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Journal of Biopharmaceutical Statistics|March 16, 2012
Dose as instrumental variable in exposure-safety analysis using count modelsJixian WangJournal of Biopharmaceutical Statistics|March 16, 2012
A portfolio-based approach to optimize proof-of-concept clinical trialsCraig Mallinckrodt, Geert Molenberghs, Charles Persinger, et al.Journal of Biopharmaceutical Statistics|March 1, 1993
Exposure analysis of dichotomous response measures in long-term studiesK E Peace, W H CarterJournal of Biopharmaceutical Statistics|March 1, 1993
Analysis of multivariate parallel-line bioassay with composite responses and composite doses, using canonical correlationsW Yuan, A M KshirsagarJournal of Biopharmaceutical Statistics|March 1, 1993
Evaluation of parametric and nonparametric two one-sided tests procedures for assessing bioequivalence of average bioavailabilityJ P Liu, C S WengJournal of Biopharmaceutical Statistics|May 1, 1996
Sample sizes for experiments with multivariate repeated measuresX Guo, W D JohnsonJournal of Biopharmaceutical Statistics|May 1, 1996
Baseline balance and conditional size: a reply to Overall et alS SennJournal of Biopharmaceutical Statistics|July 1, 1996
Application of response surface methodology and factorial designs to clinical trials for drug combination developmentW H StewartJournal of Biopharmaceutical Statistics|July 1, 1996
A note on assessing the superiority of a combination drug with a specific alternativeS M Snapinn, S K SarkarJournal of Biopharmaceutical Statistics|July 1, 1996
Two-stage designs for the logistic regression model in single-agent bioassaysW R Myers, R H Myers, W H Carter, et al.Pageof 216