Guy A. Rouleau
Montreal, QC, Canada
Last Updated: 09/26/2026
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Found 491 publications
Lack of genetic evidence for a role of SLC25A46 in alpha-synucleinopathies.
Journal: Journal of Parkinson's disease
Published: August 06, 2026
Erratum: Consequences of the Novel ALS-Associated KIF5A Variant c.2993-6C>A for Exon 27 Splicing and Axonal Transport of SFPQ.
Journal: Neurology. Genetics
Published: July 24, 2026
Oligogenic variants in NEK1 and ATXN2 in amyotrophic lateral sclerosis: report of two cases and review of the literature.
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: June 10, 2026
Ancestry-specific and multi-ancestry genome-wide association studies of restless legs syndrome.
Journal: medRxiv : the preprint server for health sciences
Published: May 18, 2026
Polygenic and spatial insights into the genetic uniqueness of essential tremor using common variants.
Journal: Journal of the neurological sciences
Published: February 16, 2026
Shared Pathogenic Pathways Between REM Sleep Behavior Disorder and Neurodegenerative and Psychiatric Disorders.
Journal: medRxiv : the preprint server for health sciences
Published: February 12, 2026
Shared Pathogenic Pathways Between REM Sleep Behavior Disorder and Neurodegenerative and Psychiatric Disorders.
Journal: medRxiv : the preprint server for health sciences
Published: February 12, 2026
Lack of genetic evidence for a role of SLC25A46 in alpha-synucleinopathies.
Journal: medRxiv : the preprint server for health sciences
Published: February 06, 2026
An Exploratory Analysis of Essential Tremor and Associated Phenotypes.
Journal: Tremor and other hyperkinetic movements (New York, N.Y.)
Published: January 19, 2026
Using multi-trait polygenic scores to predict lithium responsiveness in patients with bipolar disorder.
Journal: medRxiv : the preprint server for health sciences
Published: January 16, 2026
The world federation of neurology and its global engagement with the World Health Organization and the United Nations economic and social council.
Journal: Journal of the neurological sciences
Published: December 22, 2025
Distinct patterns of de novo coding variants contribute to Tourette Syndrome etiology.
Journal: bioRxiv : the preprint server for biology
Published: November 24, 2025
Last Updated: 09/26/2026