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

Towns, Clodagh; Richer, Madeleine; Jasaityte, Simona; Stafford, Eleanor J; Joubert, Julie; Antar, Tarek; Martinez-Carrasco, Alejandro; ... Global Parkinson’s Genetics Program (GP2); + view all (2023) Defining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2). npj Parkinson's Disease , 9 , Article 131. 10.1038/s41531-023-00533-w. Green open access

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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.

Type: Article
Title: Defining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2)
Location: United States
Open access status: An open access version is available from UCL Discovery
DOI: 10.1038/s41531-023-00533-w
Publisher version: https://doi.org/10.1038/s41531-023-00533-w
Language: English
Additional information: This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
Keywords: Clinical genetics, Cognitive ageing, Parkinson's disease
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Clinical and Movement Neurosciences
URI: https://discovery.ucl.ac.uk/id/eprint/10177271
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