Association of genetic risk variants with expression of proximal genes identifies novel susceptibility genes for cardiovascular disease.
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TM6SF2 is a regulator of liver fat metabolism influencing triglyceride secretion and hepatic lipid droplet contentAbdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1Genetics of coronary artery diseaseGenetic loci on chromosome 5 are associated with circulating levels of interleukin-5 and eosinophil count in a European population with high risk for cardiovascular disease.Prioritizing Approaches to Engage Community Members and Build Trust in Biobanks: A Survey of Attitudes and Opinions of Adults within Outpatient Practices at the University of MarylandMultiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular diseaseA genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease.Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosisMultiple Hepatic Regulatory Variants at the GALNT2 GWAS Locus Associated with High-Density Lipoprotein CholesterolNew Insights Into Aortic Diseases: A Report From the Third International Meeting on Aortic Diseases (IMAD3)Validation study of candidate single nucleotide polymorphisms associated with left ventricular hypertrophy in the Korean population.Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulationMapping Novel Pathways in Cardiovascular Disease Using eQTL Data: The Past, Present, and Future of Gene Expression AnalysisNetwork-based analysis of genome wide association data provides novel candidate genes for lipid and lipoprotein traits.Functional Analysis of the Coronary Heart Disease Risk Locus on Chromosome 21q22.Mapping of 79 loci for 83 plasma protein biomarkers in cardiovascular disease.SORBS1 gene, a new candidate for diabetic nephropathy: results from a multi-stage genome-wide association study in patients with type 1 diabetes.Intima-media thickness of the descending aorta in patients with bicuspid aortic valve.Whole Exome Sequencing to Identify Genetic Variants Associated with Raised Atherosclerotic Lesions in Young Persons.Common genetic determinants of lung function, subclinical atherosclerosis and risk of coronary artery diseaseThe chromosome 9p21.3 coronary heart disease risk allele is associated with altered gene expression in normal heart and vascular tissuesFunctional analysis of two PLA2G2A variants associated with secretory phospholipase A2-IIA levels.Use of allele-specific FAIRE to determine functional regulatory polymorphism using large-scale genotyping arraysNovel genetic approach to investigate the role of plasma secretory phospholipase A2 (sPLA2)-V isoenzyme in coronary heart disease: modified Mendelian randomization analysis using PLA2G5 expression levelsGenome-wide association studies in atherosclerosisAnalysis of multiple association studies provides evidence of an expression QTL hub in gene-gene interaction network affecting HDL cholesterol levels.Meta-analysis of 65,734 individuals identifies TSPAN15 and SLC44A2 as two susceptibility loci for venous thromboembolismEffect of High-Density Lipoprotein Metabolic Pathway Gene Variations and Risk Factors on Neovascular Age-Related Macular Degeneration and Polypoidal Choroidal Vasculopathy in China.Genome-wide studies of gene expression relevant to coronary artery diseaseImpact of common variation in bone-related genes on type 2 diabetes and related traitsLarge-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways.Vaccination against T-cell epitopes of native ApoB100 reduces vascular inflammation and disease in a humanized mouse model of atherosclerosis.Expression of ceramide-metabolising enzymes in subcutaneous and intra-abdominal human adipose tissue.A gene-centric study of common carotid artery remodelling.Large-scale association analysis identifies new risk loci for coronary artery diseaseA sequence variant associated with sortilin-1 (SORT1) on 1p13.3 is independently associated with abdominal aortic aneurysmNLRP3 Inflammasome Expression and Activation in Human Atherosclerosis.Association of TERC and OBFC1 haplotypes with mean leukocyte telomere length and risk for coronary heart disease.Genetic associations with expression for genes implicated in GWAS studies for atherosclerotic cardiovascular disease and blood phenotypes.Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci.
P2860
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P2860
Association of genetic risk variants with expression of proximal genes identifies novel susceptibility genes for cardiovascular disease.
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունիսին 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
Association of genetic risk va ...... es for cardiovascular disease.
@ast
Association of genetic risk va ...... es for cardiovascular disease.
@en
Association of genetic risk va ...... es for cardiovascular disease.
@nl
type
label
Association of genetic risk va ...... es for cardiovascular disease.
@ast
Association of genetic risk va ...... es for cardiovascular disease.
@en
Association of genetic risk va ...... es for cardiovascular disease.
@nl
prefLabel
Association of genetic risk va ...... es for cardiovascular disease.
@ast
Association of genetic risk va ...... es for cardiovascular disease.
@en
Association of genetic risk va ...... es for cardiovascular disease.
@nl
P2093
P50
P1476
Association of genetic risk va ...... es for cardiovascular disease.
@en
P2093
Anders Gabrielsen
BiKE and ASAP study groups
Ekaterina Chernogubova
Ferdinand van't Hooft
Gabrielle Paulsson-Berne
Göran K Hansson
Hanna E Agardh
P304
P356
10.1161/CIRCGENETICS.110.948935
P577
2010-06-19T00:00:00Z