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Selected
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Selected Publications

    1. Wang TH, Lee YS, Chen ES, Kong WH, Chen LK, Hsueh DW, Wei ML, Wang HS, Lee YS. Establishment of cDNA microarray analysis at the Genomic Medicine Research Core Laboratory (GMRCL) of Chang Gung Memorial Hospital. Chang Gung Medical Journal (2004) 27: 243-60.
    2. Peng HH, Wang TH, Hsueh DW, Chang SD, Soong YK. Prenatal diagnosis of partial trisomy 12q: clinical presentations and outcome. Prenatal Diagnosis (2005) 25: 470-474.
    3. Wang TH, Chang YL, Peng HH, Wang ST, Lu HW, Teng SH, Chang SD, Wang HS. Rapid detection of fetal aneuploidy using proteomics approaches on amniotic fluid supernatant. Prenatal Diagnosis (2005): 25: 559-566.
    4. Wu WM, Tsai HJ, Pang JH, Wang TH, Wang HS, Hong HS, Lee YS. Linear allele-specific long-range amplification: a novel method of long-range molecular haplotyping. Human Mutation. (2005) 26:393-4.
    5. Lee YS, Chen CH, Chao A, Chen ES, Wei ML, Chen LK, Yang KD, Lin MC, Wang YH, Liu JW, Eng HL, Chiang PC, Wu TS, Tsao KC, Huang CG, Tien YJ, Wang TH, Wang HS, Lee YS. Molecular signature of clinical severity in recovering patients with severe acute respiratory syndrome coronavirus (SARS-CoV). BMC Genomics (2005) 6: 132.
    6. Wu CM, Lee YS, Wang TH, Lee LY, Kong WH, Chen ES, Wei ML, Liang Y, Hwang TL. Identification of differential gene expression between intestinal and diffuse gastric cancer using cDNA microarray. Oncology Reports (2006) 15: 57-64.
    7. Chao A, Wang TH, Lee YS, Hsueh S, Chao AS, Chang TC, Kung WH, Huang SL, Chao FY, Wei ML, Lai CH. Molecular characterization of adenocarcinoma and squamous carcinoma of the uterine cervix using microarray analysis of gene expression. International Journal of Cancer (2006) 119: 91-98.
    8. Peng HH, Wang CJ, Wang TH, Chang SD. Prenatal diagnosis of de novo interstitial 2q14.2-2q21.3 deletion assisted by array-based comparative genomic hybridization. Journal of Reproductive Medicine (2006) 51: 438-442.
    9. Peng HH, Wang TH, Chao AS, Chang YL, Shieh SC, Chang SD. Klippel-Trenaunay-Weber syndrome involving fetal thigh: prenatal presentations and outcomes. Prenatal Diagnosis 2006; 26: 825-830
    10. Chao A, Lee YS, Chao AS, Wang TH, Chang SD. Microarray-based comparative genomic hybridization analysis of Wolf-Hirschhorn syndrome in a fetus with deletion of 4p15.3 to 4pter. Birth Defects Research (part A): Clinical and Molecular Teratology. (2006) 76: 739-43.
    11. Peng HH, Kuo PL, Chao AS, Wang TH, Chang YL, Soong YK, Chang SD. Discordant semilobar holoprosencephaly in monozygotic twins with de novo inv dup(15) marker chromosome and de novo mutation on SHH gene. Fetal Diagnosis and Therapy (2007) 22: 389-393.
    12. Chang KP, Hao SP, Liu CT, Cheng MH, Chang YL, Lee YS, Wang TH, Tsai CN. Promoter polymorphisms of DNMT3B and the risk of head and neck squamous cell carcinoma in Taiwan: A case-control study. Oral Oncology. (2007) 43: 345-351.
    13. Tsai MS, Hwang SM, Chen KD, Lee YS, Hsu LW, Chang YJ, Wang CN, Peng HH, Chang YL, Chao AS, Chang SD, Lee KD, Wang TH, Wang HS, Soong YK. Functional network analysis on the transcriptomes of mesenchymal stem cells derived from amniotic fluid, amniotic membrane, cord blood, and bone marrow. Stem Cells. (2007) 25: 2511-2523.
    14. Wang TH, Chao A. Microarray analysis of gene expression of cancer to guide the use of chemotherapeutics. Taiwanese Journal of Obstetrics and Gynecology. (2007) 46: 222-229.
    15. Chang JT, Chan SH, Lin CY, Lin TY, Wang HM, Liao CT, Wang TH, Lee LY, Cheng AJ. Differentially expressed genes in radioresistant nasopharyngeal cancer cells: gp96 and GDF15. Molecular Cancer Therapeutics (2007) 6: 2271¡V2279.
    16. Peng HH, Chang SD, Chao AS, Wang TH, Chang YL. Discordance of fetal genotype or phenotype in monozygotic twins: a report of 2 cases. Journal of Reproductive Medicine. 2007; 52: 849-851.
    17. Chao A, Wang TH, Lai CH. Overview of microarray analysis of gene expression and its applications to cervical cancer investigation. Taiwanese Journal of Obstetrics and Gynecology. (2007) 46: 363-373.
    18. Shaw SW, Chen CP, Cheng PJ, Wang TH, Hou JW, Lin CT, Chang SD, Hwa HL, Lin JL, Chao AS, Soong YK, Hsieh FJ. Gene dosage change of TPTE and BAGE2 and breakpoint analysis in Robertsonian Down syndrome. Journal of Human Genetics. (2008) 53:136¡V143.
    19. Lee YS, Tsai CN, Tsai CL, Chang SD, Hsueh DW, Liu JT, Ma CC, Lin SH, Wang TH, Wang HS. Comparison of whole genome amplification methods for further quantitative analysis with microarray-based comparative genomic hybridization. Taiwanese Journal of Obstetrics and Gynecology. (2008) 47: 32-41.
    20. Chao A, Wang TH, Lee YS, Hong JH, Tsai CN, Chen CK, Tsai CS, Chao AS, Lai CH. Analysis of functional groups of differentially expressed genes in the peripheral blood of patients with cervical cancer undergoing concurrent chemoradiation treatment. Radiation Research (2008) 169, 76-86.
    21. Lee YS, Chao A, Chao AS, Chang SD, Chen CH, Wu WM, Wang TH, Wang HS. CGcgh: A tool for molecular karyotyping using DNA microarray-based comparative genomic hybridization (array-CGH). Journal of Biomedical Science (2008) 15: 687-696.
    22. Chang KP, Hao SP, Tsang NM, Chang YL, Cheng MH, Liu CT, Lee YS, Tsai CL, Lee TJ, Wang TH, Tsai CN. Oncology Reports. (2008) 19: 217-222.
    23. Wang TH, Chao AS, Chen JK, Chao A, Chang YL, Cheng PJ, Chang SD, Wang HS. Network Analyses of differentially expressed proteins in amniotic fluid supernatant associated with abnormal human karyotypes. Fertility and Sterility (2009) 92: 96-107.
    24. Lee YS, Chen CH, Tsai CN, Tsai CL, Chao A, Wang TH. Microarray labeling extension values: laboratory signatures for Affymetrix GeneChips. Nucleic Acids Research, 2009, 37 (8): e61. pp.1¡V12.
    25. Wang TH, Wang HS. A primer of genome-wide association study (GWAS) for clinicians. Taiwanese Journal of Obstetrics and Gynecology. (2009) 48: 89-95.
    26. Soong YK, Wang TH, Lee YS, Chen CP, Chang CL, Ho SY, Chao AS, Cheng PJ, Chang SD. Genome-wide detection of uinparental disomy in a fetus with intrauterine growth restriction using genotyping microarrays. Taiwanese Journal of Obstetrics and Gynecology. (2009) 48: 152-158.
    27. Lee MS, Sun MT, Pang ST, Ueng SWN, Chen SC, Hwang TL, Wang TH. Evaluation of differentially expressed genes by shear stress in human osteoarthritic chondrocytes in vitro. Chang Gung Medical Journal (2009) 32: 42-50.
    28. Kang CJ, Chen YJ, Liao CT, Wang HM, Chang JT, Lin CY, Lee LY, Wang TH, Yen TC, Shen CR, Chen IH, Chiu CC, Cheng AJ. Transcriptome profiling and network pathway analysis of genes associated with invasive phenotype in oral cancer. Cancer Letters (2009) 284: 131-140.
    29. Chao A, Tsai CL, Wei PC, Hsueh S, Chao AS, Wang CJ, Tsai CN, Lee YS, Wang TH, Lai CH. Decreased expression of microRNA-199b increases protein levels of SET (protein phosphatase 2A inhibitor) in human choriocarcinoma. Cancer Letters. (2010) 291: 99-107.
    30. Chang KP, Kao HK, Liang Y, Cheng MH, Chang YL, Liu SC, Lin YC, Ko TY, Lee YS, Tsai CL, Wang TH, Hao SP, Tsai CN. Overexpression of Activin A in Oral Squamous Cell Carcinoma: Association with Poor Prognosis and Tumor Progression. Ann Surg Oncol. (2010) 17: 1945-1956.
    31. Cheng WC, Tsai ML, Chang CW, Huang CL, Chen CR, Shu WY, Lee YS, Wang TH, Hong JH, Li CY, Hsu IC. Microarray meta-analysis database (M2DB): a uniformly pre-processed, quality controlled, and manually curated human clinical microarray database. BMC Bioinformatics (2010), 11:421.
    32. Wang HS, Cheng BH, Wu HM, Yen CF, Liu CT, Chao A, Wang TH. A mutant single nucleotide polymorphism of follicle-stimulating hormone receptor is associated with a lower risk of endometriosis. Fertility and Sterility (2011) 95 (1): 455-7.