SwePub
Sök i LIBRIS databas

  Utökad sökning

id:"swepub:oai:lup.lub.lu.se:ec5104a4-9e7c-4017-96e7-49f87c680243"
 

Sökning: id:"swepub:oai:lup.lub.lu.se:ec5104a4-9e7c-4017-96e7-49f87c680243" > Replication of a No...

Replication of a Novel Parkinson's Locus in a European Ancestry Population

Grover, Sandeep (författare)
University of Tübingen
Kumar-Sreelatha, Ashwin Ashok (författare)
University of Tübingen
Bobbili, Dheeraj R (författare)
visa fler...
May, Patrick (författare)
Domenighetti, Cloé (författare)
Versailles Saint-Quentin-en-Yvelines University
Sugier, Pierre-Emmanuel (författare)
Versailles Saint-Quentin-en-Yvelines University
Schulte, Claudia (författare)
University Hospital Münster
Elbaz, Alexis (författare)
Versailles Saint-Quentin-en-Yvelines University
Krüger, Rejko (författare)
University Hospital of Tubingen
Gasser, Thomas (författare)
University Hospital Münster
Sharma, Manu (författare)
University of Tübingen
Puschmann, Andreas (creator_code:cre_t)
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 Hospital
Hellberg, Clara (creator_code:cre_t)
Lund University,Lunds universitet,Klinisk neurogenetik,Forskargrupper vid Lunds universitet,Clinical Neurogenetics,Lund University Research Groups,Skåne University Hospital
visa färre...
 (creator_code:org_t)
 
2021-03-24
2021
Engelska.
Ingår i: Movement Disorders. - : Wiley. - 0885-3185 .- 1531-8257. ; 36:7, s. 1689-1695
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • 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.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)

Nyckelord

Asian People/genetics
Cohort Studies
Ethnicity
Genetic Predisposition to Disease/genetics
Genome-Wide Association Study
Humans
Parkinson Disease/genetics
Risk Factors

Publikations- och innehållstyp

art (ämneskategori)
ref (ämneskategori)

Hitta via bibliotek

Till lärosätets databas

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy