Pages that link to "Item:Q5717155"
From MaRDI portal
The following pages link to Combining Multiple Comparisons and Modeling Techniques in Dose‐Response Studies (Q5717155):
Displaying 46 items.
- Optimal designs for comparing curves (Q292879) (← links)
- Optimal discriminating designs for several competing regression models (Q355119) (← links)
- Robust \(T\)-optimal discriminating designs (Q385757) (← links)
- Simultaneous confidence bounds in monotone dose-response studies (Q393545) (← links)
- Adaptive isotonic estimation of the minimum effective and peak doses in the presence of covariates (Q419309) (← links)
- Response-adaptive dose-finding under model uncertainty (Q641106) (← links)
- Optimal designs for dose-response models with linear effects of covariates (Q1663125) (← links)
- Identification of minimum effective dose based on ratio of a normally distributed data under heteroscedasticity (Q2138246) (← links)
- Random-effects meta-analysis of phase I dose-finding studies using stochastic process priors (Q2233150) (← links)
- On optimal designs for clinical trials: an updated review (Q2301225) (← links)
- A comparative study of the dose-response analysis with application to the target dose estimation (Q2323265) (← links)
- Exact simultaneous confidence intervals for a finite set of contrasts of three, four or five generally correlated normal means (Q2359467) (← links)
- On construction of the smallest one-sided confidence interval for the difference of two proportions (Q2380102) (← links)
- Exact simultaneous confidence bands for quadratic and cubic polynomial regression with applications in dose response study (Q2803539) (← links)
- Dose response signal detection under model uncertainty (Q2809526) (← links)
- Dose-response curve estimation: a semiparametric mixture approach (Q2893416) (← links)
- Practical considerations for using functional uniform prior distributions for dose-response estimation in clinical trials (Q2931052) (← links)
- Adaptive dose-finding: Proof of concept with type I error control (Q3056472) (← links)
- Sequential Methods in Multi-Arm Clinical Trials (Q3068083) (← links)
- Adaptive Dc-optimal designs for dose finding based on a continuous efficacy endpoint (Q3076087) (← links)
- Many-to-one comparison of nonlinear growth curves for Washington's Red Delicious apple (Q3168311) (← links)
- Testing effect of a drug using multiple nested models for the dose–response (Q3459939) (← links)
- Unimodal regression using Bernstein–Schoenberg splines and penalties (Q3465354) (← links)
- A Two-Stage Stepwise Estimation Procedure (Q3506484) (← links)
- Stepwise Confidence Intervals for Monotone Dose–Response Studies (Q3530108) (← links)
- A finite sample comparison of nonparametric estimates of the effective dose in quantal bioassay (Q3589957) (← links)
- Bayesian Nonparametric Estimation of Continuous Monotone Functions with Applications to Dose–Response Analysis (Q3623757) (← links)
- Comparison of different approaches for dose response analysis (Q4626710) (← links)
- Multiple confidence intervals for selected parameters adjusted for the false coverage rate in monotone dose–response microarray experiments (Q5280189) (← links)
- Dose‐finding methods for Phase I clinical trials using pharmacokinetics in small populations (Q5280197) (← links)
- Likelihood ratio tests for a dose‐response effect using multiple nonlinear regression models (Q5347418) (← links)
- Combining Multiple Comparisons and Modeling Techniques in Dose‐Response Studies (Q5717155) (← links)
- Leadership in Statistics: Increasing Our Value and Visibility (Q5868170) (← links)
- The Tukey trend test: Multiplicity adjustment using multiple marginal models (Q6055568) (← links)
- Adaptive dose‐response studies to establish proof‐of‐concept in learning‐phase clinical trials (Q6068332) (← links)
- Identifying Alert Concentrations Using a Model-Based Bootstrap Approach (Q6079691) (← links)
- Model selection characteristics when using MCP‐Mod for dose–response gene expression data (Q6089914) (← links)
- DROID: dose-ranging approach to optimizing dose in oncology drug development (Q6589229) (← links)
- Statistical considerations in model-based dose finding for binary responses under model uncertainty (Q6615891) (← links)
- A class of computational methods to reduce selection bias when designing phase 3 clinical trials (Q6618489) (← links)
- Bayesian hierarchical EMAX model for dose-response in early phase efficacy clinical trials (Q6624678) (← links)
- A comparative study of in vitro dose-response estimation under extreme observations (Q6625339) (← links)
- Optimal adaptive allocation using deep reinforcement learning in a dose-response study (Q6626773) (← links)
- Generalized multiple contrast tests in dose-response studies (Q6627492) (← links)
- cLRT-Mod: an efficient methodology for pharmacometric model-based analysis of longitudinal phase II dose finding studies under model uncertainty (Q6627793) (← links)
- A straightforward meta-analysis approach for oncology phase I dose-finding studies (Q6628513) (← links)
