Skin–Heart Connection
Fractal Dimension of Hypertrophic Cardiomyopathy Trabeculation
Truncating Plakophilin-2 Mutations in Arrhythmogenic Cardiomyopathy Are Associated With Protein Haploinsufficiency in Both Myocardium and Epidermis
Abnormal Cardiac Formation in Hypertrophic Cardiomyopathy
A Mutation Causing Brugada Syndrome Identifies a Mechanism for Altered Autonomic and Oxidant Regulation of Cardiac Sodium Currents
A Point Mutation in Myh10 Causes Major Defects in Heart Development and Body Wall Closure
Mechanical Unloading Promotes Myocardial Energy Recovery in Human Heart Failure
Cytochrome P450 Gene Variants, Race, and Mortality Among Clopidogrel-Treated Patients After Acute Myocardial Infarction
Genome-Wide Association Study Identifies Variants in Casein Kinase II (CSNK2A2) to be Associated With Leukocyte Telomere Length in a Punjabi Sikh Diabetic Cohort
Familial Transmission of Venous Thromboembolism
Lipoprotein(a) Levels, Genotype, and Incident Aortic Valve Stenosis
Induction of MicroRNA-21 With Exogenous Hydrogen Sulfide Attenuates Myocardial Ischemic and Inflammatory Injury in Mice
Genome-Wide Association Study of Plasma N6 Polyunsaturated Fatty Acids Within the Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
Following-Up Genome-Wide Association Study Signals
Strategies to Design and Analyze Targeted Sequencing Data
Sequence Variation in TMEM18 in Association With Body Mass Index
ADAM19 and HTR4 Variants and Pulmonary Function
Sequencing of 2 Subclinical Atherosclerosis Candidate Regions in 3669 Individuals
Sequencing of SCN5A Identifies Rare and Common Variants Associated With Cardiac Conduction
Association of Levels of Fasting Glucose and Insulin With Rare Variants at the Chromosome 11p11.2-MADD Locus
Genetics of Ischemic Stroke in Young Adults
MicroRNA Therapy for the Failing Heart
Obesity Genetics and Epigenetics
Correction
Correction
Correction