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Biometrics|July 6, 2019
An adaptive trial design to optimize dose-schedule regimes with delayed outcomesRuitao Lin, Peter F Thall, Ying YuanBayesian Analysis|July 16, 2021
A Phase I-II Basket Trial Design to Optimize Dose-Schedule Regimes Based on Delayed OutcomesRuitao Lin, Peter F Thall, Ying YuanJournal of the American Statistical Association|May 18, 2022
BAGS: A Bayesian Adaptive Group Sequential Trial Design With Subgroup-Specific Survival ComparisonsRuitao Lin, Peter F Thall, Ying YuanThe Annals of Applied Statistics|November 4, 2022
BAYESIAN HIERARCHICAL RANDOM-EFFECTS META-ANALYSIS AND DESIGN OF PHASE I CLINICAL TRIALSRuitao Lin, Haolun Shi, Guosheng Yin, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|September 19, 2023
Novel Clinical Trial Designs with Dose Optimization to Improve Long-term OutcomesPeter F Thall, Yong Zang, Andrew G Chapple, et al.Biometrics|February 16, 2024
A generalized phase 1-2-3 design integrating dose optimization with confirmatory treatment comparisonYong Zang, Peter F Thall, Ying YuanPharmaceutical Statistics|April 11, 2023
Generalized phase I-II designs to increase long term therapeutic success ratePeter F Thall, Yong Zang, Ying YuanPharmaceutical Statistics|July 19, 2022
A Bayesian piecewise exponential phase II design for monitoring a time-to-event endpointYun Qing, Peter F Thall, Ying YuanJournal of Biopharmaceutical Statistics|July 2, 2019
On the relative efficiency of model-assisted designs: a conditional approachRuitao Lin, Ying YuanBiostatistics (Oxford, England)|April 16, 2019
Time-to-event model-assisted designs for dose-finding trials with delayed toxicityRuitao Lin, Ying YuanPageof 198