OOIR: Observatory of International Research

Papers

(The H4-Index of Circulation-Genomic and Precision Medicine is 26. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2022-08-01 to 2026-08-01.)

Article	Citations
Editorial Board	69
Relationships of Circulating Plasma Metabolites With the QT Interval in a Large Population Cohort	63
Cardiac Troponin C E135A Variant Impairs Myofilament Response to PKA Phosphorylation and Is Associated With Autosomal Dominant Dilated Cardiomyopathy With Diastolic Dysfunction	60
Compound Heterozygous Truncating Variants in the BAG5 Gene As a Cause of Early-Onset Dilated Cardiomyopathy	39
Accelerated Epigenetic Aging Is Associated With Multiple Cardiometabolic, Hematologic, and Renal Abnormalities: A Project Baseline Health Substudy	38
Diagnostic Yield of Exome Sequencing in Patients With Congenital Heart Disease From Southern Africa	38
Investigation of Copy Number Variation in South African Patients With Congenital Heart Defects	37
Polygenic Scoring for Detection of Ascending Thoracic Aortic Dilation	35
Multi-Ancestry Polygenic Risk Score for Coronary Heart Disease Based on an Ancestrally Diverse Genome-Wide Association Study and Population-Specific Optimization	33
Mechanistic Pathways Underlying Genetic Predisposition to Atrial Fibrillation Are Associated With Different Cardiac Phenotypes and Cardioembolic Stroke Risk	31
Metabolomic and Proteomic Signatures of Cardiorespiratory Fitness for Predicting All-Cause Mortality and Non-Communicable Disease Risk: A Prospective Study in the UK Biobank	31
Calmodulinopathy Associated Long QT Syndrome, Hypertrophic Cardiomyopathy With Excessive Trabeculation in a 14-Year-Old Girl Presenting With Ventricular Fibrillation	30
PRDM16 Deletion Is Associated With Sex-dependent Cardiomyopathy and Cardiac Mortality: A Translational, Multi-Institutional Cohort Study	30
Role of TBX20 Truncating Variants in Dilated Cardiomyopathy and Left Ventricular Noncompaction	30
Plasma Protein Profile Associated With a Family History of Early-Onset Coronary Heart Disease	30
Low-Cost High-Throughput Genotyping for Diagnosing Familial Hypercholesterolemia	29
Multisite Validation of a Functional Assay to Adjudicate SCN5A Brugada Syndrome–Associated Variants	29
Prediction of Coronary Artery Disease and Major Adverse Cardiovascular Events Using Clinical and Genetic Risk Scores for Cardiovascular Risk Factors	28
DMD-Associated Dilated Cardiomyopathy: Genotypes, Phenotypes, and Phenocopies	28
Polygenic Prediction of Nongoal Response to Statin Therapy	28
Mechanisms of RBM20 Cardiomyopathy: Insights From Model Systems	28
Proactive Variant Effect Mapping Aids Diagnosis in Pediatric Cardiac Arrest	27
Genotype-Phenotype Taxonomy of Hypertrophic Cardiomyopathy	27
Childhood Hypertrophic Cardiomyopathy Caused by Beta-Myosin Heavy Chain Variants Is Associated With a More Obstructive but Less Arrhythmogenic Phenotype Than Myosin-Binding Protein C Disease	26
Hereditary Hemorrhagic Telangiectasia Prevalence Estimates Calculated From GnomAD Allele Frequencies of Predicted Pathogenic Variants in ENG and	26

Editors and Editorial Board