Published in Nat Genet on March 06, 2011
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Gene-centric meta-analyses of 108 912 individuals confirm known body mass index loci and reveal three novel signals. Hum Mol Genet (2012) 1.37
A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex. Circ Cardiovasc Genet (2012) 1.35
Genome-wide association study of coronary artery disease in the Japanese. Eur J Hum Genet (2011) 1.32
Homocysteine and coronary heart disease: meta-analysis of MTHFR case-control studies, avoiding publication bias. PLoS Med (2012) 1.27
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Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies. Circ Cardiovasc Genet (2011) 1.26
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. Nat Genet (2016) 1.22
Genetic basis of atherosclerosis: insights from mice and humans. Circ Res (2012) 1.14
Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases. PLoS Genet (2012) 1.14
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Genome-wide association study in a Lebanese cohort confirms PHACTR1 as a major determinant of coronary artery stenosis. PLoS One (2012) 1.03
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Genetics of coronary artery calcification among African Americans, a meta-analysis. BMC Med Genet (2013) 0.99
Induction of lysosomal biogenesis in atherosclerotic macrophages can rescue lipid-induced lysosomal dysfunction and downstream sequelae. Arterioscler Thromb Vasc Biol (2014) 0.98
Incorporating a Genetic Risk Score Into Coronary Heart Disease Risk Estimates: Effect on Low-Density Lipoprotein Cholesterol Levels (the MI-GENES Clinical Trial). Circulation (2016) 0.97
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ADAMTS7 cleavage and vascular smooth muscle cell migration is affected by a coronary-artery-disease-associated variant. Am J Hum Genet (2013) 0.97
The IL-33-ST2L pathway is associated with coronary artery disease in a Chinese Han population. Am J Hum Genet (2013) 0.96
Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study. BMC Med Genet (2013) 0.95
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Arguing the case for the autotaxin-lysophosphatidic acid-lipid phosphate phosphatase 3-signaling nexus in the development and complications of atherosclerosis. Arterioscler Thromb Vasc Biol (2014) 0.94
Lipid-induced epigenomic changes in human macrophages identify a coronary artery disease-associated variant that regulates PPAP2B Expression through Altered C/EBP-beta binding. PLoS Genet (2015) 0.94
Genetic associations with expression for genes implicated in GWAS studies for atherosclerotic cardiovascular disease and blood phenotypes. Hum Mol Genet (2013) 0.93
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Coronary heart disease in Indian Asians. Glob Cardiol Sci Pract (2014) 0.91
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Assessment of the value of a genetic risk score in improving the estimation of coronary risk. Atherosclerosis (2012) 0.91
Cohort Profile: the Corogene study. Int J Epidemiol (2011) 0.89
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort. Eur J Hum Genet (2013) 0.89
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Higher plasma CXCL12 levels predict incident myocardial infarction and death in chronic kidney disease: findings from the Chronic Renal Insufficiency Cohort study. Eur Heart J (2013) 0.88
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Prediction of ischemic events on the basis of transcriptomic and genomic profiling in patients undergoing carotid endarterectomy. Mol Med (2012) 0.87
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Lysosomal acid lipase: at the crossroads of normal and atherogenic cholesterol metabolism. Front Cell Dev Biol (2015) 0.86
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The SH2B1 obesity locus is associated with myocardial infarction in diabetic patients and with NO synthase activity in endothelial cells. Atherosclerosis (2011) 0.86
GREGOR: evaluating global enrichment of trait-associated variants in epigenomic features using a systematic, data-driven approach. Bioinformatics (2015) 0.86
Common genetic determinants of lung function, subclinical atherosclerosis and risk of coronary artery disease. PLoS One (2014) 0.85
Pathway analysis of body mass index genome-wide association study highlights risk pathways in cardiovascular disease. Sci Rep (2015) 0.85
The impact of genome-wide association studies on the pathophysiology and therapy of cardiovascular disease. EMBO Mol Med (2016) 0.83
Polymorphisms in catechol-O-methyltransferase modify treatment effects of aspirin on risk of cardiovascular disease. Arterioscler Thromb Vasc Biol (2014) 0.83
Adapt-Mix: learning local genetic correlation structure improves summary statistics-based analyses. Bioinformatics (2015) 0.83
Regulation of histone modifying enzymes by the ubiquitin-proteasome system. Biochim Biophys Acta (2014) 0.83
Quantitative phosphoproteomics unveils temporal dynamics of thrombin signaling in human endothelial cells. Blood (2014) 0.83
Joint effect of insulin signaling genes on cardiovascular events and on whole body and endothelial insulin resistance. Atherosclerosis (2012) 0.83
Atherosclerosis and Alzheimer--diseases with a common cause? Inflammation, oxysterols, vasculature. BMC Geriatr (2014) 0.82
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Lysophosphatidic acid and cardiovascular disease: seeing is believing. J Lipid Res (2013) 0.82
Association of genetic variants of the α-kinase 1 gene with myocardial infarction in community-dwelling individuals. Biomed Rep (2013) 0.82
Design of a randomized controlled trial of disclosing genomic risk of coronary heart disease: the Myocardial Infarction Genes (MI-GENES) study. BMC Med Genomics (2015) 0.81
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A common variant on chromosome 9p21 affects the risk of myocardial infarction. Science (2007) 18.96
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