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Simon L Girard

Showing results (11-20 of 39) with videos related to

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Behavioral and Brain Functions : BBF|February 22, 2013
Investigation of rare variants in LRP1, KPNA1, ALS2CL and ZNF480 genes in schizophrenia patients reflects genetic heterogeneity of the diseaseLoubna Jouan, Simon L Girard, Sylvia Dobrzeniecka, et al.
Annals of Clinical and Translational Neurology|June 9, 2022
Assessment of burden and segregation profiles of CNVs in patients with epilepsyClaudia Moreau, Frédérique Tremblay, Stefan Wolking, et al.
Neurology. Genetics|April 28, 2020
Polygenic risk scores of several subtypes of epilepsies in a founder populationClaudia Moreau, Rose-Marie Rébillard, Stefan Wolking, et al.
Parkinsonism & Related Disorders|May 16, 2019
Genome-wide estimates of heritability and genetic correlations in essential tremorMonica Diez-Fairen, Sara Bandres-Ciga, Gabrielle Houle, et al.
Plos Genetics|October 16, 2025
Rare diseases load through the study of a regional populationÉlisa Michel, Claudia Moreau, Laurence Gagnon, et al.
Annals of Neurology|June 29, 2011
Restless legs syndrome-associated MEIS1 risk variant influences iron homeostasisHélène Catoire, Patrick A Dion, Lan Xiong, et al.
Plos One|June 4, 2015
Mutation burden of rare variants in schizophrenia candidate genesSimon L Girard, Patrick A Dion, Cynthia V Bourassa, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 24, 2008
Autosomal-dominant locus for Restless Legs Syndrome in French-Canadians on chromosome 16p12.1Anastasia Levchenko, Jacques-Yves Montplaisir, Géraldine Asselin, et al.
European Journal of Human Genetics : EJHG|October 29, 2015
De novo variants in sporadic cases of childhood onset schizophreniaAmirthagowri Ambalavanan, Simon L Girard, Kwangmi Ahn, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 1, 2018
Exome sequencing of sporadic childhood-onset schizophrenia suggests the contribution of X-linked genes in malesAmirthagowri Ambalavanan, Boris Chaumette, Sirui Zhou, et al.
Pageof 4

Showing results (11-20 of 39) with videos related to

Sort By:
Pageof 4
Behavioral and Brain Functions : BBF|February 22, 2013
Investigation of rare variants in LRP1, KPNA1, ALS2CL and ZNF480 genes in schizophrenia patients reflects genetic heterogeneity of the diseaseLoubna Jouan, Simon L Girard, Sylvia Dobrzeniecka, et al.
Annals of Clinical and Translational Neurology|June 9, 2022
Assessment of burden and segregation profiles of CNVs in patients with epilepsyClaudia Moreau, Frédérique Tremblay, Stefan Wolking, et al.
Neurology. Genetics|April 28, 2020
Polygenic risk scores of several subtypes of epilepsies in a founder populationClaudia Moreau, Rose-Marie Rébillard, Stefan Wolking, et al.
Parkinsonism & Related Disorders|May 16, 2019
Genome-wide estimates of heritability and genetic correlations in essential tremorMonica Diez-Fairen, Sara Bandres-Ciga, Gabrielle Houle, et al.
Plos Genetics|October 16, 2025
Rare diseases load through the study of a regional populationÉlisa Michel, Claudia Moreau, Laurence Gagnon, et al.
Annals of Neurology|June 29, 2011
Restless legs syndrome-associated MEIS1 risk variant influences iron homeostasisHélène Catoire, Patrick A Dion, Lan Xiong, et al.
Plos One|June 4, 2015
Mutation burden of rare variants in schizophrenia candidate genesSimon L Girard, Patrick A Dion, Cynthia V Bourassa, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 24, 2008
Autosomal-dominant locus for Restless Legs Syndrome in French-Canadians on chromosome 16p12.1Anastasia Levchenko, Jacques-Yves Montplaisir, Géraldine Asselin, et al.
European Journal of Human Genetics : EJHG|October 29, 2015
De novo variants in sporadic cases of childhood onset schizophreniaAmirthagowri Ambalavanan, Simon L Girard, Kwangmi Ahn, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 1, 2018
Exome sequencing of sporadic childhood-onset schizophrenia suggests the contribution of X-linked genes in malesAmirthagowri Ambalavanan, Boris Chaumette, Sirui Zhou, et al.
Pageof 4