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Author Details

Dan M Roden
Vanderbilt University Medical Center
1980
764
125
Andrej Sali (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
36524479Transcriptional Dysregulation Underlies Both Monogenic Arrhythmia Syndrome and Common Modifiers of Cardiac Repolarization.Circulation2023
37758692Proteomic and genetic analyses of influenza A viruses identify pan-viral host targets.Nat Commun2023
37669985Demonstrating paths for unlocking the value of cloud genomics through cross cohort analysis.Nat Commun2023
37561600The <i>All of Us</i> Data and Research Center: Creating a Secure, Scalable, and Sustainable Ecosystem for Biomedical Research.Annu Rev Biomed Data Sci2023
37905118Determinants of mosaic chromosomal alteration fitness.medRxiv2023
37662324Clinical consequences of a polygenic predisposition to benign lower white blood cell counts: Consequences of benign WBC count genetics.medRxiv2023
37662265WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE.medRxiv2023
37903185The Shape of Ventricular Tachycardia.Circulation2023
38065071Genomic medicine year in review: 2023.Am J Hum Genet2023
37547012PheMIME: An Interactive Web App and Knowledge Base for Phenome-Wide, Multi-Institutional Multimorbidity Analysis.medRxiv2023
37883362Correction: Hypertension genetic risk score is associated with burden of coronary heart disease among patients referred for coronary angiography.PLoS One2023
37541168Laboratory and demographic predictors of functional assay positive status in suspected heparin-induced thrombocytopenia: A multicenter retrospective cohort study.Thromb Res2023
37732247ParSE-seq: A Calibrated Multiplexed Assay to Facilitate the Clinical Classification of Putative Splice-altering Variants.medRxiv2023
37930895Next-generation phenotyping: introducing phecodeX for enhanced discovery research in medical phenomics.Bioinformatics2023
37495323Pulmonary Vein Myocardial Sleeve Length and its Association With Sex and 4q25/PITX2 Genotype.JACC Clin Electrophysiol2023
37461512Leveraging Generative AI to Prioritize Drug Repurposing Candidates: Validating Identified Candidates for Alzheimer's Disease in Real-World Clinical Datasets.medRxiv2023
37046083Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.Nature2023
37046000Author Correction: Association of step counts over time with the risk of chronic disease in the All of Us Research Program.Nat Med2023
37071725Familial Hypercholesterolemia in the Electronic Medical Records and Genomics Network: Prevalence, Penetrance, Cardiovascular Risk, and Outcomes After Return of Results.Circ Genom Precis Med2023
37034657The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young.medRxiv2023
37164047Multicenter clinical and functional evidence reclassifies a recurrent noncanonical filamin C splice-altering variant.Heart Rhythm2023
37163006Detection of distant familial relatedness in biobanks for identification of undiagnosed carriers of a Mendelian disease variant: application to Long QT syndrome.medRxiv2023
37396334Cardiac Sarcoidosis and a Likely Pathogenic <i>TTN</i> Variant in a Patient Presenting With Ventricular Tachycardia.JACC Case Rep2023
37162834High-throughput functional mapping of variants in an arrhythmia gene, <i>KCNE1</i>, reveals novel biology.bioRxiv2023
36621880Returning integrated genomic risk and clinical recommendations: The eMERGE study.Genet Med2023
36716194Proactive Variant Effect Mapping Aids Diagnosis in Pediatric Cardiac Arrest.Circ Genom Precis Med2023
36472455Interactive network-based clustering and investigation of multimorbidity association matrices with associationSubgraphs.Bioinformatics2023
36540997Predictive models for abdominal aortic aneurysms using polygenic scores and PheWAS-derived risk factors.Pac Symp Biocomput2023
36496179Continuous Bayesian variant interpretation accounts for incomplete penetrance among Mendelian cardiac channelopathies.Genet Med2023
36458881Association of Longitudinal Activity Measures and Diabetes Risk: An Analysis From the National Institutes of Health All of Us Research Program.J Clin Endocrinol Metab2023
34930020Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study.Circulation2022
35617362Arrhythmias as Presentation of Genetic Cardiomyopathy.Circ Res2022
35544069Mortality Among Patients With Early-Onset Atrial Fibrillation and Rare Variants in Cardiomyopathy and Arrhythmia Genes.JAMA Cardiol2022
35377938ABO O blood group as a risk factor for platelet reactivity in heparin-induced thrombocytopenia.Blood2022
35672414The 3D mutational constraint on amino acid sites in the human proteome.Nat Commun2022
35642720Frequency of benign neutropenia among Black versus White individuals undergoing a bone marrow assessment.J Cell Mol Med2022
35396991Comparing medical history data derived from electronic health records and survey answers in the All of Us Research Program.J Am Med Inform Assoc2022
35533259Genome-wide association study of platelet factor 4/heparin antibodies in heparin-induced thrombocytopenia.Blood Adv2022
35751511Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci.Eur Heart J2022
35485600A research agenda to support the development and implementation of genomics-based clinical informatics tools and resources.J Am Med Inform Assoc2022
35656995Genetic Determinants of Body Mass Index and Fasting Glucose Are Mediators of Grade 1 Diastolic Dysfunction.J Am Heart Assoc2022
35446370Association of Pathogenic Variants in Hereditary Cancer Genes With Multiple Diseases.JAMA Oncol2022
35385311Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential.Sci Adv2022
36459977Genomic Medicine Year in Review: 2022.Am J Hum Genet2022
36372681Quantifying the phenome-wide disease burden of obesity using electronic health records and genomics.Obesity (Silver Spring)2022
36197721Functional Assays Reclassify Suspected Splice-Altering Variants of Uncertain Significance in Mendelian Channelopathies.Circ Genom Precis Med2022
36216933Association of step counts over time with the risk of chronic disease in the All of Us Research Program.Nat Med2022
33779357Loperamide Induced Recurrent Torsades de Pointes: A Case Report.J Pharm Pract2022
35226188Uterine fibroid polygenic risk score (PRS) associates and predicts risk for uterine fibroid.Hum Genet2022
35013250Integrating gene expression and clinical data to identify drug repurposing candidates for hyperlipidemia and hypertension.Nat Commun2022
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Collaborators

Joshua C Denny
Vanderbilt University
Co-authored papers 152
Marylyn D Ritchie
Center for Systems Genomics, Pennsylvania State University, University Park
Co-authored papers 59
Christian M Shaffer
Vanderbilt University
Co-authored papers 56
Jonathan D Mosley
Vanderbilt University Medical Center
Co-authored papers 52
Gail P Jarvik
University of Washington Medical Center
Co-authored papers 44
Sara L Van Driest
National Institutes of Health
Co-authored papers 44
Moore Benjamin Shoemaker
Vanderbilt University Medical Center
Co-authored papers 43
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Mayo Clinic
Co-authored papers 40
Lisa Bastarache
Vanderbilt University Medical Center
Co-authored papers 39
Peter Weeke
Rigshospitalet, University of Copenhagen
Co-authored papers 38
Quinn S Wells
Vanderbilt University Medical Center
Co-authored papers 38
Jill M Pulley
Vanderbilt University School of Medicine
Co-authored papers 37
Dana C Crawford
Cleveland Institute for Computational Biology, Case Western Reserve University
Co-authored papers 36
Marc S Williams
University of Washington Medical Center
Co-authored papers 35
Alfred L George
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Co-authored papers 33
Rex L Chisholm
Center for Genetic Medicine, Feinberg School of Medicine, Northwestern University
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Charles M Stein
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Josh F Peterson
Vanderbilt University Medical Center
Co-authored papers 29
David R Crosslin
University of Washington Medical Center
Co-authored papers 29
Melissa A Basford
Vanderbilt University
Co-authored papers 28
Teri A Manolio
National Human Genome Research Institute
Co-authored papers 28
Wei-Qi Wei
Vanderbilt University Medical Center
Co-authored papers 28
Andrew M Glazer
Vanderbilt University
Co-authored papers 28
Eric B Larson
University of Washington
Co-authored papers 27
Catherine A McCarty
University of Minnesota Medical School, 1035 University Drive duluth
Co-authored papers 27
Jennifer A Pacheco
University of Pennsylvania
Co-authored papers 26
Erica Bowton
Institute for Clinical and Translational Research, Vanderbilt University
Co-authored papers 25
Jonathan S Schildcrout
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Co-authored papers 23
Christopher G Chute
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Release 1.2