Items where Author is "Cook, EH"

Liu, L and Sabo, A and Neale, BM and Nagaswamy, U and Stevens, C and Lim, E and Bodea, CA and Muzny, D and Reid, JG and Banks, E and Coon, H and DePristo, M and Dinh, H and Fennel, T and Flannick, J and Gabriel, S and Garimella, K and Gross, S and Hawes, A and Lewis, L and Makarov, V and Maguire, J and Newsham, I and Poplin, R and Ripke, S and Shakir, K and Samocha, KE and Wu, Y and Boerwinkle, E and Buxbaum, JD and Cook, EH and Devlin, B and Schellenberg, GD and Sutcliffe, JS and Daly, MJ and Gibbs, RA and Roeder, K (2013) Analysis of Rare, Exonic Variation amongst Subjects with Autism Spectrum Disorders and Population Controls. PLoS Genetics, 9 (4). ISSN 1553-7390

Klei, L and Sanders, SJ and Murtha, MT and Hus, V and Lowe, JK and Willsey, AJ and Moreno-De-Luca, D and Yu, TW and Fombonne, E and Geschwind, D and Grice, DE and Ledbetter, DH and Lord, C and Mane, SM and Martin, CL and Martin, DM and Morrow, EM and Walsh, CA and Melhem, NM and Chaste, P and Sutcliffe, JS and State, MW and Cook, EH and Roeder, K and Devlin, B (2012) Common genetic variants, acting additively, are a major source of risk for autism. Molecular Autism, 3 (1).

Bucan, M and Abrahams, BS and Wang, K and Glessner, JT and Herman, EI and Sonnenblick, LI and Alvarez Retuerto, AI and Imielinski, M and Hadley, D and Bradfield, JP and Kim, C and Gidaya, NB and Lindquist, I and Hutman, T and Sigman, M and Kustanovich, V and Lajonchere, CM and Singleton, A and Kim, J and Wassink, TH and McMahon, WM and Owley, T and Sweeney, JA and Coon, H and Nurnberger, JI and Li, M and Cantor, RM and Minshew, NJ and Sutcliffe, JS and Cook, EH and Dawson, G and Buxbaum, JD and Grant, SFA and Schellenberg, GD and Geschwind, DH and Hakonarson, H (2009) Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes. PLoS Genetics, 5 (6). ISSN 1553-7390