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Simon L Girard

Showing results (31-40 of 39) with videos related to

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The Journal of Clinical Investigation|February 3, 2015
Functional variants of POC5 identified in patients with idiopathic scoliosisShunmoogum A Patten, Patricia Margaritte-Jeannin, Jean-Claude Bernard, et al.
Epilepsia|March 7, 2020
Testing association of rare genetic variants with resistance to three common antiseizure medicationsStefan Wolking, Claudia Moreau, Anne T Nies, et al.
Nature Communications|February 3, 2026
A multi-ancestry genetic reference for the Quebec populationPeyton McClelland, Georgette Femerling, Rose Laflamme, et al.
Medrxiv : the Preprint Server for Health Sciences|June 4, 2025
A multi-ancestry genetic reference for the Quebec populationPeyton McClelland, Georgette Femerling, Rose Laflamme, et al.
JAMA Neurology|January 4, 2022
Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysisCalwing Liao, Charles-Etienne Castonguay, Karl Heilbron, et al.
Brain : a Journal of Neurology|November 1, 2016
Genome-wide association study in essential tremor identifies three new lociStefanie H Müller, Simon L Girard, Franziska Hopfner, et al.
American Journal of Human Genetics|November 4, 2017
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic EncephalopathiesFadi F Hamdan, Candace T Myers, Patrick Cossette, et al.
Plos Genetics|November 9, 2013
Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architectureLea K Davis, Dongmei Yu, Clare L Keenan, et al.
The American Journal of Psychiatry|August 27, 2014
Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCDDongmei Yu, Carol A Mathews, Jeremiah M Scharf, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
The Journal of Clinical Investigation|February 3, 2015
Functional variants of POC5 identified in patients with idiopathic scoliosisShunmoogum A Patten, Patricia Margaritte-Jeannin, Jean-Claude Bernard, et al.
Epilepsia|March 7, 2020
Testing association of rare genetic variants with resistance to three common antiseizure medicationsStefan Wolking, Claudia Moreau, Anne T Nies, et al.
Nature Communications|February 3, 2026
A multi-ancestry genetic reference for the Quebec populationPeyton McClelland, Georgette Femerling, Rose Laflamme, et al.
Medrxiv : the Preprint Server for Health Sciences|June 4, 2025
A multi-ancestry genetic reference for the Quebec populationPeyton McClelland, Georgette Femerling, Rose Laflamme, et al.
JAMA Neurology|January 4, 2022
Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysisCalwing Liao, Charles-Etienne Castonguay, Karl Heilbron, et al.
Brain : a Journal of Neurology|November 1, 2016
Genome-wide association study in essential tremor identifies three new lociStefanie H Müller, Simon L Girard, Franziska Hopfner, et al.
American Journal of Human Genetics|November 4, 2017
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic EncephalopathiesFadi F Hamdan, Candace T Myers, Patrick Cossette, et al.
Plos Genetics|November 9, 2013
Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architectureLea K Davis, Dongmei Yu, Clare L Keenan, et al.
The American Journal of Psychiatry|August 27, 2014
Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCDDongmei Yu, Carol A Mathews, Jeremiah M Scharf, et al.
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