Nobuyuki Enzan
Okawa, Japan
Last Updated: 09/26/2026
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Found 55 publications
Integrating multi-ancestry common and rare variant mapping accelerates therapeutic target discovery.
Integrating multi-ancestry common and rare variant mapping accelerates therapeutic target discovery.
Journal: medRxiv : the preprint server for health sciences
Published: July 17, 2026
Machine Learning Reveals the Contribution of Rare Genetic Variants and Enhances Risk Prediction for Coronary Artery Disease in the Japanese Population.
Journal: Circulation. Genomic and precision medicine
Published: June 04, 2026
Genetically Mediated Differences in LDL Cholesterol and Risk of Venous Thromboembolism.
Journal: Journal of the American College of Cardiology
Published: April 06, 2026
Prognostic and exploratory neurohormonal correlates of hypochloraemia in heart failure: a multicentre cohort study.
Journal: Heart (British Cardiac Society)
Published: February 18, 2026
Temporal comparison of clinical practice and outcomes in heart failure: the JROADHF and JROADHF-NEXT studies.
Journal: European heart journal
Published: December 04, 2025
Impact of Tricuspid Regurgitation on the Prognosis of Heart Failure With Preserved Ejection Fraction: Insights From the JROADHF.
Journal: Circulation reports
Published: December 03, 2025
Multi-trait polygenic risk scores improve genomic prediction of atrial fibrillation across diverse ancestries.
Journal: Nature communications
Published: September 25, 2025
Last Updated: 09/26/2026