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TitleAssociate Professor
InstitutionMD Anderson
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    1. Luo X, Sturgis EM, Yang Z, Sun Y, Wei P, Liu Z, Wei Q, Li G. Lymphocyte telomere length predicts clinical outcomes of HPV-positive oropharyngeal cancer patients after definitive radiotherapy. Carcinogenesis. 2019 Jul 06; 40(6):735-741. PMID: 30721961.
      View in: PubMed
    2. Khogeer H, Rahman H, Jain N, Angelova EA, Yang H, Quesada A, Ok CY, Sui D, Wei P, Al Fattani A, Pierce S, Loghavi S, Lamb A, Hu P, Thakral B, Kanagal-Shamanna R, Jorgensen JL, Jabbour EJ, Kantarjian HM, Medeiros LJ, Khoury JD. Early T precursor acute lymphoblastic leukaemia/lymphoma shows differential immunophenotypic characteristics including frequent CD33 expression and in vitro response to targeted CD33 therapy. Br J Haematol. 2019 Aug; 186(4):538-548. PMID: 31115909.
      View in: PubMed
    3. Guo CC, Majewski T, Zhang L, Yao H, Bondaruk J, Wang Y, Zhang S, Wang Z, Lee JG, Lee S, Cogdell D, Zhang M, Wei P, Grossman HB, Kamat A, Duplisea JJ, Ferguson JE, Huang H, Dadhania V, Gao J, Dinney C, Weinstein JN, Baggerly K, McConkey D, Czerniak B. Dysregulation of EMT Drives the Progression to Clinically Aggressive Sarcomatoid Bladder Cancer. Cell Rep. 2019 05 07; 27(6):1781-1793.e4. PMID: 31067463.
      View in: PubMed
    4. Ma Y, Wei P. FunSPU: A versatile and adaptive multiple functional annotation-based association test of whole-genome sequencing data. PLoS Genet. 2019 04; 15(4):e1008081. PMID: 31034468.
      View in: PubMed
    5. Majewski T, Yao H, Bondaruk J, Chung W, Lee S, Lee JG, Zhang S, Cogdell D, Yang G, Choi W, Dinney C, Grossman HB, Logothetis C, Scherer SE, Guo CC, Zhang L, Wei P, Weinstein JN, Issa JP, Baggerly K, McConkey DJ, Czerniak B. Whole-Organ Genomic Characterization of Mucosal Field Effects Initiating Bladder Carcinogenesis. Cell Rep. 2019 02 19; 26(8):2241-2256.e4. PMID: 30784602.
      View in: PubMed
    6. Yang T, Chen H, Tang H, Li D, Wei P. A powerful and data-adaptive test for rare-variant-based gene-environment interaction analysis. Stat Med. 2019 03 30; 38(7):1230-1244. PMID: 30460711.
      View in: PubMed
    7. Zhang S, Wang Y, Bondaruk J, Majewski T, Yao H, Lee S, Lee JG, Cogdell D, Lotan Y, Dinney C, Wei P, Baggerly K, Czerniak B. Detection of Bladder Cancer in Urine Sediments by a Novel Multicolor Fluorescence In Situ Hybridization (Quartet) Test. Eur Urol Focus. 2019 Jul; 5(4):664-675. PMID: 29428551.
      View in: PubMed
    8. Quesada AE, Medeiros LJ, Desai PA, Lin P, Westin JR, Hawsawi HM, Wei P, Tang G, Seegmiller AC, Reddy NM, Yin CC, Wang W, Xu J, Miranda RN, Zuo Z, Li S. Increased MYC copy number is an independent prognostic factor in patients with diffuse large B-cell lymphoma. Mod Pathol. 2017 12; 30(12):1688-1697. PMID: 28776574.
      View in: PubMed
    9. Tang H, Wei P, Chang P, Li Y, Yan D, Liu C, Hassan M, Li D. Genetic polymorphisms associated with pancreatic cancer survival: a genome-wide association study. Int J Cancer. 2017 08 15; 141(4):678-686. PMID: 28470677.
      View in: PubMed
    10. Zhu L, Sturgis EM, Lu Z, Zhang H, Wei P, Wei Q, Li G. Association between miRNA-binding site polymorphisms in double-strand break repair genes and risk of recurrence in patients with squamous cell carcinomas of the non-oropharynx. Carcinogenesis. 2017 04 01; 38(4):432-438. PMID: 28334093.
      View in: PubMed
    11. Wei P, Cao Y, Zhang Y, Xu Z, Kwak IY, Boerwinkle E, Pan W. On Robust Association Testing for Quantitative Traits and Rare Variants. G3 (Bethesda). 2016 12 07; 6(12):3941-3950. PMID: 27678522.
      View in: PubMed
    12. Kim T, Wei P. Incorporating ENCODE information into association analysis of whole genome sequencing data. BMC Proc. 2016; 10(Suppl 7):257-261. PMID: 27980646.
      View in: PubMed
    13. Xu L, Tang H, El-Naggar AK, Wei P, Sturgis EM. Genetic variants in DNA double-strand break repair genes and risk of salivary gland carcinoma: a case-control study. PLoS One. 2015; 10(6):e0128753. PMID: 26035306.
      View in: PubMed
    14. Xu L, Tang H, Chen DW, El-Naggar AK, Wei P, Sturgis EM. Genome-wide association study identifies common genetic variants associated with salivary gland carcinoma and its subtypes. Cancer. 2015 Jul 15; 121(14):2367-74. PMID: 25823930.
      View in: PubMed
    15. Yu B, Li AH, Muzny D, Veeraraghavan N, de Vries PS, Bis JC, Musani SK, Alexander D, Morrison AC, Franco OH, Uitterlinden A, Hofman A, Dehghan A, Wilson JG, Psaty BM, Gibbs R, Wei P, Boerwinkle E. Association of Rare Loss-Of-Function Alleles in HAL, Serum Histidine: Levels and Incident Coronary Heart Disease. Circ Cardiovasc Genet. 2015 Apr; 8(2):351-5. PMID: 25575548.
      View in: PubMed
    16. Tang H, Wei P, Duell EJ, Risch HA, Olson SH, Bueno-de-Mesquita HB, Gallinger S, Holly EA, Petersen G, Bracci PM, McWilliams RR, Jenab M, Riboli E, Tjønneland A, Boutron-Ruault MC, Kaaks R, Trichopoulos D, Panico S, Sund M, Peeters PH, Khaw KT, Amos CI, Li D. Axonal guidance signaling pathway interacting with smoking in modifying the risk of pancreatic cancer: a gene- and pathway-based interaction analysis of GWAS data. Carcinogenesis. 2014 May; 35(5):1039-45. PMID: 24419231.
      View in: PubMed
    17. Zhang C, Sturgis EM, Zheng H, Song X, Wei P, Jin L, Chao L, Wei Q, Li G. Genetic variants in TNF-a promoter are predictors of recurrence in patients with squamous cell carcinoma of oropharynx after definitive radiotherapy. Int J Cancer. 2014 Apr 15; 134(8):1907-15. PMID: 24122460.
      View in: PubMed
    18. Tang H, Wei P, Duell EJ, Risch HA, Olson SH, Bueno-de-Mesquita HB, Gallinger S, Holly EA, Petersen GM, Bracci PM, McWilliams RR, Jenab M, Riboli E, Tjønneland A, Boutron-Ruault MC, Kaaks R, Trichopoulos D, Panico S, Sund M, Peeters PH, Khaw KT, Amos CI, Li D. Genes-environment interactions in obesity- and diabetes-associated pancreatic cancer: a GWAS data analysis. Cancer Epidemiol Biomarkers Prev. 2014 Jan; 23(1):98-106. PMID: 24136929.
      View in: PubMed
    19. Jin L, Sturgis EM, Zhang Y, Huang Z, Wei P, Guo W, Wang Z, Wei Q, Song X, Li G. Genetic variants in p53-related genes confer susceptibility to second primary malignancy in patients with index squamous cell carcinoma of head and neck. Carcinogenesis. 2013 Jul; 34(7):1551-7. PMID: 23508638.
      View in: PubMed
    20. Identification of an Association of TNFAIP3 Polymorphisms with Matrix Metalloproteinase Expression in Fibroblasts in an Integrative Study of Systemic Sclerosis-Associated Genetic and Environmental Factors. Arthritis and Rheumatology. 68:749-760.
    21. Network-based genomic discovery. Journal of the Royal Statistical Society. Series C: Applied Statistics. 59:105-125.
    22. Site disparities in apoptotic variants as predictors of risk for second primary malignancy in patients with squamous cell carcinoma of the head and neck. BMC Cancer. 16.
    23. Genetic variants in DNA double-strand break repair genes and risk of salivary gland carcinoma. PLoS One. 10.
    24. On robust association testing for quantitative traits and rare variants. G3: Genes, Genomes, Genetics. 6:3941-3950.
    25. Bayesian Inference on Risk Differences. Statistics in Biopharmaceutical Research. 5:142-155.
    26. Bayesian joint modeling of multiple gene networks and diverse genomic data to identify target genes of a transcription factor. Annals of Applied Statistics. 4:334-355.
    27. An adaptive two-sample test for high-dimensional means. Biometrika. 103:609-624.
    28. Impact of age and auto antibody status on the gene expression of scleroderma fibroblasts in response to silica stimulation. European Journal of Inflammation. 11:631-639.
    29. Comparison and integration of deleteriousness prediction methods for nonsynonymous SNVs in whole exome sequencing studies. Human Molecular Genetics. 24:2125-2137.
    30. Mendelian randomization analysis of a time-varying exposure for binary disease outcomes using functional data analysis methods. Genetic Epidemiology. 40:744-755.
    31. A semiparametric model for vQTL mapping. Biometrics.
    32. The impact of multiple single day blood pressure readings on cardiovascular risk estimation. European Journal of Preventive Cardiology. 23:1529-1536.
    33. A Powerful Pathway-Based Adaptive Test for Genetic Association with Common or Rare Variants. American Journal of Human Genetics. 97:86-98.
    34. Association of Rare Loss-Of-Function Alleles in HAL, Serum Histidine. Circulation: Cardiovascular Genetics. 8:351-355.
    35. WGSA. Journal of Medical Genetics. 53:111-112.
    36. Cancer Informatics. 14:209-218.
    37. FLAGS. Genetics. 202:919-929.
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