Are Double Mutations Double Trouble?
Local Ancestry Association, Admixture Mapping, and Ongoing Challenges
Identification of Cadherin 2 (CDH2) Mutations in Arrhythmogenic Right Ventricular Cardiomyopathy
Screening of the Filamin C Gene in a Large Cohort of Hypertrophic Cardiomyopathy Patients
Nonfamilial Hypertrophic Cardiomyopathy : Prevalence, Natural History, and Clinical Implications
Prevalence and Clinical Implication of Double Mutations in Hypertrophic Cardiomyopathy : Revisiting the Gene-Dose Effect
Additional Candidate Genes for Human Atherosclerotic Disease Identified Through Annotation Based on Chromatin Organization
Admixture Mapping of Subclinical Atherosclerosis and Subsequent Clinical Events Among African Americans in 2 Large Cohort Studies
Socioeconomic Status Interacts with the Genetic Effect of a Chromosome 9p21.3 Common Variant to Influence Coronary Artery Calcification and Incident Coronary Events in the Heinz Nixdorf Recall Study (Risk Factors, Evaluation of Coronary Calcium, and Lifestyle)
Genome-Wide Association Study Meta-Analysis of Long-Term Average Blood Pressure in East Asians
Investigating the Genetic Architecture of the PR Interval Using Clinical Phenotypes
Heritability of the Severity of the Metabolic Syndrome in Whites and Blacks in 3 Large Cohorts
Genetic Analysis of Venous Thromboembolism in UK Biobank Identifies the ZFPM2 Locus and Implicates Obesity as a Causal Risk Factor
Delivering Clinical Grade Sequencing and Genetic Test Interpretation for Cardiovascular Medicine
Potential Impact and Study Considerations of Metabolomics in Cardiovascular Health and Disease : A Scientific Statement From the American Heart Association