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Fadi F. Hamdan | Researchclopedia

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Fadi F. Hamdan

Centre Hospitalier Universitaire Sainte-Justine

116

Works

9,094

Citations

49

h-index

80

i10-index

Research Topics

Genetics and Neurodevelopmental Disorders Genomics and Rare Diseases Receptor Mechanisms and Signaling

Affiliations

University of Basrah2025–2025

National Institutes of Health2001–2009

Cervantes Institute2025–2025

Baylor College of Medicine2016–2016

Centre Hospitalier Universitaire Sainte-Justine2008–2026

Top Works

High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies

Fadi F. Hamdan,Candace T. Myers,et al.

2017451 citations

Genomic variations and chromosomal abnormalities

Neuropeptides and Animal Physiology

De Novo Mutations in Moderate or Severe Intellectual Disability

Fadi F. Hamdan,Myriam Srour,et al.

2014415 citations

De novo mutations in the gene encoding the synaptic scaffolding protein <i>SHANK3</i> in patients ascertained for schizophrenia

Julie Gauthier,Nathalie Champagne,et al.

2010379 citations

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

Fadi F. Hamdan,Julie Gauthier,et al.

2011349 citations

Mutations in <i>SYNGAP1</i> in Autosomal Nonsyndromic Mental Retardation

Fadi F. Hamdan,Julie Gauthier,et al.

2009346 citations

SHANK1 Deletions in Males with Autism Spectrum Disorder

Daisuke Sato,Anath C. Lionel,et al.

2012322 citations

Novel de novo SHANK3 mutation in autistic patients

Julie Gauthier,Dan Spiegelman,et al.

2008321 citations

Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia

Amélie Piton,J Gauthier,et al.

2010318 citations

A critical role for β cell M3 muscarinic acetylcholine receptors in regulating insulin release and blood glucose homeostasis in vivo

Dinesh Gautam,Sung‐Jun Han,et al.

2006283 citations