Darbar, Dawood
University of Illinois Chicago
19 papers on CoChatORCID 0000-0002-4103-5977
Most cited papers
- Verified
The mutational constraint spectrum quantified from variation in 141,456 humans
Karczewski, K. J., Francioli, L. C., Tiao, G., Cummings, B. B., Alföldi, J., Wang, Q., Collins, R. L., Laricchia, K. M., Ganna, A., Birnbaum, D. P., et al. (2020) · Nature
Genomics and Rare DiseasesGenetic Associations and Epidemiology
Cited by 9,434
- Verified
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
Taliun, D., Harris, D. N., Kessler, M. D., Carlson, J., Szpiech, Z. A., Torres, R., Taliun, S. A. G., Corvelo, A., Gogarten, S. M., Kang, H. M., et al. (2021) · Nature
Genetic Associations and EpidemiologyGenomics and Rare Diseases
Cited by 2,213
- Verified
A genomic mutational constraint map using variation in 76,156 human genomes
Chen, S., Francioli, L. C., Goodrich, J. K., Collins, R. L., Kanai, M., Wang, Q., Alföldi, J., Watts, N. A., Vittal, C., Gauthier, L. D., et al. (2024) · Nature
Genomics and Rare DiseasesGenetic Associations and Epidemiology
Cited by 1,727
- Verified
A structural variation reference for medical and population genetics
Collins, R. L., Brand, H., Karczewski, K. J., Zhao, X., Alföldi, J., Francioli, L. C., Khera, A. V., Lowther, C., Gauthier, L. D., Wang, H., et al. (2020) · Nature
Genomic variations and chromosomal abnormalitiesGenomics and Rare Diseases
Cited by 1,037
- Verified
Inherited causes of clonal haematopoiesis in 97,691 whole genomes
Bick, A. G., Weinstock, J. S., Nandakumar, S. K., Fulco, C. P., Bao, E. L., Zekavat, S. M., Szeto, M. D., Liao, X., Leventhal, M. J., Nasser, J., et al. (2020) · Nature
Acute Myeloid Leukemia ResearchGenetic Associations and Epidemiology
Cited by 733
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Meta-analysis identifies six new susceptibility loci for atrial fibrillation
Ellinor, P. T., Lunetta, K. L., Albert, C. M., Glazer, N. L., Ritchie, M. D., Smith, A. V., Arking, D. E., Müller-Nurasyid, M., Krijthe, B. P., Lubitz, S. A., et al. (2012) · Nature Genetics
Atrial Fibrillation Management and OutcomesGenetic Associations and Epidemiology
Cited by 601
- Verified
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke
Gudbjartsson, D. F., Holm, H., Gretarsdottir, S., Thorleifsson, G., Walters, G. B., Thorgeirsson, G., Gulcher, J., Mathiesen, E. B., Njølstad, I., Nyrnes, A., et al. (2009) · Nature Genetics
Atrial Fibrillation Management and OutcomesGenetic Associations and Epidemiology
Cited by 489
- Verified
Common variants in KCNN3 are associated with lone atrial fibrillation
Ellinor, P. T., Lunetta, K. L., Glazer, N. L., Pfeufer, A., Alonso, A., Chung, M. K., Sinner, M. F., de Bakker, P. I. W., Mueller, M., Lubitz, S. A., et al. (2010) · Nature Genetics
Cardiac electrophysiology and arrhythmiasAtrial Fibrillation Management and Outcomes
Cited by 485
- Verified · note
Metabolic Syndrome and Risk of Development of Atrial Fibrillation: The Niigata Preventive Medicine Study
Watanabe, H., Tanabe, N., Watanabe, T., Darbar, D., Roden, D. M., Sasaki, S., & Aizawa, Y. (2008) · Circulation
Atrial Fibrillation Management and OutcomesDiabetes, Cardiovascular Risks, and Lipoproteins
Cited by 427
- Verified
Cardiac Sodium Channel ( SCN5A ) Variants Associated with Atrial Fibrillation
Darbar, D., Kannankeril, P. J., Donahue, B. S., Kucera, G., Stubblefield, T., Haines, J. L., George, A. L., & Roden, D. M. (2008) · Circulation
Cardiac electrophysiology and arrhythmiasAtrial Fibrillation Management and Outcomes
Cited by 334
- Verified
Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation
Sinner, M. F., Tucker, N. R., Lunetta, K. L., Ozaki, K., Smith, J. G., Trompet, S., Bis, J. C., Lin, H., Chung, M. K., Nielsen, J. B., et al. (2014) · Circulation
Cardiac electrophysiology and arrhythmiasAtrial Fibrillation Management and Outcomes
Cited by 205
- Verified
Early-Onset Atrial Fibrillation and the Prevalence of Rare Variants in Cardiomyopathy and Arrhythmia Genes
Yoneda, Z. T., Anderson, K. C., Quintana, J. A., O’Neill, M. J., Sims, R. A., Glazer, A. M., Shaffer, C. M., Crawford, D. M., Stricker, T., Ye, F., et al. (2021) · JAMA Cardiology
Cardiac electrophysiology and arrhythmiasAtrial Fibrillation Management and Outcomes
Cited by 192
- Verified
Relation of the Severity of Obstructive Sleep Apnea in Response to Anti-Arrhythmic Drugs in Patients With Atrial Fibrillation or Atrial Flutter
Monahan, K., Brewster, J., Wang, L., Parvez, B., Goyal, S., Roden, D. M., & Darbar, D. (2012) · The American Journal of Cardiology
Obstructive Sleep Apnea ResearchAtrial Fibrillation Management and Outcomes
Cited by 170
- Verified
Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation
Ritchie, M. D., Rowan, S., Kucera, G., Stubblefield, T., Blair, M., Carter, S., Roden, D. M., & Darbar, D. (2012) · Journal of the American College of Cardiology
Cardiac electrophysiology and arrhythmiasAtrial Fibrillation Management and Outcomes
Cited by 91
- Verified
Exaggerated QT prolongation after cardioversion of atrial fibrillation
Choy, A. M. J., Darbar, D., Dell’Orto, S., & Roden, D. M. (1999) · Journal of the American College of Cardiology
Atrial Fibrillation Management and OutcomesCardiac electrophysiology and arrhythmias
Cited by 89
- Verified
Relation of morbid obesity and female gender to risk of procedural complications in patients undergoing atrial fibrillation ablation
Shoemaker, M. B., Muhammad, R., Farrell, M., Parvez, B., White, B. W., Streur, M., Stubblefield, T., Rytlewski, J., Parvathaneni, S., Nagarakanti, R., et al. (2013) · The American Journal of Cardiology
Atrial Fibrillation Management and OutcomesCardiac Arrhythmias and Treatments
Cited by 63
- Verified
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways
Young, W. J., Lahrouchi, N., Isaacs, A., Duong, T., Foco, L., Ahmed, F., Brody, J. A., Salman, R., Noordam, R., Benjamins, J.-W., et al. (2022) · Nature Communications
Cardiac electrophysiology and arrhythmiasGenetic Associations and Epidemiology
Cited by 49
- Verified
Human induced pluripotent stem cell-derived atrial cardiomyocytes carrying an SCN5A mutation identify nitric oxide signaling as a mediator of atrial fibrillation
Hong, L., Zhang, M., Ly, O. T., Chen, H., Sridhar, A., Lambers, E., Chalazan, B., Youn, S.-W., Maienschein-Cline, M., Feferman, L., et al. (2021) · Stem Cell Reports
Cardiac electrophysiology and arrhythmiasPluripotent Stem Cells Research
Cited by 44
- Verified
Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program
Cade, B. E., Lee, J., Sofer, T., Wang, H., Zhang, M., Chen, H., Gharib, S. A., Gottlieb, D. J., Guo, X., Lane, J. M., et al. (2021) · Genome Medicine
Obstructive Sleep Apnea ResearchGenetic Associations and Epidemiology
Cited by 33
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