| Issue Date | Title | Author(s) | Relation | scopus | WOS | Fulltext/Archive link |
| 2013 | A genome-wide association analysis identifies novel susceptibility loci for coronary arterial lesions in patients with Kawasaki disease. | Lin, MT; Hsu, CL; Taiwan Pediatric CV Group; Chen, PL; Yang, WS; Wang, JK; Fann, CS; Wu, MH | TRANSLATIONAL RESEARCH S1931-5244(13)00040-6. | | | |
| 2010 | A genome-wide association study identifies new loci for ACE activity: potential implications for response to ACE inhibitor. | Chung, CM; Wang, RY; Chen, JW; Fann, CS; Leu, HB; Ho, HY; Ting, CT; Lin, TH; Sheu, SH; Tsai, WC; Chen, JH; Jong, YS; Lin, SJ; Chen, YT; Pan, WH. | PHARMACOGENOMICS JOURNAL 10(6):537-44 | | | |
| 2003 | A genome-wide scan using tree-based association analysis for candidate loci related to fasting plasma glucose levels. | Chen, CH; Chang, CJ; Yang, WS; Chen, CL; Fann, CS | BMC genetics 4(Suppl 1), S65 | | | |
| 2009 | A genome-wide survey of copy number variations in Han Chinese residing in Taiwan. | Lin, CH; Lin, YC; Wu, JY; Pan, WH; Chen, YT; Fann, CS | GENOMICS 94(4):241-6 | | | |
| 2009 | A novel tool for individual haplotype inference using mixed data. | Lin, CP; Fann, CS | JOURNAL OF BIOMEDICAL SCIENCE 2;16:52 | | | |
| 2015 | A splicing-regulatory polymorphism in DRD2 disrupts ZRANB2 binding, impairs cognitive functioning and increases risk for schizophrenia in six Han Chinese samples. | Cohen, OS; Weickert, TW; Hess, JL; Paish, LM; McCoy, SY; Rothmond, DA; Galletly, C; Liu, D; Weinberg, DD; Huang, XF; 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, CH; Chang, WH; Hwu, HG; Liu, CM; Liu, YL; Wen, CC; Fann, CS; Chang, CC; Kanazawa, T; Middleton, FA; Duncan, TM; Faraone, SV; Weickert, CS; Tsuang, MT; Glatt, SJ. | MOLECULAR PSYCHIATRY 21, 975-982 | | | |
| 2011 | ANXA7, PPP3CB, DNAJC9, and ZMYND17 genes at chromosome 10q22 associated with the subgroup of schizophrenia with deficits in attention and executive function. | Liu, CM; Fann, CS; Chen, CY; Liu, YL; Oyang, YJ; Yang, WC; Chang, CC; Wen, CC; Chen, WJ; Hwang, TJ; Hsieh, MH; Liu, CC; Faraone, SV; Tsuang, MT; Hwu, HG. | BIOLOGICAL PSYCHIATRY 70(1), 51-58 | | | |
| 2002 | Association between markers in chromosomal region 17q23 and young onset hypertension: a TDT study. | Wu, SY; Fann, CS; Jou, YS; Chen, JW; Pan, WH | Journal of medical genetics 39(1), 42-44 | | | |
| 2009 | Association of the 3' region of COMT with schizophrenia in Taiwan. | Chien, YL; Liu, CM; Fann, CS; Liu, YL; Hwu, HG | Journal of the Formosan Medical Association 108(4):301-309 | | | |
| 2011 | Comprehensive Genotyping in Two Homogeneous Graves' Disease Samples Reveals Major and Novel HLA Association Alleles. | Chen, PL; Fann, CS; Chu, CC; Chang, CC; Chang, SW; Hsieh, HY; Lin, M; Yang, WS; Chang, TC. | PLoS One. 6(1), e16635 | | | |
| 2018 | Comprehensive Human Leukocyte Antigen Genotyping of Patients With Type 1 Diabetes Mellitus in Taiwan | Tung, YC; Fann, CS; Chang, CC; Chu, CC; Yang, WS; Hwu, WL; Chen, PL; Tsai, WY | PEDIATRIC DIABETES 19(4), 699-706 | | | |
| 2012 | Constructing endophenotypes of complex diseases using non-negative matrix factorization and adjusted rand index. | Wang, HM; Hsiao, CL; Hsieh, AR; Lin, YC; Fann, CS | PLoS One 7(7), e40996 | | | |
| 2005 | Construction of endophenotypes for complex diseases in the presence of heterogeneity. | Chen, CH; Kuo, CL; Lin, MC; Liang, YJ; Fann, CS | BMC genetics 6(Suppl 1), S139 | | | |
| 2010 | Diverse associations between ESR1 polymorphism and breast cancer development and progression. | Ding, SL; Yu, JC; Chen, ST; Hsu, GC; Hsu, HM; Ho, JY; Lin, YH; Chang, CC; Fann, CS; Cheng, CW; Wu, PE; Shen, CY | Clin Cancer Res 16(13), 3473-84 | | | |
| 2013 | DRD2 haplotype associated with negative symptoms and sustained attention deficits in Han Chinese with schizophrenia in Taiwan. | Chien, YL; Hwu, HG; Fann, CS; Chang, CC; Tsuang, MT; Liu, CM. | JOURNAL OF HUMAN GENETICS 58(4):229-32 | | | |
| 2010 | Ectopic and high CXCL13 chemokine expression in myasthenia gravis with thymic lymphoid hyperplasia. | Shiao, YM; Lee, CC; Hsu, YH; Huang, SF; Lin, CY; Li, LH; Fann, CS; Tsai, CY; Tsai, SF; Chiu, HC. | Journal of Neuroimmunology 221(1-2), 101-106. | | | |
| 2016 | First step of precision medicine for antithyroid drug-induced agranulocytosis. | Chen, PL; Fann, CS; Shih, HZ; Yang, WS; Chang, TC | The Lancet Diabetes & Endocrinology 4(6), 473-474 | | | |
| 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, YC; Kuo, SH; Yang, YC; Chen, JP; Hsu, PN; Lin, CW; Chen, LT; Cheng, AL; Fann, CS; Lin, JT; Wu, MS | Blood Cancer Journal 4, eXX | | | |
| 2010 | Genetic variants of IL-6 and its receptor are not associated with schizophrenia in Taiwan. | Liu, YL; Liu, CM; Fann, CS; Yang, WC; Chen, YH; Tseng, LJ; Liu, SK; Hsieh, MH; Hwang, TJ; Chan, HY; Chen, JJ; Chen, WJ; Hwu, HG. | NEUROSCIENCE LETTERS 468(3):330-3 | | | |
| 2006 | Han Chinese cell and genome bank in Taiwan: purpose, design and ethical considerations. | Pan, WH; Fann, CS; Wu, JY; Hung, YT; Ho, MS; Tai, TH; Chen, YJ; Liao, CJ; Yang, ML; Cheng, AT; Chen, YT | Human heredity 61(1), 27-30 | | | |
