Navid A. Nafissi

Navid A. Nafissi

Cardiac Electrophysiology | Cardiology

1237 Harding Place
Charlotte, NC 28204

Last Updated: 09/26/2026

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Found 15 publications

Rare coding variant architecture and gene discovery from 130,000 sequenced cases of atrial fibrillation.

Rare coding variant architecture and gene discovery from 130,000 sequenced cases of atrial fibrillation.

Journal: Research square

Published: May 18, 2026

Rare coding variant architecture and gene discovery from 130,000 sequenced cases of atrial fibrillation.

Rare coding variant architecture and gene discovery from 130,000 sequenced cases of atrial fibrillation.

Journal: Research square

Published: May 18, 2026

Clonal hematopoiesis associates with prevalent and incident cardiometabolic disease in a cardiac catheterization cohort.

Clonal hematopoiesis associates with prevalent and incident cardiometabolic disease in a cardiac catheterization cohort.

Journal: PloS one

Published: August 20, 2025

Clonal Hematopoiesis Associates with Prevalent and Incident Cardiometabolic Disease in High-Risk Individuals.

Clonal Hematopoiesis Associates with Prevalent and Incident Cardiometabolic Disease in High-Risk Individuals.

Journal: medRxiv : the preprint server for health sciences

Published: January 27, 2025

Meta-Analysis of Genome-Wide Association Studies Reveals Genetic Mechanisms of Supraventricular Arrhythmias.

Meta-Analysis of Genome-Wide Association Studies Reveals Genetic Mechanisms of Supraventricular Arrhythmias.

Journal: Circulation. Genomic and precision medicine

Published: May 28, 2024

The impact of common and rare genetic variants on bradyarrhythmia development.

The impact of common and rare genetic variants on bradyarrhythmia development.

Journal: Nature genetics

Published: September 24, 2023

Left Atrial Appendage Occlusion Devices: Are We Isolating the Right Population?

Left Atrial Appendage Occlusion Devices: Are We Isolating the Right Population?

Journal: The American journal of cardiology

Published: June 04, 2023

Prevalence and Phenotypic Burden of Monogenic Arrhythmias Using Integration of Electronic Health Records With Genetics.

Prevalence and Phenotypic Burden of Monogenic Arrhythmias Using Integration of Electronic Health Records With Genetics.

Journal: Circulation. Genomic and precision medicine

Published: September 22, 2022

Expanding the Molecular Autopsy to Uncover Occult Cardiomyopathy: Concealed to Revealed.

Expanding the Molecular Autopsy to Uncover Occult Cardiomyopathy: Concealed to Revealed.

Journal: Journal of the American College of Cardiology

Published: September 13, 2022

Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases.

Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases.

Journal: Nature genetics

Published: March 12, 2022

Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk.

Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk.

Journal: Nature genetics

Published: March 03, 2022

Differentiation of Human Induced Pluripotent Stem Cells into Epicardial-Like Cells.

Differentiation of Human Induced Pluripotent Stem Cells into Epicardial-Like Cells.

Journal: Methods in molecular biology (Clifton, N.J.)

Published: August 29, 2020

Showing 1-12 of 15

Last Updated: 09/26/2026