オープン アクセスを義務付けられた論文 - Patrick A. Dion詳細
一般には非公開: 25 件
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TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
E Kabashi, PN Valdmanis, P Dion, D Spiegelman, BJ McConkey, ...
Nature genetics 40 (5), 572-574, 2008
委任: Canadian Institutes of Health Research
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Dissection of genetic factors associated with amyotrophic lateral sclerosis
CS Leblond, HM Kaneb, PA Dion, GA Rouleau
Experimental neurology 262, 91-101, 2014
委任: Canadian Institutes of Health Research
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Recent advances in the genetics of amyotrophic lateral sclerosis
PN Valdmanis, H Daoud, PA Dion, GA Rouleau
Current neurology and neuroscience reports 9 (3), 198-205, 2009
委任: Canadian Institutes of Health Research, Fonds de recherche du Québec - Santé
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Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis
CS Leblond, Z Gan-Or, D Spiegelman, SB Laurent, A Szuto, ...
Neurobiology of aging 37, 209. e17-209. e21, 2016
委任: Canadian Institutes of Health Research, Genome Canada
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Molecular aspects of hereditary spastic paraplegia
A Noreau, PA Dion, GA Rouleau
Experimental cell research 325 (1), 18-26, 2014
委任: Canadian Institutes of Health Research
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Association of paraoxonase gene cluster polymorphisms with ALS in France, Quebec, and Sweden
PN Valdmanis, E Kabashi, A Dyck, P Hince, J Lee, P Dion, M D'Amour, ...
Neurology 71 (7), 514-520, 2008
委任: Canadian Institutes of Health Research
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Parkinson’s disease genetic loci in rapid eye movement sleep behavior disorder
Z Gan-Or, SL Girard, A Noreau, CS Leblond, JF Gagnon, I Arnulf, ...
Journal of Molecular Neuroscience 56, 617-622, 2015
委任: Canadian Institutes of Health Research, Fonds de recherche du Québec - Santé …
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Analysis of DNAJC13 mutations in French-Canadian/French cohort of Parkinson's disease
JP Ross, N Dupre, Y Dauvilliers, S Strong, A Ambalavanan, ...
Neurobiology of aging 45, 212. e13-212. e17, 2016
委任: Canadian Institutes of Health Research, Natural Sciences and Engineering …
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LRRK2 mutations in Parkinson disease; a sex effect or lack thereof? A meta-analysis
Z Gan-Or, CS Leblond, V Mallett, A Orr-Urtreger, PA Dion, GA Rouleau
Parkinsonism & related disorders 21 (7), 778-782, 2015
委任: Canadian Institutes of Health Research, Natural Sciences and Engineering …
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Identification of novel FUS mutations in sporadic cases of amyotrophic lateral sclerosis
VV Belzil, H Daoud, J St-Onge, A Desjarlais, JP Bouchard, N Dupre, ...
Amyotrophic Lateral Sclerosis 12 (2), 113-117, 2011
委任: Canadian Institutes of Health Research
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Rare susceptibility variants for bipolar disorder suggest a role for G protein-coupled receptors
C Cruceanu, JF Schmouth, SG Torres-Platas, JP Lopez, A Ambalavanan, ...
Molecular psychiatry 23 (10), 2050-2056, 2018
委任: Genome Canada
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Analysis of DPP6 and FGGY as candidate genes for amyotrophic lateral sclerosis
H Daoud, PN Valdmanis, PA Dion, GA Rouleau
Amyotrophic Lateral Sclerosis 11 (4), 389-391, 2010
委任: Canadian Institutes of Health Research
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Genetics of essential tremor: from phenotype to genes, insights from both human and mouse studies
JF Schmouth, PA Dion, GA Rouleau
Progress in Neurobiology 119, 1-19, 2014
委任: Canadian Institutes of Health Research
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Analysis of functional GLO1 variants in the BTBD9 locus and restless legs syndrome
Z Gan-Or, S Zhou, A Ambalavanan, CS Leblond, P Xie, A Johnson, ...
Sleep medicine 16 (9), 1151-1155, 2015
委任: Canadian Institutes of Health Research, Natural Sciences and Engineering …
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Cellular expression of the K+–Cl− cotransporter KCC3 in the central nervous system of mouse
M Shekarabi, A Salin-Cantegrel, J Laganière, R Gaudet, P Dion, ...
Brain research 1374, 15-26, 2011
委任: Canadian Institutes of Health Research
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Oligogenicity, C9orf72 expansion, and variant severity in ALS
JP Ross, CS Leblond, SB Laurent, D Spiegelman, A Dionne-Laporte, ...
Neurogenetics 21, 227-242, 2020
委任: Canadian Institutes of Health Research
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Teneurin transmembrane protein 4 is not a cause for essential tremor in a Canadian population
G Houle, JF Schmouth, CS Leblond, A Ambalavanan, D Spiegelman, ...
Movement Disorders 32 (2), 292-295, 2017
委任: Canadian Institutes of Health Research
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Exome sequencing of sporadic childhood‐onset schizophrenia suggests the contribution of X‐linked genes in males
A Ambalavanan, B Chaumette, S Zhou, P Xie, Q He, D Spiegelman, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 180 …, 2019
委任: US National Institutes of Health, Canadian Institutes of Health Research …
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Multiomics analyses identify genes and pathways relevant to essential tremor
C Liao, F Sarayloo, D Rochefort, G Houle, F Akçimen, Q He, AD Laporte, ...
Movement Disorders 35 (7), 1153-1162, 2020
委任: Canadian Institutes of Health Research, Natural Sciences and Engineering …
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Diagnostic yield of whole exome sequencing for adults with ataxia: a Brazilian perspective
FF da Graça, TM Peluzzo, LC Bonadia, ARM Martinez, F Diniz de Lima, ...
The Cerebellum 21 (1), 49-54, 2022
委任: Fundação de Amparo à Pesquisa do Estado de São Paulo
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