Defining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2).
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BORIS DOI
Date of Publication
September 12, 2023
Publication Type
Article
Contributor
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 | |
Tan, Manuela M X | |
Iwaki, Hirotaka | |
Morris, Huw R |
Subject(s)
Series
NPJ Parkinson's disease
ISSN or ISBN (if monograph)
2373-8057
Publisher
Nature Publishing Group
Language
English
Publisher DOI
PubMed ID
37699923
Description
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.
File(s)
| File | File Type | Format | Size | License | Publisher/Copright statement | Content | |
|---|---|---|---|---|---|---|---|
| s41531-023-00533-w.pdf | text | Adobe PDF | 1.32 MB | published |