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Jay P Ross

Showing results (21-30 of 51) with videos related to

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Plos One|November 15, 2019
Mineral absorption is an enriched pathway in a brain region of restless legs syndrome patients with reduced MEIS1 expressionFaezeh Sarayloo, Alexandre Dionne-Laporte, Helene Catoire, et al.
Medrxiv : the Preprint Server for Health Sciences|January 3, 2024
Genomic analysis identifies risk factors in restless legs syndromeFulya Akçimen, Ruth Chia, Sara Saez-Atienzar, et al.
Sleep|October 31, 2019
Genetic and epidemiological characterization of restless legs syndrome in QuébecFulya Akçimen, Jay P Ross, Faezeh Sarayloo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 28, 2023
Rare-variant and polygenic analyses of amyotrophic lateral sclerosis in the French-Canadian genomeJay P Ross, Fulya Akçimen, Calwing Liao, et al.
Annals of Neurology|July 30, 2024
Genomic Analysis Identifies Risk Factors in Restless Legs SyndromeFulya Akçimen, Ruth Chia, Sara Saez-Atienzar, et al.
Annals of Neurology|August 27, 2025
TARDBP (TDP-43) Knock-in Zebrafish Display a Late-Onset Motor Phenotype and Loss of Large Spinal Cord Motor NeuronsZiyaan A Harji, Christian J Rampal, Esteban C Rodríguez, et al.
Human Genomics|April 18, 2019
Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansionRossella Spataro, Maria Kousi, Sali M K Farhan, et al.
Plos Genetics|February 6, 2023
Spinal cord extracts of amyotrophic lateral sclerosis spread TDP-43 pathology in cerebral organoidsYoshitaka Tamaki, Jay P Ross, Paria Alipour, et al.
European Journal of Human Genetics : EJHG|August 14, 2014
VPS35 and DNAJC13 disease-causing variants in essential tremorAlex Rajput, Jay P Ross, Cecily Q Bernales, et al.
Frontiers in Genetics|December 12, 2019
Investigation of the <i>RFC1</i> Repeat Expansion in a Canadian and a Brazilian Ataxia Cohort: Identification of Novel ConformationsFulya Akçimen, Jay P Ross, Cynthia V Bourassa, et al.
Pageof 6

Showing results (21-30 of 51) with videos related to

Sort By:
Pageof 6
Plos One|November 15, 2019
Mineral absorption is an enriched pathway in a brain region of restless legs syndrome patients with reduced MEIS1 expressionFaezeh Sarayloo, Alexandre Dionne-Laporte, Helene Catoire, et al.
Medrxiv : the Preprint Server for Health Sciences|January 3, 2024
Genomic analysis identifies risk factors in restless legs syndromeFulya Akçimen, Ruth Chia, Sara Saez-Atienzar, et al.
Sleep|October 31, 2019
Genetic and epidemiological characterization of restless legs syndrome in QuébecFulya Akçimen, Jay P Ross, Faezeh Sarayloo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 28, 2023
Rare-variant and polygenic analyses of amyotrophic lateral sclerosis in the French-Canadian genomeJay P Ross, Fulya Akçimen, Calwing Liao, et al.
Annals of Neurology|July 30, 2024
Genomic Analysis Identifies Risk Factors in Restless Legs SyndromeFulya Akçimen, Ruth Chia, Sara Saez-Atienzar, et al.
Annals of Neurology|August 27, 2025
TARDBP (TDP-43) Knock-in Zebrafish Display a Late-Onset Motor Phenotype and Loss of Large Spinal Cord Motor NeuronsZiyaan A Harji, Christian J Rampal, Esteban C Rodríguez, et al.
Human Genomics|April 18, 2019
Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansionRossella Spataro, Maria Kousi, Sali M K Farhan, et al.
Plos Genetics|February 6, 2023
Spinal cord extracts of amyotrophic lateral sclerosis spread TDP-43 pathology in cerebral organoidsYoshitaka Tamaki, Jay P Ross, Paria Alipour, et al.
European Journal of Human Genetics : EJHG|August 14, 2014
VPS35 and DNAJC13 disease-causing variants in essential tremorAlex Rajput, Jay P Ross, Cecily Q Bernales, et al.
Frontiers in Genetics|December 12, 2019
Investigation of the <i>RFC1</i> Repeat Expansion in a Canadian and a Brazilian Ataxia Cohort: Identification of Novel ConformationsFulya Akçimen, Jay P Ross, Cynthia V Bourassa, et al.
Pageof 6