It’s Never Too Early to Look
A Modern Approach to Classify Missense Mutations in Cardiac Channelopathy Genes
Spongious Hypertrophic Cardiomyopathy in Patients With Mutations in the Four-and-a-Half LIM Domain 1 Gene
Subtle Abnormalities in Contractile Function Are an Early Manifestation of Sarcomere Mutations in Dilated Cardiomyopathy
BMPR2 Mutations Influence Phenotype More Obviously in Male Patients With Pulmonary Arterial Hypertension
Phylogenetic and Physicochemical Analyses Enhance the Classification of Rare Nonsynonymous Single Nucleotide Variants in Type 1 and 2 Long-QT Syndrome
Matrix Metalloproteinase-9 Genotype as a Potential Genetic Marker for Abdominal Aortic Aneurysm
Exome Sequencing Identifies 2 Rare Variants for Low High-Density Lipoprotein Cholesterol in an Extended Family
Pooled DNA Resequencing of 68 Myocardial Infarction Candidate Genes in French Canadians
Gene-Targeted Analysis of Copy Number Variants Identifies 3 Novel Associations With Coronary Heart Disease Traits
Diagnostic and Prognostic Performance of Myeloperoxidase Plasma Levels Compared With Sensitive Troponins in Patients Admitted With Acute Onset Chest Pain
Genetic Basis of Familial Valvular Heart Disease
A Clinical Approach to Inherited Arrhythmias
Chasing Cysteine Oxidative Modifications
High-Resolution Separation of Cardiovascular Proteomes
Transforming Growth factor β2 Mutations and Familial Thoracic Aortic Aneurysms
Increasing Power
Cardiovascular Risk Factors