鍾明怡 副教授

退休副教授、榮總兼任副研究員
鍾明怡
Ming-yi Chungoid
phone 02-55683265
mail mychung@nycu.edu.tw
address 榮總致德樓8樓R871
1993 Bacaner Research Award in Basic Medical Science, Minnesota Medical Foundation
  • Nov, 2013-present 臺北榮民總醫院 醫學研究部 兼任副研究員
  • Aug, 2006-present 國立陽明交通大學 生命科學系暨基因體科學研究所 副教授
  • Aug, 2005-Oct, 2013 臺北榮民總醫院 教學研究部 兼任副研究員
  • Aug, 2005-Jul, 2006 國立陽明大學 遺傳學研究所 副教授
  • Aug, 2002-Jul, 2005 國立陽明大學 遺傳學研究所 兼任副教授
  • May, 1997-Aug, 2005 臺北榮民總醫院 教學研究部 副研究員
  • Oct, 1994-May, 1997 臺北榮民總醫院 病理檢驗部臨床細胞遺傳實驗室 約聘技術師
  • 1994 美國明尼蘇達大學 分子遺傳臨床細胞遺傳 博士後研究
  • 1993 美國明尼蘇達大學 (University of Minnesota, Minneapolis) 病理生物 (Pathobiology) 博士
  • 1990 美國明尼蘇達大學 臨床實驗科學 (Clinical Laboratory Science) 碩士
  • 1987 國立臺灣大學 醫事技術學系 學士 
分子遺傳學、細胞遺傳學、醫學遺傳學
  • 遺傳學概論
  • 基因體學
  • 醫學遺傳學
  • 黃斑失養症之表現形與基因形間的關係。
  • 家族性滲漏性玻璃體視網膜病變基因在NDP/wnt/β-catenin singaling pathway與 angiogenesis中的角色。
  • 10q26基因多型性在老年性黃斑部病變的角色。
利用分子遺傳學方法找尋並了解基因在致病機轉中所扮演的角色。
科技部 < MOST109-2314-B-010 -013 >家族性滲漏性玻璃體視網膜病變之分子遺傳學研究 4(2020/08/01-2021/07/31
  1. Chung, M.Y.*, Chen SJ, Jiang YJ (2021) Phenotype Variability in the Patients of Familial Exudative Vitreoretinopathy: the RCBTB1 case. Curr Eye Res 46 (12):1931. doi:10.1080/02713683.2021.1924383
  2. Chen PC, Huang HY,Chung, M.Y., Pan CC (2021) Ossifying low grade endometrial stromal sarcoma with PHF1-BRD8 fusion. Cancer Genet 256-257:81-85. doi:10.1016/j.cancergen.2021.04.00
  3. Wu CC, Hsieh MY, Lee CK, Chuang SY, Chung, M.Y.*, Lin CC (2019) Dimethylarginine Dimethylaminohydrolase 1 Polymorphisms and Venous Intimal Hyperplasia in Hemodialysis Patients. American journal of nephrology 50 (6):454-464. doi:10.1159/000503949
  4. Liao KW, Chang CH, Tsai MS, Chien LC, Chung, M.Y., Mao IF, Tsai YA, Chen ML (2018) Associations between urinary total arsenic levels, fetal development, and neonatal birth outcomes: A cohort study in Taiwan. The Science of the total environment 612:1373-1379. doi:10.1016/j.scitotenv.2017.08.312
  5. Chen S-P, Fuh J-L, Chung, M.Y.1, Lin Y-C, Liao Y-C, Wang Y-F, Hsu C-L, Yang U-C, Lin M-W, Chiou J-J, Wang P-J, Chen P-K, Fan P-C, Wu J-Y, Chen Y-T, Kao L-S, Fann CS-J, Wang S-J (2018) Genome-wide association study identifies novel susceptibility loci for migraine in Han Chinese resided in Taiwan. Cephalalgia : an international journal of headache 38 (3):466-475. doi:doi:10.1177/0333102417695105
  6. Chang CH, Yu CJ, Du JC, Chiou HC, Chen HC, Yang W,Chung, M.Y., Chen YS, Hwang B, Mao IF, Chen ML (2018) The interactions among organophosphate pesticide exposure, oxidative stress, and genetic polymorphisms of dopamine receptor D4 increase the risk of attention deficit/hyperactivity disorder in children. Environmental research 160:339-346. doi:10.1016/j.envres.2017.10.011
  7. Yu CJ, Du JC, Chiou HC, Yang SH, Liao KW, Yang W, Chung, M.Y., Chien LC, Hwang B, Chen ML (2016) Attention Deficit/Hyperactivity Disorder and Urinary Nonylphenol Levels: A Case-Control Study in Taiwanese Children. PloS one 11 (2):e0149558. doi:10.1371/journal.pone.0149558
  8. Yu CJ, Du JC, Chiou HC, Feng CC, Chung, M.Y., Yang W, Chen YS, Chien LC, Hwang B, Chen ML (2016) Sugar-Sweetened Beverage Consumption Is Adversely Associated with Childhood Attention Deficit/Hyperactivity Disorder. International journal of environmental research and public health 13 (7):E678. doi:10.3390/ijerph13070678
  9. Yu CJ, Du JC, Chiou HC, Chung, M.Y., Yang W, Chen YS, Fuh MR, Chien LC, Hwang B, Chen ML (2016) Increased risk of attention-deficit/hyperactivity disorder associated with exposure to organophosphate pesticide in Taiwanese children. Andrology 4 (4):695-705. doi:10.1111/andr.12183
  10. Wu JH, Liu JH, Ko YC, Wang CT, Chung YC, Chu KC, Liu TT, Chao HM, Jiang YJ, Chen SJ, Chung, M.Y.* (2016) Haploinsufficiency of RCBTB1 is associated with Coats disease and familial exudative vitreoretinopathy. Human molecular genetics 25 (8):1637-1647. doi:10.1093/hmg/ddw041
  11. Lee KH, Tsai WJ, Chen YW, Yang WC, Lee CY, Ou SM, Chen YT, Chien CC, Lee PC, Chung, M.Y.*, Lin CC (2016) Genotype polymorphisms of genes regulating nitric oxide synthesis determine long-term arteriovenous fistula patency in male hemodialysis patients. Renal failure 38 (2):228-237. doi:10.3109/0886022X.2015.1120096
  12. Fuh JL, Chung, M.Y.1, Yao SC, Chen PK, Liao YC, Hsu CL, Wang PJ, Wang YF, Chen SP, Fann CS, Kao LS, Wang SJ (2016) Susceptible genes of restless legs syndrome in migraine. Cephalalgia : an international journal of headache 36 (11):1028-1037. doi:10.1177/0333102415620907
  13. Chen YW, Wu YT, Lin JS, Yang WC, Hsu YH, Lee KH, Ou SM, Chen YT, Shih CJ, Lee PC, Chan CH, Chung, M.Y.*, Lin CC (2016) Association of Genetic Polymorphisms of Renin-Angiotensin-Aldosterone System-Related Genes with Arterio-Venous Fistula Malfunction in Hemodialysis Patients. International journal of molecular sciences 17 (6). doi:10.3390/ijms17060833
  14. Tseng SH, Cheng CY, Huang MZ, Chung, M.Y.*, Su TS (2013) Modulation of formation of the 3'-end of the human argininosuccinate synthetase mRNA by GT-repeat polymorphism. International journal of biochemistry and molecular biology 4 (4):179-190
  15. Lin CC, Chung, M.Y., Yang WC, Lin SJ, Lee PC (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. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 28 (5):1284-1293. doi:10.1093/ndt/gfs608.
  16. Chang CF, Lu TM, Yang WC, Lin SJ, Lin CC, Chung, M.Y.* (2013) Gene polymorphisms of interleukin-10 and tumor necrosis factor-alpha are associated with contrast-induced nephropathy. American journal of nephrology 37 (2):110-117. doi:10.1159/000346528
  17. Lin CS, Wang LS, Chang SC, Chou TY, Hsu WH, Liu CS, Lee MH, Chung, M.Y., Wei YH (2012) Associated microsatellite alterations in mitochondrial DNA and in TP53 in thoracic esophageal squamous cell carcinoma. Oncology reports 28 (1):69-76. doi:10.3892/or.2012.1761
  18. Lee YC, Durr A, Majczenko K, Huang YH, Liu YC, Lien CC, Tsai PC, Ichikawa Y, Goto J, Monin ML, Li JZ, Chung, M.Y., 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. Ann Neurol 72 (6):859-869. doi:10.1002/ana.23701
  19. Hsu CP, Lin SJ, Chung, M.Y., Lu TM (2012) Asymmetric dimethylarginine predicts clinical outcomes in ischemic chronic heart failure. Atherosclerosis 225 (2):504-510. doi:10.1016/j.atherosclerosis.2012.09.040
  20. Chiang CH, Lin MW, Chung, M.Y., Yang UC (2012) The association between the IL-4, ADRbeta2 and ADAM 33 gene polymorphisms and asthma in the Taiwanese population. Journal of the Chinese Medical Association : JCMA 75 (12):635-643. doi:10.1016/j.jcma.2012.08.012
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