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Dr. Wang joined the Division of Biostatistics in year 2002. He also holds a joint appointment at the Human and Molecular Genetics Center (HMGC).
Dr. Wang's research interests are in statistical genetics. Recent work includes modeling and linkage/association mapping of quantitative trait loci (QTL) and disease genes using polymorphic genetic markers, haplotype analyses of single nucleotide polymorphisms (SNPs).
Recent Publications
Wang T and Sheng ZH (1996) Asymptotic stationarity of discrete-time stochastic neural networks. Neural Networks, 9: 957-963.
Bilusic M, Bataillard A, Tschannen M, Gao L, Barreto N, Vincent M, Wang T, Jacob HJ, Sassard J, and Kwitek AE (2004) Hypertension and related phenotypes cluster on chromosome 2, 13 and 17 in the Lyon Hypertensive (LH) rat. Hypertension, 44: 695-701.
Kugathasan S, Loizides A, Babusukumar U, McGuire E, Wang T, Hooper P, Nebel J, Kofman G, Noel R, Broeckel U, Tolia V (2005) Comparative Phenotypic and CARD15 Mutational analysis among African American, Hispanic, and White Children with Crohn's disease. Inflamm Bowel Dis , 11 (7): 631-638.
Zeng ZB, Wang T and Zou W (2005) Modeling quantitative trait loci and interpretation of models. Genetics, 169: 1711-1725.
Babusukumar U, Wang T, McGuire E, Miranda A, Broeckel U, Kugathasan S (2006) Contribution of OCTN variants within the IBD5 locus in pediatric onset Crohn’s disease. Am J Gastroenterol, 101 (6): 1354-1361.
Wang T and Zeng ZB (2006) Models and partition of variance for quantitative trait loci with epistasis and linkage disequilibrium. BMC Genetics, 7: article 9.
Wang T, Weir B and Zeng ZB (2006) A population-based latent variable approach for association mapping of quantitative trait loci. Annals Hum Genetics, 70 (4): 506-523.
Biank V, Friedrichs F, Babusukumar U, Wang T, Stoll M, Broeckel U, and Kugathasan S (2007) DLG5 R30Q Variant is a female-specific protective factor in pediatric onset Crohn’s disease. Am J Gastroenterol, 102 (2): 391-398.
Koukouritaki SB, Poch MT, Henderson MC, Siddens LK, Krueger SK, VanDyke JE, Williams DE, Pajewski NM, Wang T, and Hines RN (2007) Identification and functional analysis of common human flavin-containing monooxygenase 3 (FMO3) genetic variants. J Pharmacol Exp Ther, 320 (1): 266-273. |