Catey Bunce

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All published works
Action Title Year Authors
+ Common Statistical Issues in Ophthalmic Research 2022 Catey Bunce
Gabriela Czanner
+ Protocol amendments summary 2021 Daniel Fp Larkin
Kashfia Chowdhury
Caroline J Doré
Catey Bunce
Jennifer Burr
Emilia Caverly
Lisa French
Dimitra Kopsini
Anne Klepacz
Mathew K. Raynor
+ Survival Analysis vs Longitudinal Modeling With Multiple Imputation—a False Dichotomy—Reply 2021 Catey Bunce
Dun Jack Fu
Irene Stratton
+ PDF Chat The adaptive designs CONSORT extension (ACE) statement: a checklist with explanation and elaboration guideline for reporting randomised trials that use an adaptive design 2020 Munyaradzi Dimairo
Philip Pallmann
James Wason
Susan Todd
Thomas Jaki
Steven A. Julious
Adrian Mander
Christopher J. Weir
Franz Koenig
Marc K. Walton
+ PDF Chat Selective recruitment designs for improving observational studies using electronic health records 2020 James E. Barrett
Sera Aylin Cakiroglu
Catey Bunce
Anoop D Shah
Spiros Denaxas
+ Selective recruitment designs for improving observational studies using electronic health records 2019 James E. Barrett
Sera Aylin Cakiroglu
Catey Bunce
Anoop D Shah
Spiros Denaxas
+ Statistical analysis and design in ophthalmology: Toward optimizing your data 2019 Gabriela Czanner
Catey Bunce
+ Selective recruitment designs for improving observational studies using electronic health records 2019 James E. Barrett
Sera Aylin Cakiroglu
Catey Bunce
Anoop Shah
Spiros Denaxas
+ PDF Chat Ophthalmic statistics note 8: missing data—exploring the unknown 2015 Catey Bunce
Ana Quartilho
Nick Freemantle
Caroline J Doré
+ PDF Chat Certification figures and their accuracy 2015 Ana Quartilho
Antra Zekite
W Xing
Mohamed Loutfi
Catey Bunce
Richard Wormald
+ RIPOSTE: a framework for improving the design and analysis of laboratory-based research 2015 Nicholas G. D. Masca
E. Hensor
Victoria Cornelius
Francesca M. Buffa
Helen M. Marriott
James Eales
Michael Messenger
Amy E. Anderson
Chris Boot
Catey Bunce
+ RIPOSTE: a framework for improving the design and analysis of laboratory-based research Lack of reproducibility is an ongoing problem in some areas of the biomedical sciences. 2015 Nicholas G. D. Masca
E. Hensor
Victoria Cornelius
Francesca M. Buffa
Helen M. Marriott
James Eales
Michael Messenger
Amy E. Anderson
Chris Boot
Catey Bunce
+ PDF Chat Ophthalmic statistics note 5: diagnostic tests—sensitivity and specificity 2014 Luke J. Saunders
Haogang Zhu
Catey Bunce
Caroline J Doré
Nick Freemantle
David P. Crabb
+ PDF Chat Ophthalmic statistics note: the perils of dichotomising continuous variables 2014 Phillippa Cumberland
Gabriela Czanner
Catey Bunce
Caroline J Doré
Nick Freemantle
Marta García‐Fiñana
+ Attention should be given to multiplicity issues in systematic reviews 2008 Ralf Bender
Catey Bunce
Mike Clarke
Simon Gates
Stefan Lange
Nathan L. Pace
Kristian Thorlund
Common Coauthors
Commonly Cited References
Action Title Year Authors # of times referenced
+ Strategy for intention to treat analysis in randomised trials with missing outcome data 2011 Ian R. White
Nicholas J. Horton
James R. Carpenter
r. i. m. a. s. statistics
Stuart J. Pocock
2
+ The Revised CONSORT Statement for Reporting Randomized Trials: Explanation and Elaboration 2001 D G Altman
2
+ PDF Chat The CONSORT statement: revised recommendations for improving the quality of reports of parallel-group randomised trials 2001 David Moher
Kenneth F. Schulz
Douglas G. Altman
2
+ PDF Chat Deriving chemosensitivity from cell lines: Forensic bioinformatics and reproducible research in high-throughput biology 2009 Keith Baggerly
Kevin R. Coombes
2
+ PDF Chat Analysing randomised controlled trials with missing data: Choice of approach affects conclusions 2012 Shona Fielding
Peter Fayers
Craig Ramsay
2
+ PDF Chat Multiple Imputation 2015 Peng Li
Elizabeth A. Stuart
David B. Allison
2
+ PDF Chat Reporting recommendations for tumor marker prognostic studies (REMARK): explanation and elaboration 2012 Douglas G. Altman
Lisa M. McShane
Willi Sauerbrei
Sheila E. Taube
2
+ Assessing Individual Agreement 2007 Huiman X. Barnhart
Andrzej S. Kosinski
Michael Haber
2
+ Practical and statistical issues in missing data for longitudinal patient-reported outcomes 2013 Melanie L. Bell
Diane L. Fairclough
2
+ PDF Chat Increasing value and reducing waste in research design, conduct, and analysis 2014 John P. A. Ioannidis
Sander Greenland
Mark A. Hlatky
Muin J. Khoury
Malcolm Macleod
David Moher
Kenneth F. Schulz
Robert Tibshirani
2
+ PDF Chat Learning from our GWAS mistakes: from experimental design to scientific method 2012 Christophe G Lambert
Lynsey Black
2
+ PDF Chat Missing data 2007 Douglas G. Altman
Martin Bland
2
+ Designing Multi-arm Multi-stage Clinical Studies 2014 Thomas Jaki
1
+ Effect Measures for Meta‒Analysis of Trials with Binary Outcomes 2001 Jonathan J Deeks
Douglas G. Altman
1
+ The Design of Experiments 1935 Ronald Aylmer Fisher
1
+ PDF Chat Bivariate random-effects meta-analysis and the estimation of between-study correlation 2007 Richard D. Riley
Keith R. Abrams
Alex J. Sutton
Paul C. Lambert
John R. Thompson
1
+ Going Beyond the Grand Mean: Subgroup Analysis in Meta‐Analysis of Randomised Trials 2001 George Davey Smith
Matthias Egger
1
+ PDF Chat No solution yet for combining two independent studies in the presence of heterogeneity 2015 Andrea Gonnermann
Theodor Framke
Anika Großhennig
Armin Koch
1
+ Confidentiality and Trial Integrity Issues for Adaptive Designs 2006 Paul Gallo
1
+ Adaptive Dunnett tests for treatment selection 2007 Franz Koenig
Werner Brannath
Frank Bretz
Martin Posch
1
+ PDF Chat CONSORT for Reporting Randomized Controlled Trials in Journal and Conference Abstracts: Explanation and Elaboration 2008 Sally Hopewell
Mike Clarke
David Moher
Elizabeth Wager
Philippa Middleton
Douglas G. Altman
Kenneth F. Schulz
1
+ Sample size adjustment based on promising interim results and its application in confirmatory clinical trials 2015 YH Joshua Chen
Caiyan Li
KK Gordon Lan
1
+ Stochastically curtailed tests in long–term clinical trials 1982 K. K. Gordon Lan
Richard Simon
Max Halperin
1
+ Trial sequential analysis may establish when firm evidence is reached in cumulative meta-analysis 2007 Jørn Wetterslev
Kristian Thorlund
Jesper Brok
Christian Gluud
1
+ Testing multiple statistical hypotheses resulted in spurious associations: a study of astrological signs and health 2006 Peter C. Austin
Muhammad Mamdani
David N. Juurlink
Janet E. Hux
1
+ One‐ and two‐stage design proposals for a phase II trial comparing three active treatments with control using an ordered categorical endpoint 2008 John Whitehead
Thomas Jaki
1
+ Parameter estimation following group sequential hypothesis testing 1990 Scott S. Emerson
Thomas R. Fleming
1
+ Similarities and Differences of Bayesian Designs and Adaptive Designs for Medical Devices: A Regulatory View 2013 Gregory Campbell
1
+ Stopping a trial early – and then what? 2012 Janet Wittes
1
+ Statistical Principles for Clinical Trials 1998 Robert R. Kay
1
+ Group Sequential Methods with Applications to Clinical Trials 1999 Christopher Jennison
Bruce W. Turnbull
1
+ Sample Size Tables for Clinical Studies 2008 David Machin
Michael J. Campbell
Say Beng Tan
Sze Huey Tan
1
+ PDF Chat Adaptive sample size modification in clinical trials: start small then ask for more? 2015 Christopher Jennison
Bruce W. Turnbull
1
+ Benefit–risk assessment: the use of clinical utility index 2010 Danièle Ouellet
1
+ The advantages and disadvantages of adaptive designs for clinical trials 2004 Péter Bauer
Werner Brannath
1
+ PDF Chat Optimal multistage designs for randomised clinical trials with continuous outcomes 2011 James Wason
Adrian Mander
Simon G. Thompson
1
+ Better Reporting of Harms in Randomized Trials: An Extension of the CONSORT Statement 2004 John P. A. Ioannidis
1
+ Designed Extension of Studies Based on Conditional Power 1995 Michael A. Proschan
Sally Hunsberger
1
+ PDF Chat Flexible sequential designs for multi‐arm clinical trials 2014 Dominic Magirr
Nigel Stallard
Thomas Jaki
1
+ Monitoring clinical trials: Conditional or predictive power? 1986 David J. Spiegelhalter
Laurence S. Freedman
Patrick R. Blackburn
1
+ PDF Chat Simulation study for evaluating the performance of response-adaptive randomization 2014 Yining Du
Xuan Wang
J. Jack Lee
1
+ Multiple Testing in Clinical Trials 2005 Alexei Dmitrienko
Jason C. Hsu
1
+ Sampling of Populations: Methods and Applications 1992 Eric R. Ziegel
Patrick Lévy
S. Lemeshaw
1
+ Cumulating evidence from randomized trials: Utilizing sequential monitoring boundaries for cumulative meta-analysis 1997 Janice Pogue
Salim Yusuf
1
+ Confirmatory Clinical Trials with an Adaptive Design 2006 Armin Koch
1
+ Blinded Sample Size Reestimation in Multiarmed Clinical Trials 2000 Meinhard Kieser
Tim Friede
1
+ Coordinating Data Monitoring Committees and Adaptive Clinical Trial Designs 2008 Jay Herson
1
+ Sequential Treatment Assignment with Balancing for Prognostic Factors in the Controlled Clinical Trial 1975 Stuart J. Pocock
Richard Simon
1
+ PDF Chat Three steps to writing adaptive study protocols in the early phase clinical development of new medicines 2014 Ulrike Lorch
Martin O’Kane
Jӧrg Täubel
1
+ Combining different phases in the development of medical treatments within a single trial 1999 Péter Bauer
Meinhard Kieser
1