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Sitki Cem Parlar

Showing results (1-10 of 12) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|November 15, 2025
GBA1 Variants with Unknown Classification Are Modest Contributors to Parkinson's Disease SusceptibilitySitki Cem Parlar, Yoomin Lee, Ziv Gan-Or
Movement Disorders : Official Journal of the Movement Disorder Society|January 4, 2023
Classification of GBA1 Variants in Parkinson's Disease: The GBA1-PD BrowserSitki Cem Parlar, Francis P Grenn, Jonggeol Jeffrey Kim, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Lack of genetic evidence for a role of SLC25A46 in alpha-synucleinopathiesHan Yu, Sitki Cem Parlar, Konstantin Senkevich, et al.
Medrxiv : the Preprint Server for Health Sciences|June 10, 2024
Are rare heterozygous <i>SYNJ1</i> variants associated with Parkinson's disease?Konstantin Senkevich, Sitki Cem Parlar, Cloe Chantereault, et al.
NPJ Parkinson'S Disease|October 25, 2024
Are rare heterozygous SYNJ1 variants associated with Parkinson's disease?Konstantin Senkevich, Sitki Cem Parlar, Cloe Chantereault, et al.
NPJ Parkinson'S Disease|April 29, 2025
LRRK2 rare-variant per-domain genetic burden in Parkinson's Disease: association confined to the kinase domainSitki Cem Parlar, Konstantin Senkevich, Eric Yu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 11, 2026
Rare-Variant Burden across Lysosomal Genes Implicates Sialylation and Ganglioside Metabolism in Parkinson's DiseaseKonstantin Senkevich, Sitki Cem Parlar, Cloe Chantereault, et al.
Medrxiv : the Preprint Server for Health Sciences|February 27, 2026
Rare-variant burden across lysosomal genes implicates sialylation and ganglioside metabolism in Parkinson's diseaseKonstantin Senkevich, Sitki Cem Parlar, Cloe Chantereault, et al.
HGG Advances|December 11, 2025
Lack of association between G6PD variants and Parkinson diseaseLeah V Chifamba, Sitki Cem Parlar, Lang Liu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 23, 2026
The GBA1 p.E427K (p.E388K) Variant Is a Risk Factor for Synucleinopathies: A Meta-AnalysisLeah V Chifamba, Sitki Cem Parlar, Emma N Somerville, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Movement Disorders : Official Journal of the Movement Disorder Society|November 15, 2025
GBA1 Variants with Unknown Classification Are Modest Contributors to Parkinson's Disease SusceptibilitySitki Cem Parlar, Yoomin Lee, Ziv Gan-Or
Movement Disorders : Official Journal of the Movement Disorder Society|January 4, 2023
Classification of GBA1 Variants in Parkinson's Disease: The GBA1-PD BrowserSitki Cem Parlar, Francis P Grenn, Jonggeol Jeffrey Kim, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Lack of genetic evidence for a role of SLC25A46 in alpha-synucleinopathiesHan Yu, Sitki Cem Parlar, Konstantin Senkevich, et al.
Medrxiv : the Preprint Server for Health Sciences|June 10, 2024
Are rare heterozygous <i>SYNJ1</i> variants associated with Parkinson's disease?Konstantin Senkevich, Sitki Cem Parlar, Cloe Chantereault, et al.
NPJ Parkinson'S Disease|October 25, 2024
Are rare heterozygous SYNJ1 variants associated with Parkinson's disease?Konstantin Senkevich, Sitki Cem Parlar, Cloe Chantereault, et al.
NPJ Parkinson'S Disease|April 29, 2025
LRRK2 rare-variant per-domain genetic burden in Parkinson's Disease: association confined to the kinase domainSitki Cem Parlar, Konstantin Senkevich, Eric Yu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 11, 2026
Rare-Variant Burden across Lysosomal Genes Implicates Sialylation and Ganglioside Metabolism in Parkinson's DiseaseKonstantin Senkevich, Sitki Cem Parlar, Cloe Chantereault, et al.
Medrxiv : the Preprint Server for Health Sciences|February 27, 2026
Rare-variant burden across lysosomal genes implicates sialylation and ganglioside metabolism in Parkinson's diseaseKonstantin Senkevich, Sitki Cem Parlar, Cloe Chantereault, et al.
HGG Advances|December 11, 2025
Lack of association between G6PD variants and Parkinson diseaseLeah V Chifamba, Sitki Cem Parlar, Lang Liu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 23, 2026
The GBA1 p.E427K (p.E388K) Variant Is a Risk Factor for Synucleinopathies: A Meta-AnalysisLeah V Chifamba, Sitki Cem Parlar, Emma N Somerville, et al.
Pageof 2