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Lior Greenbaum

Showing results (71-80 of 103) with videos related to

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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.
European Journal of Medical Genetics|May 30, 2018
Increased yield of full GBA sequencing in Ashkenazi Jews with Parkinson's diseaseJennifer A Ruskey, Lior Greenbaum, Léanne Roncière, 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.
Journal of the Neurological Sciences|July 5, 2024
The yield of genetic workup for middle-aged and elderly patients with neurological disorders in a real-world settingNoga Lempel, Shahar Shelly, Odelia Chorin, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 24, 2020
Analysis of Heterozygous PRKN Variants and Copy-Number Variations in Parkinson's DiseaseEric Yu, Uladzislau Rudakou, Lynne Krohn, et al.
Neurobiology of Aging|November 26, 2020
Association study of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's diseasePrabhjyot Saini, Uladzislau Rudakou, Eric Yu, 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.
European Journal of Neurology|January 29, 2025
Hereditary Transthyretin Amyloidosis in Israel: Genetic Landscape and Clinical CharacteristicsAmir Dori, Odelia Chorin, Noa Ruhrman-Shahar, 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.
Pageof 11

Showing results (71-80 of 103) with videos related to

Sort By:
Pageof 11
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.
European Journal of Medical Genetics|May 30, 2018
Increased yield of full GBA sequencing in Ashkenazi Jews with Parkinson's diseaseJennifer A Ruskey, Lior Greenbaum, Léanne Roncière, 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.
Journal of the Neurological Sciences|July 5, 2024
The yield of genetic workup for middle-aged and elderly patients with neurological disorders in a real-world settingNoga Lempel, Shahar Shelly, Odelia Chorin, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 24, 2020
Analysis of Heterozygous PRKN Variants and Copy-Number Variations in Parkinson's DiseaseEric Yu, Uladzislau Rudakou, Lynne Krohn, et al.
Neurobiology of Aging|November 26, 2020
Association study of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's diseasePrabhjyot Saini, Uladzislau Rudakou, Eric Yu, 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.
European Journal of Neurology|January 29, 2025
Hereditary Transthyretin Amyloidosis in Israel: Genetic Landscape and Clinical CharacteristicsAmir Dori, Odelia Chorin, Noa Ruhrman-Shahar, 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.
Pageof 11