Iftikhar J. Kullo

Mayo Clinic — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

82h-index25.3kcitations584works6.42yr avg
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Research Topics

Genetic Associations and Epidemiology(127), Lipoproteins and Cardiovascular Health(89), Genomics and Rare Diseases(63), Peripheral Artery Disease Management(59), BRCA gene mutations in cancer(56)

Publications574 total

Healthcare professionals’ experiences returning monogenic, polygenic, and integrated risk results in the eMERGE study
Human Genetics and Genomics Advances·2025Open Access
Author Correction: Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrum
Nature Genetics·2025Open Access
Recommendations for responsible use of population descriptors in polygenic risk score development
Nature Genetics·2025· 1 citedOpen Access
Exome Sequencing Enhances Screening for Familial Hypercholesterolemia Within a Multi-Site Healthcare System
Circulation Genomic and Precision Medicine·2025
Admixture Mapping of Lipid Traits in Hispanic Americans
Journal of the American Heart Association·2025Open Access
Abstract 4366483: Multi-omic Characterization of Clonal Hematopoiesis of Indeterminate Potential (CHIP) in the ISCHEMIA (International Study of Comparative Health Effectiveness with Medical and Invasive Approaches) Trials Biorepository
Circulation·2025
Abstract 4370594: Associations Between Chronic Kidney Disease and Inflammatory Biomarkers in the Genetic Epidemiology Network of Arteriopathy Cohort
Circulation·2025
Abstract 4369800: Association of Inflammatory Hypertension with Left Ventricular Hypertrophy in Black Adults from the Genetic Epidemiology Network of Arteriopathy Study
Circulation·2025
Abstract 4369684: Mitochondrial DNA Copy Number (mtDNA-CN): Associations with Mortality and Gene Expression in the International Study of Comparative Health Effectiveness with Medical and Invasive Approaches (ISCHEMIA) Biorepository
Circulation·2025
Brachial-Ankle Pulse Wave Velocity Is Associated with Kidney Function Decline in Adults Undergoing Cardiovascular Disease Screening
Kidney360·2025· 1 citedOpen Access
Clinical use of polygenic risk scores: current status, barriers and future directions
Nature Reviews Genetics·2025· 9 cited
From GWAS to Translational Insights: Comprehensive Genetic Analysis of Nephrotic Syndrome from Multiple Populations
2025Open Access
Transformer patient embedding using electronic health records enables patient stratification and progression analysis
npj Digital Medicine·2025· 4 citedOpen Access
Development of gene-specific ACMG/AMP guidelines for the interpretation of APOB and PCSK9 variants in familial hypercholesterolemia
Atherosclerosis·2025Open Access
Data sharing in the PRIMED Consortium: Design, implementation, and recommendations for future policymaking
The American Journal of Human Genetics·2025· 2 citedOpen Access
Covering medical care costs for participants in the eMERGE Network: Challenges for equity and implementation
Genetics in Medicine·2025· 1 cited
Clonal Hematopoiesis of Indeterminate Potential in Chronic Coronary Disease: A Report From the ISCHEMIA Trials Biorepository
Circulation Genomic and Precision Medicine·2025Open Access
Recognition and management of persistent chylomicronemia: A joint expert clinical consensus by the National Lipid Association and the American Society for Preventive Cardiology
American Journal of Preventive Cardiology·2025· 6 citedOpen Access
Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrum
Nature Genetics·2025· 14 cited
Epidemiology and longitudinal course of chylomicronemia: Insights from NHANES and a large health care system
Journal of clinical lipidology·2025· 8 cited
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Frequent Co-authors

Gail P. Jarvik(16), Marylyn D. Ritchie(14), Christopher G. Chute(13), Joshua C. Denny(11), Jennifer A. Pacheco(10), David R. Crosslin(10), Teri A. Manolio(9), Rex L. Chisholm(9), Dan M. Roden(9), Rongling Li(9), Catherine A. McCarty(8), David Carrell(7), Jyotishman Pathak(7), Suzette J. Bielinski(7), Håkon Håkonarson(7), Ozan Dikilitas(7), Luke V. Rasmussen(6), Eric B. Larson(6), Yan V. Sun(6), Daniel J. Schaid(6)