Antoine Duquette
Affiliations: | Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States |
Area:
Neurogenetics, neurodegenerative disorders, Parkinson's disease, hereditary ataxiasGoogle:
"Antoine Duquette"Mean distance: 17.37 (cluster 31) | S | N | B | C | P |
Parents
Sign in to add mentor| Edward Fon | grad student | 2008- | Montreal Neurological Institute and Hospital, McGill University |
| Mel B. Feany | grad student | 2011- | Brigham and Women's Hospital |
| Bernard Brais | grad student | 2002-2005 | Université de Montréal |
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Publications
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| Chen S, Ashton C, Sakalla R, et al. (2024) Neuroradiological findings in GAA- ataxia (SCA27B): more than cerebellar atrophy. Medrxiv : the Preprint Server For Health Sciences |
| Audet S, Triassi V, Gelinas M, et al. (2024) Integration of multi-omics technologies for molecular diagnosis in ataxia patients. Frontiers in Genetics. 14: 1304711 |
| Alshimemeri S, Abo Alsamh D, Zhou L, et al. (2023) Demographics and Clinical Characteristics of Autosomal Dominant Spinocerebellar Ataxia in Canada. Movement Disorders Clinical Practice. 10: 440-451 |
| Pellerin D, Danzi MC, Wilke C, et al. (2022) Deep Intronic GAA Repeat Expansion in Late-Onset Cerebellar Ataxia. The New England Journal of Medicine |
| Labrecque M, Touma L, Bhérer C, et al. (2021) Estimated prevalence of Niemann-Pick type C disease in Quebec. Scientific Reports. 11: 22621 |
| Touma L, Labrecque M, Tetreault M, et al. (2021) Identification and Classification of Rare Variants in NPC1 and NPC2 in Quebec. Scientific Reports. 11: 10344 |
| Duquette A, Brais B, Bouchard JP, et al. (2013) Clinical presentation and early evolution of spastic ataxia of Charlevoix-Saguenay. Movement Disorders : Official Journal of the Movement Disorder Society. 28: 2011-4 |
| Thiffault I, Dicaire MJ, Tetreault M, et al. (2013) Diversity of ARSACS mutations in French-Canadians. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 40: 61-6 |
| Srour M, Philibert M, Dion MH, et al. (2009) Familial congenital mirror movements: report of a large 4-generation family. Neurology. 73: 729-31 |
| Nahas SA, Duquette A, Roddier K, et al. (2007) Ataxia-oculomotor apraxia 2 patients show no increased sensitivity to ionizing radiation. Neuromuscular Disorders : Nmd. 17: 968-9 |