Publication:

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls (2010)

Author(s): Walker M; Isaacs JD; Ferrier IN; Mansfield J; Craddock N; Hurles ME; Cardin N; Pearson RD; Plagnol V; Robson S; Vukcevic D; Barnes C; Conrad DF; Giannoulatou E; Holmes C; Marchini JL; Stirrups K; Tobin MD; Wain LV; Yau C; Aerts J; Ahmad T; Andrews TD; Arbury H; Attwood A; Auton A; Ball SG; Balmforth AJ; Barrett JC; Barroso I; Barton A; Bennett AJ; Bhaskar S; Blaszczyk K; Bowes J; Brand OJ; Braund PS; Bredin F; Breen G; Brown MJ; Bruce IN; Bull J; Burren OS; Burton J; Byrnes J; Caesar S; Clee CM; Coffey AJ; Connell JMC; Cooper JD; Dominiczak AF; Downes K; Drummond HE; Dudakia D; Dunham A; Ebbs B; Eccles D; Edkins S; Edwards C; Elliot A; Emery P; Evans DM; Evans G; Eyre S; Farmer A; Feuk L; Fitzgerald T; Flynn E; Forbes A; Forty L; Franklyn JA; Freathy RM; Gibbs P; Gilbert P; Gokumen O; Gordon-Smith K; Gray E; Green E; Groves CJ; Grozeva D; Gwilliam R; Hall A; Hammond N; Hardy M; Harrison P; Hassanali N; Hebaishi H; Hines S; Hinks A; Hitman GA; Hocking L; Howard E; Howard P; Howson JMM; Hughes D; Hunt S; Jain M; Jewell DP; Johnson T; Jolley JD; Jones IR; Jones LA; Kirov G; Langford CF; Lango-Allen H; Lathrop GM; Lee J; Lee KL; Lees C; Lewis K; Lindgren CM; Maisuria-Armer M; Maller J; Martin P; Massey DCO; McArdle WL; McGuffin P; McLay KE; Mentzer A; Mimmack ML; Morgan AE; Morris AP; Mowat C; Myers S; Newman W; Nimmo ER; O'Donovan MC; Onipinla A; Onyiah I; Ovington NR; Owen MJ; Palin K; Parnell K; Pernet D; Perry JRB; Phillips A; Pinto D; Prescott NJ; Prokopenko I; Quail MA; Rafelt S; Rayner NW; Redon R; Reid DM; Renwick A; Ring SM; Robertson N; Russell E; St Clair D; Sambrook JG; Sanderson JD; Schuilenburg H; Scott CE; Scott R; Seal S; Shaw-Hawkins S; Shields BM; Simmonds MJ; Smyth DJ; Somaskantharajah E; Spanova K; Steer S; Stephens J; Stevens HE; Stone MA; Su Z; Symmons DPM; Thompson JR; Thomson W; Travers ME; Turnbull C; Valsesia A; Walker NM; Wallace C; Warren-Perry M; Watkins NA; Webster J; Weedon MN; Wilson AG; Woodburn M; Wordsworth BP; Young AH; Zeggini E; Carter NP; Frayling TM; Lee C; McVean G; Munroe PB; Palotie A; Sawcer SJ; Scherer SW; Strachan DP; Tyler-Smith C; Brown MA; Burton PR; Caulfield MJ; Compston A; Farrall M; Gough SCL; Hall AS; Hattersley AT; Hill AVS; Mathew CG; Pembrey M; Satsangi J; Stratton MR; Worthington J; Deloukas P; Duncanson A; Kwiatkowski DP; McCarthy MI; Ouwehand WH; Parkes M; Rahman N; Todd JA; Samani NJ; Donnelly P

    Notes: The Wellcome Trust Case Control Consortium

      • Date: 01-04-2010
      • Journal: Nature
      • Volume: 464
      • Issue: 7289
      • Pages: 713-720
      • Publisher: Nature Publishing Group
      • Publication type: Article
      • Bibliographic status: Published

      Keywords: COPY-NUMBER VARIATION LARGE-SCALE SUSCEPTIBILITY POLYMORPHISMS DELETION CCL3L1 SCHIZOPHRENIA DUPLICATIONS HERITABILITY PSORIASIS

      Staff

      Dr John Mansfield
      Senior Lecturer/Consultant