Academic Journal
Q1Circulation: Genomic and Precision Medicine
About Circulation: Genomic and Precision Medicine
Circulation: Genomic and Precision Medicine is a scholarly journal published by Lippincott Williams and Wilkins. SCImago 2025 lists it in Q1, with an SJR of 1.84 and H-index of 107.
Coverage: 2018-2026. Research categories: Cardiology and Cardiovascular Medicine (Q1); Genetics (Q1); Genetics (clinical) (Q1).
Source-backed journal facts
Topics in published research
Cardiomyopathy and Myosin Studies; Genetic Associations and Epidemiology; Cardiac electrophysiology and arrhythmias; Congenital heart defects research; Genomics and Rare Diseases; Cardiovascular Effects of Exercise.
OpenAlex classifies topics from published works. These topics are not the publisher’s official aims and scope.
Source: OpenAlex source record. Retrieved 2026-10-03. Source record updated 2026-10-02. OpenAlex metrics are different from SCImago metrics and the Clarivate Journal Impact Factor.
Journal Metrics
Quartile, SJR and the listed SCImago H-index use the 2025 imported SCImago dataset. A quartile may vary by subject category. Values without a source or reporting year are unverified historical entries. Verify the current Journal Impact Factor with Clarivate or the publisher before using it.
Aims & Scope
The publisher’s official aims and scope have not yet been verified for this profile. Use the journal website to check subject fit and accepted article types before submitting.
Recent Research Articles
Latest publications matched automatically by ISSN.
Cardiologist-Delivered Genetic Testing in 482 Patients With Cardiomyopathy: The Infrastructure Needed for Mainstream Testing at Scale
Omid Kiamanesh, Susan Christian, Robert Miller, Kristin Lyons et al.
2026-10-02 · DOI: 10.1161/circgen.126.005782Personalized Nutrition for Hypertension: Current Evidence and Future Directions
Phoebe Cheong, Cass Mangan, Erin D. Clarke, Jordan Stanford et al.
2026-10-02 · DOI: 10.1161/circgen.125.005566Decoding Long Noncoding RNAs in Cardiac Development and Congenital Heart Disease: Recent Advances and Clinical Perspectives
Ying Zhang, Aldons J. Lusis, Marlin Touma
2026-10-02 · DOI: 10.1161/circgen.125.005691FLNC -Related Cardiomyopathies in an Admixed Population: Expanding the Genotype-Phenotype Spectrum and Clinical Correlates
Natalia Quintella Sangiorgi Olivetti, Luciana Sacilotto, Julia de Barros Negri Ferreira, Silas Furquim et al.
2026-10-02 · DOI: 10.1161/circgen.126.005733Homozygous TNNC1-A8V Causes Impaired Diastolic Function and Restrictive Cardiomyopathy in Children and Mice
Paula Nieto Morales, Enya Dewars, Amanda M. Mascarenhas, Mary Silzer et al.
2026-09-30 · DOI: 10.1161/circgen.125.005599Genomic Yield of Long-Read Sequencing in Congenital Heart Disease
Robert Lesurf, Anjali Jain, Nour Hanafi, Aleksandra Mitina et al.
2026-09-30 · DOI: 10.1161/circgen.125.005305Polygenic Risk Scores of Coronary Heart Disease in Chronic Kidney Disease Population: The CRIC Study
Quan Sun, Amarnath Marthi, Jia Wen, Bridget M. Lin et al.
2026-09-30 · DOI: 10.1161/circgen.126.005684Rare Cardiac Genetic Variation Is Associated With Postoperative Atrial Fibrillation
Zhanlin Chen, Anirudha S. Chandrabhatla, Anna Pfenniger, Tom Liu et al.
2026-09-30 · DOI: 10.1161/circgen.125.005688Genomic Readiness in Cardiology: Gaps in Awareness, Confidence, and Risk Literacy: Results From the PLATO Cross-Sectional Survey
Ruofei (Trophy) Chen, Adam J. Nelson, Stephen J. Nicholls
2026-09-28 · DOI: 10.1161/circgen.126.005831Gene-Corrected Human iPSC–Derived Cardiomyocytes and Skeletal Muscles Reveal Partial Dystrophin Dp427 Preservation and Cardiac Dp116 Expression in Duchenne Muscular Dystrophy Patient With a Splice-Site Mutation in Intron 68 (c.9975-1G>T)
Marta Białobrzeska, Marta Przymuszała, Paweł Ferdek, Iryna Viestia et al.
2026-09-25 · DOI: 10.1161/circgen.125.005376Clinical Characteristics and Outcomes of Hypertrophic Cardiomyopathy Associated With Thin Filament Variants: Insights From the SHaRe Registry
Alessia Argirò, Joshua Meisner, Eric Adler, Edoardo Bertero et al.
2026-09-24 · DOI: 10.1161/circgen.126.005696Comparing Cardiac Genetic Testing Pathways: Impacts on Access, Informed Choice, and Decisional Satisfaction
Susan Christian, Tallia C. Belcher, Marc Benoit, Alicia Chan et al.
2026-09-24 · DOI: 10.1161/circgen.126.005829Effects of Polygenic Risk Scores and Physical Activity on Blood Pressure Trajectories in Childhood, Adolescence, and Young Adulthood
Tian Xie, Shili Luo, Chris H.L. Thio, Marloes Cardol et al.
2026-09-24 · DOI: 10.1161/circgen.125.004307Cardiomyopathy and Sudden Cardiac Death as a Rare Presentation of Mucolipidosis Type III in a Family With Compound Heterozygous Variants in GNPTAB
Natalie Stewart, Natasha Henden, Carlos C. Smith-Díaz, Jennifer Rigby et al.
2026-08 · DOI: 10.1161/circgen.126.005703Diagnostic Yield of Exome Sequencing in Patients With Congenital Heart Disease From Southern Africa
Timothy F. Spracklen, Thomas Aldersley, John Lawrenson, Paul Human et al.
2026-08 · DOI: 10.1161/circgen.125.005463Novel Truncating Variant c.1222DupC in RBM20 Causes Cardiomyopathy Consistent With Haploinsufficiency
Priyanka Pant, Yong Huang, Zakiya Ghouse, Fang Bai et al.
2026-08 · DOI: 10.1161/circgen.125.005471Rare KDR Variants Define a Distinct Genetic Contribution to Congenital Heart Disease
Feria A. Ladha, Paul Avillach, Alexander R. Opotowsky, Aldweib Nael et al.
2026-08 · DOI: 10.1161/circgen.125.005659Functional and Molecular Characterization of Novel GDF2 ( BMP9 ) and BMP10 Variants From the French PAH and HHT Cohorts
Agnès Desroches-Castan, Léa Beurier-Soulat, Maud Tusseau, Florence Coulet et al.
2026-08 · DOI: 10.1161/circgen.125.005626Integrated Genomic and Transcriptomic Study Reveals MAPK11 and PER1 as Important Obesity Susceptibility Genes in a High-Risk Hispanic/Latino Population
Daeeun Kim, Hannah G. Polikowsky, Heather M. Highland, Hung-Hsin Chen et al.
2026-08 · DOI: 10.1161/circgen.125.005298Metabolic Task Analysis Reveals Distinct Metabotypes in End-Stage Dilated Cardiomyopathy
Bastien S.C. Nihant, Job A.J. Verdonschot, Sonia Bălan, Eva Thielecke et al.
2026-08 · DOI: 10.1161/circgen.125.005366Reviews
Community Reviews
Version History
September 25, 2026 at 7:13 am
September 25, 2026