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Statistics in Medicine
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January 3, 2013
Designing exploratory cancer trials using change in tumour size as primary endpoint
Thomas Jaki, Valérie André, Ting-Li Su, et al.
Statistics in Medicine
|
September 22, 2007
Incorporating intermediate binary responses into interim analyses of clinical trials: a comparison of four methods
Anne Whitehead, Marina Roshini Sooriyarachchi, John Whitehead, et al.
Pharmaceutical Statistics
|
November 4, 2006
Bayesian decision procedures for binary and continuous bivariate dose-escalation studies
Yinghui Zhou, John Whitehead, Elisa Bonvini, et al.
Statistics in Medicine
|
June 25, 2014
Bayesian methods for the design and interpretation of clinical trials in very rare diseases
Lisa V Hampson, John Whitehead, Despina Eleftheriou, et al.
Statistics in Medicine
|
December 5, 2008
Updating our aims and scope for the future
Ralph B D'Agostino, Vern Farewell, Joel B Greenhouse, et al.
Statistics in Medicine
|
November 19, 2004
Design considerations in the sequential analysis of matched case-control data
M Fazil Baksh, Susan Todd, John Whitehead, et al.
Statistics in Medicine
|
January 7, 2006
Sequential genome-wide association studies for monitoring adverse events in the clinical evaluation of new drugs
Patrick Kelly, Nigel Stallard, Yinghui Zhou, et al.
Statistics in Medicine
|
November 6, 2007
Sequentially testing for a gene-drug interaction in a genomewide analysis
Patrick Kelly, Yinghui Zhou, John Whitehead, et al.
Journal of Biopharmaceutical Statistics
|
November 21, 2007
A Bayesian approach for dose-escalation in a Phase I clinical trial incorporating pharmacodynamic endpoints
John Whitehead, Yinghui Zhou, Lisa Hampson, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 24, 2023
Perspectives on valuing water quality improvements using stated preference methods
Ian J Bateman, Bonnie Keeler, Sheila M Olmstead, et al.
Page
of 8
Search research articles
Search
Showing results (41-50 of 74) with videos related to
Sort By:
Page
of 8
Statistics in Medicine
|
January 3, 2013
Designing exploratory cancer trials using change in tumour size as primary endpoint
Thomas Jaki, Valérie André, Ting-Li Su, et al.
Statistics in Medicine
|
September 22, 2007
Incorporating intermediate binary responses into interim analyses of clinical trials: a comparison of four methods
Anne Whitehead, Marina Roshini Sooriyarachchi, John Whitehead, et al.
Pharmaceutical Statistics
|
November 4, 2006
Bayesian decision procedures for binary and continuous bivariate dose-escalation studies
Yinghui Zhou, John Whitehead, Elisa Bonvini, et al.
Statistics in Medicine
|
June 25, 2014
Bayesian methods for the design and interpretation of clinical trials in very rare diseases
Lisa V Hampson, John Whitehead, Despina Eleftheriou, et al.
Statistics in Medicine
|
December 5, 2008
Updating our aims and scope for the future
Ralph B D'Agostino, Vern Farewell, Joel B Greenhouse, et al.
Statistics in Medicine
|
November 19, 2004
Design considerations in the sequential analysis of matched case-control data
M Fazil Baksh, Susan Todd, John Whitehead, et al.
Statistics in Medicine
|
January 7, 2006
Sequential genome-wide association studies for monitoring adverse events in the clinical evaluation of new drugs
Patrick Kelly, Nigel Stallard, Yinghui Zhou, et al.
Statistics in Medicine
|
November 6, 2007
Sequentially testing for a gene-drug interaction in a genomewide analysis
Patrick Kelly, Yinghui Zhou, John Whitehead, et al.
Journal of Biopharmaceutical Statistics
|
November 21, 2007
A Bayesian approach for dose-escalation in a Phase I clinical trial incorporating pharmacodynamic endpoints
John Whitehead, Yinghui Zhou, Lisa Hampson, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 24, 2023
Perspectives on valuing water quality improvements using stated preference methods
Ian J Bateman, Bonnie Keeler, Sheila M Olmstead, et al.
Page
of 8