Towns, Clodagh; Richer, Madeleine; Jasaityte, Simona; Stafford, Eleanor J; Joubert, Julie; Antar, Tarek; Martinez-Carrasco, Alejandro; Makarious, Mary B; Casey, Bradford; Vitale, Dan; Levine, Kristin; Leonard, Hampton; Pantazis, Caroline B; Screven, Laurel A; Hernandez, Dena G; Wegel, Claire E; Solle, Justin; Nalls, Mike A; Blauwendraat, Cornelis; Singleton, Andrew B; ... (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. Nature Publishing Group 10.1038/s41531-023-00533-w
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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: |
Journal Article (Original Article) |
|---|---|
Division/Institute: |
04 Faculty of Medicine > Department of Gynaecology, Paediatrics and Endocrinology (DFKE) > Clinic of Human Genetics |
Subjects: |
600 Technology > 610 Medicine & health |
ISSN: |
2373-8057 |
Publisher: |
Nature Publishing Group |
Language: |
English |
Submitter: |
André Schaller |
Date Deposited: |
04 Jan 2024 11:54 |
Last Modified: |
04 Jan 2024 12:02 |
Publisher DOI: |
10.1038/s41531-023-00533-w |
PubMed ID: |
37699923 |
Additional Information: |
Christiane Zweier is part of the Collaborators: Global Parkinson’s Genetic Program (GP2) |
BORIS DOI: |
10.48350/189662 |
URI: |
https://boris.unibe.ch/id/eprint/189662 |
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