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●蔡輔仁教授

中文姓名：蔡輔仁

英文姓名：FUU-JEN TSAI

性別：男

學歷：中國醫藥大學醫學士

中國醫藥大學附設醫院中醫研究所博士

經歷：中國醫藥大學附設醫院兒科住院醫師

中國醫藥大學附設醫院兒科總醫師

現任：中國醫藥大學醫學中心兒童醫院院長

中國醫藥大學附設醫院兒科部小兒遺傳科主治醫師

中國醫藥大學附設醫院小兒遺傳科主任

中國醫藥大學附設醫院基因醫學部主任

中國醫藥大學專任教授

中國醫藥大學中醫學院院長

專科醫師：

兒科專科醫師

醫學遺傳學專科醫師

兒科內分泌及新陳代謝次專科醫師

新生兒科專科醫師

兒童重症醫學次專科醫師

重症醫學會專科醫師

主治疾病：一般兒科、小兒遺傳及新陳代謝內分泌疾病

1. Chen HY, Chen WC, Tsai HD, Hsu CD, Tsai FJ*, Tsai CH. Relation of the estrogen receptor alpha gene microsatellite polymorphism to bone mineral density and the susceptibility to osteoporosis in postmenopausal Chinese women in Taiwan. Maturitas. 2001; 30;40 :143-50.[SCI]

2. Chen HY, Tsai HD, Chen WC, Wu JY, Tsai FJ*, Tsai CH. Relation of polymorphism in the promotor region for the human osteocalcin gene to bone mineral density and occurrence of osteoporosis in postmenopausal Chinese women in Taiwan. J Clin Lab Anal. 2001; 15: 251-5. [SCI]

3. Chen WC, Chen HY, Hsu CD, Wu JY, Tsai FJ*. No association of vitamin D receptor gene BsmI polymorphisms with calcium oxalate stone formation. Mol Urol. 2001; 5: 7-10. [SCI]

4. Chen WC, Chen HY, Lu HF, Hsu CD, Tsai FJ*. Association of the vitamin D receptor gene start codon Fok I polymorphism with calcium oxalate stone disease. BJU Int. 2001; 87(3):168-71. [SCI]

5. Chen WC, Chen HY, Wu JY, Chen YT, Tsai FJ*. Osteocalcin gene Hind III polymorphism is not correlated with calcium oxalate stone disease. Urol Res 2001; 29: 98-101. [SCI]

6. Chen WC, Lin HS, Tsai FJ*, Li CW. Effects of Tamm-Horsfall protein and albumin on the inhibition of free radicals. Urol Int. 2001; 67: 305-9. [SCI]

7. Chen WC, Lu HF, Chen HY, Hsu CD, Tsai FJ*. Arginine form of p21 gene codon 31 is less prominent in patients with calcium oxalate stone. Urol Res. 2001; 29: 94-7. [SCI]

8. Chen WC, Wu HC, Chen HY, Wu MC, Hsu CD, Tsai FJ*. Interleukin-1beta gene and receptor antagonist gene polymorphisms in patients with calcium oxalate stones. Urol Res. 2001; 29: 321-4. [SCI]

9. Chen WC, Wu HC, Lin WC, Wu MC, Hsu CD, Tsai FJ*. The association of androgen- and oestrogen-receptor gene polymorphisms with urolithiasis in men. BJU Int. 2001; 88: 432-6. [SCI]

10. Chen WC, Wu HC, Lu HF, Chen HY, Tsai FJ*. Calcitonin receptor gene polymorphism: a possible genetic marker for patients with calcium oxalate stones. Eur Urol. 2001; 39: 716-9. [SCI]

11. Hsheih YY, Tsai FJ*, Chang CC, Chen WC, Tsai CH, Tsai HD, Lin CC. P21 gene codon 31 arginine/serine polymorphism: Non-association with endometriosis. J Clin Lab Anal. 2001; 15: 184-7. [SCI]

12. Hsieh YY, Chang CC, Tsai FJ*, Wu JY, Shi YR, Tsai HD, Tsai CH. Polymorphisms for interleukin-1 beta (IL-1 beta)-511 promoter, IL-1 beta exon 5, and IL-1 receptor antagonist: nonassociation with endometriosis. J Assist Reprod Genet. 2001; 18: 506-11. [SCI]

13. Hsieh YY, Chang CC, Tsai FJ*, Wu JY, Tsai CH, Tsai HD. Androgen receptor trinucleotide polymorphism in endometriosis. Fertil Steril. 2001; 76: 412-3. [SCI]

14. Hsieh YY, Tsai FJ*, Chang CC, Chen WC, Tsai CH, Tsai HD, Lin CC. p21 gene codon 31 arginine/serine polymorphism: non-association with endometriosis. J Clin Lab Anal. 2001; 15: 184-7. [SCI]

15. Hsieh YY, Wu JY, Chang CC, Tsai FJ*, Lee CC, Tsai HD, Tsai CH. Prenatal diagnosis of oculocutaneous albinism two mutations located at the same allele.Prenat Diagn. 2001; 21: 200-1. [SCI]

16. Huang CM, Tsai FJ*, Wu JY, Wu MC. Interleukin-1beta and interleukin-1 receptor antagonist gene polymorphisms in rheumatoid arthritis. Scand J Rheumatol. 2001; 30: 225-8. [SCI]

17. Lai CC, Tsai CH, Tsai FJ*, Lee CC, Lin WD. Rapid monitoring assay of congenital adrenal hyperplasia with microbore high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots. Rapid Commun Mass Spectrom. 2001; 15: 2145-51. [SCI]

18. Lee HJ, Cho DY, Tsai FJ, Shen WC. Antley-Bixler syndrome, description of two new cases and review of the literature. Pediatr Neurosurg. 2001; 34: 33-9. [SCI]

19. Lin WD, Shi YR, Tsai FJ, Lee CC, Lin HJ, Wu JY. Identification of a polymorphism (D168N) in the XRP2 gene in Chinese. Hum Mutat. 2001; 17: 354. [SCI]

20. Lin WD, Wu JY, Hsu HB, Tsai FJ*, Lee CC, Tsai CH. Mutation analysis of a family with hereditary hemorrhagic telangiectasia associated with hepatic arteriovenous malformation. J Formos Med Assoc. 2001; 100: 817-9. [SCI]

21. Shi YR, Wu JY, Tsai FJ*, Lee CC, Tsai CH. A 651-665delinsTT mutation in EXT1 causes hereditary multiple exostoses. Hum Mutat 2001; 17: 158. [SCI]

22. Shi YR, Wu JY, Tsai FJ*, Lee CC, Tsai CH. A new polymorphism (c28C>A) of EXT2 gene identified in a Taiwan Chinese family. Hum Mutat. 2001; 17(4): 356. [SCI]

23. Tsai CH, Lin WD, Tsai FJ, Peng CT, Wu JY. Pitfalls of PCR-based genotyping in patients with 21-hydroxylase deficiency. Acta Paediatr Taiwan. 2001; 42: 145-50. [SCI]

24. Tsai FJ*, Wu JY, Yang CF, Tsai CH. Further evidence that fibroblast growth factor receptor 2 mutations cause Antley-Bixler syndrome. Acta Paediatr 2001; 90: 595-7. [SCI]

25. Tsai FJ*, Yang CF, Wu JY, Tsai CH, Lee CC. Mutation analysis of Crouzon syndrome and identification of one novel mutation in Taiwanese patients. Pediatr Int. 2001; 43: 263-6. [SCI]

26. Wu JY, Wu MC, Lee CC, Tsai FJ*. Identification of a novel three-nucleotide insertion mutation (c.841-842insTGA) in the acid beta-glucosidase gene of a Taiwan Chinese patient with type II Gaucher disease. Hum Mutat. 2001; 17(3): 238. [SCI]

27. Wu MC, Wu JY, Lee CC, Tsai CH, Tsai FJ*. A novel polymorphism (c288C>T) of the NPHS2 gene identified in a Taiwan Chinese family. Hum Mutat. 2001; 17(1): 81-2. [SCI]

28. Yang CF, Tsai FJ*, Lin SP, Lee CC, Wu JY. A novel in-frame deletion mutation (c106-111del) identified in a Taiwan Chinese patient with type IVA mucopolysaccharidosis. Hum Mutat. 2001; 18: 254. [SCI]

29. Yang CF, Wu JY, Lin SP, Tsai FJ*. Mucopolysaccharidosis type VI: Report of two Taiwanese patients and identification of one novel mutation. J Formos Med Assoc. 2001; 100: 820-3. [SCI]

30. Chou IC, Tsai FJ*, Yu MT, Tsai CH. Smith-Magenis syndrome with bilateral vesicoureteral reflux: a case report. J Formos Med Assoc. 2002; 101(10): 726-8. [SCI]

31. Hung CM, Wu MC, WU JY, Tsai FJ*. No association of interleukin-4 gene polymorphisms in Chinese patients with rheumatoid arthritis in Taiwan. Clin Exp Rheumatol. 2002; 20(6): 871-2. [SCI]

32. Shi YR, Wu JY, Hsu YA, Lee CCm Tsai CH, Tsai FJ*. Mutation Screening of the EXT Genes in Patients with Hereditary Multiple Exostoses in Taiwan.Genet Test. 2002; 6(3): 237-43.[SCI]

33. Chou HT, Hung JS, Chen YT, Shi YR, Tsai FJ*. Association between angiotensinogen gene M235T polymorphism and mitral valve prolapse syndrome in Taiwan Chinese.J Heart Valve Dis. 2002; 11(6): 830-6. [SCI]

34. Chen Wc, Wu HC, Hsu CD, Chen HY, Tsai FJ*. p21 gene codon 31 polymorphism is associated with bladder cancer. Urol Oncol. 2002; 7(2): 63-6. [SCI]

35. Shi YR, Lee CC, Hsu YA, Wang CH, Tsai FJ*. A novel nonsense mutation of the sedlin gene in a family with spondyloepiphyseal dysplasia tarda. Hum Hered. 2002; 54(1): 54-6. [SCI]

36. Lin WD, Wu JY, Tsai FJ*, Gau MT, Lee CC. Type identification of autosomal dominant polycystic kidney disease by analysis of fluorescent short tandem repeat markers. J Formos Med Assoc. 2002; 101(8): 567-71. [SCI]

37. Tsai FJ*, Chou IC, Hsieh YY, Lee CC, Lin CC, Tsai CH. Interleukin-4 intron 3 polymorphism is not related to susceptibility to febrile seizures. Pediatr Neurol. 2002; 27(4): 271-4. [SCI]

38. Chou IC, Tsai FJ*, Hunang CC, Lin CC, Tsai CH. The voltage-gated potassium channel KCNQ2 in Taiwanese children with febrile convulsions. Neuroreport. 2002: 28; 13(15): 1971-3. [SCI]

39. Hsieh YY, Lin WC, Chang CC, Tsai FJ*, Yu MT, Tsai HD, Tsai CH. Turner syndrome with pseudodicentric Y chromosome mosaicism. J Assist Reprod Genet. 2002; 19(6): 302-3. [SCI]

40. Chou HT, Shi YR, Hsu Y, Tsai FJ*. Lack of association between transforming growth factor-beta1 gene polymorphisms and mitral valve prolapse in Taiwan Chinese. J Heart Valve Dis. 2002; 11(4): 478-84 [SCI]

41. Huang CM, Wu MC, Wu JY, Tsai FJ*. Interleukin-1 receptor antagonist gene polymorphism in chinese patients with systemic lupus erythematosus. Clin Rheumatol. 2002; 21(3): 255-7. [SCI]

42. Lin HJ, Chen WC, Tsai FJ*, Tsai SW. Distributions of p53 codon 72 polymorphism in primary open angle glaucoma. Br J Ophthalmol. 2002; 86(7):767-70. [SCI]

43. Huang CM, Wu MC, Wu JY, Tsai FJ*. No association of vitamin D receptor gene start codon fok 1 polymorphisms in Chinese patients with systemic lupus erythematosus. J Rheumatol. 2002; 29(6): 1211-3. [SCI]

44. Tsai FJ*, Hsieh YY, Chang CC, Lin CC, Tsai CH. Polymorphisms for interleukin 1 beta exon 5 and interleukin 1 receptor antagonist in Taiwanese children with febrile convulsions.Arch Pediatr Adolesc Med. 2002; 156(6):545-8. [SCI]

45. Wang TJ, Huang CB, Tsai FJ, Wu JY, Lai RBm, Hsiao M. Mutation in the FGFR2 gene in a Taiwanese patient with Beare-Stevenson cutis gyrata syndrome. Clin Genet. 2002; 61(3): 218-21. [SCI]

46. Chou HT, Shi YR, Wu JY, Tsai FJ*. Angiotensin II type 1 receptor gene adenine/cytosine1166 polymorphism is not associated with mitral valve prolapse syndrome in Taiwan Chinese. Circ J. 2002; 66(2): 163-6. [SCI]

47. Shi YR, Hsieh KS, Wu JY, Lee CC, Tsai CH, Tsai FJ*. Molecular analysis of syndromic congenital heart disease using short tandem repeat markers and semiquantitative polymerase chain reaction method. Pediatr Int. 2002; 44(3): 264-8. [SCI]

48. Tsai MH, Chen WC, Tsai FJ*. Correlation of p21 gene codon 31 polymorphism and TNF-alpha gene polymorphism with nasopharyngeal carcinoma. J Clin Lab Anal. 2002; 16(3):146-50. [SCI]

49. Hsieh YY, Chang CC, Tsai FJ*, Hsu Y, Tsai HD, Tsai CH. Polymorphisms for interleukin-4 (IL-4) -590 promoter, IL-4 intron3, and tumor necrosis factor alpha -308 promoter: non-association with endometriosis. J Clin Lab Anal. 2002; 16(3): 121-6. [SCI]

50. Huang CM, Wu MC, Wu JY, Tsai FJ*. Lack of association of interleukin-1beta gene polymorphisms in Chinese patients with systemic lupus erythematosus. Rheumatol Int. 2002; 21(5): 173-5. [SCI]

51. Chen HY, Chen WC, Hsu CD, Tsai FJ*, Tsai CH. Relation of vitamin D receptor FokI start codon polymorphism to bone mineral density and occurrence of osteoporosis in postmenopausal women in Taiwan. Acta Obstet Gynecol Scand. 2002; 81(2): 93-8. [SCI]

52. Chang JG, Liu HC, Shih MC, Liu SC, Chan WL, Tsai FJ. Unstable Hb Perth in a Taiwanese subject: a T-->C substitution at codon 32 of the beta-globin gene creates an MspI site. Hemoglobin. 2002; 26(1): 91-4. [SCI]

53. Chang JG, Lee LS, Chen CM, Shih MC, Wu MC, Tsai FJ, Liang DC. Molecular analysis of thiopurine S-methyltransferase alleles in South-east Asian populations. Pharmacogenetics. 2002; 12(3): 191-5. [SCI]

54. Huang CM, Wu MC, Wu JY, Tsai FJ*. Association of vitamin D receptor gene BsmI polymorphisms in Chinese patients with systemic lupus erythematosus. Lupus. 2002;11(1):31-4. [SCI]

55. Tsai FJ, Lin CC, Lu HF, Chen HY, Chen WC. Urokinase gene 3'-UTR T/C polymorphism is associated with urolithiasis. Urology. 2002; 59(3): 458-61. [SCI]

56. Wu JY, Shu SG, Yang CF, Lee CC, Tsai FJ*. Mutation analysis of thyroid peroxidase gene in Chinese patients with total iodide organification defect: identification of five novel mutations. J Endocrinol. 2002; 172(3): 627-35. [SCI]

57. Chen HY, Chen WC, Hsu CD, Tsai FJ*, Tsai CH, Li CW. Relation of BsmI vitamin D receptor gene polymorphism to bone mineral density and occurrence of osteoporosis in postmenopausal Chinese women in Taiwan. Osteoporos Int. 2001; 12(12): 1036-41. [SCI]

58. Lai CC, Tsai Ch, Tsai FJ*, Wu JY, Lin WD, Lee CC. Rapid screening assay of congenital adrenal hyperplasia by measuring 17 alpha-hydroxyprogesterone with high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots. J Clin Lab Anal. 2002; (1): 20-5. [SCI]

59. Lai CC, Tsai CH, Tsai FJ*, Wu JY, Lin WD, Lee CC. Monitoring of congenital adrenal hyperplasia by microbore HPLC-electrospray ionization tandem mass spectrometry of dried blood spots. Clin Chem. 2002; 48(2): 354-6. [SCI]

60. Tsai MH, Lin CD, Hsieh YY, Chang FC, Tsai FJ*, Chen WC, Tsai CH. Prognostic significance of the proline form of p53 codon 72 polymorphism in nasopharyngeal carcinoma. Laryngoscope. 2002; 112(1): 116-9. [SCI]

61. Chang CC, Hsieh YY, Tsai FJ*, Tsai CH, Tsai HD, Lin CC. The proline form of p53 codon 72 polymorphism is associated with endometriosis. Fertil Steril. 2002; 77(1): 43-5. [SCI]

62. Chou HT, Shi YR, Chang CT, Tsai FJ*. The polymorphisms of codon 727 and 52 of thyroid-stimulating hormone receptor gene are not associated with mitral valve prolapse syndrome in Taiwan Chinese. Jpn Heart J. 2002 Nov;43(6):655-66. [SCI]

63. Shi YR, Hsieh KS, Wu JY, Lee CC, Tsai CH, Yu MT, Chang JS, Tsai FJ*. Genetic analysis of chromosome 22q11.2 markers in congenital heart disease. J Clin Lab Anal. 2003; 17(1): 28-35. [SCI]

64. Hsieh YY, Chang CC, Tsai FJ*, Tsai HD, Yeh LS, Lin CC, Tsai CH. Estrogen receptor thymine-adenine dinucleotide repeat polymorphism is associated with susceptibility to leiomyoma. Fertil Steril. 2003; 79(1): 96-9. [SCI]

65. Chou HT, Chen YT, Shi YR, Tsai FJ*. Association between angiotensin I-converting enzyme gene insertion/deletion polymorphism and mitral valve prolapse syndrome. Am Heart J. 2003; 145(1): 169-73. [SCI]

66. Huang CM, Hang LW, Chen CL, Wu JY, Tsai FJ*. Polymorphisms of TAP1 transporter genes in Chinese patients with systemic lupus erythematosus in Taiwan. Rheumatol Int. 2003 Jun 21 [SCI]

67. Lee HH, Chang SF, Tsai FJ, Tsai LP, Lin CY. Mutation of IVS2 -12A/C>G in combination with 707-714delGAGACTAC in the CYP21 gene is caused by deletion of the C4-CYP21 repeat module with steroid 21-hydroxylase deficiency. J Clin Endocrinol Metab. 2003 Jun;88(6):2726-9. [SCI]

68. Tsai FJ, Chen WC, Chen HY, Tsai CH. The ALUI Calcitonin Receptor Gene Polymorphism (TT) Is Associated with Low Bone Mineral Density and Susceptibility to Osteoporosis in Postmenopausal Women. Gynecol Obstet Invest. 2003;55(2):82-7. [SCI]

69. Huang CM, Tsai JJ, Tsai FJ*, Chen WC, Chen CL. Insulin-like growth factor-II gene ApaI polymorphism was not associated with systemic lupus erythematosus. Lupus. 2003;12(5):423-4. [SCI]

70. Lo SF, Huang CM, Wu MC, Wu JY, Tsai FJ*. Lack of association of tumor necrosis factor alpha gene polymorphism in patients with rheumatoid arthritis in central Taiwan.
Rheumatol Int. 2003 May 16 [SCI]

71. Chou IC, Peng CT, Tsai FJ*, Huang CC, Shi YR, Tsai CH. The lack of association between febrile convulsions and polymorphisms in SCN1A. Epilepsy Res. 2003 Apr;54(1):53-7. [SCI]

72. Tsai FJ, Wu HC, Chen HY, Lu HF, Hsu CD, Chen WC. Association of E-Cadherin Gene 3'-UTR C/T Polymorphism with Calcium Oxalate Stone Disease. Urol Int. 2003;70(4):278-81. [SCI]

73. Chiang D, Chiang HC, Chen WC, Tsai FJ. Prediction of stone disease by discriminant analysis and artificial neural networks in genetic polymorphisms: a new method. BJU Int. 2003 May;91(7):661-6. [SCI]

74. Chou IC, Peng CT, Huang CC, Tsai JJ, Tsai FJ*, Tsai CH. Association analysis of gamma 2 subunit of gamma- aminobutyric acid type A receptor polymorphisms with febrile seizures.
Pediatr Res. 2003 Jul;54(1):26-9. [SCI]

75. Hang LW, Hsia TC, Chen WC, Chen HY, Tsai FJ*. TAP1 gene AccI polymorphism is associated with atopic bronchial asthma. J Clin Lab Anal. 2003; 17(2):57-60. [SCI]

76. Chen HY, Chen WC, Wu MC, Tsai FJ*, Tsai CH. Androgen receptor (AR) gene microsatellite polymorphism in postmenopausal women: correlation to bone mineral density and susceptibility to osteoporosis. Eur J Obstet Gynecol Reprod Biol. 2003 Mar 26;107(1):52-6. [SCI]

77. Lin HJ, Tsai FJ*, Chen WC, Shi YR, Hsu Y, Tsai SW. Association of tumour necrosis factor alpha -308 gene polymorphism with primary open-angle glaucoma in Chinese.
Eye. 2003 Jan;17(1):31-4. [SCI]

78. Chou HT, Shi YR, Hsu Y, Tsai FJ*. Lack of association of genetic polymorphisms in the interleukin-1beta, interleukin-1 receptor antagonist, interleukin-4 and interleukin-10 genes with mitral valve prolapse in Taiwan Chinese. J Heart Valve Dis. 2003 Jan;12(1):38-44. [SCI]

79. Chen CP, Chem SR, Lin SP, Wang W, Tsai FJ. Prenatal identification of a G338E mutation in FGFR2 in a fetus without sonographic appearance of craniosynostosis. Prenat Diagn. 2003 Feb;23(2):175-6. [SCI]

80. Chen HY, Chen WC, Wu MC, Tsai FJ*, Lin CC. Interleukin-1beta and interleukin-1 receptor antagonist gene polymorphism in postmenopausal women: correlation to bone mineral density and susceptibility to osteoporosis. Maturitas. 2003 Jan 30;44(1):49-54. [SCI]

81. Wu HC, Lin CC, Chen WC, Chen HY, Tsai FJ*. Osteocalcin gene HindIII C/T polymorphism is a biomarker for prostate cancer and responsiveness to hormone therapy. Eur Urol. 2003 Feb;43(2):197-200. [SCI]

85. Tsai MH, Chen WC, Chen HY, Tsai FJ*. Urokinase gene 3'-UTR T/C polymorphism is associated with oral cancer. J Clin Lab Anal. 2004; 18(5):276-9. [SCI]

87. Hsieh YY, Chang CC, Tsai FJ*, Lin CC, Chen JM, Tsai CH. Glutathione S-transferase M1*null genotype but not myeloperoxidase promoter G-463A polymorphism is associated with higher susceptibility to endometriosis. Mol Hum Reprod. 2004; 10(10):713-7. [SCI]

88. Hsieh YY, Chang CC, Tsai FJ*, Yeh LS, Lin CC, Peng CT. T allele for VEGF gene-460 polymorphism at the 5'-untranslated region: association with a higher susceptibility to endometriosis. J Reprod Med. 2004; 49(6):468-72. [SCI]

92. Chou HT, Chen YT, Wu JY, Tsai FJ*. Association between urokinase-plasminogen activator gene T4065C polymorphism and risk of mitral valve prolapse.Int J Cardiol. 2004; 96(2): 165-70. [SCI]

93. Lo SF, Huang CM, Lin HC, Tsai CH, Tsai FJ*. Association of CYP17 gene polymorphism and rheumatoid arthritis in Chinese patients in central Taiwan. Rheumatol Int. 2004 Jul 3 [SCI]

94. Huang CM, Tsai CH, Chen CL, Chan CP, Tsai FJ*. No relationship of -627 interleukin-10 promoter polymorphism in Chinese patients with rheumatoid arthritis. Rheumatol Int. 2004 Jun 25 [SCI]

95. Chou HT, Chen CH, Tsai CH, Tsai FJ. Association between transforming growth factor-beta1 gene C-509T and T869C polymorphisms and rheumatic heart disease. Am Heart J. 2004; 148(1): 181-6. [SCI]

97. Chou HT, Hung JS, Chen YT, Wu JY, Tsai FJ*. Association between COL3A1 collagen gene exon 31 polymorphism and risk of floppy mitral valve/mitral valve prolapse. Int J Cardiol. 2004; 95(2-3):299-305. [SCI]

101. Huang CM, Chen CL, Tsai JJ, Tsai CH, Tsai FJ*. Association between urokinase gene 3'-UTR T/C polymorphism and Chinese patients with rheumatoid arthritis in Taiwan. Clin Exp Rheumatol. 2004; 22(2):219-22. [SCI]

102. Huang CM, Chen CL, Tsai JJ, Tsai CH, Tsai FJ*. Association between urokinase gene 3'-UTR T/C polymorphism and Chinese patients with rheumatoid arthritis in Taiwan. Clin Exp Rheumatol. 2004; 22(2):219-22. [SCI]

103. Chen CP, Lin SP, Tzen CY, Tsai FJ, Hwu WL, Wang W. Detection of a homozygous D645E mutation of the acid alpha-glucosidase gene and glycogen deposition in tissues in a second-trimester fetus with infantile glycogen storage disease type II. Prenat Diagn. 2004; 24(3):231-2. [SCI]

105. Chou HT, Chen YT, Wu JY, Tsai FJ*. Lack of association between perlecan gene intron 6 BamHI polymorphism and risk of mitral valve prolapse in Taiwan Chinese. Jpn Heart J. 2004; 45(1):109-18. [SCI]

106. Yu MC, Huang CM, Wu MC, Wu JY, Tsai FJ*. Association of TAP2 gene polymorphisms in Chinese patients with rheumatoid arthritis. Clin Rheumatol. 2004; 23(1):35-9. [SCI]

107. Tsai FJ*, Lin HJ, Chen WC, Tsai CH, Tsai SW. A codon 31ser-arg polymorphism of the WAF-1/CIP-1/p21/tumour suppressor gene in Chinese primary open-angle glaucoma. Acta Ophthalmol Scand. 2004; 82(1):76-80. [SCI]

108.Huang CM, Hang LW, Chen CL, Wu JY, Tsai FJ*. Polymorphisms of TAP1 transporter genes in Chinese patients with systemic lupus erythematosus in Taiwan. Rheumatol Int. 2004; 24(3):130-2. [SCI]

發表具審查制之期刊論文篇數（SCI、SSCI 、AHCI及TSSCI除外）一覽表

1. Lin WD, Wu JY, Lai CC, Tsai FJ*, Tsai CH, Lin SP, Niu DM. A pilot study of neonatal screening by electrospray ionization tandem mass spectrometry in Taiwan. Acta Paediatr Taiwan. 2001; 42: 224-30. [MI]

2. Tsai FJ, Lee CC, Wu MC, Lin SP, Lin CY, Tsai CH, Kodama H, Wu JY. Mutation analysis of type II Gaucher disease in five Taiwanese children: identification of two novel mutations. Acta Paediatr Taiwan. 2001; 42: 231-5. [MI]

3. Wu KH, Yu MT, Tsai FJ*, Peng CT, Tsai CH. Monosomy of chromosome 10q26 with mild psychomotor retardation: report of one case. Acta Paediatr Taiwan. 2002; 43(3): 153-6. [MI]

4. Yang KC, Su BH, Tsai FJ, Peng CT. The comparison between capillary blood sampling and arterial blood sampling in an NICU. Acta Paediatr Taiwan. 2002; 43(3):124-6. [MI]

5. Wu KC, Chiu HH, Wang JH, Lee NS, Lin HC, Hsieh CC, Tsai FJ, Peng CT, Tseng YC. Characteristics of community-acquired methicillin-resistant Staphylococcus aureus in infants and children without known risk factors. J Microbiol Immunol Infect. 2002; 35(1): 53-6. [MI]

6. Chou CT, Tseng YC, Tsai FJ*, Lin CC, Liu CS, Peng CT, Tsai CH. Measurement of ear length in neonates, infants and preschool children in Taiwan. Acta Paediatr Taiwan. 2002; 43(1): 40-2. [MI]

7. Su BH, Lin TW, Lin HC, Tsai FJ, Peng CT. Inhaled nitric oxide in persistent pulmonary hypertension of the newborn: four-year experience in a single medical center. Acta Paediatr Taiwan. 2002 Sep-Oct; 43(5):259-64. [MI]

1. Yang CF, Tsai FJ, Lin SP, Wu JY. Molecular anlaysis of the N-acetylgalactosamine-6-sulfate s;ulfatase gene in Taiwanese patients with Mucopolysaccharidosis iva. 50th Annual Meeting. The American Society of Human Genetics. 2001. Oct. USA

2. Shi YR, Hsieh KS, Wu JY, Lee CC, Tsai CH, Tsai FJ. Molecular Analysis of Syndromic congenital Heart Disease by Using Short Tandem Repeat Polymorphic Markers. 50th Annual Meeting. The American Society of Human Genetics. 2001. Oct. USA

3. Wu JY, Yang CF, Tsai FJ. Molecular analysis of two patients with 3-hydroxy-methyl-glutaric aciduria: identification of three novel mutations including one de novo mutation. 51st Annual Meeting. The American Society of Human Genetics, 2001.oct. USA

4. Tsai FJ, Yang CF, Wu JY, Molecular analysis of GM1-gangliosidosis:identification and characterization of four novel mutations in two Taiwan Chinese patients. 51st Annual Meeting. The American Society of Human Genetics. 2002.Oct USA

5. Tsai LP, Tsou KS, Shi YR, Wu JY, Tsai FJ. Haplotype analysis in patients with velopharyngeal insufficiency (VPI)minimizes one VPI locus in 2.8Mb region of 22q11. 51st Annual Meeting. The American Society of Human Genetics. USA

6. Tsai FJ, Wu JY, Shu SG, Yang CF, Tsai CH. Mutation analysis of thyroid peroxidase gene in Taiwanese patients with total iodide organification defect. 10th International Congress of Human Genetics. 2001, May.

7. Tsai FJ, Wu JY, Tsai CH. Mutation Analysis of the EXT1 and EXT2 Genes in Patients with Hereditary Multiple Exostoses. 2002. USA

8. Wu JY, Yang CF, Tsai FJ. Characterization of Four Novel b-Galactosidase Gene Mutations and A Polymorphism in Taiwanese Patients with GM1-Gangliosidosis. 52nd Annual Meeting. The American Society of Human Genetics. 2002, Oct USA

9. Chang JG, Tsai FJ, Wang WY, Jong YJ. Treatment of spinal muscular atrophy by hydroxyurea. 52nd Annual Meeting. The American Society of Human Genetics. 2002, Oct USA

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91 91年11月 2002年國家生技醫療品質獎醫療院所類”品質金獎” 生策會

93 93年5月第三屆”罕見疾病藥物供應製造及研究發展獎勵行政院衛生署活動”傑出貢獻獎

學年	計畫名稱	補助/委託金額	計畫編號	補助/委託機構	執行期限	備註
93	一個類似鎖骨顱骨發育不良症家族的基因定位	810,000	93-2314-B-039-011-	行政院國家科學委員會	2004/8/1 至 2005/7/31	執行中
92	生長激素療效之藥理遺傳學與蛋白質體學研究（2/3）	2,620,000	92-3112-B-039-001-	行政院國家科學委員會	2003/5/1 至 2004/4/30
91	生長激素療效之藥理遺傳學研究	1,794,900	91-3112-B-039-001-	行政院國家科學委員會	2002/5/1 至 2003/4/30