| Evaluating the Clinical Validity of Hypertrophic Cardiomyopathy Genes |
36 |
| Induced Pluripotent Stem Cells for Cardiovascular Disease Modeling and Precision Medicine A Scientific Statement From the American Heart Association |
27 |
| Circulating Branched-Chain Amino Acids and Incident Cardiovascular Disease in a Prospective Cohort of US Women |
25 |
| Clinical Outcomes and Sustainability of Using CYP2C19 Genotype-Guided Antiplatelet Therapy After Percutaneous Coronary Intervention |
18 |
| Birthweight, Type 2 Diabetes Mellitus, and Cardiovascular Disease Addressing the Barker Hypothesis With Mendelian Randomization |
17 |
| Exome Sequencing in Children With Pulmonary Arterial Hypertension Demonstrates Differences Compared With Adults |
17 |
| Cardiovascular Health in Turner Syndrome A Scientific Statement From the American Heart Association |
15 |
| Chemotherapy-Related Cardiac Dysfunction A Systematic Review of Genetic Variants Modulating Individual Risk |
15 |
| Thyroid Function and Dysfunction in Relation to 16 Cardiovascular Diseases A Mendelian Randomization Study |
14 |
| High-Throughput Functional Evaluation of KCNQ1 Decrypts Variants of Unknown Significance |
13 |
| Whole-Exome Sequencing Identifies Pathogenic Variants in TJP1 Gene Associated With Arrhythmogenic Cardiomyopathy |
13 |
| Human Genetics of Obesity and Type 2 Diabetes Mellitus Past, Present, and Future |
13 |
| Polygenic Contribution in Individuals With Early-Onset Coronary Artery Disease |
12 |
| Validation of Genome-Wide Polygenic Risk Scores for Coronary Artery Disease in French Canadians |
12 |
| Large-Scale Phenome-Wide Association Study of PCSK9 Variants Demonstrates Protection Against Ischemic Stroke |
11 |
| Prospective Cardiovascular Genetics Evaluation in Spontaneous Coronary Artery Dissection |
11 |
| Impact of Apolipoprotein(a) Isoform Size on Lipoprotein(a) Lowering in the HPS2-THRIVE Study |
10 |
| Prospective Study of Epigenetic Age Acceleration and Incidence of Cardiovascular Disease Outcomes in the ARIC Study (Atherosclerosis Risk in Communities) |
10 |
| SCN5A (Na-V 1.5) Variant Functional Perturbation and Clinical Presentation Variants of a Certain Significance |
10 |
| Impact of Pathogenic FBN1 Variant Types on the Progression of Aortic Disease in Patients With Marfan Syndrome |
9 |
| Establishment of Specialized Clinical Cardiovascular Genetics Programs: Recognizing the Need and Meeting Standards: A Scientific Statement From the American Heart Association |
9 |
| A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome Data |
9 |
| Assessment and Validation of a Phenotype-Enhanced Variant Classification Framework to Promote or Demote RYR2 Missense Variants of Uncertain Significance |
9 |
| Gut Microbiome and Response to Cardiovascular Drugs |
8 |
| Outcomes of Contemporary Family Screening in Hypertrophic Cardiomyopathy |
8 |
| Rare Missense Variants in TLN1 Are Associated With Familial and Sporadic Spontaneous Coronary Artery Dissection |
8 |
| Familial Sinus Node Disease Caused by a Gain of GIRK (G-Protein Activated Inwardly Rectifying K+ Channel) Channel Function |
8 |
| Interleukin-6 Receptor Signaling and Abdominal Aortic Aneurysm Growth Rates |
8 |
| Loss-of-Function ABCC8 Mutations in Pulmonary Arterial Hypertension |
8 |
| Genetic Regulation of PCSK9 (Proprotein Convertase Subtilisin/Kexin Type 9) Plasma Levels and Its Impact on Atherosclerotic Vascular Disease Phenotypes |
7 |
| Proteomic Analysis of the Myocardium in Hypertrophic Obstructive Cardiomyopathy |
7 |
| Rare Protein-Truncating Variants in APOB, Lower Low-Density Lipoprotein Cholesterol, and Protection Against Coronary Heart Disease |
7 |
| Variants in NKX2-5 and FLNC Cause Dilated Cardiomyopathy and Sudden Cardiac Death |
7 |
| Partitioning the Pleiotropy Between Coronary Artery Disease and Body Mass Index Reveals the Importance of Low Frequency Variants and Central Nervous System-Specific Functional Elements |
7 |
| Identification of Common and Rare Genetic Variation Associated With Plasma Protein Levels Using Whole-Exome Sequencing and Mass Spectrometry |
6 |
| ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals |
6 |
| Arrhythmogenic Right Ventricular Cardiomyopathy-Associated Desmosomal Variants Are Rarely De Novo: Segregation and Haplotype Analysis of a Multinational Cohort |
6 |
| Functional Assays to Screen and Dissect Genomic Hits Doubling Down on the National Investment in Genomic Research |
6 |
| Key Value of RNA Analysis of MYBPC3 Splice-Site Variants in Hypertrophic Cardiomyopathy |
6 |
| A-Band Titin Truncation in Zebrafish Causes Dilated Cardiomyopathy and Hemodynamic Stress Intolerance |
6 |
| Effects of Delivering SLCO1B1 Pharmacogenetic Information in Randomized Trial and Observational Settings |
6 |
| Genetic Susceptibility Loci for Cardiovascular Disease and Their Impact on Atherosclerotic Plaques |
6 |
| International Triadin Knockout Syndrome Registry The Clinical Phenotype and Treatment Outcomes of Patients With Triadin Knockout Syndrome |
6 |
| Dawn of Epitranscriptomic Medicine |
6 |
| Clinical Implications of Identifying Pathogenic Variants in Individuals With Thoracic Aortic Dissection |
6 |
| 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 |
5 |
| Interactions Between Regulatory Variants in CYP7A1 (Cholesterol 7 alpha-Hydroxylase) Promoter and Enhancer Regions Regulate CYP7A1 Expression |
5 |
| CETP (Cholesteryl Ester Transfer Protein) Concentration A Genome-Wide Association Study Followed by Mendelian Randomization on Coronary Artery Disease |
5 |
| Nocturnal Atrial Fibrillation Caused by Mutation in KCND Encoding Pore-Forming (alpha) Subunit of the Cardiac Kv4.2 Potassium Channel |
5 |
| Cardiac Dysfunction in Duchenne Muscular Dystrophy Is Less Frequent in Patients With Mutations in the Dystrophin Dp116 Coding Region Than in Other Regions |
5 |
