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Journal of Biopharmaceutical Statistics|November 27, 2002
Issues related to subgroup analysis in clinical trialsLu Cui, H M James Hung, Sue Jane Wang, et al.Biometrical Journal. Biometrische Zeitschrift|September 16, 2006
A regulatory view on adaptive/flexible clinical trial designH M James Hung, Robert T O'Neill, Sue-Jane Wang, et al.Contemporary Clinical Trials|May 5, 2011
Evaluation of performance of some enrichment designs dealing with high placebo response in psychiatric clinical trialsYeh-Fong Chen, Yang Yang, H M James Hung, et al.Bioinformatics (Oxford, England)|November 27, 2004
Sample size for gene expression microarray experimentsChen-An Tsai, Sue-Jane Wang, Dung-Tsa Chen, et al.JCO Precision Oncology|August 24, 2022
Bayesian Sample Size Planning Tool for Phase I Dose-Finding TrialsXiaolei Lin, Jiaying Lyu, Shijie Yuan, et al.Pharmacogenomics|December 15, 2010
Designing pharmacogenomic studies to be fit for purposeDaniel K Burns, Arlene R Hughes, Aidan Power, et al.Molecular Systems Biology|September 17, 2009
A simple and efficient algorithm for genome-wide homozygosity analysis in diseaseWei Liu, Jinhui Ding, Jesse Raphael Gibbs, et al.Statistics in Medicine|January 10, 2003
Some fundamental issues with non-inferiority testing in active controlled trialsH M James Hung, Sue-Jane Wang, Yi Tsong, et al.Alcoholism, Clinical and Experimental Research|December 25, 2002
Short of complete abstinence: an analysis exploration of multiple drinking episodes in alcoholism treatment trialsSue-Jane Wang, Cellia J Winchell, Cynthia G McCormick, et al.Journal of Biopharmaceutical Statistics|November 9, 2010
Perspectives on the use of adaptive designs in clinical trials. Part II. Panel discussionNorbert Benda, Werner Brannath, Frank Bretz, et al.Pageof 8