Jay P Ross

Affiliations: 
McGill University, Montreal, QC, Canada 
Area:
Amyotrophic Lateral Sclerosis
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"Jay Ross"
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Publications

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Akçimen F, Chia R, Saez-Atienzar S, et al. (2024) Genomic Analysis Identifies Risk Factors in Restless Legs Syndrome. Annals of Neurology
Schmilovich Z, Bourque VR, Douard E, et al. (2024) Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability. Frontiers in Psychiatry. 15: 1369767
Akçimen F, Chia R, Saez-Atienzar S, et al. (2023) Genomic analysis identifies risk factors in restless legs syndrome. Medrxiv : the Preprint Server For Health Sciences
Schmilovich Z, Bourque VR, Douard E, et al. (2023) Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability. Medrxiv : the Preprint Server For Health Sciences
Ross JP, Akçimen F, Liao C, et al. (2023) Rare variant and polygenic analyses of amyotrophic lateral sclerosis in the French-Canadian genome. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 100967
Tamaki Y, Ross JP, Alipour P, et al. (2023) Spinal cord extracts of amyotrophic lateral sclerosis spread TDP-43 pathology in cerebral organoids. Plos Genetics. 19: e1010606
Alipour P, Senkevich K, Ross JP, et al. (2022) Investigation of the causal relationship between ALS and autoimmune disorders: a Mendelian randomization study. Bmc Medicine. 20: 382
Peretz I, Ross J, Bourassa CV, et al. (2022) Do variants in the coding regions of FOXP2, a gene implicated in speech disorder, confer a risk for congenital amusia? Annals of the New York Academy of Sciences
Castonguay CE, Liao C, Khayachi A, et al. (2022) Transcriptomic effects of propranolol and primidone converge on molecular pathways relevant to essential tremor. Npj Genomic Medicine. 7: 46
Ross JP, Akçimen F, Liao C, et al. (2022) Questioning the Association of the Dinucleotide Repeat With Amyotrophic Lateral Sclerosis. Neurology. Genetics. 8: e678
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