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Defining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2).

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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.authorMartinez-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.authorHernandez, 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.date.accessioned2024-10-25T18:40:02Z
dc.date.available2024-10-25T18:40:02Z
dc.date.issued2023-09-12
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.
dc.description.noteChristiane Zweier is part of the Collaborators: Global Parkinson’s Genetic Program (GP2)
dc.identifier.doi10.48350/189662
dc.identifier.pmid37699923
dc.identifier.publisherDOI10.1038/s41531-023-00533-w
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/171882
dc.language.isoen
dc.publisherNature Publishing Group
dc.relation.ispartofNPJ Parkinson's disease
dc.relation.issn2373-8057
dc.relation.organizationClinic of Human Genetics
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleDefining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2).
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issue1
oaire.citation.startPage131
oaire.citation.volume9
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unibe.date.licenseChanged2024-01-04 11:02:29
unibe.description.ispublishedpub
unibe.eprints.legacyId189662
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unibe.subtype.articlejournal

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