scientific article; zbMATH DE number 3322699

From MaRDI portal
Revision as of 03:55, 7 March 2024 by Import240305080351 (talk | contribs) (Created automatically from import240305080351)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)

Publication:5602015

zbMath0203.21505MaRDI QIDQ5602015

G. Barrie Wetherill

Publication date: 1963


Title: zbMATH Open Web Interface contents unavailable due to conflicting licenses.



Related Items (29)

Efficient Robbins–Monro procedure for multivariate binary dataOn a new stopping rule for stochastic approximationSequential design for binary dose-response experimentsOn D-optimal designs for binary dataOptimal Bayesian estimation of the median effective doseSequential empirical Bayesian design for sensitivity experimentsRobust and efficient estimation of effective doseEstimators and D-optimal experimental designs for mixtures of binary responsesPerformance Measures in Dose‐Finding ExperimentsBayesian sequential experimental design for binary response data with application to electromyographic experimentsAdaptive isotonic estimation of the minimum effective and peak doses in the presence of covariatesDesign issues for generalized linear models: a reviewUnnamed ItemThree-phase optimal design of sensitivity experimentsCommentary on: ``Three-phase optimal design for sensitivity experimentsCumulative cohort design for dose-findingLikelihood‐Based Experimental Design for Estimation of Ed 50Group up-and-down designs for dose-findingDose Finding for Continuous and Ordinal Outcomes with a Monotone Objective Function: A Unified ApproachSaddlepoint approach to inference for response probabilities under the logistic response modelEmpirical evaluation of a model of global psychophysical judgments. IV : Forms for the weighting functionThe application of stochastic approximation methods to the bio-assay problemA distribution‐free approach to qdantal response assaysEfficient Construction of Test Inversion Confidence Intervals Using Quantile RegressionA new sequential approximation methodAn Optimizing Up-and-Down DesignStrong consistency of maximum quasi-likelihood estimators in generalized linear models with fixed and adaptive designsOperating characteristics of the standard phase I clinical trial design.Bias induced by adaptive dose-finding designs




This page was built for publication: