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A method for testing a prespecified subgroup in clinical trials

Statistics in medicine, 2007-08, Vol.26 (19), p.3535-3549

2007

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Cowpea bruchid midgut transcriptome response to a soybean cystatin - costs and benefits of counter-defence

Insect molecular biology, 2009-02, Vol.18 (1), p.97-110

2009

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Rice small C2-domain proteins are phosphorylated by calcium-dependent protein kinase

Molecules and Cells, 2013, 35(5), , pp.381-387

2013

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Design and analysis of non-inferiority mortality trials in oncology

Statistics in medicine, 2003-01, Vol.22 (2), p.239-264

2003

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Some issues with composite endpoints in clinical trials

Fundamental & clinical pharmacology, 2005-12, Vol.19 (6), p.609-619

Chi, George Y.H.

2005

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On Sample Size and Inference for Two‐Stage Adaptive Designs

Biometrics, 2001-03, Vol.57 (1), p.172-177

2001

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Understanding the FDA Guidance on Adaptive Designs: Historical, Legal, and Statistical Perspectives

Journal of biopharmaceutical statistics, 2010-11, Vol.20 (6), p.1178-1219

2010

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Mechanical Properties and Electrical Resistance of TiNi Shape-Memory Alloy

Materials science forum, 2002-05, Vol.394-395, p.241-244

2002

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Inferiority Index and Margin in Noninferiority Trials

Statistics in biopharmaceutical research, 2011-05, Vol.3 (2), p.288-301

2011

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Physiological and Proteomics Analysis to Potassium Starvation in Rice

한국환경농학회지, 2011, 30(4), , pp.395-401

2011

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Cloning and Expression of a New Isotype of the Peroxiredoxin Gene of Chinese Cabbage and Its Comparison to 2Cys-Peroxiredoxin Isolated from the Same Plant

Biochemical and biophysical research communications, 1999-05, Vol.258 (3), p.768-771

1999

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Blends of statistical designs for dose-response studies

Communications in statistics. Theory and methods, 1994-01, Vol.23 (2), p.341-360

1994

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George Chi's Discussion of the "Executive Summary of the PhRMA Working Group on Adaptive Designs in Clinical Drug Development" By Christy Chuang-Stein, Vladimir Dragalin, Brenda Gaydos, Michael Krams, and José Pinheiro

Journal of biopharmaceutical statistics, 2006-07, Vol.16 (3), p.285-286

Chi, George Y. H.

2006

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A Ratio Test in Active Control Non-Inferiority Trials with a Time-to-Event Endpoint

Journal of biopharmaceutical statistics, 2006-03, Vol.16 (2), p.151-164

2006

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Multiple Testings: Multiple Comparisons and Multiple Endpoints

Drug information journal, 1998-10, Vol.32 (1_suppl), p.1347S-1362S

Chi, George Y. H.

1998

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Hypotheses and Type I Error in Active-Control Noninferiority Trials

Journal of biopharmaceutical statistics, 2004-12, Vol.14 (2), p.301-313

2004

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Blends of statistical designs for dose-response studies 1

Communications in statistics. Theory and methods, 1994-01, Vol.23 (2), p.341-360

1994

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Evaluation of Health-Related Quality-of-Life Measures in Oncology Drug Product Applications: Issues and Concerns

Journal of biopharmaceutical statistics, 2004-12, Vol.14 (1), p.23-30

2004

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Response Surface and Factorial Designs for Combination Antihypertensive Drugs

Drug information journal, 1990-04, Vol.24 (2), p.371-378

1990

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THE ATTRACTIVENESS OF THE CONCEPT OF A PROSPECTIVELY DESIGNED TWO-STAGE CLINICAL TRIAL

Journal of biopharmaceutical statistics, 1999-11, Vol.9 (4), p.537-547

1999

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Testing for the Existence of a Desirable Dose Combination

Biometrics, 1993-03, Vol.49 (1), p.85-94

1993

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Efficacy Evaluation for Monotherapies in Two-by-Two Factorial Trials

Biometrics, 1995-12, Vol.51 (4), p.1483-1493

1995

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On some statistical methods for analysis of combination drug studies

Communications in statistics. Theory and methods, 1994-01, Vol.23 (2), p.361-376

1994

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Designing a clinical trial to demonstrate prevention of ulcer recurrence: Modelling simulation approaches

Statistics in medicine, 1988-08, Vol.7 (8), p.877-888

1988

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Nonlinear prediction of generalized random processes

Journal of approximation theory, 1972, Vol.6 (4), p.391-403

Chi, G.Y.H

1972

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A method for testing a prespecified subgroup in clinical trials

Cowpea bruchid midgut transcriptome response to a soybean cystatin - costs and benefits of counter-defence

Rice small C2-domain proteins are phosphorylated by calcium-dependent protein kinase

Design and analysis of non-inferiority mortality trials in oncology

Some issues with composite endpoints in clinical trials

On Sample Size and Inference for Two‐Stage Adaptive Designs

Understanding the FDA Guidance on Adaptive Designs: Historical, Legal, and Statistical Perspectives

Mechanical Properties and Electrical Resistance of TiNi Shape-Memory Alloy

Inferiority Index and Margin in Noninferiority Trials

Physiological and Proteomics Analysis to Potassium Starvation in Rice

Cloning and Expression of a New Isotype of the Peroxiredoxin Gene of Chinese Cabbage and Its Comparison to 2Cys-Peroxiredoxin Isolated from the Same Plant

Blends of statistical designs for dose-response studies

George Chi's Discussion of the "Executive Summary of the PhRMA Working Group on Adaptive Designs in Clinical Drug Development" By Christy Chuang-Stein, Vladimir Dragalin, Brenda Gaydos, Michael Krams, and José Pinheiro

A Ratio Test in Active Control Non-Inferiority Trials with a Time-to-Event Endpoint

Multiple Testings: Multiple Comparisons and Multiple Endpoints

Hypotheses and Type I Error in Active-Control Noninferiority Trials

Blends of statistical designs for dose-response studies 1

Evaluation of Health-Related Quality-of-Life Measures in Oncology Drug Product Applications: Issues and Concerns

Response Surface and Factorial Designs for Combination Antihypertensive Drugs

THE ATTRACTIVENESS OF THE CONCEPT OF A PROSPECTIVELY DESIGNED TWO-STAGE CLINICAL TRIAL

Testing for the Existence of a Desirable Dose Combination

Efficacy Evaluation for Monotherapies in Two-by-Two Factorial Trials

On some statistical methods for analysis of combination drug studies

Designing a clinical trial to demonstrate prevention of ulcer recurrence: Modelling simulation approaches

Nonlinear prediction of generalized random processes

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