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The New England Journal of Medicine|February 7, 2009
Mutations in SYNGAP1 in autosomal nonsyndromic mental retardationFadi F Hamdan, Julie Gauthier, Dan Spiegelman, et al.
Nature Medicine|September 29, 2020
Neuronal defects in a human cellular model of 22q11.2 deletion syndromeThemasap A Khan, Omer Revah, Aaron Gordon, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 14, 2010
De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophreniaJulie Gauthier, Nathalie Champagne, Ronald G Lafrenière, et al.
Molecular Psychiatry|May 19, 2010
Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophreniaA Piton, J Gauthier, F F Hamdan, et al.
American Journal of Human Genetics|August 28, 2010
Direct measure of the de novo mutation rate in autism and schizophrenia cohortsPhilip Awadalla, Julie Gauthier, Rachel A Myers, et al.
Frontiers in Global Women'S Health|July 22, 2025
Research advances and future directions in female ADHD: the lifelong interplay of hormonal fluctuations with mood, cognition, and diseaseJ J Sandra Kooij, Maxime de Jong, Jessica Agnew-Blais, et al.
Science (New York, N.Y.)|March 29, 2008
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophreniaTom Walsh, Jon M McClellan, Shane E McCarthy, et al.
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