| 臺大學術典藏 |
2022-05-05T05:16:23Z |
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
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Liu Y.-L.; Fann C.S.-J.; Liu C.-M.; WEI J. CHEN; Wu J.-Y.; Hung S.-I.; Chen C.-H.; Jou Y.-S.; Liu S.-K.; Hwang T.-J.; Hsieh M.H.; 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 |
2022-05-05T05:16:19Z |
No association evidence between schizophrenia and dystrobrevin-binding protein 1 (DTNBP1) in Taiwanese families
|
Liu C.-M.; Liu Y.-L.; Fann C.S.-J.; Yang W.-C.; Wu J.-Y.; Hung S.-I.; WEI J. CHEN; Chueh C.-M.; Liu W.-M.; Liu C.-C.; Hsieh M.-H.; Hwang T.-J.; Faraone S.V.; Tsuang M.T.; Hwu H.-G. |
| 臺大學術典藏 |
2022-05-05T05:16:18Z |
Association evidence of schizophrenia with distal genomic region of NOTCH4 in Taiwanese families
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Liu C.-M.; Liu Y.-L.; Fann C.S.-J.; WEI J. CHEN; Yang W.-C.; Ouyang W.-C.; Chen C.-Y.; Jou Y.-S.; Hsieh M.-H.; Liu S.-K.; Hwang T.-J.; Faraone S.V.; Tsuang M.T.; Hwu H.-G. |
| 臺大學術典藏 |
2022-05-05T05:16:17Z |
HTF9C gene of 22q11.21 region associates with schizophrenia having deficit-sustained attention
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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.; Hsieh M.H.; Hwang T.-J.; Faraone S.V.; Tsuang M.T.; WEI J. CHEN; Hwu H.-G.; Chung-Shan |
| 臺大學術典藏 |
2022-05-05T05:16:17Z |
More evidence supports the association of PPP3CC with schizophrenia
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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.; Hsieh M.H.; Liu C.C.; Tsuang M.M.; Wu J.Y.; Jou Y.S.; Faraone S.V.; Tsuang M.T.; WEI J. CHEN; Hwu H.-G. |
| 臺大學術典藏 |
2022-05-05T05:16:15Z |
RASD2, MYH9, and CACNG2 Genes at Chromosome 22q12 Associated with the Subgroup of Schizophrenia with Non-Deficit in Sustained Attention and Executive Function
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Liu Y.-L.; Fann C.S.-J.; Liu C.-M.; WEI J. CHEN; 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. |
| 臺大學術典藏 |
2022-05-05T05:16:10Z |
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.; Hsieh M.H.; Hwang T.-J.; Chan H.-Y.; Chen J.-J.; WEI J. CHEN; Hwu H.-G. |
| 臺大學術典藏 |
2022-05-05T05:16:04Z |
ANXA7, PPP3CB, DNAJC9, and ZMYND17 genes at chromosome 10q22 associated with the subgroup of schizophrenia with deficits in attention and executive function
|
Liu C.-M.; Fann C.S.-J.; Chen C.-Y.; Liu Y.-L.; Oyang Y.-J.; Yang W.-C.; Chang C.-C.; Wen C.-C.; WEI J. CHEN; Hwang T.-J.; Hsieh M.H.; Liu C.-C.; Faraone S.V.; Tsuang M.T.; Hwu H.-G. |
| 臺大學術典藏 |
2022-05-05T05:15:47Z |
Haplotypes of the D-amino acid oxidase gene are significantly associated with schizophrenia and its neurocognitive deficits
|
Liu Y.-L.; Wang S.-C.; Hwu H.-G.; Fann C.S.-J.; Yang U.-C.; Yang W.-C.; Hsu P.-C.; Chang C.-C.; Wen C.-C.; Tsai-Wu J.-J.; Hwang T.-J.; Hsieh M.H.; Liu C.-C.; Chien Y.-L.; Fang C.-P.; Faraone S.V.; Tsuang M.T.; WEI J. CHEN; Liu C.-M. |
| 臺大學術典藏 |
2022-05-05T05:15:36Z |
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.; WEI J. CHEN; Hwang T.-J.; Hsieh M.H.; Liu C.-C.; Chien Y.-L.; Lin Y.-T.; Tsuang M.T. |
| 臺大學術典藏 |
2021-10-22T07:39:45Z |
Haplotypes of the D-amino acid oxidase gene are significantly associated with schizophrenia and its neurocognitive deficits
|
Liu Y.-L.; Wang S.-C.; HAI-GWO HWU; Fann C.S.-J.; Yang U.-C.; Yang W.-C.; Hsu P.-C.; Chang C.-C.; Wen C.-C.; Tsai-Wu J.-J.; Hwang T.-J.; Hsieh M.H.; Liu C.-C.; Chien Y.-L.; Fang C.-P.; Faraone S.V.; Tsuang M.T.; Chen W.J.; Liu C.-M. |
| 臺大學術典藏 |
2021-10-22T07:39:44Z |
A splicing-regulatory polymorphism in DRD2 disrupts ZRANB2 binding, impairs cognitive functioning and increases risk for schizophrenia in six Han Chinese samples
|
Cohen O.S.; Weickert T.W.; Hess J.L.; Paish L.M.; McCoy S.Y.; Rothmond D.A.; Galletly C.; Liu D.; Weinberg D.D.; Huang X.-F.; Xu Q.; Shen Y.; Zhang D.; Yue W.; Yan J.; Wang L.; Lu T.; He L.; Shi Y.; Xu M.; Che R.; Tang W.; Chen C.-H.; Chang W.-H.; HAI-GWO HWU; Liu C.-M.; Liu Y.-L.; Wen C.-C.; Fann C.S.-J.; Chang C.-C.; Kanazawa T.; Middleton F.A.; Duncan T.M.; Faraone S.V.; Weickert C.S.; Tsuang M.T.; Glatt S.J. |
| 臺大學術典藏 |
2021-10-22T07:39:41Z |
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.; HAI-GWO HWU; 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.; Chien Y.-L.; Lin Y.-T.; Tsuang M.T. |
| 臺大學術典藏 |
2021-09-23T08:02:18Z |
DRD2 haplotype associated with negative symptoms and sustained attention deficits in Han Chinese with schizophrenia in Taiwan
|
Chien Y.-L.; Hwu H.-G.; Fann C.S.-J.; Chang C.-C.; Tsuang M.-T.; CHIH-MIN LIU |
| 臺大學術典藏 |
2021-09-23T08:02:11Z |
Haplotypes of the D-amino acid oxidase gene are significantly associated with schizophrenia and its neurocognitive deficits
|
Liu Y.-L.; Wang S.-C.; Hwu H.-G.; Fann C.S.-J.; Yang U.-C.; Yang W.-C.; Hsu P.-C.; Chang C.-C.; Wen C.-C.; Tsai-Wu J.-J.; Hwang T.-J.; Hsieh M.H.; Liu C.-C.; Chien Y.-L.; Fang C.-P.; Faraone S.V.; Tsuang M.T.; Chen W.J.; CHIH-MIN LIU |
| 臺大學術典藏 |
2021-09-23T08:02:10Z |
A splicing-regulatory polymorphism in DRD2 disrupts ZRANB2 binding, impairs cognitive functioning and increases risk for schizophrenia in six Han Chinese samples
|
Cohen O.S.; Weickert T.W.; Hess J.L.; Paish L.M.; McCoy S.Y.; Rothmond D.A.; Galletly C.; Liu D.; Weinberg D.D.; Huang X.-F.; Xu Q.; Shen Y.; Zhang D.; Yue W.; Yan J.; Wang L.; Lu T.; He L.; Shi Y.; Xu M.; Che R.; Tang W.; Chen C.-H.; Chang W.-H.; Hwu H.-G.; CHIH-MIN LIU; Liu Y.-L.; Wen C.-C.; Fann C.S.-J.; Chang C.-C.; Kanazawa T.; Middleton F.A.; Duncan T.M.; Faraone S.V.; Weickert C.S.; Tsuang M.T.; Glatt S.J. |
| 臺大學術典藏 |
2021-09-23T08:02:07Z |
Genetic associations and expression of extra-short isoforms of disrupted-in-schizophrenia 1 in a neurocognitive subgroup of schizophrenia
|
CHIH-MIN LIU; 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.; Chien Y.-L.; Lin Y.-T.; Tsuang M.T. |
| 臺大學術典藏 |
2021-08-31T06:42:25Z |
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.; ANN-LII CHENG; Fann C.S.J.; Lin J.-T.; Wu M.-S. |
| 臺大學術典藏 |
2021-08-13T03:35:17Z |
ANXA7, PPP3CB, DNAJC9, and ZMYND17 genes at chromosome 10q22 associated with the subgroup of schizophrenia with deficits in attention and executive function
|
Liu C.-M.; Fann C.S.-J.; Chen C.-Y.; Liu Y.-L.; Oyang Y.-J.; Yang W.-C.; Chang C.-C.; Wen C.-C.; Chen W.J.; Hwang T.-J.; Hsieh M.H.; CHEN-CHUNG LIU; Faraone S.V.; Tsuang M.T.; Hwu H.-G. |
| 臺大學術典藏 |
2021-08-13T03:35:09Z |
Haplotypes of the D-amino acid oxidase gene are significantly associated with schizophrenia and its neurocognitive deficits
|
Liu Y.-L.; Wang S.-C.; Hwu H.-G.; Fann C.S.-J.; Yang U.-C.; Yang W.-C.; Hsu P.-C.; Chang C.-C.; Wen C.-C.; Tsai-Wu J.-J.; Hwang T.-J.; Hsieh M.H.; CHEN-CHUNG LIU; Chien Y.-L.; Fang C.-P.; Faraone S.V.; Tsuang M.T.; Chen W.J.; Liu C.-M. |
| 臺大學術典藏 |
2021-08-13T03:35:05Z |
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.; CHEN-CHUNG LIU; Chien Y.-L.; Lin Y.-T.; Tsuang M.T. |
| 臺大學術典藏 |
2021-07-06T08:49:47Z |
Thyrotropin receptor antibodies and a genetic hint in antithyroid drug-induced adverse drug reactions
|
LIN-CHAU CHANG; Chang C.-C.; Chen P.-L.; Wang S.-H.; Chen Y.-H.; Tsai Y.-H.; Shih S.-R.; Chiu W.-Y.; Fann C.S.-J.; Yang W.-S.; Chang T.-C. |
| 臺大學術典藏 |
2021-07-06T02:04:18Z |
Linkage of Graves' disease to the human leucocyte antigen region in the Chinese-Han population in Taiwan
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PEI-LUNG CHEN; Fann C.S.-J.; Chang C.-C.; Wu I.-L.; Chiu W.-Y.; Lin C.-Y.; Yang W.-S.; Chang T.-C. |
| 臺大學術典藏 |
2021-07-06T02:04:18Z |
Family-based association study of cytotoxic T-lymphocyte antigen-4 with susceptibility to Graves' disease in Han population of Taiwan
|
PEI-LUNG CHEN; Fann C.S.-J.; Chang C.-C.; Wu I.-L.; Chiu W.-Y.; Lin C.-Y.; Yang W.-S.; Chang T.-C. |
| 臺大學術典藏 |
2021-07-06T02:04:16Z |
Comprehensive genotyping in two homogeneous Graves' disease samples reveals major and novel HLA association alleles
|
PEI-LUNG CHEN; Fann C.-S.-J.; Chu C.-C.; Chang C.-C.; Chang S.-W.; Hsieh H.-Y.; Lin M.; Yang W.-S.; Chang T.-C. |
