Sitki C. Parlar

Montreal, QC, Canada

Last Updated: 09/26/2026

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Found 14 publications

Lack of genetic evidence for a role of SLC25A46 in alpha-synucleinopathies.

Lack of genetic evidence for a role of SLC25A46 in alpha-synucleinopathies.

Journal: Journal of Parkinson's disease

Published: August 06, 2026

Rare-Variant Burden Analysis of Dystonia Genes in Parkinson's Disease.

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.

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.

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.

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.

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.

Lack of genetic evidence for a role of SLC25A46 in alpha-synucleinopathies.

Journal: medRxiv : the preprint server for health sciences

Published: February 06, 2026

GBA1 Variants with Unknown Classification Are Modest Contributors to Parkinson's Disease Susceptibility.

GBA1 Variants with Unknown Classification Are Modest Contributors to Parkinson's Disease Susceptibility.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: September 05, 2025

Lack of association between G6PD variants and Parkinson disease.

Lack of association between G6PD variants and Parkinson disease.

Journal: HGG advances

Published: May 08, 2025

Genetic testing for Parkinson's disease in Israel: Insights from the Rostock Parkinson's Disease (ROPAD) study.

Genetic testing for Parkinson's disease in Israel: Insights from the Rostock Parkinson's Disease (ROPAD) study.

Journal: Parkinsonism & related disorders

Published: March 09, 2025

LRRK2 rare-variant per-domain genetic burden in Parkinson's Disease: association confined to the kinase domain.

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

Are rare heterozygous SYNJ1 variants associated with Parkinson's disease?

Are rare heterozygous SYNJ1 variants associated with Parkinson's disease?

Journal: medRxiv : the preprint server for health sciences

Published: June 10, 2024

Showing 1-12 of 14

Last Updated: 09/26/2026