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Simon L Girard

Showing results (21-30 of 39) with videos related to

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Plos One|October 11, 2016
Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy IndividualsSimon L Girard, Cynthia V Bourassa, Louis-Philippe Lemieux Perreault, et al.
Human Molecular Genetics|January 8, 2009
MEIS1 intronic risk haplotype associated with restless legs syndrome affects its mRNA and protein expression levelsLan Xiong, Hélène Catoire, Patrick Dion, et al.
Plos Genetics|April 13, 2018
Global characterization of copy number variants in epilepsy patients from whole genome sequencingJean Monlong, Simon L Girard, Caroline Meloche, 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.
Human Molecular Genetics|October 26, 2014
Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosisHannah M Kaneb, Andrew W Folkmann, Véronique V Belzil, et al.
Nature Genetics|July 12, 2011
Increased exonic de novo mutation rate in individuals with schizophreniaSimon L Girard, Julie Gauthier, Anne Noreau, et al.
American Journal of Human Genetics|August 7, 2012
Exome sequencing identifies FUS mutations as a cause of essential tremorNancy D Merner, Simon L Girard, Hélène Catoire, et al.
Neurobiology of Aging|May 2, 2016
The role of the melanoma gene MC1R in Parkinson disease and REM sleep behavior disorderZiv Gan-Or, Noreen Mohsin, Simon L Girard, et al.
Annals of Clinical and Translational Neurology|May 21, 2021
Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsyStefan Wolking, Claudia Moreau, Mark McCormack, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|February 16, 2026
Copy Number Variant Duplications Associated with Essential TremorMiranda Medeiros, Calwing Liao, Allison A Dilliott, et al.
Pageof 4

Showing results (21-30 of 39) with videos related to

Sort By:
Pageof 4
Plos One|October 11, 2016
Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy IndividualsSimon L Girard, Cynthia V Bourassa, Louis-Philippe Lemieux Perreault, et al.
Human Molecular Genetics|January 8, 2009
MEIS1 intronic risk haplotype associated with restless legs syndrome affects its mRNA and protein expression levelsLan Xiong, Hélène Catoire, Patrick Dion, et al.
Plos Genetics|April 13, 2018
Global characterization of copy number variants in epilepsy patients from whole genome sequencingJean Monlong, Simon L Girard, Caroline Meloche, 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.
Human Molecular Genetics|October 26, 2014
Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosisHannah M Kaneb, Andrew W Folkmann, Véronique V Belzil, et al.
Nature Genetics|July 12, 2011
Increased exonic de novo mutation rate in individuals with schizophreniaSimon L Girard, Julie Gauthier, Anne Noreau, et al.
American Journal of Human Genetics|August 7, 2012
Exome sequencing identifies FUS mutations as a cause of essential tremorNancy D Merner, Simon L Girard, Hélène Catoire, et al.
Neurobiology of Aging|May 2, 2016
The role of the melanoma gene MC1R in Parkinson disease and REM sleep behavior disorderZiv Gan-Or, Noreen Mohsin, Simon L Girard, et al.
Annals of Clinical and Translational Neurology|May 21, 2021
Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsyStefan Wolking, Claudia Moreau, Mark McCormack, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|February 16, 2026
Copy Number Variant Duplications Associated with Essential TremorMiranda Medeiros, Calwing Liao, Allison A Dilliott, et al.
Pageof 4