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Pharmaceutical Statistics|June 14, 2012
Testing bioequivalence for multiple formulations with power and sample size calculationsCheng Zheng, Jixian Wang, Lihui ZhaoPharmaceutical Statistics|February 10, 2015
Modifications of sequential designs in bioequivalence trialsCheng Zheng, Lihui Zhao, Jixian WangPharmaceutical Statistics|November 3, 2017
A simple, doubly robust, efficient estimator for survival functions using pseudo observationsJixian WangJournal of Biopharmaceutical Statistics|August 20, 2010
Many-to-one comparison after sample size reestimation for trials with multiple treatment arms and treatment selectionJixian WangJournal of Biopharmaceutical Statistics|March 16, 2012
Dose as instrumental variable in exposure-safety analysis using count modelsJixian WangPharmaceutical Statistics|December 22, 2019
Covariate adjustment for randomized controlled trials revisitedJixian WangResearch Synthesis Methods|June 11, 2015
Semiparametric hazard function estimation in meta-analysis for time to event dataJixian WangBiometrical Journal. Biometrische Zeitschrift|September 16, 2006
An adaptive two-stage design with treatment selection using the conditional error function approachJixian WangPharmaceutical Statistics|February 15, 2021
Response-adaptive trial designs with accelerated Thompson samplingJixian WangPageof 112