Brandon Chalazan

Medical Genetics
225 E Chicago Ave
Chicago, IL 60611

Last Updated: 09/26/2026

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Found 16 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

Clinical Impact of Rare Variants in Racial and Ethnic Minorities With Atrial Fibrillation.

Clinical Impact of Rare Variants in Racial and Ethnic Minorities With Atrial Fibrillation.

Journal: Circulation. Arrhythmia and electrophysiology
Published: March 31, 2026

A titin missense variant drives atrial electrical remodeling and is associated with atrial fibrillation.

A titin missense variant drives atrial electrical remodeling and is associated with atrial fibrillation.

Journal: eLife
Published: January 22, 2026

A titin missense variant drives atrial electrical remodeling and is associated with atrial fibrillation.

A titin missense variant drives atrial electrical remodeling and is associated with atrial fibrillation.

Journal: medRxiv : the preprint server for health sciences
Published: December 16, 2024

Clinical Genetic Testing for Atrial Fibrillation: Are We There Yet?

Clinical Genetic Testing for Atrial Fibrillation: Are We There Yet?

Journal: The Canadian journal of cardiology
Published: August 11, 2023

Genetic testing in monogenic early-onset atrial fibrillation.

Genetic testing in monogenic early-onset atrial fibrillation.

Journal: European journal of human genetics : EJHG
Published: August 27, 2022

Mutant ANP induces mitochondrial and ion channel remodeling in a human iPSC-derived atrial fibrillation model.

Mutant ANP induces mitochondrial and ion channel remodeling in a human iPSC-derived atrial fibrillation model.

Journal: JCI insight
Published: October 07, 2021

Association of Rare Genetic Variants and Early-Onset Atrial Fibrillation in Ethnic Minority Individuals.

Association of Rare Genetic Variants and Early-Onset Atrial Fibrillation in Ethnic Minority Individuals.

Journal: JAMA cardiology
Published: May 05, 2021

Common genetic variants associated with obesity in an African-American and Hispanic/Latino population.

Common genetic variants associated with obesity in an African-American and Hispanic/Latino population.

Journal: PloS one
Published: May 11, 2020

Human induced pluripotent stem cell-derived atrial cardiomyocytes carrying an SCN5A mutation identify nitric oxide signaling as a mediator of atrial fibrillation.

Human induced pluripotent stem cell-derived atrial cardiomyocytes carrying an SCN5A mutation identify nitric oxide signaling as a mediator of atrial fibrillation.

Journal: Stem cell reports
Published: September 25, 2019

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program.

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program.

Journal: Nature
Published: March 06, 2019
Showing 1-12 of 16

Last Updated: 09/26/2026