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J. F. Gagnon

Researcher at Université du Québec à Montréal

Publications -  17
Citations -  40

J. F. Gagnon is an academic researcher from Université du Québec à Montréal. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 1, co-authored 1 publications receiving 20 citations.

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Psychological characteristics of patients with myotonic dystrophy type 1

TL;DR: The psychological characteristics of a large cohort of patients with DM1 are described to characterize those at risk of developing a psychiatric disorder, and to compare characteristics between two DM1 phenotypes, a mild and more severe adult‐onset phenotype.
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Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects

Lynne Krohn, +105 more
TL;DR: This paper performed a genome-wide association study of RBD, identifying five RBD risk loci near SNCA, GBA, TMEM175, INPP5F, and SCARB2.
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Progression of clinical markers in prodromal Parkinson's disease and dementia with Lewy bodies: a multicentre study.

TL;DR: In this paper , the authors used linear mixed-effect modeling to estimate annual rates of clinical marker progression stratified by disease subtype, including prodromal Parkinson's disease and dementia with Lewy bodies, and calculated sample size requirements to demonstrate slowing of progression under different anticipated treatment effects.
Posted ContentDOI

Mitochondrial dysfunction underlies cortical atrophy in prodromal synucleinopathies

TL;DR: It is demonstrated that the development of atrophy in synucleinopathies is constrained by specific genes and networks, and thinning in iRBD was constrained by the brain's connectome and that it mapped onto specific networks involved in motor and planning functions.
Journal ArticleDOI

Mitochondrial function-associated genes underlie cortical atrophy in prodromal synucleinopathies.

TL;DR: In this paper , the authors performed cutting-edge imaging transcriptomics and comprehensive spatial mapping analyses in a multicentric cohort of 171 polysomnography-confirmed isolated rapid eye movement sleep behaviour disorder (iRBD) patients (67.7 ± 6.6 (49-87) years; 83% men) and 238 healthy controls (66.6 ± 7.9 (41-88) years).