Wei-Qi Wei
Wei-Qi Wei
Vanderbilt University Medical Center
Verified email at vumc.org - Homepage
Title
Cited by
Cited by
Year
Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies
W Zhou, JB Nielsen, LG Fritsche, R Dey, ME Gabrielsen, BN Wolford, ...
Nature genetics 50 (9), 1335-1341, 2018
4132018
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
2652012
Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins
I Postmus, S Trompet, HA Deshmukh, MR Barnes, X Li, HR Warren, ...
Nature communications 5 (1), 1-10, 2014
2122014
Extracting research-quality phenotypes from electronic health records to support precision medicine
WQ Wei, JC Denny
Genome Medicine 7 (41), 2015
1792015
Clinical and pharmacogenetic predictors of circulating atorvastatin and rosuvastatin concentrations in routine clinical care
MK DeGorter, RG Tirona, UI Schwarz, YH Choi, GK Dresser, N Suskin, ...
Circulation: Cardiovascular Genetics 6 (4), 400-408, 2013
1562013
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals
A Giri, JN Hellwege, JM Keaton, J Park, C Qiu, HR Warren, ES Torstenson, ...
Nature genetics 51 (1), 51-62, 2019
1472019
Combining billing codes, clinical notes, and medications from electronic health records provides superior phenotyping performance
JCD Wei-Qi Wei, Pedro L Teixeira, Huan Mo, Robert M Cronin, Jeremy L Warner
Journal of the American Medical Informatics Association, 2015
130*2015
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
1292017
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
1232018
IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes
Y Momozawa, J Dmitrieva, E Théâtre, V Deffontaine, S Rahmouni, ...
Nature communications 9 (1), 1-18, 2018
1102018
Development and evaluation of an ensemble resource linking medications to their indications
WQ Wei, RM Cronin, H Xu, TA Lasko, L Bastarache, JC Denny
Journal of the American Medical Informatics Association 20 (5), 954-961, 2013
962013
CNTRO: a semantic web ontology for temporal relation inferencing in clinical narratives
C Tao, WQ Wei, HR Solbrig, G Savova, CG Chute
AMIA annual symposium proceedings 2010, 787, 2010
922010
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
892019
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
882012
Learning from longitudinal data in electronic health record and genetic data to improve cardiovascular event prediction
J Zhao, QP Feng, P Wu, RA Lupu, RA Wilke, QS Wells, JC Denny, ...
Scientific reports 9 (1), 1-10, 2019
682019
LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving Statins
WQ Wei, X Li, Q Feng, M Kubo, IJ Kullo, PL Peissig, EW Karlson, ...
Circulation 138 (17), 1839-1849, 2018
572018
Evaluating electronic health record data sources and algorithmic approaches to identify hypertensive individuals
PL Teixeira, WQ Wei, RM Cronin, H Mo, JP VanHouten, RJ Carroll, ...
Journal of the American Medical Informatics Association 24 (1), 162-171, 2017
572017
A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease
CA Emdin, ME Haas, AV Khera, K Aragam, M Chaffin, D Klarin, G Hindy, ...
PLoS genetics 16 (4), e1008629, 2020
562020
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), 1-19, 2019
562019
Harmonizing clinical sequencing and interpretation for the eMERGE III network
H Zouk, E Venner, NJ Lennon, DM Muzny, D Abrams, S Adunyah, ...
The American Journal of Human Genetics 105 (3), 588-605, 2019
562019
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