| 臺大學術典藏 |
2020-03-17T06:23:01Z |
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 Y.-L.;Fann C.S.-J.;Liu C.-M.;Chen W.J.;Wu J.-Y.;Hung S.-I.;Chen C.-H.;Jou Y.-S.;Liu S.-K.;Hwang T.-J.;Ming-Hsien Hsieh;Ouyang W.-C.;Chan H.-Y.;Chen J.-J.;Yang W.-C.;Lin C.-Y.;Lee S.F.C.;Hwu H.-G.; Liu Y.-L.; Fann C.S.-J.; Liu C.-M.; Chen W.J.; Wu J.-Y.; Hung S.-I.; Chen C.-H.; Jou Y.-S.; Liu S.-K.; Hwang T.-J.; MING-HSIEN HSIEH; Ouyang W.-C.; Chan H.-Y.; Chen J.-J.; Yang W.-C.; Lin C.-Y.; Lee S.F.C.; Hwu H.-G. |
| 臺大學術典藏 |
2020-03-17T06:23:01Z |
Evaluation of RGS4 as a candidate gene for schizophrenia
|
Liu Y.-L.;Fann C.S.-J.;Liu C.-M.;Wu J.-Y.;Hung S.-I.;Chan H.-Y.;Chen J.-J.;Lin C.-Y.;Liu S.-K.;Ming-Hsien Hsieh;Hwang T.-J.;Ouyang W.-C.;Chen C.-Y.;Lin J.-J.;Chou F.H.-C.;Chueh C.-M.;Liu W.-M.;Tsuang M.-M.;Faraone S.V.;Tsuang M.T.;Chen W.J.;Hwu H.-G.; Liu Y.-L.; Fann C.S.-J.; Liu C.-M.; Wu J.-Y.; Hung S.-I.; Chan H.-Y.; Chen J.-J.; Lin C.-Y.; Liu S.-K.; MING-HSIEN HSIEH; Hwang T.-J.; OuYang W.-C.; Chen C.-Y.; Lin J.-J.; Chou F.H.-C.; Chueh C.-M.; Liu W.-M.; Tsuang M.-M.; Faraone S.V.; Tsuang M.T.; Chen W.J.; Hwu H.-G. |
| 臺大學術典藏 |
2020-03-17T06:23:00Z |
No association of G72 and d-amino acid oxidase genes with schizophrenia
|
Liu Y.-L.;Fann C.S.-J.;Liu C.-M.;Chang C.C.;Wu J.-Y.;Hung S.-I.;Liu S.-K.;Ming-Hsien Hsieh;Hwang T.-J.;Chan H.-Y.;Chen J.-J.;Faraone S.V.;Tsuang M.T.;Chen W.J.;Hwu H.-G.; Liu Y.-L.; Fann C.S.-J.; Liu C.-M.; Chang C.C.; Wu J.-Y.; Hung S.-I.; Liu S.-K.; MING-HSIEN HSIEH; Hwang T.-J.; Chan H.-Y.; Chen J.-J.; Faraone S.V.; Tsuang M.T.; Chen W.J.; Hwu H.-G. |
| 臺大學術典藏 |
2020-03-17T06:22:58Z |
No association evidence between schizophrenia and dystrobrevin-binding protein 1 (DTNBP1) in Taiwanese families
|
Hwu H.-G.; Tsuang M.T.; Faraone S.V.; Hwang T.-J.; MING-HSIEN HSIEH; Liu C.-C.; Chueh C.-M.; Liu W.-M.; Chen W.J.; Hung S.-I.; Wu J.-Y.; Yang W.-C.; Liu C.-M.;Liu Y.-L.;Fann C.S.-J.;Yang W.-C.;Wu J.-Y.;Hung S.-I.;Chen W.J.;Chueh C.-M.;Liu W.-M.;Liu C.-C.;Ming-Hsien Hsieh;Hwang T.-J.;Faraone S.V.;Tsuang M.T.;Hwu H.-G.; Liu C.-M.; Liu Y.-L.; Fann C.S.-J. |
| 臺大學術典藏 |
2020-03-17T06:22:57Z |
More evidence supports the association of PPP3CC with schizophrenia
|
Liu Y.L.;Fann C.S.J.;Liu C.M.;Chang C.C.;Yang W.C.;Hung S.I.;Yu S.L.;Hwang T.J.;Ming-Hsien Hsieh;Liu C.C.;Tsuang M.M.;Wu J.Y.;Jou Y.S.;Faraone S.V.;Tsuang M.T.;Chen W.J.;Hwu H.-G.; Liu Y.L.; Fann C.S.J.; Liu C.M.; Chang C.C.; Yang W.C.; Hung S.I.; Yu S.L.; Hwang T.J.; MING-HSIEN HSIEH; Liu C.C.; Tsuang M.M.; Wu J.Y.; Jou Y.S.; Faraone S.V.; Tsuang M.T.; Chen W.J.; Hwu H.-G. |
| 臺大學術典藏 |
2020-03-17T06:22:56Z |
HTF9C gene of 22q11.21 region associates with schizophrenia having deficit-sustained attention
|
Chung-Shan; Hwu H.-G.; Chen W.J.; Tsuang M.T.; Faraone S.V.; Liu Y.-L.;Fann C.S.-J.;Liu C.-M.;Ching Chang C.;Yang W.-C.;Wu J.-Y.;Hung S.-I.;Chan H.-Y.;Chen J.-J.;Ming-Hsien Hsieh;Hwang T.-J.;Faraone S.V.;Tsuang M.T.;Chen W.J.;Hwu H.-G.;Chung-Shan; Liu Y.-L.; Fann C.S.-J.; Liu C.-M.; Ching Chang C.; Yang W.-C.; Wu J.-Y.; Hung S.-I.; Chan H.-Y.; Chen J.-J.; MING-HSIEN HSIEH; Hwang T.-J. |
| 臺大學術典藏 |
2020-03-17T06:22:55Z |
RASD2, MYH9, and CACNG2 Genes at Chromosome 22q12 Associated with the Subgroup of Schizophrenia with Non-Deficit in Sustained Attention and Executive Function
|
Liu Y.-L.; Fann C.S.-J.; Liu C.-M.; Chen W.J.; Wu J.-Y.; Hung S.-I.; Chen C.-H.; Jou Y.-S.; Liu S.-K.; Hwang T.-J.; MING-HSIEN HSIEH; Chang C.C.; Yang W.-C.; Lin J.-J.; Chou F.H.-C.; Faraone S.V.; Tsuang M.T.; Hwu H.-G. |
| 臺大學術典藏 |
2020-03-17T06:22:53Z |
Genetic variants of IL-6 and its receptor are not associated with schizophrenia in Taiwan
|
Liu Y.-L.;Liu C.-M.;Fann C.S.-J.;Yang W.C.;Chen Y.-H.;Tseng L.-J.;Liu S.-K.;Ming-Hsien Hsieh;Hwang T.-J.;Chan H.-Y.;Chen J.-J.;Chen W.J.;Hwu H.-G.; Hwu H.-G.; Liu Y.-L.; Liu C.-M.; Fann C.S.-J.; Yang W.C.; Chen Y.-H.; Tseng L.-J.; Liu S.-K.; MING-HSIEN HSIEH; Hwang T.-J.; Chan H.-Y.; Chen J.-J.; Chen W.J. |
| 臺大學術典藏 |
2020-03-17T06:22:39Z |
Haplotypes of the D-amino acid oxidase gene are significantly associated with schizophrenia and its neurocognitive deficits
|
Liu C.-M.; Chen W.J.; Tsuang M.T.; Faraone S.V.; Fang C.-P.; Liu C.-C.; Chien Y.-L.; MING-HSIEN HSIEH; Hwang T.-J.; Tsai-Wu J.-J.; Wen C.-C.; Chang C.-C.; Liu Y.-L.; Wang S.-C.; Hwu H.-G.; Fann C.S.-J.; Yang U.-C.; Yang W.-C.; Hsu P.-C. |
| 臺大學術典藏 |
2020-03-03T03:36:43Z |
Genetic polymorphisms and tissue expression of interleukin-22 associated with risk and therapeutic response of gastric mucosa-associated lymphoid tissue lymphoma
|
Liao F.; Hsu Y.-C.; Kuo S.-H.; Yang Y.-C.; Chen J.-P.; Hsu P.-N.; CHUNG-WU LIN; Chen L.-T.; Cheng A.-L.; Fann C.S.J.; Lin J.-T.; Wu M.-S. |
| 臺大學術典藏 |
2019-12-04T08:44:18Z |
Erratum: HLA-B*5801 allele as a genetic marker for severe cutaneous adverse reactions caused by allopurinol (Proceedings of the National Academy of Sciences of the United States of America (March 15, 2005) 102, 11 (4134-4139))
|
Hung S.-I.;Chung W.-H.;Liou L.-B.;Chu C.-C.;Lin M.;Huang H.-P.;Lin Y.-L.;Lan J.-L.;Yang L.-C.;Hong H.-S.;Chen M.-J.;Lai P.-C.;Wu M.-S.;Chia-Yu Chu;Wang K.-H.;Chen C.-H.;Fann C.S.J.;Wu J.-Y.;Chen Y.-T.; Hung S.-I.; Chung W.-H.; Liou L.-B.; Chu C.-C.; Lin M.; Huang H.-P.; Lin Y.-L.; Lan J.-L.; Yang L.-C.; Hong H.-S.; Chen M.-J.; Lai P.-C.; Wu M.-S.; CHIA-YU CHU; Wang K.-H.; Chen C.-H.; Fann C.S.J.; Wu J.-Y.; Chen Y.-T. |
| 臺大學術典藏 |
2019-12-04T08:44:18Z |
HLA-B*5801 allele as a genetic marker for severe cutaneous adverse reactions caused by allopurinol
|
Lai P.-C.; Wu M.-S.; CHIA-YU CHU; Wang K.-H.; Chen C.-H.; Fann C.S.J.; Wu J.-Y.; Chen Y.-T.; Hung S.-L.;Chung W.-H.;Liou L.-B.;Chu C.-C.;Lin M.;Huang H.-P.;Lin Y.-L.;Lan J.-L.;Yang L.-C.;Hong H.-S.;Chen M.-J.;Lai P.-C.;Wu M.-S.;Chia-Yu Chu;Wang K.-H.;Chen C.-H.;Fann C.S.J.;Wu J.-Y.;Chen Y.-T.; Hung S.-L.; Chung W.-H.; Liou L.-B.; Chu C.-C.; Lin M.; Huang H.-P.; Lin Y.-L.; Lan J.-L.; Yang L.-C.; Hong H.-S.; Chen M.-J. |
| 臺大學術典藏 |
2019-07-09T06:52:03Z |
Genetic associations and expression of extra-short isoforms of disrupted-in-schizophrenia 1 in a neurocognitive subgroup of schizophrenia
|
Tsuang M.T.; Chien Y.-L.; Lin Y.-T.; Liu C.-C.; Hsieh M.H.; Hwang T.-J.; WWI J. CHEN; Chang C.-C.; Hsu P.-C.; Liu C.-M.;Liu Y.-L.;Hwu H.-G.;Fann C.S.-J.;Yang U.-C.;Hsu P.-C.;Chang C.-C.;Wwi J. Chen;Hwang T.-J.;Hsieh M.H.;Liu C.-C.;Chien Y.-L.;Lin Y.-T.;Tsuang M.T.; Liu C.-M.; Liu Y.-L.; Hwu H.-G.; Fann C.S.-J.; Yang U.-C. |
| 臺大學術典藏 |
2019 |
Genetic associations and expression of extra-short isoforms of disrupted-in-schizophrenia 1 in a neurocognitive subgroup of schizophrenia
|
Tsuang M.T.; Lin Y.-T.; Chien Y.-L.; Liu C.-C.; MING-HSIEN HSIEH; Hwang T.-J.; Chen W.J.; Chang C.-C.; Yang U.-C.; Hsu P.-C.; Fann C.S.-J.; Hwu H.-G.; Liu Y.-L.; Liu C.-M.; Liu C.-M.;Liu Y.-L.;Hwu H.-G.;Fann C.S.-J.;Yang U.-C.;Hsu P.-C.;Chang C.-C.;Chen W.J.;Hwang T.-J.;Ming-Hsien Hsieh;Liu C.-C.;Chien Y.-L.;Lin Y.-T.;Tsuang M.T. |
| 臺大學術典藏 |
2019 |
Genetic associations and expression of extra-short isoforms of disrupted-in-schizophrenia 1 in a neurocognitive subgroup of schizophrenia
|
Liu C.-M.;Liu Y.-L.;Hwu H.-G.;Fann C.S.-J.;Yang U.-C.;Hsu P.-C.;Chang C.-C.;Chen W.J.;Hwang T.-J.;Hsieh M.H.;Liu C.-C.;Yi-Ling Chien;Lin Y.-T.;Tsuang M.T.; Liu C.-M.; Liu Y.-L.; Hwu H.-G.; Fann C.S.-J.; Yang U.-C.; Hsu P.-C.; Chang C.-C.; Chen W.J.; Hwang T.-J.; Hsieh M.H.; Liu C.-C.; YI-LING CHIEN; Lin Y.-T.; Tsuang M.T. |
| 臺大學術典藏 |
2018-09-10T08:28:22Z |
Comprehensive genotyping in two homogeneous Graves' disease samples reveals major and novel HLA association alleles
|
Chen, P.-L.; Fann, C.-S.-J.; Chu, C.-C.; Chang, C.-C.; Chang, S.-W.; Hsieh, H.-Y.; Lin, M.; Yang, W.-S.; Chang, T.-C.; TIEN-CHUN CHANG; WEI-SHIUNG YANG; PEI-LUNG CHEN; CHEN, PEI-LUNG; FANN, CATHY SHENG-JIUAN; CHU, CHEN- CHUNG; CHANG, CHIEN-CHING; CHANG, SU-WEI; HSIEH, HSIN-YI; LIN, CHU-MARIE; YANG, WEI-SHIUNG; CHANG, TIEN-CHUN |
| 臺大學術典藏 |
2018-09-10T05:16:45Z |
Linkage evidence of schizophrenia to loci near neuregulin 1 gene on chromosome 8p21 in Taiwanese families
|
Liu, C.-M.;Hwu, H.-G.;Fann, C.S.J.;Lin, C.-Y.;Liu, Y.-L.;Ou-Yang, W.-C.;Lee, S.F.-C.Liu, Chih-Min; Hwu, Hai-Gwo; Fann, Cathy S.J.; Lin, Chin-Yu; Liu, Yu-Li; Ou-Yang, Wen-Chen; Lee, Sandy F-C; Liu, Chih-Min; HAI-GWO HWU; Hwu, Hai-Gwo; CHIH-MIN LIU; Fann, Cathy S.J.; Lin, Chin-Yu; Liu, Yu-Li; Ou-Yang, Wen-Chen; Lee, Sandy F-C |
| 臺大學術典藏 |
2018-09-10T04:28:24Z |
Linkage of schizophrenia with chromosome 1q loci in Taiwanese families
|
Hwu, H.-G.;Liu, C.-M.;Fann, C.S.-J.;Ou-Yang, W.-C.;Lee, S.F.-C.; HAI-GWO HWU; CHIH-MIN LIU |
| 臺大學術典藏 |
2018-09-10T03:44:18Z |
Linkage analysis of schizophrenia to chromosome 1q21-22 in Taiwanese families
|
Liu, C.-M.;Hwu, H.-G.;Ou-Yang, W.-C.;Lee, S.F.-C.;Fann, C.S.J.;Chu, C.-H.; CHIH-MIN LIU |
| 臺大學術典藏 |
2018-09-10T03:44:17Z |
Suggestive evidence for linkage of schizophrenia to markers at chromosome 15q13-14 in Taiwanese families
|
HAI-GWO HWU; CHIH-MIN LIU; Liu, C.-M.;Hwu, H.-G.;Lin, M.-W.;Ou-Yang, W.-C.;Lee, S.F.-C.;Fann, C.S.J.;Wong, S.-H.;Hsieh, S.-H. |
| 國立臺灣大學 |
2014 |
Genetic polymorphisms and tissue expression of interleukin-22 associated with risk and therapeutic response of gastric mucosa-associated lymphoid tissue lymphoma
|
Liao, F.; Hsu, Y-C; Kuo, S-H; Yang, Y-C; Chen, J-P; Hsu, P-N; Lin, C-W; Chen, L-T; Cheng, A-L; Fann, C. S. J.; Lin, J-T; Wu, M-S; 林肇堂; 林中梧; 郭頌鑫; 鄭安理; 吳明賢; 許秉寧 |
| 臺大學術典藏 |
2013 |
A genome-wide association analysis identifies novel susceptibility loci for coronary arterial lesions in patients with Kawasaki disease
|
Lin M.-T.;Chia-Lin Hsu;Chen P.-L.;Yang W.-S.;Wang J.-K.;Fann C.S.J.;Wu M.-H.; Lin M.-T.; CHIA-LIN HSU; Chen P.-L.; Yang W.-S.; Wang J.-K.; Fann C.S.J.; Wu M.-H. |
| 臺大學術典藏 |
2011 |
ANXA7, PPP3CB, DNAJC9, and ZMYND17 genes at chromosome 10q22 associated with the subgroup of schizophrenia with deficits in attention and executive function
|
Fann C.S.-J.; Liu C.-M.; Chen C.-Y.; Liu Y.-L.; Oyang Y.-J.; Yang W.-C.; Chang C.-C.; Wen C.-C.; Chen W.J.; Hwang T.-J.; MING-HSIEN HSIEH; Liu C.-C.; Faraone S.V.; Tsuang M.T.; Hwu H.-G. |
| 國立臺灣大學 |
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, Y.-L.; Fann, C.S.-J.; Liu, C.-M.; Chen, W.J.; Wu, J.-Y.; Hung, S.-I.; Chen, C.-H.; Jou, Y.-S.; Liu, S.-K.; Hwang, T.-J.; Hsieh, M.H.; Chang, C.C.; Yang, W.-C.; Lin, J.-J.; Chou, F.H.-C.; Faraone, S.V.; Tsuang, M.T.; Hwu, H.-G. |
| 國立臺灣大學 |
2007-08 |
Association evidence of schizophrenia with distal genomic region of NOTCH4 in Taiwanese families
|
Liu, C.-M.; Liu, Y.-L.; Fann, C.S.-J.; Chen, W.J.; Yang, W.-C.; Ouyang, W.-C.; Chen, C.-Y.; Jou, Y.-S.; Liu, S.-K.; Hsieh, M.-H.; Hwang, T.-J.; Faraone, S.V.; Tsuang, M.T.; Hwu, H.-G. |
