An X chromosome-wide association study in autism families identifies <it>TBL1X </it>as a novel autism spectrum disorder candidate gene in males

by Chung Ren-Hua, Ma Deqiong, Wang Kai, Hedges Dale J, Jaworski James M, Gilbert John R, Cuccaro Michael L, Wright Harry H, Abramson Ruth K, Konidari Ioanna, Whitehead Patrice L, Schellenberg Gerard D, Hakonarson Hakon, Haines Jonathan L, Pericak-Vance Margaret A, Martin Eden R
Published 2011-11-01

Genomic and epigenetic evidence for oxytocin receptor deficiency in autism

by Worley Gordon, Langford Cordelia F, Ellis Peter, Wright Harry H, Abramson Ruth K, Lintas Carla, Markunas Christina A, Biscocho Dhani, Johnson Jessica, Towers Aaron J, Connelly Jessica J, Gregory Simon G, Delong G Robert, Murphy Susan K, Cuccaro Michael L, Persico Antonello, Pericak-Vance Margaret A
Published 2009-10-01