De novo mutations in the gene encoding the synaptic scaffolding protein <i>SHANK3</i> in patients ascertained for schizophreniaJulie Gauthier, Yanlian Yang, Nathalie Champagne et al.|Proceedings of the National Academy of Sciences|2010Cited by 380
Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophreniaJulie Gauthier, Guy A. Rouleau, Tabrez J. Siddiqui et al.|Human Genetics|2011Cited by 284
Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human NeuronsScott C. Bell, Philippe M. Campeau, Anne Lortie et al.|The American Journal of Human Genetics|2019Cited by 91
A de novo frameshift mutation in chromodomain helicase DNA‐binding domain 8 (CHD8): A case report and literature reviewNancy D. Merner, Carl Ernst, Baudouin Forgeot d’Arc et al.|American Journal of Medical Genetics Part A|2016Cited by 46