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JIAN WANG

TitleAssistant Professor
InstitutionMD Anderson
DepartmentBiostatistics
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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. Ren Z, Shrestha M, Sakamoto T, Melkman T, Meng L, Cairns RA, Zacksenhaus E, Mak TW, Stambolic V, Minden MD, Wang JA. Opposing effects of NPM1wt and NPM1c mutants on AKT signaling in AML. Leukemia. 2020 04; 34(4):1172-1176. PMID: 31728055.
      View in: PubMed
    2. Wang J, Yu R, Shete S. X-chromosome genetic association test accounting for X-inactivation, skewed X-inactivation, and escape from X-inactivation. Genet Epidemiol. 2014 Sep; 38(6):483-93. PMID: 25043884.
      View in: PubMed
    3. Talluri R, Wang J, Shete S. Calculation of exact p-values when SNPs are tested using multiple genetic models. BMC Genet. 2014 Jun 20; 15:75. PMID: 24950707.
      View in: PubMed
    4. Wilkinson AV, Gabriel KP, Wang J, Bondy ML, Dong Q, Wu X, Shete S, Spitz MR. Sensation-seeking genes and physical activity in youth. Genes Brain Behav. 2013 Mar; 12(2):181-8. PMID: 23190435.
      View in: PubMed
    5. Reyes-Gibby CC, Wang J, Spitz M, Wu X, Yennurajalingam S, Shete S. Genetic variations in interleukin-8 and interleukin-10 are associated with pain, depressed mood, and fatigue in lung cancer patients. J Pain Symptom Manage. 2013 Aug; 46(2):161-72. PMID: 23149083.
      View in: PubMed
    6. Wang J, Spitz MR, Amos CI, Wu X, Wetter DW, Cinciripini PM, Shete S. Method for evaluating multiple mediators: mediating effects of smoking and COPD on the association between the CHRNA5-A3 variant and lung cancer risk. PLoS One. 2012; 7(10):e47705. PMID: 23077662.
      View in: PubMed
    7. Wang J, Shete S. Analysis of secondary phenotype involving the interactive effect of the secondary phenotype and genetic variants on the primary disease. Ann Hum Genet. 2012 Nov; 76(6):484-99. PMID: 22881407.
      View in: PubMed
    8. Wang J, Shete S. Testing departure from Hardy-Weinberg proportions. Methods Mol Biol. 2012; 850:77-102. PMID: 22307695.
      View in: PubMed
    9. Wang J, Shete S. Testing Hardy-Weinberg proportions in a frequency-matched case-control genetic association study. PLoS One. 2011; 6(11):e27642. PMID: 22110703.
      View in: PubMed
    10. Wilkinson AV, Bondy ML, Wu X, Wang J, Dong Q, D'Amelio AM, Prokhorov AV, Pu X, Yu RK, Etzel CJ, Shete S, Spitz MR. Cigarette experimentation in Mexican origin youth: psychosocial and genetic determinants. Cancer Epidemiol Biomarkers Prev. 2012 Jan; 21(1):228-38. PMID: 22028400.
      View in: PubMed
    11. Wang J, Shete S. Power and type I error results for a bias-correction approach recently shown to provide accurate odds ratios of genetic variants for the secondary phenotypes associated with primary diseases. Genet Epidemiol. 2011 Nov; 35(7):739-43. PMID: 21769937.
      View in: PubMed
    12. Wang J, Shete S. Estimation of odds ratios of genetic variants for the secondary phenotypes associated with primary diseases. Genet Epidemiol. 2011 Apr; 35(3):190-200. PMID: 21308766.
      View in: PubMed
    13. Wang J, Shete S. A powerful hybrid approach to select top single-nucleotide polymorphisms for genome-wide association study. BMC Genet. 2011 Jan 06; 12:3. PMID: 21211033.
      View in: PubMed
    14. Wang J, Spitz MR, Amos CI, Wilkinson AV, Wu X, Shete S. Mediating effects of smoking and chronic obstructive pulmonary disease on the relation between the CHRNA5-A3 genetic locus and lung cancer risk. Cancer. 2010 Jul 15; 116(14):3458-62. PMID: 20564069.
      View in: PubMed
    15. Wang J, Shete S. Using both cases and controls for testing hardy-weinberg proportions in a genetic association study. Hum Hered. 2010; 69(3):212-8. PMID: 20203526.
      View in: PubMed
    16. Wang J, Shete S. A test for genetic association that incorporates information about deviation from Hardy-Weinberg proportions in cases. Am J Hum Genet. 2008 Jul; 83(1):53-63. PMID: 18589394.
      View in: PubMed
    17. MAPK1/ERK2 as novel target genes for pain in head and neck cancer patients. BMC Genetics.
    18. Gene network analysis shows immune-signaling and ERK1/2 as novel genetic markers for multiple addiction phenotypes. BMC Systems Biology. 9.
    19. X-Chromosome genetic association test accounting for X-inactivation, skewed X-inactivation, and escape from X-inactivation. Genetic Epidemiology.
    20. Informative gene network for chemotherapy-induced peripheral neuropathy. BioData Mining. 8.
    21. False-negative-rate based approach selecting top single-nucleotide polymorphisms in the first stage of a two-stage genome-wide association study. Statistics and its Interface. 4:359-372.
    22. Response to Zang et al. and Han et al. American Journal of Human Genetics. 84:298-300.
    23. Genome-wide association study suggests common variants within RP11-634B7.4 gene influencing severe pre-treatment pain in head and neck cancer patients. Scientific Reports. 6.
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