(top 60%)
Impact Factor
(top 60%)
extended IF
87(top 4%)
H-Index
1,502
authors
831
papers
31,629
citations
2,783
citing journals
26,610
citing authors

Most Cited Articles of Circulation: Cardiovascular Genetics in 2016

TitleYearCitations
Epigenetic Signatures of Cigarette Smoking2016419
Treatment Gaps in Adults With Heterozygous Familial Hypercholesterolemia in the United States: Data From the CASCADE-FH Registry2016122
International Registry of Patients Carrying TGFBR1 or TGFBR2 Mutations: Results of the MAC (Montalcino Aortic Consortium)2016102
Spectrum and Prevalence of CALM1-, CALM2-, and CALM3-Encoded Calmodulin Variants in Long QT Syndrome and Functional Characterization of a Novel Long QT Syndrome-Associated Calmodulin Missense Variant, E141G201672
CD36 Is a Matrix Metalloproteinase-9 Substrate That Stimulates Neutrophil Apoptosis and Removal During Cardiac Remodeling201659
Mendelian Randomization Studies Do Not Support a Role for Vitamin D in Coronary Artery Disease201659
Nutrigenomics, the Microbiome, and Gene-Environment Interactions: New Directions in Cardiovascular Disease Research, Prevention, and Treatment: A Scientific Statement From the American Heart Association201658
Whole-Exome Molecular Autopsy After Exertion-Related Sudden Unexplained Death in the Young201656
Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction201646
Genotype-Dependent Effects of Dalcetrapib on Cholesterol Efflux and Inflammation: Concordance With Clinical Outcomes201645
Elevated Plasma Cardiac Troponin T Levels Caused by Skeletal Muscle Damage in Pompe Disease201644
Homozygous Familial Hypercholesterolemia in Spain: Prevalence and Phenotype-Genotype Relationship201640
Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease201637
Genetic Susceptibility to Lipid Levels and Lipid Change Over Time and Risk of Incident Hyperlipidemia in Chinese Populations201635
Enhancing Literacy in Cardiovascular Genetics: A Scientific Statement From the American Heart Association201635
Clinical Utility of Multimarker Genetic Risk Scores for Prediction of Incident Coronary Heart Disease: A Cohort Study Among Over 51 000 Individuals of European Ancestry201634
Systematic Characterization of Long Noncoding RNAs Reveals the Contrasting Coordination of Cis- and Trans-Molecular Regulation in Human Fetal and Adult Hearts201634
Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk201633
Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis201632
Genetic Variation in the SLC8A1 Calcium Signaling Pathway Is Associated With Susceptibility to Kawasaki Disease and Coronary Artery Abnormalities201632
International Genome-Wide Association Study Consortium Identifies Novel Loci Associated With Blood Pressure in Children and Adolescents201630
New Insights Into the Genetic Basis of Inherited Arrhythmia Syndromes201628
Decoding the Long Noncoding RNA During Cardiac Maturation: A Roadmap for Functional Discovery201628
Sudden Cardiac Arrest and Rare Genetic Variants in the Community201622
Search for Rare Copy-Number Variants in Congenital Heart Defects Identifies Novel Candidate Genes and a Potential Role for FOXC1 in Patients With Coarctation of the Aorta201621