教師簡介

代表著作

  • Wu, J.H., Liu, J.H., Ko, Y.C., Wang, C.T., Chung, Y.C., Chu, K.C., Liu, T.T., Chao, H.M., Jiang, Y.J., Chen, S.J. and Chung, M.Y. (2016) Haploinsufficiency of RCBTB1 is Associated with Coats Disease and Familial Exudative Vitreoretinopathy. Hum Mol Genet, in press.
  • Yu, C.J., Du, J.C., Chiou, H.C., Yang, S.H., Liao, K.W., Yang, W., Chung, M.Y., Chien, L.C., Hwang, B. and Chen, M.L. (2016) Attention Deficit/Hyperactivity Disorder and Urinary Nonylphenol Levels: A Case-Control Study in Taiwanese Children. PLoS One, 11, e0149558.
  • Lee, K.H., Tsai, W.J., Chen, Y.W., Yang, W.C., Lee, C.Y., Ou, S.M., Chen, Y.T., Chien, C.C., Lee, P.C., Chung, M.Y. et al. (2016) Genotype polymorphisms of genes regulating nitric oxide synthesis determine long-term arteriovenous fistula patency in male hemodialysis patients. Ren Fail, 38, 228-237.
  • Fuh, J.L., Chung, M.Y., Yao, S.C., Chen, P.K., Liao, Y.C., Hsu, C.L., Wang, P.J., Wang, Y.F., Chen, S.P., Fann, C.S. et al. (2015) Susceptible genes of restless legs syndrome in migraine. Cephalalgia, in press.
  • Tseng, S.H., Cheng, C.Y., Huang, M.Z., Chung, M.Y. and Su, T.S. (2013) Modulation of formation of the 3'-end of the human argininosuccinate synthetase mRNA by GT-repeat polymorphism. Int J Biochem Mol Biol, 4, 179-190.
  • Lin, C.C., Chung, M.Y., Yang, W.C., Lin, S.J. and Lee, P.C. (2013) Length polymorphisms of heme oxygenase-1 determine the effect of far-infrared therapy on the function of arteriovenous fistula in hemodialysis patients: a novel physicogenomic study. Nephrol Dial Transplant, 28, 1284-1293.
  • Chang, C.F., Lu, T.M., Yang, W.C., Lin, S.J., Lin, C.C. and Chung, M.Y. (2013) Gene polymorphisms of interleukin-10 and tumor necrosis factor-alpha are associated with contrast-induced nephropathy. Am J Nephrol, 37, 110-117.
  • Lin, C.S., Wang, L.S., Chang, S.C., Chou, T.Y., Hsu, W.H., Liu, C.S., Lee, M.H., Chung, M.Y. and Wei, Y.H. (2012) Associated microsatellite alterations in mitochondrial DNA and in TP53 in thoracic esophageal squamous cell carcinoma. Oncol Rep, 28, 69-76.
  • Lee YC, Durr A, Majczenko K, Huang YH, Liu YC, Lien CC, Tsai PC, Ichikawa Y, Goto J, Monin ML, Li JZ, Chung MY, Mundwiller E, Shakkottai V, Liu TT, Tesson C, Lu YC, Brice A, Tsuji S, Burmeister M, Stevanin G, Soong BW. (2012) Mutations in KCND3 cause spinocerebellar ataxia type 22. Annals of Neurology, 72, 859-869.
  • Hsu, C.P., Lin, S.J., Chung, M.Y. and Lu, T.M. (2012) Asymmetric dimethylarginine predicts clinical outcomes in ischemic chronic heart failure. Atherosclerosis, 225, 504-510.
  • Chiang, C.H., Lin, M.W., Chung, M.Y. and Yang, U.C. (2012) The association between the IL-4, ADRbeta2 and ADAM 33 gene polymorphisms and asthma in the Taiwanese population. J Chin Med Assoc, 75, 635-643.
  • Zhang, L., Su, T.P., Choi, K., Maree, W., Li, C.T., Chung, M.Y., Chen, Y.S., Bai, Y.M., Chou, Y.H., Barker, J.L. et al. (2011) P11 (S100A10) as a potential biomarker of psychiatric patients at risk of suicide. J Psychiatr Res, 45, 435-441.
  • Zhang, L., Li, C.T., Su, T.P., Hu, X.Z., Lanius, R.A., Webster, M.J., Chung, M.Y., Chen, Y.S., Bai, Y.M., Barker, J.L. et al. (2011) P11 expression and PET in bipolar disorders. J Psychiatr Res, 45, 1426-1430.
  • Lu, T.M., Lin, S.J., Lin, M.W., Hsu, C.P. and Chung, M.Y. (2011) The association of dimethylarginine dimethylaminohydrolase 1 gene polymorphism with type 2 diabetes: a cohort study. Cardiovasc Diabetol, 10, 16.
  • Lu, T.M., Chung, M.Y., Lin, M.W., Hsu, C.P. and Lin, S.J. (2011) Plasma asymmetric dimethylarginine predicts death and major adverse cardiovascular events in individuals referred for coronary angiography. Int J Cardiol, in press.
  • Lu, T.M., Chung, M.Y., Lin, C.C., Hsu, C.P. and Lin, S.J. (2011) Asymmetric dimethylarginine and clinical outcomes in chronic kidney disease. Clin J Am Soc Nephrol, 6, 1566-1572.