Clin Pract, vol. 13, pp. 3, http://dx.doi.org/10.1186/s13053-015-0025-2
2015
Bowden NA; Beveridge NJ; Ashton KA; Baines KJ; Scott RJ, 2015, 'Understanding Xeroderma Pigmentosum Complementation Groups Using Gene Expression Profiling after UV-Light Exposure.', Int J Mol Sci, vol. 16, pp. 15985 - 15996, http://dx.doi.org/10.3390/ijms160715985
2015
Scott RJ; Cavana RY; Cameron D, 2015, 'Interpersonal success factors for strategy implementation: a case study using group model building', Journal of the Operational Research Society, vol. 66, pp. 1023 - 1034, http://dx.doi.org/10.1057/jors.2014.70
2015
Cropley VL; Scarr E; Fornito A; Klauser P; Bousman CA; Scott R; Cairns MJ; Tooney PA; Pantelis C; Dean B, 2015, 'The effect of a muscarinic receptor 1 gene variant on grey matter volume in schizophrenia.', Psychiatry Res, vol. 234, pp. 182 - 187, http://dx.doi.org/10.1016/j.pscychresns.2015.09.004
2015
Blackwell C; Moscovis S; Hall S; Burns C; Scott RJ, 2015, 'Exploring the risk factors for sudden infant deaths and their role in inflammatory responses to infection.', Front Immunol, vol. 6, pp. 44, http://dx.doi.org/10.3389/fimmu.2015.00044
2015
Pan X; Bowman M; Scott RJ; Fitter J; Nicholson RC; Smith R; Zakar T, 2015, 'Methylation of the Corticotropin Releasing Hormone Gene Promoter in BeWo Cells: Relationship to Gene Activity.', Int J Endocrinol, vol. 2015, pp. 861302, http://dx.doi.org/10.1155/2015/861302
2015
Moscovis SM; Cox A; Hall ST; Burns CJ; Scott RJ; Blackwell CC, 2015, 'Effects of gender, cytokine gene polymorphisms and environmental factors on inflammatory responses.', Innate Immun, vol. 21, pp. 523 - 530, http://dx.doi.org/10.1177/1753425914553645
2015
Lener M; Wiechowska-Kozlowska A; Scott RJ; Muszynska M; Kladny J; Waloszczyk P; Rutkowska A; Sukiennicki G; Gromowski T; Jaworska-Bieniek K; van de Wetering T; Kaczmarek K; Jakubowska A; Lubinski J, 2015, 'Serum concentrations of Cu, Se, Fe and Zn in patients diagnosed with pancreatic cancer', Hereditary Cancer in Clinical Practice, vol. 13, http://dx.doi.org/10.1186/1897-4287-13-s1-a14
2015
O'Mara TA; Glubb DM; Painter JN; Cheng T; Dennis J; Australian National Endometrial Cancer Study Group (ANECS) ; Attia J; Holliday EG; McEvoy M; Scott RJ; Ashton K; Proietto T; Otton G; Shah M; Ahmed S; Healey CS; Gorman M; Martin L; National Study of Endometrial Cancer Genetics Group (NSECG) ; Hodgson S; Fasching PA; Hein A; Beckmann MW; Ekici AB; Hall P; Czene K; Darabi H; Li J; Dürst M; Runnebaum I; Hillemanns P; Dörk T; Lambrechts D; Depreeuw J; Annibali D; Amant F; Zhao H; Goode EL; Dowdy SC; Fridley BL; Winham SJ; Salvesen HB; Njølstad TS; Trovik J; Werner HMJ; Tham E; Liu T; Mints M; RENDOCAS ; Bolla MK; Michailidou K; Tyrer JP; Wang Q; Hopper JL; AOCS Group ; Peto J; Swerdlow AJ; Burwinkel B; Brenner H; Meindl A; Brauch H; Lindblom A; Chang-Claude J; Couch FJ; Giles GG; Kristensen VN; Cox A; Pharoah PDP; Dunning AM; Tomlinson I; Easton DF; Thompson DJ; Spurdle AB, 2015, 'Comprehensive genetic assessment of the ESR1 locus identifies a risk region for endometrial cancer.', Endocr Relat Cancer, vol. 22, pp. 851 - 861, http://dx.doi.org/10.1530/ERC-15-0319
2015
Moscovis SM; Gordon AE; Al Madani OM; Gleeson M; Scott RJ; Hall ST; Burns C; Blackwell C, 2015, 'Genetic and Environmental Factors Affecting TNF-α Responses in Relation to Sudden Infant Death Syndrome.', Front Immunol, vol. 6, pp. 374, http://dx.doi.org/10.3389/fimmu.2015.00374
2015
Cox AJ; Moscovis SM; Blackwell CC; Scott RJ, 2014, 'Cytokine gene polymorphism among Indigenous Australians.', Innate Immun, vol. 20, pp. 431 - 439, http://dx.doi.org/10.1177/1753425913498911
2014
Scott RJ, 2014, 'A Systems Perspective on the Natural Resources Framework: comment on Hearnshaw et al.', Policy Quarterly, vol. 10, pp. 59 - 62, http://igps.victoria.ac.nz/publications/files/3d69af7dcc4.pdf
2014
Zyluk A; Paszkowska-Szczur K; Gupta S; Scott RJ; Lubiński J; Debniak T, 2014, 'Dupuytren's disease and the risk of malignant neoplasms', Hereditary Cancer in Clinical Practice, vol. 12, http://dx.doi.org/10.1186/1897-4287-12-6
2014
Loth DW; Soler Artigas M; Gharib SA; Wain LV; Franceschini N; Koch B; Pottinger TD; Smith AV; Duan Q; Oldmeadow C; Lee MK; Strachan DP; James AL; Huffman JE; Vitart V; Ramasamy A; Wareham NJ; Kaprio J; Wang X-Q; Trochet H; Kähönen M; Flexeder C; Albrecht E; Lopez LM; de Jong K; Thyagarajan B; Alves AC; Enroth S; Omenaas E; Joshi PK; Fall T; Viñuela A; Launer LJ; Loehr LR; Fornage M; Li G; Wilk JB; Tang W; Manichaikul A; Lahousse L; Harris TB; North KE; Rudnicka AR; Hui J; Gu X; Lumley T; Wright AF; Hastie ND; Campbell S; Kumar R; Pin I; Scott RA; Pietiläinen KH; Surakka I; Liu Y; Holliday EG; Schulz H; Heinrich J; Davies G; Vonk JM; Wojczynski M; Pouta A; Johansson A; Wild SH; Ingelsson E; Rivadeneira F; Völzke H; Hysi PG; Eiriksdottir G; Morrison AC; Rotter JI; Gao W; Postma DS; White WB; Rich SS; Hofman A; Aspelund T; Couper D; Smith LJ; Psaty BM; Lohman K; Burchard EG; Uitterlinden AG; Garcia M; Joubert BR; McArdle WL; Musk AB; Hansel N; Heckbert SR; Zgaga L; van Meurs JBJ; Navarro P; Rudan I; Oh Y-M; Redline S; Jarvis DL; Zhao JH; Rantanen T; O'Connor GT; Ripatti S; Scott RJ; Karrasch S; Grallert H; Gaddis NC; Starr JM; Wijmenga C; Minster RL; Lederer DJ; Pekkanen J; Gyllensten U; Campbell H; Morris AP; Gläser S; Hammond CJ; Burkart KM; Beilby J; Kritchevsky SB; Gudnason V; Hancock DB; Williams OD; Polasek O; Zemunik T; Kolcic I; Petrini MF; Wjst M; Kim WJ; Porteous DJ; Scotland G; Smith BH; Viljanen A; Heliövaara M; Attia JR; Sayers I; Hampel R; Gieger C; Deary IJ; Boezen HM; Newman A; Jarvelin M-R; Wilson JF; Lind L; Stricker BH; Teumer A; Spector TD; Melén E; Peters MJ; Lange LA; Barr RG; Bracke KR; Verhamme FM; Sung J; Hiemstra PS; Cassano PA; Sood A; Hayward C; Dupuis J; Hall IP; Brusselle GG; Tobin MD; London SJ, 2014, 'Genome-wide association analysis identifies six new loci associated with forced vital capacity.', Nat Genet, vol. 46, pp. 669 - 677, http://dx.doi.org/10.1038/ng.3011
2014
Greenop KR; Peters S; Bailey HD; Fritschi L; Attia J; Scott RJ; Glass DC; de Klerk NH; Alvaro F; Armstrong BK; Milne E, 2014, 'Erratum to: Exposure to pesticides and the risk of childhood brain tumors', Cancer Causes & Control, vol. 25, pp. 1239 - 1240, http://dx.doi.org/10.1007/s10552-014-0418-y
2014
Paszkowska-Szczur K; Scott RJ; Górski B; Cybulski C; Kurzawski G; Dymerska D; Gupta S; Van De Wetering T; Masojć B; Kashyap A; Gapska P; Gromowski T; Kładny J; Lubiński J; Dębniak T, 2014, 'Polymorphisms in nucleotide excision repair genes and susceptibility to colorectal cancer in the Polish population', Molecular Biology Reports, http://dx.doi.org/10.1007/s11033-014-3824-z
2014
Abdullah N; Attia J; Oldmeadow C; Scott RJ; Holliday EG, 2014, 'The architecture of risk for type 2 diabetes: understanding Asia in the context of global findings.', Int J Endocrinol, vol. 2014, pp. 593982, http://dx.doi.org/10.1155/2014/593982
2014
Pluschke A; Jaaback K; Scott RJ; Lombard J; Yin H, 2014, 'Epithelioid trophoblastic tumour simulating a high grade carcinoma.', Pathology, vol. 46, pp. 248 - 250, http://dx.doi.org/10.1097/PAT.0000000000000088
2014
Avery-Kiejda KA; Braye SG; Forbes JF; Scott RJ, 2014, 'The expression of Dicer and Drosha in matched normal tissues, tumours and lymph node metastases in triple negative breast cancer.', BMC Cancer, vol. 14, pp. 253, http://dx.doi.org/10.1186/1471-2407-14-253
2014
Wan C; Latter JL; Amirshahi A; Symonds I; Finnie J; Bowden N; Scott RJ; Cunningham KA; Timms P; Beagley KW, 2014, 'Progesterone activates multiple innate immune pathways in Chlamydia trachomatis-infected endocervical cells.', Am J Reprod Immunol, vol. 71, pp. 165 - 177, http://dx.doi.org/10.1111/aji.12168
2014
Purrington KS; Slettedahl S; Bolla MK; Michailidou K; Czene K; Nevanlinna H; Bojesen SE; Andrulis IL; Cox A; Hall P; Carpenter J; Yannoukakos D; A. Haiman C; Fasching PA; Mannermaa A; Winqvist R; Brenner H; Lindblom A; Chenevix-Trench G; Benitez J; Swerdlow A; Kristensen V; Guénel P; Meindl A; Darabi H; Eriksson M; Fagerholm R; Aittomaki K; Blomqvist C; Nordestgaard BG; Nielsen SF; Flyger H; Wang X; Olswold C; Olson JE; Mulligan AM; Knight JA; Tchatchou S; Reed MWR; Cross SS; Liu J; Li J; Humphreys K; Clarke C; Scott R; Balleine R; Baxter R; Braye S; Dahlstrom J; Forbes J; Lee S; Marsh D; Morey A; Pathmanathan N; Spigelman A; Wilcken N; Yip D; Landrith S; Oeser S; Rübner M; Williams E; Ryder-Mills E; Sargus K; Colleran G; Rowan A; Jones A; Andersen DU; Arnadottir MB; Bank A; Kjeldgård D; Pita H; Alonso C; Herrero D; Álvarez N; Zamora MP; Menendez P; Lacey J; Wang S; Ma H; Lu Y; Clague J; Deapen D; Pinder R; Lee E; Schumacher F; Horn-Ross P; Reynolds P; Nelson D; Ziegler H; Wolf S; Hermann V; Hellebrand H; Engert S; Fostira F; Fountzilas G; Konstantopoulou I; Henderson BE; Le Marchand L; Ekici AB; Hartmann A, 2014, 'Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade', Human Molecular Genetics, vol. 23, pp. 6034 - 6046, http://dx.doi.org/10.1093/hmg/ddu300
2014
Wong-Brown MW; Avery-Kiejda KA; Bowden NA; Scott RJ, 2014, 'Low prevalence of germline PALB2 mutations in Australian triple-negative breast cancer.', Int J Cancer, vol. 134, pp. 301 - 305, http://dx.doi.org/10.1002/ijc.28361
2014
Moscovis SM; Hall ST; Burns CJ; Scott RJ; Blackwell CC, 2014, 'The male excess in sudden infant deaths.', Innate Immun, vol. 20, pp. 24 - 29, http://dx.doi.org/10.1177/1753425913481071
2014
Scott RJ; Fox SB; Desai J; Grieu F; Amanuel B; Garrett K; Harraway J; Cheetham G; Pattle N; Haddad A; Byron K; Rudzki B; Waring P; Iacopetta B, 2014, 'KRAS mutation testing of metastatic colorectal cancer in Australia: where are we at?', Asia Pac J Clin Oncol, vol. 10, pp. 261 - 265, http://dx.doi.org/10.1111/ajco.12201
2014
Gusev A; Lee SH; Trynka G; Finucane H; Vilhjálmsson BJ; Xu H; Zang C; Ripke S; Bulik-Sullivan B; Stahl E; Kähler AK; Hultman CM; Purcell SM; McCarroll SA; Daly M; Pasaniuc B; Sullivan PF; Neale BM; Wray NR; Raychaudhuri S; Price AL; Corvin A; Walters JTR; Farh KH; Holmans PA; Lee P; Collier DA; Huang H; Pers TH; Agartz I; Agerbo E; Albus M; Alexander M; Amin F; Bacanu SA; Begemann M; Belliveau RA; Bene J; Bergen SE; Bevilacqua E; Bigdeli TB; Black DW; Børglum AD; Bruggeman R; Buccola NG; Buckner RL; Byerley W; Cahn W; Cai G; Campion D; Cantor RM; Carr VJ; Carrera N; Catts SV; Chambert KD; Chan RCK; Chen RYL; Chen EYH; Cheng W; Cheung EFC; Chong SA; Cloninger CR; Cohen D; Cohen N; Cormican P; Craddock N; Crowley JJ; Curtis D; Davidson M; Davis KL; Degenhardt F; Del Favero J; De Lisi LE; Demontis D; Dikeos D; Dinan T; Djurovic S; Donohoe G; Drapeau E; Duan J; Dudbridge F; Durmishi N; Eichhammer P; Eriksson J; Escott-Price V; Essioux L; Fanous AH; Farrell MS; Frank J; Franke L; Freedman R; Freimer NB; Friedl M; Friedman JI; Fromer M; Genovese G; Georgieva L; Gershon ES; Giegling I; Giusti-Rodrguez P, 2014, 'Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases', American Journal of Human Genetics, vol. 95, pp. 535 - 552, http://dx.doi.org/10.1016/j.ajhg.2014.10.004
2014
Holliday EG; Attia J; Hancock S; Koloski N; McEvoy M; Peel R; D'Amato M; Agréus L; Nyhlin H; Andreasson A; Almazar AE; Saito YA; Scott RJ; Talley NJ, 2014, 'Genome-wide association study identifies two novel genomic regions in irritable bowel syndrome.', Am J Gastroenterol, vol. 109, pp. 770 - 772, http://dx.doi.org/10.1038/ajg.2014.56
2014
Holliday EG; Traylor M; Malik R; Bevan S; Maguire J; Koblar SA; Sturm J; Hankey GJ; Oldmeadow C; McEvoy M; Sudlow C; Rothwell PM; Coresh J; Hamet P; Tremblay J; Turner ST; De Andrade M; Rao M; Schmidt R; Crick PA; Robino A; Peralta CA; Jukema JW; Mitchell P; Rosas SE; Wang JJ; Scott RJ; Dichgans M; Mitchell BD; Kao WHL; Fox CS; Levi C; Attia J; Markus HS, 2014, 'Polygenic overlap between kidney function and large artery atherosclerotic stroke', Stroke, vol. 45, pp. 3508 - 3513, http://dx.doi.org/10.1161/STROKEAHA.114.006609
2014
Mirecka A; Paszkowska-Szczur K; Scott RJ; Górski B; van de Wetering T; Wokołorczyk D; Gromowski T; Serrano-Fernandez P; Cybulski C; Kashyap A; Gupta S; Gołab A; Słojewski M; Sikorski A; Lubiński J; Debniak T, 2014, 'Common variants of xeroderma pigmentosum genes and prostate cancer risk', Gene, vol. 546, pp. 156 - 161, http://dx.doi.org/10.1016/j.gene.2014.06.026
2014
Avery-Kiejda KA; Braye SG; Mathe A; Forbes JF; Scott RJ, 2014, 'Decreased expression of key tumour suppressor microRNAs is associated with lymph node metastases in triple negative breast cancer.', BMC Cancer, vol. 14, pp. 51, http://dx.doi.org/10.1186/1471-2407-14-51
2014
Smith CJA; Bensing S; Maltby VE; Zhang M; Scott RJ; Smith R; Kämpe O; Hökfelt T; Crock PA, 2014, 'Intermediate lobe immunoreactivity in a patient with suspected lymphocytic hypophysitis.', Pituitary, vol. 17, pp. 22 - 29, http://dx.doi.org/10.1007/s11102-013-0461-9
2014
Spurdle AB; Couch FJ; Parsons MT; McGuffog L; Barrowdale D; Bolla MK; Wang Q; Healey S; Schmutzler RK; Wappenschmidt B; Rhiem K; Hahnen E; Engel C; Meindl A; Ditsch N; Arnold N; Plendl H; Niederacher D; Sutter C; Wang-Gohrke S; Steinemann D; Preisler-Adams S; Kast K; Varon-Mateeva R; Ellis S; Frost D; Platte R; Perkins J; Gareth Evans D; Izatt L; Eeles R; Adlard J; Davidson R; Cole T; Scuvera G; Manoukian S; Bonanni B; Mariette F; Fortuzzi S; Viel A; Pasini B; Papi L; Varesco L; Balleine R; Nathanson KL; Domchek SM; Offitt K; Jakubowska A; Lindor N; Thomassen M; Jensen UB; Rantala J; Borg Å; Andrulis IL; Miron A; Hansen TVO; Caldes T; Neuhausen SL; Toland AE; Nevanlinna H; Montagna M; Garber J; Godwin AK; Osorio A; Factor RE; Terry MB; Rebbeck TR; Karlan BY; Southey M; Rashid MU; Tung N; Pharoah PDP; Blows FM; Dunning AM; Provenzano E; Hall P; Czene K; Schmidt MK; Broeks A; Cornelissen S; Verhoef S; Fasching PA; Beckmann MW; Ekici AB; Slamon DJ; Bojesen SE; Nordestgaard BG; Nielsen SF; Flyger H; Chang-Claude J; Flesch-Janys D; Rudolph A; Seibold P; Aittomäki K; Muranen TA; Carl Blomqvist PH; Figueroa J; Chanock SJ; Brinton L; Lissowska J, 2014, 'Refined histopathological predictors of BRCA1 and BRCA2 mutation status: A large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia', Breast Cancer Research, vol. 16, http://dx.doi.org/10.1186/s13058-014-0474-y
2014
Cox MB; Bowden NA; Scott RJ; Lechner-Scott J, 2014, 'Common genetic variants in the plasminogen activation pathway are not associated with multiple sclerosis.', Mult Scler, vol. 20, pp. 489 - 491, http://dx.doi.org/10.1177/1352458513498127
2014
Graves MC; Benton M; Lea RA; Boyle M; Tajouri L; Macartney-Coxson D; Scott RJ; Lechner-Scott J, 2014, 'Methylation differences at the HLA-DRB1 locus in CD4+ T-Cells are associated with multiple sclerosis.', Mult Scler, vol. 20, pp. 1033 - 1041, http://dx.doi.org/10.1177/1352458513516529
2014
Cairns MJ; Wang X; Atkins JR; Fillman SG; Tooney P; Scott RJ; Shannon-Weickert C; Carr V, 2014, 'Poster #M175 GENE SET ENRICHMENT OF DIFFERENTIAL EXPRESSION AND SPLICING ANALYSIS BY RNA-SEQ IN POSTMORTEM DLPFC AND PBMCS IN SCHIZOPHRENIA', Schizophrenia Research, vol. 153, pp. S254 - S254, http://dx.doi.org/10.1016/s0920-9964(14)70725-x
2014
Baines KJ; Simpson JL; Wood LG; Scott RJ; Fibbens NL; Powell H; Cowan DC; Taylor DR; Cowan JO; Gibson PG, 2014, 'Sputum gene expression signature of 6 biomarkers discriminates asthma inflammatory phenotypes.', J Allergy Clin Immunol, vol. 133, pp. 997 - 1007, http://dx.doi.org/10.1016/j.jaci.2013.12.1091
2014
Gromowski T; Masojć B; Scott RJ; Cybulski C; Górski B; Kluźniak W; Paszkowska-Szczur K; Rozmiarek A; Dębniak B; Maleszka R; Kładny J; Lubiński J; Dębniak T, 2014, 'Prevalence of the E318K and V320I MITF germline mutations in Polish cancer patients and multiorgan cancer risk-a population-based study.', Cancer Genet, vol. 207, pp. 128 - 132, http://dx.doi.org/10.1016/j.cancergen.2014.03.003
2014
Moscovis S; Hall S; Burns C; Scott R; Blackwell C, 2014, 'Development of an experimental model for assessing the effects of cigarette smoke and virus infections on inflammatory responses to bacterial antigens.', Innate Immun, vol. 20, pp. 647 - 658, http://dx.doi.org/10.1177/1753425913503893
2014
Masson AL; Talseth-Palmer BA; Evans T-J; Grice DM; Hannan GN; Scott RJ, 2014, 'Expanding the genetic basis of copy number variation in familial breast cancer.', Hered Cancer Clin Pract, vol. 12, pp. 15, http://dx.doi.org/10.1186/1897-4287-12-15
2014
Atkins JR; Wu JQ; Tooney PA; Scott RJ; Carr VJ; Cairns MJ, 2014, 'Poster #S132 COPY NUMBER VARIANT ANALYSIS ON 401 CASES OF SCHIZOPHRENIA: A SEARCH FOR CAUSAL GENES FINDS DISRUPTION IN THE NEUROGENESIS REGULATOR JAGGED 2', Schizophrenia Research, vol. 153, pp. S136 - S136, http://dx.doi.org/10.1016/s0920-9964(14)70411-6
2014
Oldmeadow C; Holliday EG; McEvoy M; Scott R; Kwok JB; Mather K; Sachdev P; Schofield PR; Attia J, 2014, 'Concordance between direct and imputed APOE genotypes using 1000 Genomes data', Journal of Alzheimer's Diseasse, vol. 42, pp. 391 - 393, http://dx.doi.org/10.3233/JAD-140846
2014
Dymerska D; Kurzawski G; Suchy J; Roomere H; Toome K; Metspalu A; Janavičius R; Elsakov P; Irmejs A; Berzina D; Miklaševičs E; Gardovskis J; Rebane E; Kelve M; Kładny J; Huzarski T; Gronwald J; Dębniak T; Byrski T; Stembalska A; Surdyka D; Siołek M; Szwiec M; Banaszkiewicz Z; Wiśniowski R; Kilar E; Scott RJ; Lubiński J, 2014, 'Lynch syndrome mutations shared by the Baltic States and Poland.', Clin Genet, vol. 86, pp. 190 - 193, http://dx.doi.org/10.1111/cge.12251
2014
Evans T-J; Milne E; Anderson D; de Klerk NH; Jamieson SE; Talseth-Palmer BA; Bowden NA; Holliday EG; Rudant J; Orsi L; Richardson E; Lavis L; Catchpoole D; Attia JR; Armstrong BK; Clavel J; Scott RJ, 2014, 'Confirmation of childhood acute lymphoblastic leukemia variants, ARID5B and IKZF1, and interaction with parental environmental exposures.', PLoS One, vol. 9, pp. e110255, http://dx.doi.org/10.1371/journal.pone.0110255
2014
Raudino A; Carr VJ; Cairns MJ; Oldmeadow C; Tooney PA; Scott RJ; Green MJ, 2014, 'Poster #S143 INTERACTIVE EFFECTS OF FKBP5 AND CHILDHOOD TRAUMA ON COGNITION IN SCHIZOPHRENIA', Schizophrenia Research, vol. 153, pp. S140 - S141, http://dx.doi.org/10.1016/s0920-9964(14)70422-0
2014
Avery-Kiejda KA; Morten B; Wong-Brown MW; Mathe A; Scott RJ, 2014, 'The relative mRNA expression of p53 isoforms in breast cancer is associated with clinical features and outcome.', Carcinogenesis, vol. 35, pp. 586 - 596, http://dx.doi.org/10.1093/carcin/bgt411
2014
Wu JQ; Green MJ; Gardiner E; Tooney P; Scott RJ; Carr VJ; Cairns MJ, 2014, 'Poster #M102 TRANSCRIPTOME ANALYSIS REVEALS DOWN-REGULATED SIGNAL TRANSDUCTION PATHWAYS IN PERIPHERAL BLOOD MONONUCLEAR CELLS FROM SCHIZOPHRENIA PATIENTS WITH COGNITIVE IMPAIRMENT', Schizophrenia Research, vol. 153, pp. S226 - S227, http://dx.doi.org/10.1016/s0920-9964(14)70652-8
2014
De Vivo I; Prescott J; Setiawan VW; Olson SH; Wentzensen N; Australian National Endometrial Cancer Study Group ; Attia J; Black A; Brinton L; Chen C; Chen C; Cook LS; Crous-Bou M; Doherty J; Dunning AM; Easton DF; Friedenreich CM; Garcia-Closas M; Gaudet MM; Haiman C; Hankinson SE; Hartge P; Henderson BE; Holliday E; Horn-Ross PL; Hunter DJ; Le Marchand L; Liang X; Lissowska J; Long J; Lu L; Magliocco AM; McEvoy M; O'Mara TA; Orlow I; Painter JN; Pooler L; Rastogi R; Rebbeck TR; Risch H; Sacerdote C; Schumacher F; Scott RJ; Sheng X; Shu X-O; Spurdle AB; Thompson D; Vanden Berg D; Weiss NS; Xia L; Xiang Y-B; Yang HP; Yu H; Zheng W; Chanock S; Kraft P, 2014, 'Genome-wide association study of endometrial cancer in E2C2.', Hum Genet, vol. 133, pp. 211 - 224, http://dx.doi.org/10.1007/s00439-013-1369-1
2014
Scott RJ; Cavana RY; Cameron D, 2014, 'Mechanisms for Understanding Mental Model Change in Group Model Building', Systems Research and Behavioral Science, vol. 33, pp. n/a - n/a, http://dx.doi.org/10.1002/sres.2303
2014
Rudnicka H; Masojc B; van de Wetering T; Debniak T; Cybulski C; Gronwald J; Scott R; Lubinski J; Gorski B, 2014, 'First recurrent large genomic rearrangement in the BRCA1 gene found in Poland.', Cancer Epidemiol, vol. 38, pp. 382 - 385, http://dx.doi.org/10.1016/j.canep.2014.05.010
2014
Moayyeri A; Hsu YH; Karasik D; Estrada K; Xiao SM; Nielson C; Srikanth P; Giroux S; Wilson SG; Zheng HF; Smith AV; Pye SR; Leo PJ; Teumer A; Hwang JY; Ohlsson C; McGuigan F; Minster RL; Hayward C; Olmos JM; Lyytikäinen LP; Lewis JR; Swart KMA; Masi L; Oldmeadow C; Holliday EG; Cheng S; Van Schoor NM; Harvey NC; Kruk M; Del Greco FM; Igl W; Trummer O; Grigoriou E; Luben R; Liu CT; Zhou Y; Oei L; Medina-Gomez C; Zmuda J; Tranah G; Brown SJ; Williams FM; Soranzo N; Jakobsdottir J; Siggeirsdottir K; Holliday KL; Hannemann A; Go MJ; Garcia M; Polasek O; Laaksonen M; Zhu K; Enneman AW; McEvoy M; Pee R; Sham PC; Jaworski M; Johansson A; Hicks AA; Pludowski P; Scott R; Dhonukshe-Rutten RAM; van Der Velde NV; Kaöhönen M; Viikari JS; Sievaönen H; Raitakari OT; González-Macías J; Hernández JL; Mellström D; Ljunggren O; Cho YS; Völker U; Nauck M; Homuth G; Völzke H; Haring R; Brown MA; McCloskey E; Nicholson GC; Eastell R; Eisman JA; Jones G; Reid IR; Dennison EM; Wark J; Boonen S; Vanderschueren D; Wu FCW; Aspelund T; Richards JB; Bauer D; Hofman A; Khaw KT; Dedoussis G; Obermayer-Pietsch B; Gyllensten U; Pramstaller PP; Lorenc RS, 2014, 'Genetic determinants of heel bone properties: Genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium', Human Molecular Genetics, vol. 23, pp. 3054 - 3068, http://dx.doi.org/10.1093/hmg/ddt675
2014
Chen J; Pande M; Huang Y-J; Wei C; Amos CI; Talseth-Palmer BA; Meldrum CJ; Chen WV; Gorlov IP; Lynch PM; Scott RJ; Frazier ML, 2013, 'Cell cycle-related genes as modifiers of age of onset of colorectal cancer in Lynch syndrome: a large-scale study in non-Hispanic white patients.', Carcinogenesis, vol. 34, pp. 299 - 306, http://dx.doi.org/10.1093/carcin/bgs344
2013
Schache M; Richardson AJ; Mitchell P; Wang JJ; Rochtchina E; Viswanathan AC; Wong TY; Saw SM; Topouzis F; Xie J; Sim X; Holliday EG; Attia J; Scott RJ; Baird PN, 2013, 'Genetic association of refractive error and axial length with 15q14 but not 15q25 in the blue mountains eye study cohort', Ophthalmology, vol. 120, pp. 292 - 297, http://dx.doi.org/10.1016/j.ophtha.2012.08.006
2013
Bowden NA; Ashton KA; Vilain RE; Avery-Kiejda KA; Davey RJ; Murray HC; Budden T; Braye SG; Zhang XD; Hersey P; Scott RJ, 2013, 'Regulators of global genome repair do not respond to DNA damaging therapy but correlate with survival in melanoma.', PLoS One, vol. 8, pp. e70424, http://dx.doi.org/10.1371/journal.pone.0070424
2013
Wong-Brown MW; McPhillips ML; Hipwell M; Pecenpetelovska G; Dooley S; Meldrum C; Scott RJ, 2013, 'cDNA analysis of the BRCA1 unclassified variant c.5194-12G>A.', Clin Genet, vol. 84, pp. 505 - 506, http://dx.doi.org/10.1111/cge.12052
2013
Sim X; Jensen RA; Ikram MK; Cotch MF; Li X; MacGregor S; Xie J; Smith AV; Boerwinkle E; Mitchell P; Klein R; Klein BEK; Glazer NL; Lumley T; McKnight B; Psaty BM; de Jong PTVM; Hofman A; Rivadeneira F; Uitterlinden AG; van Duijn CM; Aspelund T; Eiriksdottir G; Harris TB; Jonasson F; Launer LJ; Attia J; Baird PN; Harrap S; Holliday EG; Inouye M; Rochtchina E; Scott RJ; Viswanathan A; Li G; Smith NL; Wiggins KL; Kuo JZ; Taylor KD; Hewitt AW; Martin NG; Montgomery GW; Sun C; Young TL; Mackey DA; van Zuydam NR; Doney ASF; Palmer CNA; Morris AD; Rotter JI; Tai ES; Gudnason V; Vingerling JR; Siscovick DS; Wang JJ; Wong TY, 2013, 'Genetic Loci for Retinal Arteriolar Microcirculation', PLoS ONE, vol. 8, http://dx.doi.org/10.1371/journal.pone.0065804
2013
Scott RJ; Cavana RY; Cameron D, 2013, 'Evaluating immediate and long-term impacts of qualitative group model building workshops on participants' mental models', System Dynamics Review, vol. 29, pp. 216 - 236, http://dx.doi.org/10.1002/sdr.1505
2013
Köttgen A; Albrecht E; Teumer A; Vitart V; Krumsiek J; Hundertmark C; Pistis G; Ruggiero D; O'Seaghdha CM; Haller T; Yang Q; Tanaka T; Johnson AD; Kutalik Z; Smith AV; Shi J; Struchalin M; Middelberg RPS; Brown MJ; Gaffo AL; Pirastu N; Li G; Hayward C; Zemunik T; Huffman J; Yengo L; Zhao JH; Demirkan A; Feitosa MF; Liu X; Malerba G; Lopez LM; van der Harst P; Li X; Kleber ME; Hicks AA; Nolte IM; Johansson A; Murgia F; Wild SH; Bakker SJL; Peden JF; Dehghan A; Steri M; Tenesa A; Lagou V; Salo P; Mangino M; Rose LM; Lehtimäki T; Woodward OM; Okada Y; Tin A; Müller C; Oldmeadow C; Putku M; Czamara D; Kraft P; Frogheri L; Thun GA; Grotevendt A; Gislason GK; Harris TB; Launer LJ; McArdle P; Shuldiner AR; Boerwinkle E; Coresh J; Schmidt H; Schallert M; Martin NG; Montgomery GW; Kubo M; Nakamura Y; Tanaka T; Munroe PB; Samani NJ; Jacobs DR; Liu K; D'Adamo P; Ulivi S; Rotter JI; Psaty BM; Vollenweider P; Waeber G; Campbell S; Devuyst O; Navarro P; Kolcic I; Hastie N; Balkau B; Froguel P; Esko T; Salumets A; Khaw KT; Langenberg C; Wareham NJ; Isaacs A; Kraja A; Zhang Q; Wild PS; Scott RJ; Holliday EG; Org E; Viigimaa M; Bandinelli S; Metter JE; Lupo A; Trabetti E; Sorice R; Döring A; Lattka E; Strauch K; Theis F; Waldenberger M; Wichmann H-E; Davies G; Gow AJ; Bruinenberg M; LifeLines Cohort Study ; Stolk RP; Kooner JS; Zhang W; Winkelmann BR; Boehm BO; Lucae S; Penninx BW; Smit JH; Curhan G; Mudgal P; Plenge RM; Portas L; Persico I; Kirin M; Wilson JF; Mateo Leach I; van Gilst WH; Goel A; Ongen H; Hofman A; Rivadeneira F; Uitterlinden AG; Imboden M; von Eckardstein A; Cucca F; Nagaraja R; Piras MG; Nauck M; Schurmann C; Budde K; Ernst F; Farrington SM; Theodoratou E; Prokopenko I; Stumvoll M; Jula A; Perola M; Salomaa V; Shin S-Y; Spector TD; Sala C; Ridker PM; Kähönen M; Viikari J; Hengstenberg C; Nelson CP; CARDIoGRAM Consortium ; DIAGRAM Consortium ; ICBP Consortium ; MAGIC Consortium ; Meschia JF; Nalls MA; Sharma P; Singleton AB; Kamatani N; Zeller T; Burnier M; Attia J; Laan M; Klopp N; Hillege HL; Kloiber S; Choi H; Pirastu M; Tore S; Probst-Hensch NM; Völzke H; Gudnason V; Parsa A; Schmidt R; Whitfield JB; Fornage M; Gasparini P; Siscovick DS; Polašek O; Campbell H; Rudan I; Bouatia-Naji N; Metspalu A; Loos RJF; van Duijn CM; Borecki IB; Ferrucci L; Gambaro G; Deary IJ; Wolffenbuttel BHR; Chambers JC; März W; Pramstaller PP; Snieder H; Gyllensten U; Wright AF; Navis G; Watkins H; Witteman JCM; Sanna S; Schipf S; Dunlop MG; Tönjes A; Ripatti S; Soranzo N; Toniolo D; Chasman DI; Raitakari O; Kao WHL; Ciullo M; Fox CS; Caulfield M; Bochud M; Gieger C, 2013, 'Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.', Nat Genet, vol. 45, pp. 145 - 154, http://dx.doi.org/10.1038/ng.2500
2013
Talseth-Palmer BA; Wijnen JT; Barker D; Vasen HFA; Scott RJ, 2013, 'Reply to Win and Jenkins.', Int J Cancer, vol. 133, pp. 1764, http://dx.doi.org/10.1002/ijc.28178
2013
Rietveld CA; Medland SE; Derringer J; Yang J; Esko T; Martin NW; Westra HJ; Shakhbazov K; Abdellaoui A; Agrawal A; Albrecht E; Alizadeh BZ; Amin N; Barnard J; Baumeister SE; Benke KS; Bielak LF; Boatman JA; Boyle PA; Davies G; De Leeuw C; Eklund N; Evans DS; Ferhmann R; Fischer K; Gieger C; Gjessing HK; Hägg S; Harris JR; Hayward C; Holzapfel C; Ibrahim-Verbaas CA; Ingelsson E; Jacobsson B; Joshi PK; Jugessur A; Kaakinen M; Kanoni S; Karjalainen J; Kolcic I; Kristiansson K; Kutalik Z; Lahti J; Lee SH; Lin P; Lind PA; Liu Y; Lohman K; Loitfelder M; McMahon G; Vidal PM; Meirelles O; Milani L; Myhre R; Nuotio ML; Oldmeadow CJ; Petrovic KE; Peyrot WJ; Polašek O; Quaye L; Reinmaa E; Rice JP; Rizzi TS; Schmidt H; Schmidt R; Smith AV; Smith JA; Tanaka T; Terracciano A; Van Der Loos MJHM; Vitart V; Völzke H; Wellmann J; Yu L; Zhao W; Allik J; Attia JR; Bandinelli S; Bastardot F; Beauchamp J; Bennett DA; Berger K; Bierut LJ; Boomsma DI; Bültmann U; Campbell H; Chabris CF; Cherkas L; Chung MK; Cucca F; De Andrade M; De Jager PL; De Neve JE; Deary IJ; Dedoussis GV; Deloukas P; Dimitriou M; Eiríksdóttir G; Elderson MF; Eriksson JG, 2013, 'GWAS of 126,559 individuals identifies genetic variants associated with educational attainment', Science, vol. 340, pp. 1467 - 1471, http://dx.doi.org/10.1126/science.1235488
2013
Fellowes A; Meldrum C; Bell A; Scott R; Fox S, 2013, 'The clinical laboratory’s journey towards accreditation in diagnostic genomics', Pathology, vol. 45, pp. S32 - S32, http://dx.doi.org/10.1097/01.pat.0000426805.55870.ad
2013
Stambolian D; Wojciechowski R; Oexle K; Pirastu M; Li X; Raffe LJ; Cotch MF; Chew EY; Klein B; Klein R; Wong TY; Simpson CL; Klaver CCW; van Duijn CM; Verhoeven VJM; Baird PN; Vitart V; Paterson AD; Mitchell P; Saw SM; Fossarello M; Kazmierkiewicz K; Murgia F; Portas L; Schache M; Richardson A; Xie J; Wang JJ; Rochtchina E; Viswanathan AC; Hayward C; Wright AF; Polašek O; Campbell H; Rudan I; Oostra BA; Uitterlinden AG; Hofman A; Rivadeneira F; Amin N; Karssen LC; Vingerling JR; Hosseini SM; Döring A; Bettecken T; Vatavuk Z; Gieger C; Wichmann HE; Wilson JF; Fleck B; Foster PJ; Topouzis F; McGuffin P; Sim X; Inouye M; Holliday EG; Attia J; Scott RJ; Rotter JI; Meitinger T; Bailey-Wilson JE, 2013, 'Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error', Human Molecular Genetics, vol. 22, pp. 2754 - 2764, http://dx.doi.org/10.1093/hmg/ddt116
2013
Bolton KA; Ross JP; Grice DM; Bowden NA; Holliday EG; Avery-Kiejda KA; Scott RJ, 2013, 'STaRRRT: a table of short tandem repeats in regulatory regions of the human genome.', BMC Genomics, vol. 14, pp. 795, http://dx.doi.org/10.1186/1471-2164-14-795
2013
Yadav S; Cotlarciuc I; Munroe PB; Khan MS; Nalls MA; Bevan S; Cheng Y-C; Chen W-M; Malik R; McCarthy NS; Holliday EG; Speed D; Hasan N; Pucek M; Rinne PE; Sever P; Stanton A; Shields DC; Maguire JM; McEvoy M; Scott RJ; Ferrucci L; Macleod MJ; Attia J; Markus HS; Sale MM; Worrall BB; Mitchell BD; Dichgans M; Sudlow C; Meschia JF; Rothwell PM; Caulfield M; Sharma P; International Stroke Genetics Consortium , 2013, 'Genome-wide analysis of blood pressure variability and ischemic stroke.', Stroke, vol. 44, pp. 2703 - 2709, http://dx.doi.org/10.1161/STROKEAHA.113.002186
2013
Lener MR; Gupta S; Scott RJ; Tootsi M; Kulp M; Tammesoo ML; Viitak A; Metspalu A; Serrano-Fernández P; Kładny J; Jaworska-Bieniek K; Durda K; Muszyńska M; Sukiennicki G; Jakubowska A; Lubiński J, 2013, 'Can selenium levels act as a marker of colorectal cancer risk?', BMC Cancer, vol. 13, http://dx.doi.org/10.1186/1471-2407-13-214
2013
Talseth-Palmer BA; Wijnen JT; Grice DM; Scott RJ, 2013, 'Genetic modifiers of cancer risk in Lynch syndrome: a review.', Fam Cancer, vol. 12, pp. 207 - 216, http://dx.doi.org/10.1007/s10689-013-9614-2
2013
Paszkowska-Szczur K; Scott RJ; Serrano-Fernandez P; Mirecka A; Gapska P; Górski B; Cybulski C; Maleszka R; Sulikowski M; Nagay L; Lubinski J; Dębniak T, 2013, 'Xeroderma pigmentosum genes and melanoma risk.', Int J Cancer, vol. 133, pp. 1094 - 1100, http://dx.doi.org/10.1002/ijc.28123
2013
Greenop KR; Peters S; Bailey HD; Fritschi L; Attia J; Scott RJ; Glass DC; de Klerk NH; Alvaro F; Armstrong BK; Milne E, 2013, 'Exposure to pesticides and the risk of childhood brain tumors.', Cancer Causes Control, vol. 24, pp. 1269 - 1278, http://dx.doi.org/10.1007/s10552-013-0205-1
2013
Cox MB; Bowden NA; Scott RJ; Lechner-Scott J, 2013, 'Altered expression of the plasminogen activation pathway in peripheral blood mononuclear cells in multiple sclerosis: possible pathomechanism of matrix metalloproteinase activation.', Mult Scler, vol. 19, pp. 1268 - 1274, http://dx.doi.org/10.1177/1352458513475493
2013
Talseth-Palmer BA; Holliday EG; Evans TJ; McEvoy M; Attia J; Grice DM; Masson AL; Meldrum C; Spigelman A; Scott RJ, 2013, 'Continuing difficulties in interpreting CNV data: Lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients', BMC Medical Genomics, vol. 6, http://dx.doi.org/10.1186/1755-8794-6-10
2013
Masson AL; Talseth-Palmer BA; Evans T-J; Grice DM; Duesing K; Hannan GN; Scott RJ, 2013, 'Copy number variation in hereditary non-polyposis colorectal cancer.', Genes (Basel), vol. 4, pp. 536 - 555, http://dx.doi.org/10.3390/genes4040536
2013
Barzideh J; Scott RJ; Aitken RJ, 2013, 'Analysis of the global methylation status of human spermatozoa and its association with the tendency of these cells to enter apoptosis.', Andrologia, vol. 45, pp. 424 - 429, http://dx.doi.org/10.1111/and.12033
2013
Talseth-Palmer B; Wijnen JT; Brenne IS; Jagmohan-Changur S; Barker D; Ashton K; Tops C; Evans TJ; McPhillips M; Groombridge C; Suchy J; Kurzawski G; Spigelman AD; Moller P; Morreau H; Van Wezel T; Lubinski J; Vasen H; Scott RJ, 2013, 'Combined analysis of three Lynch syndrome cohorts confirms the modifying effects of 8q23.3 and 11q23.1 in MLH1 mutation carriers', International Journal of Cancer, vol. 132, pp. 1556 - 1564, http://dx.doi.org/10.1002/ijc.27843
2013
Jensen RA; Sim X; Li X; Cotch MF; Ikram MK; Holliday EG; Eiriksdottir G; Harris TB; Jonasson F; Klein BEK; Launer LJ; Smith AV; Boerwinkle E; Cheung N; Hewitt AW; Liew G; Mitchell P; Wang JJ; Attia J; Scott R; Glazer NL; Lumley T; McKnight B; Psaty BM; Taylor K; Hofman A; de Jong PTVM; Rivadeneira F; Uitterlinden AG; Tay WT; Teo YY; Seielstad M; Liu J; Cheng CY; Saw SM; Aung T; Ganesh SK; O'Donnell CJ; Nalls MA; Wiggins KL; Kuo JZ; van Duijn CM; Gudnason V; Klein R; Siscovick DS; Rotter JI; Tai ES; Vingerling J; Wong TY, 2013, 'Genome-Wide Association Study of Retinopathy in Individuals without Diabetes', PLoS ONE, vol. 8, http://dx.doi.org/10.1371/journal.pone.0054232
2013
Acikyol B; Graham RM; Trinder D; House MJ; Olynyk JK; Scott RJ; Milward EA; Johnstone DM, 2013, 'Brain transcriptome perturbations in the transferrin receptor 2 mutant mouse support the case for brain changes in iron loading disorders, including effects relating to long-term depression and long-term potentiation.', Neuroscience, vol. 235, pp. 119 - 128, http://dx.doi.org/10.1016/j.neuroscience.2013.01.014
2013
Talseth-Palmer BA; Wijnen JT; Andreassen EK; Barker D; Jagmohan-Changur S; Tops CM; Meldrum C; Spigelman A; Hes FJ; Van Wezel T; Vasen HFA; Scott RJ, 2013, 'The importance of a large sample cohort for studies on modifier genes influencing disease severity in FAP patients', Hereditary Cancer in Clinical Practice, vol. 11, http://dx.doi.org/10.1186/1897-4287-11-20
2013
Kumarasinghe N; Beveridge NJ; Gardiner E; Scott RJ; Yasawardene S; Perera A; Mendis J; Suriyakumara K; Schall U; Tooney PA, 2013, 'Gene expression profiling in treatment-naive schizophrenia patients identifies abnormalities in biological pathways involving AKT1 that are corrected by antipsychotic medication', INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY, vol. 16, pp. 1483 - 1503, http://dx.doi.org/10.1017/S1461145713000035
2013
Titmarsh CJ; Moscovis SM; Hall S; Tzanakaki G; Kesanopoulos K; Xirogianni A; Scott RJ; Blackwell CC, 2013, 'Comparison of cytokine gene polymorphisms among Greek patients with invasive meningococcal disease or viral meningitis.', J Med Microbiol, vol. 62, pp. 694 - 700, http://dx.doi.org/10.1099/jmm.0.058073-0
2013
Johnstone DM; Riveros C; Heidari M; Graham RM; Trinder D; Berretta R; Olynyk JK; Scott RJ; Moscato P; Milward EA, 2013, 'Evaluation of Different Normalization and Analysis Procedures for Illumina Gene Expression Microarray Data Involving Small Changes.', Microarrays (Basel), vol. 2, pp. 131 - 152, http://dx.doi.org/10.3390/microarrays2020131
2013
Lubiński J; Huzarski T; Jakubowska A; Gronwald J; Jaworska K; Muszyńska M; Sukiennicki G; Durda K; Cybulski C; Dębniak T; Tołoczko A; Oszurek O; Serrano-Fernandez P; Scott R; Narod S, 2012, 'Prospective observation of breast/ovarian cancer risk in BRCA1 carriers depending on serum selenium level optimized with diet', Hereditary Cancer in Clinical Practice, vol. 10, pp. A11 - A11, http://dx.doi.org/10.1186/1897-4287-10-s1-a11
2012
Nyholt DR; Low S-K; Anderson CA; Painter JN; Uno S; Morris AP; MacGregor S; Gordon SD; Henders AK; Martin NG; Attia J; Holliday EG; McEvoy M; Scott RJ; Kennedy SH; Treloar SA; Missmer SA; Adachi S; Tanaka K; Nakamura Y; Zondervan KT; Zembutsu H; Montgomery GW, 2012, 'Genome-wide association meta-analysis identifies new endometriosis risk loci.', Nat Genet, vol. 44, pp. 1355 - 1359, http://dx.doi.org/10.1038/ng.2445
2012
Johnstone DM; Graham RM; Trinder D; Riveros C; Olynyk JK; Scott RJ; Moscato P; Milward EA, 2012, 'Changes in brain transcripts related to Alzheimer's disease in a model of HFE hemochromatosis are not consistent with increased Alzheimer's disease risk.', J Alzheimers Dis, vol. 30, pp. 791 - 803, http://dx.doi.org/10.3233/JAD-2012-112183
2012
Orsi L; Rudant J; Bonaventure A; Goujon-Bellec S; Corda E; Evans T-J; Petit A; Bertrand Y; Nelken B; Robert A; Michel G; Sirvent N; Chastagner P; Ducassou S; Rialland X; Hémon D; Milne E; Scott RJ; Baruchel A; Clavel J, 2012, 'Genetic polymorphisms and childhood acute lymphoblastic leukemia: GWAS of the ESCALE study (SFCE).', Leukemia, vol. 26, pp. 2561 - 2564, http://dx.doi.org/10.1038/leu.2012.148
2012
Johnstone D; Graham RM; Trinder D; Delima RD; Riveros C; Olynyk JK; Scott RJ; Moscato P; Milward EA, 2012, 'Brain transcriptome perturbations in the Hfe(-/-) mouse model of genetic iron loading.', Brain Res, vol. 1448, pp. 144 - 152, http://dx.doi.org/10.1016/j.brainres.2012.02.006
2012
Bailey HD; Miller M; Langridge A; de Klerk NH; van Bockxmeer FM; Attia J; Scott RJ; Armstrong BK; Milne E, 2012, 'Maternal dietary intake of folate and vitamins B6 and B12 during pregnancy and the risk of childhood acute lymphoblastic leukemia.', Nutr Cancer, vol. 64, pp. 1122 - 1130, http://dx.doi.org/10.1080/01635581.2012.707278
2012
Cox MB; Ban M; Bowden NA; Baker A; Scott RJ; Lechner-Scott J, 2012, 'Potential association of vitamin D receptor polymorphism Taq1 with multiple sclerosis', Multiple Sclerosis Journal, vol. 18, pp. 16 - 22, http://dx.doi.org/10.1177/1352458511415562
2012
Milne E; Greenop KR; Scott RJ; Bailey HD; Attia J; Dalla-Pozza L; de Klerk NH; Armstrong BK, 2012, 'Parental prenatal smoking and risk of childhood acute lymphoblastic leukemia.', Am J Epidemiol, vol. 175, pp. 43 - 53, http://dx.doi.org/10.1093/aje/kwr275
2012
Ashton KA; Scurry J; Rutherford J; Otton G; Scott RJ; Bowden NA, 2012, 'Nodular prurigo of the vulva.', Pathology, vol. 44, pp. 565 - 567, http://dx.doi.org/10.1097/PAT.0b013e328354e006
2012
Kim K-T; Mossman D; Small D; J. Scott R, 2012, 'Gene Expression Profiling of Human Myeloid Leukemic MV4-11 Cells Treated with 5-Aza-2’-deoxycytidine', Journal of Cancer Therapy, vol. 03, pp. 177 - 182, http://dx.doi.org/10.4236/jct.2012.33025
2012
Scott RJ, 2012, 'Overview of genetic markers for hereditary colorectal cancer', Hereditary Cancer in Clinical Practice, vol. 10, pp. A22 - A22, http://dx.doi.org/10.1186/1897-4287-10-s4-a22
2012
Kurlapska A; Serrano-Fernández P; Starzyńska T; Małecka-Panas E; Dąbrowski GA; Dębniak T; Kurzawski G; Suchy J; Rogoza-Mateja W; Scott RJ; Lubiński J, 2012, 'Cumulative small effect genetic markers and the detection of advanced colorectal neoplasias by population screening', Hereditary Cancer in Clinical Practice, vol. 10, pp. A26 - A26, http://dx.doi.org/10.1186/1897-4287-10-s4-a26
2012
Green MI; Chia T-Y; Cairns MJ; Tooney P; Scott RJ; Carr VJ, 2012, 'Poster #113 COMT MODULATES THE EFFECTS OF LIFETIME CANNABIS USE ON COGNITION AND SYMPTOM PROFILES IN SCHIZOPHRENIA', Schizophrenia Research, vol. 136, pp. S226 - S226, http://dx.doi.org/10.1016/s0920-9964(12)70685-0
2012
Loughland CM; McCabe K; Bridge J; Henskens F; Catts S; Jablensky A; Michie P; Mowry B; Pantelis C; Schall U; Scott R; Tooney P; Duffy L; Carr V, 2012, 'THE AUSTRALIAN SCHIZOPHRENIA RESEARCH BIOBANK (ASRB): AN AUDIT OF THE FIRST FIVE-YEARS OF RECRUITMENT RESOURCE ACCESS', SCHIZOPHRENIA RESEARCH, vol. 136, pp. S249 - S250, http://dx.doi.org/10.1016/S0920-9964(12)70749-1
2012
Holliday EG; Maguire JM; Evans T-J; Golledge J; Biros E; Lewis MD; Koblar S; Jannes J; Hankey GJ; Baker R; Parsons MW; Sturm JW; Lincz LF; McEvoy M; Peel R; Moscato P; Scott RJ; Levi C; Attia J, 2012, 'Abstract 13: A Locus on Chromosome 6p21 is Associated with Large Artery Atherosclerotic Ischemic Stroke', Stroke, vol. 43, http://dx.doi.org/10.1161/str.43.suppl_1.a13
2012
Kurzawski G; Dymerska D; Serrano-Fernández P; Trubicka J; Masojć B; Jakubowska A; Scott RJ, 2012, 'DNA and RNA analyses in detection of genetic predisposition to cancer.', Hered Cancer Clin Pract, vol. 10, pp. 17, http://dx.doi.org/10.1186/1897-4287-10-17
2012
Gardiner EJ; Cairns MJ; Beveridge NJ; Liu B; Carr V; Scott R; Tooney P, 2012, 'IMMUNE-RELATED DIFFERENTIAL EXPRESSION PROFILE IN PERIPHERAL BLOOD MONONUCLEAR CELLS IN SCHIZOPHRENIA', SCHIZOPHRENIA RESEARCH, vol. 136, pp. S225 - S226, http://dx.doi.org/10.1016/S0920-9964(12)70684-9
2012
Talseth-Palmer BA; Wijnen JT; Brenne IS; Jagmohan-Changur S; Ashton KA; Tops CM; Evans T-J; McPhillips M; Groombridge C; Suchy J; Kurzawski G; Spigelman A; Møller P; Morreau HM; Van Wezel T; Lubinski J; Vasen HFA; Scott RJ, 2012, 'Chromosome 8q23.3, 10p14 and 11q23.1 variants modify colorectal cancer risk in Lynch syndrome – a combined analysis of the Australian, Dutch and Polish Lynch syndrome cohorts', Hereditary Cancer in Clinical Practice, vol. 10, pp. A32 - A32, http://dx.doi.org/10.1186/1897-4287-10-s2-a32
2012
Vilain RE; Braye SG; Scott RJ, 2012, 'BRAF and NRAS mutational status are prognostically important in thick and locally advanced cutaneous melanoma', Pathology, vol. 44, pp. S99 - S99, http://dx.doi.org/10.1016/s0031-3025(16)32887-2
2012
Kim K-T; Carroll AP; Mashkani B; Cairns MJ; Small D; Scott RJ, 2012, 'MicroRNA-16 is down-regulated in mutated FLT3 expressing murine myeloid FDC-P1 cells and interacts with Pim-1.', PLoS One, vol. 7, pp. e44546, http://dx.doi.org/10.1371/journal.pone.0044546
2012
Jakubowska A; Rozkrut D; Antoniou A; Hamann U; Scott RJ; McGuffog L; Healy S; Sinilnikova OM; Rennert G; Lejbkowicz F; Flugelman A; Andrulis IL; Glendon G; Ozcelik H; OCGN ; Thomassen M; Paligo M; Aretini P; SWE-BRCA ; Kantala J; Aroer B; von Wachenfeldt A; Liljegren A; Loman N; Herbst K; Kristoffersson U; Rosenquist R; Karlsson P; Stenmark-Askmalm M; Melin B; Nathanson KL; Domchek SM; Byrski T; Huzarski T; Gronwald J; Menkiszak J; Cybulski C; Serrano P; Osorio A; Cajal TR; Tsitlaidou M; Benítez J; Gilbert M; HEBON ; Rookus M; Aalfs CM; Kluijt I; Boessenkool-Pape JL; Meijers-Heijboer HEJ; Oosterwijk JC; van Asperen CJ; Blok MJ; Nelen MR; van den Ouweland AMW; Seynaeve C; van der Luijt RB; Devilee P; EMBRACE ; Easton DF; Peock S; Frost D; Platte R; Ellis SD; Fineberg E; Evans DG; Lalloo F; Eeles R; Jacobs C; Adlard J; Davidson R; Eccles D; Cole T; Cook J; Godwin A; Bove B; GEMO Study Collaborators ; Stoppa-Lyonnet D; Caux-Moncoutier V; Belotti M; Tirapo C; Mazoyer S; Barjhoux L; Boutry-Kryza N; Pujol P; Coupier I; Peyrat J-P; Vennin P; Muller D; Fricker J-P; Venat-Bouvet L; Johannsson OT; Isaacs C; Schmutzler R; Wappenschmidt B; Meindl A; Arnold N; Varon-Mateeva R; Niederacher D; Sutter C; Deissler H; Preisler-Adams S; Simard J; Soucy P; Durocher F; Chenevix-Trench G; Beesley J; Chen X; KConFab ; Rebbeck T; Couch F; Wang X; Lindor N; Fredericksen Z; Pankratz VS; Peterlongo P; Bonanni B; Fortuzzi S; Peissel B; Szabo C; Mai PL; Loud JT; Lubinski J; CIMBA, the Consortium of Investigators of Modifiers of BRCA1/2-Related Cancer , 2012, 'Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study.', Br J Cancer, vol. 106, pp. 2016 - 2024, http://dx.doi.org/10.1038/bjc.2012.160
2012
Smith CJA; Bensing S; Burns C; Robinson PJ; Kasperlik-Zaluska AA; Scott RJ; Kämpe O; Crock PA, 2012, 'Identification of TPIT and other novel autoantigens in lymphocytic hypophysitis: immunoscreening of a pituitary cDNA library and development of immunoprecipitation assays.', Eur J Endocrinol, vol. 166, pp. 391 - 398, http://dx.doi.org/10.1530/EJE-11-1015
2012
Green MI; Cairns MJ; Wu JQ; Dragovic M; Jablensky A; Tooney P; Scott R; Carr VJ, 2012, 'Poster #114 GENOME-WIDE SUPPORTED VARIANTS (MIR137) PREDICTS MEMBERSHIP OF A COGNITIVE SUBTYPE OF SCHIZOPHRENIA', Schizophrenia Research, vol. 136, pp. S226 - S226, http://dx.doi.org/10.1016/s0920-9964(12)70686-2
2012
Young KMN; Scurry J; Jaaback K; Bowden NA; Scott RJ, 2012, 'Bilateral dysgerminoma associated with gonadoblastoma and sex-cord stromal tumour with annular tubules in a 28-year-old fertile woman with normal karyotype.', Pathology, vol. 44, pp. 257 - 260, http://dx.doi.org/10.1097/PAT.0b013e32835140a5
2012
Reeves SG; Meldrum C; Groombridge C; Spigelman A; Suchy J; Kurzawski G; Lubinski J; Scott RJ, 2012, 'DNA repair gene polymorphisms and risk of early onset colorectal cancer in Lynch syndrome', Cancer Epidemiology, vol. 36, pp. 183 - 189, http://dx.doi.org/10.1016/j.canep.2011.09.003
2012
Long J; Zheng W; Xiang Y-B; Lose F; Thompson D; Tomlinson I; Yu H; Wentzensen N; Lambrechts D; Dörk T; Dubrowinskaja N; Goodman MT; Salvesen HB; Fasching PA; Scott RJ; Delahanty R; Zheng Y; O'Mara T; Healey CS; Hodgson S; Risch H; Yang HP; Amant F; Turmanov N; Schwake A; Lurie G; Trovik J; Beckmann MW; Ashton K; Ji B-T; Bao P-P; Howarth K; Lu L; Lissowska J; Coenegrachts L; Kaidarova D; Dürst M; Thompson PJ; Krakstad C; Ekici AB; Otton G; Shi J; Zhang B; Gorman M; Brinton L; Coosemans A; Matsuno RK; Halle MK; Hein A; Proietto A; Cai H; Lu W; Dunning A; Easton D; Gao Y-T; Cai Q; Spurdle AB; Shu X-O, 2012, 'Genome-wide association study identifies a possible susceptibility locus for endometrial cancer.', Cancer Epidemiol Biomarkers Prev, vol. 21, pp. 980 - 987, http://dx.doi.org/10.1158/1055-9965.EPI-11-1160
2012
Vilain RE; Braye SG; Scott RJ, 2012, 'BRAF and NRAS mutational status are prognostically important in thick and locally advanced cutaneous melanoma', Pathology, vol. 44, pp. S63 - S63, http://dx.doi.org/10.1016/s0031-3025(16)32760-x
2012
Green MJ; Chia T-Y; Cairns MJ; Wu JQ; Tooney P; Scott RJ; Carr VI, 2012, 'Poster #102 COMT GENOTYPE MODULATES THE EFFECTS OF CHILDHOOD ADVERSITY ON COGNITION AND SYMPTOMS IN SCHIZOPHRENIA', Schizophrenia Research, vol. 136, pp. S222 - S222, http://dx.doi.org/10.1016/s0920-9964(12)70674-6
2012
Talseth-Palmer BA; Scott RJ; Vasen HFA; Wijnen JT, 2012, '8q23.3 and 11q23.1 as modifying loci influencing the risk for CRC in Lynch syndrome.', Eur J Hum Genet, vol. 20, pp. 487 - 488, http://dx.doi.org/10.1038/ejhg.2011.232
2012
Milne E; Royle JA; Bennett LC; de Klerk NH; Bailey HD; Bower C; Miller M; Attia J; Scott RJ; Kirby M; Armstrong BK, 2011, 'Maternal consumption of coffee and tea during pregnancy and risk of childhood ALL: results from an Australian case-control study', CANCER CAUSES & CONTROL, vol. 22, pp. 207 - 218, http://dx.doi.org/10.1007/s10552-010-9688-1
2011
Dymerska D; Fernández P; Suchy J; Pławski A; Słomski R; Kąklewski K; Scott RJ; Gronwald J; Kładny J; Byrski T; Huzarski T; Lubiński J; Kurzawski G, 2011, 'Combined iPLEX and TaqMan assays to screen for 45 common mutations in Lynch syndrome and FAP patients', Hereditary Cancer in Clinical Practice, vol. 9, pp. A9 - A9, http://dx.doi.org/10.1186/1897-4287-9-s2-a9
2011
Hondow HL; Fox SB; Mitchell G; Scott RJ; Beshay V; Wong SQ; kConFab Investigators ; Dobrovic A, 2011, 'A high-throughput protocol for mutation scanning of the BRCA1 and BRCA2 genes.', BMC Cancer, vol. 11, pp. 265, http://dx.doi.org/10.1186/1471-2407-11-265
2011
Bailey HD; Armstrong BK; de Klerk NH; Fritschi L; Attia J; Scott RJ; Smibert E; Milne E, 2011, 'Exposure to professional pest control treatments and the risk of childhood acute lymphoblastic leukemia', INTERNATIONAL JOURNAL OF CANCER, vol. 129, pp. 1678 - 1688, http://dx.doi.org/10.1002/ijc.25769
2011
Patsopoulos NA; Bayer Pharma MS Genetics Working Group ; Steering Committees of Studies Evaluating IFNβ-1b and a CCR1-Antagonist ; ANZgene Consortium ; GeneMSA ; International Multiple Sclerosis Genetics Consortium ; Esposito F; Reischl J; Lehr S; Bauer D; Heubach J; Sandbrink R; Pohl C; Edan G; Kappos L; Miller D; Montalbán J; Polman CH; Freedman MS; Hartung H-P; Arnason BGW; Comi G; Cook S; Filippi M; Goodin DS; Jeffery D; O'Connor P; Ebers GC; Langdon D; Reder AT; Traboulsee A; Zipp F; Schimrigk S; Hillert J; Bahlo M; Booth DR; Broadley S; Brown MA; Browning BL; Browning SR; Butzkueven H; Carroll WM; Chapman C; Foote SJ; Griffiths L; Kermode AG; Kilpatrick TJ; Lechner-Scott J; Marriott M; Mason D; Moscato P; Heard RN; Pender MP; Perreau VM; Perera D; Rubio JP; Scott RJ; Slee M; Stankovich J; Stewart GJ; Taylor BV; Tubridy N; Willoughby E; Wiley J; Matthews P; Boneschi FM; Compston A; Haines J; Hauser SL; McCauley J; Ivinson A; Oksenberg JR; Pericak-Vance M; Sawcer SJ; De Jager PL; Hafler DA; de Bakker PIW, 2011, 'Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.', Ann Neurol, vol. 70, pp. 897 - 912, http://dx.doi.org/10.1002/ana.22609
2011
Milne E; Royle J; Bennett L; de Klerk N; Bailey H; Bower C; Miller M; Attia J; Scott R; Armstrong B, 2011, 'MATERNAL CONSUMPTION OF COFFEE AND TEA DURING PREGNANCY AND RISK OF CHILDHOOD ALL: RESULTS FROM AN AUSTRALIAN CASE-CONTROL STUDY', ISEE Conference Abstracts, vol. 2011, http://dx.doi.org/10.1289/isee.2011.00557
2011
Sawcer S; Hellenthal G; Pirinen M; Spencer CCA; Patsopoulos NA; Moutsianas L; Dilthey A; Su Z; Freeman C; Hunt SE; Edkins S; Gray E; Booth DR; Potter SC; Goris A; Band G; Oturai AB; Strange A; Saarela J; Bellenguez C; Fontaine B; Gillman M; Hemmer B; Gwilliam R; Zipp F; Jayakumar A; Martin R; Leslie S; Hawkins S; Giannoulatou E; D'Alfonso S; Blackburn H; Boneschi FM; Liddle J; Harbo HF; Perez ML; Spurkland A; Waller MJ; Mycko MP; Ricketts M; Comabella M; Hammond N; Kockum I; McCann OT; Ban M; Whittaker P; Kemppinen A; Weston P; Hawkins C; Widaa S; Zajicek J; Dronov S; Robertson N; Bumpstead SJ; Barcellos LF; Ravindrarajah R; Abraham R; Alfredsson L; Ardlie K; Aubin C; Baker A; Baker K; Baranzini SE; Bergamaschi L; Bergamaschi R; Bernstein A; Berthele A; Boggild M; Bradfield JP; Brassat D; Broadley SA; Buck D; Butzkueven H; Capra R; Carroll WM; Cavalla P; Celius EG; Cepok S; Chiavacci R; Clerget-Darpoux F; Clysters K; Comi G; Cossburn M; Cournu-Rebeix I; Cox MB; Cozen W; Cree BAC; Cross AH; Cusi D; Daly MJ; Davis E; De Bakker PIW; Debouverie M; D'Hooghe MB; Dixon K; Dobosi R; Dubois B; Ellinghaus D; Elovaara I; Esposito F, 2011, 'Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis', Nature, vol. 476, pp. 214 - 219, http://dx.doi.org/10.1038/nature10251
2011
Zacharin M; Bajpai A; Chow CW; Catto-Smith A; Stratakis C; Wong MW; Scott R, 2011, 'Gastrointestinal polyps in McCune Albright syndrome.', J Med Genet, vol. 48, pp. 458 - 461, http://dx.doi.org/10.1136/jmg.2010.086330
2011
Oldmeadow C; Riveros C; Holliday EG; Scott R; Moscato P; Wang JJ; Mitchell P; Buitendijk GHS; Vingerling JR; Klaver CCW; Klein R; Attia J, 2011, 'Sifting the wheat from the chaff: Prioritizing GWAS results by identifying consistency across analytical methods', Genetic Epidemiology, vol. 35, pp. 745 - 754, http://dx.doi.org/10.1002/gepi.20622
2011
Baines KJ; Simpson JL; Wood LG; Scott RJ; Gibson PG, 2011, 'Systemic upregulation of neutrophil α-defensins and serine proteases in neutrophilic asthma.', Thorax, vol. 66, pp. 942 - 947, http://dx.doi.org/10.1136/thx.2010.157719
2011
Maguire J; Thakkinstian A; Levi C; Lincz L; Bisset L; Sturm J; Scott R; Whyte S; Attia J, 2011, 'Impact of COX-2 rs5275 and rs20417 and GPIIIa rs5918 polymorphisms on 90-day ischemic stroke functional outcome: A novel finding', Journal of Stroke and Cerebrovascular Diseases, vol. 20, pp. 134 - 144, http://dx.doi.org/10.1016/j.jstrokecerebrovasdis.2009.10.011
2011
Vilain R; Dudding T; Braye S; Groombridge C; Meldrum C; Spigelman AD; Ackland S; Ashman L; Scott R, 2011, 'Can a familial gastrointestinal tumour syndrome be allelic with Waardenberg Syndrome?', Clinical Genetics: an international journal of genetics and molecular medicine, vol. 79, pp. 1 - 7, http://dx.doi.org/10.1111/j.1399-0004.2010.01489.x
2011
Wong MW; Nordfors C; Mossman D; Pecenpetelovska G; Avery-Kiejda KA; Talseth-Palmer B; Bowden NA; Scott RJ, 2011, 'BRIP1, PALB2, and RAD51C mutation analysis reveals their relative importance as genetic susceptibility factors for breast cancer.', Breast Cancer Res Treat, vol. 127, pp. 853 - 859, http://dx.doi.org/10.1007/s10549-011-1443-0
2011
Talseth-Palmer B; Brenne I; Ashton K; Evans T; McPhillips M; Groombridge C; Suchy J; Kurzawski G; Spigelman AD; Lubinski J; Scott R, 2011, 'Colorectal cancer susceptibility Ioci on chromosome 8q23.3 and 11q23.1 as modifiers for disease expression in lynch syndrome', Journal of Medical Genetics, vol. 48, pp. 279 - 284, http://dx.doi.org/10.1136/jmg.2010.079962
2011
Avery-Kiejda KA; Bowden NA; Croft AJ; Scurr LL; Kairupan CF; Ashton KA; Talseth-Palmer BA; Rizos H; Zhang XD; Scott RJ; Hersey P, 2011, 'P53 in human melanoma fails to regulate target genes associated with apoptosis and the cell cycle and may contribute to proliferation.', BMC Cancer, vol. 11, pp. 203, http://dx.doi.org/10.1186/1471-2407-11-203
2011
Mossman D; Scott RJ, 2011, 'Long term transcriptional reactivation of epigenetically silenced genes in colorectal cancer cells requires DNA hypomethylation and histone acetylation.', PLoS One, vol. 6, pp. e23127, http://dx.doi.org/10.1371/journal.pone.0023127
2011
Baines KJ; Simpson JL; Wood LG; Scott RJ; Gibson PG, 2011, 'Transcriptional phenotypes of asthma defined by gene expression profiling of induced sputum samples.', J Allergy Clin Immunol, vol. 127, pp. 153 - 160.e9, http://dx.doi.org/10.1016/j.jaci.2010.10.024
2011
Yotova V; Lefebvre J-F; Moreau C; Gbeha E; Hovhannesyan K; Bourgeois S; Bédarida S; Azevedo L; Amorim A; Sarkisian T; Avogbe PH; Chabi N; Dicko MH; Kou' Santa Amouzou ES; Sanni A; Roberts-Thomson J; Boettcher B; Scott RJ; Labuda D, 2011, 'An X-linked haplotype of Neandertal origin is present among all non-African populations.', Mol Biol Evol, vol. 28, pp. 1957 - 1962, http://dx.doi.org/10.1093/molbev/msr024
2011
Jaworowska E; Trubicka J; Lener MR; Masojć B; Złowocka-Perłowska E; McKay JD; Renard H; Oszutowska D; Wokołorczyk D; Lubiński J; Grodzki T; Serwatowski P; Nej-Wołosiak K; Tołoczko-Grabarek A; Sikorski A; Słojewski M; Jakubowska A; Cybulski C; Lubiński J; Scott RJ, 2011, 'Smoking related cancers and loci at chromosomes 15q25, 5p15, 6p22.1 and 6p21.33 in the Polish population.', PLoS One, vol. 6, pp. e25057, http://dx.doi.org/10.1371/journal.pone.0025057
2011
Spurdle AB; Thompson DJ; Ahmed S; Ferguson K; Healey CS; O'Mara T; Walker LC; Montgomery SB; Dermitzakis ET; Australian National Endometrial Cancer Study Group ; Fahey P; Montgomery GW; Webb PM; Fasching PA; Beckmann MW; Ekici AB; Hein A; Lambrechts D; Coenegrachts L; Vergote I; Amant F; Salvesen HB; Trovik J; Njolstad TS; Helland H; Scott RJ; Ashton K; Proietto T; Otton G; National Study of Endometrial Cancer Genetics Group ; Tomlinson I; Gorman M; Howarth K; Hodgson S; Garcia-Closas M; Wentzensen N; Yang H; Chanock S; Hall P; Czene K; Liu J; Li J; Shu X-O; Zheng W; Long J; Xiang Y-B; Shah M; Morrison J; Michailidou K; Pharoah PD; Dunning AM; Easton DF, 2011, 'Genome-wide association study identifies a common variant associated with risk of endometrial cancer.', Nat Genet, vol. 43, pp. 451 - 454, http://dx.doi.org/10.1038/ng.812
2011
Talseth-Palmer BA; Scott RJ, 2011, 'Genetic variation and its role in malignancy.', Int J Biomed Sci, vol. 7, pp. 158 - 171, https://www.ncbi.nlm.nih.gov/pubmed/23675233
2011
Dymerska D; Serrano-Fernández P; Suchy J; Pławski A; Słomski R; Kaklewski K; Scott RJ; Gronwald J; Kładny J; Byrski T; Huzarski T; Lubiński J; Kurzawski G, 2010, 'Combined iPLEX and TaqMan assays to screen for 45 common mutations in Lynch syndrome and FAP patients.', J Mol Diagn, vol. 12, pp. 82 - 90, http://dx.doi.org/10.2353/jmoldx.2010.090063
2010
McEvoy M; Smith W; D'Este C; Duke J; Peel R; Schofield P; Scott R; Byles J; Henry D; Ewald B; Hancock S; Smith D; Attia J, 2010, 'Cohort profile: The hunter community study', International Journal of Epidemiology, vol. 39, pp. 1452 - 1463, http://dx.doi.org/10.1093/ije/dyp343
2010
Holliday EG; Scott RJ; Attia J, 2010, 'Evidence-based medicine in the era of biomarkers: teaching a new dog old tricks?', Clin Pharmacol Ther, vol. 88, pp. 740 - 742, http://dx.doi.org/10.1038/clpt.2010.214
2010
Johnstone D; Graham RM; Trinder D; Scott RJ; Olynyk JK; Moscato P; Milward EA, 2010, 'O2‐07‐02: Microarray analysis of brain expression changes for genes relating to Alzheimer's disease and other neurodegenerative disorders in mouse models of iron overload', Alzheimer's & Dementia, vol. 6, pp. S112 - S112, http://dx.doi.org/10.1016/j.jalz.2010.05.347
2010
Cox AJ; Gleeson M; Pyne DB; Callister R; Fricker PA; Scott RJ, 2010, 'Cytokine gene polymorphisms and risk for upper respiratory symptoms in highly-trained athletes.', Exerc Immunol Rev, vol. 16, pp. 8 - 21, https://www.ncbi.nlm.nih.gov/pubmed/20839488
2010
Bowden NA; Ashton KA; Avery-Kiejda KA; Zhang XD; Hersey P; Scott RJ, 2010, 'Nucleotide excision repair gene expression after Cisplatin treatment in melanoma.', Cancer Res, vol. 70, pp. 7918 - 7926, http://dx.doi.org/10.1158/0008-5472.CAN-10-0161
2010
Ashton KA; Proietto A; Otton G; Symonds I; McEvoy M; Attia J; Gilbert M; Hamann U; Scott RJ, 2010, 'Polymorphisms in genes of the steroid hormone biosynthesis and metabolism pathways and endometrial cancer risk.', Cancer Epidemiol, vol. 34, pp. 328 - 337, http://dx.doi.org/10.1016/j.canep.2010.03.005
2010
Kamran Ikram M; Xueling S; Jensen RA; Cotch MF; Hewitt AW; Ikram MA; Wang JJ; Klein R; Klein BEK; Breteler MMB; Cheung N; Liew G; Mitchell P; Uitterlinden AG; Rivadeneira F; Hofman A; de Jong PTVM; van Duijn CM; Kao L; Cheng CY; Smith AV; Glazer NL; Lumley T; McKnight B; Psaty BM; Jonasson F; Eiriksdottir G; Aspelund T; Harris TB; Launer LJ; Taylor KD; Li X; Iyengar SK; Xi Q; Sivakumaran TA; MacKey DA; MacGregor S; Martin NG; Young TL; Bis JC; Wiggins KL; Heckbert SR; Hammond CJ; Andrew T; Fahy S; Attia J; Holliday EG; Scott RJ; Islam FMA; Rotter JI; McAuley AK; Boerwinkle E; Tai ES; Gudnason V; Siscovick DS; Vingerling JR; Wong TY, 2010, 'Four novel loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation In vivo', PLoS Genetics, vol. 6, pp. 1 - 12, http://dx.doi.org/10.1371/journal.pgen.1001184
2010
Baines KJ; Simpson JL; Bowden NA; Scott RJ; Gibson PG, 2010, 'Differential gene expression and cytokine production from neutrophils in asthma phenotypes.', Eur Respir J, vol. 35, pp. 522 - 531, http://dx.doi.org/10.1183/09031936.00027409
2010
Cox MB; Cairns MJ; Gandhi KS; Carroll AP; Moscovis S; Stewart GJ; Broadley S; Scott RJ; Booth DR; Lechner-Scott J; ANZgene Multiple Sclerosis Genetics Consortium , 2010, 'MicroRNAs miR-17 and miR-20a inhibit T cell activation genes and are under-expressed in MS whole blood.', PLoS One, vol. 5, pp. e12132, http://dx.doi.org/10.1371/journal.pone.0012132
2010
Talseth-Palmer B; McPhillips M; Groombridge C; Spigelman AD; Scott R, 2010, 'MSH6 and PMS2 mutation positive Australian Lynch syndrome families: novel mutations, cancer risk and age of diagnosis of colorectal cancer', Hereditary Cancer in Clinical Practice, vol. 8, pp. 1 - 10, http://dx.doi.org/10.1186/1897-4287-8-5
2010
Dudding TE; Lawrence O; Winship I; Froyen G; Vandewalle J; Scott R; Shelling AN, 2010, 'Array comparative genomic hybridization for the detection of submicroscopic copy number variations of the X chromosome in women with premature ovarian failure.', Hum Reprod, vol. 25, pp. 3159 - 3160, http://dx.doi.org/10.1093/humrep/deq284
2010
Ikram MK; Sim X; Jensen RA; Cotch MF; Hewitt AW; Ikram MA; Wang JJ; Klein R; Klein BEK; Breteler MMB; Cheung N; Liew G; Mitchell P; Uitterlinden AG; Rivadeneira F; Hofman A; de Jong PTVM; van Duijn CM; Kao L; Cheng C-Y; Smith AV; Glazer NL; Lumley T; McKnight B; Psaty BM; Jonasson F; Eiriksdottir G; Aspelund T; Harris TB; Launer LJ; Taylor KD; Li X; Iyengar SK; Xi Q; Sivakumaran TA; Mackey DA; MacGregor S; Martin NG; Young TL; Bis JC; Wiggins KL; Heckbert SR; Hammond CJ; Andrew T; Fahy S; Attia J; Holliday EG; Scott RJ; Islam FMA; Rotter JI; McAuley AK; Boerwinkle E; Tai ES; Gudnason V; Siscovick DS; Vingerling JR; Wong TY, 2010, 'Correction: Four Novel Loci (19q13, 6q24, 12q24, and 5q14) Influence the Microcirculation In Vivo', PLoS Genetics, vol. 6, http://dx.doi.org/10.1371/annotation/841bfadf-85d1-4059-894f-2863d73fa963
2010
Carr V; Loughland C; McCabe K; Nasir A; Stan C; Jablensky A; Henskens F; Michie P; Mowry B; Pantelis C; Schall U; Scott R, 2010, 'THE AUSTRALIAN SCHIZOPHRENIA RESEARCH BANK (ASRB): DEMOGRAPHIC, CLINICAL AND NEUROPSYCHOLOGICAL PROFILES FOR THE FIRST 500 PARTICIPANTS WITH SCHIZOPHRENIA', SCHIZOPHRENIA RESEARCH, vol. 117, pp. 312 - 312, http://dx.doi.org/10.1016/j.schres.2010.02.525
2010
Trubicka J; Grabowska-Kłujszo E; Suchy J; Masojć B; Serrano-Fernandez P; Kurzawski G; Cybulski C; Górski B; Huzarski T; Byrski T; Gronwald J; Złowocka E; Kładny J; Banaszkiewicz Z; Wiśniowski R; Kowalska E; Lubinski J; Scott RJ, 2010, 'Variant alleles of the CYP1B1 gene are associated with colorectal cancer susceptibility.', BMC Cancer, vol. 10, pp. 420, http://dx.doi.org/10.1186/1471-2407-10-420
2010
Tomlinson IPM; Dunlop M; Campbell H; Zanke B; Gallinger S; Hudson T; Koessler T; Pharoah PD; Niittymäki I; Tuupanen S; Aaltonen LA; Hemminki K; Lindblom A; Försti A; Sieber O; Lipton L; van Wezel T; Morreau H; Wijnen JT; Devilee P; Matsuda K; Nakamura Y; Castellví-Bel S; Ruiz-Ponte C; Castells A; Carracedo A; Ho JWC; Sham P; Hofstra RMW; Vodicka P; Brenner H; Hampe J; Schafmayer C; Tepel J; Schreiber S; Völzke H; Lerch MM; Schmidt CA; Buch S; Moreno V; Villanueva CM; Peterlongo P; Radice P; Echeverry MM; Velez A; Carvajal-Carmona L; Scott R; Penegar S; Broderick P; Tenesa A; Houlston RS, 2010, 'Erratum: COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer', British Journal of Cancer, vol. 102, pp. 455 - 455, http://dx.doi.org/10.1038/sj.bjc.6605518
2010
Ashton KA; Proietto A; Otton G; Symonds I; McEvoy M; Attia J; Scott RJ, 2010, 'Toll-like receptor (TLR) and nucleosome-binding oligomerization domain (NOD) gene polymorphisms and endometrial cancer risk.', BMC Cancer, vol. 10, pp. 382, http://dx.doi.org/10.1186/1471-2407-10-382
2010
Ghandi K; Mckay F; Cox M; Riveros C; Armstrong N; Heard R; Vucic S; Williams D; Stankovich J; Brown M; Danoy P; Stewart G; Broadley S; Moscato P; Lechner-scott J; Scott R; Booth D, 2010, 'The multiple sclerosis whole blood mRNA transcriptome and genetic associations indicate dysregulation of specific T cell pathways in pathogenesis', Human Molecular Genetics, vol. 19, pp. 2134 - 2143
2010
Scott RJ, 2010, 'Have the roles of two functional polymorphisms in breast cancer, R72P in P53 and MDM2-309 in MDM2, become clearer?', Breast Cancer Res, vol. 12, pp. 102, http://dx.doi.org/10.1186/bcr2474
2010
McCabe KL; Loughland CM; Nasir A; Catts S; Jablensky A; Henskens F; Michie P; Mowry B; Pantelis C; Schall U; Scott R; Carr V, 2010, 'THE AUSTRALIAN SCHIZOPHRENIA RESEARCH BANK (ASRB): QUALITY ASSURANCE AND CONTROL FOR A COMPREHENSIVE CLINICAL, NEUROPSYCHOLOGICAL, GENETIC AND NEUROIMAGING DATABASE FOR RESEARCHERS', SCHIZOPHRENIA RESEARCH, vol. 117, pp. 200 - 200, http://dx.doi.org/10.1016/j.schres.2010.02.269
2010
Out AA; Tops CMJ; Nielsen M; Weiss MM; van Minderhout IJHM; Fokkema IFAC; Buisine M-P; Claes K; Colas C; Fodde R; Fostira F; Franken PF; Gaustadnes M; Heinimann K; Hodgson SV; Hogervorst FBL; Holinski-Feder E; Lagerstedt-Robinson K; Olschwang S; van den Ouweland AMW; Redeker EJW; Scott RJ; Vankeirsbilck B; Grønlund RV; Wijnen JT; Wikman FP; Aretz S; Sampson JR; Devilee P; den Dunnen JT; Hes FJ, 2010, 'Leiden Open Variation Database of the MUTYH gene.', Hum Mutat, vol. 31, pp. 1205 - 1215, http://dx.doi.org/10.1002/humu.21343
2010
Attia J; Thakkinstian A; McElduff P; Milne E; Dawson S; Scott RJ; Klerk ND; Armstrong B; Thompson J, 2010, 'Detecting genotyping error using measures of degree of Hardy-Weinberg disequilibrium.', Stat Appl Genet Mol Biol, vol. 9, pp. Article - 5, http://dx.doi.org/10.2202/1544-6115.1463
2010
Tomlinson IPM; Dunlop M; Campbell H; Zanke B; Gallinger S; Hudson T; Koessler T; Pharoah PD; Niittymäki I; Tuupanen S; Aaltonen LA; Hemminki K; Lindblom A; Försti A; Sieber O; Lipton L; van Wezel T; Morreau H; Wijnen JT; Devilee P; Matsuda K; Nakamura Y; Castellví-Bel S; Ruiz-Ponte C; Castells A; Carracedo A; Ho JWC; Sham P; Hofstra RMW; Vodicka P; Brenner H; Hampe J; Schafmayer C; Tepel J; Schreiber S; Völzke H; Lerch MM; Schmidt CA; Buch S; Moreno V; Villanueva CM; Peterlongo P; Radice P; Echeverry MM; Velez A; Carvajal-Carmona L; Scott R; Penegar S; Broderick P; Tenesa A; Houlston RS, 2010, 'COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer.', Br J Cancer, vol. 102, pp. 447 - 454, http://dx.doi.org/10.1038/sj.bjc.6605338
2010
Riveros C; Mellor D; Gandhi KS; Mckay FC; Cox MB; Berretta R; Vaezpour SY; Inostroza-Ponta M; Broadley SA; Heard RN; Vucic S; Stewart GJ; Williams DW; Scott RJ; Lechner-Scott J; Booth DR; Moscato P, 2010, 'A Transcription Factor Map as Revealed by a Genome- Wide Gene Expression Analysis of Whole-Blood mRNA Transcriptome in Multiple Sclerosis', PLoS ONE, vol. 5, http://dx.doi.org/10.1371/journal.pone.0014176
2010
Jakubowska A; Gronwald J; Menkiszak J; Górski B; Huzarski T; Byrski T; Tołoczko-Grabarek A; Gilbert M; Edler L; Zapatka M; Eils R; Lubiński J; Scott RJ; Hamann U, 2010, 'BRCA1-associated breast and ovarian cancer risks in Poland: no association with commonly studied polymorphisms.', Breast Cancer Res Treat, vol. 119, pp. 201 - 211, http://dx.doi.org/10.1007/s10549-009-0390-5
2010
Mossman D; Kim K-T; Scott RJ, 2010, 'Demethylation by 5-aza-2'-deoxycytidine in colorectal cancer cells targets genomic DNA whilst promoter CpG island methylation persists.', BMC Cancer, vol. 10, pp. 366, http://dx.doi.org/10.1186/1471-2407-10-366
2010
Loughland CM; Draganic D; Mccabe K; Richards J; Nasir A; Allen J; Catts S; Jablensky J; Henskens F; Michie P; Mowry B; Pantelis C; Schall U; Scott R; Tooney P; Carr VJ, 2010, 'The Australian Schizophrenia Research Bank: A database of comprehensive clinical, endophenotypic and genetic data for aetiological studies of schizophrenia', Australian and New Zealand Journal of Psychiatry, vol. 44, pp. 1029 - 1035, http://dx.doi.org/10.3109/00048674.2010.501758
2010
Simpson JL; Baines KJ; Boyle MJ; Scott RJ; Gibson PG, 2009, 'Oncostatin M (OSM) is increased in asthma with incompletely reversible airflow obstruction.', Exp Lung Res, vol. 35, pp. 781 - 794, http://dx.doi.org/10.3109/01902140902906412
2009
Ashton KA; Proietto A; Otton G; Symonds I; McEvoy M; Attia J; Gilbert M; Hamann U; Scott RJ, 2009, 'Polymorphisms in TP53 and MDM2 combined are associated with high grade endometrial cancer.', Gynecol Oncol, vol. 113, pp. 109 - 114, http://dx.doi.org/10.1016/j.ygyno.2008.12.036
2009
Kładny J; Suchy J; Kłujszo-Grabowska E; Kacperski T; Scott RJ; Kurzawski G; Lubiński J, 2009, 'Clinical characteristics of tumors derived from colorectal cancer patients who harbor the tumor necrosis factor alpha-1031T/T and NOD2 3020insC polymorphism.', Cancer Epidemiol, vol. 33, pp. 161 - 163, http://dx.doi.org/10.1016/j.canep.2009.06.004
2009
Weidenhofer J; Scott RJ; Tooney PA, 2009, 'Investigation of the expression of genes affecting cytomatrix active zone function in the amygdala in schizophrenia: effects of antipsychotic drugs.', J Psychiatr Res, vol. 43, pp. 282 - 290, http://dx.doi.org/10.1016/j.jpsychires.2008.04.001
2009
Talseth-Palmer BA; Bowden NA; Meldrum C; Nicholl J; Thompson E; Friend K; Liebelt J; Bratkovic D; Haan E; Yu S; Scott RJ, 2009, 'A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology.', Cytogenet Genome Res, vol. 124, pp. 94 - 101, http://dx.doi.org/10.1159/000200093
2009
Reeves S; Meldrum C; Groombridge C; Spigelman AD; Suchy J; Kurzawski G; Lubinski J; McElduff S; Scott R, 2009, 'MTHFR 677 C>T and 1298 A>C polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer', European Journal of Human Genetics, vol. 17, pp. 629 - 635, http://dx.doi.org/10.1038/ejhg.2008.239
2009
Ashton KA; Proietto A; Otton G; Symonds I; Scott RJ, 2009, 'Genetic variants in MUTYH are not associated with endometrial cancer risk.', Hered Cancer Clin Pract, vol. 7, pp. 3, http://dx.doi.org/10.1186/1897-4287-7-3
2009
Attia J; Ioannidis JPA; Thakkinstian A; McEvoy M; Scott RJ; Minelli C; Thompson J; Infante-Rivard C; Guyatt G, 2009, 'How to use an article about genetic association: B: Are the results of the study valid?', JAMA, vol. 301, pp. 191 - 197, http://dx.doi.org/10.1001/jama.2008.946
2009
Cotton RGH; Al Aqeel AI; Al-Mulla F; Carrera P; Claustres M; Ekong R; Hyland VJ; Macrae FA; Marafie MJ; Paalman MH; Patrinos GP; Qi M; Ramesar RS; Scott RJ; Sijmons RH; Sobrido M-J; Vihinen M; members of the Human Variome Project Data Collection from Clinics, Data Collection from Laboratories and Publication, Credit and Incentives Working Groups , 2009, 'Capturing all disease-causing mutations for clinical and research use: toward an effortless system for the Human Variome Project.', Genet Med, vol. 11, pp. 843 - 849, http://dx.doi.org/10.1097/GIM.0b013e3181c371c5
2009
Attia J; Ioannidis JPA; Thakkinstian A; McEvoy M; Scott RJ; Minelli C; Thompson J; Infante-Rivard C; Guyatt G, 2009, 'How to use an article about genetic association: A: Background concepts.', JAMA, vol. 301, pp. 74 - 81, http://dx.doi.org/10.1001/jama.2008.901
2009
Kaput J; Cotton RGH; Hardman L; Watson M; Al Aqeel AI; Al-Aama JY; Al-Mulla F; Alonso S; Aretz S; Auerbach AD; Bapat B; Bernstein IT; Bhak J; Bleoo SL; Blöcker H; Brenner SE; Burn J; Bustamante M; Calzone R; Cambon-Thomsen A; Cargill M; Carrera P; Cavedon L; Cho YS; Chung Y-J; Claustres M; Cutting G; Dalgleish R; den Dunnen JT; Díaz C; Dobrowolski S; dos Santos MRN; Ekong R; Flanagan SB; Flicek P; Furukawa Y; Genuardi M; Ghang H; Golubenko MV; Greenblatt MS; Hamosh A; Hancock JM; Hardison R; Harrison TM; Hoffmann R; Horaitis R; Howard HJ; Barash CI; Izagirre N; Jung J; Kojima T; Laradi S; Lee Y-S; Lee J-Y; Gil-da-Silva-Lopes VL; Macrae FA; Maglott D; Marafie MJ; Marsh SGE; Matsubara Y; Messiaen LM; Möslein G; Netea MG; Norton ML; Oefner PJ; Oetting WS; O'Leary JC; de Ramirez AMO; Paalman MH; Parboosingh J; Patrinos GP; Perozzi G; Phillips IR; Povey S; Prasad S; Qi M; Quin DJ; Ramesar RS; Richards CS; Savige J; Scheible DG; Scott RJ; Seminara D; Shephard EA; Sijmons RH; Smith TD; Sobrido M-J; Tanaka T; Tavtigian SV; Taylor GR; Teague J; Töpel T; Ullman-Cullere M; Utsunomiya J; van Kranen HJ; Vihinen M; Webb E; Weber TK; Yeager M; Yeom YI; Yim S-H; Yoo H-S; Contributors to the Human Variome Project Planning Meeting , 2009, 'Planning the human variome project: the Spain report.', Hum Mutat, vol. 30, pp. 496 - 510, http://dx.doi.org/10.1002/humu.20972
2009
Australia and New Zealand Multiple Sclerosis Genetics Consortium (ANZgene) , 2009, 'Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20.', Nat Genet, vol. 41, pp. 824 - 828, http://dx.doi.org/10.1038/ng.396
2009
Gapska P; Scott RJ; Serrano-Fernandez P; Huzarski T; Byrski T; Kładny J; Gronwald J; Górski B; Cybulski C; Lubinski J; Debniak T, 2009, 'Vitamin D receptor variants and breast cancer risk in the Polish population.', Breast Cancer Res Treat, vol. 115, pp. 629 - 633, http://dx.doi.org/10.1007/s10549-008-0107-1
2009
Gapska P; Scott RJ; Serrano-Fernandez P; Mirecka A; Rassoud I; Górski B; Cybulski C; Huzarski T; Byrski T; Nagay L; Maleszka R; Sulikowski M; Lubinski J; Debniak T, 2009, 'Vitamin D receptor variants and the malignant melanoma risk: a population-based study.', Cancer Epidemiol, vol. 33, pp. 103 - 107, http://dx.doi.org/10.1016/j.canep.2009.06.006
2009
Baines KJ; Simpson JL; Scott RJ; Gibson PG, 2009, 'Immune responses of airway neutrophils are impaired in asthma.', Exp Lung Res, vol. 35, pp. 554 - 569, http://dx.doi.org/10.1080/01902140902777490
2009
Lubiński J; Korzeń M; Górski B; Cybulski C; Debniak T; Jakubowska A; Jaworska K; Wokołorczyk D; Medrek K; Matyjasik J; Huzarski T; Byrski T; Gronwald J; Masojć B; Lener M; Szymańska A; Szymańska-Pasternak J; Serrano-Fernàndez P; Piegat A; Uciński R; Domagała P; Domagała W; Chosia M; Kładny J; Górecka B; Narod S; Scott R, 2009, 'Genetic contribution to all cancers: the first demonstration using the model of breast cancers from Poland stratified by age at diagnosis and tumour pathology.', Breast Cancer Res Treat, vol. 114, pp. 121 - 126, http://dx.doi.org/10.1007/s10549-008-9974-8
2009
Attia J; Ioannidis JPA; Thakkinstian A; McEvoy M; Scott RJ; Minelli C; Thompson J; Infante-Rivard C; Guyatt G, 2009, 'How to use an article about genetic association: C: What are the results and will they help me in caring for my patients?', JAMA, vol. 301, pp. 304 - 308, http://dx.doi.org/10.1001/jama.2008.993
2009
Ashton KA; Proietto A; Otton G; Symonds I; McEvoy M; Attia J; Gilbert M; Hamann U; Scott RJ, 2009, 'Estrogen receptor polymorphisms and the risk of endometrial cancer.', BJOG, vol. 116, pp. 1053 - 1061, http://dx.doi.org/10.1111/j.1471-0528.2009.02185.x
2009
Milne E; Royle JA; de Klerk NH; Blair E; Bailey H; Cole C; Attia J; Scott RJ; Armstrong BK, 2009, 'Fetal growth and risk of childhood acute lymphoblastic leukemia: results from an Australian case-control study.', Am J Epidemiol, vol. 170, pp. 221 - 228, http://dx.doi.org/10.1093/aje/kwp117
2009
Whitehall V; Tran K; Umapathy A; Grieu F; Hewitt C; Evans T-J; Ismail T; Li WQ; Collins P; Ravetto P; Leggett B; Salto-Tellez M; Soong R; Fox S; Scott RJ; Dobrovic A; Iacopetta B, 2009, 'A Multicenter Blinded Study to Evaluate KRAS Mutation Testing Methodologies in the Clinical Setting', JOURNAL OF MOLECULAR DIAGNOSTICS, vol. 11, pp. 543 - 552, http://dx.doi.org/10.2353/jmoldx.2009.090057
2009
Lubiński J; Sijmons RH; Scott RJ, 2009, 'Hereditary Cancer in Clinical Practice transfers to BioMed Central', Hereditary Cancer in Clinical Practice, vol. 7, http://dx.doi.org/10.1186/1897-4287-7-1
2009
Froyen G; Corbett M; Vandewalle J; Jarvela I; Lawrence O; Meldrum C; Bauters M; Govaerts K; Vandeleur L; Van Esch H; Chelly J; Sanlaville D; van Bokhoven H; Ropers HH; Laumonnier F; Ranieri E; Schwartz CE; Abidi F; Tarpey PS; Futreal PA; Whibley A; Raymond FL; Stratton MR; Fryns JP; Scott R; Peippo M; Sipponen M; Partington M; Mowat D; Field M; Hackett A; Marynen P; Turner G; Gécz J, 2008, 'Submicroscopic Duplications of the Hydroxysteroid Dehydrogenase HSD17B10 and the E3 Ubiquitin Ligase HUWE1 Are Associated with Mental Retardation', American Journal of Human Genetics, vol. 82, pp. 432 - 443, http://dx.doi.org/10.1016/j.ajhg.2007.11.002
2008
Reeves SG; Mossman D; Meldrum CJ; Kurzawski G; Suchy J; Lubinski J; Scott RJ, 2008, 'The -149C>T SNP within the DeltaDNMT3B gene, is not associated with early disease onset in hereditary non-polyposis colorectal cancer.', Cancer Lett, vol. 265, pp. 39 - 44, http://dx.doi.org/10.1016/j.canlet.2008.02.005
2008
Foster R; Byrnes E; Meldrum C; Griffith R; Ross G; Upjohn E; Braue A; Scott R; Varigos G; Ferrao P; Ashman L, 2008, 'Association of paediatric mastocytosis with a polymorphism resulting in an amino acid substitution (M541L) in the transmembrane domain of c-KIT, Brit', British Journal of Dermatology, vol. 159, pp. 1160 - 1169, http://dx.doi.org/10.1111/j.1365-2133.2008.08827.x
2008
Reeves SG; Rich D; Meldrum CJ; Colyvas K; Kurzawski G; Suchy J; Lubinski J; Scott RJ, 2008, 'IGF1 is a modifier of disease risk in hereditary non-polyposis colorectal cancer.', Int J Cancer, vol. 123, pp. 1339 - 1343, http://dx.doi.org/10.1002/ijc.23668
2008
Debniak T; van de Wetering T; Scott R; Nagay L; Cybulski C; Górski B; Jakubowska A; Gronwald J; Masojć B; Huzarski T; Byrski T; Nej-Wołosiak K; Kładny J; Maleszka R; Lubinski J, 2008, 'Low prevalence of CDKN2A/ARF mutations among early-onset cancers of breast, pancreas and malignant melanoma in Poland.', Eur J Cancer Prev, vol. 17, pp. 389 - 391, http://dx.doi.org/10.1097/CEJ.0b013e3282f75eb1
2008
Simpson JL; Powell H; Boyle MJ; Scott RJ; Gibson PG, 2008, 'Clarithromycin targets neutrophilic airway inflammation in refractory asthma.', Am J Respir Crit Care Med, vol. 177, pp. 148 - 155, http://dx.doi.org/10.1164/rccm.200707-1134OC
2008
Talseth-Palmer BA; Bowden NA; Hill A; Meldrum C; Scott RJ, 2008, 'Whole genome amplification and its impact on CGH array profiles.', BMC Res Notes, vol. 1, pp. 56, http://dx.doi.org/10.1186/1756-0500-1-56
2008
Jakubowska A; Gronwald J; Menkiszak J; Górski B; Huzarski T; Byrski T; Edler L; Lubiński J; Scott RJ; Hamann U, 2008, 'The VEGF_936_C>T 3'UTR polymorphism reduces BRCA1-associated breast cancer risk in Polish women.', Cancer Lett, vol. 262, pp. 71 - 76, http://dx.doi.org/10.1016/j.canlet.2007.11.029
2008
Ashton KA; Proietto A; Otton G; Symonds I; McEvoy M; Attia J; Gilbert M; Hamann U; Scott RJ, 2008, 'The influence of the Cyclin D1 870 G>A polymorphism as an endometrial cancer risk factor.', BMC Cancer, vol. 8, pp. 272, http://dx.doi.org/10.1186/1471-2407-8-272
2008
Dudding T; Heron J; Thakkinstian A; Nurk E; Golding J; Pembrey M; Ring SM; Attia J; Scott RJ, 2008, 'Factor V Leiden is associated with pre-eclampsia but not with fetal growth restriction: a genetic association study and meta-analysis.', J Thromb Haemost, vol. 6, pp. 1869 - 1875, http://dx.doi.org/10.1111/j.1538-7836.2008.03134.x
2008
Talseth BA; Ashton KA; Meldrum C; Suchy J; Kurzawski G; Lubinski J; Scott RJ, 2008, 'Aurora-A and Cyclin D1 polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer.', Int J Cancer, vol. 122, pp. 1273 - 1277, http://dx.doi.org/10.1002/ijc.23177
2008
Beveridge NJ; Tooney PA; Carroll AP; Gardiner E; Bowden N; Scott RJ; Tran N; Dedova I; Cairns MJ, 2008, 'Dysregulation of miRNA 181b in the temporal cortex in schizophrenia', Human Molecular Genetics, vol. 17, pp. 1156 - 1168, http://dx.doi.org/10.1093/hmg/ddn005
2008
Johnstone D; Graham R; Trinder D; Scott R; Olynyk J; Milward E, 2008, 'P3-230: Alterations in the expression of genes important in Alzheimer's disease (APP, presenilin 1, tau) in the HFE knockout mouse model of the iron disorder hemochromatosis', Alzheimer's & Dementia, vol. 4, pp. T588 - T588, http://dx.doi.org/10.1016/j.jalz.2008.05.1797
2008
Debniak T; Scott RJ; Górski B; Cybulski C; van de Wetering T; Serrano-Fernandez P; Huzarski T; Byrski T; Nagay L; Debniak B; Kowalska E; Jakubowska A; Gronwald J; Wokolorczyk D; Maleszka R; Kładny J; Lubinski J, 2008, 'Common variants of DNA repair genes and malignant melanoma.', Eur J Cancer, vol. 44, pp. 110 - 114, http://dx.doi.org/10.1016/j.ejca.2007.10.006
2008
Scott R; Crooks R; Meldrum C, 2008, 'Gene symbol: STK11. Disease: Peutz-Jeghers Syndrome.', Hum Genet, vol. 124, pp. 300, https://www.ncbi.nlm.nih.gov/pubmed/18846624
2008
Złowocka E; Cybulski C; Górski B; Debniak T; Słojewski M; Wokołorczyk D; Serrano-Fernández P; Matyjasik J; van de Wetering T; Sikorski A; Scott RJ; Lubiński J, 2008, 'Germline mutations in the CHEK2 kinase gene are associated with an increased risk of bladder cancer.', Int J Cancer, vol. 122, pp. 583 - 586, http://dx.doi.org/10.1002/ijc.23099
2008
Scott RJ, 2008, 'Modifier genes and HNPCC: variable phenotypic expression in HNPCC and the search for modifier genes.', Eur J Hum Genet, vol. 16, pp. 531 - 532, http://dx.doi.org/10.1038/ejhg.2008.46
2008
Avery-Kiejda KA; Zhang XD; Adams LJ; Scott RJ; Vojtesek B; Lane DP; Hersey P, 2008, 'Small molecular weight variants of p53 are expressed in human melanoma cells and are induced by the DNA-damaging agent cisplatin.', Clin Cancer Res, vol. 14, pp. 1659 - 1668, http://dx.doi.org/10.1158/1078-0432.CCR-07-1422
2008
Jakubowska A; Gronwald J; Menkiszak J; Górski B; Huzarski T; Byrski T; Benner A; Lubiński J; Scott RJ; Hamann U, 2008, 'Ovarian cancer risk in Polish BRCA1 mutation carriers is not associated with the prohibitin 3' untranslated region polymorphism.', BMC Cancer, vol. 8, pp. 90, http://dx.doi.org/10.1186/1471-2407-8-90
2008
Suchy J; Kłujszo-Grabowska E; Kładny J; Cybulski C; Wokołorczyk D; Szymańska-Pasternak J; Kurzawski G; Scott RJ; Lubiński J, 2008, 'Inflammatory response gene polymorphisms and their relationship with colorectal cancer risk.', BMC Cancer, vol. 8, pp. 112, http://dx.doi.org/10.1186/1471-2407-8-112
2008
Alberici P; Gaspar C; Franken P; Gorski MM; de Vries I; Scott RJ; Ristimäki A; Aaltonen LA; Fodde R, 2008, 'Smad4 haploinsufficiency: a matter of dosage.', Pathogenetics, vol. 1, pp. 2, http://dx.doi.org/10.1186/1755-8417-1-2
2008
Jaworowska E; Serrano-Fernández P; Tarnowska C; Lubiński J; Brzosko M; Flicinski J; Masojc B; Matyjasik J; Scott RJ; Narod SA; Lubiński J, 2008, 'Familial association of laryngeal, lung, stomach and early-onset breast cancer.', Breast Cancer Res Treat, vol. 112, pp. 359 - 361, http://dx.doi.org/10.1007/s10549-007-9869-0
2008
Bowden NA; Scott RJ; Tooney PA, 2008, 'Altered gene expression in the superior temporal gyrus in schizophrenia.', BMC Genomics, vol. 9, pp. 199, http://dx.doi.org/10.1186/1471-2164-9-199
2008
Jakubowska A; Gronwald J; Menkiszak J; Górski B; Huzarski T; Byrski T; Edler L; Lubinski J; Scott RJ; Hamann U, 2007, 'Integrin beta3 Leu33Pro polymorphism increases BRCA1-associated ovarian cancer risk.', J Med Genet, vol. 44, pp. 408 - 411, http://dx.doi.org/10.1136/jmg.2006.047498
2007
Simpson JL; Grissell TV; Douwes J; Scott RJ; Boyle MJ; Gibson PG, 2007, 'Innate immune activation in neutrophilic asthma and bronchiectasis.', Thorax, vol. 62, pp. 211 - 218, http://dx.doi.org/10.1136/thx.2006.061358
2007
Jaworowska E; Serrano-Fernández P; Tarnowska C; Lubiński J; Kram A; Masojc B; Scott R; Lubiński J, 2007, 'Clinical and epidemiological features of familial laryngeal cancer in Poland.', Cancer Detect Prev, vol. 31, pp. 270 - 275, http://dx.doi.org/10.1016/j.cdp.2006.06.007
2007
Jakubowska A; Gronwald J; Górski B; Huzarski T; Byrski T; Benner A; Lubiński J; Scott RJ; Hamann U, 2007, 'The 3' untranslated region C > T polymorphism of prohibitin is a breast cancer risk modifier in Polish women carrying a BRCA1 mutation.', Breast Cancer Res Treat, vol. 104, pp. 67 - 74, http://dx.doi.org/10.1007/s10549-006-9389-3
2007
Bowden NA; Scott RJ; Tooney PA, 2007, 'Altered expression of regulator of G-protein signalling 4 (RGS4) mRNA in the superior temporal gyrus in schizophrenia.', Schizophr Res, vol. 89, pp. 165 - 168, http://dx.doi.org/10.1016/j.schres.2006.09.003
2007
Talseth BA; Meldrum C; Suchy J; Kurzawski G; Lubinski J; Scott RJ, 2007, 'MDM2 SNP309 T>G alone or in combination with the TP53 R72P polymorphism does not appear to influence disease expression and age of diagnosis of colorectal cancer in HNPCC patients.', Int J Cancer, vol. 120, pp. 563 - 565, http://dx.doi.org/10.1002/ijc.22339
2007
Mhaidat NM; Zhang XD; Allen J; Avery-Kiejda KA; Scott RJ; Hersey P, 2007, 'Temozolomide induces senescence but not apoptosis in human melanoma cells', BRITISH JOURNAL OF CANCER, vol. 97, pp. 1225 - 1233, http://dx.doi.org/10.1038/sj.bjc.6604017
2007
Attia J; Thakkinstian A; Wang Y; Lincz L; Parsons M; Sturm J; McGettigan P; Scott R; Meldrum C; Levi C, 2007, 'The PAI-1 4G/5G Gene Polymorphism and Ischemic Stroke: An Association Study and Meta-Analysis', Journal of Stroke and Cerebrovascular Diseases, vol. 16, pp. 173 - 179, http://dx.doi.org/10.1016/j.jstrokecerebrovasdis.2007.03.002
2007
Talseth BA; Meldrum C; Suchy J; Kurzawski G; Lubinski J; Scott RJ, 2007, 'Lack of association between genetic polymorphisms in cytokine genes and disease expression in patients with hereditary non-polyposis colorectal cancer.', Scand J Gastroenterol, vol. 42, pp. 628 - 632, http://dx.doi.org/10.1080/00365520601106699
2007
Jakubowska A; Gronwald J; Menkiszak J; Górski B; Huzarski T; Byrski T; Edler L; Lubiński J; Scott RJ; Hamann U, 2007, 'Methylenetetrahydrofolate reductase polymorphisms modify BRCA1-associated breast and ovarian cancer risks.', Breast Cancer Res Treat, vol. 104, pp. 299 - 308, http://dx.doi.org/10.1007/s10549-006-9417-3
2007
Kairupan C; Scott RJ, 2007, 'Base excision repair and the role of MUTYH.', Hered Cancer Clin Pract, vol. 5, pp. 199 - 209, http://dx.doi.org/10.1186/1897-4287-5-4-199
2007
Lubinski J; Korzen M; Gorski B; Cybulski C; Debniak T; Jakubowska A; Medrek K; Matyjasik J; Huzarski T; Byrski T; Gronwald J; Masojc B; Lener M; Szymanska A; Szymanska-Pasternak J; Fernandez PS; Wokolorczyk D; Piegat A; Ucinski M; Domagala P; Kladny J; Gorecka B; Scott R; Narod S, 2007, 'Breast cancer susceptibility genes.', J BUON, vol. 12 Suppl 1, pp. S23 - S29, https://www.ncbi.nlm.nih.gov/pubmed/17935274
2007
Jakubowska A; Gronwald J; Menkiszak J; Górski B; Huzarski T; Byrski T; Edler L; Lubiñski J; Scott RJ; Hamann U, 2007, 'The RAD51 135 G>C polymorphism modifies breast cancer and ovarian cancer risk in Polish BRCA1 mutation carriers.', Cancer Epidemiol Biomarkers Prev, vol. 16, pp. 270 - 275, http://dx.doi.org/10.1158/1055-9965.EPI-06-0562
2007
Scott RJ, 2007, 'Response to “Variability in the clinical phenotype among families with HNPCC”: The potential importance of the location of the mutation in the gene by Dr. Prathap Bandipalliam', International Journal of Cancer, vol. 120, pp. 2278 - 2278, http://dx.doi.org/10.1002/ijc.22347
2007
Matyjasik J; Cybulski C; Masojć B; Jakubowska A; Serrano-Fernandez P; Górski B; Debniak T; Huzarski T; Byrski T; Gronwald J; Złowocka E; Narod SA; Scott R; Lubinski J, 2007, 'CYP1B1 and predisposition to breast cancer in Poland.', Breast Cancer Res Treat, vol. 106, pp. 383 - 388, http://dx.doi.org/10.1007/s10549-007-9500-4
2007
Bowden NA; Croft A; Scott RJ, 2007, 'Gene expression profiling in familial adenomatous polyposis adenomas and desmoid disease.', Hered Cancer Clin Pract, vol. 5, pp. 79 - 96, http://dx.doi.org/10.1186/1897-4287-5-2-79
2007
Reeves S; Meldrum C; Scott RJ, 2006, 'Re: IGF-1 gene polymorphism and risk for hereditary nonpolyposis colorectal cancer.', J Natl Cancer Inst, vol. 98, pp. 1664 - 1665, http://dx.doi.org/10.1093/jnci/djj452
2006
Debniak T; Scott RJ; Huzarski T; Byrski T; Masojć B; van de Wetering T; Serrano-Fernandez P; Górski B; Cybulski C; Gronwald J; Debniak B; Maleszka R; Kładny J; Bieniek A; Nagay L; Haus O; Grzybowska E; Wandzel P; Niepsuj S; Narod SA; Lubinski J, 2006, 'XPD common variants and their association with melanoma and breast cancer risk.', Breast Cancer Res Treat, vol. 98, pp. 209 - 215, http://dx.doi.org/10.1007/s10549-005-9151-2
2006
Talseth BA; Meldrum C; Suchy J; Kurzawski G; Lubinski J; Scott RJ, 2006, 'Age of diagnosis of colorectal cancer in HNPCC patients is more complex than that predicted by R72P polymorphism in TP53.', Int J Cancer, vol. 118, pp. 2479 - 2484, http://dx.doi.org/10.1002/ijc.21661
2006
Ashton KA; Meldrum CJ; McPhillips ML; Suchy J; Kurzawski G; Lubinski J; Scott RJ, 2006, 'The Association of the COMT V158M Polymorphism with Endometrial/Ovarian Cancer in HNPCC Families Adhering to the Amsterdam Criteria.', Hered Cancer Clin Pract, vol. 4, pp. 94 - 102, http://dx.doi.org/10.1186/1897-4287-4-2-94
2006
Debniak T; Cybulski C; Kurzawski G; Górski B; Huzarski T; Byrski T; Gronwald J; Suchy J; Masojć B; Mierzejewski M; Lener M; Teodorczyk U; Medrek K; Złowocka E; Grabowska-Kłujszo E; Nej-Wołosiak K; Szymańska A; Szymańska-Pasternak J; Matyjasik J; Wetering TVD; Jakubowska A; Oszurek O; Tołoczko-Grabarek A; Castaneda J; Scott R; Narod SA; Lubiński J, 2006, 'Low-risk Genes and Multi-organ Cancer Risk in the Polish Population.', Hered Cancer Clin Pract, vol. 4, pp. 52 - 55, http://dx.doi.org/10.1186/1897-4287-4-1-52
2006
Hitchins MP; Suter CM; Wong J; Cheong K; Hawkins NJ; Leggett B; Scott R; Spigelman AD; Tomlinson IP; Martin DI; Ward RL, 2006, 'Germline epimutations of APC are not associated with inherited colorectal polyposis', Gut, vol. 55, pp. 586 - 587, http://dx.doi.org/10.1136/gut.2005.087486
2006
Talseth BA; Meldrum C; Suchy J; Kurzawski G; Lubinski J; Scott RJ, 2006, 'Genetic polymorphisms in xenobiotic clearance genes and their influence on disease expression in hereditary nonpolyposis colorectal cancer patients.', Cancer Epidemiol Biomarkers Prev, vol. 15, pp. 2307 - 2310, http://dx.doi.org/10.1158/1055-9965.EPI-06-0040
2006
Masojć B; Mierzejewski M; Cybulski C; van de Wetering T; Debniak T; Górski B; Jaworowska E; Tarnowska C; Lenner M; Scott RJ; Lubiński J, 2006, 'Cancer Familial Aggregation (CFA) and G446A polymorphism in ARLTS1 gene.', Breast Cancer Res Treat, vol. 99, pp. 59 - 62, http://dx.doi.org/10.1007/s10549-006-9180-5
2006
Moscovis SM; Gordon AE; Al Madani OM; Gleeson M; Scott RJ; Roberts-Thomson J; Hall ST; Weir DM; Busuttil A; Blackwell CC, 2006, 'IL6 G-174C associated with sudden infant death syndrome in a Caucasian Australian cohort.', Hum Immunol, vol. 67, pp. 819 - 825, http://dx.doi.org/10.1016/j.humimm.2006.07.010
2006
Bowden NA; Weidenhofer J; Scott RJ; Schall U; Todd J; Michie PT; Tooney PA, 2006, 'Preliminary investigation of gene expression profiles in peripheral blood lymphocytes in schizophrenia.', Schizophr Res, vol. 82, pp. 175 - 183, http://dx.doi.org/10.1016/j.schres.2005.11.012
2006
Debniak T; Scott R; Masojc B; Serrano-Fernández P; Huzarski T; Byrski T; Debniak B; Górski B; Cybulski C; Medrek K; Kurzawski G; van de Wetering T; Maleszka R; Kładny J; Lubinski J, 2006, 'MC1R common variants, CDKN2A and their association with melanoma and breast cancer risk.', Int J Cancer, vol. 119, pp. 2597 - 2602, http://dx.doi.org/10.1002/ijc.22210
2006
Mossman D; Scott RJ, 2006, 'Epimutations, inheritance and causes of aberrant DNA methylation in cancer.', Hered Cancer Clin Pract, vol. 4, pp. 75 - 80, http://dx.doi.org/10.1186/1897-4287-4-2-75
2006
Suchy J; Kurzawski G; Jakubowska K; Rać ME; Safranow K; Kładny J; Rzepka-Górska I; Chosia M; Czeszyńska B; Oszurek O; Scott RJ; Lubiński J, 2006, 'Frequency and nature of hMSH6 germline mutations in Polish patients with colorectal, endometrial and ovarian cancers.', Clin Genet, vol. 70, pp. 68 - 70, http://dx.doi.org/10.1111/j.1399-0004.2006.00630.x
2006
Lener MR; Oszutowska D; Castaneda J; Kurzawski G; Suchy J; Nej-Wołosiak K; Byrski T; Huzarski T; Gronwald J; Szymańska A; Szymańska-Pasternak J; Grodzki T; Serwatowski P; Bre Borowicz G; Scott RJ; Lubiński J, 2006, 'Prevalence of the NOD2 3020insC mutation in aggregations of breast and lung cancer.', Breast Cancer Res Treat, vol. 95, pp. 141 - 145, http://dx.doi.org/10.1007/s10549-005-9057-z
2006
Jaworowska E; Masojć B; Tarnowska C; Brzosko M; Fliciński J; Serrano-Fernandez P; Matyjasik J; Amernik K; Scott RJ; Lubiński J, 2006, 'Association between early-onset breast and laryngeal cancers.', Breast Cancer Res Treat, vol. 97, pp. 215 - 219, http://dx.doi.org/10.1007/s10549-005-9116-5
2006
Scott R; Moscovis S; Hall S; Gleeson M; Roberts-Thomson J; Blackwell C, 2006, 'The influence of infection on cytokine gene polymorphisms in evolution', Before Farming, vol. 2006, pp. 1 - 7, http://dx.doi.org/10.3828/bfarm.2006.2.1
2006
Kurzawski G; Suchy J; Lener M; Kłujszo-Grabowska E; Kładny J; Safranow K; Jakubowska K; Jakubowska A; Huzarski T; Byrski T; Debniak T; Cybulski C; Gronwald J; Oszurek O; Oszutowska D; Kowalska E; Góźdź S; Niepsuj S; Słomski R; Pławski A; Łacka-Wojciechowska A; Rozmiarek A; Fiszer-Maliszewska Ł; Bebenek M; Sorokin D; Sasiadek MM; Stembalska A; Grzebieniak Z; Kilar E; Stawicka M; Godlewski D; Richter P; Brozek I; Wysocka B; Limon J; Jawień A; Banaszkiewicz Z; Janiszewska H; Kowalczyk J; Czudowska D; Scott RJ; Lubiński J, 2006, 'Germline MSH2 and MLH1 mutational spectrum including large rearrangements in HNPCC families from Poland (update study).', Clin Genet, vol. 69, pp. 40 - 47, http://dx.doi.org/10.1111/j.1399-0004.2006.00550.x
2006
Weidenhofer J; Bowden NA; Scott RJ; Tooney PA, 2006, 'Altered gene expression in the amygdala in schizophrenia: up-regulation of genes located in the cytomatrix active zone.', Mol Cell Neurosci, vol. 31, pp. 243 - 250, http://dx.doi.org/10.1016/j.mcn.2005.09.013
2006
Simpson JL; Scott R; Boyle MJ; Gibson PG, 2006, 'Inflammatory subtypes in asthma: assessment and identification using induced sputum.', Respirology, vol. 11, pp. 54 - 61, http://dx.doi.org/10.1111/j.1440-1843.2006.00784.x
2006
Debniak T; Scott RJ; Huzarski T; Byrski T; Rozmiarek A; Debniak B; Górski B; Cybulski C; Medrek K; Mierzejewski M; Masojc B; Matyjasik J; Złowocka E; Teodorczyk U; Lener M; Klujszo-Grabowska E; Nej-Wołosiak K; Jaworowska E; Oszutowska D; Szymańska A; Szymańska J; Castaneda J; van de Wetering T; Suchy J; Kurzawski G; Oszurek O; Narod S; Lubinski J, 2006, 'CDKN2A common variant and multi-organ cancer risk--a population-based study.', Int J Cancer, vol. 118, pp. 3180 - 3182, http://dx.doi.org/10.1002/ijc.21760
2006
Bowden NA; Tooney PA; Scott RJ, 2006, 'Gene expression profiling of xeroderma pigmentosum.', Hered Cancer Clin Pract, vol. 4, pp. 103 - 110, http://dx.doi.org/10.1186/1897-4287-4-2-103
2006
Milne E; van Bockxmeer FM; Robertson L; Brisbane JM; Ashton LJ; Scott RJ; Armstrong BK, 2006, 'Buccal DNA collection: comparison of buccal swabs with FTA cards.', Cancer Epidemiol Biomarkers Prev, vol. 15, pp. 816 - 819, http://dx.doi.org/10.1158/1055-9965.EPI-05-0753
2006
Blackwell CC; Moscovis SM; Gordon AE; Al Madani OM; Hall ST; Gleeson M; Scott RJ; Roberts-Thomson J; Weir DM; Busuttil A, 2005, 'Cytokine responses and sudden infant death syndrome: genetic, developmental, and environmental risk factors.', J Leukoc Biol, vol. 78, pp. 1242 - 1254, http://dx.doi.org/10.1189/jlb.0505253
2005
Scott RJ; Meldrum CJ, 2005, 'Missense mutations in cancer predisposing genes: can we make sense of them?', Hered Cancer Clin Pract, vol. 3, pp. 123 - 127, http://dx.doi.org/10.1186/1897-4287-3-3-123
2005
Ashton KA; Meldrum CJ; McPhillips ML; Kairupan CF; Scott RJ, 2005, 'Frequency of the Common MYH Mutations (G382D and Y165C) in MMR Mutation Positive and Negative HNPCC Patients.', Hered Cancer Clin Pract, vol. 3, pp. 65 - 70, http://dx.doi.org/10.1186/1897-4287-3-2-65
2005
Weber W; Scott RJ, 2005, 'Case report: familial gastric cancer and chordoma in the same family.', Hered Cancer Clin Pract, vol. 3, pp. 81 - 84, http://dx.doi.org/10.1186/1897-4287-3-2-81
2005
McPhillips M; Meldrum CJ; Creegan R; Edkins E; Scott RJ, 2005, 'Deletion Mutations in an Australian Series of HNPCC Patients.', Hered Cancer Clin Pract, vol. 3, pp. 43 - 47, http://dx.doi.org/10.1186/1897-4287-3-1-43
2005
Debniak T; Scott RJ; Huzarski T; Byrski T; Rozmiarek A; Debniak B; Załuga E; Maleszka R; Kładny J; Górski B; Cybulski C; Gronwald J; Kurzawski G; Lubinski J, 2005, 'CDKN2A common variants and their association with melanoma risk: a population-based study.', Cancer Res, vol. 65, pp. 835 - 839, https://www.ncbi.nlm.nih.gov/pubmed/15705881
2005
Simpson JL; Scott RJ; Boyle MJ; Gibson PG, 2005, 'Differential proteolytic enzyme activity in eosinophilic and neutrophilic asthma.', Am J Respir Crit Care Med, vol. 172, pp. 559 - 565, http://dx.doi.org/10.1164/rccm.200503-369OC
2005
Gronwald J; Jauch A; Cybulski C; Schoell B; Böhm-Steuer B; Lener M; Grabowska E; Górski B; Jakubowska A; Domagała W; Chosia M; Scott RJ; Lubiński J, 2005, 'Comparison of genomic abnormalities between BRCAX and sporadic breast cancers studied by comparative genomic hybridization.', Int J Cancer, vol. 114, pp. 230 - 236, http://dx.doi.org/10.1002/ijc.20723
2005
Hitchins MP; Williams RA; Cheong KF; Halani N; Lin V; Packham D; Ku S; Buckle AD; Hawkins NJ; Burn J, 2005, 'MLH1 Germline Epimutations as a Factor in Hereditary Nonpolyposis Colorectal Cancer', Gastroenterology, vol. 129, pp. 1392 - 1399, http://dx.doi.org/10.1053/j.gastro.2005.09.003
2005
Debniak T; Górski B; Scott RJ; Cybulski C; Medrek K; Zowocka E; Kurzawski G; Debniak B; Kadny J; Bielecka-Grzela S; Maleszka R; Lubiński J, 2004, 'Germline mutation and large deletion analysis of the CDKN2A and ARF genes in families with multiple melanoma or an aggregation of malignant melanoma and breast cancer.', Int J Cancer, vol. 110, pp. 558 - 562, http://dx.doi.org/10.1002/ijc.20163
2004
Blackwell CC; Moscovis SM; Gordon AE; Al Madani OM; Hall ST; Gleeson M; Scott RJ; Roberts-Thomson J; Weir DM; Busuttil A, 2004, 'Ethnicity, infection and sudden infant death syndrome.', FEMS Immunol Med Microbiol, vol. 42, pp. 53 - 65, http://dx.doi.org/10.1016/j.femsim.2004.06.007
2004
Gawdis-Wojnarska B; Brzosko M; Fliciński J; Marlicz K; Starzyńska T; Scott RJ; Lubiński J, 2004, 'Nuclear pedigree criteria for the identification of individuals suspected to be at risk of an inherited predisposition to gastric cancer.', Hered Cancer Clin Pract, vol. 2, pp. 65 - 68, http://dx.doi.org/10.1186/1897-4287-2-2-65
2004
Scott RJ, 2004, 'DNA double strand break repair and its association with inherited predispositions to breast cancer.', Hered Cancer Clin Pract, vol. 2, pp. 37 - 43, http://dx.doi.org/10.1186/1897-4287-2-1-37
2004
Moscovis SM; Gordon AE; Hall ST; Gleeson M; Scott RJ; Roberts-Thomsom J; Weir DM; Busuttil A; Blackwell CC, 2004, 'Interleukin 1-beta responses to bacterial toxins and sudden infant death syndrome.', FEMS Immunol Med Microbiol, vol. 42, pp. 139 - 145, http://dx.doi.org/10.1016/j.femsim.2004.06.005
2004
Kurzawski G; Suchy J; Kładny J; Grabowska E; Mierzejewski M; Jakubowska A; Debniak T; Cybulski C; Kowalska E; Szych Z; Domagała W; Scott RJ; Lubiński J, 2004, 'The NOD2 3020insC mutation and the risk of colorectal cancer.', Cancer Res, vol. 64, pp. 1604 - 1606, http://dx.doi.org/10.1158/0008-5472.can-03-3791
2004
Scott RJ; Ashton KA, 2004, 'Familial breast and bowel cancer: does it exist?', Hered Cancer Clin Pract, vol. 2, pp. 25 - 29, http://dx.doi.org/10.1186/1897-4287-2-1-25
2004
2004, 'Presymptomatic DNA Testing in BRCA1/2. Invited reactions from the field on the van Oostrom and Tibben paper', Hereditary Cancer in Clinical Practice, vol. 2, pp. 107 - 107, http://dx.doi.org/10.1186/1897-4287-2-3-107
2004
Moscovis SM; Gordon AE; Al Madani OM; Gleeson M; Scott RJ; Roberts-Thomson J; Hall ST; Weir DM; Busuttil A; Blackwell CC, 2004, 'Interleukin-10 and sudden infant death syndrome.', FEMS Immunol Med Microbiol, vol. 42, pp. 130 - 138, http://dx.doi.org/10.1016/j.femsim.2004.06.020
2004
2004, 'DNA mismatch repair genes and hereditary non-polyposis colorectal cancer.', J Gastroenterol Hepatol, vol. 19, pp. 465 - 466, http://dx.doi.org/10.1111/j.1440-1746.2004.03425.x
2004
Marazita ML; Murray JC; Lidral AC; Arcos-Burgos M; Cooper ME; Goldstein T; Maher BS; Daack-Hirsch S; Schultz R; Mansilla MA; Field LL; Liu Y-E; Prescott N; Malcolm S; Winter R; Ray A; Moreno L; Valencia C; Neiswanger K; Wyszynski DF; Bailey-Wilson JE; Albacha-Hejazi H; Beaty TH; McIntosh I; Hetmanski JB; Tunçbilek G; Edwards M; Harkin L; Scott R; Roddick LG, 2004, 'Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35.', Am J Hum Genet, vol. 75, pp. 161 - 173, http://dx.doi.org/10.1086/422475
2004
Smith CJA; Crock PA; King BR; Meldrum CJ; Scott RJ, 2004, 'Phenotype-genotype correlations in a series of wolfram syndrome families.', Diabetes Care, vol. 27, pp. 2003 - 2009, http://dx.doi.org/10.2337/diacare.27.8.2003
2004
Scott RJ; Crooks R; Rose L; Attia J; Thakkinstian A; Thomas L; Spigelman AD; Meldrum CJ, 2004, 'Germline Missense Changes in the APC Gene and Their Relationship to Disease.', Hered Cancer Clin Pract, vol. 2, pp. 81 - 91, http://dx.doi.org/10.1186/1897-4287-2-2-81
2004
Liu X; Sinn H-P; Ulmer HU; Scott RJ; Hamann U, 2004, 'Intronic TP53 Germline Sequence Variants Modify the Risk in German Breast/Ovarian Cancer Families.', Hered Cancer Clin Pract, vol. 2, pp. 139 - 145, http://dx.doi.org/10.1186/1897-4287-2-3-139
2004
Górski B; Debniak T; Masojć B; Mierzejewski M; Medrek K; Cybulski C; Jakubowska A; Kurzawski G; Chosia M; Scott R; Lubiński J, 2003, 'Germline 657del5 mutation in the NBS1 gene in breast cancer patients.', Int J Cancer, vol. 106, pp. 379 - 381, http://dx.doi.org/10.1002/ijc.11231
2003
Scott RJ, 2003, 'Familial Adenomatous Polyposis (FAP) and Other Polyposis Syndromes', Hereditary Cancer in Clinical Practice, vol. 1, pp. 19 - 19, http://dx.doi.org/10.1186/1897-4287-1-1-19
2003
Meldrum CJ; McPhillips M; Crooks R; Thomas L; Edkins T; Creegan R; Miller E; Agrez M; Scott RJ, 2003, 'A Comparison Between Denaturing Gradient Gel Electrophoresis and Denaturing High Performance Liquid Chromatography in Detecting Mutations in Genes Associated with Hereditary Non-Polyposis Colorectal Cancer (HNPCC) and the Identification of 9 New Mutations Previously Unidentified by DGGE', Hereditary Cancer in Clinical Practice, vol. 1, pp. 39 - 39, http://dx.doi.org/10.1186/1897-4287-1-1-39
2003
Lubiński W; Kurzawski G; Suchy J; Szych Z; Penkala K; Palacz O; Scott RJ; Lubiński J, 2003, 'Electro-oculographic and electroretinographic studies in HNPCC gene mutation carriers.', Ophthalmic Res, vol. 35, pp. 281 - 294, http://dx.doi.org/10.1159/000072149
2003
Jakubowska A; Scott R; Menkiszak J; Gronwald J; Byrski T; Huzarski T; Górski B; Cybulski C; Debniak T; Kowalska E; Starzyńska T; Ławniczak M; Narod S; Lubinski J, 2003, 'A high frequency of BRCA2 gene mutations in Polish families with ovarian and stomach cancer.', Eur J Hum Genet, vol. 11, pp. 955 - 958, http://dx.doi.org/10.1038/sj.ejhg.5201064
2003
Kurzawski G; Safranow K; Suchy J; Chlubek D; Scott RJ; Lubiński J, 2002, 'Mutation analysis of MLH1 and MSH2 genes performed by denaturing high-performance liquid chromatography.', J Biochem Biophys Methods, vol. 51, pp. 89 - 100, http://dx.doi.org/10.1016/s0165-022x(02)00003-9
2002
Scott R; Crooks R; Meldrum C; Smith CJ; Mowat DR; McPhillips M; Spigelman A, 2002, 'Mutation analysis of the STK11/LKB1 gene and clinical characteristics of an Australian series of Peutz-Jeghers syndrome patients', Clinical Geriatrics, vol. 62, pp. 282 - 287, http://dx.doi.org/10.1034/j.1399-0004.2002.620405.x
2002
Ward RL; Meldrum C; Williams R; Mokany E; Scott R; Turner J; Hawkins NJ; Burgess B; Groombridge C; Spigelman A, 2002, 'Impact of microsatellite testing and mismatch repair protein expression on the clinical interpretation of genetic testing in hereditary non-polyposis colorectal cancer', Journal of Cancer Research and Clinical Oncology, vol. 128, pp. 403 - 411, http://dx.doi.org/10.1007/s00432-002-0361-2
2002
Scott RJ; Vajdic CM; Armstrong BK; Ainsworth CJ; Meldrum CJ; Aitken JF; Kricker A, 2002, 'BRCA2 mutations in a population-based series of patients with ocular melanoma', International Journal of Cancer, vol. 102, pp. 188 - 191, http://dx.doi.org/10.1002/ijc.10693
2002
Niu J; Dorahy DJ; Gu X; Scott RJ; Draganic B; Ahmed N; Agrez MV, 2002, 'Integrin expression in colon cancer cells is regulated by the cytoplasmic domain of the beta6 integrin subunit.', Int J Cancer, vol. 99, pp. 529 - 537, http://dx.doi.org/10.1002/ijc.10397
2002
Hamann U; Liu X; Lange S; Ulmer HU; Benner A; Scott RJ, 2002, 'Contribution of BRCA2 germline mutations to hereditary breast/ovarian cancer in Germany.', J Med Genet, vol. 39, pp. E12, http://dx.doi.org/10.1136/jmg.39.3.e12
2002
Jakubowska A; Nej K; Huzarski T; Scott RJ; Lubiński J, 2002, 'BRCA2 gene mutations in families with aggregations of breast and stomach cancers.', Br J Cancer, vol. 87, pp. 888 - 891, http://dx.doi.org/10.1038/sj.bjc.6600562
2002
Gu X; Niu J; Dorahy DJ; Scott R; Agrez MV, 2002, 'Integrin alpha(v)beta6-associated ERK2 mediates MMP-9 secretion in colon cancer cells.', Br J Cancer, vol. 87, pp. 348 - 351, http://dx.doi.org/10.1038/sj.bjc.6600480
2002
Ahmed N; Niu J; Dorahy DJ; Gu X; Andrews S; Meldrum CJ; Scott RJ; Baker MS; Macreadie IG; Agrez MV, 2002, 'Direct integrin alphavbeta6-ERK binding: implications for tumour growth.', Oncogene, vol. 21, pp. 1370 - 1380, http://dx.doi.org/10.1038/sj.onc.1205286
2002
Scott R; McPhillips M; Meldrum C; Fitzgerald PE; Adams K; Spigelman A; du Sart D; Tucker K; Kirk J, 2001, 'Hereditary Nonpolyposis Colorectal Cancer in 95 Families: Differences and Similarities between Mutation-Positive and Mutation-Negative Kindreds', American Journal of Human Genetics, vol. 68, pp. 118 - 127, http://dx.doi.org/10.1086/316942
2001
Jakubowska A; Górski B; Kurzawski G; Debniak T; Hadaczek P; Cybulski C; Kladny J; Oszurek O; Scott RJ; Lubinski J, 2001, 'Optimization of experimental conditions for RNA-based sequencing of MLH1 and MSH2 genes.', Hum Mutat, vol. 17, pp. 52 - 60, http://dx.doi.org/10.1002/1098-1004(2001)17:1<52::AID-HUMU6>3.0.CO;2-E
2001
Jakubowska A; Górski B; Byrski T; Huzarski T; Gronwald J; Menkiszak J; Cybulski C; Debniak T; Hadaczek P; Scott RJ; Lubinski J, 2001, 'Detection of germline mutations in the BRCA1 gene by RNA-based sequencing.', Hum Mutat, vol. 18, pp. 149 - 156, http://dx.doi.org/10.1002/humu.1164
2001
Connor JR; Milward EA; Moalem S; Sampietro M; Boyer P; Percy ME; Vergani C; Scott RJ; Chorney M, 2001, 'Is hemochromatosis a risk factor for Alzheimer's disease?', J Alzheimers Dis, vol. 3, pp. 471 - 477, http://dx.doi.org/10.3233/jad-2001-3506
2001
Scott RJ, 2001, 'Reply to Vasen et al.', The American Journal of Human Genetics, vol. 68, pp. 1534 - 1535, http://dx.doi.org/10.1086/320614
2001
Nasioulas S; Jones IT; St John DJ; Scott RJ; Forrest SM; McKinlay Gardner RJ, 2001, 'Profuse familial adenomatous polyposis with an adenomatous polyposis coli exon 3 mutation.', Fam Cancer, vol. 1, pp. 3 - 7, http://dx.doi.org/10.1023/a:1011570523343
2001
Church JM; Guldenschuh I; Hurlimann R; Muller A; Ammann R; Mullhaupt B; Zala G-F; Flury R; Seelentag W; Roth J; Meyenberger C; Fried M; Hoppeler T; Dobbie Z; Spigelman AD; Scott RJ, 2001, 'Invited commentary', Diseases of the Colon & Rectum, vol. 44, pp. 1097 - 1099, http://dx.doi.org/10.1007/bf02234628
2001
Humar B; Müller H; Scott RJ, 2001, 'Cell cycle dependent DNA break increase in ataxia telangiectasia lymphoblasts after radiation exposure.', Mol Pathol, vol. 54, pp. 347 - 350, http://dx.doi.org/10.1136/mp.54.5.347
2001
Scott RJ; Meldrum C; Crooks R; Spigelman AD; Kirk J; Tucker K; Koorey D; Hunter Family Cancer Service , 2001, 'Familial adenomatous polyposis: More evidence for disease diversity and genetic heterogeneity', Gut, vol. 48, pp. 508 - 514, http://dx.doi.org/10.1136/gut.48.4.508
2001
Ritz MF; Lechner-Scott J; Scott RJ; Fuhr P; Malik N; Erne B; Taylor V; Suter U; Schaeren-Wiemers N; Steck AJ, 2000, 'Characterisation of autoantibodies to peripheral myelin protein 22 in patients with hereditary and acquired neuropathies.', J Neuroimmunol, vol. 104, pp. 155 - 163, http://dx.doi.org/10.1016/s0165-5728(99)00250-7
2000
Ritz M; Lechner‐Scott J; Scott R; Fuhr P; Malik N; Erne B; Taylor V; Suter U; Schaeren‐Wiemers N; Steck ; AJ. , 2000, 'CHARACTERISATION OF AUTOANTIBODIES TO PERIPHERAL MYELIN PROTEIN 22 IN PATIENTS WITH HEREDITARY AND ACQUIRED NEUROPATHIES', Journal of the Peripheral Nervous System, vol. 5, pp. 239 - 239, http://dx.doi.org/10.1111/j.1529-8027.2000.22-13.x
2000
Ritz M; Lechner-Scott J; Scott R; Fuhr P; Malik N; Erne B; Taylor V; Suter U; Schaeren-Wiemers N; Steck ; AJ. , 2000, 'CHARACTERISATION OF AUTOANTIBODIES TO PERIPHERAL MYELIN PROTEIN 22 IN PATIENTS WITH HEREDITARY AND ACQUIRED NEUROPATHIES', Journal of the Peripheral Nervous System, vol. 5, pp. 239 - 239, http://dx.doi.org/10.1046/j.1529-8027.2000.00022-13.x
2000
Heinimann K; Scott RJ; Buerstedde JM; Weber W; Siebold K; Attenhofer M; Müller H; Dobbie Z, 1999, 'Influence of selection criteria on mutation detection in patients with hereditary nonpolyposis colorectal cancer.', Cancer, vol. 85, pp. 2512 - 2518, http://dx.doi.org/10.1002/(sici)1097-0142(19990615)85:12<2512::aid-cncr4>3.0.co;2-g
1999
Heinimann K; Scott RJ; Chappuis P; Weber W; Müller H; Dobbie Z; Hutter P, 1999, 'N-acetyltransferase 2 influences cancer prevalence in hMLH1/hMSH2 mutation carriers.', Cancer Res, vol. 59, pp. 3038 - 3040, https://www.ncbi.nlm.nih.gov/pubmed/10397239
1999
Heinimann K; Müllhaupt B; Weber W; Attenhofer M; Scott RJ; Fried M; Martinoli S; Müller H; Dobbie Z, 1998, 'Phenotypic differences in familial adenomatous polyposis based on APC gene mutation status.', Gut, vol. 43, pp. 675 - 679, http://dx.doi.org/10.1136/gut.43.5.675
1998
Lakhani SR; Jacquemier J; Sloane JP; Gusterson BA; Anderson TJ; van de Vijver MJ; Farid LM; Venter D; Antoniou A; Storfer-Isser A; Smyth E; Steel CM; Haites N; Scott RJ; Goldgar D; Neuhausen S; Daly PA; Ormiston W; McManus R; Scherneck S; Ponder BA; Ford D; Peto J; Stoppa-Lyonnet D; Bignon YJ; Struewing JP; Spurr NK; Bishop DT; Klijn JG; Devilee P; Cornelisse CJ; Lasset C; Lenoir G; Barkardottir RB; Egilsson V; Hamann U; Chang-Claude J; Sobol H; Weber B; Stratton MR; Easton DF, 1998, 'Multifactorial analysis of differences between sporadic breast cancers and cancers involving BRCA1 and BRCA2 mutations.', J Natl Cancer Inst, vol. 90, pp. 1138 - 1145, http://dx.doi.org/10.1093/jnci/90.15.1138
1998
Neuhausen SL; Godwin AK; Gershoni-Baruch R; Schubert E; Garber J; Stoppa-Lyonnet D; Olah E; Csokay B; Serova O; Lalloo F; Osorio A; Stratton M; Offit K; Boyd J; Caligo MA; Scott RJ; Schofield A; Teugels E; Schwab M; Cannon-Albright L; Bishop T; Easton D; Benitez J; King MC; Ponder BA; Weber B; Devilee P; Borg A; Narod SA; Goldgar D, 1998, 'Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study.', Am J Hum Genet, vol. 62, pp. 1381 - 1388, http://dx.doi.org/10.1086/301885
1998
Maier D; Zhang Z; Taylor E; Hamou MF; Gratzl O; Van Meir EG; Scott RJ; Merlo A, 1998, 'Somatic deletion mapping on chromosome 10 and sequence analysis of PTEN/MMAC1 point to the 10q25-26 region as the primary target in low-grade and high-grade gliomas.', Oncogene, vol. 16, pp. 3331 - 3335, http://dx.doi.org/10.1038/sj.onc.1201832
1998
Ford D; Easton DF; Stratton M; Narod S; Goldgar D; Devilee P; Bishop DT; Weber B; Lenoir G; Chang-Claude J; Sobol H; Teare MD; Struewing J; Arason A; Scherneck S; Peto J; Rebbeck TR; Tonin P; Neuhausen S; Barkardottir R; Eyfjord J; Lynch H; Ponder BA; Gayther SA; Zelada-Hedman M, 1998, 'Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium.', Am J Hum Genet, vol. 62, pp. 676 - 689, http://dx.doi.org/10.1086/301749
1998
Scott RJ; Taeschner W; Heinimann K; Müller H; Dobbie Z; Morgenthaler S; Hoffmann F; Peterli B; Meyer UA, 1997, 'Association of extracolonic manifestations of familial adenomatous polyposis with acetylation phenotype in a large FAP kindred.', Eur J Hum Genet, vol. 5, pp. 43 - 49, https://www.ncbi.nlm.nih.gov/pubmed/9156320
1997
Hamann U; Häner M; Stosiek U; Bastert G; Scott RJ, 1997, 'Low frequency of BRCA1 germline mutations in 45 German breast/ovarian cancer families.', J Med Genet, vol. 34, pp. 884 - 888, http://dx.doi.org/10.1136/jmg.34.11.884
1997
Heinimann K; Müller H; Weber W; Scott RJ, 1997, 'Disease expression in Swiss hereditary non-polyposis colorectal cancer (HNPCC) kindreds.', Int J Cancer, vol. 74, pp. 281 - 285, http://dx.doi.org/10.1002/(sici)1097-0215(19970620)74:3<281::aid-ijc8>3.0.co;2-v
1997
Hamann U; Brauch H; Garvin AM; Bastert G; Scott RJ, 1997, 'German family study on hereditary breast and/or ovarian cancer: germline mutation analysis of the BRCA1 gene.', Genes Chromosomes Cancer, vol. 18, pp. 126 - 132, https://www.ncbi.nlm.nih.gov/pubmed/9115962
1997
Maier D; Comparone D; Taylor E; Zhang Z; Gratzl O; Van Meir EG; Scott RJ; Merlo A, 1997, 'New deletion in low-grade oligodendroglioma at the glioblastoma suppressor locus on chromosome 10q25-26.', Oncogene, vol. 15, pp. 997 - 1000, http://dx.doi.org/10.1038/sj.onc.1201209
1997
Garvin AM; Eppenberger U; Müller H; Eppenberger-Castori S; Scott RJ, 1997, 'BRCA1 mutations found in archived early onset breast tumours.', Eur J Cancer, vol. 33, pp. 683 - 686, http://dx.doi.org/10.1016/s0959-8049(96)00499-6
1997
Scott RJ, 1997, 'DNA Mismatch Repair and Hereditary Nonpolyposis Colorectal Cancer', Oncology Research and Treatment, vol. 20, pp. 42 - 47, http://dx.doi.org/10.1159/000218895
1997
Dobbie Z; Heinimann K; Bishop DT; Müller H; Scott RJ, 1997, 'Identification of a modifier gene locus on chromosome 1p35-36 in familial adenomatous polyposis.', Hum Genet, vol. 99, pp. 653 - 657, http://dx.doi.org/10.1007/s004390050423
1997
Garvin AM; Attenhofer-Haner M; Scott RJ, 1997, 'BRCA1 and BRCA2 mutation analysis in 86 early onset breast/ovarian cancer patients.', J Med Genet, vol. 34, pp. 990 - 995, http://dx.doi.org/10.1136/jmg.34.12.990
1997
Lechner-Scott J; Steck AJ; Scott RJ, 1997, '[Genetic studies in neurology].', Schweiz Med Wochenschr, vol. 127, pp. 1141 - 1153, https://www.ncbi.nlm.nih.gov/pubmed/9312837
1997
Scott RJ, 1997, 'Cancer genes: Functional aspects', European Journal of Cancer, vol. 33, pp. 1706 - 1707, http://dx.doi.org/10.1016/s0959-8049(97)00259-1
1997
Shattuck-Eidens D, 1997, 'BRCA1 Sequence Analysis in Women at High Risk for Susceptibility Mutations', JAMA, vol. 278, pp. 1242 - 1242, http://dx.doi.org/10.1001/jama.1997.03550150046034
1997
Humar B; Müller H; Scott RJ, 1997, 'Elevated frequency of p53-independent apoptosis after irradiation increases levels of DNA breaks in ataxia telangiectasia lymphoblasts.', Int J Radiat Biol, vol. 72, pp. 257 - 269, http://dx.doi.org/10.1080/095530097143257
1997
Dobbie Z; Spycher M; Mary JL; Häner M; Guldenschuh I; Hürliman R; Amman R; Roth J; Müller H; Scott RJ, 1996, 'Correlation between the development of extracolonic manifestations in FAP patients and mutations beyond codon 1403 in the APC gene.', J Med Genet, vol. 33, pp. 274 - 280, http://dx.doi.org/10.1136/jmg.33.4.274
1996
Merlo A; Rochlitz C; Scott R, 1996, 'Survival of patients with Turcot's syndrome and glioblastoma.', N Engl J Med, vol. 334, pp. 736 - 737, http://dx.doi.org/10.1056/NEJM199603143341118
1996
Garvin AM; Spycher M; Häner M; Torhorst J; Müller H; Herrmann R; Rochlitz C; Weber W; Scott RJ, 1996, 'BRCA1 mutations in a selected series of breast/ovarian cancer patients.', J Med Genet, vol. 33, pp. 721 - 725, http://dx.doi.org/10.1136/jmg.33.9.721
1996
Dobbie Z; Müller H; Scott RJ, 1996, 'Secretory phospholipase A2 does not appear to be associated with phenotypic variation in familial adenomatous polyposis.', Hum Genet, vol. 98, pp. 386 - 390, http://dx.doi.org/10.1007/s004390050226
1996
Scott RJ; Froggatt NJ; Trembath RC; Evans DG; Hodgson SV; Maher ER, 1996, 'Familial infiltrative fibromatosis (desmoid tumours) (MIM135290) caused by a recurrent 3' APC gene mutation.', Hum Mol Genet, vol. 5, pp. 1921 - 1924, http://dx.doi.org/10.1093/hmg/5.12.1921
1996
Scott RJ; van der Luijt R; Spycher M; Mary JL; Muller A; Hoppeler T; Haner M; Muller H; Martinoli S; Brazzola PL, 1996, 'Novel germline APC gene mutation in a large familial adenomatous polyposis kindred displaying variable phenotypes.', Gut, vol. 38, pp. 794, https://www.ncbi.nlm.nih.gov/pubmed/8707134
1996
GARVIN AM; HANER M; MULLER H; WEBER W; TORHORST J; SCOTT RJ, 1996, 'BRCA1 AND BRCA2 MUTATION DETECTION IN A SELECTED SERIES OF BREAST CANCER PATIENTS', European Journal of Cancer Prevention, vol. 5, pp. 101 - 101, http://dx.doi.org/10.1097/00008469-199612002-00016
1996
van der Luijt RB; Meera Khan P; Vasen HF; Breukel C; Tops CM; Scott RJ; Fodde R, 1996, 'Germline mutations in the 3' part of APC exon 15 do not result in truncated proteins and are associated with attenuated adenomatous polyposis coli.', Hum Genet, vol. 98, pp. 727 - 734, http://dx.doi.org/10.1007/s004390050293
1996
Hutter P; Couturier A; Scott RJ; Alday P; Delozier-Blanchet C; Cachat F; Antonarakis SE; Joris F; Gaudin M; D'Amato L; Buerstedde JM, 1996, 'Complex genetic predisposition to cancer in an extended HNPCC family with an ancestral hMLH1 mutation.', J Med Genet, vol. 33, pp. 636 - 640, http://dx.doi.org/10.1136/jmg.33.8.636
1996
Garvin AM; Mueller H; Eppenberger-Castori S; Eppenberger UR; Scott RJ, 1996, 'Informed consent and BRCA1 mutation detection in archived breast tumor specimens.', Lancet, vol. 347, pp. 1189, http://dx.doi.org/10.1016/s0140-6736(96)90647-9
1996
Scott RJ; van der Luijt R; Spycher M; Mary JL; Müller A; Hoppeler T; Haner M; Müller H; Martinoli S; Brazzola PL, 1995, 'Novel germline APC gene mutation in a large familial adenomatous polyposis kindred displaying variable phenotypes.', Gut, vol. 36, pp. 731 - 736, http://dx.doi.org/10.1136/gut.36.5.731
1995
Buerstedde JM; Alday P; Torhorst J; Weber W; Müller H; Scott R, 1995, 'Detection of new mutations in six out of 10 Swiss HNPCC families by genomic sequencing of the hMSH2 and hMLH1 genes.', J Med Genet, vol. 32, pp. 909 - 912, http://dx.doi.org/10.1136/jmg.32.11.909
1995
Lechner-Scott JS; Scott RJ; Steck AJ; Kappos L, 1995, '[Hereditary motor and sensory neuropathies. Clinical and molecular genetic aspects].', Schweiz Arch Neurol Psychiatr (1985), vol. 146, pp. 157 - 167, https://www.ncbi.nlm.nih.gov/pubmed/8533057
1995
Mary JL; Bishop T; Kolodner R; Lipford JR; Kane M; Weber W; Torhorst J; Müller H; Spycher M; Scott RJ, 1994, 'Mutational analysis of the hMSH2 gene reveals a three base pair deletion in a family predisposed to colorectal cancer development.', Hum Mol Genet, vol. 3, pp. 2067 - 2069, https://www.ncbi.nlm.nih.gov/pubmed/7874129
1994
Rey JP; Scott R; Müller H, 1994, 'Apoptosis is not involved in the hypersensitivity of Fanconi anemia cells to mitomycin C.', Cancer Genet Cytogenet, vol. 75, pp. 67 - 71, http://dx.doi.org/10.1016/0165-4608(94)90218-6
1994
Müller H; Scott RJ, 1994, 'How common is hereditary cancer?', Ann Med, vol. 26, pp. 173 - 175, http://dx.doi.org/10.3109/07853899409147886
1994
Müller H; Scott R; Weber W; Meier R, 1994, 'Colorectal cancer: lessons for genetic counselling and care for families.', Clin Genet, vol. 46, pp. 106 - 114, http://dx.doi.org/10.1111/j.1399-0004.1994.tb04212.x
1994
Dobbie Z; Spycher M; Hürliman R; Ammann R; Ammann T; Roth J; Müller A; Müller H; Scott RJ, 1994, 'Mutational analysis of the first 14 exons of the adenomatous polyposis coli (APC) gene.', Eur J Cancer, vol. 30A, pp. 1709 - 1713, http://dx.doi.org/10.1016/0959-8049(94)00294-f
1994
Vermeulen W; Scott RJ; Rodgers S; Müller HJ; Cole J; Arlett CF; Kleijer WJ; Bootsma D; Hoeijmakers JH; Weeda G, 1994, 'Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3.', Am J Hum Genet, vol. 54, pp. 191 - 200, https://www.ncbi.nlm.nih.gov/pubmed/8304337
1994
Scott RJ; Müller H, 1993, 'Familial and genetic aspects of colorectal carcinogenesis.', Eur J Cancer, vol. 29A, pp. 2163 - 2167, http://dx.doi.org/10.1016/0959-8049(93)90056-l
1993
Scott RJ; Krummenacher F; Mary JL; Weber W; Spycher M; Müller H, 1993, '[Hereditary p53 mutation in a patient with multiple tumors: significance for genetic counseling].', Schweiz Med Wochenschr, vol. 123, pp. 1287 - 1292, https://www.ncbi.nlm.nih.gov/pubmed/8393584
1993
Scott RJ; Itin P; Kleijer WJ; Kolb K; Arlett C; Muller H, 1993, 'Xeroderma pigmentosum-Cockayne syndrome complex in two patients: absence of skin tumors despite severe deficiency of DNA excision repair.', J Am Acad Dermatol, vol. 29, pp. 883 - 889, http://dx.doi.org/10.1016/0190-9622(93)70263-s
1993
Rey JP; Scott R; Müller H, 1993, 'Induction and removal of interstrand crosslinks in the ribosomal RNA genes of lymphoblastoid cell lines from patients with Fanconi anemia.', Mutat Res, vol. 289, pp. 171 - 180, http://dx.doi.org/10.1016/0027-5107(93)90067-p
1993
Müller H; Scott R, 1992, 'Hereditary conditions in which the loss of heterozygosity may be important.', Mutat Res, vol. 284, pp. 15 - 24, http://dx.doi.org/10.1016/0027-5107(92)90021-s
1992
Scott R, 1992, 'IL-2 Approval Recommended by FDA Panel', JNCI Journal of the National Cancer Institute, vol. 84, pp. 226 - 227, http://dx.doi.org/10.1093/jnci/84.4.226-a
1992
Scott R, 1992, 'Dermatologists warn nation of increased skin cancer risk.', J Natl Cancer Inst, vol. 84, pp. 1696, http://dx.doi.org/10.1093/jnci/84.22.1696
1992
Müller H; Mosimann S; Gebhardt M; Scott R; Spycher M; Weber W, 1992, '[Tumor diseases in families of 600 breast cancer patients with special reference to familial adenocarcinomatosis and the Li-Fraumeni-/SBLA syndrome].', Helv Chir Acta, vol. 59, pp. 239 - 245, https://www.ncbi.nlm.nih.gov/pubmed/1526835
1992
Scott R, 1991, 'Commission urges stronger leadership against AIDS.', J Natl Cancer Inst, vol. 83, pp. 1449, http://dx.doi.org/10.1093/jnci/83.20.1449
1991
Scott RJ; Hall PA; Haldane JS; van Noorden S; Price Y; Lane DP; Wright NA, 1991, 'A comparison of immunohistochemical markers of cell proliferation with experimentally determined growth fraction.', J Pathol, vol. 165, pp. 173 - 178, http://dx.doi.org/10.1002/path.1711650213
1991
Scott RJ; English V; Noguchi T; Tanaka T; Yeoh GC, 1988, 'Pyruvate kinase isoenzyme transitions in cultures of fetal rat hepatocytes.', Cell Differ Dev, vol. 25, pp. 109 - 118, http://dx.doi.org/10.1016/0922-3371(88)90004-4
1988
Scott R; Yeoh GC, 1984, 'A requirement for DNA synthesis in foetal hepatocyte differentiation. Effect of cytosine arabinoside on the appearance of the liver isoenzyme of pyruvate kinase.', Differentiation, vol. 28, pp. 49 - 52, http://dx.doi.org/10.1111/j.1432-0436.1984.tb00265.x
1984
Scott RJ; Yeoh GC, 1983, 'Appearance of the liver form of pyruvate kinase in differentiating cultured foetal hepatocytes.', Differentiation, vol. 25, pp. 64 - 69, http://dx.doi.org/10.1111/j.1432-0436.1984.tb01339.x
1983
Reports
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Working Papers
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Scott RJ, 2016, Theoretical foundations of department chief executive performance appraisals, http://dx.doi.org10.13140/RG.2.1.4702.1049
2016
Scott RJ, 2016, The performance relationship between department chief executives and the State Services Commission in New Zealand., http://dx.doi.org10.13140/RG.2.1.4299.4162/1
2016
Scott RJ, 2016, Case studies in collaborating for better public services, http://dx.doi.orghttp://10.0.51.84/RG.2.1.3232.8081
2016
Scott RJ, 2016, Collective impact in the Public Sector: the New Zealand Results approach, http://dx.doi.org10.13140/RG.2.1.2839.5929
2016
Other
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Fazekas-Lavu M; Parker A; Spigelman AD; Scott RJ; Epstein RJ; Jensen M; Samaras K, 2017, Thyroid cancer in a patient with lynch syndrome – case report and literature review, http://dx.doi.org/10.2147/TCRM.S121812
2017
Organisational units
lensSchool of Business
lensPublic Service Research Group
Sub Theme
lensPublic Service Management