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dc.contributor.authorTowns, Clodagh
dc.contributor.authorRicher, Madeleine
dc.contributor.authorJasaityte, Simona
dc.contributor.authorStafford, Eleanor J.
dc.contributor.authorJoubert, Julie
dc.contributor.authorAntar, Tarek
dc.contributor.authorMartínez Carrasco, Alejandro
dc.contributor.authorMakarious, Mary B.
dc.contributor.authorCasey, Bradford
dc.contributor.authorVitale, Dan
dc.contributor.authorLevine, Kristin
dc.contributor.authorLeonard, Hampton
dc.contributor.authorPantazis, Caroline B.
dc.contributor.authorScreven, Laurel A.
dc.contributor.authorHernández, Dena G.
dc.contributor.authorWegel, Claire E.
dc.contributor.authorSolle, Justin
dc.contributor.authorNalls, Mike A.
dc.contributor.authorBlauwendraat, Cornelis
dc.contributor.authorSingleton, Andrew B.
dc.contributor.authorTan, Manuela M. X.
dc.contributor.authorIwaki, Hirotaka
dc.contributor.authorMorris, Huw R.
dc.contributor.authorCubo Delgado, Esther 
dc.contributor.authorGlobal Parkinson's Genetics Program
dc.date.accessioned2024-03-19T12:40:06Z
dc.date.available2024-03-19T12:40:06Z
dc.date.issued2023-09
dc.identifier.urihttp://hdl.handle.net/10259/8851
dc.description.abstractThe 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.mimetypeapplication/pdf
dc.language.isoenges
dc.publisherSpringer Natureen
dc.relation.ispartofnpj Parkinson's Disease. 2023, V. 9, n. 1en
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.otherSistema nervioso-Enfermedadeses
dc.subject.otherNervous system-Diseasesen
dc.subject.otherMedicinaes
dc.subject.otherMedicineen
dc.subject.otherNeurologíaes
dc.subject.otherNeurologyen
dc.titleDefining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)en
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.relation.publisherversionhttps://doi.org/10.1038/s41531-023-00533-wes
dc.identifier.doi10.1038/s41531-023-00533-w
dc.identifier.essn2373-8057
dc.journal.titlenpj Parkinson's Diseaseen
dc.volume.number9es
dc.issue.number1es
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones


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