Dawood Darbar

17PUBLICATIONS
290CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Cardiology (incl. cardiovascular diseases)Circuits and systemsOther European languagesBiomaterials
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Publications (17)

|May 18, 2026
Rare coding variant architecture and gene discovery from 130,000 sequenced cases of atrial fibrillation.

|Mar 31, 2026
Clinical Impact of Rare Variants in Racial and Ethnic Minorities With Atrial Fibrillation.

Michael C Hill, Brandon Chalazan, Shashank Sandu

|Jan 22, 2026
A titin missense variant drives atrial electrical remodeling and is associated with atrial fibrillation.

Mahmud Arif Pavel, Hanna Chen, Michael Hill

|Mar 06, 2025
Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk.

Seung Hoan Choi, Sean J Jurgens, Ling Xiao

|Oct 03, 2024
Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height.

Gareth Hawkes, Robin N Beaumont, Zilin Li

|May 24, 2024
Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes.

Rebecca Keener, Surya B Chhetri, Carla J Connelly

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Frequent Collaborators

8 joint publications

Jennifer Brody

8 joint publications

Susan R Heckbert

7 joint publications

Charles Kooperberg

6 joint publications

Joshua C Bis