| Publication | Date of Publication | Type |
|---|
| A quantitative framework to inform extrapolation decisions in children | 2025-01-22 | Paper |
| Group sequential designs for clinical trials when the maximum sample size is uncertain | 2025-01-02 | Paper |
| Validation of predicted individual treatment effects in out of sample respondents | 2024-12-12 | Paper |
| Recurrent events modelling of haemophilia bleeding events | 2024-11-27 | Paper |
| An information theoretic phase I--II design for molecularly targeted agents that does not require an assumption of monotonicity | 2024-11-21 | Paper |
| Subgroup analysis of treatment effects for misclassified biomarkers with time-to-event data | 2024-11-21 | Paper |
| Point estimation for adaptive trial designs. I: A methodological review | 2024-10-30 | Paper |
| Dose finding studies for therapies with late-onset toxicities: a comparison study of designs | 2024-10-30 | Paper |
| Practical implementation of the partial ordering continual reassessment method in a phase I combination-schedule dose-finding trial | 2024-10-30 | Paper |
| An order restricted multi-arm multi-stage clinical trial design | 2024-10-29 | Paper |
| Estimation of treatment effects following a sequential trial of multiple treatments | 2024-10-29 | Paper |
| Improving safety of the continual reassessment method via a modified allocation rule | 2024-10-29 | Paper |
| Optimizing subgroup selection in two-stage adaptive enrichment and umbrella designs | 2024-10-29 | Paper |
| Online error rate control for platform trials | 2024-10-28 | Paper |
| Point estimation for adaptive trial designs. II: Practical considerations and guidance | 2024-10-28 | Paper |
| A Bayesian multi-arm multi-stage clinical trial design incorporating information about treatment ordering | 2024-10-28 | Paper |
| Adding experimental treatment arms to multi-arm multi-stage platform trials in progress | 2024-10-14 | Paper |
| A multi-arm multi-stage platform design that allows preplanned addition of arms while still controlling the family-wise error | 2024-10-14 | Paper |
| A comparison of Bayesian information borrowing methods in basket trials and a novel proposal of modified exchangeability‐nonexchangeability method | 2024-03-04 | Paper |
| Bayesian Sample Size Determination Using Commensurate Priors to Leverage Preexperimental Data | 2023-10-30 | Paper |
| A novel statistical test for treatment differences in clinical trials using a response‐adaptive forward‐looking Gittins Index Rule | 2023-10-30 | Paper |
| Generalisations of a Bayesian decision-theoretic randomisation procedure and the impact of delayed responses | 2022-07-22 | Paper |
| An Information Theoretic Approach for Selecting Arms in Clinical Trials | 2022-07-08 | Paper |
| An evaluation of the bootstrap for model validation in mixture models | 2022-06-28 | Paper |
| Loss functions in restricted parameter spaces and their Bayesian applications | 2022-02-24 | Paper |
| Using a dose‐finding benchmark to quantify the loss incurred by dichotomization in Phase II dose‐ranging studies | 2021-07-09 | Paper |
| Assessing Systemic Drug Exposure in Repeated Dose Toxicity Studies in the Case of Complete and Incomplete Sampling | 2020-09-28 | Paper |
| Instrumental variable estimation in semi‐parametric additive hazards models | 2020-02-07 | Paper |
| A flexible design for advanced Phase I/II clinical trials with continuous efficacy endpoints | 2020-02-03 | Paper |
| A DIAGNOSTIC TOOL FOR CHECKING ASSUMPTIONS OF REGRESSION MIXTURE MODELS | 2019-12-05 | Paper |
| Confidence regions for treatment effects in subgroups in biomarker stratified designs | 2019-02-28 | Paper |
| A Bayesian adaptive design for clinical trials in rare diseases | 2018-08-14 | Paper |
| A review of the deterministic and diffusion approximations for stochastic chemical reaction networks | 2017-11-07 | Paper |
| An information-theoretic approach for selecting arms in clinical trials | 2017-08-08 | Paper |
| Loss Functions in Restricted Parameter Spaces and Their Bayesian Applications | 2017-06-07 | Paper |
| Statistical evaluation of toxicological assays with zero or near-to-zero proportions or counts in the concurrent negative control group: a tutorial | 2014-11-14 | Paper |
| A hybrid method to estimate the minimum effective dose for monotone and non‐monotone dose–response relationships | 2014-06-17 | Paper |
| Simultaneous confidence intervals that are compatible with closed testing in adaptive designs | 2014-01-17 | Paper |
| Using regression mixture models with non-normal data: examining an ordered polytomous approach | 2013-11-15 | Paper |
| A generalized Dunnett test for multi-arm multi-stage clinical studies with treatment selection | 2012-06-18 | Paper |
| Symmetric maximum kernel likelihood estimation | 2011-02-03 | Paper |
