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Peng Wei
Peng Wei
Professor, The University of Texas MD Anderson Cancer Center
Verified email at mdanderson.org - Homepage
Title
Cited by
Cited by
Year
Comparison and integration of deleteriousness prediction methods for nonsynonymous SNVs in whole exome sequencing studies
C Dong, P Wei, X Jian, R Gibbs, E Boerwinkle, K Wang, X Liu
Human Molecular Genetics, 2015
10752015
Hydroxycarbamide versus chronic transfusion for maintenance of transcranial doppler flow velocities in children with sickle cell anaemia-TCD With Transfusions Changing to …
RE Ware, BR Davis, WH Schultz, RC Brown, B Aygun, S Sarnaik, I Odame, ...
The Lancet, 2016
4682016
A powerful and adaptive association test for rare variants
W Pan, J Kim, Y Zhang, X Shen, P Wei
Genetics, 2014
1912014
Current challenges and new opportunities for gene-environment interaction studies of complex diseases
K McAllister, LE Mechanic, C Amos, H Aschard, IA Blair, N Chatterjee, ...
American journal of epidemiology 186 (7), 753-761, 2017
1712017
Activation of endothelial and coagulation systems in left ventricular assist device recipients
R John, S Panch, J Hrabe, P Wei, A Solovey, L Joyce, R Hebbel
The Annals of thoracic surgery 88 (4), 1171-1179, 2009
1222009
WGSA: an annotation pipeline for human genome sequencing studies
X Liu, S White, B Peng, AD Johnson, JA Brody, AH Li, Z Huang, A Carroll, ...
Journal of Medical Genetics, 2016
1072016
Assessment of luminal and basal phenotypes in bladder cancer
CB Guo CC, Bondaruk J, Yao H, Wang Z, Zhang L, Lee S, Lee JG, Cogdell D ...
Scientific Reports 10, 2020
1062020
Site disparities in apoptotic variants as predictors of risk for second primary malignancy in patients with squamous cell carcinoma of the head and neck
Y Sun, W Yu, EM Sturgis, P Wei, D Lei, Q Wei, X Song, G Li
BMC Cancer, 2016
102*2016
Incorporating gene networks into statistical tests for genomic data via a spatially correlated mixture model
P Wei, W Pan
Bioinformatics 24 (3), 404-411, 2008
1012008
Dysregulation of EMT drives the progression to clinically aggressive sarcomatoid bladder cancer
CC Guo, T Majewski, L Zhang, H Yao, J Bondaruk, Y Wang, S Zhang, ...
Cell reports 27 (6), 1781-1793. e4, 2019
982019
An adaptive two-sample test for high-dimensional means
G Xu, L Lin, P Wei, W Pan
Biometrika 103 (3), 609-624, 2016
932016
Common and rare von Willebrand factor (VWF) coding variants, von Willebrand factor levels, and factor VIII levels in African Americans: the NHLBI exome sequencing project
JM Johnsen, PL Auer, AC Morrison, S Jiao, P Wei, J Haessler, K Fox, ...
Blood 122 (4), 590-597, 2013
87*2013
Insights into Pancreatic Cancer Etiology from Pathway Analysis of Genome-Wide Association Study Data
P Wei, H Tang, D Li
PLoS ONE 7 (10), e46887, 2012
872012
Dietary inflammatory potential in relation to the gut microbiome: results from a cross-sectional study
J Zheng, KL Hoffman, JS Chen, N Shivappa, A Sood, GJ Browman, ...
British Journal of Nutrition 124 (9), 931-942, 2020
752020
A Powerful Framework for Integrating eQTL and GWAS Summary Data
Z Xu, C Wu, P Wei, W Pan
Genetics, 2017
722017
Genetic endothelial systems biology of sickle stroke risk
L Chang Milbauer, P Wei, J Enenstein, A Jiang, CA Hillery, JP Scott, ...
Blood, The Journal of the American Society of Hematology 111 (7), 3872-3879, 2008
652008
A powerful pathway-based adaptive test for genetic association with common or rare variants
W Pan, IY Kwak, P Wei
American Journal of Human Genetics, 2015
642015
Persistent IDH1/2 mutations in remission can predict relapse in patients with acute myeloid leukemia
CY Ok, S Loghavi, D Sui, P Wei, R Kanagal-Shamanna, CC Yin, Z Zuo, ...
Haematologica 104 (2), 305, 2019
622019
A versatile omnibus test for detecting mean and variance heterogeneity
Y Cao, P Wei, M Bailey, JSK Kauwe, TJ Maxwell, ...
Genetic epidemiology 38 (1), 51-59, 2014
612014
Increased MYC copy number is an independent prognostic factor in patients with diffuse large B-cell lymphoma
AE Quesada, LJ Medeiros, PA Desai, P Lin, JR Westin, HM Hawsawi, ...
Modern Pathology 30 (12), 1688-1697, 2017
542017
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