Myriam Srour

De Novo Mutations in Moderate or Severe Intellectual Disability

Fadi F. Hamdan, Myriam Srour, José‐Mario Capo‐Chichi et al. · PLoS Genetics · 2014 · 411 citations · Full text

Genetic Diseases, Mendelian Disorder, Genetic Disorder +13

Excess of De Novo Deleterious Mutations in Genes Associated with Glutamatergic Systems in Nonsyndromic Intellectual Disability

Fadi F. Hamdan, Julie Gauthier, Yoichi Araki et al. · The American Journal of Human Genetics · 2011 · 348 citations

Genes Associated, Genetic Disorder, Genetics +8

Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development

Silvia Cappello, Mary Jane Gray, Caroline Badouel et al. · Nature Genetics · 2013 · 276 citations

Molecular Neuroscience, Developmental Biology, Signaling Pathway +7

Screening for Developmental Delay in the Setting of a Community Pediatric Clinic: A Prospective Assessment of Parent-Report Questionnaires

David Rydz, Myriam Srour, Maryam Oskoui et al. · PEDIATRICS · 2006 · 254 citations

KIF1A, an Axonal Transporter of Synaptic Vesicles, Is Mutated in Hereditary Sensory and Autonomic Neuropathy Type 2

Jean‐Baptiste Rivière, Siriram Ramalingam, Valérie Lavastre et al. · The American Journal of Human Genetics · 2011 · 203 citations · Full text

Synaptic Plasticity, Neuromuscular Junction, Molecular Neuroscience +15