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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
9862018
Precision medicine, AI, and the future of personalized health care
KB Johnson, WQ Wei, D Weeraratne, ME Frisse, K Misulis, K Rhee, ...
Clinical and translational science 14 (1), 86-93, 2021
4722021
The power of genetic diversity in genome-wide association studies of lipids
SE Graham, SL Clarke, KHH Wu, S Kanoni, GJM Zajac, S Ramdas, ...
Nature 600 (7890), 675-679, 2021
3912021
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
3582019
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
3282019
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
3262012
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
3012017
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), 5068, 2014
2782014
Extracting research-quality phenotypes from electronic health records to support precision medicine
WQ Wei, JC Denny
Genome Medicine 7 (41), 2015
2522015
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), 2427, 2018
2122018
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
2082013
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
202*2015
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), 717, 2019
1922019
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
1922018
Genome-wide modeling of polygenic risk score in colorectal cancer risk
M Thomas, LC Sakoda, M Hoffmeister, EA Rosenthal, JK Lee, ...
The American journal of human genetics 107 (3), 432-444, 2020
1372020
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
1302020
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
1262019
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
1242013
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
1172012
Use of genetic variants related to antihypertensive drugs to inform on efficacy and side effects
D Gill, MK Georgakis, F Koskeridis, L Jiang, Q Feng, WQ Wei, ...
Circulation 140 (4), 270-279, 2019
1142019
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