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D. Roden · SciRah

Researcher profile · Semantic Scholar

D. Roden

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D. Roden — researcher profile on SciRah

h-index: 127
Works: 843
Citations: 65K

Most-cited papers

Assessing the contribution of rare variants to complex trait heritability from whole genome sequence data
Pierrick Wainschtein, D. Jain, Zhili Zheng, L. Cupples +46 more
2022Nature Genetics279 citations Open access
Semantic Scholar
Association of step counts over time with the risk of chronic disease in the All of Us Research Program
H. Master, J. Annis, Shih-Wun Huang, J. Beckman +8 more
2022Nature Medicine188 citations Open access
Semantic Scholar
Early-Onset Atrial Fibrillation and the Prevalence of Rare Variants in Cardiomyopathy and Arrhythmia Genes
Z. Yoneda, Katherine C. Anderson, Joseph A. Quintana, M. O’Neill +14 more
2021JAMA cardiology151 citations Open access
Semantic Scholar
Phenome-Wide Association Studies
L. Bastarache, J. Denny, D. Roden
2022Journal of the American Medical Association (JAMA)139 citations Open access
Semantic Scholar
Genome-wide association analyses identify novel Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
J. Barc, R. Tadros, C. Glinge, David Y. Chiang +152 more
2022Nature Genetics114 citations Open access
Semantic Scholar
Returning integrated genomic risk and clinical recommendations: the eMERGE study
Jodell E. Linder, Aimee Allworth, Harris T. Bland, P. Caraballo +102 more
2023Genetics in Medicine106 citations Open access
Semantic Scholar
Aberrant activation of TCL1A promotes stem cell expansion in clonal hematopoiesis
J. Weinstock, J. Gopakumar, B. Burugula, M. Uddin +107 more
2023Nature106 citations Open access
Semantic Scholar
Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential
T. Nakao, A. Bick, M. Taub, S. Zekavat +116 more
2022Science Advances76 citations Open access
Semantic Scholar
Deep learning analysis of electrocardiogram for risk prediction of drug-induced arrhythmias and diagnosis of long QT syndrome.
Edi Prifti, Ahmad Fall, Giovanni E. Davogustto, A. Pulini +11 more
2021European Heart Journal71 citations Open access
Semantic Scholar
Anticancer drug-induced life-threatening ventricular arrhythmias: a World Health Organization pharmacovigilance study.
J. Salem, L. Nguyen, J. Moslehi, S. Ederhy +4 more
2021European Heart Journal68 citations Open access
Semantic Scholar
The All of Us Data and Research Center - Creating a Secure, Scalable, and Sustainable Ecosystem for Biomedical Research
K. Mayo, M. Basford, R. Carroll, Moira Dillon +31 more
2023Annual Review of Biomedical Data Science67 citations Open access
Semantic Scholar
Next-generation phenotyping: introducing phecodeX for enhanced discovery research in medical phenomics
Megan M. Shuey, William W. Stead, Ida Aka, April L. Barnado +23 more
2023medRxiv67 citations Open access
Semantic Scholar
ARRHYTHMIAS AS PRESENTATION OF GENETIC CARDIOMYOPATHY
J. Laws, Megan C. Lancaster, M. Ben Shoemaker, W. Stevenson +7 more
2022Circulation Research64 citations Open access
Semantic Scholar
Proteomic and genetic analyses of influenza A viruses identify pan-viral host targets
Kelsey M. Haas, Michael J. McGregor, Mehdi Bouhaddou, B. Polacco +51 more
2023Nature Communications60 citations Open access
Semantic Scholar
Integrating gene expression and clinical data to identify drug repurposing candidates for hyperlipidemia and hypertension
Patrick Wu, Qi-Ping Feng, V. Kerchberger, Scott D. Nelson +9 more
2022Nature Communications58 citations Open access
Semantic Scholar
Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes
A. Bick, J. Weinstock, Satish K. Nandakumar, Charles P. Fulco +131 more
2021Nature50 citations Open access
Semantic Scholar
Mortality Among Patients With Early-Onset Atrial Fibrillation and Rare Variants in Cardiomyopathy and Arrhythmia Genes
Z. Yoneda, Katherine C. Anderson, Fei Ye, Joseph A. Quintana +18 more
2022JAMA cardiology49 citations Open access
Semantic Scholar
Shared Decision Making in Cardiac Electrophysiology Procedures and Arrhythmia Management
M. Chung, A. Fagerlin, Paul J. Wang, Tinuola B. Ajayi +38 more
2021Circulation: Arrhythmia and Electrophysiology44 citations Open access
Semantic Scholar
Association of Pathogenic Variants in Hereditary Cancer Genes With Multiple Diseases.
Chen-Jie Zeng, L. Bastarache, Ran Tao, E. Venner +29 more
2022JAMA Oncology41 citations Open access
Semantic Scholar
The 3D mutational constraint on amino acid sites in the human proteome
Bian Li, D. Roden, J. Capra
2022Nature Communications39 citations Open access
Semantic Scholar
Association Between a Common, Benign Genotype and Unnecessary Bone Marrow Biopsies Among African American Patients.
S. L. Van Driest, Noura S. Abul-Husn, J. Glessner, L. Bastarache +14 more
2021JAMA Internal Medicine34 citations Open access
Semantic Scholar
Arrhythmia variant associations and reclassifications in the eMERGE-III sequencing study
A. Glazer, Giovanni E. Davogustto, C. Shaffer, Carlos G. Vanoye +46 more
2021medRxiv29 citations Open access
Semantic Scholar
Predictive Accuracy of a Polygenic Risk Score for Postoperative Atrial Fibrillation After Cardiac Surgery
M. Kertai, J. Mosley, Jing He, A. Ramakrishnan +5 more
2021Circulation Genomic and Precision Medicine25 citations Open access
Semantic Scholar
The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network
K. Leppig, A. Rahm, P. Appelbaum, S. Aufox +41 more
2022Genetics in Medicine24 citations Open access
Semantic Scholar
Molecular characterization and investigation of the role of genetic variation in phenotypic variability and response to treatment in a large pediatric Marfan syndrome cohort
J. Meester, Silke Peeters, Lotte J. F. Van Den Heuvel, G. Vandeweyer +23 more
2022Genetics in Medicine24 citations Open access
Semantic Scholar
Transcriptional dysregulation underlies both a monogenic arrhythmia syndrome and common modifier of cardiac repolarization
K. Bersell, Tao Yang, J. Mosley, A. Glazer +30 more
2022Circulation23 citations
Semantic Scholar
Quinidine in the Management of Recurrent Ventricular Arrhythmias: A Reappraisal.
D. Li, Z. Cox, T. Richardson, Arvindh N. Kanagasundram +6 more
2021JACC Clinical Electrophysiology22 citations Open access
Semantic Scholar
Dominant negative effects of SCN5A missense variants
M. O’Neill, Ayesha Muhammad, Bian Li, Y. Wada +5 more
2021bioRxiv22 citations Open access
Semantic Scholar
Demonstrating paths for unlocking the value of cloud genomics through cross cohort analysis
N. Deflaux, M. Selvaraj, H. Condon, Kelsey Mayo +13 more
2023Nature Communications19 citations Open access
Semantic Scholar
Common ancestry-specific ion channel variants predispose to drug-induced arrhythmias
Y. Wada, Tao Yang, C. Shaffer, Laura L. Daniel +6 more
2022Circulation19 citations Open access
Semantic Scholar
Management of Congenital Long QT Syndrome: Commentary from the Experts
E. Kaufman, L. Eckhardt, M. Ackerman, P. Aziz +20 more
2021Circulation: Arrhythmia and Electrophysiology19 citations Open access
Semantic Scholar
DDIWAS: High-throughput electronic health record-based screening of drug-drug interactions
Patrick Wu, Scott D. Nelson, Juan Zhao, C. Stone +10 more
2021J. Am. Medical Informatics Assoc.18 citations Open access
Semantic Scholar
Functional Assays Reclassify Suspected Splice-Altering Variants of Uncertain Significance in Mendelian Channelopathies
M. O’Neill, Y. Wada, L. Hall, Devyn W. Mitchell +2 more
2022bioRxiv17 citations Open access
Semantic Scholar
ABO O blood group as a risk factor for platelet reactivity in heparin-induced thrombocytopenia
J. Karnes, J. Rollin, Jason B. Giles, Kiana L. Martinez +19 more
2022Blood17 citations Open access
Semantic Scholar
Association of longitudinal activity measures and diabetes risk: an analysis from the NIH All of Us Research Program.
A. S. Perry, J. Annis, H. Master, M. Nayor +9 more
2022Journal of Clinical Endocrinology and Metabolism16 citations Open access
Semantic Scholar
Continuous Bayesian Variant Interpretation Accounts for Incomplete Penetrance among Mendelian Cardiac Channelopathies
M. O’Neill, Luca Sala, I. Denjoy, Y. Wada +15 more
2022medRxiv16 citations Open access
Semantic Scholar
High-throughput functional mapping of variants in an arrhythmia gene, KCNE1, reveals novel biology
Ayesha Muhammad, Maria E. Calandranis, Bian Li, T. Yang +9 more
2023bioRxiv14 citations Open access
Semantic Scholar
Familial Hypercholesterolemia in the eMERGE Network: Prevalence, Penetrance, Cardiovascular Risk, and Outcomes after Return of Results
O. Dikilitas, Alborz Sherafati, Seyedmohammad Saadatagah, Benjamin A. Satterfield +21 more
2023Circulation Genomic and Precision Medicine13 citations Open access
Semantic Scholar
Veratridine Can Bind to a Site at the Mouth of the Channel Pore at Human Cardiac Sodium Channel NaV1.5
Alican Gulsevin, A. Glazer, Tiffany Shields, B. Kroncke +2 more
2022International Journal of Molecular Sciences13 citations Open access
Semantic Scholar
Uterine fibroid polygenic risk score (PRS) associates and predicts risk for uterine fibroid
Jacqueline A. Piekos, J. Hellwege, Yan-Fei Zhang, E. Torstenson +11 more
2022Human Genetics13 citations Open access
Semantic Scholar
Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci.
J. Ghouse, V. Tragante, Ayesha Muhammad, G. Ahlberg +23 more
2022European Heart Journal12 citations Open access
Semantic Scholar
Clinical Management of Brugada Syndrome: Commentary From the Experts
Michael J. Cutler, L. Eckhardt, Elizabeth S. Kaufman, E. Arbelo +24 more
2023Circulation: Arrhythmia and Electrophysiology11 citations Open access
Semantic Scholar
Frequency of benign neutropenia among Black versus White individuals undergoing a bone marrow assessment
S. Borinstein, David Agamasu, J. Schildcrout, L. Bastarache +6 more
2022Journal of Cellular and Molecular Medicine11 citations Open access
Semantic Scholar
Phenotyping coronavirus disease 2019 during a global health pandemic: Lessons learned from the characterization of an early cohort
Sarah Delozier, S. Bland, M. McPheeters, Q. Wells +9 more
2021Journal of Biomedical Informatics11 citations Open access
Semantic Scholar
Estimating the Post-Test Probability of Long QT Syndrome Diagnosis for Rare KCNH2 Variants
Krystian Kozek, Y. Wada, Luca Sala, I. Denjoy +26 more
2021Circulation Genomic and Precision Medicine10 citations Open access
Semantic Scholar
Proactive Variant Effect Mapping Aids Diagnosis in Pediatric Cardiac Arrest
Brendan J Floyd, Jochen Weile, P. Kannankeril, A. Glazer +6 more
2023Circulation Genomic and Precision Medicine9 citations Open access
Semantic Scholar
Genome-wide association study of platelet factor 4/heparin antibodies in heparin-induced thrombocytopenia
Jason B. Giles, H. Steiner, J. Rollin, C. Shaffer +16 more
2022Blood Advances9 citations Open access
Semantic Scholar
Comparing medical history data derived from electronic health records and survey answers in the All of Us Research Program
Lina M. Sulieman, R. Cronin, R. Carroll, Karthik Natarajan +5 more
2022J. Am. Medical Informatics Assoc.9 citations Open access
Semantic Scholar
High-throughput framework for genetic analyses of adverse drug reactions using electronic health records
Neil S. Zheng, C. Stone, Lan Jiang, C. Shaffer +9 more
2021PLoS Genetics9 citations Open access
Semantic Scholar
Genetic thyroid stimulating hormone regulation of atrial fibrillation risk is mediated through an effect on height.
Mingjian Shi, Alireza Manouchehri, C. Shaffer, N. Vaitinadin +8 more
2021Journal of Clinical Endocrinology and Metabolism9 citations Open access
Semantic Scholar

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