Last Updated: 09/26/2026
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Found 25 publications
Prevalence and Clinical Impact of Pathogenic Variants in Cardiomyopathy Genes Among Individuals with Cardiac Conduction Disorders.
Journal: medRxiv : the preprint server for health sciences
Published: June 29, 2026
Association of Common Ancestry-Enriched Variants With Cardiomyopathy and Arrhythmias.
Journal: Circulation
Published: May 27, 2026
RBM20 Truncating Variants and Human Cardiomyopathy.
Journal: JAMA cardiology
Published: April 08, 2026
Mapping the Functional Landscape of KCNQ1 to Define Ion Channel Mechanisms and Arrhythmia Risk.
Journal: medRxiv : the preprint server for health sciences
Published: December 25, 2025
The functional landscape of coding variation in the familial hypercholesterolemia gene LDLR.
Journal: Science (New York, N.Y.)
Published: October 30, 2025
The functional landscape of coding variation in the familial hypercholesterolemia gene LDLR.
Journal: Science (New York, N.Y.)
Published: October 30, 2025
Creating an atlas of variant effects to resolve variants of uncertain significance and guide cardiovascular medicine.
Journal: Nature reviews. Cardiology
Published: August 04, 2025
The Therapeutic Impact of Genetic Evaluation in an Atrial Fibrillation Precision Medicine Clinic.
Journal: medRxiv : the preprint server for health sciences
Published: April 08, 2025
Genetic evaluation of early-onset atrial fibrillation: impact on patient management.
Journal: European heart journal
Published: March 31, 2025
A Polygenic Predictor of Baseline QTc is Associated With Sotalol-Induced QT Prolongation.
Journal: Circulation
Published: December 09, 2024
Multiplexed Assays of Variant Effect and Automated Patch Clamping Improve KCNH2-LQTS Variant Classification and Cardiac Event Risk Stratification.
Journal: Circulation
Published: September 24, 2024
Clinical Characteristics and Outcomes in Patients With Atrial Fibrillation and Pathogenic TTN Variants.
Journal: JACC. Clinical electrophysiology
Published: May 23, 2024
Last Updated: 09/26/2026