Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Patrick A Dion

Showing results (71-80 of 188) with videos related to

Pageof 19
Sort By:
Proceedings of the National Academy of Sciences of the United States of America|July 24, 2019
Genetic architecture and adaptations of Nunavik InuitSirui Zhou, Pingxing Xie, Amélie Quoibion, et al.
Neurobiology of Aging|February 25, 2012
Analysis of the SORT1 gene in familial amyotrophic lateral sclerosisVéronique V Belzil, Catherine André-Guimont, Marie-Renée Atallah, et al.
Neurogenetics|May 10, 2020
Oligogenicity, C9orf72 expansion, and variant severity in ALSJay P Ross, Claire S Leblond, Sandra B Laurent, et al.
Molecular Psychiatry|May 2, 2025
Transcriptomic and epigenomic consequences of heterozygous loss-of-function mutations in AKAP11, a shared risk gene for bipolar disorder and schizophreniaNargess Farhangdoost, Calwing Liao, Yumin Liu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 28, 2016
SYNE1 mutations cause autosomal-recessive ataxia with retained reflexes in Brazilian patientsMaria Thereza Drumond Gama, Gabrielle Houle, Anne Noreau, et al.
Annals of the New York Academy of Sciences|August 18, 2022
Do variants in the coding regions of FOXP2, a gene implicated in speech disorder, confer a risk for congenital amusia?Isabelle Peretz, Jay Ross, Cynthia V Bourassa, et al.
Nature Genetics|March 20, 2026
Single-cell expression QTL analyses of the human cerebellum reveal vulnerability of oligodendrocytes in essential tremorCharles-Etienne Castonguay, Farah Aboasali, Miranda Medeiros, et al.
Medrxiv : the Preprint Server for Health Sciences|May 18, 2026
Ancestry-specific and multi-ancestry genome-wide association studies of restless legs syndromeFulya Akçimen, Miranda Medeiros, Katie L J Cederberg, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|August 23, 2011
Glucocerebrosidase mutations in a French-Canadian Parkinson's disease cohortAnne Noreau, Jean-Baptiste Rivière, Sabrina Diab, et al.
American Journal of Human Genetics|December 13, 2006
Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegiaPaul N Valdmanis, Inge A Meijer, Annie Reynolds, et al.
Pageof 19

Showing results (71-80 of 188) with videos related to

Sort By:
Pageof 19
Proceedings of the National Academy of Sciences of the United States of America|July 24, 2019
Genetic architecture and adaptations of Nunavik InuitSirui Zhou, Pingxing Xie, Amélie Quoibion, et al.
Neurobiology of Aging|February 25, 2012
Analysis of the SORT1 gene in familial amyotrophic lateral sclerosisVéronique V Belzil, Catherine André-Guimont, Marie-Renée Atallah, et al.
Neurogenetics|May 10, 2020
Oligogenicity, C9orf72 expansion, and variant severity in ALSJay P Ross, Claire S Leblond, Sandra B Laurent, et al.
Molecular Psychiatry|May 2, 2025
Transcriptomic and epigenomic consequences of heterozygous loss-of-function mutations in AKAP11, a shared risk gene for bipolar disorder and schizophreniaNargess Farhangdoost, Calwing Liao, Yumin Liu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 28, 2016
SYNE1 mutations cause autosomal-recessive ataxia with retained reflexes in Brazilian patientsMaria Thereza Drumond Gama, Gabrielle Houle, Anne Noreau, et al.
Annals of the New York Academy of Sciences|August 18, 2022
Do variants in the coding regions of FOXP2, a gene implicated in speech disorder, confer a risk for congenital amusia?Isabelle Peretz, Jay Ross, Cynthia V Bourassa, et al.
Nature Genetics|March 20, 2026
Single-cell expression QTL analyses of the human cerebellum reveal vulnerability of oligodendrocytes in essential tremorCharles-Etienne Castonguay, Farah Aboasali, Miranda Medeiros, et al.
Medrxiv : the Preprint Server for Health Sciences|May 18, 2026
Ancestry-specific and multi-ancestry genome-wide association studies of restless legs syndromeFulya Akçimen, Miranda Medeiros, Katie L J Cederberg, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|August 23, 2011
Glucocerebrosidase mutations in a French-Canadian Parkinson's disease cohortAnne Noreau, Jean-Baptiste Rivière, Sabrina Diab, et al.
American Journal of Human Genetics|December 13, 2006
Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegiaPaul N Valdmanis, Inge A Meijer, Annie Reynolds, et al.
Pageof 19