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S LEBLOND

Showing results (51-60 of 94) with videos related to

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Neurobiology of Aging|May 30, 2016
Analysis of DNAJC13 mutations in French-Canadian/French cohort of Parkinson's diseaseJay P Ross, Nicolas Dupre, Yves Dauvilliers, et al.
Molecular Neurobiology|October 14, 2018
Absence of Mutation Enrichment for Genes Phylogenetically Conserved in the Olivocerebellar Motor Circuitry in a Cohort of Canadian Essential Tremor CasesJean-François Schmouth, Gabrielle Houle, Amirthagowri Ambalavanan, et al.
Sleep Medicine|August 24, 2015
Analysis of functional GLO1 variants in the BTBD9 locus and restless legs syndromeZiv Gan-Or, Sirui Zhou, Amirthagowri Ambalavanan, et al.
Communications Biology|September 12, 2019
Social and non-social autism symptoms and trait domains are genetically dissociableVarun Warrier, Roberto Toro, Hyejung Won, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 4, 2017
Teneurin transmembrane protein 4 is not a cause for essential tremor in a Canadian populationGabrielle Houle, Jean-François Schmouth, Claire S Leblond, et al.
Neurobiology of Aging|October 24, 2015
Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosisClaire S Leblond, Ziv Gan-Or, Dan Spiegelman, et al.
Neurology. Genetics|December 26, 2018
No rare deleterious variants from <i>STK32B</i>, <i>PPARGC1A</i>, and <i>CTNNA3</i> are associated with essential tremorGabrielle Houle, Amirthagowri Ambalavanan, Jean-François Schmouth, et al.
Scientific Reports|January 16, 2019
Altered spinogenesis in iPSC-derived cortical neurons from patients with autism carrying de novo SHANK3 mutationsLaura Gouder, Aline Vitrac, Hany Goubran-Botros, et al.
BMC Medical Genetics|December 5, 2013
Heterozygous FA2H mutations in autism spectrum disordersIsabelle Scheid, Anna Maruani, Guillaume Huguet, et al.
NPJ Genomic Medicine|January 25, 2019
Both rare and common genetic variants contribute to autism in the Faroe IslandsClaire S Leblond, Freddy Cliquet, Coralie Carton, et al.
Pageof 10

Showing results (51-60 of 94) with videos related to

Sort By:
Pageof 10
Neurobiology of Aging|May 30, 2016
Analysis of DNAJC13 mutations in French-Canadian/French cohort of Parkinson's diseaseJay P Ross, Nicolas Dupre, Yves Dauvilliers, et al.
Molecular Neurobiology|October 14, 2018
Absence of Mutation Enrichment for Genes Phylogenetically Conserved in the Olivocerebellar Motor Circuitry in a Cohort of Canadian Essential Tremor CasesJean-François Schmouth, Gabrielle Houle, Amirthagowri Ambalavanan, et al.
Sleep Medicine|August 24, 2015
Analysis of functional GLO1 variants in the BTBD9 locus and restless legs syndromeZiv Gan-Or, Sirui Zhou, Amirthagowri Ambalavanan, et al.
Communications Biology|September 12, 2019
Social and non-social autism symptoms and trait domains are genetically dissociableVarun Warrier, Roberto Toro, Hyejung Won, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 4, 2017
Teneurin transmembrane protein 4 is not a cause for essential tremor in a Canadian populationGabrielle Houle, Jean-François Schmouth, Claire S Leblond, et al.
Neurobiology of Aging|October 24, 2015
Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosisClaire S Leblond, Ziv Gan-Or, Dan Spiegelman, et al.
Neurology. Genetics|December 26, 2018
No rare deleterious variants from <i>STK32B</i>, <i>PPARGC1A</i>, and <i>CTNNA3</i> are associated with essential tremorGabrielle Houle, Amirthagowri Ambalavanan, Jean-François Schmouth, et al.
Scientific Reports|January 16, 2019
Altered spinogenesis in iPSC-derived cortical neurons from patients with autism carrying de novo SHANK3 mutationsLaura Gouder, Aline Vitrac, Hany Goubran-Botros, et al.
BMC Medical Genetics|December 5, 2013
Heterozygous FA2H mutations in autism spectrum disordersIsabelle Scheid, Anna Maruani, Guillaume Huguet, et al.
NPJ Genomic Medicine|January 25, 2019
Both rare and common genetic variants contribute to autism in the Faroe IslandsClaire S Leblond, Freddy Cliquet, Coralie Carton, et al.
Pageof 10