Ridha Joober - Concepedia

Author

Ridha Joober

Also Known As

F Fathalli, Joober Ridha, Joober, Ridha, Patricia Boksa, R JOOBER, R Joober, R. Joober, RIDHA JOOBER, Ridha Joober, S2D team

584

Publications

18.3K

Citations

H-Index

199

Concepts

All Affiliations

McGill University Douglas Mental Health University Institute Université de Montréal Douglas College Montreal Neurological Institute and Hospital

About

Ridha Joober is an author at McGill University specializing in medicine, psychiatry, and social sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	48	132	7.9K
2	Health Sciences	8	8	523
3	Education	2	2	104
4	Arts	1	1	28
5	Engineering	1	1	80

Ridha Joober

289

Publications

15.2K

Citations

H-Index

Page 1

	Year	Citations
Increased exonic de novo mutation rate in individuals with schizophrenia Simon Girard, Julie Gauthier, Anne Noreau, Nature Genetics Risk PredictionPsychiatryGenetic DisorderGeneticsPsychiatric Genetics	2011	442
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
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia Clyde Francks, Shinji Maegawa, Juha Laurén, Molecular Psychiatry ChromatinPsychiatryGenetic DisorderGeneticsPsychiatric Genetics	2007	357
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
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
Prediction of Level of Serotonin 2A Receptor Binding by Serotonin Receptor 2A Genetic Variation in Postmortem Brain Samples From Subjects Who Did or Did Not Commit Suicide Gustavo Turecki, Richard Brière, Karen M. Dewar, American Journal of Psychiatry	1999	276
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
Direct Measure of the De Novo Mutation Rate in Autism and Schizophrenia Cohorts Philip Awadalla, Julie Gauthier, Rachel A. Myers, The American Journal of Human Genetics PsychiatrySyndromic AutismGeneticsPsychiatric GeneticsGenetic Epidemiology	2010	248
De Novo Mutations in FOXP1 in Cases with Intellectual Disability, Autism, and Language Impairment Fadi F. Hamdan, Hussein Daoud, Daniel Rochefort, The American Journal of Human Genetics Neurodevelopmental DisordersGenetic DisorderGeneticsFragile X SpectrumLanguage Impairment	2010	233

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