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R. Carroll · SciRah

Researcher profile · Semantic Scholar

R. Carroll

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R. Carroll — researcher profile on SciRah

h-index: 37
Works: 94
Citations: 9,780

Most-cited papers

A gene-based association method for mapping traits using reference transcriptome data
E. Gamazon, H. Wheeler, Kaanan P. Shah, S. Mozaffari +7 more
2015Nature Genetics1,792 citations Open access
Semantic Scholar
Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data
J. Denny, L. Bastarache, M. Ritchie, R. Carroll +32 more
2013Nature Biotechnology1,004 citations Open access
Semantic Scholar
A catalog of genetic loci associated with kidney function from analyses of a million individuals
M. Wuttke, Yong Li, Man Li, Karsten B. Sieber +324 more
2019Nature Genetics767 citations Open access
Semantic Scholar
Genetics of rheumatoid arthritis contributes to biology and drug discovery
Yukinori Okada, Di Wu, G. Trynka, T. Raj +91 more
2013Nature756 citations Open access
Semantic Scholar
Mapping ICD-10 and ICD-10-CM Codes to Phecodes: Workflow Development and Initial Evaluation
Patrick Wu, A. Gifford, Xiangrui Meng, Xue Li +8 more
2019JMIR Medical Informatics485 citations Open access
Semantic Scholar
R PheWAS: data analysis and plotting tools for phenome-wide association studies in the R environment
R. Carroll, L. Bastarache, J. Denny
2014Bioinform.449 citations Open access
Semantic Scholar
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
A. Tin, J. Marten, Victoria L. Halperin Kuhns, Yong Li +222 more
2019Nature Genetics365 citations Open access
Semantic Scholar
Evaluating phecodes, clinical classification software, and ICD-9-CM codes for phenome-wide association studies in the electronic health record
Wei-Qi Wei, L. Bastarache, R. Carroll, Joy Marlo +5 more
2017PLoS ONE346 citations Open access
Semantic Scholar
The All of Us Research Program: Data quality, utility, and diversity
Andrea H. Ramirez, Lina M. Sulieman, David J. Schlueter, Alese E. Halvorson +44 more
2022Patterns331 citations Open access
Semantic Scholar
Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis
K. Ishigaki, S. Sakaue, C. Terao, Yang Luo +86 more
2022Nature Genetics281 citations Open access
Semantic Scholar
Portability of an algorithm to identify rheumatoid arthritis in electronic health records
R. Carroll, W. Thompson, A. Eyler, A. Mandelin +16 more
2012J. Am. Medical Informatics Assoc.233 citations Open access
Semantic Scholar
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
A. Teumer, Yong Li, Sahar Ghasemi, B. Prins +182 more
2019Nature Communications195 citations Open access
Semantic Scholar
Increased monocyte count as a cellular biomarker for poor outcomes in fibrotic diseases: a retrospective, multicentre cohort study
Madeleine K. D. Scott, K. Quinn, Qin Li, R. Carroll +20 more
2019The Lancet Respiratory Medicine194 citations Open access
Semantic Scholar
Phenotype risk scores identify patients with unrecognized Mendelian disease patterns
L. Bastarache, Jacob J. Hughey, S. Hebbring, Joy Marlo +23 more
2018Science192 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
Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in Diabetes
A. Teumer, A. Tin, R. Sorice, M. Gorski +122 more
2015Diabetes160 citations Open access
Semantic Scholar
GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network
B. Namjou, T. Lingren, Yongbo Huang, S. Parameswaran +26 more
2019BMC Medicine152 citations Open access
Semantic Scholar
Integration of Sequence Data from a Consanguineous Family with Genetic Data from an Outbred Population Identifies PLB1 as a Candidate Rheumatoid Arthritis Risk Gene
Y. Okada, D. Diogo, J. Greenberg, Faten Mouassess +44 more
2014PLoS ONE125 citations Open access
Semantic Scholar
Inverting the model of genomics data sharing with the NHGRI Genomic Data Science Analysis, Visualization, and Informatics Lab-space
M. Schatz, Anthony A. Philippakis, E. Afgan, E. Banks +24 more
2022Cell Genomics124 citations Open access
Semantic Scholar
Naïve Electronic Health Record phenotype identification for Rheumatoid arthritis.
R. Carroll, A. Eyler, J. Denny
2011AMIA ... Annual Symposium proceedings. AMIA Symposium122 citations
Semantic Scholar
Applying active learning to high-throughput phenotyping algorithms for electronic health records data.
Yukun Chen, R. Carroll, Eugenia R. McPeek Hinz, A. Shah +3 more
2013JAMIA Journal of the American Medical Informatics Association115 citations Open access
Semantic Scholar
Evaluating electronic health record data sources and algorithmic approaches to identify hypertensive individuals
P. L. Teixeira, Wei-Qi Wei, R. Cronin, Huan Mo +12 more
2017J. Am. Medical Informatics Assoc.88 citations Open access
Semantic Scholar
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline
M. Gorski, Bettina Jung, Yong Li, P. Matías-García +127 more
2020Kidney International85 citations Open access
Semantic Scholar
Identifying Lupus Patients in Electronic Health Records: Development and Validation of Machine Learning Algorithms and Application of Rule-Based Algorithms
A. Jorge, V. Castro, A. Barnado, V. Gainer +10 more
2019Seminars in Arthritis & Rheumatism73 citations Open access
Semantic Scholar
The eMERGE Genotype Set of 83,717 Subjects Imputed to ~40 Million Variants Genome Wide and Association with the Herpes Zoster Medical Record Phenotype
I. Stanaway, T. O. Hall, E. Rosenthal, M. Palmer +36 more
2018Genetic Epidemiology71 citations
Semantic Scholar
Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index
R. Cronin, Julie R. Field, Y. Bradford, C. Shaffer +31 more
2014Frontiers in Genetics68 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
Facilitating phenotype transfer using a common data model
G. Hripcsak, N. Shang, P. Peissig, Luke V. Rasmussen +18 more
2019Journal of Biomedical Informatics66 citations Open access
Semantic Scholar
Representing Knowledge Consistently Across Health Systems
S. Rosenbloom, R. Carroll, J. Warner, Michael E. Matheny +1 more
2017Yearbook of Medical Informatics59 citations Open access
Semantic Scholar
Genetic variation in the HLA region is associated with susceptibility to herpes zoster
D. Crosslin, D. Carrell, A. Burt, D. S. Kim +33 more
2014Genes and Immunity58 citations Open access
Semantic Scholar
An atlas of genetic variation linking pathogen-induced cellular traits to human disease
Liuyang Wang, Kelly J. Pittman, Jeffrey R. Barker, Raul E. Salinas +17 more
2018Cell Host and Microbe50 citations Open access
Semantic Scholar
SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function.
Man Li, Yong Li, Olivia Weeks, Vladan Mijatovic +152 more
2017Journal of the American Society of Nephrology49 citations Open access
Semantic Scholar
Developing and Evaluating Mappings of ICD-10 and ICD-10-CM Codes to Phecodes
Patrick Wu, A. Gifford, Xiangrui Meng, Xue Li +8 more
2018bioRxiv48 citations Open access
Semantic Scholar
A polygenic and phenotypic risk prediction for Polycystic Ovary Syndrome evaluated by Phenome-wide association studies
Yoonjung Yoonie Joo, K. Actkins, J. Pacheco, A. Basile +25 more
2019bioRxiv47 citations Open access
Semantic Scholar
Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies
M. Gorski, H. Rasheed, A. Teumer, Laurent F. Thomas +172 more
2022Kidney International44 citations Open access
Semantic Scholar
Clinical Pharmacogenetics of Cytochrome P450-Associated Drugs in Children
Ida Aka, Christiana J Bernal, R. Carroll, Angela C. Maxwell-Horn +2 more
2017Journal of Personalized Medicine44 citations Open access
Semantic Scholar
Uncovering exposures responsible for birth season – disease effects: a global study
M. Boland, Pradipta Parhi, Li Li, R. Miotto +15 more
2017J. Am. Medical Informatics Assoc.40 citations Open access
Semantic Scholar
A case study evaluating the portability of an executable computable phenotype algorithm across multiple institutions and electronic health record environments
J. Pacheco, Luke V. Rasmussen, Richard C. Kiefer, T. Campion +20 more
2018J. Am. Medical Informatics Assoc.35 citations Open access
Semantic Scholar
Workshop proceedings: GWAS summary statistics standards and sharing
Jacqueline A. L. MacArthur, A. Buniello, Laura W. Harris, J. Hayhurst +15 more
2021Cell Genomics34 citations Open access
Semantic Scholar
Heritability and genome-wide association study of benign prostatic hyperplasia (BPH) in the eMERGE network
J. Hellwege, S. Stallings, E. Torstenson, R. Carroll +18 more
2019Scientific Reports33 citations Open access
Semantic Scholar
CYP2C19 Phenotype and Risk of Proton Pump Inhibitor–Associated Infections
Christiana J Bernal, Ida Aka, R. Carroll, Joseph R. Coco +4 more
2019Pediatrics33 citations Open access
Semantic Scholar
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals
T. Winkler, Humaira Rasheed, A. Teumer, M. Gorski +310 more
2022Communications Biology28 citations Open access
Semantic Scholar
Phenome-wide association study identifies marked increased in burden of comorbidities in African Americans with systemic lupus erythematosus
A. Barnado, R. Carroll, C. Casey, Lee Wheless +2 more
2018Arthritis Research & Therapy28 citations Open access
Semantic Scholar
Diversity and Scale: Genetic Architecture of 2,068 Traits in the VA Million Veteran Program
A. Verma, J. Huffman, Alex A. Rodriguez, Mitchell Conery +64 more
2023medRxiv27 citations Open access
Semantic Scholar
CYP2D6 genotype and adverse events to risperidone in children and adolescents
K. Oshikoya, Katelyn M. Neely, R. Carroll, Ida Aka +3 more
2019Pediatric Research27 citations Open access
Semantic Scholar
Adverse Events Associated with Risperidone Use in Pediatric Patients: A Retrospective Biobank Study
K. Oshikoya, R. Carroll, Ida Aka, D. Roden +1 more
2019Drugs - Real World Outcomes22 citations Open access
Semantic Scholar
The phenotype-genotype reference map: Improving biobank data science through replication
L. Bastarache, Sarah Delozier, A. Pandit, Jing He +9 more
2022bioRxiv17 citations Open access
Semantic Scholar
Comparison 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
R. Cronin, Alese E. Halvorson, Cassie Springer, Xiao-Ke Feng +11 more
2021J. Am. Medical Informatics Assoc.17 citations Open access
Semantic Scholar
Characterizing variability of electronic health record-driven phenotype definitions
P. Brandt, A. Kho, Yuan Luo, J. Pacheco +21 more
2022J. Am. Medical Informatics Assoc.16 citations
Semantic Scholar
Managing re-identification risks while providing access to the All of Us research program
Weiyi Xia, M. Basford, R. Carroll, E. Clayton +7 more
2023J. Am. Medical Informatics Assoc.15 citations Open access
Semantic Scholar

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