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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00004350naa a2200553 4500
001oai:lup.lub.lu.se:ec5104a4-9e7c-4017-96e7-49f87c680243
003SwePub
008230831s2021 | |||||||||||000 ||eng|
024a https://lup.lub.lu.se/record/ec5104a4-9e7c-4017-96e7-49f87c6802432 URI
024a https://doi.org/10.1002/mds.285462 DOI
040 a (SwePub)lu
041 a engb eng
042 9 SwePub
072 7a art2 swepub-publicationtype
072 7a ref2 swepub-contenttype
100a Grover, Sandeepu University of Tübingen4 aut
2451 0a Replication of a Novel Parkinson's Locus in a European Ancestry Population
264 c 2021-03-24
264 1b Wiley,c 2021
520 a 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.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Neurologi0 (SwePub)302072 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Neurology0 (SwePub)302072 hsv//eng
653 a Asian People/genetics
653 a Cohort Studies
653 a Ethnicity
653 a Genetic Predisposition to Disease/genetics
653 a Genome-Wide Association Study
653 a Humans
653 a Parkinson Disease/genetics
653 a Risk Factors
700a Kumar-Sreelatha, Ashwin Ashoku University of Tübingen4 aut
700a Bobbili, Dheeraj R4 aut
700a May, Patrick4 aut
700a Domenighetti, Cloéu Versailles Saint-Quentin-en-Yvelines University4 aut
700a Sugier, Pierre-Emmanuelu Versailles Saint-Quentin-en-Yvelines University4 aut
700a Schulte, Claudiau University Hospital Münster4 aut
700a Elbaz, Alexisu Versailles Saint-Quentin-en-Yvelines University4 aut
700a Krüger, Rejkou University Hospital of Tubingen4 aut
700a Gasser, Thomasu University Hospital Münster4 aut
700a Sharma, Manuu University of Tübingen4 aut
700a Puschmann, Andreasu Lund 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 Hospital4 cre0 (Swepub:lu)med-aps
700a Hellberg, Clarau Lund University,Lunds universitet,Klinisk neurogenetik,Forskargrupper vid Lunds universitet,Clinical Neurogenetics,Lund University Research Groups,Skåne University Hospital4 cre0 (Swepub:lu)ala10che
710a University of Tübingenb Versailles Saint-Quentin-en-Yvelines University4 org
710a COURAGE-PD Consortium
773t Movement Disordersd : Wileyg 36:7, s. 1689-1695q 36:7<1689-1695x 0885-3185x 1531-8257
856u http://dx.doi.org/10.1002/mds.28546x freey FULLTEXT
856u https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.28546
8564 8u https://lup.lub.lu.se/record/ec5104a4-9e7c-4017-96e7-49f87c680243
8564 8u https://doi.org/10.1002/mds.28546

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