Ronald G. Lafrenière

Author

Also Known As

J.J. Chen, P Drapeau, R G Lafreniere, R G Lafrenière, R Lafrenière, R. G. Lafreniere, R. Lafreniere, R.G. Lafreniere, R.G. Lafrenière, Ronald G Lafrenière

Publications

8.3K

Citations

H-Index

Concepts

All Affiliations

McGill University Université de Montréal Centre Hospitalier de l’Université de Montréal Stanford University Montreal Children's Hospital

About

Ronald G. Lafrenière is an author at McGill University specializing in medicine, genetics, and neurogenetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	24	28	6K
2	Social Sciences	5	5	357
3	Public Health	3	3	246
4	Engineering	2	2	1.3K
5	Natural Sciences	1	1	107

Ronald G. Lafrenière

Publications

7.5K

Citations

H-Index

Page 1

	Year	Citations
A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome Carolyn J. Brown, Andrea Ballabio, James L. Rupert, Nature ChromatinDevelopmental BiologyGenetic DisorderGeneticsInactive X Chromosome	1991	1.5K
The human XIST gene: Analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus Carolyn J. Brown, Brian Hendrich, Jim L. Rupert, Cell ChromatinSystems BiologyEngineeringGeneticsRna Biology	1992	1.3K
Localization of the X inactivation centre on the human X chromosome in Xq13 Carolyn J. Brown, Ronald G. Lafrenière, Vicki E. C. Powers, Nature ChromatinChromosome DynamicsDevelopmental BiologyX Inactivation CentreCytogenetics	1991	382
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
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
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

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