Konstantin A. Senkevich
Montreal, QC, Canada
Last Updated: 09/26/2026
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Found 88 publications
Lack of genetic evidence for a role of SLC25A46 in alpha-synucleinopathies.
Journal: Journal of Parkinson's disease
Published: August 06, 2026
Genome-wide association studies identify genetic determinants of synucleinopathy biomarkers.
Journal: Research square
Published: July 17, 2026
Glucocerebrosidase dysfunction in GBA1 carriers: insights from blood and macrophage analyses.
Journal: Molecular biology reports
Published: May 21, 2026
Rare-Variant Burden Analysis of Dystonia Genes in Parkinson's Disease.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: April 04, 2026
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
Lack of genetic evidence for a role of SLC25A46 in alpha-synucleinopathies.
Journal: medRxiv : the preprint server for health sciences
Published: February 06, 2026
Genome-wide association studies identify genetic determinants of synucleinopathy biomarkers.
Journal: medRxiv : the preprint server for health sciences
Published: January 08, 2026
Exploring MAPT-containing H1 and H2 haplotypes in Parkinson's disease across diverse populations.
Journal: medRxiv : the preprint server for health sciences
Published: December 31, 2025
Exploring MAPT-containing H1 and H2 haplotypes in Parkinson's disease across diverse populations.
Journal: NPJ Parkinson's disease
Published: November 24, 2025
Last Updated: 09/26/2026