Accelerating Medicines Partnership: Parkinson's Disease. Genetic Resource

Background Whole‐genome sequencing data are available from several large studies across a variety of diseases and traits. However, massive storage and computation resources are required to use these data, and to achieve sufficient power for discoveries, harmonization of multiple cohorts is critical....

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Vydáno v:	Movement disorders Ročník 36; číslo 8; s. 1795 - 1804
Hlavní autoři:	Iwaki, Hirotaka, Leonard, Hampton L., Makarious, Mary B., Bookman, Matt, Landin, Barry, Vismer, David, Casey, Bradford, Gibbs, J. Raphael, Hernandez, Dena G., Blauwendraat, Cornelis, Vitale, Daniel, Song, Yeajin, Kumar, Dinesh, Dalgard, Clifton L., Sadeghi, Mahdiar, Dong, Xianjun, Misquitta, Leonie, Scholz, Sonja W., Scherzer, Clemens R., Nalls, Mike A., Biswas, Shameek, Singleton, Andrew B.
Médium:	Journal Article
Jazyk:	angličtina
Vydáno:	Hoboken, USA John Wiley & Sons, Inc 01.08.2021 Wiley Subscription Services, Inc
Témata:	clinical Cohort Studies genetics Genomes Genotyping Humans LRRK2 protein Movement disorders Mutation Neurodegenerative diseases open science Parkinson Disease - drug therapy Parkinson Disease - genetics Parkinson's disease Polygenic inheritance Population studies Regular Issue Whole genome sequencing United States > US open science clinical Parkinson's disease genetics
ISSN:	0885-3185, 1531-8257, 1531-8257
On-line přístup:	Získat plný text
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