3.8 Article

A Genome-Wide Association Scan of RR and QT Interval Duration in 3 European Genetically Isolated Populations The EUROSPAN Project

期刊

CIRCULATION-CARDIOVASCULAR GENETICS
卷 2, 期 4, 页码 322-U48

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/CIRCGENETICS.108.833806

关键词

genetics; heart rate; population

资金

  1. European Commission [018947 (LSHG-CT-2006-01947)]
  2. Croatian Ministry of Science, Education and Sport [108-1080315-0302]
  3. Ministry of Health of the Autonomous Province of Bolzano
  4. South Tyrolean Sparkasse Foundation
  5. Scottish Executive Health Department
  6. Royal Society
  7. Wellcome Trust
  8. Netherlands Organization for Scientific Research (NWO) [91203014]
  9. Russian Foundation for Basic Research (NWO-RFBR) [047.017.043]
  10. Center of Medical Systems Biology (CMSB)
  11. Netherlands Genomics Initiative
  12. Chief Scientist Office [CZB/4/710] Funding Source: researchfish
  13. Medical Research Council [MC_U127561128] Funding Source: researchfish
  14. MRC [MC_U127561128] Funding Source: UKRI

向作者/读者索取更多资源

Background-We set out to identify common genetic determinants of the length of the RR and QT intervals in 2325 individuals from isolated European populations. Methods and Results-We analyzed the heart rate at rest, measured as the RR interval, and the length of the corrected QT interval for association with 318 237 single-nucleotide polymorphisms. The RR interval was associated with common variants within GPR133, a G-protein-coupled receptor (rs885389, P = 3.9 x 10(-8)). The QT interval was associated with the earlier reported NOS1AP gene (rs2880058, P = 2.00 x 10(-10)) and with a region on chromosome 13 (rs2478333, P = 4.34 x 10(-8)), which is 100 kb from the closest known transcript LOC730174 and has previously not been associated with the length of the QT interval. Conclusion-Our results suggested an association between the RR interval and GPR133 and confirmed an association between the QT interval and NOS1AP. (Circ Cardiovasc Genet. 2009; 2: 322-328.)

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