|
Taiwan Academic Institutional Repository >
Browse by Author
|
"fann csj"
Showing items 6-30 of 31 (2 Page(s) Totally) 1 2 > >> View [10|25|50] records per page
中國醫藥大學 |
2011-05 |
Genome-wide Association study of bipolar I disorder in the Han Chinese population.
|
(Lee MTM); (Chen CH); (Lee CS); (Chen CC); (Chong MY); (Ouyang WC); (Chiu NY); (Chuo LJ); (Chen CY); (Tan HKL); 藍先元(Hsien-Yuan Lane); (Chang TJ); (Lin CH); (Jou SH); (Hou YM); (Feng J); (Lai TJ); (Tung CL); (Chen TJ); (Chang CJ); (Lung FW); (Chen CK); (Shiah IS); (Liu CY); (Teng PR); (Chen KH); (Shen LJ); (Cheng CS); (Chang TP); (Li CF); (Chou CH); (Chen CY); (Wang KHT); (Fann CSJ); (Wu JY); (Chen YT); (Cheng ATA)* |
國家衛生研究院 |
2010-04-15 |
Ectopic and high CXCL13 chemokine expression in myasthenia gravis with thymic lymphoid hyperplasia
|
Shiao, YM;Lee, CC;Hsu, YH;Huang, SF;Lin, CY;Li, LH;Fann, CSJ;Tsai, CY;Tsai, SF;Chiu, HC |
國家衛生研究院 |
2010-01-14 |
Genetic variants of IL-6 and its receptor are not associated with schizophrenia in Taiwan
|
Liu, YL;Liu, CM;Fann, CSJ;Yang, WC;Chen, YH;Tseng, LJ;Liu, SK;Hsieh, MH;Hwang, TJ;Chan, HY;Chen, JJ;Chen, WJ;Hwu, HG |
中國醫藥大學 |
2010 |
Genome-wide Association study of bipolar I disorder in the Han Chinese population.
|
(Lee MTM); (Chen CH); (Lee CS); (Chen CC); (Chong MY); (Ouyang WC); (Chiu NY); (Chuo LJ); (Chen CY); (Tan HKL); 藍先元(Hsien-Yuan Lane); (Chang TJ); (Lin CH); (Jou SH); (Hou YM); (Feng J); (Lai TJ); (Tung CL); (Chen TJ); (Chang CJ); (Lung FW); (Chen CK); (Shiah IS); (Liu CY); (Teng PR); (Chen KH); (Shen LJ); (Cheng CS); (Chang TP); (Li CF); (Chou CH); (Chen CY); (Wang KHT); (Fann CSJ); (Wu JY); (Chen YT); (Cheng ATA)* |
國立臺灣大學 |
2009-11 |
Clustering by neurocognition for fine-mapping of the schizophrenia susceptibility loci on chromosome 6p
|
Lin, S-H; Liu, CM; Liu, YL; Fann, CSJ; Hsiao, PC; Wu, JY; Hung, SI; Chen, CH; Wu, HM; Jou, YS; Liu, SK; Hwang, TJ; Hsieh, MH; Chang, CC; Yang, WC; Lin, JJ; Chou, FHC; Faraone, SV; Tsuang, MT; Hwu, HG; Chen, WJ |
國家衛生研究院 |
2009-04 |
Association of the 3'region of COMT with Schizophrenia in Taiwan
|
Chien, YL;Liu, CM;Fann, CSJ;Liu, YL;Hwu, HG |
國家衛生研究院 |
2008-11 |
RASD2, MYH9, and CACNG2 Genes at Chromosome 22q12 Associated with the Subgroup of Schizophrenia with Non-Deficit in Sustained Attention and Executive Function
|
Liu, YL;Fann, CSJ;Liu, CM;Chen, WJ;Wu, JY;Hung, SI;Chen, CH;Jou, YS;Liu, SK;Hwang, TJ;Hsieh, MH;Chang, CC;Yang, WC;Lin, JJ;Chou, FHC;Faraone, SV;Tsuang, MT;Hwu, HG |
國家衛生研究院 |
2007-12 |
HTF9C gene of 22q11.21 region associates with schizophrenia having deficit-sustained attention
|
Liu, YL; Fann, CSJ; Liu, CM; Chang, CC; Yang, WC; Wu, JY; Hung, SL; Chan, HY; Chen, JJ; Hsieh, MH; Hwang, TJ; Faraone, SV; Tsuang, MT; Chen, WJ; Hwu, HG |
國家衛生研究院 |
2007-10 |
More evidence supports the association of PPP3CC with schizophrenia
|
Liu, YL; Fann, CSJ; Liu, CM; Chang, CC; Yang, WC; Hung, SI; Yu, SL; Hwang, TJ; Hsieh, MH; Liu, CC; Tsuang, MM; Wu, JY; Jou, YS; Faraone, SV; Tsuang, MT; Chen, WJ; Hwu, HG |
國家衛生研究院 |
2007-07 |
No association evidence between schizophrenia and dystrobrevin-binding protein 1 (DTNBP1) in Taiwanese families
|
Liu, CM; Liu, YL; Fann, CSJ; Yang, WC; Wu, JY; Hung, SI; Chen, WJ; Chueh, CM; Liu, WM; Liu, CC; Hsieh, MH; Hwang, TJ; Faraone, SV; Tsuang, MT; Hwu, HG |
國家衛生研究院 |
2006-10 |
No association of G72 and D-amino acid oxidase genes with schizophrenia
|
Liu, YL; Fann, CSJ; Liu, CM; Chang, CC; Wu, JY; Hung, SI; Liu, SK; Hsieh, MH; Hwang, TJ; Chan, HY; Chen, JJ; Faraone, SV; Tsuang, MT; Chen, WJ; Hwu, HG |
國家衛生研究院 |
2006-10 |
Systematic mutation screening study for DISC1 and NRG1 in schizophrenia
|
Liu, CM;Hwu, HG;Liu, YL;Yang, UC;Hsu, PC;Fann, CSJ;Yang, WC |
國家衛生研究院 |
2006-10 |
Systematic SNP polymorphism screening for schizophrenia candidate gene of calcium channel, voltage-dependent, gamma subunit (CACNG2)
|
Hwu, HG;Liu, CM;Fann, CSJ;Tsai, HF;Yang, UC;Hsu, PC;Liu, YL |
國家衛生研究院 |
2006-09-15 |
A single nucleotide polymorphism fine mapping study of chromosome 1q42.1 reveals the vulnerability genes for schizophrenia, GNPAT and DISC1: Association with impairment of sustained attention
|
Liu, YL; Fann, CSJ; Liu, CM; Chen, WJ; Wu, JY; Hung, SL; Chen, CH; Jou, YS; Liu, SK; Hwang, TJ; Hsieh, MH; Ouyang, WC; Chan, HY; Chen, JJ; Yang, WC; Lin, CY; Lee, SFC; Hwu, HG |
國家衛生研究院 |
2005-06-02 |
Type II collagen gene variants and inherited osteonecrosis of the femoral head
|
Liu, YF; Chen, WM; Lin, YF; Yang, RC; Lin, MW; Li, LH; Chang, YH; Jou, YS; Lin, PY; Su, JS; Huang, SF; Hsiao, KJ; Fann, CSJ; Hwang, HW; Chen, YT; Tsai, SF |
中國醫藥大學 |
2005 |
Construction of endophenotypes for complex diseases in the presence of heterogeneity
|
Chen, CH; Kuo, CL; Lin, MCP; Liang, YJ; Fann, CSJ |
中國醫藥大學 |
2005 |
A functional polymorphism in the promoter region of the tryptophan hydroxylase gene is associated with alcohol dependence in one aboriginal group in Taiwan
|
Sun, HS; Fann, CSJ; Lane, HY; Chang, YT; Chang, CJ; Liu, YL; Cheng, ATA |
中國醫藥大學 |
2005 |
HLA-B*5801 allele as a genetic marker for severe cutaneous adverse reactions caused by allopurinol
|
Hung, SL; Chung, WH; Liou, LB; Chu, CC; Lin, M; Huang, HP; Lin, YL; Lan, JL; Yang, LC; Hong, HS; Chen, MJ; Lai, PC; Wu, MS; Chu, CY; Wang, KH; Chen, CH; Fann, CSJ; Wu, JY; Chen, YT |
中國醫藥大學 |
2005 |
HLA-B*5801 allele as a genetic marker for severe cutaneous adverse reactions caused by allopurinol
|
Hung, SL; Chung, WH; Liou, LB; Chu, CC; Lin, M; Huang, HP; Lin, YL; Lan, JL; Yang, LC; Hong, HS; Chen, MJ; Lai, PC; Wu, MS; Chu, CY; Wang, KH; Chen, CH; Fann, CSJ; Wu, JY; Chen, YT |
國家衛生研究院 |
2004-08 |
Autosomal dominant avascular necrosis of femoral head in two Taiwanese pedigrees and linkage to chromosome 12q13
|
Chen, WM; Liu, YF; Lin, MW; Chen, IC; Lin, PY; Lin, GL; Jou, YS; Lin, YT; Fann, CSJ; Wu, JY; Hsiao, KJ; Tsai, SF |
中國醫藥大學 |
2004 |
Autosomal dominant avascular necrosis of femoral head in two Taiwanese pedigrees and linkage to chromosome 12q13
|
Chen, WM; Liu, YF; Lin, MW; Chen, IC; Lin, PY; Lin, GL; Jou, YS; Lin, YT; Fann, CSJ; Wu, JY; Hsiao, KJ; Tsai, SF |
中國醫藥大學 |
2004 |
Autosomal dominant avascular necrosis of femoral head in two Taiwanese pedigrees and linkage to chromosome 12q13
|
Chen, WM; Liu, YF; Lin, MW; Chen, IC; Lin, PY; Lin, GL; Jou, YS; Lin, YT; Fann, CSJ; Wu, JY; Hsiao, KJ; Tsai, SF |
國家衛生研究院 |
2003-11 |
Young-onset hypertension in Chinese is linked to STRP marker of lipoprotein lipase (LPL) and associated with its haplotype
|
Pan, W;Chen, P;Jou, Y;Fann, CSJ;Chen, J;Chung, C;Chen, Y;Wu, S;Kang, M;Lin, C |
國家衛生研究院 |
2002-11 |
Clinical implications of chromosomal abnormalities in gastric adenocarcinomas
|
Wu, CW; Chen, GD; Fann, CSJ; Lee, AFY; Chi, CW; Liu, JM; Weier, U; Chen, JY |
國家衛生研究院 |
2002-01 |
Association between markers in chromosomal region 17q23 and young onset hypertension: a TDT study
|
Wu, SY; Fann, CSJ; Jou, YS; Chen, JW; Pan, WH |
Showing items 6-30 of 31 (2 Page(s) Totally) 1 2 > >> View [10|25|50] records per page
|