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J Raphael

Showing results (441-450 of 488) with videos related to

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The Lancet. Neurology|August 15, 2015
Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling studyMike A Nalls, Cory Y McLean, Jacqueline Rick, et al.
Neurobiology of Aging|June 13, 2017
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseasesCornelis Blauwendraat, Faraz Faghri, Lasse Pihlstrom, et al.
Annals of Neurology|January 25, 2023
Genome-Wide Analysis of Structural Variants in Parkinson DiseaseKimberley J Billingsley, Jinhui Ding, Pilar Alvarez Jerez, et al.
Biorxiv : the Preprint Server for Biology|January 7, 2025
Long-read sequencing of hundreds of diverse brains provides insight into the impact of structural variation on gene expression and DNA methylationKimberley J Billingsley, Melissa Meredith, Kensuke Daida, et al.
Annals of Neurology|November 7, 2025
Association between Human Leukocyte Antigen Alleles and Neuropathological Outcomes in Lewy Body DiseaseMarios Gavrielatos, Michael G Heckman, Alexandra I Soto-Beasley, et al.
Nature Neuroscience|April 2, 2014
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosisJanel O Johnson, Erik P Pioro, Ashley Boehringer, et al.
Cell Genomics|March 23, 2023
The Foundational Data Initiative for Parkinson Disease: Enabling efficient translation from genetic maps to mechanismElisangela Bressan, Xylena Reed, Vikas Bansal, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 9, 2019
Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and α-synuclein mechanismsCornelis Blauwendraat, Karl Heilbron, Costanza L Vallerga, et al.
Neurobiology of Aging|January 21, 2014
Missense variant in TREML2 protects against Alzheimer's diseaseBruno A Benitez, Sheng Chih Jin, Rita Guerreiro, et al.
Blood|November 8, 2019
Therapy-induced mutations drive the genomic landscape of relapsed acute lymphoblastic leukemiaBenshang Li, Samuel W Brady, Xiaotu Ma, et al.
Pageof 49

Showing results (441-450 of 488) with videos related to

Sort By:
Pageof 49
The Lancet. Neurology|August 15, 2015
Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling studyMike A Nalls, Cory Y McLean, Jacqueline Rick, et al.
Neurobiology of Aging|June 13, 2017
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseasesCornelis Blauwendraat, Faraz Faghri, Lasse Pihlstrom, et al.
Annals of Neurology|January 25, 2023
Genome-Wide Analysis of Structural Variants in Parkinson DiseaseKimberley J Billingsley, Jinhui Ding, Pilar Alvarez Jerez, et al.
Biorxiv : the Preprint Server for Biology|January 7, 2025
Long-read sequencing of hundreds of diverse brains provides insight into the impact of structural variation on gene expression and DNA methylationKimberley J Billingsley, Melissa Meredith, Kensuke Daida, et al.
Annals of Neurology|November 7, 2025
Association between Human Leukocyte Antigen Alleles and Neuropathological Outcomes in Lewy Body DiseaseMarios Gavrielatos, Michael G Heckman, Alexandra I Soto-Beasley, et al.
Nature Neuroscience|April 2, 2014
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosisJanel O Johnson, Erik P Pioro, Ashley Boehringer, et al.
Cell Genomics|March 23, 2023
The Foundational Data Initiative for Parkinson Disease: Enabling efficient translation from genetic maps to mechanismElisangela Bressan, Xylena Reed, Vikas Bansal, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 9, 2019
Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and α-synuclein mechanismsCornelis Blauwendraat, Karl Heilbron, Costanza L Vallerga, et al.
Neurobiology of Aging|January 21, 2014
Missense variant in TREML2 protects against Alzheimer's diseaseBruno A Benitez, Sheng Chih Jin, Rita Guerreiro, et al.
Blood|November 8, 2019
Therapy-induced mutations drive the genomic landscape of relapsed acute lymphoblastic leukemiaBenshang Li, Samuel W Brady, Xiaotu Ma, et al.
Pageof 49