Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium
about
Combined analysis of three genome-wide association studies on vWF and FVIII plasma levelsCohort Profile: TwinsUK and healthy ageing twin studyFive years of GWAS discoveryvon Willebrand disease: clinical and laboratory lessons learned from the large von Willebrand disease studiesHemostatic factors and risk of coronary heart disease in general populations: new prospective study and updated meta-analysesThe molecular characterization of von Willebrand disease: good in partsRare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWFGenome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2.Population genomics of cardiometabolic traits: design of the University College London-London School of Hygiene and Tropical Medicine-Edinburgh-Bristol (UCLEB) ConsortiumGenetics of venous thrombosis: insights from a new genome wide association studyIdentification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studiesGenome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosisGene-centric approach identifies new and known loci for FVIII activity and VWF antigen levels in European Americans and African Americans.Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project.Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study.Characterizing polymorphisms and allelic diversity of von Willebrand factor gene in the 1000 GenomesSafety and prolonged activity of recombinant factor VIII Fc fusion protein in hemophilia A patients.Syntaxin-binding protein STXBP5 inhibits endothelial exocytosis and promotes platelet secretion.Estimation and partition of heritability in human populations using whole-genome analysis methods.Gene-centric association signals for haemostasis and thrombosis traits identified with the HumanCVD BeadChip.Association between polymorphisms in the coagulation factor VII gene and coronary heart disease risk in different ethnicities: a meta-analysisA phenomics-based strategy identifies loci on APOC1, BRAP, and PLCG1 associated with metabolic syndrome phenotype domains.Functional architecture of Weibel-Palade bodies.Third Åland islands conference on von Willebrand disease, 26-28 September 2012: meeting report.Elevated factor VIII levels and risk of venous thrombosis.Platelet secretion and hemostasis require syntaxin-binding protein STXBP5.Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide associationEffect of genetic variation in STXBP5 and STX2 on von Willebrand factor and bleeding phenotype in type 1 von Willebrand disease patients.Mapping the N-glycome of human von Willebrand factor.Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study.A variant in the ABO gene explains the variation in soluble E-selectin levels-results from dense genotyping in two independent populations.Genetic sequence analysis of inherited bleeding diseases.Genome partitioning of genetic variation for complex traits using common SNPsGenetic predictors of fibrin D-dimer levels in healthy adults.Genetic determinants of plasma von Willebrand factor antigen levels: a target gene SNP and haplotype analysis of ARIC cohort.Genetic variation within the anticoagulant, procoagulant, fibrinolytic and innate immunity pathways as risk factors for venous thromboembolismGenetic variation associated with plasma von Willebrand factor levels and the risk of incident venous thrombosis.Performance related factors are the main determinants of the von Willebrand factor response to exhaustive physical exercise.A gene-centric association scan for Coagulation Factor VII levels in European and African Americans: the Candidate Gene Association Resource (CARe) ConsortiumNovel loci involved in platelet function and platelet count identified by a genome-wide study performed in children.
P2860
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P2860
Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium
description
2010 nî lūn-bûn
@nan
2010 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի մարտին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Novel associations of multiple ...... enome Epidemiology) Consortium
@ast
Novel associations of multiple ...... enome Epidemiology) Consortium
@en
type
label
Novel associations of multiple ...... enome Epidemiology) Consortium
@ast
Novel associations of multiple ...... enome Epidemiology) Consortium
@en
prefLabel
Novel associations of multiple ...... enome Epidemiology) Consortium
@ast
Novel associations of multiple ...... enome Epidemiology) Consortium
@en
P2093
P2860
P50
P1433
P1476
Novel associations of multiple ...... enome Epidemiology) Consortium
@en
P2093
Aaron R Folsom
Alan F Wright
Andrew D Johnson
Angela Silveira
Ann Rumley
Barbara McKnight
Christopher J O'Donnell
Cornelia M Van Duijn
David P Strachan
Edwin G Bovill
P2860
P304
P356
10.1161/CIRCULATIONAHA.109.869156
P407
P50
P577
2010-03-15T00:00:00Z