Academia Sinica Life Science Library -- Publications

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Publications

Inst. of Biomedical Sciences - 范盛娟 FANN, CATHY S.J.

Journal

1.Winsvold BS, Harder AVE, Ran C, Chalmer MA, Dalmasso MC, Ferkingstad E, Tripathi KP, Bacchelli E, Børte S, Fourier C, Petersen AS, Vijfhuizen LS, Magnusson SH, O'Connor E, Bjornsdottir G, Häppölä P, Wang YF, Callesen I, Kelderman T, Gallardo VJ, de Boer I, Olofsgård FJ, Heinze K, Lund N, Thomas LF, Hsu CL, Pirinen M, Hautakangas H, Ribasés M, Guerzoni S, Sivakumar P, Yip J, Heinze A, Küçükali F, Ostrowski SR, Pedersen OB, Kristoffersen ES, Martinsen AE, Artigas MS, Lagrata S, Cainazzo MM, Adebimpe J, Quinn O, Göbel C, Cirkel A, Volk AE, Heilmann-Heimbach S, Skogholt AH, Gabrielsen ME, Wilbrink LA, Danno D, Mehta D, Guðbjartsson DF; HUNT All-In Headache, The International Headache Genetics Consortium, DBDS Genomic Consortium; Rosendaal FR, Willems van Dijk K, Fronczek R, Wagner M, Scherer M, Göbel H, Sleegers K, Sveinsson OA, Pani L, Zoli M, Ramos-Quiroga JA, Dardiotis E, Steinberg A, Riedel-Heller S, Sjöstrand C, Thorgeirsson TE, Stefansson H, Southgate L, Trembath RC, Vandrovcova J, Noordam R, Paemeleire K, Stefansson K, Fann CS, Waldenlind E, Tronvik E, Jensen RH, Chen SP, Houlden H, Terwindt GM, Kubisch C, Maestrini E, Vikelis M, Pozo-Rosich P, Belin AC, Manjit Matharu, Arn M J M van den Maagdenberg, Thomas F Hansen, Alfredo Ramirez, John-Anker Zwart; International Consortium for Cluster Headache Genetics. Cluster Headache Genomewide Association Study and Meta-Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor. Ann Neurol.. 2023-07, 07-24, 2023-07. [JCR]　[WOS]
Chen TH, Hsu HC, You JF, Lai CC, Tsou YK, Hsu CL, Fann CSJ, Chien RN, Chang ML. Extracellular Nicotinamide Phosphoribosyltransferase as a Surrogate Marker of Prominent Malignant Potential in Colonic Polyps: A 2-Year Prospective Study. Cancers.. 15(6):1702., 1702-1702, 2023-03. [JCR]　[WOS]
Lian IB, Sie JJ, Chang CC, Fann CSJ, Huang CH. Effects of insomnia and non-vasomotor menopausal symptoms on coronary heart disease risk: a mendelian randomization study. Heliyon.. 9(2):e13569, e13569-e13569, 2023-02. [JCR]　[WOS]
Chen SP, Hsu CL, Wang YF, Yang FC, Chen TH, Huang JH, Pan LH, Fuh JL, Chang HC, Lee YL, Chang HC, Lee KH, Chang YC, Fann CS*, Wang SJ. Genome-wide analyses identify novel risk loci for cluster headache in Han Chinese residing in Taiwan. J Headache Pain.. 23(1), 147, 2022-11-21. [JCR]　[WOS]
Lee CJ, Chen TH, Lim AMW, Chang CC, Sie JJ, Chen PL, Chang SW, Wu SJ, Hsu CL, Hsieh AR, Yang WS, Fann CSJ*. Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Commun Biol.. 5(1), 1175, 2022-11-03. [JCR]　[WOS]
Geevimaan K, Guo JY, Shen CN, Jiang JK, Fann CSJ, Hwang MJ, Shui JW, Lin HT, Wang MJ, Shih HC, Li AF, Chang SC, Yang SH, Chen JY. Patient-Derived Organoid Serves as a Platform for Personalized Chemotherapy in Advanced Colorectal Cancer Patients. Front Oncol.. 12, 883437, 2022-06-01. [JCR]　[WOS]
Jiang YJ, Fann CS, Fuh JL, Chung MY, Huang HY, Chu KC, Wang YF, Hsu CL, Kao LS, Chen SP, Wang SJ. Genome-wide analysis identified novel susceptible genes of restless legs syndrome in migraineurs. J Headache Pain. 23(1), 39-39, 2022-03. [JCR]　[WOS]
Tsao YC, Wang SJ, Hsu CL, Wang YF, Fuh JL, Chen SP, Fann CS. Genome-wide association study reveals susceptibility loci for self-reported headache in a large community-based Asian population. Cephalalgia.. 42(3), 229-238, 2022-03. [JCR]　[WOS]
Liu CM, Liu CL, Hu KW, Tseng VS, Chang SL, Lin YJ, Lo LW, Chung FP, Chao TF, Tuan TC, Liao JN, Lin CY, Chang TY, Fann CS, Higa S, Yagi N, Hu YF, Chen SA. A Deep Learning-enabled Electrocardiogram Model for the Identification of a Rare Inherited Arrhythmia: Brugada Syndrome. Canadian Journal of Cardiology. 38(2), 152-159, 2022-02. [JCR]　[WOS]
Chang ML, Chang SW, Chen SC, Chien RN, Hsu CL, Chang MY, Fann CSJ*. Genetic Association of Hepatitis C-Related Mixed Cryoglobulinemia: A 10-Year Prospective Study of Asians Treated with Antivirals. Viruses. 13(3):464. doi: 10.3390/v13030464., 464-464, 2021-12. [JCR]　[WOS]
Wu LS, Huang MC, Chen CK, Shen CY, Fann CS, Lin CY, Lin CC, Cheng AT. Genome-Wide Association Study of Lithium-Induced Dry Mouth in Bipolar I Disorder. Journal of Personalized Medicine. 11(12):1265., 1265-1265, 2021-12. [JCR]　[WOS]
Hsieh AR, Fann CSJ, Lin HC, Tai J, Hsieh SY, Tai DI. Hepatitis B virus persistent infection-related single nucleotide polymorphisms in HLA regions are associated with viral load in hepatoma families. WORLD JOURNAL OF GASTROENTEROLOGY. 27(37), 6262-6276, 2021-10. [JCR]　[WOS]
Ip PP, Li Q, Lin WH, Chang CC, Fann CS, Chen HY, Liu FT, Lebrilla CB, Yang CC, Liao F. Analysis of site-specific glycan profiles of serum proteins in patients with multiple sclerosis or neuromyelitis optica spectrum disorder - a pilot study. Glycobiology. 31(9), 1230-1238, 2021-09. [JCR]　[WOS]
Li WY, Huang SW, Wang SF, Liu HF, Chou CH, Wu SJ, Huang HD, Lu PL, Fann CSJ, Chen M, Chen YH, Chen YA. Source identification of HIV-1 transmission in three lawsuits Using Ultra-Deep pyrosequencing and phylogenetic analysis. Journal of Microbiology, Immunology and Infection. 54(4), 596-605, 2021-08. [JCR]　[WOS]
Wu LS, Huang MC, Fann CS, Lane HY, Kuo CJ, Chiu WC, Kwok PY, Cheng AT. Genome-wide association study of early-onset bipolar I disorder in the Han Taiwanese population. Translational Psychiatry. 11(1), 301-301, 2021-05. [JCR]　[WOS]
Chang ML, Lin YS, Chang MY, Hsu CL, Chien RN, Fann CS*. Accelerated cardiovascular risk after viral clearance in hepatitis C patients with the NAMPT-rs61330082 TT genotype: An 8-year prospective cohort study. Virulence. 12(1), 270-280, 2021-01-15. [JCR]　[WOS]
Horpaopan Sukanya, Fann Cathy S. J., Lathrop Mark, Ott Jurg. Shared genomic segment analysis with equivalence testing. Genetic Epidemiology. 44(7), 741-747, 2020-10. [JCR]　[WOS]
Ai-Ru Hsieh, Jia Jyun Sie, Chien Ching Chang, Jurg Ott, Ie-Bin Lian*, Cathy SJ Fann*. Maximal Segmental Score method for localizing recessive disease variants based on sequence data. Frontiers in Genetics.. 11, 2020-06. [JCR]　[WOS]
Ling YH, Chen SP, Fann CS, Wang SJ, Wang YF. TRPM8 genetic variant is associated with chronic migraine and allodynia. J Headache Pain.. 20(1):115., 2019-12-16. [JCR]　[WOS]
Hsieh AR, Chen LS, Li YJ, Fann CSJ*. Determining population stratification and subgroup effects in association studies of rare genetic variants for nicotine dependence. Psychiatric Genetics. 29(4):111-119, 2019-08. [JCR]　[WOS]
Liu Chih-Min, Liu Yu-Li, Hwu Hai-Gwo, Fann Cathy Shen-Jang, Yang Ueng-Cheng, Hsu Pei-Chun, Chang Chien-Ching, Chen Wei J., Hwang Tzung-Jeng, Hsieh Ming H., Liu Chen-Chung, Chien Yi-Ling, Lin Yi-Tin, Tsuang Ming T. Genetic associations and expression of extra-short isoforms of disrupted-in-schizophrenia 1 in a neurocognitive subgroup of schizophrenia. Journal of Human Genetics. 64(7),653-663, 2019-07. [JCR]　[WOS]
Imai-Okazaki A, Li Y, Horpaopan S, Riazalhosseini Y, Garshasbi M, Mosse YP, Zhang D, Schrauwen I, Sharma A, Fann CSJ, Leal SM, Lathrop M, Ott J. Heterozygosity mapping for human dominant trait variants. Hum Mutat.. 40(7):996-1004., 2019-07. [JCR]　[WOS]
Wang W, Fann CSJ, Yang SH, Chen HH, Chen CY. Weight loss and metabolic improvements in obese patients undergoing gastric banding and gastric banded plication: A comparison. Nutrition. 57,290-299., 2019-01. [JCR]　[WOS]
Chang LC, Chang CC, Chen PL, Wang SH, Chen YH, Tsai YH, Shih SR, Chiu WY, Fann CS*, Yang WS*, Chang TC*. Thyrotropin receptor antibodies and a genetic hint in antithyroid drug-induced adverse drug reactions. Expert Opin Drug Saf.. 17(8), 775-784, 2018-08. [JCR]　[WOS]
Tung YC, Fann CS, Chang CC, Chu CC, Yang WS, Hwu WL, Chen PL, Tsai WY. Comprehensive HLA genotyping of patients with type 1 diabetes mellitus in Taiwan. PEDIATRIC DIABETES. 19(4), 699-706, 2018-07. [JCR]　[WOS]
Ip Peng-Peng, Chung Chen-Yen, Chang Chien-Ching, Lee Yu-Fang, Wang Hui-Min, Lian Ie-Bin, Fann Cathy Shen-Jang, Yang Chi-Chao, Liao Fang. Differentiation of remitting neuromyelitis optica spectrum disorders from multiple sclerosis by integrating parameters from serum proteins and lymphocyte subsets. J Neuroimmunol.. 318, 45-52, 2018-05. [JCR]　[WOS]
Chen SP, Fuh JL, Chung MY, Lin YC, Loai YC, Wang YF, Hsu CL, Yang YC, Lin MW, Chiou JJ,Wang PJ, Chen PK, Fan PC, Wu JY, Chen YT, Kao LS, Fann CSJ*, Wang SJ*. Genome-wide Association Study Identifies Novel Susceptibility Loci for Migraine in Han Chinese Resided in Taiwan. CEPHALALGIA. 38(3),466-475, 2018-03. [JCR]　[WOS]
Hsieh AR, Chen DP, Chattopadhyay AS, Li YJ, Chang CC, Fann CSJ. A non-threshold region-specific method for detecting rare variants in complex diseases. PLOS ONE. 12(11), e0188566., 2017-11. [JCR]　[WOS]
Spracklen CN, Chen P, Kim YJ, Wang X, Cai H, Li S, Long J, Wu Y, Wang YX, Takeuchi F, Wu JY, Jung KJ, Hu C, Akiyama K, Zhang Y, Moon S, Johnson TA, Li H, Dorajoo R, He M, Cannon ME, Roman TS, Salfati E, Lin KH, Guo X, Sheu WH, Absher D, Adair LS, Assimes TL, Aung T, Cai Q, Chang LC, Chen CH, Chien LH, Chuang LM, Chuang SC, Du S, Fan Q, Fann CS, Feranil AB, Friedlander Y, Gordon-Larsen P, Gu D, Gui L, Guo Z, Heng CK, Hixson J, Hou X, Hsiung CA, Hu Y, Hwang MY, Hwu CM, Isono M, Juang JJ, Khor CC, Kim YK, Koh WP, Kubo M, Lee IT, Lee SJ, Lee WJ, Liang KW, Lim B, Lim SH, Liu J, Nabika T, Pan WH, Peng H, Quertermous T, Sabanayagam C, Sandow K, Shi J, Sun L, Tan PC, Tan SP, Taylor KD, Teo YY, Toh SA, Tsunoda T, van Dam RM, Wang A, Wang F, Wang J, Wei WB, Xiang YB, Yao J, Yuan JM, Zhang R, Zhao W, Chen YI, Rich SS, Rotter JI, Wang TD, Wu T, Lin X, Han BG, Tanaka T, Cho YS, Katsuya T, Jia W, Jee SH, Chen YT, Kato N, Jonas JB, Cheng CY, Shu XO, He J, Zheng W, Wong TY, Huang W, Kim BJ, Tai ES, Mohlke KL, Sim X. Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels. HUMAN MOLECULAR GENETICS. 26(9), 1770-1784, 2017-05. [JCR]　[WOS]
Hsieh AR, Fann CS, Yeh CT, Lin HC, Wan SY, Chen YC, Hsu CL, Tai J, Lin SM, Tai DI. Effects of sex and generation on hepatitis B viral load in families with hepatocellular carcinoma. WORLD JOURNAL OF GASTROENTEROLOGY. 23(5), 876-884, 2017-02. [JCR]　[WOS]
Chen DP, Lin YC, Fann CS. Methods for identifying differentially methylated regions for sequence- and array-based data. Briefing in Functional Genomics. 15(6), 485-490, 2016-11. [JCR]　[WOS]
Chen PL, Fann CS, Shih HZ, Yang WS, Chang TC. First step of precision medicine for antithyroid drug-induced agranulocytosis. The Lancet Diabetes & Endocrinology. 4(6), 473-474, 2016-05. [JCR]　[WOS]
Liu YL, Wang SC, Hwu HG, Fann CS, Yang UC, Yang WC, Hsu PC, Chang CC, Wen CC, Tsai-Wu JJ, Hwang TJ, Hsieh MH, Liu CC, Chien YL, Fang CP, Faraone SV, Tsuang MT, Chen WJ, Liu CM. Haplotypes of the D-Amino Acid Oxidase Gene Are Significantly Associated with Schizophrenia and Its Neurocognitive Deficits. PLoS One. 11(3), e0150435, 2016-03. [JCR]　[WOS]
Sengupta Chattopadhyay A, Lin YC, Hsieh AR, Chang CC, Lian IB, Fann CS. Using propensity score adjustment method in genetic association studies. COMPUTATIONAL BIOLOGY AND CHEMISTRY. 62, 1-11, 2016-03. [JCR]　[WOS]
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. A splicing-regulatory polymorphism in DRD2 disrupts ZRANB2 binding, impairs cognitive functioning and increases risk for schizophrenia in six Han Chinese samples. MOLECULAR PSYCHIATRY. 21, 975-982, 2016. [JCR]　[WOS]
Fuh JL, Chung MY, Yao SC, Chen PK, Liao YC, Hsu CL, Wang PJ, Wang YF, Chen SP, Fann CS, Kao LS, Wang SJ. Susceptible genes of restless legs syndrome in migraine. CEPHALALGIA. 35(12-13)S6, OR18, 2015-12. [JCR]　[WOS]
Chang CJ, Chou T, Fann CS. PCN121 – Clinical, Mediciation and Economical Outcome Research of Advanced Colorectal Cancer Relapse Using Reimbursement and Cancer Registry Databases. VALUE IN HEALTH. 18(7), A451, 2015-11. [JCR]　[WOS]
Chang CJ, Chou T, Chang S, Chien L, Fann CS. PCN318 – Impact on Time Gap Between Approval and Reimbursement of Target Therapy to Advanced Colorectal Cancer. VALUE IN HEALTH. 18(7), A486-A487, 2015-11. [JCR]　[WOS]
Pei-Lung Chen, Shyang-Rong Shih, Pei-Wen Wang, Ying-Chao Lin, Chen-Chung Chu, Jung-Hsin Lin, Szu-Chi Chen, 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, Cathy Shen-Jang Fann*, Wei-Shiung Yang and Tien-Chun Chang. Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study. Nature Communications. 6, 7633, 2015-05. [JCR]　[WOS]
Leu HB, Chung CM, Lin SJ, Chiang KM, Yang HC, Ho HY, Ting CT, Lin TH, Sheu SH, Tsai WC, Chen JH, Yin WH, Chiu TY, Chen CI, Fann CS, Chen YT, Pan WH, Chen JW. Association of circadian genes with diurnal blood pressure changes and non-dipper essential hypertension: a genetic association with young-onset hypertension. HYPERTENSION RESEARCH. 38(2), 155-162, 2015-02. [JCR]　[WOS]
Shu-Chen Chang, Chee-Jen Chang*, Yu-Jr Lin, Ie-Bin Lian, Cathy S.J. Fann*. Use of a failure probability constraint to suggest an initial dose in a Phase I cancer clinical trial. JOURNAL OF FOOD AND DRUG ANALYSIS. 22(4), 556-562, 2014-12. [JCR]　[WOS]
Liao F, Hsu YC, Kuo SH, Yang YC, Chen JP, Hsu PN, Lin CW, Chen LT, Cheng AL, Fann CS, Lin JT, Wu MS. Genetic polymorphisms and tissue expression of interleukin-22 associated with risk and therapeutic response of gastric mucosa-associated lymphoid tissue lymphoma. BLOOD CANCER JOURNAL. 4, eXX, 2014-10. [JCR]　[WOS]
Lin YC, Hsieh AR, Hsiao CL, Wu SJ, Wang HM, Lian IB, Fann C. Identifying rare and common disease associated variants in genomic data using Parkinson¿s disease as a model. JOURNAL OF BIOMEDICAL SCIENCE. 21(1), 88, 2014-08. [JCR]　[WOS]
Chang SW, Fann CS, Su WH, Wang YC, Weng CC, Yu CJ, Hsu CL, Hsieh AR, Chien RN, Chu CM, Tai DI. A genome-wide association study on chronic HBV infection and its clinical progression in male Han-Taiwanese. PLoS One. 9(6), e99724, 2014-06. [JCR]　[WOS]
Ching-Lin Hsiao, Ai-Ru Hsieh, Ie-Bin Lian, Ying-Chao Lin, Hui-Min Wang, Cathy S.J. Fann. A novel method for identification and quantification of consistently differentially methylated regions. PLoS One. 9(5), e97513, 2014-05. [JCR]　[WOS]
Hsieh AR, Chang SW, Chen PL, Chu CC, Hsiao CL, Yang WS, Chang CC, Wu JY, Chen YT, Chang TC, Fann CS. Predicting HLA genotypes using unphased and flanking single-nucleotide polymorphisms in Han Chinese population. BMC genomics. 15, 81, 2014-01. [JCR]　[WOS]
Sengupta Chattopadhyay A, Hsiao CL, Chang CC, Lian IeB, Fann CS. Summarizing techniques that combine three non-parametric scores to detect disease-associated 2-way SNP-SNP interactions. Ge. GENE. 533(1), 304-312, 2014-01. [JCR]　[WOS]
Liao HC, Huang YH, Chen YJ, Kao SM, Lin HY, Huang CK, Liu HC, Hsu TR, Lin SP, Yang CF, Fann CS, Chiu PC, Hsieh KS, Fu YC, Ke YY, Lin CY, Tsai FJ, Wang CH, Chao MC, Yu WC, Chiang CC, Niu DM. Plasma globotriaosylsphingosine (lysoGb3) could be a biomarker for Fabry disease with a Chinese hotspot late-onset mutation (IVS4+919G>A). Clin Chim Acta.. 426, 114-120, 2013-11. [JCR]　[WOS]
Chien YL, Hwu HG, Fann CS, Chang CC, Tsuang MT, Liu CM. DRD2 haplotype associated with negative symptoms and sustained attention deficits in Han Chinese with schizophrenia in Taiwan. JOURNAL OF HUMAN GENETICS. 58(4), 229-232, 2013-04. [JCR]　[WOS]
Chung CM, Wang RY, Fann CS, Chen JW, Jong YS, Jou YS, Yang HC, Kang CS, Chen CC, Chang HC, Pan WH. . Fine-mapping angiotensin-converting enzyme gene: separate QTLs identified for hypertension and for ACE activity. . PLoS One. 8(3), e56119, 2013-03. [JCR]　[WOS]
Yang HC, Liu CM, Liu YL, Chen CW, Chang CC, Fann CS, Chiou JJ, Yang UC, Chen CH, Faraone SV, Tsuang MT, Hwu HG. . The DAO Gene Is Associated with Schizophrenia and Interacts with Other Genes in the Taiwan Han Chinese Population. . PLoS One. 8(3), e60099, 2013-03. [JCR]　[WOS]
Lin M, Hsu C; TAIWAN PEDIATRIC CV GROUP, Chen P, Yang W, Wang J, Fann CS*, Wu M: . A genome-wide association analysis identifies novel susceptibility loci for coronary arterial lesions in patients with Kawasaki disease. . TRANSLATIONAL RESEARCH. 161(6), 513-515, 2013-01. [JCR]　[WOS]
Okada Y, Sim X, Go M, Wu J, Gu D, Takeuchi F, Takahashi A, Maeda S, Tsunoda T, Chen P, Lim S, Wong T, Liu J, Young T, Aung T, Seielstad M, Teo Y, Kim Y, Lee J, Han B, Kang D, Chen CH, Tsai F, Chang L, Fann CS, et al.,The KidneyGen Consortium; The CKDGen Consortium, Albrecht E; The GUGC consortium, et al.,: . Meta-analysis identifies multiple loci associated with kidney function-related traits in ease Asian populations. . NATURE GENETICS. 44(8), 904-909, 2012-12. [JCR]　[WOS]
Lin YC, Hsiao CL, Hsieh AR, Lian IeB, Fann CS. Using maximal segmental score in genome-wide association studies. GENETIC EPIDEMIOLOGY. 36(6), 594-601, 2012-09. [JCR]　[WOS]
Wang HM, Hsiao CL, Hsieh AR, Lin YC, Fann CS. Constructing endophenotypes of complex diseases using non-negative matrix factorization and adjusted rand index. . PLoS One. 7(7), e40996, 2012-07. [JCR]　[WOS]
Wen W, Cho YS, Zheng W, Dorajoo R, Kato N, Qi L, Chen CH, Delahanty RJ, Okada Y, Tabara Y, Gu D, Zhu D, Haiman CA, Mo Z, Gao YT, Saw SM, Go MJ, Takeuchi F, Chang LC, Kokubo Y, Liang J, Hao M, Le Marchand L, Zhang Y, Hu Y, Wong TY, Long J, Han BG, Kubo M, Yamamoto K, Su MH, Miki T, Henderson BE, Song H, Tan A, He J, Ng DP, Cai Q, Tsunoda T, Tsai FJ, Iwai N, Chen GK, Shi J, Xu J, Sim X, Xiang YB, Maeda S, Ong RT, Li C, Nakamura Y, Aung T, Kamatani N, Liu JJ, Lu W, Yokota M, Seielstad M, Fann CS; Genetic Investigation of ANthropometric Traits (GIANT) Consortium, Wu JY, Lee JY, Hu FB, Tanaka T, Tai ES, Shu XO. Meta-analysis identifies common variants associated with body mass index in east Asians. NATURE GENETICS. 44(3), 307-U112, 2012-02. [JCR]　[WOS]
Wu DB, Chang CJ, Huang YC, Wen YW, Wu CL, Fann CS. Cost-effectiveness analysis of pneumococcal conjugate vaccine in Taiwan: a transmission dynamic modeling approach. VALUE IN HEALTH. 15(1 Suppl), S15-S19, 2012-01. [JCR]　[WOS]
Lee MT, Chen CH, Lee CS, Chen CC, Chong MY, Ouyang WC, Chiu NY, Chuo LJ, Chen CY, Tan HK, Lane HY, Chang TJ, Lin CH, Jou SH, Hou YM, Feng J, Lai TJ, Tung CL, Chen TJ, Chang CJ, Lung FW, Chen CK, Shiah IS, Liu CY, Teng PR, Chen KH, Shen LJ, Cheng CS, Chang TP, Li CF, Chou CH, Chen CY, Wang KH, Fann CS, Wu JY, Chen YT, Cheng AT. Genome-wide association study of bipolar I disorder in the Han Chinese population. MOLECULAR PSYCHIATRY. 16(5), 548-556, 2011-08. [JCR]　[WOS]
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. ANXA7, PPP3CB, DNAJC9, and ZMYND17 genes at chromosome 10q22 associated with the subgroup of schizophrenia with deficits in attention and executive function. BIOLOGICAL PSYCHIATRY. 70(1), 51-58, 2011-07. [JCR]　[WOS]
Ai-Ru Hsieh, Ching-Lin Hsiao, Su-Wei Chang, Hui-Min Wang, Cathy SJ Fann,. On the use of multifactor dimensionality reduction (MDR) and classification and regression tree (CART) to identify haplotype-haplotype interactions in genetic studies. Genomics.. 97(2), 77-85., 2011-02. [JCR]　[WOS]
Chen PL, Fann CS, Chu CC, Chang CC, Chang SW, Hsieh HY, Lin M, Yang WS, Chang TC. Comprehensive Genotyping in Two Homogeneous Graves' Disease Samples Reveals Major and Novel HLA Association Alleles. PLoS One.. 6(1), e16635, 2011-01. [JCR]　[WOS]
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. A genome-wide association study identifies new loci for ACE activity: potential implications for response to ACE inhibitor. PHARMACOGENOMICS JOURNAL. 10(6):537-44, 2010-12. [JCR]　[WOS]
Ding SL, Yu JC, Chen ST, Hsu GC, Hsu HM, Ho JY, Lin YH, Chang CC, Fann CS, Cheng CW, Wu PE, Shen CY. Diverse associations between ESR1 polymorphism and breast cancer development and progression. Clin Cancer Res. 16(13), 3473-84, 2010-07. [JCR]　[WOS]
Shiao YM, Lee CC, Hsu YH, Huang SF, Lin CY, Li LH, Fann CS, Tsai CY, Tsai SF, Chiu HC. Ectopic and high CXCL13 chemokine expression in myasthenia gravis with thymic lymphoid hyperplasia. Journal of Neuroimmunology. 221(1-2), 101-106., 2010-04. [JCR]　[WOS]
Tsai FJ, Yang CF, Chen CC, Chuang LM, Lu CH, Chang CT, Wang TY, Chen RH, Shiu CF, Liu YM, Chang CC, Chen P, Chen CH, Fann CS, Chen YT, Wu JY. A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese. PLoS genetics. 6(2):e1000847, 2010-02. [JCR]　[WOS]
Hsiao CL, Lian IB, Hsieh AR, Fann CS. Modeling expression quantitative trait loci in data combining ethnic populations. BMC BIOINFORMATICS. 11(1):111, 2010-02. [JCR]　[WOS]
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. Genetic variants of IL-6 and its receptor are not associated with schizophrenia in Taiwan. NEUROSCIENCE LETTERS. 468(3):330-3, 2010-01. [JCR]　[WOS]
Lin CH, Lin YC, Wu JY, Pan WH, Chen YT, Fann CS . A genome-wide survey of copy number variations in Han Chinese residing in Taiwan. GENOMICS. 94(4):241-6, 2009-10. [JCR]　[WOS]
Chen HH, Lee WJ, Fann CS, Bouchard C, Pan WH . Severe obesity is associated with novel single nucleotide polymorphisms of the ESR1 and PPARgamma locus in Han Chinese. AMERICAN JOURNAL OF CLINICAL NUTRITION. 90(2), 255-262, 2009-08. [JCR]　[WOS]
Lin CP, Fann CS. A novel tool for individual haplotype inference using mixed data. JOURNAL OF BIOMEDICAL SCIENCE. 2;16:52, 2009-06. [JCR]　[WOS]
Yang HC, Liang YJ, Wu YL, Chung CM, Chiang KM, Ho HY, Ting CT, Lin TH, Sheu SH, Tsai WC, Chen JH, Leu HB, Yin WH, Chiu TY, Chen CI, Fann CS, Wu JY, Lin TN, Lin SJ, Chen YT, Chen JW, Pan WH. Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan. PLoS ONE. 4(5):e5459, 2009-05. [JCR]　[WOS]
Chien YL, Liu CM, Fann CS, Liu YL, Hwu HG. Association of the 3' region of COMT with schizophrenia in Taiwan. Journal of the Formosan Medical Association. 108(4):301-309, 2009-04. [JCR]　[WOS]
Chen P, Jou YS, Fann CS, Chen JW, Chung CM, Lin CY, Wu SY, Kang MJ, Chen YC, Jong YS, Lo HM, Kang CS, Chen CC, Chang HC, Huang NK, Wu YL, Pan WH. Lipoprotein lipase variants associated with an endophenotype of hypertension: hypertension combined with elevated triglycerides. Hum Mutat. 30(1), 49-55, 2009-01. [JCR]　[WOS]
Lin CH, Li LH, Ho SF, Chuang TP, Wu JY, Chen YT, Fann CS. A large-scale survey of genetic copy number variations among Han Chinese residing in Taiwan. BMC Genet. 9(1), 92, 2008-12. [JCR]　[WOS]
Lin CH, Huang MC, Li LH, Wu JY, Chen YT, Fann CSJ. Genome-wide copy number analysis using copy number inferring tool (CNIT) and DNA pooling. Hum Mutat.. 29(8), 1055-1062, 2008-08. [JCR]　[WOS]
Lian IB, Lin YH, Lin YC, Yang HC, Chang CJ, Fann CS. Using the Longest Significance Run to Estimate Region-Specific P-values in Genetic Association Mapping Studies. . BMC Bioinformatics. 9(1),246, 2008-05. [JCR]　[WOS]
C. F. Yang, W. L. Hwu, L. C. Yang, W. H. Chung, Y. H. Chien, C. F. Hung, H. C. Chen, P. J. Tsai, C. S. J. Fann, F. Liao and Y. T. Chen. A promoter sequence variant of ZNF750 is linked with familial psoriasis. J Invest Dermatol. (in press), 2008. [JCR]　[WOS]
P. L. Chen, C. S. J. Fann, C. C. Chang, I. L. Wu, W. Y. Chiu, W. S. Yang and T. C. Chang. Family-based association study of cytotoxic T-lymphocyte antigen-4 with susceptibility to Graves' disease in Han population of Taiwan. Genes Immun. 9(2), 87-92, 2008. [JCR]　[WOS]
R. Y. Wang, C. M. Chung, C. S. J. Fann, H. C. Yang, J. W. Chen, Y. S. Jong, Y. S. Jou, H. M. Lo, F. M. Ho, C. S. Kang, C. C. Chen, H. C. Chang, S. K. Shyue and W. H. Pan. Genome-wide scan for quantitative ACE activity in Taiwan young-onset hypertension study. Hum Hered. 65(2), 85-90, 2008. [JCR]　[WOS]
Yang HC, Hsieh HY, Fann CS. Kernel-based association test. Genetics. 179(2),1057-68, 2008. [JCR]　[WOS]
H. C. Yang, M. C. Huang, L. H. Li, C. H. Lin, A. L. Yu, M. B. Diccianni, J. Y. Wu, Y. T. Chen and C. S. J. Fann. MPDA: microarray pooled DNA analyzer. BMC Bioinformatics. 9(1), 196, 2008. [JCR]　[WOS]
Liu YL, Fann CS, Liu CM, Chen WJ, Wu JY, Hung SI, Chen CH, Jou YS, Liu SK, Hwang TJ, Hsieh MH, Chang CC, Yang WC, Lin JJ, Chou FH, Faraone SV, Tsuang MT, Hwu HG. RASD2, MYH9, and CACNG2 Genes at Chromosome 22q12 Associated with the Subgroup of Schizophrenia with Non-Deficit in Sustained Attention and Executive Function. Biol Psychiatry. 64,789-796, 2008. [JCR]　[WOS]
I.B. Lian, C.J. Chang , Y.J. Liang, M.J. Yang and C.S.J. Fann. Identifying differentially expressed genes in dye-swapped microarray experiments of small sample size. COMPUTATIONAL STATISTICS & DATA ANALYSIS. 51(5), 2602-2620, 2007-02. [JCR]　[WOS]
C. M. Liu, Y. L. Liu, C. S. J. Fann, W. J. Chen, W. C. Yang, W. C. Ouyang, C. Y. Chen, Y. S. Jou, M. H. Hsieh, S. K. Liu, T. J. Hwang, S. V. Faraone, M. T. Tsuang and H. G. Hwu. Association evidence of schizophrenia with distal genomic region of NOTCH4 in Taiwanese families. Genes Brain Behav. 6(6), 497-502, 2007. [JCR]　[WOS]
Yang HC, Fann CS. Association mapping using pooled DNA. Methods in Molecular Biology. 376, 161-175, 2007. [JCR]　[WOS]
H. M. Lachman, C. S. J. Fann, M. Bartzis, O. L. Evgrafov, R. N. Rosenthal, E. V. Nunes, C. Miner, M. Santana, J. Gaffney, A. Riddick, C. L. Hsu, and J. Knowles. Genomewide suggestive linkage of opioid dependence to chromosome 14q. HUMAN MOLECULAR GENETICS. 16(11), 1327-1334, 2007. [JCR]　[WOS]
Y. L. Liu, C. S. J. Fann, C. M. Liu, C. C. Chang, W. C. Yang, J. Y. Wu, S. I. Hung, H. Y. Chan, J. J. Chen, M. H. Hsieh, T. J. Hwang, S. V. Faraone, M. T. Tsuang, W. J. Chen and H. G. Hwu. HTF9C gene of 22q11.21 region associates with schizophrenia having deficit-sustained attention. Psychiat Genet. 17(6), 333-338, 2007. [JCR]　[WOS]
P. L. Chen, C. S. J. Fann, C. C. Chang, I. L. Wu, W. Y. Chiu, C. Y. Lin, W. S. Yang, and T. C. Chang. Linkage of Graves' disease to the human leucocyte antigen region in the Chinese-Han population in Taiwan. Clin Endocrin. 66(5), 646-651, 2007. [JCR]　[WOS]
Y. L. Liu, C. S. Fann, C. M. Liu, C. C. Chang, W. C. Yang, S. I. Hung, S. L. Yu, T. J. Hwang, M. H. Hsieh, C. C. Liu, M. M. Tsuang, J. Y. Wu, Y. S. Jou, S. V. Faraone, M. T. Tsuang, W. J. Chen and H. G. Hwu. More evidence supports the association of PPP3CC with schizophrenia. Mol Psychiatry. 12(10), 966-974, 2007. [JCR]　[WOS]
C. M. Liu, Y. L. Liu, C. S. J. Fann, W. C. Yang, J. Y. Wu, S. I. Hung, W. J. Chen, C. M. Chueh, W. M. Liu, C. C. Liu, M. H. Hsieh, T. J. Hwang, S. V. Faraone, M. T. Tsuang, and H. G. Hwu. No association evidence between schizophrenia and dystrobrevin-binding protein 1 (DTNBP1) in Taiwanese families. SCHIZOPHRENIA RESEARCH. 93(1-3), 391-398, 2007. [JCR]　[WOS]
H. C. Yang, C. H. Lin, S. I. Hung and C.S.J. Fann. A comparison of individual genotyping and pooled DNA analysis for polymorphism validation prior to large-scale genetic studies. Ann Hum Genet. 70, 350-359, 2006. [JCR]　[WOS]
H. C. Yang, C. H. Lin, C. L. Hsu, S. I. Hung, J. Y. Wu, W. H. Pan, Y. T. Chen and C.S.J. Fann. A comparison of major histocompatibility complex SNPs in Han Chinese residing in Taiwan and Caucasians. J Biomed Sci. 13, 489-498, 2006. [JCR]　[WOS]
H. C. Yang, Y. J. Liang, M. C. Huang, L. H. Li, C. H. Lin, J. Y. Wu, Y. T. Chen and C. S. J. Fann. A genome-wide study of preferential amplification/hybridization in microarray-based pooled DNA experiments. Nucleic Acids Res. 34(15), e106, 2006. [JCR]　[WOS]
Y. L. Liu, C. S. J. Fann, C. M. Liu, J. W. Wu, S. I. Hung, C. H. Chen, Y. S. Jou, S. K. Liu, T. J. Hwang, M. H. Hsieh, W. C. Ouyang, H. Y. Chan, J. J. Chen, W. C. Yang, C. Y. Lin, S. F. C. Lee and H. W. Hwu. 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. Biol Psychiatry. 60(6), 554-562, 2006. [JCR]　[WOS]
H. C. Yang, C. Y. Lin and C. S. J. Fann. A sliding-window weighted linkage disequilibrium test. Genet Epidemiol. 30(6), 531-545, 2006. [JCR]　[WOS]
Y. L. Liu, C. S. J. Fann, C. M. Liu, J. Y. Wu, S. I. Hung, H. Y. Chan, J. J. Chen, C. C. Pan, S. K. Liu, M. H. Hsieh, T. J. Hwang, W. C. Ouyang, C. Y. Chen, J. J. Lin, F. H. Chou, C. M. Chueh, W. M. Liu, M. M. Tsuang, S. V. Faraone, M. T. Tsuang, W. J. Chen and H. G. Hwu. Absence of significant associations between four AKT1 SNP markers and schizophrenia in the Taiwanese population. Psychiatric Genetics. 16, 39-41, 2006. [JCR]　[WOS]
Y. L. Liu, F. C. Shen-Jang, C. M. Liu, J. Y. Wu, S. I. Hung, H. Y. Chan, J. J. Chen, C. Y. Lin, S. K. Liu, M. H. Hsieh, T. J. Hwang, W. C. Ouyang, C. Y. Chen, J. J. Lin, F. H. Chou, C. M. Chueh, W. M. Liu, M. M. Tsuang, S. V. Faraone, M. T. Tsuang, W. J. Chen and H. G. Hwu. Evaluation of RGS4 as a candidate gene for schizophrenia. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics. 141, 418-420, 2006. [JCR]　[WOS]
W. H. Pan, C. S. J. Fann, J. Y. Wu, Y. T. Hung, M. S. Ho, T. H. Tai, Y. J. Chen, C. J. Liao, M. L. Yang, A. T. A. Cheng and Y. T. Chen. Han Chinese Cell and Genome Bank in Taiwan: Purpose, Design and Ethical Considerations. Hum Hered. 61, 27-30, 2006. [JCR]　[WOS]
C.C. Lin, W.C. Yang, S.J. Lin, T.W. Chen, W.S. Lee, C.F. Chang, P.C. Lee, S.D. Lee, T.S. Su, C.S.J. Fann and M.Y. Chung. Length polymorphism in heme oxygenase-1 is associated with arteriovenous fistula patency in hemodialysis patients. Kidney International. 69, 165~172, 2006. [JCR]　[WOS]
W.J. Chen, J.Y. Yang, J.H. Lin, C.S.J. Fann, V. Osyetrov, C.C. King, A.Y.M. Chen, H.L. Chang, H.W. Kuo, F. Liao and M.S. Ho. Nasopharyngeal shedding of severe acute respiratory syndrome-associated virus (SARS-CoV) is associated with genetic polymorphisms. Clinical Infectious Diseases. 42, 1561-1569, 2006. [JCR]　[WOS]
Y. L. Liu, C. S. J. Fann, C. M. Liu, C. C. Chang, J. Y. Wu, S. I. Hung, S. K. Liu, M. H. Hsieh, T. J. Hwang, H. Y. Chan, J. J. Chen, S. V. Faraone, M. T. Tsuang, W. J. Chen and H. G. Hwu. No association of G72 and D-amino acid oxidase genes with schizophrenia. Schizophrenia Research. 87(1-3), 15-20, 2006. [JCR]　[WOS]
H. C. Yang, C. C. Pan, C. Y. Lin and C. S. J. Fann. PDA: pooled DNA analyzer. BMC Bioinformatics. 7, 233, 2006. [JCR]　[WOS]
C. C. Lin, C. S. J. Fann and M. Y. Chung. Response to 'Hardy-Weinberg equilibrium and control subjects'. Kidney Int. 70, 1375, 2006. [JCR]　[WOS]
H. S. Sun, C. S. Fann, H. Y. Lane, Y. T. Chang, C. J. Chang, Y. L. Liu, W. Y. Yu and A. T. Cheng. A functional polymorphism in the promoter region of the tryptophan hydroxylase gene is associated with alcohol dependence in one aboriginal group in Taiwan. Alcohol Clin Exp Res. 29, 1月7日, 2005. [JCR]　[WOS]
H.C. Yang, C.C. Chang, C.Y. Lin, C.L. Chen, C.Y. Lin and C.S.J Fann. A genome-wide scanning and fine mapping study of COGA data. BMC Genetics. 6, S30, 2005. [JCR]　[WOS]
Y.L. Lo, J.C. Yu, S.T. Chen, H.C. Yang, C.S.J. Fann, Y.C. Mau and C.Y. Shen. Breast cancer risk associated with genotypic polymorphism of the mitosis-regulating gene Aurora-A/STK15/BTAK. International Journal of Cancer. 115, 276~283, 2005. [JCR]　[WOS]
C.H. Chen, C.L. Kuo, M.C.P. Lin, Y.J. Liang and C.S.J. Fann. Construction of endophenotypes for complex diseases in the presence of heterogeneity. BMC Genetics. 6, S139, 2005. [JCR]　[WOS]
Hung SI, Chung WH, Liou LB, Chu CC, Lin M, Huang HP, Lin YL, Lan JL, Yang LC, Hong HS, Chen MJ, Lai PC, Wu MS, Chu CY, Wang KH, Chen CH, Fann CS, Wu JY, Chen YT. HLA-B*5801 allele as a genetic marker for severe cutaneous adverse reactions caused by allopurinol. Proceedings of the National Academy of Sciences of the United States of America. 102, 4134-4139, 2005. [JCR]　[WOS]
C.M. Liu, H.G. Hwu, C.S.J. Fann, C.Y. Lin, Y.L. Liu, W.C. Ou-Yang and S.F. Lee. Linkage evidence of schizophrenia to loci near neuregulin 1 gene on chromosome 8p21 in Taiwanese families. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics. 134B, 79-83, 2005. [JCR]　[WOS]
P. Chen, Y. S. Jou, C. S. J. Fann, J. W. Chen, S. Y. Wu and W. H. Pan. Lipoprotein lipase gene is linked and associated with hypertension in Taiwan young-onset hypertension genetic study. J Biomed Sci. 12, 651-658, 2005. [JCR]　[WOS]
W. L. Hwu, C. F. Yang, C. S. Fann, C. L. Chen, T. F. Tsai, Y. H. Chien, S. C. Chiang, C. H. Chen, S. I. Hung, J. Y. Wu and Y. T. Chen. Mapping of psoriasis to 17q terminus. J Med Genet. 42, 152-158, 2005. [JCR]　[WOS]
H.C. Yang, C.C. Pan, R.C.Y. Luand, C.S.J. Fann. New adjustment factors and sample size calculation in a DNA-pooling experiment with preferential amplification. Genetics. 169, 399-410, 2005. [JCR]　[WOS]
Y. F. Liu, W. M. Chen, Y. F. Lin, R. C. Yang, M. W. Lin, L. H. Li, Y. H. Chang, J. S. Jou, P. Y. Lin, J. S. Su, S. F. Huang, K. J. Hsiao, C. S. Fann, H. W. Hwang, Y. T. Chen and S. F. Tsai. Type II collagen gene variants and inherited osteonecrosis of the frmoral head. New England Journal of Medicine. 352, 2294-2301, 2005. [JCR]　[WOS]
W. M. Chen, Y. F. Liu, M. W. Lin, I. C. Chen, P. Y. Lin, G. L. Lin, Y. S. Jou, Y. T. Lin, C. S. Fann, J. Y. Wu, K. J. Hsiao and S. F. Tsai. Autosomal dominant avascular necrosis of femoral head in two Taiwanese pedigrees and linkage to chromosome 12q13. Am J Hum Genet. 75, 310-317, 2004. [JCR]　[WOS]
E. W. Loe, C. S. Fann, Y. T. Chang, C. J. and A. T. Cheng. Endogenous opioid receptor genes and alcohol dependence among Taiwanese Han. Alcohol Clin Exp Res. 28, 15-19, 2004. [JCR]　[WOS]
Chen CH, Chang CJ, Yang WS, Chen CL, Fann CS. A genome-wide scan using tree-based association analysis for candidate loci related to fasting plasma glucose levels. BMC GENETICS. 4 (Suppl 1), S65, 2003-12. [JCR]　[WOS]
H. G. Hwu, C. M. Liu, C. S. Fann, W. C. Ou-Yang and S. F. Lee. Linkage of schizophrenia with chromosome 1q loci in Taiwanese families. Mol Psychiatry. 8, 445-452, 2003. [JCR]　[WOS]
C.S.J. Fann, C. J. Chang, W. C. Chou and I. B. Lian. On the tail probability of the longest well-matching run. Statistics & Probability Letters. 63, 267-274, 2003. [JCR]　[WOS]
P. Stopkova, T. Saito, C. S. Fann, D. F. Papolos, J. Vevera, I. Paclt, I. Zukov, R. Stryjer, R. D. Strous and H. M. Lachman. Polymorphism screening of PIP5K2A: a candidate gene for chromosome 10p-linked psychiatric disorders. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics. 123B, 50-58, 2003. [JCR]　[WOS]
Y. M. Lin, H. C. Yang, T. J. Lai, C. S. Fann and H. S. Sun. Receptor mediated effect of serotonergic transmission in patients with bipolar affective disorder. J Med Genet. 40, 781-786, 2003. [JCR]　[WOS]
C.S.J. Fann, J. Y. Chen, C. W. Wu and C. W. Chi. Reply to: Regarding clinical implications of chromosomal abnormalities in gastric adenocarcinomas. Genes Chromosomes & Cancer. 38, 204-206, 2003. [JCR]　[WOS]
S. Y. Wu, C. S. Fann, Y. S. Jou, J. W. Chen and W. H. Pan. Association between markers in chromosomal region 17q23 and young onset hypertension: a TDT study. J Med Genet. 39, 42-44, 2002. [JCR]　[WOS]
Y. T. Chang, H. S. Sun, C. S. Fann, C. J. Chang, Z. H. Liao, J. L. Huang, E. W. Loh, W. Y. Yu and A. T. Cheng. Association of the gamma-aminobutyric acid A receptor gene cluster with alcohol dependence in Taiwanese Han. Mol Psychiatry. 7, 828-829, 2002. [JCR]　[WOS]
H. F. Sun, Y. T. Chang, C. S. Fann, C. J. Chang, Y. H. Chen, Y. P. Hsu, W. Y. Yu and A. T. Cheng. Association study of novel human serotonin 5-HT(1B) polymorphisms with alcohol dependence in Taiwanese Han. Biol Psychiatry. 51, 896-901, 2002. [JCR]　[WOS]
T. J. Lai, C. Y. Wu, C.S.J. Fann, T. M. Chen and S. S. Sun. Association Study of the Tryptophan Hydroxylase Gene Polymorephism and Bipolar Affective Disorder In Taiwan. J Genet Mol Biol. 13, 101-104, 2002. [JCR]　[WOS]
C. W. Wu, G. D. Chen, C. S. Fann, A. F. Lee, C. W. Chi, J. M. Liu, U. Weier and J. Y. Chen. Clinical implications of chromosomal abnormalities in gastric adenocarcinomas. Genes Chromosomes Cancer. 35, 219-231, 2002. [JCR]　[WOS]
Z. Harish, A. C. Bregante, C. Morgan, C. S. Fann, C. M. Callaghan, M. A. Witt, K. A. Levinson and W. B. Caspe. A comprehensive inner-city asthma program reduces hospital and emergency room utilization. Annals of Allergy Asthma & Immunology. 86, 185-189, 2001. [JCR]　[WOS]
D. L. Brown, C. S. Fann and C. J. Chang. Meta-analysis of effectiveness and safety of abciximab versus eptifibatide or tirofiban in percutaneous coronary intervention. Am J Cardiol. 87, 537-541, 2001. [JCR]　[WOS]
T. Saito, F. Guan, D. F. Papolos, S. Lau, M. Klein, C. S. Fann and H. M. Lachman. Mutation analysis of SYNJ1: a possible candidate gene for chromosome 21q22-linked bipolar disorder. Mol Psychiatry. 6, 387-395, 2001. [JCR]　[WOS]
M. L. Huang, L. Y. Chiu, W. H. Pan, C. M. Yang, C. Y. Hu, D. B. Lin, C.S. J. Fann and M. S. Ho. Negative association between HLA-A2 and a low antibody response to hepatitis B vaccine in Bunun ethnic children. J Genet Mol Biol. 12, 151-160, 2001. [JCR]　[WOS]
T. Saito, F. Guan, D. F. Papolos, N. Rajouria, C. S. Fann and H. M. Lachman. Polymorphism in SNAP29 gene promoter region associated with schizophrenia. Mol Psychiatry. 6, 193-201, 2001. [JCR]　[WOS]
C. N. Wu, Y. C. Lin, C. Fann, N. S. Liao, S. R. Shih and M. S. Ho. Protection against lethal enterovirus 71 infection in newborn mice by passive immunization with subunit VP1 vaccines and inactivated virus. Vaccine. 20, 895-904, 2001. [JCR]　[WOS]
C. M. Liu, H. G. Hwu, M. W. Lin, W. C. Ou-Yang, S. F. Lee, C. S. Fann, S. H. Wong and S. H. Hsieh. Suggestive evidence for linkage of schizophrenia to markers at chromosome 15q13-14 in Taiwanese families. American Journal of Medical Genetics. 105(8), 658-661, 2001. [JCR]　[WOS]
C. J. Chang, C. S. Fann. Using data mining to address heterogeneity in the Southampton data. Genet Epidemiol. 21 Suppl 1, S180-185, 2001. [JCR]　[WOS]
D. L. Brown, C. S. Fann and C. J. Chang. Effect of glycoprotein IIb/IIIa inhibitors on the individual components of composite endpoints used in clinical trials of unstable angina and non-Q-wave myocardial infarction. Cardiovascular Drugs and Therapy. 14, 253-258, 2000. [JCR]　[WOS]
W. H. Pan, J. W. Chen, C. Fann, Y. S. Jou and S. Y. Wu. Linkage analysis with candidate genes: the Taiwan young-onset hypertension genetic study. Hum Genet. 107, 210-215, 2000. [JCR]　[WOS]
S. Wassertheil-Smoller, C.S.J. Fann, R. M. Allman, H. R. Black, G. H. Camel, B. Davis, K. Masaki, S. Pressel, R. Prineas, J. Stamler and T. M. Vogt. Relation of low body mass to death and stroke in the systolic hypertension in the elderly program. Arch Intern Med. 160, 494-500, 2000. [JCR]　[WOS]
C. S. Fann, Y. Y. Shugart, H. Lachman, A. Collins and C. J. Chang. The impact of redefining affection status for alcoholism on affected-sib-pair analysis. Genet Epidemiol. 17 Suppl 1, S151-156, 1999. [JCR]　[WOS]
E. I. Ginns, P. St Jean, R. A. Philibert, M. Galdzicka, P. Damschroder-Williams, B. Thiel, R. T. Long, L. J. Ingraham, H. Dalwaldi, M. A. Murray, M. Ehlert, S. Paul, B. G. Remortel, A. P. Patel, M. C. Anderson, C. Shaio, E. Lau, I. Dymarskaia, B. M. Martin, B. Stubblefield, K. M. Falls, J. P. Carulli, T. P. Keith, C. S. Fann, S. M. Paul and et al. A genome-wide search for chromosomal loci linked to mental health wellness in relatives at high risk for bipolar affective disorder among the Old Order Amish. Proceedings of the National Academy of Sciences of the United States of America. 95, 15531-15536, 1998. [JCR]　[WOS]
W. Li, C. S. Fann and J. Ott. Low-order polynomial trends of female-to-male map distance ratios along human chromosomes. Hum Hered. 48, 266-270, 1998. [JCR]　[WOS]
F. Haghighi, W. Li and C. S. Fann. Affected-sib-pair analyses of bipolar disorder using data on chromosome 18. Genet Epidemiol. 14, 641-646, 1997. [JCR]　[WOS]
Fann CS, Ott J. Parsimonious estimation of sex-specific map distances by stepwise maximum likelihood regression. GENOMICS. 29(3), 571-575, 1995-10. [JCR]　[WOS]
Pauls DL, Ott J, Paul SM, Allen CR, Fann CS, Carulli JP, Falls KM, Bouthillier CA, Gravius TC, Keith TP, et al. Linkage analyses of chromosome 18 markers do not identify a major susceptibility locus for bipolar affective disorder in the Old Order Amish. AMERICAN JOURNAL OF HUMAN GENETICS. 57(3), 636-643, 1995-09. [JCR]　[WOS]

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