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Author Details

Robert J Carroll
Vanderbilt University Medical Center
2011
62
29
PMIDPaper TitleJournal TitlePublished Year
36765713Correlates of Taxane-Induced Neuropathy, an Electronic Health Record Based Observational Study.Cancers (Basel)2023
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
37662278Developing and Evaluating Pediatric Phecodes (Peds-Phecodes) for High-Throughput Phenotyping Using Electronic Health Records.medRxiv2023
37607538The phenotype-genotype reference map: Improving biobank data science through replication.Am J Hum Genet2023
37425708Diversity and Scale: Genetic Architecture of 2,068 Traits in the VA Million Veteran Program.medRxiv2023
37046000Author Correction: Association of step counts over time with the risk of chronic disease in the All of Us Research Program.Nat Med2023
36474423Characterizing variability of electronic health record-driven phenotype definitions.J Am Med Inform Assoc2023
36809550Managing re-identification risks while providing access to the All of Us research program.J Am Med Inform Assoc2023
34864995Inference-based correction of multi-site height and weight measurement data in the All of Us research program.J Am Med Inform Assoc2022
35697829Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.Commun Biol2022
35396991Comparing medical history data derived from electronic health records and survey answers in the All of Us Research Program.J Am Med Inform Assoc2022
36372681Quantifying the phenome-wide disease burden of obesity using electronic health records and genomics.Obesity (Silver Spring)2022
36333501Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis.Nat Genet2022
36216933Association of step counts over time with the risk of chronic disease in the All of Us Research Program.Nat Med2022
35090449Under-specification as the source of ambiguity and vagueness in narrative phenotype algorithm definitions.BMC Med Inform Decis Mak2022
33420026Lossless integration of multiple electronic health records for identifying pleiotropy using summary statistics.Nat Commun2021
36082306Workshop proceedings: GWAS summary statistics standards and sharing.Cell Genom2021
34547180Racial disparity in taxane-induced neutropenia among cancer patients.Cancer Med2021
33404595Comparison of family health history in surveys vs electronic health record data mapped to the observational medical outcomes partnership data model in the All of Us Research Program.J Am Med Inform Assoc2021
33137338Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline.Kidney Int2021
32386537Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic Groups.Am J Hum Genet2020
30298529The eMERGE genotype set of 83,717 subjects imputed to ~40â¿¿million variants genome wide and association with the herpes zoster medical record phenotype.Genet Epidemiol2019
31672532Automated grouping of medical codes via multiview banded spectral clustering.J Biomed Inform2019
31699831CYP2C19 Phenotype and Risk of Proton Pump Inhibitor-Associated Infections.Pediatrics2019
31553307Mapping ICD-10 and ICD-10-CM Codes to Phecodes: Workflow Development and Initial Evaluation.JMIR Med Inform2019
31311600GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network.BMC Med2019
30988330Heritability and genome-wide association study of benign prostatic hyperplasia (BPH) in the eMERGE network.Sci Rep2019
30774981A phenome-wide association study to discover pleiotropic effects of <i>PCSK9</i>, <i>APOB</i>, and <i>LDLR</i>.NPJ Genom Med2019
31152163A catalog of genetic loci associated with kidney function from analyses of a million individuals.Nat Genet2019
30919267Adverse Events Associated with Risperidone Use in Pediatric Patients: A Retrospective Biobank Study.Drugs Real World Outcomes2019
30935881Increased monocyte count as a cellular biomarker for poor outcomes in fibrotic diseases: a retrospective, multicentre cohort study.Lancet Respir Med2019
30459343Unfolding of hidden white blood cell count phenotypes for gene discovery using latent class mixed modeling.Genes Immun2019
30477398Phenome-wide association study identifies dsDNA as a driver of major organ involvement in systemic lupus erythematosus.Lupus2019
30665626Identifying lupus patients in electronic health records: Development and validation of machine learning algorithms and application of rule-based algorithms.Semin Arthritis Rheum2019
29036387Uncovering exposures responsible for birth season - disease effects: a global study.J Am Med Inform Assoc2018
29912272Evaluating statistical approaches to leverage large clinical datasets for uncovering therapeutic and adverse medication effects.Bioinformatics2018
30124903A case study evaluating the portability of an executable computable phenotype algorithm across multiple institutions and electronic health record environments.J Am Med Inform Assoc2018
30092202An Atlas of Genetic Variation Linking Pathogen-Induced Cellular Traits to Human Disease.Cell Host Microbe2018
29636090Phenome-wide association study identifies marked increased in burden of comorbidities in African Americans with systemic lupus erythematosus.Arthritis Res Ther2018
29481723Phenome-Wide Association Studies Uncover a Novel Association of Increased Atrial Fibrillation in Male Patients With Systemic Lupus Erythematosus.Arthritis Care Res (Hoboken)2018
29590070Phenotype risk scores identify patients with unrecognized Mendelian disease patterns.Science2018
27497800Evaluating electronic health record data sources and algorithmic approaches to identify hypertensive individuals.J Am Med Inform Assoc2017
29099060Clinical Pharmacogenetics of Cytochrome P450-Associated Drugs in Children.J Pers Med2017
29063555Representing Knowledge Consistently Across Health Systems.Yearb Med Inform2017
28686612Evaluating phecodes, clinical classification software, and ICD-9-CM codes for phenome-wide association studies in the electronic health record.PLoS One2017
27589350Phenome-Wide Association Study of Rheumatoid Arthritis Subgroups Identifies Association Between Seronegative Disease and Fibromyalgia.Arthritis Rheumatol2017
27920155<i>SOS2</i> and <i>ACP1</i> Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function.J Am Soc Nephrol2017
27860419Reply.Arthritis Rheumatol2017
27390187Developing Electronic Health Record Algorithms That Accurately Identify Patients With Systemic Lupus Erythematosus.Arthritis Care Res (Hoboken)2017
26831199Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.Nat Commun2016
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Collaborators

Vanderbilt University
Co-authored papers 41
Vanderbilt University Medical Center
Co-authored papers 16
Vanderbilt University Medical Center
Co-authored papers 14
University of Washington Medical Center
Co-authored papers 11
Mayo Clinic
Co-authored papers 10
University of Washington Medical Center
Co-authored papers 10
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Co-authored papers 9
Biomedical and Translational Informatics Institute
Co-authored papers 9
Vanderbilt University Medical Center
Co-authored papers 9
Kaiser Permanente Washington Health Research Institute
Co-authored papers 9
University of Pennsylvania
Co-authored papers 8
Hasso Plattner Institute for Digital Health at Mount Sinai
Co-authored papers 8
The Center for Applied Genomics, Children's Hospital of Philadelphia
Co-authored papers 8
Center for Systems Genomics, Pennsylvania State University, University Park
Co-authored papers 8
Center for Precision Medicine Research, Marshfield Clinic Research Institute
Co-authored papers 8
Co-authored papers 7
Vanderbilt University School of Medicine
Co-authored papers 7
Co-authored papers 6
Northwestern University Feinberg School of Medicine
Co-authored papers 6
Institute of Genetic Epidemiology, Medical Center-University of Freiburg
Co-authored papers 6
University of Regensburg
Co-authored papers 6
Baylor College of Medicine
Co-authored papers 6
Co-authored papers 6
University of Regensburg
Co-authored papers 6
National Institutes of Health
Co-authored papers 6
University Medicine Greifswald
Co-authored papers 6
Vanderbilt University
Co-authored papers 6
Co-authored papers 6
Co-authored papers 6
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