https://scholars.lib.ntu.edu.tw/handle/123456789/639057
標題: | Defining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2) | 作者: | 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 CHIN-HSIEN LIN |
公開日期: | 12-九月-2023 | 卷: | 9 | 期: | 1 | 起(迄)頁: | 131 | 來源出版物: | NPJ Parkinson's disease | 摘要: | 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. |
URI: | https://scholars.lib.ntu.edu.tw/handle/123456789/639057 | ISSN: | 2373-8057 | DOI: | 10.1038/s41531-023-00533-w |
顯示於: | 醫學院附設醫院 (臺大醫院) |
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