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Plos One|October 14, 2014
Sample size determination for individual bioequivalence inferenceChieh Chiang, Chin-Fu Hsiao, Jen-Pei LiuPharmaceutical Statistics|February 27, 2010
An alternative phase II/III design for continuous endpointsWong-Shian Huang, Jen-pei Liu, Chin-Fu HsiaoJournal of Computational Biology : a Journal of Computational Molecular Cell Biology|November 25, 2005
Evaluation of experimental designs for two-color cDNA microarraysChu-Wen Yang, Chin-Fu Hsiao, Chen-Kung ChouJournal of Biopharmaceutical Statistics|October 31, 2003
A group sequential approach to evaluation of bridging studiesChin-Fu Hsiao, Jia-Zhen Xu, Jen-Pei LiuJournal of Biopharmaceutical Statistics|February 11, 2005
A two-stage design for bridging studiesChin-Fu Hsiao, Jia-Zhen Xu, Jen-Pei LiuJournal of Biopharmaceutical Statistics|September 6, 2012
Design and evaluation of multiregional trials with heterogeneous treatment effect across regionsChi-Tian Chen, H M James Hung, Chin-Fu HsiaoPlos One|July 1, 2017
Sample size determination for a specific region in multiregional clinical trials with multiple co-primary endpointsWong-Shian Huang, Hui-Nien Hung, Toshimitsu Hamasaki, et al.Journal of Biopharmaceutical Statistics|September 6, 2012
Statistical methods for bridging studiesShein-Chung Chow, Chieh Chiang, Jen-pei Liu, et al.Journal of Biopharmaceutical Statistics|May 25, 2010
Sample size determination for a specific region in a multiregional trialFeng-Shou Ko, Hsiao-Hui Tsou, Jen-Pei Liu, et al.Journal of Biopharmaceutical Statistics|January 16, 2007
Use of prior information for Bayesian evaluation of bridging studiesChin-Fu Hsiao, Yu-Yi Hsu, Hsiao-Hui Tsou, et al.Pageof 32