Cited 9 times in

Defining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2)

Authors
 Clodagh Towns  ;  Madeleine Richer  ;  Simona Jasaityte  ;  Eleanor J Stafford  ;  Julie Joubert  ;  Tarek Antar  ;  Alejandro Martinez-Carrasco  ;  Mary B Makarious  ;  Bradford Casey  ;  Dan Vitale  ;  Kristin Levine  ;  Hampton Leonard  ;  Caroline B Pantazis  ;  Laurel A Screven  ;  Dena G Hernandez  ;  Claire E Wegel  ;  Justin Solle  ;  Mike A Nalls  ;  Cornelis Blauwendraat  ;  Andrew B Singleton  ;  Manuela M X Tan  ;  Hirotaka Iwaki  ;  Huw R Morris  ;  Global Parkinson’s Genetics Program (GP2) 
Citation
 NPJ PARKINSONS DISEASE, Vol.9(1) : 131, 2023-12 
Journal Title
NPJ PARKINSONS DISEASE
Issue Date
2023-12
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. © 2023, Springer Nature Limited.
Files in This Item:
T999202451.pdf Download
DOI
10.1038/s41531-023-00533-w
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Neurology (신경과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Yun Joong(김윤중) ORCID logo https://orcid.org/0000-0002-2956-1552
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/198251
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