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Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)
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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10497609/ https://www.ncbi.nlm.nih.gov/pubmed/37699923 http://dx.doi.org/10.1038/s41531-023-00533-w |
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author | Towns, Clodagh Richer, Madeleine Jasaityte, Simona Stafford, Eleanor J. Joubert, Julie Antar, Tarek Martinez-Carrasco, Alejandro Makarious, Mary B. Casey, Bradford Vitale, Dan Levine, Kristin Leonard, Hampton Pantazis, Caroline B. Screven, Laurel A. Hernandez, Dena G. Wegel, Claire E. Solle, Justin Nalls, Mike A. Blauwendraat, Cornelis Singleton, Andrew B. Tan, Manuela M. X. Iwaki, Hirotaka Morris, Huw R. |
author_facet | Towns, Clodagh Richer, Madeleine Jasaityte, Simona Stafford, Eleanor J. Joubert, Julie Antar, Tarek Martinez-Carrasco, Alejandro Makarious, Mary B. Casey, Bradford Vitale, Dan Levine, Kristin Leonard, Hampton Pantazis, Caroline B. Screven, Laurel A. Hernandez, Dena G. Wegel, Claire E. Solle, Justin Nalls, Mike A. Blauwendraat, Cornelis Singleton, Andrew B. Tan, Manuela M. X. Iwaki, Hirotaka Morris, Huw R. |
author_sort | Towns, Clodagh |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-10497609 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104976092023-09-14 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 Makarious, Mary B. Casey, Bradford Vitale, Dan Levine, Kristin Leonard, Hampton Pantazis, Caroline B. Screven, Laurel A. Hernandez, Dena G. Wegel, Claire E. Solle, Justin Nalls, Mike A. Blauwendraat, Cornelis Singleton, Andrew B. Tan, Manuela M. X. Iwaki, Hirotaka Morris, Huw R. NPJ Parkinsons Dis Brief Communication 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. Nature Publishing Group UK 2023-09-12 /pmc/articles/PMC10497609/ /pubmed/37699923 http://dx.doi.org/10.1038/s41531-023-00533-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Brief Communication Towns, Clodagh Richer, Madeleine Jasaityte, Simona Stafford, Eleanor J. Joubert, Julie Antar, Tarek Martinez-Carrasco, Alejandro Makarious, Mary B. Casey, Bradford Vitale, Dan Levine, Kristin Leonard, Hampton Pantazis, Caroline B. Screven, Laurel A. Hernandez, Dena G. Wegel, Claire E. Solle, Justin Nalls, Mike A. Blauwendraat, Cornelis Singleton, Andrew B. Tan, Manuela M. X. Iwaki, Hirotaka Morris, Huw R. Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2) |
title | Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2) |
title_full | Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2) |
title_fullStr | Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2) |
title_full_unstemmed | Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2) |
title_short | Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2) |
title_sort | defining the causes of sporadic parkinson’s disease in the global parkinson’s genetics program (gp2) |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10497609/ https://www.ncbi.nlm.nih.gov/pubmed/37699923 http://dx.doi.org/10.1038/s41531-023-00533-w |
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