| Year |
Citation |
Score |
| 2024 |
Audet S, Triassi V, Gelinas M, Legault-Cadieux N, Ferraro V, Duquette A, Tetreault M. Integration of multi-omics technologies for molecular diagnosis in ataxia patients. Frontiers in Genetics. 14: 1304711. PMID 38239855 DOI: 10.3389/fgene.2023.1304711 |
0.571 |
|
| 2023 |
Alshimemeri S, Abo Alsamh D, Zhou L, Furtado S, Kraft S, Bruno V, Duquette A, Brais B, Suchowersky O, Munhoz RP, Slow E. Demographics and Clinical Characteristics of Autosomal Dominant Spinocerebellar Ataxia in Canada. Movement Disorders Clinical Practice. 10: 440-451. PMID 36949783 DOI: 10.1002/mdc3.13666 |
0.49 |
|
| 2022 |
Pellerin D, Danzi MC, Wilke C, Renaud M, Fazal S, Dicaire MJ, Scriba CK, Ashton C, Yanick C, Beijer D, Rebelo A, Rocca C, Jaunmuktane Z, Sonnen JA, Larivière R, ... ... Duquette A, et al. Deep Intronic GAA Repeat Expansion in Late-Onset Cerebellar Ataxia. The New England Journal of Medicine. PMID 36516086 DOI: 10.1056/NEJMoa2207406 |
0.586 |
|
| 2021 |
Labrecque M, Touma L, Bhérer C, Duquette A, Tétreault M. Estimated prevalence of Niemann-Pick type C disease in Quebec. Scientific Reports. 11: 22621. PMID 34799641 DOI: 10.1038/s41598-021-01966-0 |
0.536 |
|
| 2021 |
Touma L, Labrecque M, Tetreault M, Duquette A. Identification and Classification of Rare Variants in NPC1 and NPC2 in Quebec. Scientific Reports. 11: 10344. PMID 33990640 DOI: 10.1038/s41598-021-89630-5 |
0.557 |
|
| 2013 |
Duquette A, Brais B, Bouchard JP, Mathieu J. Clinical presentation and early evolution of spastic ataxia of Charlevoix-Saguenay. Movement Disorders : Official Journal of the Movement Disorder Society. 28: 2011-4. PMID 23913799 DOI: 10.1002/Mds.25604 |
0.552 |
|
| 2013 |
Thiffault I, Dicaire MJ, Tetreault M, Huang KN, Demers-Lamarche J, Bernard G, Duquette A, Larivière R, Gehring K, Montpetit A, McPherson PS, Richter A, Montermini L, Mercier J, Mitchell GA, et al. Diversity of ARSACS mutations in French-Canadians. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 40: 61-6. PMID 23250129 DOI: 10.1017/S0317167100012968 |
0.643 |
|
| 2009 |
Srour M, Philibert M, Dion MH, Duquette A, Richer F, Rouleau GA, Chouinard S. Familial congenital mirror movements: report of a large 4-generation family. Neurology. 73: 729-31. PMID 19720981 DOI: 10.1212/Wnl.0B013E3181B59Bda |
0.364 |
|
| 2007 |
Nahas SA, Duquette A, Roddier K, Gatti RA, Brais B. Ataxia-oculomotor apraxia 2 patients show no increased sensitivity to ionizing radiation. Neuromuscular Disorders : Nmd. 17: 968-9. PMID 17720498 DOI: 10.1016/J.Nmd.2007.06.464 |
0.586 |
|
| 2006 |
Tétreault M, Duquette A, Thiffault I, Bherer C, Jarry J, Loisel L, Banwell B, D'Anjou G, Mathieu J, Robitaille Y, Vanasse M, Brais B. A new form of congenital muscular dystrophy with joint hyperlaxity maps to 3p23-21. Brain : a Journal of Neurology. 129: 2077-84. PMID 16760198 DOI: 10.1093/Brain/Awl146 |
0.543 |
|
| 2005 |
Duquette A, Roddier K, McNabb-Baltar J, Gosselin I, St-Denis A, Dicaire MJ, Loisel L, Labuda D, Marchand L, Mathieu J, Bouchard JP, Brais B. Mutations in senataxin responsible for Quebec cluster of ataxia with neuropathy. Annals of Neurology. 57: 408-14. PMID 15732101 DOI: 10.1002/Ana.20408 |
0.605 |
|
| 2003 |
Stumpf E, Masson H, Duquette A, Berthelet F, McNabb J, Lortie A, Lesage J, Montplaisir J, Brais B, Cossette P. Adult Alexander disease with autosomal dominant transmission: a distinct entity caused by mutation in the glial fibrillary acid protein gene. Archives of Neurology. 60: 1307-12. PMID 12975300 DOI: 10.1001/Archneur.60.9.1307 |
0.61 |
|
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