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

Global Parkinson’s Genetics Program (GP2), Huw R. Morris*

*Corresponding author for this work

Research output: Contribution to journalArticleResearchpeer-review

4 Citations (Scopus)

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.

Original languageEnglish
Article number131
Journalnpj Parkinson's Disease
Volume9
Issue number1
DOIs
Publication statusPublished - 12 Sept 2023
Externally publishedYes

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