Towns, Clodagh, Richer, Madeleine, Jasaityte, Simona, Stafford, Eleanor J, Joubert, Julie, Antar, Tarek, Martinez-Carrasco, Alejandro, Makarious, Mary B, Casey, Bradford, Vitale, Dan et al (show 14 more authors)
(2023)
Defining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2).
NPJ Parkinson's disease, 9 (1).
p. 131.
Abstract
The Global Parkinson's Genetics Program (GP2) will genotype over 150,000 participants from around the world, and integrate genetic and clinical data for use in large-scale analyses to dramatically expand our understanding of the genetic architecture of PD. This report details the workflow for cohort integration into the complex arm of GP2, and together with our outline of the monogenic hub in a companion paper, provides a generalizable blueprint for establishing large scale collaborative research consortia.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | Global Parkinson’s Genetics Program (GP2) |
| Divisions: | Faculty of Health and Life Sciences Faculty of Health and Life Sciences > Institute of Systems, Molecular and Integrative Biology |
| Depositing User: | Symplectic Admin |
| Date Deposited: | 26 Mar 2024 10:26 |
| Last Modified: | 26 Mar 2024 15:29 |
| DOI: | 10.1038/s41531-023-00533-w |
| Open Access URL: | https://doi.org/10.1038/s41531-023-00533-w |
| Related URLs: | |
| URI: | https://livrepository.liverpool.ac.uk/id/eprint/3179947 |
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