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S Faye Williamson

Showing results (1-10 of 10) with videos related to

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Biometrics|July 20, 2019
A response-adaptive randomization procedure for multi-armed clinical trials with normally distributed outcomesS Faye Williamson, Sofía S Villar
Computational Statistics & Data Analysis|June 14, 2022
Generalisations of a Bayesian decision-theoretic randomisation procedure and the impact of delayed responsesS Faye Williamson, Peter Jacko, Thomas Jaki
Clinical Trials (London, England)|February 12, 2025
Hybrid sample size calculations for cluster randomised trials using assuranceS Faye Williamson, Svetlana V Tishkovskaya, Kevin J Wilson
Computational Statistics & Data Analysis|June 21, 2017
A Bayesian adaptive design for clinical trials in rare diseasesS Faye Williamson, Peter Jacko, Sofía S Villar, et al.
Diagnostic and Prognostic Research|August 18, 2023
Sample size determination for point-of-care COVID-19 diagnostic tests: a Bayesian approachS Faye Williamson, Cameron J Williams, B Clare Lendrem, et al.
Statistics in Medicine|April 11, 2022
Bayesian sample size determination for diagnostic accuracy studiesKevin J Wilson, S Faye Williamson, A Joy Allen, et al.
Journal of Clinical Epidemiology|July 5, 2022
Subgroup analyses in randomized controlled trials frequently categorized continuous subgroup informationS Faye Williamson, Michael J Grayling, Adrian P Mander, et al.
Statistics in Biopharmaceutical Research|June 30, 2021
Efficient Adaptive Designs for Clinical Trials of Interventions for COVID-19Nigel Stallard, Lisa Hampson, Norbert Benda, et al.
Trials|October 5, 2023
Medicines and Healthcare products Regulatory Agency's "Consultation on proposals for legislative changes for clinical trials": a response from the Trials Methodology Research Partnership Adaptive Designs Working Group, with a focus on data sharingMartin Law, Dominique-Laurent Couturier, Babak Choodari-Oskooei, et al.
Trials|November 22, 2023
Correction: Medicines and Healthcare products Regulatory Agency's "Consultation on proposals for legislative changes for clinical trials": a response from the Trials Methodology Research Partnership Adaptive Designs Working Group, with a focus on data sharingMartin Law, Dominique-Laurent Couturier, Babak Choodari-Oskooei, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Biometrics|July 20, 2019
A response-adaptive randomization procedure for multi-armed clinical trials with normally distributed outcomesS Faye Williamson, Sofía S Villar
Computational Statistics & Data Analysis|June 14, 2022
Generalisations of a Bayesian decision-theoretic randomisation procedure and the impact of delayed responsesS Faye Williamson, Peter Jacko, Thomas Jaki
Clinical Trials (London, England)|February 12, 2025
Hybrid sample size calculations for cluster randomised trials using assuranceS Faye Williamson, Svetlana V Tishkovskaya, Kevin J Wilson
Computational Statistics & Data Analysis|June 21, 2017
A Bayesian adaptive design for clinical trials in rare diseasesS Faye Williamson, Peter Jacko, Sofía S Villar, et al.
Diagnostic and Prognostic Research|August 18, 2023
Sample size determination for point-of-care COVID-19 diagnostic tests: a Bayesian approachS Faye Williamson, Cameron J Williams, B Clare Lendrem, et al.
Statistics in Medicine|April 11, 2022
Bayesian sample size determination for diagnostic accuracy studiesKevin J Wilson, S Faye Williamson, A Joy Allen, et al.
Journal of Clinical Epidemiology|July 5, 2022
Subgroup analyses in randomized controlled trials frequently categorized continuous subgroup informationS Faye Williamson, Michael J Grayling, Adrian P Mander, et al.
Statistics in Biopharmaceutical Research|June 30, 2021
Efficient Adaptive Designs for Clinical Trials of Interventions for COVID-19Nigel Stallard, Lisa Hampson, Norbert Benda, et al.
Trials|October 5, 2023
Medicines and Healthcare products Regulatory Agency's "Consultation on proposals for legislative changes for clinical trials": a response from the Trials Methodology Research Partnership Adaptive Designs Working Group, with a focus on data sharingMartin Law, Dominique-Laurent Couturier, Babak Choodari-Oskooei, et al.
Trials|November 22, 2023
Correction: Medicines and Healthcare products Regulatory Agency's "Consultation on proposals for legislative changes for clinical trials": a response from the Trials Methodology Research Partnership Adaptive Designs Working Group, with a focus on data sharingMartin Law, Dominique-Laurent Couturier, Babak Choodari-Oskooei, et al.
Pageof 1