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Lack of Association Between GBA Mutations and Motor Complications in European and American Parkinson's Disease Cohorts

dc.contributor.authorMaple-Grodem, Jodi
dc.contributor.authorPaul, Kimberly C.
dc.contributor.authorDalen, Ingvild
dc.contributor.authorNgo, Kathie J.
dc.contributor.authorWong, Darice
dc.contributor.authorMacleod, Angus D.
dc.contributor.authorCounsell, Carl E.
dc.contributor.authorBackstrom, David
dc.contributor.authorForsgren, Lars
dc.contributor.authorTysnes, Ole-Bjorn
dc.contributor.authorKusters, Cynthia D. J.
dc.contributor.authorFogel, Brent L.
dc.contributor.authorBronstein, Jeff M.
dc.contributor.authorRitz, Beate
dc.contributor.authorAlves, Guido
dc.date.accessioned2021-11-15T16:24:01Z
dc.date.available2021-11-15T16:24:01Z
dc.date.issued2021-10-12
dc.identifier.citationMaple-Grodem , J , Paul , K C , Dalen , I , Ngo , K J , Wong , D , Macleod , A D , Counsell , C E , Backstrom , D , Forsgren , L , Tysnes , O-B , Kusters , C D J , Fogel , B L , Bronstein , J M , Ritz , B & Alves , G 2021 , ' Lack of Association Between GBA Mutations and Motor Complications in European and American Parkinson's Disease Cohorts ' , Journal of Parkinson's Disease , vol. 11 , no. 4 , pp. 1569-1578 . https://doi.org/10.3233/JPD-212657en
dc.identifier.issn1877-7171
dc.identifier.otherPURE: 208629847
dc.identifier.otherPURE UUID: 7caf54e6-1907-41ec-a92b-cceffa80665f
dc.identifier.otherWOS: 000708976600006
dc.identifier.otherScopus: 85117367436
dc.identifier.urihttps://hdl.handle.net/2164/17503
dc.descriptionACKNOWLEDGMENTS The authors would like to thank all of the patients and controls for participation in each of the studies. Equally, we thank all members of each of the study groups and other personnel for their contributions. Funding sources for the respective studies are as follows: The Norwegian ParkWest study has been funded by the Research Council of Norway (177966), the Western Norway Regional Health Authority (911218), the Norwegian Parkinson’s Research Foundation, and Rebergs Legacy. PINE study was supported by Parkinson’s UK (G0502, G0914, G1302), Scottish Government Chief Scientist Office, BMA Doris Hillier Award, the BUPA Foundation, NHS Grampian Endowments, and RS MacDonald Trust. The NYPUM study has been funded by the Swedish Medical Research Council, the Swedish Parkinson’s disease Association, the Swedish Parkinson’s Foundation, Parkinson Research Foundation, Erling Persson Foundation, Kempe Foundation, the Swedish Brain Foundation (Hjarnfonden), and the Vasterbotten County Council. AAS, JMG and GA are supported by the Research Council of Norway (287842). BLF acknowledges support through donations to the UCLA Clinical Neurogenomics Research Center. CK is supported by the NIH grant F32AG063442. The PEG study was supported by NIH/NIEHS grants R01-ES010544 and U54-ES012078. Publication of this manuscript was supported under the The Michael J. Fox Foundation: 2021 RFA: Accelerating Publication of Parkinson’s Disease Replication Data.en
dc.format.extent10
dc.language.isoeng
dc.relation.ispartofJournal of Parkinson's Diseaseen
dc.rights© 2021 – The authors. Published by IOS Press. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC 4.0). https://creativecommons.org/licenses/by-nc/4.0/en
dc.subjectGBAen
dc.subjectParkinson's diseaseen
dc.subjectmotor complicationsen
dc.subjectdyskinesiasen
dc.subjectmotor fluctuationsen
dc.subjectLEVODOPA-INDUCED DYSKINESIAen
dc.subjectGLUCOCEREBROSIDASE MUTATIONSen
dc.subjectCLINICAL-FEATURESen
dc.subjectRISKen
dc.subjectGENEen
dc.subjectPROGRESSIONen
dc.subjectFREQUENCYen
dc.subjectDEMENTIAen
dc.subjectGENOTYPEen
dc.subjectDECLINEen
dc.subjectR Medicine (General)en
dc.subjectParkinson's UKen
dc.subjectG0502en
dc.subjectG0914en
dc.subjectG1302en
dc.subjectChief Scientist Office (CSO)en
dc.subjectOtheren
dc.subjectSupplementary Informationen
dc.subjecthttps://dx.doi.org/10.3233/JPD-212657en
dc.subject.lccR1en
dc.titleLack of Association Between GBA Mutations and Motor Complications in European and American Parkinson's Disease Cohortsen
dc.typeJournal articleen
dc.contributor.institutionUniversity of Aberdeen.Medicine, Medical Sciences & Nutritionen
dc.contributor.institutionUniversity of Aberdeen.Chronic Disease Research Groupen
dc.contributor.institutionUniversity of Aberdeen.Other Applied Health Sciencesen
dc.contributor.institutionUniversity of Aberdeen.Institute of Applied Health Sciencesen
dc.description.statusPeer revieweden
dc.description.versionPublisher PDFen
dc.identifier.doihttps://doi.org/10.3233/JPD-212657
dc.identifier.vol11en
dc.identifier.iss4en


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