10 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Liao C, Sarayloo F, Vuokila V, Rochefort D, Akçimen F, Diamond S, Houle G, Laporte AD, Spiegelman D, He Q, Catoire H, Dion PA, Rouleau GA. Transcriptomic Changes Resulting From Overexpression Identify Pathways Potentially Relevant to Essential Tremor. Frontiers in Genetics. 11: 813. PMID 32849812 DOI: 10.3389/fgene.2020.00813  0.76
2020 Liao C, Sarayloo F, Rochefort D, Houle G, Akçimen F, He Q, Laporte AD, Spiegelman D, Poewe W, Berg D, Müller S, Hopfner F, Deuschl G, Kuhlenbäeumer G, Rajput A, et al. Multiomics Analyses Identify Genes and Pathways Relevant to Essential Tremor. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 32249994 DOI: 10.1002/mds.28031  0.76
2020 Beaudin M, Sellami L, Martel C, Touzel-Deschênes L, Houle G, Martineau L, Lacroix K, Lavallée A, Chrestian N, Rouleau GA, Gros-Louis F, Laforce R, Dupré N. Characterization of the phenotype with cognitive impairment and protein mislocalization in SCA34. Neurology. Genetics. 6: e403. PMID 32211516 DOI: 10.1212/NXG.0000000000000403  0.56
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  0.76
2019 Diez-Fairen M, Bandres-Ciga S, Houle G, Nalls MA, Girard SL, Dion PA, Blauwendraat C, Singleton AB, Rouleau GA, Pastor P. Genome-wide estimates of heritability and genetic correlations in essential tremor. Parkinsonism & Related Disorders. PMID 31085086 DOI: 10.1016/j.parkreldis.2019.05.002  0.76
2018 Liao C, Houle G, He Q, Laporte AD, Girard SL, Dion PA, Rouleau GA. Investigating the association and causal relationship between restless legs syndrome and essential tremor. Parkinsonism & Related Disorders. PMID 30366831 DOI: 10.1016/j.parkreldis.2018.10.022  0.76
2018 Schmouth JF, Houle G, Ambalavanan A, Leblond CS, Spiegelman D, Laurent SB, Bourassa CV, Panisset M, Chouinard S, Dupré N, Vilariño-Güell C, Rajput A, Dion PA, Rouleau GA. Absence of Mutation Enrichment for Genes Phylogenetically Conserved in the Olivocerebellar Motor Circuitry in a Cohort of Canadian Essential Tremor Cases. Molecular Neurobiology. PMID 30315477 DOI: 10.1007/s12035-018-1369-1  0.76
2017 Houle G, Ambalavanan A, Schmouth JF, Leblond CS, Spiegelman D, Laurent SB, Bourassa CV, Grayson C, Panisset M, Chouinard S, Dupré N, Vilariño-Güell C, Rajput A, Girard SL, Dion PA, et al. No rare deleterious variants from , , and are associated with essential tremor. Neurology. Genetics. 3: e195. PMID 30584593 DOI: 10.1212/NXG.0000000000000195  0.76
2017 Houle G, Schmouth JF, Leblond CS, Ambalavanan A, Spiegelman D, Laurent SB, Bourassa CV, Panisset M, Chouinard S, Dupré N, Vilariño-Güell C, Rajput A, Dion PA, Rouleau GA. Teneurin transmembrane protein 4 is not a cause for essential tremor in a Canadian population. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 28158909 DOI: 10.1002/mds.26753  0.76
2016 Gama MT, Houle G, Noreau A, Dionne-Laporte A, Dion PA, Rouleau GA, Barsottini OG, Pedroso JL. SYNE1 mutations cause autosomal-recessive ataxia with retained reflexes in Brazilian patients. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 27671794 DOI: 10.1002/mds.26810  0.76
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