Publication:
The Parkinson's Disease Genome-Wide Association Study Locus Browser.

dc.contributor.authorGrenn, Francis P
dc.contributor.authorKim, Jonggeol J
dc.contributor.authorMakarious, Mary B
dc.contributor.authorIwaki, Hirotaka
dc.contributor.authorIllarionova, Anastasia
dc.contributor.authorBrolin, Kajsa
dc.contributor.authorKluss, Jillian H
dc.contributor.authorSchumacher-Schuh, Artur F
dc.contributor.authorLeonard, Hampton
dc.contributor.authorFaghri, Faraz
dc.contributor.authorBillingsley, Kimberley
dc.contributor.authorKrohn, Lynne
dc.contributor.authorHall, Ashley
dc.contributor.authorDiez-Fairen, Monica
dc.contributor.authorPeriñán, Maria Teresa
dc.contributor.authorFoo, Jia Nee
dc.contributor.authorSandor, Cynthia
dc.contributor.authorWebber, Caleb
dc.contributor.authorFiske, Brian K
dc.contributor.authorGibbs, J Raphael
dc.contributor.authorNalls, Mike A
dc.contributor.authorSingleton, Andrew B
dc.contributor.authorBandres-Ciga, Sara
dc.contributor.authorReed, Xylena
dc.contributor.authorBlauwendraat, Cornelis
dc.contributor.authorInternational Parkinson's Disease Genomics Consortium (IPDGC)
dc.date.accessioned2023-02-09T09:39:35Z
dc.date.available2023-02-09T09:39:35Z
dc.date.issued2020-08-31
dc.description.abstractParkinson's disease (PD) is a neurodegenerative disease with an often complex component identifiable by genome-wide association studies. The most recent large-scale PD genome-wide association studies have identified more than 90 independent risk variants for PD risk and progression across more than 80 genomic regions. One major challenge in current genomics is the identification of the causal gene(s) and variant(s) at each genome-wide association study locus. The objective of the current study was to create a tool that would display data for relevant PD risk loci and provide guidance with the prioritization of causal genes and potential mechanisms at each locus. We included all significant genome-wide signals from multiple recent PD genome-wide association studies including themost recent PD risk genome-wide association study, age-at-onset genome-wide association study, progression genome-wide association study, and Asian population PD risk genome-wide association study. We gathered data for all genes 1 Mb up and downstream of each variant to allow users to assess which gene(s) are most associated with the variant of interest based on a set of self-ranked criteria. Multiple databases were queried for each gene to collect additional causal data. We created a PD genome-wide association study browser tool (https://pdgenetics.shinyapps.io/GWASBrowser/) to assist the PD research community with the prioritization of genes for follow-up functional studies to identify potential therapeutic targets. Our PD genome-wide association study browser tool provides users with a useful method of identifying potential causal genes at all known PD risk loci from large-scale PD genome-wide association studies. We plan to update this tool with new relevant data as sample sizes increase and new PD risk loci are discovered. © 2020 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society. This article has been contributed to by US Government employees and their work is in the public domain in the USA.
dc.identifier.doi10.1002/mds.28197
dc.identifier.essn1531-8257
dc.identifier.pmcPMC7754106
dc.identifier.pmid32864809
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754106/pdf
dc.identifier.unpaywallURLhttps://movementdisorders.onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.28197
dc.identifier.urihttp://hdl.handle.net/10668/16180
dc.issue.number11
dc.journal.titleMovement disorders : official journal of the Movement Disorder Society
dc.journal.titleabbreviationMov Disord
dc.language.isoen
dc.organizationInstituto de Biomedicina de Sevilla-IBIS
dc.organizationHospital Universitario Virgen del Rocío
dc.page.number2056-2067
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, N.I.H., Extramural
dc.pubmedtypeResearch Support, N.I.H., Intramural
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectGWAS
dc.subjectParkinson's disease
dc.subjectprioritization
dc.subject.meshAge of Onset
dc.subject.meshGenetic Predisposition to Disease
dc.subject.meshGenome-Wide Association Study
dc.subject.meshHumans
dc.subject.meshNeurodegenerative Diseases
dc.subject.meshParkinson Disease
dc.subject.meshRisk Factors
dc.titleThe Parkinson's Disease Genome-Wide Association Study Locus Browser.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number35
dspace.entity.typePublication

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