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Dan Vitale

Showing results (21-30 of 50) with videos related to

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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.
Neurology. Genetics|February 25, 2025
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.
NPJ Parkinson'S Disease|September 12, 2023
Defining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2)Clodagh Towns, Madeleine Richer, Simona Jasaityte, et al.
Medrxiv : the Preprint Server for Health Sciences|June 10, 2024
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.
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.
NPJ Parkinson'S Disease|March 26, 2025
The LRRK2 p.L1795F variant causes Parkinson's disease in the European populationLara M Lange, Kristin Levine, Susan H Fox, et al.
Biorxiv : the Preprint Server for Biology|November 28, 2024
CNV-Finder: Streamlining Copy Number Variation DiscoveryNicole Kuznetsov, Kensuke Daida, Mary B Makarious, et al.
NPJ Parkinson'S Disease|April 2, 2022
Multi-modality machine learning predicting Parkinson's diseaseMary B Makarious, Hampton L Leonard, Dan Vitale, et al.
Medrxiv : the Preprint Server for Health Sciences|December 11, 2023
Insights into Ancestral Diversity in Parkinsons Disease Risk: A Comparative Assessment of Polygenic Risk ScoresPaula Saffie Awad, Mary B Makarious, Inas Elsayed, et al.
Pageof 5

Showing results (21-30 of 50) with videos related to

Sort By:
Pageof 5
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.
Neurology. Genetics|February 25, 2025
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.
NPJ Parkinson'S Disease|September 12, 2023
Defining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2)Clodagh Towns, Madeleine Richer, Simona Jasaityte, et al.
Medrxiv : the Preprint Server for Health Sciences|June 10, 2024
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.
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.
NPJ Parkinson'S Disease|March 26, 2025
The LRRK2 p.L1795F variant causes Parkinson's disease in the European populationLara M Lange, Kristin Levine, Susan H Fox, et al.
Biorxiv : the Preprint Server for Biology|November 28, 2024
CNV-Finder: Streamlining Copy Number Variation DiscoveryNicole Kuznetsov, Kensuke Daida, Mary B Makarious, et al.
NPJ Parkinson'S Disease|April 2, 2022
Multi-modality machine learning predicting Parkinson's diseaseMary B Makarious, Hampton L Leonard, Dan Vitale, et al.
Medrxiv : the Preprint Server for Health Sciences|December 11, 2023
Insights into Ancestral Diversity in Parkinsons Disease Risk: A Comparative Assessment of Polygenic Risk ScoresPaula Saffie Awad, Mary B Makarious, Inas Elsayed, et al.
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