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00925njm 22002777a 4500 dc Towns, Clodagh author Richer, Madeleine author Jasaityte, Simona author Stafford, Eleanor J. author Joubert, Julie author Antar, Tarek author Martínez Carrasco, Alejandro author Makarious, Mary B. author Casey, Bradford author Vitale, Dan author Levine, Kristin author Leonard, Hampton author Pantazis, Caroline B. author Screven, Laurel A. author Hernández, Dena G. author Wegel, Claire E. author Solle, Justin author Nalls, Mike A. author Blauwendraat, Cornelis author Singleton, Andrew B. author Tan, Manuela M. X. author Iwaki, Hirotaka author Morris, Huw R. author Cubo Delgado, Esther author Global Parkinson's Genetics Program author 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. http://hdl.handle.net/10259/8851 10.1038/s41531-023-00533-w 2373-8057 Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)