Publication List of Kwang-Jen Hsiao, Ph.D. (¿½ ¼s ¤¯ ±Ð ±Â)


 
 Scientific Publications (1997 - 2004)

 
67.
 Chen CH, Liu MY, Wei FC, Koong FJ, Hwu HG, Hsiao KJ.  Further evidence of no association between Ser9Gly polymorphism of dopamine D3 receptor gene and schizophrenia.  Am J Med Genet 1997;74:40-3.


68. Zhang M, Hsiao KJ, Su TS, Chao HK, Chen RG, Gu XF.  Two novel mutations in phenylalanine hydroxylase gene and in vitro expression analysis on Arg252Gln.  Chin Med Sci J 1997;12:22-5.


69. Chen CH, Wei FC, Koong FJ, Hsiao KJ.  Association of TaqI a polymorphism of dopamine D2 receptor gene and tardive dyskinesia in schizophrenia.  Biol Psychiatry 1997;41:827-9.


70. Chen CH, Lee YR, Wei FC, Koong FJ, Hwu HG, Hsiao KJ.  Association study of N1aIII and MspI genetic polymorphisms of Catechol-O-Methyltransferase gene and susceptibility to schizophrenia.  Biol Psychiatry 1997;41:985-7.


71. Jeng MJ, Lin CY, Soong WJ, Hsiao KJ, Hwang B, Chiang SH.  Neonatal thyroid function is unaffected by maternal topical iodine disinfection for cesarean section or vaginal delivery.  Clin Pediat 1997;2:109-11.


72. Jeng MJ, Lin CY, Soong WJ, Hsiao KJ, Hwang B, Chiang SH.  Neonatal thyroid function is unaffected by single treatment with different preparations of povidone-iodine on wide skin surface.  Acta Paed Sin 1997;38:28-31.


73. Chou P, Li CL, Kuo HS, Hsiao KJ, Tsai ST.  Comparison of the prevalence in two diabetes surveys in Pu-Li, Taiwan, 1987-88 and 1991-92.  Diabetes Res Clin Pr 1997;38:61-7.


74. Lin CM, Tan Y, Lee YM, Chang CC, Hsiao KJ.  Expression of human phenylalanine hydroxylase activity in T lymphocyte of classical phenylketonuria children by retroviral-mediated gene transfer.  J Inher Metab Dis 1997;20:742-54.


75. Liu XQ, Liu TT, Hsiao KJ, Zhang M, Zhang YF, Ye J, Chen RG, Gu XF.  Identification of mutation gene in atypical phenylketonuria.  Chin J Med Genet 1997;6:351-3. (in Chinese)


76. Chen CH, Lee YR, Wei FC, Koong FJ, Hwu HG, Hsiao KJ.  Lack of allelic association between 102T/C polymorphism of serotonin receptor type 2A gene and schizophrenia in Chinese.  Psychiatr Genet 1997;7:35-8.


77. Liu TT, Hsiao KJ, Lu SF, Wu SJ, Wu KF, Chiang SH, Liu XQ, Chen RG, Yu WM.  Mutation analysis of the 6-pyruvoyl-tetrahydropterin synthase gene in Chinese hyperphenylalaninemia caused by tetrahydrobiopterin synthesis deficiency.  Hum Mutat 1998;11:76-83.


78. Liu TT, Lu SF, Hsiao KJ.  Genomic Structure of 6-Pyruvoyl-tetrahydropterin Synthase Gene and a T/C Polymorphism Detected in Chinese.  J Biomed Lab Sci 1998;10:39-47.


79. Chen CH, Shyu PW, Wu SJ, Sheu SS, Desnick RJ, Hsiao KJ.  Identification of a novel point mutation (S65T) in a -galactosidase A gene in Chinese patients with Fabry disease.  Mutations in Brief no. 169 (1998) Online,   Hum Mutat 1998;11:328-30.


80. Tang DJ, Ma XQ, Song CY, Lin BH, Wu SJ, Chiang SH, Hsiao KJ.  Glucose-6-phosphate dehydrogenase mutations among Cantonese revealed by polymerase chain reaction using dried blood spots.  Chin J Hematol 1998;4:189-91. (in Chinese)


81. Jeng MJ, Lin CY, Soong WJ, Hsiao KJ, Hwang BT, Ghiang SH.  The effect of povidone-iodine on thyroid function of neonates wiyh different birth sizes.  Acta Paed Sin 1998;39:371-5.


82. Chen CH, Chiu YL, Wei FC, Koong FJ, Liu HC, Shaw CK, Hwu HG, Hsiao KJ.  High seroprevalence of Borna virus infection in schizophrenic patients, family members and mental health workers in Taiwan.  Mol Psychiatry 1999;4:33-8.


83. Hong CJ, Song HL, Lai HC, Tsai, SJ, Hsiao KJ.  Methanol/acetone treatment helps the amplification of FMR1 CGG repeat fragment in dried blood spots from Guthrie cards.  Lancet 1999;353: 1153-4.


84. Tsai MT, Shaw CK, Hsiao KJ, Chen CH.  Genetic association study of a polymorphic CAG repeats array of calcium-activated potassium channel (KCNN3) gene and schizophrenia among the Chinese population from Taiwan.  Mol Psychiatry 1999;4:271-3.


85. Chen CH, Chiu YL, Shaw CK, Tsai MT, Hwang AL, Hsiao KJ.  Detection of Borna disease virus RNA from peripheral blood cells in schizophrenic patients and mental health workers.  Mol Psychiatry 1999;4:566-71.


86. Hsiao KJ, Liu TT, Liu MY, Wu KF, Chiang SH, Wu SJ.  Human gene mutations, Gene Symbol: PTS, Disease: Hyperphenylalaninemia.  Hum Genet 1999;104:115.


87. Cheung KL, Tang NLS, Hsiao KJ, Law LK, Wong W, Ng PC, Pang CP, Applegarth DA, Fok TF, Hjelm NM.  Classical galactosaemia in Chinese: A case report and review of disease incidence.  J Paediatr Child Health 1999;35:399-400.


88. Chen CH, Lee YR, Chung MY, Wei FC, Koong FJ, Shaw CK, Yeh JI, Hsiao KJ.  Systematic mutation analysis of the catechol O-methyltransferase gene as a candidate gene for schizophrenia.  Am J Psychiatry 1999;156:1273-5.


89. Hwu WL, Wang PJ, Hsiao KJ, Wang TR, Chiou YW, Lee YM.  Dopa-responsive dystonia induced by a recessive GTP cyclohydrolase I mutation.  Hum Genet 1999;105:226-30.


90. Chang CC, Hsiao KJ, Lee YM, Lin CM.  Towards metabolic sink therapy for mut methylmalonic acidaemia: Correction of methylmalonyl-CoA mutase deficiency in T lymphocytes from a mut methylmalonic acidaemia child by retroviral-mediated gene transfer.  J Inher Metab Dis 1999;22:773-87.


91. Chang CC, Hsiao KJ, Chen ML, Lin CM.  Towards metabolic sink therapy for mut methylmalonic acidaemia: Retrovirus-mediated transfer of the human methylmalonyl-CoA mutase cDNA into peripheral blood progenitor cells of a child with mut methylmalonic acidaemia.  J Inher Metab Dis 1999;22:951-2.


92. Liu XQ, Hsiao KJ, Gu XF, Liu TT, Zhang YF, Ye J, Zhang M, Chen RG.  A novel missense mutation in 6-pyruvoyl-tetrahydropterin synthase gene.  Chin J Med Genet. 1999;16:342. (in Chinese)


93.
 Chiang SH, Wu SJ, Wu KF, Hsiao KJ.  Neonatal screening for glucose-6-phosphate dehydrogenase deficiency in Taiwan.  Southeast Asian J Trop Med Public Health 1999;30: Suppl 2:72-4.


94. Hsiao KJ, Chang YH, Liu TT, Chiang SH, Yang YL.  Human gene mutations, Gene Symbol: PTS, Disease:  Hyperphenylalaninemia. Accession Number: H971533, H971534.  Hum Genet 2000;106:151.


95.
 Yang Y, Qi Y, Chao HT, Lee HH, Hsiao KJ, et al.  Prenatal diagnosis of congenital adrenal hyperplasia with 21-hydroxylase deficiency.  Chin J Pediatr 2000;38:766-8. (in Chinese)


96. Chao HK, Hsiao KJ, Su TS.  A silent mutation induces exon skipping in the phenylalanine hydroxylase gene in phenylketonuria.  Hum Genet  2001;108:14-9.


97. Hsiao KJ, Chiu YH, Chang YH, Chiang SH, Liu TT.  Human gene mutations, Gene Symbol: PTS, Disease: Hyperphenylalaninemia, Accession Number: H971855.  Hum Genet 2001;108:176.


98.
 Hsu HC, Lee YM, Yang CF, Hsiao KJ, Liu TT, Ho CK, Ho CH, Wang SY, Liu WT.  Detection of Kaposi's sarcoma-associated herpesvirus in bone marrow biopsy samples from Taiwanese patients with multiple myeloma.  Cancer 2001;91:1409-13.


99. Okano Y, Asada M, Fujimoto A, Ohtake A, Murayama K, Hsiao KJ, Chich K, Yang Y, Cao Q, Reichardt JKV, Niihra S, Imamura T, Yamano T.  A genetic factor for agerelated cataract: identification and characterization of a novel galactokinase variant "Osaka" in Asians.  Am J Hum Genet 2001;68:1036-42.


100. Liu TT, Chang YH, Chiang SH, Yang YL, Yu WM, Hsiao KJ.  Identification of three novel 6-pyruvoyl-tetrahydropterin synthase gene mutation (226C>T, IVS3+1G>A, 116-119delTGTT) in Chinese hyperphenylalaninemia cause by tetrahydrobiopterin synthesis deficiency.  Mutation in Brief no. 425 (2001) Online.  Hum Mutat 2001;18:83.


101. Liu TT, Chiang SH, Wu SJ, Hsiao KJ.  Tetrahydrobiopterin deficient hyperphenylalaninemia in the Chinese.  Clin Chim Acta 2001;313:157-69.


102. Chen CH, Chen WY, Liu HL, Liu TT, Tsou AP, Lin CY, Chao T, Qi, Y, Hsiao KJ.  Identification of mutations in vasopressin 2 receptor gene causing nephrogenic diabetes insipidus in Chinese patients.  J Hum Genet 2002; 47:66-73.


103. Chen KJ, Chao HK, Hsiao KJ, Su TS.  Identification and characterization of a novel liver-specific enhancer of the human phenylalanine hydroxylase gene.   Hum Genet 2002;110:235-43.


104.
 Tsai MT, Hung CC, Tsai CY, Liu MY, Su YC, Chen YH, Hsiao KJ, Chen CH.  Mutation analysis of synapsin III gene in schizophrenia.  Am J Med Genet 2002;114:79-83.


105.
 Chen YM, Rey WY, Lan YC, Lai SF, Huang YC, Wu SI, Liu TT, Hsiao KJ.  Antibody reactivity to HIV-1 Vpu in HIV-1/AIDS patients on highly active antiretroviral therapy.  J Biomed Sci 2003;10:266-275.


106.
 Kobayashi K, Lu YB, Li MX, Nishi I, Hsiao KJ, Choeh K, Yang YL, Hwu WL, Reichardt JKV, Palmilerl F, Okano Y, Saheki T.  Screening of nine SLC25A13 mutations: their frequency in patients with citrin deficiency and high carrier rates in Asia populations.  Mol Genet Metab 2003;80:356-9.


107.
 Liu XQ, Zhang YF, Liu TT, Gu XF, Hsiao KJ, Bao KR, Yu LH.  Genotype and phenotype correlation in Chinese patients with Wilson's Disease.  Chin J Pediatr 2003;41:35-8. (in Chinese)


108.
 Liu XQ, Zhang YF, Liu TT, Hsiao KJ, Zhang JM, Gu XF, Bao KR, Yu LH, Wang MX.  Correlation of ATP7B genotype with phenotype in Chinese patients with Wilson disease.  World J Gastroenterol 2004;10:590-3.


109.
 Saheki T, Kobayashi K, Iijima M, Horiuchi M, Begum L, Jalil MA, Li MX, Lu YB, Ushikai M, Tabata A, Moriyama M, Hsiao KJ, Yang Y.  Adult-onset type II citrullinemia and idiopathic neonatal hepatitis caused by citrin deficiency: involvement of the aspartate glutamate carrier for urea synthesis and maintenance of the urea cycle.  Mol Genet Metab 2004;81:S20-6.


110.
 The International Chimpanzee Chromosome 22 Consortium.  DNA sequence and comparative analysis of chimpanzee chromosome 22.  Nature 2004;429:382-8.


111.
 Bartholomay LC, Cho WL, Rocheleau TA, Boyle JP, Beck ET,  Fuchs JF, Liss P, Rusch M, Butler KM, Wu RCC, Lin SP, Kuo HY, Tsao IY, Huang CY, Liu TT, Hsiao KJ, Tsai SF, Yang UC, Nappi AJ, Perna NT, Chen CC, Christensen BM.  Toward a description of the transcriptomes of immune-activated hemocytes from the mosquito vectors, Aedes aegypti and Armigeres subalbatus.  Infect Immun 2004;72:4114-26.


112.
 Wu KH, Tzung TY, Ro LS, Hsiao KJ.  A novel mutation (c.1072_1074delGAG) in the alpha-galactosidase A gene detected in a Taiwanese family with Fabry disease.  Acta Derm Venereol 2004; (in press)


113.
 Chen WM, Liu YF, Lin MW, Chen IC, Lin PY, Lin GL, Jou YS, Lin YT, Fan CSJ, Wu JY, Hsiao KJ, Tsai SF.  Report of pedigrees of autosomal dominant avascular necrosis of femoral head and linkage to chromosome 12q13.  Am J Hum Genet 2004;75:310-7.

 
 
 Scientific Publications  1977 - 1996  1997 - 2004
 Conference Abstracts     1975 - 1996  1997 - 2004
 Other Publications

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Updated on Aug. 18, 2004 by K.-J.Hsiao    ¿½ ¼s ¤¯ ±Ð ±Â