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Journal of Biopharmaceutical Statistics|October 31, 2017
Design, data monitoring, and analysis of clinical trials with co-primary endpoints: A reviewToshimitsu Hamasaki, Scott R Evans, Koko AsakuraJournal of Biopharmaceutical Statistics|September 22, 2017
Estimating the Optimal Personalized Treatment Strategy Based on Selected Variables to Prolong Survival via Random Survival Forest with Weighted BootstrapJincheng Shen, Lu Wang, Stephanie Daignault, et al.Journal of Biopharmaceutical Statistics|September 22, 2017
Biomarker enrichment considerations in oncology early development single-arm studiesHong Tian, Kevin LiuJournal of Biopharmaceutical Statistics|September 7, 2017
Definitions and statistical properties of master protocols for personalized medicine in oncologyLindsay A Renfro, Sumithra J MandrekarJournal of Biopharmaceutical Statistics|February 9, 2018
Optimal dose selection accounting for patient subpopulations in a randomized Phase II trial to maximize the success probability of a subsequent Phase III trialFumihiro Takahashi, Satoshi MoritaJournal of Biopharmaceutical Statistics|March 16, 2018
Multiplicity-Adjusted Confidence Limits in Risk Assessment with Quantal Response DataLucy KernsJournal of Biopharmaceutical Statistics|March 20, 2018
Determining sample size for a binary diagnostic test in the presence of verification biasGuogen Shan, Hua Zhang, Tao JiangJournal of Biopharmaceutical Statistics|March 28, 2018
Approximate confidence intervals for the likelihood ratios of a binary diagnostic test in the presence of partial disease verificationM A Montero-Alonso, J A Roldán-NofuentesJournal of Biopharmaceutical Statistics|July 9, 2008
Using adaptive tests for the analysis of repeated measurementsT W O'GormanJournal of Biopharmaceutical Statistics|July 9, 2008
Generalizability in nongaussian longitudinal clinical trial data based on generalized linear mixed modelsTony Vangeneugden, Geert Molenberghs, Annouschka Laenen, et al.Pageof 219