Fadi F. Hamdan - Concepedia

Author

Fadi F. Hamdan

Also Known As

F F Hamdan, F. F. Hamdan, F.F. Hamdan, F.Q. HAMDAN, FADI F. HAMDAN, Fadi F Hamdan, Fadi F. Hamdan, Fadi Hamdan, Fadi. F. Hamdan, Fadi F. Hamdan

115

Publications

Citations

H-Index

Concepts

All Affiliations

Université de Montréal Centre Hospitalier Universitaire Sainte-Justine McGill University Montreal Neurological Institute and Hospital Centre Hospitalier de l’Université de Montréal

About

Fadi F. Hamdan is an author at Université de Montréal specializing in medicine, genetics, and neurogenetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	34	39	4.9K
2	Social Sciences	8	8	1.2K
3	Natural Sciences	7	7	322
4	Biochemistry	4	4	500
5	Public Health	2	2	120

Fadi F. Hamdan

Publications

8.2K

Citations

H-Index

Page 1

	Year	Citations
De Novo Mutations in Moderate or Severe Intellectual Disability Fadi F. Hamdan, Myriam Srour, José‐Mario Capo‐Chichi, PLoS Genetics Genetic DiseasesMendelian DisorderGenetic DisorderMedicineGenetics	2014	411
De novo mutations in the gene encoding the synaptic scaffolding protein <i>SHANK3</i> in patients ascertained for schizophrenia Julie Gauthier, Nathalie Champagne, Ronald G. Lafrenière, Proceedings of the National Academy of Sciences	2010	379
Excess of De Novo Deleterious Mutations in Genes Associated with Glutamatergic Systems in Nonsyndromic Intellectual Disability Fadi F. Hamdan, Julie Gauthier, Yoichi Araki, The American Journal of Human Genetics Genes AssociatedGenetic DisorderGeneticsPsychiatric GeneticsNonsyndromic Intellectual Disability	2011	348
Mutations in <i>SYNGAP1</i> in Autosomal Nonsyndromic Mental Retardation Fadi F. Hamdan, Julie Gauthier, Dan Spiegelman, New England Journal of Medicine	2009	342
Novel de novo SHANK3 mutation in autistic patients Julie Gauthier, Dan Spiegelman, Amélie Piton, American Journal of Medical Genetics Part B Neuropsychiatric Genetics	2008	320
SHANK1 Deletions in Males with Autism Spectrum Disorder Daisuke Sato, Anath C. Lionel, Claire S. Leblond, The American Journal of Human Genetics Shank1 DeletionsSyndromic AutismPsychiatryAutism	2012	320
Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia Amélie Piton, J Gauthier, Fadi F. Hamdan, Molecular Psychiatry Systematic ResequencingX-chromosome Synaptic GenesGenetic DisorderGeneticsPsychiatric Genetics	2010	315
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, Fadi F. Hamdan, Cell Metabolism Molecular PharmacologyInsulin SignalingSignal TransductionMolecular PhysiologyBiochemistry	2006	282
Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia Julie Gauthier, Tabrez J. Siddiqui, Huashan Peng, Human Genetics Autism Spectrum DisordersSyndromic AutismGeneticsGenetic DisorderPsychiatric Genetics	2011	275
Mutations in<i>SYNGAP1</i>Cause Intellectual Disability, Autism, and a Specific Form of Epilepsy by Inducing Haploinsufficiency Martin H. Berryer, Fadi F. Hamdan, Laura L. Klitten, Human Mutation GeneticsPathologyDisease-causing Point MutationsDisease Gene IdentificationSynaptic Signaling	2012	270

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