De novo mutations revealed by whole-exome sequencing are strongly associated with autism

Stephan Sanders, Michael T. Murtha(Yale University), Abha R. Gupta(Yale University), John D. Murdoch(Yale University), Melanie J. Raubeson(Yale University), A. Jeremy Willsey(Yale University), A. Gulhan Ercan‐Sencicek(Yale University), Nicholas M. DiLullo(Yale University), Neelroop Parikshak, Jason L. Stein, Michael F. Walker(Yale University), G Ober(Yale University), Nicole A. Teran(Yale University), Youeun Song(Yale University), Paul El-Fishawy(Yale University), Ryan Murtha(Yale University), Murim Choi(Yale University), John D. Overton(Yale University), Robert Bjornson(Yale University), Nicholas Carriero(Yale University), Kyle A. Meyer(Yale University), Kaya Bilgüvar(Yale University), Shrikant Mane(Center for Genomic Science), Nenad Šestan(Yale University), Richard P. Lifton(Yale University), Murat Günel(Center for Human Genetics), Kathryn Roeder(Carnegie Mellon University), Daniel H. Geschwind, Bernie Devlin(University of Pittsburgh), Matthew W. State(Yale University)
Nature
April 3, 2012
Cited by 2,159

Abstract


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