학술논문
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
Document Type
Artikel
Author
Fu, JM; Satterstrom, FK; Peng, MS; Brand, H; Collins, RL; Dong, S; Wamsley, B; Klei, L; Wang, L; Hao, SP; Stevens, CR; Cusick, C; Babadi, M; Banks, E; Collins, B; Dodge, S; Gabriel, SB; Gauthier, L; Lee, SK; Liang, L; Ljungdahl, A; Mahjani, B; Sloofman, L; Smirnov, AN; Barbosa, M; Betancur, C; Brusco, A; Chung, BHY; Cook, EH; Cuccaro, ML; Domenici, E; Ferrero, GB; Gargus, JJ; Herman, GE; Hertz-Picciotto, I; Maciel, P; Manoach, DS; Passos-Bueno, MR; Persico, AM; Renieri, A; Sutcliffe, JS; Tassone, F; Trabetti, E; Campos, G; Cardaropoli, S; Carli, D; Chan, MCY; Fallerini, C; Giorgio, E; Girardi, AC; Hansen-Kiss, E; Lee, SL; Lintas, C; Ludena, Y; Nguyen, R; Pavinato, L; Pericak-Vance, M; Pessah, IN; Schmidt, RJ; Smith, M; Costa, CIS; Trajkova, S; Wang, JYT; Yu, MHC; Cutler, DJ; De Rubeis, S; Buxbaum, JD; Daly, MJ; Devlin, B; Roeder, K; Sanders, SJ; Talkowski, ME
Source
Nature genetics. 54(9):1320
Subject
Language
English
English
English
ISSN
1546-1718