4.2(top 5%)
2-year impact
5.4(top 5%)
3-year impact
5.0(top 5%)
5-year impact
3.6(top 5%)
10-year impact
833(top 20%)
papers
41.3K(top 10%)
citations
98(top 5%)
h-index
4.4(top 5%)
extended IF
1.0K
all documents
41.8K
doc citations
150(top 5%)
g-index

Top Articles

#TitleJournalYearCitations
1Circulating MicroRNA-208b and MicroRNA-499 Reflect Myocardial Damage in Cardiovascular DiseaseCirculation: Cardiovascular Genetics2010654
2Epigenetic Signatures of Cigarette SmokingCirculation: Cardiovascular Genetics2016630
3Quantitative Serum Nuclear Magnetic Resonance Metabolomics in Cardiovascular Epidemiology and GeneticsCirculation: Cardiovascular Genetics2015570
4Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) ConsortiumCirculation: Cardiovascular Genetics2009488
5Increased MicroRNA-1 and MicroRNA-133a Levels in Serum of Patients With Cardiovascular Disease Indicate Myocardial DamageCirculation: Cardiovascular Genetics2011479
6Clinical Presentation, Long-Term Follow-Up, and Outcomes of 1001 Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patients and Family MembersCirculation: Cardiovascular Genetics2015398
7Association of a Peripheral Blood Metabolic Profile With Coronary Artery Disease and Risk of Subsequent Cardiovascular EventsCirculation: Cardiovascular Genetics2010387
8Whole Exome Sequencing to Identify a Novel Gene (Caveolin-1) Associated With Human Pulmonary Arterial HypertensionCirculation: Cardiovascular Genetics2012319
9Ethical and Practical Guidelines for Reporting Genetic Research Results to Study ParticipantsCirculation: Cardiovascular Genetics2010298
10Association Between Shortened Leukocyte Telomere Length and Cardiometabolic OutcomesCirculation: Cardiovascular Genetics2015284
11Multiple Genetic Loci Influence Serum Urate Levels and Their Relationship With Gout and Cardiovascular Disease Risk FactorsCirculation: Cardiovascular Genetics2010269
12SCN5A Mutations and the Role of Genetic Background in the Pathophysiology of Brugada SyndromeCirculation: Cardiovascular Genetics2009262
13PITX2c Is Expressed in the Adult Left Atrium, and Reducing Pitx2c Expression Promotes Atrial Fibrillation Inducibility and Complex Changes in Gene ExpressionCirculation: Cardiovascular Genetics2011254
14Circulating MicroRNAs as Biomarkers and Potential Paracrine Mediators of Cardiovascular DiseaseCirculation: Cardiovascular Genetics2010241
15Lipoprotein(a) Levels, Genotype, and Incident Aortic Valve StenosisCirculation: Cardiovascular Genetics2014232
16A Mutation in the β3 Subunit of the Cardiac Sodium Channel Associated With Brugada ECG PhenotypeCirculation: Cardiovascular Genetics2009230
17Genetic Determinants of Statin-Induced Low-Density Lipoprotein Cholesterol ReductionCirculation: Cardiovascular Genetics2012227
18PITX2 Insufficiency Leads to Atrial Electrical and Structural Remodeling Linked to ArrhythmogenesisCirculation: Cardiovascular Genetics2011215
19High Incidence of the Cardiac Variant of Fabry Disease Revealed by Newborn Screening in the Taiwan Chinese PopulationCirculation: Cardiovascular Genetics2009212
20Compound and Digenic Heterozygosity Predicts Lifetime Arrhythmic Outcome and Sudden Cardiac Death in Desmosomal Gene–Related Arrhythmogenic Right Ventricular CardiomyopathyCirculation: Cardiovascular Genetics2013212
21Elevated CD14 ++ CD16 − Monocytes Predict Cardiovascular EventsCirculation: Cardiovascular Genetics2012207
22Coding Sequence Rare Variants Identified in MYBPC3 , MYH6 , TPM1 , TNNC1 , and TNNI3 From 312 Patients With Familial or Idiopathic Dilated CardiomyopathyCirculation: Cardiovascular Genetics2010204
23The Importance of Genetic Counseling, DNA Diagnostics, and Cardiologic Family Screening in Left Ventricular Noncompaction CardiomyopathyCirculation: Cardiovascular Genetics2010199
24DNA Methylation Map of Human AtherosclerosisCirculation: Cardiovascular Genetics2014199
25Comprehensive Desmosome Mutation Analysis in North Americans With Arrhythmogenic Right Ventricular Dysplasia/CardiomyopathyCirculation: Cardiovascular Genetics2009192
26A Genetic Risk Score Is Associated With Incident Cardiovascular Disease and Coronary Artery CalciumCirculation: Cardiovascular Genetics2012183
27Hypophosphatemia, Hyperphosphaturia, and Bisphosphonate Treatment Are Associated With Survival Beyond Infancy in Generalized Arterial Calcification of InfancyCirculation: Cardiovascular Genetics2008180
28Gain-of-Function Mutations in TRPM4 Cause Autosomal Dominant Isolated Cardiac Conduction DiseaseCirculation: Cardiovascular Genetics2010180
29Prevalence of Sarcomere Protein Gene Mutations in Preadolescent Children With Hypertrophic CardiomyopathyCirculation: Cardiovascular Genetics2009176
30Treatment Gaps in Adults With Heterozygous Familial Hypercholesterolemia in the United StatesCirculation: Cardiovascular Genetics2016176
31Comparative Lipidomics Profiling of Human Atherosclerotic PlaquesCirculation: Cardiovascular Genetics2011175
32Genome-Wide Screen for Metabolic Syndrome Susceptibility Loci Reveals Strong Lipid Gene Contribution But No Evidence for Common Genetic Basis for Clustering of Metabolic Syndrome TraitsCirculation: Cardiovascular Genetics2012175
33miR-143 and miR-145Circulation: Cardiovascular Genetics2011173
34Cardiovascular EpigeneticsCirculation: Cardiovascular Genetics2010172
35Polymorphism in the CETP Gene Region, HDL Cholesterol, and Risk of Future Myocardial InfarctionCirculation: Cardiovascular Genetics2009170
36Dynamic MicroRNA Expression Programs During Cardiac Differentiation of Human Embryonic Stem CellsCirculation: Cardiovascular Genetics2010167
37Sarcomere Gene Mutations in Isolated Left Ventricular Noncompaction Cardiomyopathy Do Not Predict Clinical PhenotypeCirculation: Cardiovascular Genetics2011166
38Comprehensive Whole-Genome and Candidate Gene Analysis for Response to Statin Therapy in the Treating to New Targets (TNT) CohortCirculation: Cardiovascular Genetics2009165
39Genome-Wide Association Study of Plasma N6 Polyunsaturated Fatty Acids Within the Cohorts for Heart and Aging Research in Genomic Epidemiology ConsortiumCirculation: Cardiovascular Genetics2014165
40Association of Genome-Wide Variation With the Risk of Incident Heart Failure in Adults of European and African AncestryCirculation: Cardiovascular Genetics2010162
41Nonfamilial Hypertrophic CardiomyopathyCirculation: Cardiovascular Genetics2017162
42Novel Calmodulin Mutations Associated With Congenital Arrhythmia SusceptibilityCirculation: Cardiovascular Genetics2014160
43Correlation of Peripheral-Blood Gene Expression With the Extent of Coronary Artery StenosisCirculation: Cardiovascular Genetics2008158
44Mutations in the Sarcomere Gene MYH7 in Ebstein AnomalyCirculation: Cardiovascular Genetics2011157
45Clinical and Pharmacogenetic Predictors of Circulating Atorvastatin and Rosuvastatin Concentrations in Routine Clinical CareCirculation: Cardiovascular Genetics2013157
46International Registry of Patients Carrying TGFBR1 or TGFBR2 MutationsCirculation: Cardiovascular Genetics2016157
47Outcome in Phospholamban R14del CarriersCirculation: Cardiovascular Genetics2014154
48Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) StudyCirculation: Cardiovascular Genetics2010153
49First Analysis of the Relation Between CYP2C19 Genotype and Pharmacodynamics in Patients Treated With Ticagrelor Versus ClopidogrelCirculation: Cardiovascular Genetics2010152
50Pharmacogenomic Determinants of the Cardiovascular Effects of DalcetrapibCirculation: Cardiovascular Genetics2015150