Lange, Lara and Avenali, Micol and Ellis, Melina and Illarionova, Anastasia J. and Sarmiento, Ignacio Keller and Tan, Ai-Huey and Madoev, Harutyun and Galandra, Caterina and Junker, Johanna and Roopnarain, Karisha and Solle, Justin and Wegel, Claire and Fang, Zih-Hua and Heutink, Peter R. and Kumar, Kishore and Lim, Shen-Yang and Valente, Enza Maria and Nalls, Mike and Blauwendraat, Cornelis and Singleton, Andrew and Mencacci, Niccolo and Lohmann, Katja and Klein, Christine and Program, Global Parkinsons Genetic (2023) Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2). NPJ Parkinson's Disease, 9 (1). ISSN 2373-8057, DOI https://doi.org/10.1038/s41531-023-00526-9.
Full text not available from this repository.Abstract
The Monogenic Network of the Global Parkinson's Genetics Program (GP2) aims to create an efficient infrastructure to accelerate the identification of novel genetic causes of Parkinson's disease (PD) and to improve our understanding of already identified genetic causes, such as reduced penetrance and variable clinical expressivity of known disease-causing variants. We aim to perform short- and long-read whole-genome sequencing for up to 10,000 patients with parkinsonism. Important features of this project are global involvement and focusing on historically underrepresented populations.
| Item Type: | Article |
|---|---|
| Funders: | Aligning Science Across Parkinson's (ASAP), Michael J Fox Foundation, Aligning Science Against Parkinson's (ASAP) initiative |
| Uncontrolled Keywords: | Monogenic Network; Global Parkinson's Genetics Program (GP2); Parkinson's disease (PD) |
| Subjects: | R Medicine > RC Internal medicine > RC0321 Neuroscience. Biological psychiatry. Neuropsychiatry |
| Divisions: | Faculty of Medicine |
| Depositing User: | Ms. Juhaida Abd Rahim |
| Date Deposited: | 30 Oct 2025 08:00 |
| Last Modified: | 30 Oct 2025 08:00 |
| URI: | http://eprints.um.edu.my/id/eprint/48713 |
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