2026-04-29T00:13:06Zhttps://riubu.ubu.es/oai/request

oai:riubu.ubu.es:10259/88512024-03-20T01:05:14Zcom_10259_4219com_10259_5086com_10259_2604col_10259_4220

Towns, Clodagh Richer, Madeleine Jasaityte, Simona Stafford, Eleanor J. Joubert, Julie Antar, Tarek Martínez Carrasco, Alejandro Makarious, Mary B. Casey, Bradford Vitale, Dan Levine, Kristin Leonard, Hampton Pantazis, Caroline B. Screven, Laurel A. Hernández, Dena G. Wegel, Claire E. Solle, Justin Nalls, Mike A. Blauwendraat, Cornelis Singleton, Andrew B. Tan, Manuela M. X. Iwaki, Hirotaka Morris, Huw R. Cubo Delgado, Esther Global Parkinson's Genetics Program 2023-09 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. application/pdf http://hdl.handle.net/10259/8851 eng Springer Nature Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2) info:eu-repo/semantics/article TEXT RIUBU. Repositorio Institucional de la Universidad de Burgos Hispana