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Abel Kho
Abel Kho
Professor, Northwestern University
Verified email at nm.org
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Cited by
Year
Defining the role of common variation in the genomic and biological architecture of adult human height
AR Wood, T Esko, J Yang, S Vedantam, TH Pers, S Gustafsson, AY Chu, ...
Nature genetics 46 (11), 1173-1186, 2014
21242014
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
10312013
Validation of electronic medical record-based phenotyping algorithms: results and lessons learned from the eMERGE network
KM Newton, PL Peissig, AN Kho, SJ Bielinski, RL Berg, V Choudhary, ...
Journal of the American Medical Informatics Association 20 (e1), e147-e154, 2013
4272013
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
A Mahajan, CN Spracklen, W Zhang, MCY Ng, LE Petty, H Kitajima, ...
Nature genetics 54 (5), 560-572, 2022
3752022
Electronic medical records for genetic research: results of the eMERGE consortium
AN Kho, JA Pacheco, PL Peissig, L Rasmussen, KM Newton, N Weston, ...
Science translational medicine 3 (79), 79re1-79re1, 2011
3662011
Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study
AN Kho, MG Hayes, L Rasmussen-Torvik, JA Pacheco, WK Thompson, ...
Journal of the American Medical Informatics Association 19 (2), 212-218, 2012
3402012
Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome-and phenome-wide studies
JC Denny, DC Crawford, MD Ritchie, SJ Bielinski, MA Basford, Y Bradford, ...
The American Journal of Human Genetics 89 (4), 529-542, 2011
3032011
Electronic health records-driven phenotyping: challenges, recent advances, and perspectives
J Pathak, AN Kho, JC Denny
Journal of the American Medical Informatics Association 20 (e2), e206-e211, 2013
2912013
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
2452012
Comparative effectiveness of aspirin dosing in cardiovascular disease
WS Jones, H Mulder, LM Wruck, MJ Pencina, S Kripalani, D Muñoz, ...
New England Journal of Medicine 384 (21), 1981-1990, 2021
2202021
Rubik: Knowledge guided tensor factorization and completion for health data analytics
Y Wang, R Chen, J Ghosh, JC Denny, A Kho, Y Chen, BA Malin, J Sun
Proceedings of the 21th ACM SIGKDD international conference on knowledge …, 2015
2122015
Genome-and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk
MD Ritchie, JC Denny, RL Zuvich, DC Crawford, JS Schildcrout, ...
Circulation 127 (13), 1377-1385, 2013
1972013
A genome-and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects
K Shameer, JC Denny, K Ding, H Jouni, DR Crosslin, M De Andrade, ...
Human genetics 133, 95-109, 2014
1632014
The All of Us Research Program: data quality, utility, and diversity
AH Ramirez, L Sulieman, DJ Schlueter, A Halvorson, J Qian, ...
Patterns 3 (8), 2022
1482022
Design and implementation of a privacy preserving electronic health record linkage tool in Chicago
AN Kho, JP Cashy, KL Jackson, AR Pah, S Goel, J Boehnke, ...
Journal of the American Medical Informatics Association 22 (5), 1072-1080, 2015
1482015
Desiderata for computable representations of electronic health records-driven phenotype algorithms
H Mo, WK Thompson, LV Rasmussen, JA Pacheco, G Jiang, R Kiefer, ...
Journal of the American Medical Informatics Association 22 (6), 1220-1230, 2015
1462015
Importance of multi-modal approaches to effectively identify cataract cases from electronic health records
PL Peissig, LV Rasmussen, RL Berg, JG Linneman, CA McCarty, ...
Journal of the American Medical Informatics Association 19 (2), 225-234, 2012
1392012
Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network
DR Crosslin, A McDavid, N Weston, SC Nelson, X Zheng, E Hart, ...
Human genetics 131, 639-652, 2012
1362012
PCORnet® 2020: current state, accomplishments, and future directions
CB Forrest, KM McTigue, AF Hernandez, LW Cohen, H Cruz, K Haynes, ...
Journal of Clinical Epidemiology 129, 60-67, 2021
1232021
Impact of data fragmentation across healthcare centers on the accuracy of a high-throughput clinical phenotyping algorithm for specifying subjects with type 2 diabetes mellitus
WQ Wei, CL Leibson, JE Ransom, AN Kho, PJ Caraballo, HS Chai, ...
Journal of the American Medical Informatics Association 19 (2), 219-224, 2012
1232012
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