| Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
|
1
|
A common variant on chromosome 9p21 affects the risk of myocardial infarction.
|
Science
|
2007
|
18.96
|
|
2
|
A branched-chain amino acid-related metabolic signature that differentiates obese and lean humans and contributes to insulin resistance.
|
Cell Metab
|
2009
|
11.46
|
|
3
|
Large-scale association analysis identifies new risk loci for coronary artery disease.
|
Nat Genet
|
2012
|
7.59
|
|
4
|
Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction.
|
Nat Genet
|
2009
|
6.83
|
|
5
|
The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm.
|
Nat Genet
|
2008
|
6.72
|
|
6
|
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease.
|
N Engl J Med
|
2016
|
3.88
|
|
7
|
Relationships between circulating metabolic intermediates and insulin action in overweight to obese, inactive men and women.
|
Diabetes Care
|
2009
|
3.69
|
|
8
|
Effect of CYP2C19 and ABCB1 single nucleotide polymorphisms on outcomes of treatment with ticagrelor versus clopidogrel for acute coronary syndromes: a genetic substudy of the PLATO trial.
|
Lancet
|
2010
|
3.55
|
|
9
|
Differential metabolic impact of gastric bypass surgery versus dietary intervention in obese diabetic subjects despite identical weight loss.
|
Sci Transl Med
|
2011
|
3.20
|
|
10
|
The SLCO1B1*5 genetic variant is associated with statin-induced side effects.
|
J Am Coll Cardiol
|
2009
|
3.10
|
|
11
|
Sex Differences in Demographics, Risk Factors, Presentation, and Noninvasive Testing in Stable Outpatients With Suspected Coronary Artery Disease: Insights From the PROMISE Trial.
|
JACC Cardiovasc Imaging
|
2016
|
2.36
|
|
12
|
Genetically determined height and coronary artery disease.
|
N Engl J Med
|
2015
|
2.24
|
|
13
|
Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies.
|
J Am Coll Cardiol
|
2010
|
2.17
|
|
14
|
Red cell distribution width, C-reactive protein, the complete blood count, and mortality in patients with coronary disease and a normal comparison population.
|
Clin Chim Acta
|
2011
|
1.83
|
|
15
|
Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm.
|
Nat Genet
|
2010
|
1.79
|
|
16
|
Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease.
|
Am J Hum Genet
|
2007
|
1.55
|
|
17
|
Current Science on Consumer Use of Mobile Health for Cardiovascular Disease Prevention: A Scientific Statement From the American Heart Association.
|
Circulation
|
2015
|
1.48
|
|
18
|
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
|
|
19
|
GATA2 is associated with familial early-onset coronary artery disease.
|
PLoS Genet
|
2006
|
1.32
|
|
20
|
Comprehensive genetic analysis of the platelet activating factor acetylhydrolase (PLA2G7) gene and cardiovascular disease in case-control and family datasets.
|
Hum Mol Genet
|
2008
|
1.21
|
|
21
|
Branched chain amino acids are novel biomarkers for discrimination of metabolic wellness.
|
Metabolism
|
2013
|
1.20
|
|
22
|
Pharmacogenetic predictors of statin-mediated low-density lipoprotein cholesterol reduction and dose response.
|
Circ Cardiovasc Genet
|
2008
|
1.17
|
|
23
|
Genetic effects in the leukotriene biosynthesis pathway and association with atherosclerosis.
|
Hum Genet
|
2009
|
1.04
|
|
24
|
Association between the chromosome 9p21 locus and angiographic coronary artery disease burden: a collaborative meta-analysis.
|
J Am Coll Cardiol
|
2013
|
1.02
|
|
25
|
Biomarkers and cardiovascular disease: determining causality and quantifying contribution to risk assessment.
|
JAMA
|
2009
|
1.01
|
|
26
|
Risk factors for 1-year mortality after thoracic endovascular aortic repair.
|
J Thorac Cardiovasc Surg
|
2012
|
0.99
|
|
27
|
Validation study of genetic associations with coronary artery disease on chromosome 3q13-21 and potential effect modification by smoking.
|
Ann Hum Genet
|
2009
|
0.96
|
|
28
|
Genetic and functional association of FAM5C with myocardial infarction.
|
BMC Med Genet
|
2008
|
0.96
|
|
29
|
Rationale and design of the Duke Electrophysiology Genetic and Genomic Studies (EPGEN) biorepository.
|
Am Heart J
|
2009
|
0.93
|
|
30
|
Metabolic profiles predict adverse events after coronary artery bypass grafting.
|
J Thorac Cardiovasc Surg
|
2012
|
0.93
|
|
31
|
Fine mapping of a linkage peak with integration of lipid traits identifies novel coronary artery disease genes on chromosome 5.
|
BMC Genet
|
2012
|
0.92
|
|
32
|
Aging-related atherosclerosis is exacerbated by arterial expression of tumor necrosis factor receptor-1: evidence from mouse models and human association studies.
|
Hum Mol Genet
|
2010
|
0.92
|
|
33
|
Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease.
|
Hum Genet
|
2011
|
0.91
|
|
34
|
Taking cardiovascular genetic association studies to the next level.
|
J Am Coll Cardiol
|
2007
|
0.89
|
|
35
|
The S1103Y cardiac sodium channel variant is associated with implantable cardioverter-defibrillator events in blacks with heart failure and reduced ejection fraction.
|
Circ Cardiovasc Genet
|
2011
|
0.89
|
|
36
|
Effect of heparin administration on metabolomic profiles in samples obtained during cardiac catheterization.
|
Circ Cardiovasc Genet
|
2011
|
0.89
|
|
37
|
Gene-smoking interactions in multiple Rho-GTPase pathway genes in an early-onset coronary artery disease cohort.
|
Hum Genet
|
2013
|
0.88
|
|
38
|
Prevalence and management of hypertension in acute coronary syndrome patients varies by sex: observations from the Sibrafiban versus aspirin to Yield Maximum Protection from ischemic Heart events postacute cOroNary sYndromes (SYMPHONY) randomized clinical trials.
|
Am Heart J
|
2005
|
0.88
|
|
39
|
Predictors of mortality in patients with chronic kidney disease and an implantable defibrillator: an EPGEN substudy.
|
Europace
|
2011
|
0.87
|
|
40
|
Comprehensive analysis of LAMC1 genetic variants in advanced pelvic organ prolapse.
|
Am J Obstet Gynecol
|
2012
|
0.86
|
|
41
|
Genome-wide linkage analysis of quantitative biomarker traits of osteoarthritis in a large, multigenerational extended family.
|
Arthritis Rheum
|
2010
|
0.85
|
|
42
|
Epigenetic regulation of COL15A1 in smooth muscle cell replicative aging and atherosclerosis.
|
Hum Mol Genet
|
2013
|
0.84
|
|
43
|
Exploration of a hypothesized independent association of a common 9p21.3 gene variant and ischemic stroke in patients with and without angiographic coronary artery disease.
|
Cerebrovasc Dis
|
2010
|
0.83
|
|
44
|
Matrix metalloproteinase-9 genetic polymorphisms and the risk for advanced pelvic organ prolapse.
|
Obstet Gynecol
|
2012
|
0.83
|
|
45
|
Systems Genetics Analysis of Genome-Wide Association Study Reveals Novel Associations Between Key Biological Processes and Coronary Artery Disease.
|
Arterioscler Thromb Vasc Biol
|
2015
|
0.83
|
|
46
|
Race and sex differences in small-molecule metabolites and metabolic hormones in overweight and obese adults.
|
OMICS
|
2013
|
0.82
|
|
47
|
Closing the gap: treating hypertension in women.
|
Cardiol Rev
|
2008
|
0.82
|
|
48
|
Association of Roadway Proximity with Fasting Plasma Glucose and Metabolic Risk Factors for Cardiovascular Disease in a Cross-Sectional Study of Cardiac Catheterization Patients.
|
Environ Health Perspect
|
2015
|
0.81
|
|
49
|
Polymorphisms associated with in vitro aspirin resistance are not associated with clinical outcomes in patients with coronary artery disease who report regular aspirin use.
|
Am Heart J
|
2011
|
0.80
|
|
50
|
Inverse association of general joint hypermobility with hand and knee osteoarthritis and serum cartilage oligomeric matrix protein levels.
|
Arthritis Rheum
|
2008
|
0.80
|
|
51
|
Genome-wide linkage analysis of cardiovascular disease biomarkers in a large, multigenerational family.
|
PLoS One
|
2013
|
0.78
|
|
52
|
Potential Impact and Study Considerations of Metabolomics in Cardiovascular Health and Disease: A Scientific Statement From the American Heart Association.
|
Circ Cardiovasc Genet
|
2017
|
0.77
|
|
53
|
Characterizing the phenotype of advanced pelvic organ prolapse.
|
Female Pelvic Med Reconstr Surg
|
2012
|
0.76
|
|
54
|
SLCO1B1 genetic variants, long-term low-density lipoprotein cholesterol levels and clinical events in patients following cardiac catheterization.
|
Pharmacogenomics
|
2015
|
0.75
|
|
55
|
Biomarker bonanza?
|
J Am Coll Cardiol
|
2010
|
0.75
|
|
56
|
Postmenopausal hormone use in women with acute coronary syndromes.
|
J Womens Health (Larchmt)
|
2004
|
0.75
|
|
57
|
Training cardiovascular specialists in imaging: a curriculum based on fundamental concepts required for multimodal imaging.
|
Am Heart J
|
2007
|
0.75
|
|
58
|
Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.
|
Nat Genet
|
2017
|
0.75
|