Wei-Qi Wei
Wei-Qi Wei
Vanderbilt University Medical Center
Bestätigte E-Mail-Adresse bei - Startseite
Zitiert von
Zitiert von
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
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
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
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
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
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
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
Extracting research-quality phenotypes from electronic health records to support precision medicine
WQ Wei, JC Denny
Genome Medicine 7 (41), 2015
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
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
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
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
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
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
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
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
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
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
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
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
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