| Year |
Citation |
Score |
| 2023 |
Akçimen F, Chia R, Saez-Atienzar S, Ruffo P, Rasheed M, Ross JP, Liao C, Ray A, Dion PA, Scholz SW, Rouleau GA, Traynor BJ. Genomic analysis identifies risk factors in restless legs syndrome. Medrxiv : the Preprint Server For Health Sciences. PMID 38168192 DOI: 10.1101/2023.12.19.23300211 |
0.755 |
|
| 2023 |
Schmilovich Z, Bourque VR, Douard E, Huguet G, Poulain C, Ross JP, Alipour P, Castonguay CÉ, Younis N, Jean-Louis M, Saci Z, Pausova Z, Paus T, Schuman G, Porteous D, et al. 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. PMID 38076919 DOI: 10.1101/2023.11.29.23299190 |
0.395 |
|
| 2023 |
Ross JP, Akçimen F, Liao C, Kwan K, Phillips DE, Schmilovich Z, Spiegelman D, Genge A, Dupré N, Dion PA, Farhan SMK, Rouleau GA. 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. PMID 37638500 DOI: 10.1016/j.gim.2023.100967 |
0.796 |
|
| 2023 |
Tamaki Y, Ross JP, Alipour P, Castonguay CÉ, Li B, Catoire H, Rochefort D, Urushitani M, Takahashi R, Sonnen JA, Stifani S, Dion PA, Rouleau GA. Spinal cord extracts of amyotrophic lateral sclerosis spread TDP-43 pathology in cerebral organoids. Plos Genetics. 19: e1010606. PMID 36745687 DOI: 10.1371/journal.pgen.1010606 |
0.398 |
|
| 2022 |
Alipour P, Senkevich K, Ross JP, Spiegelman D, Manousaki D, Dion PA, Rouleau GA. Investigation of the causal relationship between ALS and autoimmune disorders: a Mendelian randomization study. Bmc Medicine. 20: 382. PMID 36320012 DOI: 10.1186/s12916-022-02578-9 |
0.424 |
|
| 2022 |
Peretz I, Ross J, Bourassa CV, Perreault LL, Dion PA, Weiss MW, Felezeu M, Rouleau GA, Dubé MP. 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. PMID 35980667 DOI: 10.1111/nyas.14883 |
0.648 |
|
| 2022 |
Castonguay CE, Liao C, Khayachi A, Liu Y, Medeiros M, Houle G, Ross JP, Dion PA, Rouleau GA. Transcriptomic effects of propranolol and primidone converge on molecular pathways relevant to essential tremor. Npj Genomic Medicine. 7: 46. PMID 35927430 DOI: 10.1038/s41525-022-00318-9 |
0.79 |
|
| 2022 |
Ross JP, Akçimen F, Liao C, Spiegelman D, Weisburd B, Dupré N, Dion PA, Rouleau GA, Farhan SMK. Questioning the Association of the Dinucleotide Repeat With Amyotrophic Lateral Sclerosis. Neurology. Genetics. 8: e678. PMID 35923349 DOI: 10.1212/NXG.0000000000000678 |
0.781 |
|
| 2022 |
Salmon K, Ross JP, Bertone V, Gobbo M, Anoja N, Karamchandani J, Dion PA, Rouleau GA, Genge A. The value of testing for ATXN2 intermediate repeat expansions in routine clinical practice for amyotrophic lateral sclerosis. European Journal of Human Genetics : Ejhg. PMID 35864146 DOI: 10.1038/s41431-022-01146-2 |
0.312 |
|
| 2022 |
Liao C, Vuokila V, Catoire H, Akçimen F, Ross JP, Bourassa CV, Dion PA, Meijer IA, Rouleau GA. Transcriptome-wide association study reveals increased neuronal FLT3 expression is associated with Tourette's syndrome. Communications Biology. 5: 289. PMID 35354918 DOI: 10.1038/s42003-022-03231-0 |
0.793 |
|
| 2022 |
Hop PJ, Zwamborn RAJ, Hannon E, Shireby GL, Nabais MF, Walker EM, van Rheenen W, van Vugt JJFA, Dekker AM, Westeneng HJ, Tazelaar GHP, van Eijk KR, Moisse M, Baird D, Al Khleifat A, ... ... Ross JP, et al. Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS. Science Translational Medicine. 14: eabj0264. PMID 35196023 DOI: 10.1126/scitranslmed.abj0264 |
0.442 |
|
| 2022 |
van Rheenen W, van der Spek RAA, Bakker MK, van Vugt JJFA, Hop PJ, Zwamborn RAJ, de Klein N, Westra HJ, Bakker OB, Deelen P, Shireby G, Hannon E, Moisse M, Baird D, Restuadi R, ... ... Ross JP, et al. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology. Nature Genetics. PMID 35102318 DOI: 10.1038/s41588-022-01020-3 |
0.482 |
|
| 2022 |
Roy V, Ross JP, Pépin R, Cortez Ghio S, Brodeur A, Touzel Deschênes L, Le-Bel G, Phillips DE, Milot G, Dion PA, Guérin S, Germain L, Berthod F, Auger FA, Rouleau GA, et al. Moyamoya Disease Susceptibility Gene Regulates Endothelial Barrier Function. Stroke. STROKEAHA120032691. PMID 34991336 DOI: 10.1161/STROKEAHA.120.032691 |
0.464 |
|
| 2022 |
Liao C, Castonguay CE, Heilbron K, Vuokila V, Medeiros M, Houle G, Akçimen F, Ross JP, Catoire H, Diez-Fairen M, Kang J, Mueller SH, Girard SL, Hopfner F, Lorenz D, et al. Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis. Jama Neurology. PMID 34982113 DOI: 10.1001/jamaneurol.2021.4781 |
0.787 |
|
| 2021 |
van Rheenen W, van der Spek RAA, Bakker MK, van Vugt JJFA, Hop PJ, Zwamborn RAJ, de Klein N, Westra HJ, Bakker OB, Deelen P, Shireby G, Hannon E, Moisse M, Baird D, Restuadi R, ... ... Ross JP, et al. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology. Nature Genetics. 53: 1636-1648. PMID 34873335 DOI: 10.1038/s41588-021-00973-1 |
0.561 |
|
| 2021 |
Oliveira LM, Rastin T, Nimmo GAM, Ross JP, Dion PA, Zhang M, Nevay DL, Arkadir D, Gotkine M, Barnett C, Shoesmith CL, Zimran A, Rogaeva EA, Zinman L, Rouleau GA, et al. Occurrence of Amyotrophic Lateral Sclerosis in Type 1 Gaucher Disease. Neurology. Genetics. 7: e600. PMID 34017912 DOI: 10.1212/NXG.0000000000000600 |
0.446 |
|
| 2021 |
Estiar MA, Yu E, Haj Salem I, Ross JP, Mufti K, Akçimen F, Leveille E, Spiegelman D, Ruskey JA, Asayesh F, Dagher A, Yoon G, Tarnopolsky M, Boycott KM, Dupre N, et al. Evidence for Non-Mendelian Inheritance in Spastic Paraplegia 7. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 33598982 DOI: 10.1002/mds.28528 |
0.73 |
|
| 2020 |
Akçimen F, Ross JP, Liao C, Spiegelman D, Dion PA, Rouleau GA. Expanded CAG Repeats in ATXN1, ATXN2, ATXN3, and HTT in the 1000 Genomes Project. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 33159825 DOI: 10.1002/mds.28341 |
0.762 |
|
| 2020 |
Liao C, Akçimen F, Diez-Fairen M, Houle G, Ross JP, Schmilovich Z, Spiegelman D, Vuokila V, Catoire H, Meijer IA, Pastor P, Rajput A, Dion PA, Rouleau GA. Assessing the NOTCH2NLC GGC expansion in European patients with essential tremor. Brain : a Journal of Neurology. PMID 33146671 DOI: 10.1093/brain/awaa291 |
0.726 |
|
| 2020 |
Course MM, Gudsnuk K, Smukowski SN, Winston K, Desai N, Ross JP, Sulovari A, Bourassa CV, Spiegelman D, Couthouis J, Yu CE, Tsuang DW, Jayadev S, Kay MA, Gitler AD, et al. Evolution of a Human-Specific Tandem Repeat Associated with ALS. American Journal of Human Genetics. PMID 32750315 DOI: 10.1016/J.Ajhg.2020.07.004 |
0.506 |
|
| 2020 |
Akçimen F, Sarayloo F, Liao C, Ross JP, Oliveira RB, Dion PA, Rouleau GA. Transcriptome-wide association study for restless legs syndrome identifies new susceptibility genes. Communications Biology. 3: 373. PMID 32651461 DOI: 10.1038/s42003-020-1105-z |
0.757 |
|
| 2020 |
Ross JP, Dion PA, Rouleau GA. Exome sequencing in genetic disease: recent advances and considerations. F1000research. 9. PMID 32431803 DOI: 10.12688/F1000Research.19444.1 |
0.473 |
|
| 2020 |
Ross JP, Leblond CS, Laurent SB, Spiegelman D, Dionne-Laporte A, Camu W, Dupré N, Dion PA, Rouleau GA. Oligogenicity, C9orf72 expansion, and variant severity in ALS. Neurogenetics. PMID 32385536 DOI: 10.1007/S10048-020-00612-7 |
0.547 |
|
| 2019 |
Akçimen F, Ross JP, Bourassa CV, Liao C, Rochefort D, Gama MTD, Dicaire MJ, Barsottini OG, Brais B, Pedroso JL, Dion PA, Rouleau GA. Investigation of the Repeat Expansion in a Canadian and a Brazilian Ataxia Cohort: Identification of Novel Conformations. Frontiers in Genetics. 10: 1219. PMID 31824583 DOI: 10.3389/Fgene.2019.01219 |
0.771 |
|
| 2019 |
Sarayloo F, Dionne-Laporte A, Catoire H, Rochefort D, Houle G, Ross JP, Akçimen F, Barros Oliveira R, Turecki G, Dion PA, Rouleau GA. Mineral absorption is an enriched pathway in a brain region of restless legs syndrome patients with reduced MEIS1 expression. Plos One. 14: e0225186. PMID 31725784 DOI: 10.1371/Journal.Pone.0225186 |
0.73 |
|
| 2019 |
Akçimen F, Ross JP, Sarayloo F, Liao C, De Barros Oliveira R, Ruskey JA, Bourassa CV, Dion PA, Xiong L, Gan-Or Z, Rouleau GA. Genetic and epidemiological characterization of restless legs syndrome in Québec. Sleep. PMID 31665514 DOI: 10.1093/Sleep/Zsz265 |
0.747 |
|
| 2019 |
Ross JP, Leblond CS, Catoire H, Volkening K, Strong M, Zinman L, Robertson J, Dion PA, Rouleau GA. Somatic expansion of the hexanucleotide repeat does not occur in ALS spinal cord tissues. Neurology. Genetics. 5: e317. PMID 31041398 DOI: 10.1212/Nxg.0000000000000317 |
0.415 |
|
| 2019 |
Spataro R, Kousi M, Farhan SMK, Willer JR, Ross JP, Dion PA, Rouleau GA, Daly MJ, Neale BM, La Bella V, Katsanis N. Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion. Human Genomics. 13: 19. PMID 30992063 DOI: 10.1186/S40246-019-0203-9 |
0.551 |
|
| 2018 |
Li J, Ruskey JA, Arnulf I, Dauvilliers Y, Hu MTM, Högl B, Leblond CS, Zhou S, Ambalavanan A, Ross JP, Bourassa CV, Spiegelman D, Laurent SB, Stefani A, Charley Monaca C, et al. Full sequencing and haplotype analysis of MAPT in Parkinson's disease and rapid eye movement sleep behavior disorder. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 29756641 DOI: 10.1002/Mds.27385 |
0.651 |
|
| 2018 |
Zhou S, Gan-Or Z, Ambalavanan A, Lai D, Xie P, Bourassa CV, Strong S, Ross JP, Dionne-Laporte A, Spiegelman D, Dupré N, Foroud TM, Xiong L, Dion PA, Rouleau GA. Genome-wide association analysis identifies new candidate risk loci for familial intracranial aneurysm in the French-Canadian population. Scientific Reports. 8: 4356. PMID 29531279 DOI: 10.1038/S41598-018-21603-7 |
0.714 |
|
| 2018 |
Ross JP, Mohtashami S, Leveille E, Johnson AM, Xiong L, Dion PA, Fon E, Dauvilliers Y, Dupré N, Rouleau GA, Gan-Or Z. Association study of essential tremor genetic loci in Parkinson's disease. Neurobiology of Aging. PMID 29398123 DOI: 10.1016/J.Neurobiolaging.2018.01.001 |
0.547 |
|
| 2017 |
Sadovnick AD, Traboulsee AL, Zhao Y, Bernales CQ, Encarnacion M, Ross JP, Yee IM, Criscuoli MG, Vilariño-Güell C. Genetic modifiers of multiple sclerosis progression, severity and onset. Clinical Immunology (Orlando, Fla.). 180: 100-105. PMID 28501589 DOI: 10.1016/J.Clim.2017.05.009 |
0.363 |
|
| 2017 |
Ross JP, Dupré N, Dauvilliers Y, Strong S, Dionne-Laporte A, Dion PA, Rouleau GA, Gan-Or Z. RIC3 variants are not associated with Parkinson's disease in French-Canadians and French. Neurobiology of Aging. PMID 28153381 DOI: 10.1016/J.Neurobiolaging.2017.01.005 |
0.533 |
|
| 2016 |
Gan-Or Z, Montplaisir JY, Ross JP, Poirier J, Warby SC, Arnulf I, Strong S, Dauvilliers Y, Leblond CS, Hu MT, Högl B, Stefani A, Monaca CC, De Cock VC, Boivin M, et al. The dementia-associated APOE ε4 allele is not associated with rapid eye movement sleep behavior disorder. Neurobiology of Aging. PMID 27814994 DOI: 10.1016/J.Neurobiolaging.2016.10.002 |
0.499 |
|
| 2016 |
Wang Z, Sadovnick AD, Traboulsee AL, Ross JP, Bernales CQ, Encarnacion M, Yee IM, de Lemos M, Greenwood T, Lee JD, Wright G, Ross CJ, Zhang S, Song W, Vilariño-Güell C. Case-Control Studies Are Not Familial Studies. Neuron. 92: 339-341. PMID 27764669 DOI: 10.1016/J.Neuron.2016.09.053 |
0.446 |
|
| 2016 |
Mallett V, Ross JP, Alcalay RN, Ambalavanan A, Sidransky E, Dion PA, Rouleau GA, Gan-Or Z. GBA p.T369M substitution in Parkinson disease: Polymorphism or association? A meta-analysis. Neurology. Genetics. 2: e104. PMID 27648471 DOI: 10.1212/Nxg.0000000000000104 |
0.462 |
|
| 2016 |
Wang Z, Sadovnick AD, Traboulsee AL, Ross JP, Bernales CQ, Encarnacion M, Yee IM, de Lemos M, Greenwood T, Lee JD, Wright G, Ross CJ, Zhang S, Song W, Vilariño-Güell C. Nuclear Receptor NR1H3 in Familial Multiple Sclerosis. Neuron. 90: 948-954. PMID 27253448 DOI: 10.1016/J.Neuron.2016.04.039 |
0.368 |
|
| 2016 |
Ross JP, Dupre N, Dauvilliers Y, Strong S, Ambalavanan A, Spiegelman D, Dionne-Laporte A, Pourcher E, Langlois M, Boivin M, Leblond CS, Dion PA, Rouleau GA, Gan-Or Z. Analysis of DNAJC13 mutations in French-Canadian/French cohort of Parkinson's disease. Neurobiology of Aging. PMID 27236598 DOI: 10.1016/J.Neurobiolaging.2016.04.023 |
0.491 |
|
| 2016 |
Sadovnick AD, Traboulsee AL, Bernales CQ, Ross JP, Forwell AL, Yee IM, Guillot-Noel L, Fontaine B, Cournu-Rebeix I, Alcina A, Fedetz M, Izquierdo G, Matesanz F, Hilven K, Dubois B, et al. Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients. G3 (Bethesda, Md.). PMID 27194806 DOI: 10.1534/G3.116.030841 |
0.391 |
|
| 2016 |
Forwell AL, Bernales CQ, Ross JP, Yee IM, Encarnacion M, Lee JD, Sadovnick AD, Traboulsee AL, Vilariño-Güell C. Analysis of CH25H in multiple sclerosis and neuromyelitis optica. Journal of Neuroimmunology. 291: 70-2. PMID 26857497 DOI: 10.1016/J.Jneuroim.2015.12.014 |
0.402 |
|
| 2015 |
Rajput A, Ross JP, Bernales CQ, Rayaprolu S, Soto-Ortolaza AI, Ross OA, van Gerpen J, Uitti RJ, Wszolek ZK, Rajput AH, Vilariño-Güell C. VPS35 and DNAJC13 disease-causing variants in essential tremor. European Journal of Human Genetics : Ejhg. 23: 887-8. PMID 25118025 DOI: 10.1038/Ejhg.2014.164 |
0.403 |
|
| 2014 |
Traboulsee AL, Bernales CQ, Ross JP, Lee JD, Sadovnick AD, Vilariño-Güell C. Genetic variants in IL2RA and IL7R affect multiple sclerosis disease risk and progression. Neurogenetics. 15: 165-9. PMID 24770783 DOI: 10.1007/S10048-014-0403-3 |
0.433 |
|
| 2014 |
Bernales CQ, Ross JP, Lee JD, Zhao Y, Sadovnick AD, Traboulsee AL, Vilariño-Güell C. Progressive multiple sclerosis does not associate with rs996343 and rs2046748. Multiple Sclerosis (Houndmills, Basingstoke, England). 20: 766-7. PMID 24368757 DOI: 10.1177/1352458513517280 |
0.312 |
|
| 2014 |
Ross JP, Bernales CQ, Lee JD, Sadovnick AD, Traboulsee AL, Vilariño-Güell C. Analysis of CYP27B1 in multiple sclerosis. Journal of Neuroimmunology. 266: 64-6. PMID 24308945 DOI: 10.1016/J.Jneuroim.2013.11.006 |
0.353 |
|
| 2014 |
Ross JP, Rayaprolu S, Bernales CQ, Soto-Ortolaza AI, van Gerpen J, Uitti RJ, Wszolek ZK, Rajput A, Rajput AH, Rajput ML, Ross OA, Vilariño-Güell C. SLC1A2 rs3794087 does not associate with essential tremor Neurobiology of Aging. 35. PMID 24139280 DOI: 10.1016/J.Neurobiolaging.2013.09.022 |
0.447 |
|
| 2014 |
Rajput A, Rajput AH, Rajput ML, Encarnacion M, Bernales CQ, Ross JP, Farrer MJ, Vilariño-Güell C. Identification of FUS p.R377W in essential tremor. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 21: 361-3. PMID 23834483 DOI: 10.1111/Ene.12231 |
0.385 |
|
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