Bernard Brais, M.D., Ph.D., M.Phil.
Affiliations: | Université de Montréal, Montréal, Canada |
Area:
Neurogenetics, neurodegenerative disorders, neuromuscular disorders, hereditary ataxiasGoogle:
"Bernard Brais"Mean distance: 18.64 (cluster 28)
Children
Sign in to add trainee| Antoine Duquette | grad student | 2002-2005 | Université de Montréal |
| Veronique Bolduc | grad student | 2011 | Université de Montréal |
| Martine Tetreault | grad student | 2013 | 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 |
| Pellerin D, Danzi MC, Renaud M, et al. (2024) Spinocerebellar ataxia 27B: A novel, frequent and potentially treatable ataxia. Clinical and Translational Medicine. 14: e1504 |
| Alkhalifa A, Chen S, Hasiloglu ZI, et al. (2023) White matter abnormalities in 15 subjects with SPG76. Journal of Neurology |
| Hengel H, Pellerin D, Wilke C, et al. (2023) As Frequent as Polyglutamine Spinocerebellar Ataxias: SCA27B in a Large German Autosomal Dominant Ataxia Cohort. Movement Disorders : Official Journal of the Movement Disorder Society. 38: 1557-1558 |
| 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 |
| Coutelier M, Jacoupy M, Janer A, et al. (2021) NPTX1 mutations trigger endoplasmic reticulum stress and cause autosomal dominant cerebellar ataxia. Brain : a Journal of Neurology |
| Gauquelin L, Hartley T, Tarnopolsky M, et al. (2020) Channelopathies Are a Frequent Cause of Genetic Ataxias Associated with Cerebellar Atrophy. Movement Disorders Clinical Practice. 7: 940-949 |
| Nicolau S, Choquet K, Bareke E, et al. (2020) A molecular diagnosis of LGMDR1 established by RNA sequencing. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 1-11 |
| Pellerin D, Ellezam B, Korathanakhun P, et al. (2020) Multi-system proteinopathy associated with a G156S mutation in a French Canadian family. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 1-11 |