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; Martínez Carrasco, Alejandro; Makarious, Mary B.; Casey, Bradford; Vitale, Dan; Levine, Kristin; Leonard, Hampton; Pantazis, Caroline B.; Screven, Laurel A.; Hernández, Dena G.; Wegel, Claire E.; Solle, Justin; Nalls, Mike A.; Blauwendraat, Cornelis; Singleton, Andrew B.; Tan, Manuela M. X.; Iwaki, Hirotaka; Morris, Huw R.; Cubo Delgado, Esther; Global Parkinson's Genetics Program

doi:10.1038/s41531-023-00533-w

dc.contributor.author	Towns, Clodagh
dc.contributor.author	Richer, Madeleine
dc.contributor.author	Jasaityte, Simona
dc.contributor.author	Stafford, Eleanor J.
dc.contributor.author	Joubert, Julie
dc.contributor.author	Antar, Tarek
dc.contributor.author	Martínez Carrasco, Alejandro
dc.contributor.author	Makarious, Mary B.
dc.contributor.author	Casey, Bradford
dc.contributor.author	Vitale, Dan
dc.contributor.author	Levine, Kristin
dc.contributor.author	Leonard, Hampton
dc.contributor.author	Pantazis, Caroline B.
dc.contributor.author	Screven, Laurel A.
dc.contributor.author	Hernández, Dena G.
dc.contributor.author	Wegel, Claire E.
dc.contributor.author	Solle, Justin
dc.contributor.author	Nalls, Mike A.
dc.contributor.author	Blauwendraat, Cornelis
dc.contributor.author	Singleton, Andrew B.
dc.contributor.author	Tan, Manuela M. X.
dc.contributor.author	Iwaki, Hirotaka
dc.contributor.author	Morris, Huw R.
dc.contributor.author	Cubo Delgado, Esther
dc.contributor.author	Global Parkinson's Genetics Program
dc.date.accessioned	2024-03-19T12:40:06Z
dc.date.available	2024-03-19T12:40:06Z
dc.date.issued	2023-09
dc.identifier.uri	http://hdl.handle.net/10259/8851
dc.description.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.	en
dc.format.mimetype	application/pdf
dc.language.iso	eng	es
dc.publisher	Springer Nature	en
dc.relation.ispartof	npj Parkinson's Disease. 2023, V. 9, n. 1	en
dc.rights	Atribución 4.0 Internacional	*
dc.rights.uri	http://creativecommons.org/licenses/by/4.0/	*
dc.subject.other	Sistema nervioso-Enfermedades	es
dc.subject.other	Nervous system-Diseases	en
dc.subject.other	Medicina	es
dc.subject.other	Medicine	en
dc.subject.other	Neurología	es
dc.subject.other	Neurology	en
dc.title	Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)	en
dc.type	info:eu-repo/semantics/article	es
dc.rights.accessRights	info:eu-repo/semantics/openAccess	es
dc.relation.publisherversion	https://doi.org/10.1038/s41531-023-00533-w	es
dc.identifier.doi	10.1038/s41531-023-00533-w
dc.identifier.essn	2373-8057
dc.journal.title	npj Parkinson's Disease	en
dc.volume.number	9	es
dc.issue.number	1	es
dc.type.hasVersion	info:eu-repo/semantics/publishedVersion	es

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