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機構 日期 題名 作者
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 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

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