2026-04-29T02:55:44Zhttps://riubu.ubu.es/oai/requestoai:riubu.ubu.es:10259/88512024-03-20T01:05:14Zcom_10259_4219com_10259_5086com_10259_2604col_10259_4220
Repositorio Institucional de la Universidad de Burgos
author
Towns, Clodagh
author
Richer, Madeleine
author
Jasaityte, Simona
author
Stafford, Eleanor J.
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Joubert, Julie
author
Antar, Tarek
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Martínez Carrasco, Alejandro
author
Makarious, Mary B.
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Casey, Bradford
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Vitale, Dan
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Levine, Kristin
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Leonard, Hampton
author
Pantazis, Caroline B.
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Screven, Laurel A.
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Hernández, Dena G.
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Wegel, Claire E.
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Solle, Justin
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Nalls, Mike A.
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Blauwendraat, Cornelis
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Singleton, Andrew B.
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Tan, Manuela M. X.
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Iwaki, Hirotaka
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Morris, Huw R.
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Cubo Delgado, Esther
author
Global Parkinson's Genetics Program
2024-03-19T12:40:06Z
2024-03-19T12:40:06Z
2023-09
http://hdl.handle.net/10259/8851
10.1038/s41531-023-00533-w
2373-8057
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.
eng
Atribución 4.0 Internacional
Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)
info:eu-repo/semantics/article
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URL
https://riubu.ubu.es/bitstream/10259/8851/1/Towns-npjpd_2023.pdf
File
MD5
19acf53fe81bc49d5ee62621f5579fc3
1385839
application/pdf
Towns-npjpd_2023.pdf