Dawood Darbar

发表

Identifying UMLS concepts from ECG Impressions using Knowledge Map

Randolph A. Miller, S. Trent Rosenbloom, Joshua C. Denny, 2005, AMIA.

Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation.

Thomas Meitinger, Dan M Roden, Josée Dupuis, 2008, European heart journal.

Pharmacogenomics of atrial fibrillation

Nancy J. Brown, Marylyn D. Ritchie, Dan M. Roden, 2005 .

Genetic and Clinical Risk Prediction Model for Postoperative Atrial Fibrillation

Dan M Roden, William S Bush, Dawood Darbar, 2015, Circulation. Arrhythmia and electrophysiology.

Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals

Tariq Ahmad, Patrick F. Sullivan, Andres Metspalu, 2020, Nature Communications.

Drug-Induced Long QT Syndrome

Dan M Roden, Dawood Darbar, D. Roden, 2010, Pharmacological Reviews.

Functional modeling in zebrafish demonstrates that the atrial-fibrillation-associated gene GREM2 regulates cardiac laterality, cardiomyocyte differentiation and atrial rhythm

Dan M. Roden, M. Benjamin Shoemaker, Dawood Darbar, 2012, Disease Models & Mechanisms.

A clinical prediction model to estimate risk for 30-day adverse events in emergency department patients with symptomatic atrial fibrillation.

Dan M Roden, Cathy A Jenkins, Frank E Harrell, 2009, Annals of emergency medicine.

Genome-Wide Assessment for Genetic Variants Associated with Ventricular Dysfunction after Primary Coronary Artery Bypass Graft Surgery

Dan M. Roden, Christine E. Seidman, Kuang-Yu Liu, 2011, PloS one.

Familial atrial fibrillation is a genetically heterogeneous disorder.

Douglas L Packer, Dawood Darbar, Timothy M Olson, 2003, Journal of the American College of Cardiology.

A new paradigm for predicting risk of Torsades de Pointes during drug development: Commentary on: “Improved prediction of drug‐induced Torsades de Pointes through simulations of dynamics and machine learning algorithms”

Mark McCauley, Dawood Darbar, D. Darbar, 2016, Clinical pharmacology and therapeutics.

A rare variant in MYH6 is associated with high risk of sick sinus syndrome

Dan M Roden, Kari Stefansson, Gudmar Thorleifsson, 2011, Nature Genetics.

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

Brian E. Cade, Zachary A. Szpiech, Shannon Kelly, 2019, Nature.

Common Variants in KCNN3 are Associated with Lone Atrial Fibrillation

Thomas Meitinger, Andres Metspalu, Dan M. Roden, 2010, Nature Genetics.

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

Claude Bouchard, William Wheeler, Peter Kraft, 2014 .

Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation

Gonçalo Abecasis, Dan M Roden, Christopher M Haggerty, 2018, JAMA.

Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals

Tariq Ahmad, Patrick F. Sullivan, Andres Metspalu, 2019, bioRxiv.

Electrophysiologic Characterization of Calcium Handling in Human Induced Pluripotent Stem Cell-Derived Atrial Cardiomyocytes

Eleonora Savio-Galimberti, Dawood Darbar, Jalees Rehman, 2018, Stem cell reports.