Stephen L. George

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All published works
Action Title Year Authors
+ Assessment of treatment effect heterogeneity for multiregional randomized clinical trials 2024 Haotian Zhuang
Xiaofei Wang
Stephen L. George
+ Futility monitoring for randomized clinical trials with non-proportional hazards: An optimal conditional power approach 2023 Xiaofei Wang
Stephen L. George
+ Commentary on Harun et al.: The use of historical controls in randomized clinical trials 2023 Stephen L. George
+ PDF Chat Design and analysis of biomarker-integrated clinical trials with adaptive threshold detection and flexible patient enrichment 2020 Ting Wang
Xiaofei Wang
Stephen L. George
Haibo Zhou
+ A signature enrichment design with Bayesian adaptive randomization 2020 Fang Xia
Stephen L. George
Jing Ning
Liang Li
Xuelin Huang
+ PDF Chat Bias-adjusted Kaplan–Meier survival curves for marginal treatment effect in observational studies 2019 Xiaofei Wang
Fangfang Bai
Herbert Pang
Stephen L. George
+ Enriched Biomarker‐Driven Clinical Trials 2019 Xiaofei Wang
Jianwen Cai
Stephen L. George
+ PDF Chat Auxiliary variable–enriched biomarker‐stratified design 2018 Ting Wang
Xiaofei Wang
Haibo Zhou
Jianwen Cai
Stephen L. George
+ PDF Chat On Enrichment Strategies for Biomarker Stratified Clinical Trials 2017 Xiaofei Wang
Jingzhu Zhou
Ting Wang
Stephen L. George
+ PDF Chat Time‐dependent classification accuracy curve under marker‐dependent sampling 2016 Zhaoyin Zhu
Xiaofei Wang
Paramita Saha‐Chaudhuri
Andrzej S. Kosinski
Stephen L. George
+ A Multi-State Model for Designing Clinical Trials for Testing Overall Survival Allowing for Crossover after Progression 2016 Fang Xia
Stephen L. George
Xiaofei Wang
+ A Multi-State Model for Designing Clinical Trials for Testing Overall Survival Allowing for Crossover after Progression 2016 Fang Xia
Stephen L. George
Xiaofei Wang
+ PDF Chat Problematic trial detection in ClinicalTrials.gov 2015 Chris Hartgerink
Stephen L. George
+ PDF Chat A Multi-State Model for Designing Clinical Trials for Testing Overall Survival Allowing for Crossover after Progression 2015 Fang Xia
Stephen L. George
Xiaofei Wang
+ A Multi-state Model for Designing Clinical Trials for Testing Overall Survival Allowing for Crossover after Progression 2015 M.S. Fang Xia
Stephen L. George
Xiaofei Wang
+ PDF Chat Estimation of AUC or Partial AUC Under Test-Result-Dependent Sampling 2012 Xiaofei Wang
Junling Ma
Stephen L. George
Haibo Zhou
+ PDF Chat ROC curve estimation under test-result-dependent sampling 2012 Xiangyu Wang
JinHua Ma
Stephen L. George
+ Targeted Clinical Trials 2011 Stephen L. George
Xiaofei Wang
+ PDF Chat Multiple testing of treatment‐effect‐modifying biomarkers in a randomized clinical trial with a survival endpoint 2011 Stefan Michiels
Richard F. Potthoff
Stephen L. George
+ PDF Chat Clinical Trials Data Collection: When Less Is More 2010 Daniel J. Sargent
Stephen L. George
+ PDF Chat A permutation-based multiple testing method for time-course microarray experiments 2009 Insuk Sohn
Kouros Owzar
Stephen L. George
Sujong Kim
Sin‐Ho Jung
+ PDF Chat Sample size calculation for microarray experiments with blocked one-way design 2009 Sin‐Ho Jung
Insuk Sohn
Stephen L. George
Liping Feng
Phyllis C. Leppert
+ PDF Chat Between-Arm Comparisons in Randomized Phase II Trials 2009 Sin‐Ho Jung
Stephen L. George
+ PDF Chat Flexible Phase I Clinical Trials: Allowing for Nonbinary Toxicity Response and Removal of Other Common Limitations 2009 Richard F. Potthoff
Stephen L. George
+ PDF Chat Statistical Issues in Translational Cancer Research 2008 Stephen L. George
+ Design of Clinical Trials of Targeted Therapy 2007 Stephen L. George
+ PDF Chat Randomized Clinical Trial Design for Assessing Noninferiority When Superiority Is Expected 2007 Boris Freidlin
Edward L. Korn
Stephen L. George
Robert J. Gray
+ Phase I Clinical Trials With Non-Binary Toxicity Response 2007 Richard F. Potthoff
Stephen L. George
+ <i>p</i>-Value Calculation for Multistage Phase II Cancer Clinical Trials 2006 Sin‐Ho Jung
Kouros Owzar
Stephen L. George
Taiyeong Lee
+ Rejoinder 2006 Sin‐Ho Jung
Kouros Owzar
Stephen L. George
Taiyeong Lee
+ Processes to Activate Phase III Clinical Trials in a Cooperative Oncology Group: The Case of Cancer and Leukemia Group B 2006 David M. Dilts
Alan B. Sandler
Matthew J. Baker
Steven K. Cheng
Stephen L. George
Kathleen S. Karas
Stephen McGuire
Gourija S. Menon
Jason Reusch
Debbie Sawyer
+ Controversies in the Early Reporting of a Clinical Trial in Early Breast Cancer 2006 Stephen L. George
Mark R. Green
+ A general formulation for a one-sided group sequential design 2005 Barry Kurt Moser
Stephen L. George
+ Sample Size Calculation for Simulation-Based Multiple-Testing Procedures 2005 Heejung Bang
Sin‐Ho Jung
Stephen L. George
+ A multiple testing procedure to associate gene expression levels with survival 2005 Sin‐Ho Jung
Kouros Owzar
Stephen L. George
+ Strength of accumulating evidence and data monitoring committee decision making 2004 Stephen L. George
Boris Freidlin
Edward L. Korn
+ PDF Chat Managing Accrual in Cooperative Group Clinical Trials 2004 Todd L. Demmy
Joyce M. Yasko
Deborah Collyar
Mira L. Katz
Carol Krasnov
Margaret J. Borwhat
Anne Battershell
Stephen L. George
+ Fulfillment of the uncertainty principle in cancer clinical trials 2004 Steven Joffe
David P. Harrington
Stephen L. George
Ezekiel J. Emanuel
L. Budzinski
Jane C. Weeks
+ Fulfillment of the uncertainty principle in cancer clinical trials 2004 Steven Joffe
David P. Harrington
Stephen L. George
Ezekiel J. Emanuel
L. Budzinski
J. C. Weeks
+ Should statisticians reporting to data monitoring committees be independent of the trial sponsor and leadership? 2004 Susan S. Ellenberg
Stephen L. George
+ Data monitoring and large apparent treatment effects 2004 Edward L. Korn
Boris Freidlin
Stephen L. George
+ Admissible two‐stage designs for phase II cancer clinical trials 2004 Sin‐Ho Jung
Taiyeong Lee
KyungMann Kim
Stephen L. George
+ PDF Chat Selection Bias, Phase II Trials, and the FDA Accelerated Approval Process 2003 Stephen L. George
+ An Introduction to Randomized Controlled Clinical Trials. J. N. S. Matthews, Arnold, London, U.K., 2000. Number of pages: xiv + 189. Price: £19.99. ISBN 0‐340‐761431 2001 Stephen L. George
+ Detecting treatment‐by‐centre interaction in multi‐centre clinical trials 2001 Richard F. Potthoff
Bercedis L. Peterson
Stephen L. George
+ Detecting treatment-by-centre interaction in multi-centre clinical trials 2001 Richard F. Potthoff
B. Peterson
Stephen L. George
+ Fraud in Medical Research 2000 Jonas Ranstam
Marc Buyse
Stephen L. George
Stephen Evans
Nancy L. Geller
Bruno Scherrer
Emmanuel Lesaffre
Gordon Murray
Lutz Edler
Jane L. Hutton
+ Surrogate Endpoints in Cancer Clinical Trials 2000 Stephen L. George
+ PDF Chat The role of biostatistics in the prevention, detection and treatment of fraud in clinical trials 1999 Marc Buyse
Stephen L. George
Stephen Evans
Nancy L. Geller
Jonas Ranstam
Bruno Scherrer
Emmanuel Lesaffre
Gordon Murray
Lutz Edler
Jane L. Hutton
+ Data Monitoring Committees and Interim Monitoring Guidelines 1999 Boris Freidlin
Edward L. Korn
Stephen L. George
+ Statistical reviewing policies of medical journals 1998 Steven N. Goodman
Douglas G. Altman
Stephen L. George
+ Reducing patient eligibility criteria in cancer clinical trials. 1996 Stephen L. George
+ Stopping a clinical trial early: Frequentist and bayesian approaches applied to a CALGB trial in non‐small‐cell lung cancer 1994 Stephen L. George
Chengchang Li
Donald A. Berry
Mark R. Green
+ Discussion of ‘sequential methods based on the boundaries approach for the clinical comparison of survival times’ 1994 Stephen L. George
+ The case against independent monitoring committees 1994 David Harrington
John J. Crowley
Stephen L. George
Thomas F. Pajak
Carol Redmond
Sam Wieand
+ Statistical Considerations and Modeling of Clinical Utility of Tumor Markers 1994 Stephen L. George
+ Sample size requirements and length of study for testing interaction in a 1 × k factorial design when time-to-failure is the outcome 1993 Bercedis L. Peterson
Stephen L. George
+ A survey of monitoring practices in cancer clinical trials 1993 Stephen L. George
+ Quantitative estimation of the thermal dose-modifying factor for cis-diamminedichloroplatinum (CDDP) in tumour-bearing dogs 1992 Rodney L. Page
Donald Ε. Thrall
Stephen L. George
G. Sylvester Price
Greta L. Heidner
Margaret C. McEntee
Carol Novotney
Marlene Hauck
Mark W. Dewhirst
+ The bootstrap and identification of prognostic factors via cox's proportional hazards regression model 1985 Chen‐Hsin Chen
Stephen L. George
+ Replicated Paired Comparisons between Two Objects: The (k,r)-Series 1974 Stephen L. George
+ Planning the size and duration of a clinical trial studying the time to some critical event 1974 Stephen L. George
M. M. Desu
+ A First Course in Statistics 1972 Stephen L. George
+ A First Course in Statistics 1972 Stephen L. George
F. N. David
+ Evaluation of empirical Bayes estimators for small numbers of past samples 1971 Stephen L. George
Common Coauthors
Commonly Cited References
Action Title Year Authors # of times referenced
+ PDF Chat Randomized Clinical Trials With Biomarkers: Design Issues 2010 Boris Freidlin
Lisa M. McShane
Edward L. Korn
6
+ PDF Chat Clinical Trial Designs for Predictive Biomarker Validation: Theoretical Considerations and Practical Challenges 2009 Sumithra J. Mandrekar
Daniel J. Sargent
5
+ PDF Chat Estimation of AUC or Partial AUC Under Test-Result-Dependent Sampling 2012 Xiaofei Wang
Junling Ma
Stephen L. George
Haibo Zhou
5
+ Sample size requirements and length of study for testing interaction in a 1 × k factorial design when time-to-failure is the outcome 1993 Bercedis L. Peterson
Stephen L. George
5
+ Approaches to evaluation of treatment effect in randomized clinical trials with genomic subset 2007 Sue‐Jane Wang
Robert T. O’Neill
Hung Hung
5
+ PDF Chat Design and Inference for Cancer Biomarker Study with an Outcome and Auxiliary‐Dependent Subsampling 2009 Xiaofei Wang
Haibo Zhou
5
+ Planning the size and duration of a clinical trial studying the time to some critical event 1974 Stephen L. George
M. M. Desu
5
+ Clinical Trial Designs for Predictive Marker Validation in Cancer Treatment Trials 2005 Daniel J. Sargent
Barbara A. Conley
Carmen J. Allegra
Laurence Collette
5
+ PDF Chat Evaluating the Efficiency of Targeted Designs for Randomized Clinical Trials 2004 Richard Simon
Aboubakar Maitournam
5
+ The asymptotic properties of nonparametric tests for comparing survival distributions 1981 David Schoenfeld
4
+ PDF Chat Improving cost‐effectiveness of epidemiological studies via designed missingness strategies 2010 Warren Strauss
Louise Ryan
Michele Morara
Nicole Iroz‐Elardo
Mark D. Davis
Matthew Cupp
Marcia Nishioka
James J. Quackenboss
Warren Galke
HalĂ»k Özkaynak
4
+ Resampling-Based Multiple Testing: Examples and Methods for p-Value Adjustment. 1994 Michael A. Martin
Peter H. Westfall
S. Stanley Young
4
+ PDF Chat On Enrichment Strategies for Biomarker Stratified Clinical Trials 2017 Xiaofei Wang
Jingzhu Zhou
Ting Wang
Stephen L. George
4
+ PDF Chat ROC curve estimation under test-result-dependent sampling 2012 Xiangyu Wang
JinHua Ma
Stephen L. George
4
+ Monitoring clinical trials: Conditional or predictive power? 1986 David J. Spiegelhalter
Laurence S. Freedman
Patrick R. Blackburn
4
+ PDF Chat The Use of Genomics in Clinical Trial Design 2008 Richard Simon
4
+ PDF Chat Sample size calculation for multiple testing in microarray data analysis 2004 Sin‐Ho Jung
Heejung Bang
S. Stanley Young
4
+ PDF Chat Adaptive Signature Design: An Adaptive Clinical Trial Design for Generating and Prospectively Testing A Gene Expression Signature for Sensitive Patients 2005 Boris Freidlin
Richard Simon
4
+ Optimal design for epidemiological studies subject to designed missingness 2007 Michele Morara
Louise Ryan
E. Andrés Houseman
Warren Strauss
4
+ Data Monitoring Committees and Interim Monitoring Guidelines 1999 Boris Freidlin
Edward L. Korn
Stephen L. George
4
+ PDF Chat On the efficiency of targeted clinical trials 2004 A. Maitournam
Richard Simon
4
+ Design and Analysis of Phase I Clinical Trials 1989 Barry E. Storer
3
+ Enrichment design with patient population augmentation 2015 Bo Yang
Yijie Zhou
Lanju Zhang
Lu Cui
3
+ Biased sampling designs to improve research efficiency: Factors influencing pulmonary function over time in children with asthma 2015 Jonathan S. Schildcrout
Paul J. Rathouz
Leila R. Zelnick
Shawn Garbett
Patrick J. Heagerty
3
+ Designs for Group Sequential Phase II Clinical Trials 1987 M N Chang
Terry M. Therneau
H. Samuel Wieand
S. Stephen
3
+ PDF Chat Optimal two-stage designs for phase II clinical trials 1989 Richard Simon
3
+ Repeated Significance Tests on Accumulating Data 1969 P. Armitage
C. K. McPherson
Beverley Charles Rowe
3
+ Comparison of Statistical Analysis Plans in Randomize-All Phase III Trials with a Predictive Biomarker 2014 Shigeyuki Matsui
Yuki Choai
Takahiro Nonaka
3
+ PDF Chat Using Bayesian modeling in frequentist adaptive enrichment designs 2017 Noah Simon
Richard Simon
3
+ A Semiparametric Empirical Likelihood Method for Biased Sampling Schemes with Auxiliary Covariates 2006 Xiaofei Wang
Haibo Zhou
3
+ Biomarkers and surrogate endpoints: Preferred definitions and conceptual framework 2001 Arthur J. Atkinson
Wayne A. Colburn
Victor G. DeGruttola
David L. DeMets
Gregory J. Downing
Daniel F. Hoth
John A. Oates
Carl C. Peck
Robert T. Schooley
Bert Spilker
3
+ Group sequential methods in the design and analysis of clinical trials 1977 Stuart J. Pocock
3
+ PDF Chat Statistical Issues in Translational Cancer Research 2008 Stephen L. George
3
+ PDF Chat An Approach to Evaluating and Comparing Biomarkers for Patient Treatment Selection 2014 Holly Janes
Marshall Brown
Ying Huang
Margaret S. Pepe
3
+ Group Sequential Methods with Applications to Clinical Trials 1999 Christopher Jennison
Bruce W. Turnbull
3
+ PDF Chat Adaptive enrichment designs for clinical trials 2013 Noah Simon
Richard H. Simon
3
+ On the estimation of the binomial probability in multistage clinical trials 2004 Sin‐Ho Jung
Kyung Mann Kim
3
+ A Semiparametric Empirical Likelihood Method for Data from an Outcome-Dependent Sampling Scheme with a Continuous Outcome 2002 Haibo Zhou
Mark A. Weaver
Jing Qin
Matthew P. Longnecker
M. C. Wang
3
+ Testing for Qualitative Interactions between Treatment Effects and Patient Subsets 1985 Mitchell H. Gail
Richard Simon
3
+ Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing 1995 Yoav Benjamini
Yosef Hochberg
3
+ Graphical Search for Two-Stage Designs for Phase II Clinical Trials 2001 Sin‐Ho Jung
Mark Carey
Kyung Mann Kim
3
+ Resampling-Based Multiple Testing: Examples and Methods for p-Value Adjustment 1993 Yogendra P. Chaubey
Peter H. Westfall
Stefano Young
3
+ PDF Chat A Direct Approach to False Discovery Rates 2002 John D. Storey
3
+ Regression modelling strategies for improved prognostic prediction 1984 Frank E. Harrell
Kerry L. Lee
Robert M. Califf
David B. Pryor
Robert A. Rosati
3
+ Continual Reassessment Method: A Practical Design for Phase 1 Clinical Trials in Cancer 1990 John O’Quigley
Margaret S. Pepe
Lloyd D. Fisher
3
+ A Multiple Testing Procedure for Clinical Trials 1979 Peter C. O’Brien
Thomas R. Fleming
3
+ PDF Chat Empirical Likelihood and General Estimating Equations 1994 Qin Jin
Jerry Lawless
3
+ A comment on futility monitoring 2002 Boris Freidlin
Edward L. Korn
3
+ PDF Chat Measuring the Performance of Markers for Guiding Treatment Decisions 2011 Holly Janes
Margaret S. Pepe
Patrick M. Bossuyt
William E. Barlow
3
+ The Statistical Evaluation of Medical Tests for Classification and Prediction 2005 Margaret S. Pepe
2