Circulation-genomic And Precision Medicine

Effects of Delivering SLCO1B1 Pharmacogenetic Information in Randomized Trial and Observational Settings

Genetic Susceptibility Loci for Cardiovascular Disease and Their Impact on Atherosclerotic Plaques

International Triadin Knockout Syndrome Registry The Clinical Phenotype and Treatment Outcomes of Patients With Triadin Knockout Syndrome

Dawn of Epitranscriptomic Medicine

Clinical Implications of Identifying Pathogenic Variants in Individuals With Thoracic Aortic Dissection

Tailoring the American College of Medical Genetics and Genomics and the Association for Molecular Pathology Guidelines for the Interpretation of Sequenced Variants in the FBN1 Gene for Marfan Syndrome Proposal for a Disease- and Gene-Specific Guideline

Interactions Between Regulatory Variants in CYP7A1 (Cholesterol 7 alpha-Hydroxylase) Promoter and Enhancer Regions Regulate CYP7A1 Expression

CETP (Cholesteryl Ester Transfer Protein) Concentration A Genome-Wide Association Study Followed by Mendelian Randomization on Coronary Artery Disease

Nocturnal Atrial Fibrillation Caused by Mutation in KCND Encoding Pore-Forming (alpha) Subunit of the Cardiac Kv4.2 Potassium Channel

Cardiac Dysfunction in Duchenne Muscular Dystrophy Is Less Frequent in Patients With Mutations in the Dystrophin Dp116 Coding Region Than in Other Regions