Schizophrenia-risk variant rs6994992 in the neuregulin-1 gene on brain developmental trajectories in typically developing children

por Douet, V, Chang, L, Pritchett, A, Lee, K, Keating, B, Bartsch, H, Jernigan, T L, Dale, A, Akshoomoff, N, Murray, S, Bloss, C, Kennedy, D N, Amaral, D, Gruen, J, Kaufmann, W E, Casey, B J, Sowell, E, Ernst, T
Publicado 2014

Genome-wide association study of shared components of reading disability and language impairment

por Eicher, J D, Powers, N R, Miller, L L, Akshoomoff, N, Amaral, D G, Bloss, C S, Libiger, O, Schork, N J, Darst, B F, Casey, B J, Chang, L, Ernst, T, Frazier, J, Kaufmann, W E, Keating, B, Kenet, T, Kennedy, D, Mostofsky, S, Murray, S S, Sowell, E R, Bartsch, H, Kuperman, J M, Brown, T T, Hagler, D J, Dale, A M, Jernigan, T L, St Pourcain, B, Davey Smith, G, Ring, S M, Gruen, J R
Publicado 2013

Evidence for the role of EPHX2 gene variants in anorexia nervosa

por Scott-Van Zeeland, A A, Bloss, C S, Tewhey, R, Bansal, V, Torkamani, A, Libiger, O, Duvvuri, V, Wineinger, N, Galvez, L, Darst, B F, Smith, E N, Carson, A, Pham, P, Phillips, T, Villarasa, N, Tisch, R, Zhang, G, Levy, S, Murray, S, Chen, W, Srinivasan, S, Berenson, G, Brandt, H, Crawford, S, Crow, S, Fichter, M M, Halmi, K A, Johnson, C, Kaplan, A S, La Via, M, Mitchell, J E, Strober, M, Rotondo, A, Treasure, J, Woodside, D B, Bulik, C M, Keel, P, Klump, K L, Lilenfeld, L, Plotnicov, K, Topol, E J, Shih, P B, Magistretti, P, Bergen, A W, Berrettini, W, Kaye, W, Schork, N J
Publicado 2014