Matches in UGent Biblio for { <https://biblio.ugent.be/publication/2107434#aggregation> ?p ?o. }
- aggregation classification "A1".
- aggregation creator B334198.
- aggregation creator B334199.
- aggregation creator B334200.
- aggregation creator B334201.
- aggregation creator B334202.
- aggregation creator B334203.
- aggregation creator B334204.
- aggregation creator B334205.
- aggregation creator B334206.
- aggregation creator B334207.
- aggregation creator B334208.
- aggregation creator B334209.
- aggregation creator B334210.
- aggregation creator B334211.
- aggregation creator B334212.
- aggregation creator B334213.
- aggregation creator B334214.
- aggregation creator B334215.
- aggregation creator B334216.
- aggregation creator B334217.
- aggregation creator B334218.
- aggregation creator B334219.
- aggregation creator B334220.
- aggregation creator B334221.
- aggregation creator B334222.
- aggregation creator B334223.
- aggregation creator B334224.
- aggregation creator B334225.
- aggregation creator B334226.
- aggregation creator B334227.
- aggregation creator B334228.
- aggregation creator B334229.
- aggregation creator B334230.
- aggregation creator B334231.
- aggregation creator B334232.
- aggregation creator B334233.
- aggregation creator B334234.
- aggregation creator B334235.
- aggregation creator B334236.
- aggregation creator B334237.
- aggregation creator B334238.
- aggregation creator B334239.
- aggregation creator B334240.
- aggregation creator B334241.
- aggregation creator B334242.
- aggregation creator B334243.
- aggregation creator B334244.
- aggregation creator B334245.
- aggregation creator B334246.
- aggregation creator B334247.
- aggregation creator B334248.
- aggregation creator B334249.
- aggregation creator B334250.
- aggregation creator B334251.
- aggregation creator B334252.
- aggregation creator B334253.
- aggregation creator B334254.
- aggregation creator B334255.
- aggregation creator B334256.
- aggregation creator B334257.
- aggregation creator B334258.
- aggregation creator B334259.
- aggregation creator B334260.
- aggregation creator B334261.
- aggregation creator B334262.
- aggregation creator B334263.
- aggregation creator person.
- aggregation creator person.
- aggregation creator person.
- aggregation creator person.
- aggregation creator person.
- aggregation creator person.
- aggregation creator person.
- aggregation creator person.
- aggregation creator person.
- aggregation date "2012".
- aggregation format "application/pdf".
- aggregation hasFormat 2107434.bibtex.
- aggregation hasFormat 2107434.csv.
- aggregation hasFormat 2107434.dc.
- aggregation hasFormat 2107434.didl.
- aggregation hasFormat 2107434.doc.
- aggregation hasFormat 2107434.json.
- aggregation hasFormat 2107434.mets.
- aggregation hasFormat 2107434.mods.
- aggregation hasFormat 2107434.rdf.
- aggregation hasFormat 2107434.ris.
- aggregation hasFormat 2107434.txt.
- aggregation hasFormat 2107434.xls.
- aggregation hasFormat 2107434.yaml.
- aggregation isPartOf urn:issn:1942-325X.
- aggregation language "eng".
- aggregation rights "I have transferred the copyright for this publication to the publisher".
- aggregation subject "Medicine and Health Sciences".
- aggregation title "Common genetic variation in the 3'-BCL11B gene desert is associated with carotid-femoral pulse wave velocity and excess cardiovascular disease risk: the AortaGen Consortium".
- aggregation abstract "BACKGROUND: Carotid-femoral pulse wave velocity (CFPWV) is a heritable measure of aortic stiffness that is strongly associated with increased risk for major cardiovascular disease events. METHODS AND RESULTS: We conducted a meta-analysis of genome-wide association data in 9 community-based European ancestry cohorts consisting of 20 634 participants. Results were replicated in 2 additional European ancestry cohorts involving 5306 participants. Based on a preliminary analysis of 6 cohorts, we identified a locus on chromosome 14 in the 3'-BCL11B gene desert that is associated with CFPWV (rs7152623, minor allele frequency=0.42, beta=-0.075+/-0.012 SD/allele, P=2.8x10(-10); replication beta=-0.086+/-0.020 SD/allele, P=1.4x10(-6)). Combined results for rs7152623 from 11 cohorts gave beta=-0.076+/-0.010 SD/allele, P=3.1x10(-15). The association persisted when adjusted for mean arterial pressure (beta=-0.060+/-0.009 SD/allele, P=1.0x10(-11)). Results were consistent in younger (<55 years, 6 cohorts, n=13 914, beta=-0.081+/-0.014 SD/allele, P=2.3x10(-9)) and older (9 cohorts, n=12 026, beta=-0.061+/-0.014 SD/allele, P=9.4x10(-6)) participants. In separate meta-analyses, the locus was associated with increased risk for coronary artery disease (hazard ratio=1.05; confidence interval=1.02-1.08; P=0.0013) and heart failure (hazard ratio=1.10, CI=1.03-1.16, P=0.004). CONCLUSIONS: Common genetic variation in a locus in the BCL11B gene desert that is thought to harbor 1 or more gene enhancers is associated with higher CFPWV and increased risk for cardiovascular disease. Elucidation of the role this novel locus plays in aortic stiffness may facilitate development of therapeutic interventions that limit aortic stiffening and related cardiovascular disease events.".
- aggregation authorList BK629791.
- aggregation endPage "90".
- aggregation issue "1".