OOIR: Observatory of International Research

Papers

(The H4-Index of Circulation-Genomic and Precision Medicine is 20. 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 2021-04-01 to 2025-04-01.)

Article	Citations
MYH7 p.Glu903Gln Is a Pathogenic Variant Associated With Hypertrophic Cardiomyopathy	154
Multiomic Profiling in Black and White Populations Reveals Novel Candidate Pathways in Left Ventricular Hypertrophy and Incident Heart Failure Specific to Black Adults	106
Evaluating the Cardiometabolic Efficacy and Safety of Lipoprotein Lipase Pathway Targets in Combination With Approved Lipid-Lowering Targets: A Drug Target Mendelian Randomization Study	90
Compound Heterozygous Truncating Variants in the BAG5 Gene As a Cause of Early-Onset Dilated Cardiomyopathy	72
Retraction of: Systematic Evaluation of KCNQ1 variant using ACMG/AMP Guidelines and Risk Stratification in Long QT Syndrome Type 1	67
Pregnancy Outcomes in Females With Dilated Cardiomyopathy–Associated Rare Genetic Variants	55
Oligogenic Architecture of Rare Noncoding Variants Distinguishes 4 Congenital Heart Disease Phenotypes	50
Pharmacogenomics of the Efficacy and Safety of Colchicine in COLCOT	40
Clinical Characteristics of SCN5A p.R965C Carriers: A Common Founder Variant Predisposing to Brugada Syndrome in Thailand	33
Genome-Wide De Novo Variants in Congenital Heart Disease Are Not Associated With Maternal Diabetes or Obesity	31
How Normal Is Low-Normal Left Ventricular Ejection Fraction in Familial Dilated Cardiomyopathy?	30
Reproductive Carrier Screening: Identifying Families at Risk for Familial Hypercholesterolemia in the United States	27
Polygenic Risk and Coronary Artery Disease Severity	27
Genetically Predicted Pulse Pressure and Risk of Abdominal Aortic Aneurysm: A Mendelian Randomization Analysis	23
Mulibrey Nanism and the Real Time Use of Genome and Biobank Engines to Inform Clinical Care in an Ultrarare Disease	23
Hidden Risk: Arrhythmogenic Genes in the General Population	23
Rare Genetic Variants Associated With Sudden Cardiac Arrest in the Young: A Prospective, Population-Based Study	22
Cardioinformatics Advancements in Healthcare and Biotechnology	22
Editorial Board	21
Correction to: Coassin et al, Genome-Wide Characterization of a Highly Penetrant Form of Hyperlipoprotein(a)emia Associated With Genetically Elevated Cardiovascular Risk	21
Dynamic Importance of Genomic and Clinical Risk for Coronary Artery Disease Over the Life Course	20
Prognostic Implications Between hsCRP and CYP2C19 Genotype in Patients From East Asia: Insights From the PTRG-DES Consortium	20
Lipoprotein(a) Atherosclerotic Cardiovascular Disease Risk Score Development and Prediction in Primary Prevention From Real-World Data	20
Recent Advances on the Genetics of Spontaneous Coronary Artery Dissection	20