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Replication of a No...
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Grover, SandeepUniversity of Tübingen
(author)
Replication of a Novel Parkinson's Locus in a European Ancestry Population
- Article/chapterEnglish2021
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LIBRIS-ID:oai:lup.lub.lu.se:ec5104a4-9e7c-4017-96e7-49f87c680243
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https://lup.lub.lu.se/record/ec5104a4-9e7c-4017-96e7-49f87c680243URI
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https://doi.org/10.1002/mds.28546DOI
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Language:English
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Summary in:English
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Subject category:art swepub-publicationtype
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Subject category:ref swepub-contenttype
Notes
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BACKGROUND: A recently published East Asian genome-wide association study of Parkinson;s disease (PD) reported 2 novel risk loci, SV2C and WBSCR17.OBJECTIVES: The objective of this study were to determine whether recently reported novel SV2C and WBSCR17 loci contribute to the risk of developing PD in European and East Asian ancestry populations.METHODS: We report an association analysis of recently reported variants with PD in the COURAGE-PD cohort (9673 PD patients; 8465 controls) comprising individuals of European and East Asian ancestries. In addition, publicly available summary data (41,386 PD patients; 476,428 controls) were pooled.RESULTS: Our findings confirmed the role of the SV2C variant in PD pathogenesis (rs246814, COURAGE-PD PEuropean = 6.64 × 10-4 , pooled PD P = 1.15 × 10-11 ). The WBSCR17 rs9638616 was observed as a significant risk marker in the East Asian pooled population only (P = 1.16 × 10-8 ).CONCLUSIONS: Our comprehensive study provides an up-to-date summary of recently detected novel loci in different PD populations and confirmed the role of SV2C locus as a novel risk factor for PD irrespective of the population or ethnic group analyzed. © 2021 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
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Kumar-Sreelatha, Ashwin AshokUniversity of Tübingen
(author)
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Bobbili, Dheeraj R
(author)
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May, Patrick
(author)
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Domenighetti, CloéVersailles Saint-Quentin-en-Yvelines University
(author)
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Sugier, Pierre-EmmanuelVersailles Saint-Quentin-en-Yvelines University
(author)
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Schulte, ClaudiaUniversity Hospital Münster
(author)
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Elbaz, AlexisVersailles Saint-Quentin-en-Yvelines University
(author)
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Krüger, RejkoUniversity Hospital of Tubingen
(author)
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Gasser, ThomasUniversity Hospital Münster
(author)
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Sharma, ManuUniversity of Tübingen
(author)
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Puschmann, AndreasLund University,Lunds universitet,Neurologi, Lund,Sektion IV,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Klinisk neurogenetik,Forskargrupper vid Lunds universitet,Neurology, Lund,Section IV,Department of Clinical Sciences, Lund,Faculty of Medicine,Clinical Neurogenetics,Lund University Research Groups,Skåne University Hospital(Swepub:lu)med-aps
(creator_code:cre_t)
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Hellberg, ClaraLund University,Lunds universitet,Klinisk neurogenetik,Forskargrupper vid Lunds universitet,Clinical Neurogenetics,Lund University Research Groups,Skåne University Hospital(Swepub:lu)ala10che
(creator_code:cre_t)
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University of TübingenVersailles Saint-Quentin-en-Yvelines University
(creator_code:org_t)
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COURAGE-PD Consortium
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In:Movement Disorders: Wiley36:7, s. 1689-16950885-31851531-8257
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Grover, Sandeep
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May, Patrick
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Schulte, Claudia
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Elbaz, Alexis
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Krüger, Rejko
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Hellberg, Clara
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