臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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機構	日期	題名	作者
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	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.
臺大學術典藏	2021-07-06T02:04:15Z	A genome-wide association analysis identifies novel susceptibility loci for coronary arterial lesions in patients with Kawasaki disease	Lin M.-T.; Hsu C.-L.; PEI-LUNG CHEN; Yang W.-S.; Wang J.-K.; Fann C.S.J.; Wu M.-H.
臺大學術典藏	2021-07-06T02:04:12Z	Predicting HLA genotypes using unphased and flanking single-nucleotide polymorphisms in Han Chinese population	Hsieh A.-R.; Chang S.-W.; PEI-LUNG CHEN; Chu C.-C.; Hsiao C.-L.; Yang W.-S.; Chang C.-C.; Wu J.-Y.; Chen Y.-T.; Chang T.-C.; Fann C.S.J.
臺大學術典藏	2021-07-06T02:04:08Z	Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study	PEI-LUNG CHEN; Shih S.-R.; Wang P.-W.; Lin Y.-C.; Chu C.-C.; Lin J.-H.; Chen S.-C.; Chang C.-C.; Huang T.-S.; Tsai K.S.; Tseng F.-Y.; Wang C.-Y.; Lu J.-Y.; Chiu W.-Y.; Chang C.-C.; Chen Y.-H.; Chen Y.-T.; Fann C.S.-J.; Yang W.-S.; Chang T.-C.
臺大學術典藏	2021-07-06T02:04:05Z	First step towards precision medicine for antithyroid drug-induced agranulocytosis	Pei-Lung Chen;Fann C.S.-J.;Shih S.-R.;Yang W.-S.;Chang T.-C.; PEI-LUNG CHEN; Fann C.S.-J.; Shih S.-R.; Yang W.-S.; Chang T.-C.
臺大學術典藏	2021-07-06T02:04:01Z	Comprehensive human leukocyte antigen genotyping of patients with type 1 diabetes mellitus in Taiwan	Tung Y.-C.; Fann C.S.-J.; Chang C.-C.; Chu C.-C.; Yang W.-S.; Hwu W.-L.; PEI-LUNG CHEN; Tsai W.-Y.
臺大學術典藏	2021-07-06T02:04:00Z	Thyrotropin receptor antibodies and a genetic hint in antithyroid drug-induced adverse drug reactions	Chang L.-C.; Chang C.-C.; PEI-LUNG CHEN; 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	2021-07-03T03:35:22Z	Lipoprotein lipase gene is linked and associated with hypertension in Taiwan young-onset hypertension genetic study	PEI-JER CHEN; Jou Y.-S.; Fann C.S.J.; Chen J.-W.; Wu S.-Y.; Pan W.-H.
臺大學術典藏	2021-07-03T03:34:58Z	Lipoprotein lipase variants associated with an endophenotype of hypertension: Hypertension combined with elevated triglycerides	PEI-JER CHEN; Jou Y.-S.; Fann C.S.J.; Chen J.-W.; Chung C.-M.; Lin C.-Y.; Wu S.-Y.; Kang M.-J.; Chen Y.-C.; Jong Y.-S.; Lo H.-M.; Kang C.-S.; Chen C.-C.; Chang H.-C.; Huang N.-K.; Wu Y.-L.; Pan W.-H.
臺大學術典藏	2021-07-03T03:34:44Z	A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese	Tsai F.-J.; Yang C.-F.; Chen C.-C.; Chuang L.-M.; Lu C.-H.; Chang C.-T.; Wang T.-Y.; Chen R.-H.; Shiu C.-F.; Liu Y.-M.; Chang C.-C.; PEI-JER CHEN; Chen C.-H.; Fann C.S.J.; Chen Y.-T.; Wu J.-Y.
臺大學術典藏	2021-07-02T02:35:56Z	Linkage of Graves' disease to the human leucocyte antigen region in the Chinese-Han population in Taiwan	Chen P.-L.; Fann C.S.-J.; Chang C.-C.; Wu I.-L.; Chiu W.-Y.; Lin C.-Y.; WEI-SHIUNG YANG; Chang T.-C.
臺大學術典藏	2021-07-02T02:35:53Z	Family-based association study of cytotoxic T-lymphocyte antigen-4 with susceptibility to Graves' disease in Han population of Taiwan	Chen P.-L.; Fann C.S.-J.; Chang C.-C.; Wu I.-L.; Chiu W.-Y.; Lin C.-Y.; WEI-SHIUNG YANG; Chang T.-C.
臺大學術典藏	2021-07-02T02:35:44Z	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.; WEI-SHIUNG YANG; Chang T.-C.
臺大學術典藏	2021-07-02T02:35:38Z	A genome-wide association analysis identifies novel susceptibility loci for coronary arterial lesions in patients with Kawasaki disease	Lin M.-T.; Hsu C.-L.; Chen P.-L.; WEI-SHIUNG YANG; Wang J.-K.; Fann C.S.J.; Wu M.-H.
臺大學術典藏	2021-07-02T02:35:33Z	Predicting HLA genotypes using unphased and flanking single-nucleotide polymorphisms in Han Chinese population	Hsieh A.-R.; Chang S.-W.; Chen P.-L.; Chu C.-C.; Hsiao C.-L.; WEI-SHIUNG YANG; Chang C.-C.; Wu J.-Y.; Chen Y.-T.; Chang T.-C.; Fann C.S.J.
臺大學術典藏	2021-07-02T02:35:27Z	Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study	Chen P.-L.; Shih S.-R.; Wang P.-W.; Lin Y.-C.; Chu C.-C.; Lin J.-H.; Chen S.-C.; Chang C.-C.; Huang T.-S.; Tsai K.S.; Tseng F.-Y.; Wang C.-Y.; Lu J.-Y.; Chiu W.-Y.; Chang C.-C.; Chen Y.-H.; Chen Y.-T.; Fann C.S.-J.; WEI-SHIUNG YANG; Chang T.-C.

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