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Controlled Clinical Trials|December 14, 2004
Statistical comparison of random allocation methods in cancer clinical trialsAtsushi Hagino, Chikuma Hamada, Isao Yoshimura, et al.Journal of Human Genetics|August 19, 2006
The confidence interval of allelic odds ratios under the Hardy-Weinberg disequilibriumYasunori Sato, Hideki Suganami, Chikuma Hamada, et al.Statistical Applications in Genetics and Molecular Biology|December 4, 2009
Statistical screening method for genetic factors influencing susceptibility to common diseases in a two-stage genome-wide association studyYasunori Sato, Nan Laird, Hideki Suganami, et al.International Journal of Clinical Oncology|April 25, 2009
The role of meta-analysis in cancer clinical trialsChikuma HamadaJournal of Toxicologic Pathology|February 27, 2018
Statistical analysis for toxicity studiesChikuma HamadaPharmaceutical Statistics|August 17, 2018
A Bayesian hierarchal modeling approach to shortening phase I/II trials of anticancer drug combinationsShinjo Yada, Chikuma HamadaTherapeutic Innovation & Regulatory Science|September 19, 2018
Adaptive Seamless Design for Establishing Pharmacokinetic and Efficacy Equivalence in Developing BiosimilarsRyuji Uozumi, Chikuma HamadaPharmaceutical Statistics|November 29, 2016
Application of Bayesian hierarchical models for phase I/II clinical trials in oncologyShinjo Yada, Chikuma HamadaContemporary Clinical Trials Communications|April 27, 2018
Analyses of drug combinations using missing data shortens trial periods in phase I/II oncology trialsShinjo Yada, Chikuma HamadaJournal of Biopharmaceutical Statistics|February 17, 2016
Interim decision-making strategies in adaptive designs for population selection using time-to-event endpointsRyuji Uozumi, Chikuma HamadaPageof 13