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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.author김윤중-
dc.date.accessioned2024-03-22T05:51:17Z-
dc.date.available2024-03-22T05:51:17Z-
dc.date.issued2023-12-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/198251-
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. © 2023, Springer Nature Limited.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherNature Publishing Group-
dc.relation.isPartOfNPJ PARKINSONS DISEASE-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleDefining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2)-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Neurology (신경과학교실)-
dc.contributor.googleauthorClodagh Towns-
dc.contributor.googleauthorMadeleine Richer-
dc.contributor.googleauthorSimona Jasaityte-
dc.contributor.googleauthorEleanor J Stafford-
dc.contributor.googleauthorJulie Joubert-
dc.contributor.googleauthorTarek Antar-
dc.contributor.googleauthorAlejandro Martinez-Carrasco-
dc.contributor.googleauthorMary B Makarious-
dc.contributor.googleauthorBradford Casey-
dc.contributor.googleauthorDan Vitale-
dc.contributor.googleauthorKristin Levine-
dc.contributor.googleauthorHampton Leonard-
dc.contributor.googleauthorCaroline B Pantazis-
dc.contributor.googleauthorLaurel A Screven-
dc.contributor.googleauthorDena G Hernandez-
dc.contributor.googleauthorClaire E Wegel-
dc.contributor.googleauthorJustin Solle-
dc.contributor.googleauthorMike A Nalls-
dc.contributor.googleauthorCornelis Blauwendraat-
dc.contributor.googleauthorAndrew B Singleton-
dc.contributor.googleauthorManuela M X Tan-
dc.contributor.googleauthorHirotaka Iwaki-
dc.contributor.googleauthorHuw R Morris-
dc.contributor.googleauthorGlobal Parkinson’s Genetics Program (GP2)-
dc.identifier.doi10.1038/s41531-023-00533-w-
dc.contributor.localIdA00796-
dc.relation.journalcodeJ04109-
dc.identifier.eissn2373-8057-
dc.identifier.pmid37699923-
dc.contributor.alternativeNameKim, Yun Joong-
dc.contributor.affiliatedAuthor김윤중-
dc.citation.volume9-
dc.citation.number1-
dc.citation.startPage131-
dc.identifier.bibliographicCitationNPJ PARKINSONS DISEASE, Vol.9(1) : 131, 2023-12-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Neurology (신경과학교실) > 1. Journal Papers
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