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Chien-Ching Chang
Researcher at Academia Sinica
Publications - 26
Citations - 583
Chien-Ching Chang is an academic researcher from Academia Sinica. The author has contributed to research in topics: Single-nucleotide polymorphism & Haplotype. The author has an hindex of 14, co-authored 25 publications receiving 526 citations.
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Journal ArticleDOI
Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study
Pei-Lung Chen,Shyang-Rong Shih,Pei-Wen Wang,Ying-Chao Lin,Chen-Chung Chu,Jung-Hsin Lin,Jung-Hsin Lin,Szu-Chi Chen,Ching-Chung Chang,Ching-Chung Chang,Tien-Shang Huang,Keh-Sung Tsai,Fen-Yu Tseng,Chih-Yuan Wang,Jin-Ying Lu,Wei-Yih Chiu,Chien-Ching Chang,Yu-Hsuan Chen,Yuan-Tsong Chen,Yuan-Tsong Chen,Cathy S.J. Fann,Wei-Shiung Yang,Tien-Chun Chang +22 more
TL;DR: A two-stage association study on two separate subject sets, using direct human leukocyte antigen genotyping and SNP-based genome-wide association study, shows results that could be useful for antithyroid-induced agranulocytosis and potentially for agranulateosis caused by other chemicals.
Journal ArticleDOI
More evidence supports the association of PPP3CC with schizophrenia.
Yu-Li Liu,Cathy S.J. Fann,Chih-Min Liu,Chien-Ching Chang,Wei-Chih Yang,Shuen-Iu Hung,Shuen-Iu Hung,Sung-Liang Yu,Tzung-Jeng Hwang,Ming H. Hsieh,C-M Liu,Min-Min Tsuang,J Wu,Yuh-Shan Jou,Stephen V. Faraone,Ming T. Tsuang,Ming T. Tsuang,Wei J. Chen,H-G Hwu +18 more
TL;DR: The results suggest that PPP3CC gene may be a true susceptibility gene for schizophrenia.
Journal ArticleDOI
Comprehensive genotyping in two homogeneous Graves' disease samples reveals major and novel HLA association alleles.
Pei-Lung Chen,Cathy S.J. Fann,Cathy S.J. Fann,Chen-Chung Chu,Chien-Ching Chang,Su-Wei Chang,Hsin-Yi Hsieh,Marie Lin,Wei-Shiung Yang,Tien-Chun Chang +9 more
TL;DR: These GD-associated alleles identified in ethnic Chinese Hans, and those identified in other Asian studies, are totally distinct from the known associated alleles in Caucasians.
Journal ArticleDOI
RASD2, MYH9, and CACNG2 Genes at Chromosome 22q12 Associated with the Subgroup of Schizophrenia with Non-Deficit in Sustained Attention and Executive Function
Yu-Li Liu,Cathy S.J. Fann,Chih-Min Liu,Wei J. Chen,Jer-Yuarn Wu,Shuen-Iu Hung,Chun-Houh Chen,Yuh-Shan Jou,Shi-Kai Liu,Tzung-Jeng Hwang,Ming H. Hsieh,Chien-Ching Chang,Wei-Chih Yang,Wei-Chih Yang,Jin-Jia Lin,Frank Huang-Chih Chou,Stephen V. Faraone,Ming T. Tsuang,Ming T. Tsuang,Hai-Gwo Hwu +19 more
TL;DR: The genes RASD2, MYH9, and CACNG2 might be vulnerability genes for neuropsychologically defined subgroups of schizophrenic patients.
Journal ArticleDOI
No association of G72 and d-amino acid oxidase genes with schizophrenia
Yu-Li Liu,Cathy S.J. Fann,Chih-Min Liu,Chien-Ching Chang,Jer-Yuarn Wu,Shuen-Iu Hung,Shih-Kai Liu,Ming H. Hsieh,Tzung-Jeng Hwang,Hung-Yu Chan,Jiahn-Jyh Chen,Stephen V. Faraone,Ming T. Tsuang,Ming T. Tsuang,Wei J. Chen,Hai-Gwo Hwu +15 more
TL;DR: The genes of D-amino acid oxidase (DAAO) activator (DAOA or G72; 13q34) and DAAO (12q24) have been suggested as candidate genes and involved in the N-methyl-D-aspartate receptor regulation pathway for schizophrenia.