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citing journals

Top Articles

#TitleJournalYearCitations
1A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery diseaseNature Genetics20152,178
2Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation studyLancet, The20121,992
3Large-scale association analysis identifies 13 new susceptibility loci for coronary artery diseaseNature Genetics20111,724
4Multiple Rare Alleles Contribute to Low Plasma Levels of HDL CholesterolScience20041,041
5Association analyses based on false discovery rate implicate new loci for coronary artery diseaseNature Genetics2017597
6Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarctionNature2015591
7A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortiumNature Genetics2009490
8Genetic Variants Influencing Circulating Lipid Levels and Risk of Coronary Artery DiseaseArteriosclerosis, Thrombosis, and Vascular Biology2010374
9Shared Genetic Susceptibility to Ischemic Stroke and Coronary Artery DiseaseStroke2014311
10Genetics of Coronary Artery DiseaseCirculation Research2016301
11Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery DiseaseJournal of the American College of Cardiology2017222
12Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysisLancet Neurology, The2017202
13From The Cover: The highly conserved cardiac glycoside binding site of Na,K-ATPase plays a role in blood pressure regulationProceedings of the National Academy of Sciences of the United States of America2005172
14Genes and Coronary Artery DiseaseJournal of the American College of Cardiology2012139
15Gene Dosage of the Common Variant 9p21 Predicts Severity of Coronary Artery DiseaseJournal of the American College of Cardiology2010134
16Rare Copy Number Variants Contribute to Congenital Left-Sided Heart DiseasePLoS Genetics2012121
17Genome-wide association study and targeted metabolomics identifies sex-specific association of CPS1 with coronary artery diseaseNature Communications2016111
18The selective peroxisome proliferator-activated receptor alpha modulator (SPPARMα) paradigm: conceptual framework and therapeutic potentialCardiovascular Diabetology2019108
19Hepatic Lipase, High Density Lipoproteins, and HypertriglyceridemiaAmerican Journal of Pathology2011101
20The Keap1–Nrf2 Stress Response Pathway Promotes Mitochondrial Hyperfusion Through Degradation of the Mitochondrial Fission Protein Drp1Antioxidants and Redox Signaling201796
21In vivo and in vitro examination of the functional significances of novel lamin gene mutations in heart failure patientsJournal of Medical Genetics200591
22Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studiesEuropean Heart Journal201290
23Improved Prediction of Cardiovascular Disease Based on a Panel of Single Nucleotide Polymorphisms Identified Through Genome-Wide Association StudiesCirculation: Cardiovascular Genetics201088
24Relations between lipoprotein(a) concentrations, LPA genetic variants, and the risk of mortality in patients with established coronary heart disease: a molecular and genetic association studyLancet Diabetes and Endocrinology,the201788
25Plasma PCSK9 Levels Are Elevated with Acute Myocardial Infarction in Two Independent Retrospective Angiographic StudiesPLoS ONE201479
26Functional interaction between COL4A1/COL4A2 and SMAD3 risk loci for coronary artery diseaseAtherosclerosis201557
27Genome-wide identification of circulating-miRNA expression quantitative trait loci reveals the role of several miRNAs in the regulation of cardiometabolic phenotypesCardiovascular Research201956
28Clinical and Genetic Association of Serum Ceruloplasmin With Cardiovascular RiskArteriosclerosis, Thrombosis, and Vascular Biology201255
299p21 and the Genetic Revolution for Coronary Artery DiseaseClinical Chemistry201254
30Functional Analysis of a Novel Genome-Wide Association Study Signal in SMAD3 That Confers Protection From Coronary Artery DiseaseArteriosclerosis, Thrombosis, and Vascular Biology201649
319p21.3 Coronary Artery Disease Risk Variants Disrupt TEAD Transcription Factor–Dependent Transforming Growth Factor β Regulation of p16 Expression in Human Aortic Smooth Muscle CellsCirculation201548
32Obesity shows preserved plasma proteome in large independent clinical cohortsScientific Reports201847
33Genome-Wide Association Studies of Hypertension: Have They Been Fruitful?Journal of Cardiovascular Translational Research201046
34Cardiac myosin binding protein C regulates postnatal myocyte cytokinesisProceedings of the National Academy of Sciences of the United States of America201544
35Influence of Pro12Ala peroxisome proliferator-activated receptor γ2 polymorphism on glucose response to exercise training in type 2 diabetesDiabetologia200541
36SPG7 Variant Escapes Phosphorylation-Regulated Processing by AFG3L2, Elevates Mitochondrial ROS, and Is Associated with Multiple Clinical PhenotypesCell Reports201440
37Functional Genomics of the 9p21.3 Locus for Atherosclerosis: Clarity or Confusion?Current Cardiology Reports201440
38Runs of Homozygosity: Association with Coronary Artery Disease and Gene Expression in Monocytes and MacrophagesAmerican Journal of Human Genetics201538
39Differential effects of glyoxalase 1 overexpression on diabetic atherosclerosis and renal dysfunction in streptozotocin-treated, apolipoprotein E-deficient micePhysiological Reports201435
40A prospective randomized evaluation of a pharmacogenomic approach to antiplatelet therapy among patients with ST-elevation myocardial infarction: the RAPID STEMI studyPharmacogenomics Journal201635
41Adiposity significantly modifies genetic risk for dyslipidemiaJournal of Lipid Research201433
42A genetic basis for coronary artery diseaseTrends in Cardiovascular Medicine201533
43Gene–environment interaction in dyslipidemiaCurrent Opinion in Lipidology201533
44Partitioning the heritability of coronary artery disease highlights the importance of immune-mediated processes and epigenetic sites associated with transcriptional activityCardiovascular Research201731
45Extracellular Nucleotides Inhibit Insulin Receptor Signaling, Stimulate Autophagy and Control Lipoprotein SecretionPLoS ONE201227
46Increased genetic risk for obesity in premature coronary artery diseaseEuropean Journal of Human Genetics201627
47Regulation of MFGE8 by the intergenic coronary artery disease locus on 15q26.1Atherosclerosis201927
48Functional characterization of a promoter polymorphism that drives ACSL5 gene expression in skeletal muscle and associates with diet‐induced weight lossFASEB Journal200926
49Two Chromosome 9p21 Haplotype Blocks Distinguish Between Coronary Artery Disease and Myocardial Infarction RiskCirculation: Cardiovascular Genetics201326
50Genetic variants primarily associated with type 2 diabetes are related to coronary artery disease riskAtherosclerosis201526