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Top Articles

#TitleJournalYearCitations
1Circulating MicroRNA-208b and MicroRNA-499 Reflect Myocardial Damage in Cardiovascular DiseaseCirculation: Cardiovascular Genetics2010683
2Epigenetic Signatures of Cigarette SmokingCirculation: Cardiovascular Genetics2016678
3Quantitative Serum Nuclear Magnetic Resonance Metabolomics in Cardiovascular Epidemiology and GeneticsCirculation: Cardiovascular Genetics2015624
4Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) ConsortiumCirculation: Cardiovascular Genetics2009519
5Increased MicroRNA-1 and MicroRNA-133a Levels in Serum of Patients With Cardiovascular Disease Indicate Myocardial DamageCirculation: Cardiovascular Genetics2011497
6Association of a Peripheral Blood Metabolic Profile With Coronary Artery Disease and Risk of Subsequent Cardiovascular EventsCirculation: Cardiovascular Genetics2010390
7Clinical Presentation, Long-Term Follow-Up, and Outcomes of 1001 Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patients and Family MembersCirculation: Cardiovascular Genetics2015370
8Whole Exome Sequencing to Identify a Novel Gene (Caveolin-1) Associated With Human Pulmonary Arterial HypertensionCirculation: Cardiovascular Genetics2012333
9Ethical and Practical Guidelines for Reporting Genetic Research Results to Study ParticipantsCirculation: Cardiovascular Genetics2010328
10Multiple Genetic Loci Influence Serum Urate Levels and Their Relationship With Gout and Cardiovascular Disease Risk FactorsCirculation: Cardiovascular Genetics2010285
11Association Between Shortened Leukocyte Telomere Length and Cardiometabolic OutcomesCirculation: Cardiovascular Genetics2015277
12PITX2c Is Expressed in the Adult Left Atrium, and Reducing Pitx2c Expression Promotes Atrial Fibrillation Inducibility and Complex Changes in Gene ExpressionCirculation: Cardiovascular Genetics2011267
13SCN5A Mutations and the Role of Genetic Background in the Pathophysiology of Brugada SyndromeCirculation: Cardiovascular Genetics2009262
14Circulating MicroRNAs as Biomarkers and Potential Paracrine Mediators of Cardiovascular DiseaseCirculation: Cardiovascular Genetics2010262
15A Mutation in the β3 Subunit of the Cardiac Sodium Channel Associated With Brugada ECG PhenotypeCirculation: Cardiovascular Genetics2009232
16Genetic Determinants of Statin-Induced Low-Density Lipoprotein Cholesterol ReductionCirculation: Cardiovascular Genetics2012231
17PITX2 Insufficiency Leads to Atrial Electrical and Structural Remodeling Linked to ArrhythmogenesisCirculation: Cardiovascular Genetics2011221
18Lipoprotein(a) Levels, Genotype, and Incident Aortic Valve StenosisCirculation: Cardiovascular Genetics2014219
19Coding Sequence Rare Variants Identified in MYBPC3 , MYH6 , TPM1 , TNNC1 , and TNNI3 From 312 Patients With Familial or Idiopathic Dilated CardiomyopathyCirculation: Cardiovascular Genetics2010218
20Elevated CD14 ++ CD16 Monocytes Predict Cardiovascular EventsCirculation: Cardiovascular Genetics2012217
21High Incidence of the Cardiac Variant of Fabry Disease Revealed by Newborn Screening in the Taiwan Chinese PopulationCirculation: Cardiovascular Genetics2009214
22Compound and Digenic Heterozygosity Predicts Lifetime Arrhythmic Outcome and Sudden Cardiac Death in Desmosomal Gene–Related Arrhythmogenic Right Ventricular CardiomyopathyCirculation: Cardiovascular Genetics2013209
23DNA Methylation Map of Human AtherosclerosisCirculation: Cardiovascular Genetics2014207
24The Importance of Genetic Counseling, DNA Diagnostics, and Cardiologic Family Screening in Left Ventricular Noncompaction CardiomyopathyCirculation: Cardiovascular Genetics2010205
25Gain-of-Function Mutations in TRPM4 Cause Autosomal Dominant Isolated Cardiac Conduction DiseaseCirculation: Cardiovascular Genetics2010200
26A Genetic Risk Score Is Associated With Incident Cardiovascular Disease and Coronary Artery CalciumCirculation: Cardiovascular Genetics2012196
27Comprehensive Desmosome Mutation Analysis in North Americans With Arrhythmogenic Right Ventricular Dysplasia/CardiomyopathyCirculation: Cardiovascular Genetics2009195
28miR-143 and miR-145Circulation: Cardiovascular Genetics2011189
29Polymorphism in the CETP Gene Region, HDL Cholesterol, and Risk of Future Myocardial InfarctionCirculation: Cardiovascular Genetics2009186
30Cardiovascular EpigeneticsCirculation: Cardiovascular Genetics2010186
31Genome-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 Genetics2012182
32Hypophosphatemia, Hyperphosphaturia, and Bisphosphonate Treatment Are Associated With Survival Beyond Infancy in Generalized Arterial Calcification of InfancyCirculation: Cardiovascular Genetics2008181
33Comparative Lipidomics Profiling of Human Atherosclerotic PlaquesCirculation: Cardiovascular Genetics2011177
34Prevalence of Sarcomere Protein Gene Mutations in Preadolescent Children With Hypertrophic CardiomyopathyCirculation: Cardiovascular Genetics2009176
35Association of Genome-Wide Variation With the Risk of Incident Heart Failure in Adults of European and African AncestryCirculation: Cardiovascular Genetics2010176
36Dynamic MicroRNA Expression Programs During Cardiac Differentiation of Human Embryonic Stem CellsCirculation: Cardiovascular Genetics2010176
37Correlation of Peripheral-Blood Gene Expression With the Extent of Coronary Artery StenosisCirculation: Cardiovascular Genetics2008175
38Comprehensive Whole-Genome and Candidate Gene Analysis for Response to Statin Therapy in the Treating to New Targets (TNT) CohortCirculation: Cardiovascular Genetics2009170
39Treatment Gaps in Adults With Heterozygous Familial Hypercholesterolemia in the United StatesCirculation: Cardiovascular Genetics2016170
40Clinical and Pharmacogenetic Predictors of Circulating Atorvastatin and Rosuvastatin Concentrations in Routine Clinical CareCirculation: Cardiovascular Genetics2013168
41Sarcomere Gene Mutations in Isolated Left Ventricular Noncompaction Cardiomyopathy Do Not Predict Clinical PhenotypeCirculation: Cardiovascular Genetics2011167
42Novel Calmodulin Mutations Associated With Congenital Arrhythmia SusceptibilityCirculation: Cardiovascular Genetics2014165
43Genome-Wide Association Study of Plasma N6 Polyunsaturated Fatty Acids Within the Cohorts for Heart and Aging Research in Genomic Epidemiology ConsortiumCirculation: Cardiovascular Genetics2014164
44First Analysis of the Relation Between CYP2C19 Genotype and Pharmacodynamics in Patients Treated With Ticagrelor Versus ClopidogrelCirculation: Cardiovascular Genetics2010163
45Multiethnic Genome-Wide Association Study of Cerebral White Matter Hyperintensities on MRICirculation: Cardiovascular Genetics2015162
46Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) StudyCirculation: Cardiovascular Genetics2010159
47Pharmacogenomic Determinants of the Cardiovascular Effects of DalcetrapibCirculation: Cardiovascular Genetics2015158
48Targeted Next-Generation Sequencing for the Molecular Genetic Diagnostics of CardiomyopathiesCirculation: Cardiovascular Genetics2011155
49Mutations in the Sarcomere Gene MYH7 in Ebstein AnomalyCirculation: Cardiovascular Genetics2011153
50Modeling of Arrhythmogenic Right Ventricular Cardiomyopathy With Human Induced Pluripotent Stem CellsCirculation: Cardiovascular Genetics2013153