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Mina Ryten

Showing results (151-160 of 176) with videos related to

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Annals of Neurology|January 25, 2023
Genome-Wide Analysis of Structural Variants in Parkinson DiseaseKimberley J Billingsley, Jinhui Ding, Pilar Alvarez Jerez, et al.
Nature Structural & Molecular Biology|December 12, 2024
African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in GBA1Pilar Álvarez Jerez, Peter Wild Crea, Daniel M Ramos, et al.
NPJ Parkinson'S Disease|June 20, 2025
A community-led initiative to de-risk and advance Parkinson's disease therapeutic targetsAlexandra Vaiana, Jonathan Behr, Ryan Birol, et al.
Neuron|November 26, 2020
Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral SclerosisRamita Dewan, Ruth Chia, Jinhui Ding, et al.
Nature Communications|December 5, 2022
Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effectsLynne Krohn, Karl Heilbron, Cornelis Blauwendraat, et al.
Nature|December 17, 2013
Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's diseaseCarlos Cruchaga, Celeste M Karch, Sheng Chih Jin, et al.
Cell Genomics|June 30, 2023
Genome-wide structural variant analysis identifies risk loci for non-Alzheimer's dementiasKarri Kaivola, Ruth Chia, Jinhui Ding, et al.
Nature|February 26, 2025
Rare disease gene association discovery in the 100,000 Genomes ProjectValentina Cipriani, Letizia Vestito, Emma F Magavern, et al.
Medrxiv : the Preprint Server for Health Sciences|January 10, 2024
Rare disease gene association discovery from burden analysis of the 100,000 Genomes Project dataValentina Cipriani, Letizia Vestito, Emma F Magavern, et al.
Neuron|September 28, 2011
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTDAlan E Renton, Elisa Majounie, Adrian Waite, et al.
Pageof 18

Showing results (151-160 of 176) with videos related to

Sort By:
Pageof 18
Annals of Neurology|January 25, 2023
Genome-Wide Analysis of Structural Variants in Parkinson DiseaseKimberley J Billingsley, Jinhui Ding, Pilar Alvarez Jerez, et al.
Nature Structural & Molecular Biology|December 12, 2024
African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in GBA1Pilar Álvarez Jerez, Peter Wild Crea, Daniel M Ramos, et al.
NPJ Parkinson'S Disease|June 20, 2025
A community-led initiative to de-risk and advance Parkinson's disease therapeutic targetsAlexandra Vaiana, Jonathan Behr, Ryan Birol, et al.
Neuron|November 26, 2020
Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral SclerosisRamita Dewan, Ruth Chia, Jinhui Ding, et al.
Nature Communications|December 5, 2022
Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effectsLynne Krohn, Karl Heilbron, Cornelis Blauwendraat, et al.
Nature|December 17, 2013
Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's diseaseCarlos Cruchaga, Celeste M Karch, Sheng Chih Jin, et al.
Cell Genomics|June 30, 2023
Genome-wide structural variant analysis identifies risk loci for non-Alzheimer's dementiasKarri Kaivola, Ruth Chia, Jinhui Ding, et al.
Nature|February 26, 2025
Rare disease gene association discovery in the 100,000 Genomes ProjectValentina Cipriani, Letizia Vestito, Emma F Magavern, et al.
Medrxiv : the Preprint Server for Health Sciences|January 10, 2024
Rare disease gene association discovery from burden analysis of the 100,000 Genomes Project dataValentina Cipriani, Letizia Vestito, Emma F Magavern, et al.
Neuron|September 28, 2011
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTDAlan E Renton, Elisa Majounie, Adrian Waite, et al.
Pageof 18