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Clinical Trials (London, England)|June 6, 2019
Quantifying time-varying cause-specific hazard and subdistribution hazard ratios with competing risks dataGuoqing Diao, Joseph G Ibrahim
Biometrics|May 21, 2019
Semiparametric frailty models for zero-inflated event count data in the presence of informative dropoutGuoqing Diao, Donglin Zeng, Kuolung Hu, et al.
Statistics in Medicine|August 25, 2022
Synthesizing studies for comparing different treatment sequences in clinical trialsGuoqing Diao, Haijun Ma, Donglin Zeng, et al.
Journal of Biopharmaceutical Statistics|February 14, 2018
Biomarker threshold adaptive designs for survival endpointsGuoqing Diao, Jun Dong, Donglin Zeng, et al.
Journal of Biopharmaceutical Statistics|March 14, 2017
On inference of control-based imputation for analysis of repeated binary outcomes with missing dataFei Gao, Guanghan Liu, Donglin Zeng, et al.
Journal of Biopharmaceutical Statistics|March 20, 2025
Improving power in adaptive expansion of biomarker populations in phase 3 clinical trialsGuoqing Diao, Xun Jiang, Donglin Zeng, et al.
Journal of Biopharmaceutical Statistics|March 16, 2017
Statistical design of noninferiority multiple region clinical trials to assess global and consistent treatment effectsGuoqing Diao, Donglin Zeng, Joseph G Ibrahim, et al.
Statistics and Its Interface|August 29, 2020
Bayesian flexible hierarchical skew heavy-tailed multivariate meta regression models for individual patient data with applicationsSungduk Kim, Ming-Hui Chen, Joseph Ibrahim, et al.
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