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Journal of Biopharmaceutical Statistics|June 23, 2004
Hypotheses and type I error in active-control noninferiority trialsGang Chen, Yong-Cheng Wang, George Y H ChiJournal of Biopharmaceutical Statistics|April 6, 2006
A ratio test in active control non-inferiority trials with a time-to-event endpointYong-Cheng Wang, Gang Chen, George Y H ChiJournal of Biopharmaceutical Statistics|March 19, 2004
Evaluation of health-related quality-of-life measures in oncology drug product applications: issues and concernsRajeshwari Sridhara, Gang Chen, George Y H Chi, et al.Statistics in Medicine|January 10, 2003
Design and analysis of non-inferiority mortality trials in oncologyMark Rothmann, Ning Li, Gang Chen, et al.Fundamental & Clinical Pharmacology|November 30, 2005
Some issues with composite endpoints in clinical trialsGeorge Y H ChiStatistics in Medicine|February 3, 2007
A method for testing a prespecified subgroup in clinical trialsYang Song, George Y H ChiJournal of Biopharmaceutical Statistics|November 9, 2010
Understanding the FDA guidance on adaptive designs: historical, legal, and statistical perspectivesQing Liu, George Y H ChiContemporary Clinical Trials Communications|May 9, 2018
On clinical trials with a high placebo response rateGeorge Y H Chi, Yihan Li, Yanning Liu, et al.Journal of Molecular Modeling|June 5, 2014
Mechanistic exploration of the catalytic cycles for the CO oxidation by O2 over FeO(1-3) application of the energetic span modelHuan-Jiang Wang, Yong-Cheng WangStatistics in Medicine|February 21, 2012
An entropy-based nonparametric test for the validation of surrogate endpointsXiaopeng Miao, Yong-Cheng Wang, Ashis GangopadhyayPageof 767