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Robert Carroll
Robert Carroll
Assistant Professor, Vanderbilt University Medical Center
在 vanderbilt.edu 的电子邮件经过验证
标题
引用次数
引用次数
年份
Genetics of rheumatoid arthritis contributes to biology and drug discovery
Y Okada, D Wu, G Trynka, T Raj, C Terao, K Ikari, Y Kochi, K Ohmura, ...
Nature 506 (7488), 376-381, 2014
24972014
A gene-based association method for mapping traits using reference transcriptome data
ER Gamazon, HE Wheeler, KP Shah, SV Mozaffari, K Aquino-Michaels, ...
Nature genetics 47 (9), 1091-1098, 2015
16232015
Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data
JC Denny, L Bastarache, MD Ritchie, RJ Carroll, R Zink, JD Mosley, ...
Nature biotechnology 31 (12), 1102-1111, 2013
10072013
A catalog of genetic loci associated with kidney function from analyses of a million individuals
M Wuttke, Y Li, M Li, KB Sieber, MF Feitosa, M Gorski, A Tin, L Wang, ...
Nature genetics 51 (6), 957-972, 2019
6252019
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
C Pattaro, A Teumer, M Gorski, AY Chu, M Li, V Mijatovic, M Garnaas, ...
Nature communications 7 (1), 10023, 2016
4892016
R PheWAS: data analysis and plotting tools for phenome-wide association studies in the R environment
RJ Carroll, L Bastarache, JC Denny
Bioinformatics 30 (16), 2375-2376, 2014
3822014
Mapping ICD-10 and ICD-10-CM codes to phecodes: workflow development and initial evaluation
P Wu, A Gifford, X Meng, X Li, H Campbell, T Varley, J Zhao, R Carroll, ...
JMIR medical informatics 7 (4), e14325, 2019
3552019
Evaluating phecodes, clinical classification software, and ICD-9-CM codes for phenome-wide association studies in the electronic health record
WQ Wei, LA Bastarache, RJ Carroll, JE Marlo, TJ Osterman, ER Gamazon, ...
PloS one 12 (7), e0175508, 2017
3202017
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
A Tin, J Marten, VL Halperin Kuhns, Y Li, M Wuttke, H Kirsten, KB Sieber, ...
Nature genetics 51 (10), 1459-1474, 2019
2972019
Portability of an algorithm to identify rheumatoid arthritis in electronic health records
RJ Carroll, WK Thompson, AE Eyler, AM Mandelin, T Cai, RM Zink, ...
Journal of the American Medical Informatics Association 19 (e1), e162-e169, 2012
2422012
Increased monocyte count as a cellular biomarker for poor outcomes in fibrotic diseases: a retrospective, multicentre cohort study
MKD Scott, K Quinn, Q Li, R Carroll, H Warsinske, F Vallania, S Chen, ...
The Lancet Respiratory Medicine 7 (6), 497-508, 2019
2042019
Phenotype risk scores identify patients with unrecognized Mendelian disease patterns
L Bastarache, JJ Hughey, S Hebbring, J Marlo, W Zhao, WT Ho, ...
Science 359 (6381), 1233-1239, 2018
1972018
Genome-wide association studies identify genetic loci associated with albuminuria in diabetes
A Teumer, A Tin, R Sorice, M Gorski, NC Yeo, AY Chu, M Li, Y Li, ...
Diabetes 65 (3), 803-817, 2016
1712016
Effect of oral methylprednisolone on decline in kidney function or kidney failure in patients with IgA nephropathy: the TESTING randomized clinical trial
J Lv, MG Wong, MA Hladunewich, V Jha, LS Hooi, H Monaghan, M Zhao, ...
Jama 327 (19), 1888-1898, 2022
1592022
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
A Teumer, Y Li, S Ghasemi, BP Prins, M Wuttke, T Hermle, A Giri, ...
Nature communications 10 (1), 4130, 2019
1592019
Naïve electronic health record phenotype identification for rheumatoid arthritis
RJ Carroll, AE Eyler, JC Denny
AMIA annual symposium proceedings 2011, 189, 2011
1522011
GA4GH: International policies and standards for data sharing across genomic research and healthcare
HL Rehm, AJH Page, L Smith, JB Adams, G Alterovitz, LJ Babb, ...
Cell genomics 1 (2), 2021
1482021
Experiments and model for serration statistics in low-entropy, medium-entropy and high-entropy alloys
R Carroll, C Lee, CW Tsai, JW Yeh, J Antonaglia, BAW Brinkman, ...
Scientific reports 5 (1), 16997, 2015
1412015
GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network
B Namjou, T Lingren, Y Huang, S Parameswaran, BL Cobb, IB Stanaway, ...
BMC medicine 17, 1-19, 2019
1302019
Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis
K Ishigaki, S Sakaue, C Terao, Y Luo, K Sonehara, K Yamaguchi, ...
Nature genetics 54 (11), 1640-1651, 2022
1292022
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