Mutations in <i>SYNGAP1</i> in Autosomal Nonsyndromic Mental RetardationFadi F. Hamdan, Jacques L. Michaud, Julie Gauthier et al.|New England Journal of Medicine|2009Cited by 352
Excess of De Novo Deleterious Mutations in Genes Associated with Glutamatergic Systems in Nonsyndromic Intellectual DisabilityFadi F. Hamdan, Jacques L. Michaud, Sylvia Dobrzeniecka et al.|The American Journal of Human Genetics|2011Cited by 352
De novo <i>STXBP1</i> mutations in mental retardation and nonsyndromic epilepsyFadi F. Hamdan, Jacques L. Michaud, Amélie Piton et al.|Annals of Neurology|2009Cited by 148
Intellectual disability without epilepsy associated with STXBP1 disruptionFadi F. Hamdan, Jacques L. Michaud, Julie Gauthier et al.|European Journal of Human Genetics|2011Cited by 97