Pages that link to "Item:Q3506509"
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The following pages link to Determining the Effective Sample Size of a Parametric Prior (Q3506509):
Displaying 39 items.
- Bayesian sample size determination for binary regression with a misclassified covariate and no gold standard (Q693273) (← links)
- On divergence measures leading to Jeffreys and other reference priors (Q899027) (← links)
- Bayesian models and decision algorithms for complex early phase clinical trials (Q903294) (← links)
- Meta-analytic-predictive use of historical variance data for the design and analysis of clinical trials (Q1658139) (← links)
- Web-based statistical tools for the analysis and design of clinical trials that incorporate historical controls (Q1663106) (← links)
- Control of type I error rates in Bayesian sequential designs (Q1738139) (← links)
- A phase I-II basket trial design to optimize dose-schedule regimes based on delayed outcomes (Q2057378) (← links)
- Bayesian hierarchical random-effects meta-analysis and design of phase I clinical trials (Q2080762) (← links)
- The Wasserstein impact measure (WIM): a practical tool for quantifying prior impact in Bayesian statistics (Q2157491) (← links)
- Random-effects meta-analysis of phase I dose-finding studies using stochastic process priors (Q2233150) (← links)
- Borrowing strength and borrowing index for Bayesian hierarchical models (Q2291343) (← links)
- Effective sample size for a mixture prior (Q2667587) (← links)
- Robust meta‐analytic‐predictive priors in clinical trials with historical control information (Q3465388) (← links)
- The Effective Sample Size (Q5080443) (← links)
- Graphical prior elicitation in univariate models (Q5085071) (← links)
- Inference and Decision Making for 21st-Century Drug Development and Approval (Q5868274) (← links)
- Iterated multisource exchangeability models for individualized inference with an application to mobile sensor data (Q6050943) (← links)
- Elastic priors to dynamically borrow information from historical data in clinical trials (Q6055896) (← links)
- Prior effective sample size in phase II clinical trials with mixed binary and continuous responses (Q6068062) (← links)
- DICE: A Bayesian model for early dose finding in phase I trials with multiple treatment courses (Q6068878) (← links)
- Optimality of testing procedures for survival data in the nonproportional hazards setting (Q6074503) (← links)
- Bayesian dose regimen assessment in early phase oncology incorporating pharmacokinetics and pharmacodynamics (Q6079344) (← links)
- The phoropter method: a stochastic graphical procedure for prior elicitation in univariate data models (Q6101006) (← links)
- Quantifying observed prior impact (Q6121775) (← links)
- Bayesian dynamic borrowing of historical information with applications to the analysis of large-scale assessments (Q6160305) (← links)
- BEAST: Bayesian hybrid design with flexible sample size adaptation for time-to-event endpoints (Q6560579) (← links)
- Bayesian gamma processes for optimizing condition-based maintenance under uncertainty (Q6574722) (← links)
- Discussion of: ``Specifying prior distributions in reliability applications'': towards new formal rules for informative prior elicitation? (Q6581566) (← links)
- SAM: self-adapting mixture prior to dynamically borrow information from historical data in clinical trials (Q6589223) (← links)
- Practical approaches to Bayesian sample size determination in non-inferiority trials with binary outcomes (Q6617468) (← links)
- REDOMA: Bayesian random-effects dose-optimization meta-analysis using spike-and-slab priors (Q6618357) (← links)
- A group-sequential randomized trial design utilizing supplemental trial data (Q6622279) (← links)
- A Bayesian adaptive marker-stratified design for molecularly targeted agents with customized hierarchical modeling (Q6627181) (← links)
- Bayesian leveraging of historical control data for a clinical trial with time-to-event endpoint (Q6627508) (← links)
- Propensity-score-based meta-analytic predictive prior for incorporating real-world and historical data (Q6627979) (← links)
- Bayesian modeling of a bivariate toxicity outcome for early phase oncology trials evaluating dose regimens (Q6628011) (← links)
- Bayesian semiparametric prior for historical control borrowing in clinical trials (Q6628120) (← links)
- Unit information prior for adaptive information borrowing from multiple historical datasets (Q6628251) (← links)
- Dose finding studies for therapies with late-onset toxicities: a comparison study of designs (Q6629421) (← links)
