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

Towns, Clodagh; Richer, Madeleine; Joubert, Julie; Antar, Tarek; Levine, Kristin; Screven, Laurel A.; Wegel, Claire E.; Solle, Justin; Tan, Manuela M. X.; Global Parkinsons Genetics Program

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.

Más información

Título según WOS: ID WOS:001188490300001 Not found in local WOS DB
Título según SCOPUS: Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)
Título de la Revista: npj Parkinson's Disease
Volumen: 9
Número: 1
Editorial: Nature Research
Fecha de publicación: 2023
Idioma: English
DOI:

10.1038/s41531-023-00533-w

Notas: ISI, SCOPUS