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机构 日期 题名 作者
國家衛生研究院 2016-06 FamPipe: An automatic analysis pipeline for analyzing sequencing data in families for disease studies Chung, RH;Tsai, WY;Kang, CY;Yao, PJ;Tsai, HJ;Chen, CH
國家衛生研究院 2016-02 SeqSIMLA2_exact: Simulate multiple disease sites in large pedigrees with given disease status for diseases with low prevalence Yao, PJ;Chung, RH
國家衛生研究院 2015-08-18 Effect of common genetic variants of growth arrest-specific 6 gene on insulin resistance, obesity and type 2 diabetes in an Asian population Hsieh, CH;Chung, RH;Lee, WJ;Lin, MW;Chuang, LM;Quertermous, T;Assimes, T;Hung, YJ;Yu, YW
國家衛生研究院 2015-05-15 A multi-SNP association test for complex diseases incorporating an optimal P-value threshold algorithm in nuclear families Wang, YT;Sung, PY;Lin, PL;Yu, YW;Chung, RH
國家衛生研究院 2015-01 SeqSIMLA2: Simulating correlated quantitative traits accounting for shared environmental effects in user-specified pedigree structure Chung, RH;Tsai, WY;Hsieh, CH;Hung, KY;Hsiung, CA;Hauser, ER
國家衛生研究院 2014-09-22 Family-based association test using both common and rare variants and accounting for directions of effects for sequencing data Chung, RH;Tsai, WY;Martin, ER
國家衛生研究院 2014-06-17 Identification of rare variants for hypertension with incorporation of linkage information Chiu, YF;Chung, RH;Lee, CY;Kao, HY;Hou, L;Hsu, FC
國家衛生研究院 2014-04 The association of genetic polymorphisms in the kappa-opioid receptor 1 gene with body weight, alcohol use, and withdrawal symptoms in patients with methadone maintenance Wang, SC;Tsou, HH;Chung, RH;Chang, YS;Fang, CP;Chen, CH;Ho, IK;Kuo, HW;Liu, SC;Shih, YH;Wu, HY;Huang, BH;Lin, KM;Chen, AC;Hsiao, CF;Liu, YL
國家衛生研究院 2013-09-04 Pathway-PDT: A flexible pathway analysis tool for nuclear families Park, YS;Schmidt, M;Martin, ER;Pericak-Vance, MA;Chung, RH
國家衛生研究院 2013-06-20 SeqSIMLA: A sequence and phenotype simulation tool for complex disease studies Chung, RH;Shih, CC

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