Large scale association analysis of novel genetic loci for coronary artery disease.
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Reduced cholesterol and triglycerides in mice with a mutation in Mia2, a liver protein that localizes to ER exit sitesCardiovascular genomicsEpigenome-guided analysis of the transcriptome of plaque macrophages during atherosclerosis regression reveals activation of the Wnt signaling pathwayAdditive influence of genetic predisposition and conventional risk factors in the incidence of coronary heart disease: a population-based study in GreecePopulation genomics of cardiometabolic traits: design of the University College London-London School of Hygiene and Tropical Medicine-Edinburgh-Bristol (UCLEB) ConsortiumThe rs1333049 polymorphism on locus 9p21.3 and extreme longevity in Spanish and Japanese cohorts.Implications of genetic polymorphisms in inflammation-induced atherosclerosisPheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene-disease associations.Replication of putative susceptibility loci from genome-wide association studies associated with coronary atherosclerosis in Chinese Han population.Genome-wide association analysis of incident coronary heart disease (CHD) in African Americans: a short reportA genetic risk variant for myocardial infarction on chromosome 6p24 is associated with impaired central hemodynamic indexes.Genome-wide assessment for genetic variants associated with ventricular dysfunction after primary coronary artery bypass graft surgery.Joint effects of common genetic variants from multiple genes and pathways on the risk of premature coronary artery diseaseStromal cell-derived factor 1 as a biomarker of heart failure and mortality risk.Genotype-informed estimation of risk of coronary heart disease based on genome-wide association data linked to the electronic medical record.Early identification of cardiovascular risk using genomics and proteomics.Monocyte gene expression signature of patients with early onset coronary artery disease.Genetic copy number variants in myocardial infarction patients with hyperlipidemia.Sortilin: an unusual suspect in cholesterol metabolism: from GWAS identification to in vivo biochemical analyses, sortilin has been identified as a novel mediator of human lipoprotein metabolism.Genome-wide association study of coronary artery disease.Genetic causes of myocardial infarction: new insights from genome-wide association studies.The genetics of normal platelet reactivity.Genetic markers enhance coronary risk prediction in men: the MORGAM prospective cohortsAssessment of the 9p21.3 locus in severity of coronary artery disease in the presence and absence of type 2 diabetes.Genome-wide linkage scan identifies two novel genetic loci for coronary artery disease: in GeneQuest families.Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study: A Genome-wide association meta-analysis involving more than 22 000 cases and 60 000 controls.Genome-wide association studies in atherosclerosisGenetics of coronary artery disease - a clinician's perspectiveAssociation of SNP rs17465637 on chromosome 1q41 and rs599839 on 1p13.3 with myocardial infarction in an American caucasian population.Genetic polymorphism rs6922269 in the MTHFD1L gene is associated with survival and baseline active vitamin B12 levels in post-acute coronary syndromes patients.The impact of coronary artery disease risk loci on ischemic heart failure severity and prognosis: association analysis in the COntrolled ROsuvastatin multiNAtional trial in heart failure (CORONA).Comparative analysis of genome-wide association studies signals for lipids, diabetes, and coronary heart disease: Cardiovascular Biomarker Genetics Collaboration.The effect of hepatic lipase on coronary artery disease in humans is influenced by the underlying lipoprotein phenotypeEffect of 9p21 genetic variation on coronary heart disease is not modified by other risk markers. The Atherosclerosis Risk in Communities (ARIC) StudyAssociation of a genetic risk score with prevalent and incident myocardial infarction in subjects undergoing coronary angiography.Lack of association between four SNPs in the SLC22A3-LPAL2-LPA gene cluster and coronary artery disease in a Chinese Han population: a case control study.Genetic predisposition to coronary heart disease and stroke using an additive genetic risk score: a population-based study in Greece.Genetics of coronary artery disease: focus on genome-wide association studies.Analysis of recently identified dyslipidemia alleles reveals two loci that contribute to risk for carotid artery disease.The Relationship Between Coronary Artery Disease and Genetic Polymorphisms of Melanoma Inhibitory Activity 3.
P2860
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P2860
Large scale association analysis of novel genetic loci for coronary artery disease.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
2009年论文
@zh
2009年论文
@zh-cn
name
Large scale association analysis of novel genetic loci for coronary artery disease.
@ast
Large scale association analysis of novel genetic loci for coronary artery disease.
@en
type
label
Large scale association analysis of novel genetic loci for coronary artery disease.
@ast
Large scale association analysis of novel genetic loci for coronary artery disease.
@en
prefLabel
Large scale association analysis of novel genetic loci for coronary artery disease.
@ast
Large scale association analysis of novel genetic loci for coronary artery disease.
@en
P2093
P2860
P50
P1476
Large scale association analysis of novel genetic loci for coronary artery disease.
@en
P2093
C Hengstenberg
Coronary Artery Disease Consortium
J Thompson
N J Samani
R McGinnis
P2860
P304
P356
10.1161/ATVBAHA.108.181388
P407
P577
2009-01-22T00:00:00Z