Jennifer A. Ruskey
Montreal, QC, Canada
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 61 publications
The GBA1 p.E427K (p.E388K) Variant is a Risk Factor for Synucleinopathies: A Meta-Analysis.
Journal: medRxiv : the preprint server for health sciences
Published: March 27, 2026
The GBA1 p.E427K (p.E388K) Variant Is a Risk Factor for Synucleinopathies: A Meta-Analysis.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: March 18, 2026
Rare-Variant Burden across Lysosomal Genes Implicates Sialylation and Ganglioside Metabolism in Parkinson's Disease.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: March 10, 2026
Rare-variant burden across lysosomal genes implicates sialylation and ganglioside metabolism in Parkinson's disease.
Journal: medRxiv : the preprint server for health sciences
Published: February 27, 2026
Genome-wide association study of REM sleep behavior disorder in Parkinson's disease.
Journal: NPJ Parkinson's disease
Published: June 30, 2025
Lack of association between G6PD variants and Parkinson disease.
Journal: HGG advances
Published: May 08, 2025
Correction: The Parkinson's disease risk gene cathepsin B promotes fibrillar alpha-synuclein clearance, lysosomal function and glucocerebrosidase activity in dopaminergic neurons.
Journal: Molecular neurodegeneration
Published: December 19, 2024
LRRK2 rare-variant per-domain genetic burden in Parkinson's Disease: association confined to the kinase domain.
Journal: NPJ Parkinson's disease
Published: October 13, 2024
Lack of epistatic interaction of SNCA with APOE in synucleinopathies.
Journal: Brain communications
Published: August 22, 2024
Genome-wide association study of glucocerebrosidase activity modifiers.
Journal: Research square
Published: June 17, 2024
Are rare heterozygous SYNJ1 variants associated with Parkinson's disease?
Journal: medRxiv : the preprint server for health sciences
Published: June 10, 2024
Are rare heterozygous SYNJ1 variants associated with Parkinson's disease?
Journal: NPJ Parkinson's disease
Published: May 29, 2024
Last Updated: 09/26/2026