Individual common variants exert weak effects on the risk for autism spectrum disorderspi.
Anney R; Klei L; Pinto D; Almeida J; Bacchelli E; Baird G; Bolshakova N; Bölte S; Bolton PF; Bourgeron T; Brennan S; Brian J; Casey J; Conroy J; Correia C; Corsello C; Crawford EL; de Jonge M; Delorme R; Duketis E; Duque F; Estes A; Farrar P; Fernandez BA; Folstein SE; Fombonne E; Gilbert J; Gillberg C; Glessner JT; Green A; Green J; Guter SJ; Heron EA; Holt R; Howe JL; Hughes G; Hus V; Igliozzi R; Jacob S; Kenny GP; Kim C; Kolevzon A; Kustanovich V; Lajonchere CM; Lamb JA; Law-Smith M; Leboyer M; Le Couteur A; Leventhal BL; Liu XQ; Lombard F; Lord C; Lotspeich L; Lund SC; Magalhaes TR; Mantoulan C; McDougle CJ; Melhem NM; Merikangas A; Minshew NJ; Mirza GK; Munson J; Noakes C; Nygren G; Papanikolaou K; Pagnamenta AT; Parrini B; Paton T; Pickles A; Posey DJ; Poustka F; Ragoussis J; Regan R; Roberts W; Roeder K; Roge B; Rutter ML; Schlitt S; Shah N; Sheffield VC; Soorya L; Sousa I; Stoppioni V; Sykes N; Tancredi R; Thompson AP; Thomson S; Tryfon A; Tsiantis J; Van Engeland H; Vincent JB; Volkmar F; Vorstman JA; Wallace S; Wing K; Wittemeyer K; Wood S; Zurawiecki D; Zwaigenbaum L; Bailey AJ; Battaglia A; Cantor RM; Coon H; Cuccaro ML; Dawson G; Ennis S; Freitag CM; Geschwind DH; Haines JL; Klauck SM; McMahon WM; Maestrini E; Miller J; Monaco AP; Nelson SF; Nurnberger JI Jr; Oliveira G; Parr JR; Pericak-Vance MA; Piven J; Schellenberg GD; Scherer SW; Vicente AM; Wassink TH; Wijsman EM; Betancur C; Buxbaum JD; Cook EH; Gallagher L; Gill M; Hallmayer J; Paterson AD; Sutcliffe JS; Szatmari P; Vieland VJ; Hakonarson H; Devlin B; Human Molecular Genetics, 2012, vol. 21, issue 21, p 4781, ISSN 14602083. ISBN 14602083.

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