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Mike Nalls

Showing results (21-30 of 52) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|July 17, 2025
MEDICATION EXPOSURE AND NEURODEGENERATIVE DISEASE RISK ACROSS NATIONAL BIOBANKSKristin S Levine, Lana Sargent, Emma N Somerville, et al.
Neurology. Genetics|May 14, 2021
Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor SubtypesIsabel Alfradique-Dunham, Rami Al-Ouran, Rainer von Coelln, et al.
Biorxiv : the Preprint Server for Biology|July 9, 2025
Haplotype-Resolved DNA Methylation at the <i>APOE</i> Locus identifies Allele-Specific Epigenetic Signatures Relevant to Alzheimer's Disease RiskRylee M Genner, Melissa Meredith, Abraham Moller, et al.
NPJ Parkinson'S Disease|September 13, 2023
Author Correction: Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2)Lara M Lange, Micol Avenali, Melina Ellis, et al.
American Journal of Human Genetics|December 16, 2014
Meta-analysis of correlated traits via summary statistics from GWASs with an application in hypertensionXiaofeng Zhu, Tao Feng, Bamidele O Tayo, et al.
Plos One|May 19, 2017
Multiple modality biomarker prediction of cognitive impairment in prospectively followed de novo Parkinson diseaseChelsea Caspell-Garcia, Tanya Simuni, Duygu Tosun-Turgut, et al.
NPJ Parkinson'S Disease|June 27, 2023
Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2)Lara M Lange, Micol Avenali, Melina Ellis, et al.
Neurology. Genetics|June 11, 2025
Erratum: The Neurodegenerative Disease Knowledge Portal: Propelling Discovery Through the Sharing of Neurodegenerative Disease Genomic ResourcesAllison A Dilliott, Maria C Costanzo, Sara Bandres-Ciga, et al.
Medrxiv : the Preprint Server for Health Sciences|April 29, 2026
Bridging Genetics and Precision Medicine in Parkinson's Disease through GP2Kajsa Atterling Brolin, Lara M Lange, Emily Navarro-Jones, et al.
Research Square|October 7, 2024
The <i>LRRK2</i> p.L1795F variant causes Parkinson's disease in the European populationLara M Lange, Kristin Levine, Susan H Fox, et al.
Pageof 6

Showing results (21-30 of 52) with videos related to

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Pageof 6
Medrxiv : the Preprint Server for Health Sciences|July 17, 2025
MEDICATION EXPOSURE AND NEURODEGENERATIVE DISEASE RISK ACROSS NATIONAL BIOBANKSKristin S Levine, Lana Sargent, Emma N Somerville, et al.
Neurology. Genetics|May 14, 2021
Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor SubtypesIsabel Alfradique-Dunham, Rami Al-Ouran, Rainer von Coelln, et al.
Biorxiv : the Preprint Server for Biology|July 9, 2025
Haplotype-Resolved DNA Methylation at the <i>APOE</i> Locus identifies Allele-Specific Epigenetic Signatures Relevant to Alzheimer's Disease RiskRylee M Genner, Melissa Meredith, Abraham Moller, et al.
NPJ Parkinson'S Disease|September 13, 2023
Author Correction: Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2)Lara M Lange, Micol Avenali, Melina Ellis, et al.
American Journal of Human Genetics|December 16, 2014
Meta-analysis of correlated traits via summary statistics from GWASs with an application in hypertensionXiaofeng Zhu, Tao Feng, Bamidele O Tayo, et al.
Plos One|May 19, 2017
Multiple modality biomarker prediction of cognitive impairment in prospectively followed de novo Parkinson diseaseChelsea Caspell-Garcia, Tanya Simuni, Duygu Tosun-Turgut, et al.
NPJ Parkinson'S Disease|June 27, 2023
Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2)Lara M Lange, Micol Avenali, Melina Ellis, et al.
Neurology. Genetics|June 11, 2025
Erratum: The Neurodegenerative Disease Knowledge Portal: Propelling Discovery Through the Sharing of Neurodegenerative Disease Genomic ResourcesAllison A Dilliott, Maria C Costanzo, Sara Bandres-Ciga, et al.
Medrxiv : the Preprint Server for Health Sciences|April 29, 2026
Bridging Genetics and Precision Medicine in Parkinson's Disease through GP2Kajsa Atterling Brolin, Lara M Lange, Emily Navarro-Jones, et al.
Research Square|October 7, 2024
The <i>LRRK2</i> p.L1795F variant causes Parkinson's disease in the European populationLara M Lange, Kristin Levine, Susan H Fox, et al.
Pageof 6