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Part I Bayesian Methods In Biomedical Research |
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1 An Application of Bayesian Approach for Testing Non-inferiority Case Studies in Vaccine Trials |
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3 | (14) |
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2 Bayesian Design of Noninferiority Clinical Trials with Co-primary Endpoints and Multiple Dose Comparison |
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17 | (18) |
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3 Bayesian Functional Mixed Models for Survival Responses with Application to Prostate Cancer |
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35 | (26) |
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Veerabhadran Baladandayuthapan |
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4 Bayesian Predictive Approach to Early Termination for Enriched Enrollment Randomized Withdrawal Trials |
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61 | (14) |
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Part II Diagnostic Medicine and Classification |
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5 Estimation of ROC Curve with Multiple Types of Missing Gold Standard |
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75 | (14) |
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6 Group Sequential Methods for Comparing Correlated Receiver Operating Characteristic Curves |
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89 | (20) |
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7 Nonparametric Covariate Adjustment for the Youden Index |
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109 | (24) |
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8 Comparative Effectiveness Research Using Meta-Analysis to Evaluate and Summarize Diagnostic Accuracy |
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133 | (16) |
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Part III Innovative Clinical Trial Designs and Analysis |
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9 Some Characteristics of the Varying-Stage Adaptive Phase II/III Clinical Trial Design |
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149 | (14) |
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10 Collective Evidence in Drug Evaluation |
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163 | (22) |
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11 Applications of Probability of Study Success in Clinical Drug Development |
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185 | (12) |
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12 Treatment Effect Estimation in Adaptive Clinical Trials: A Review |
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197 | (6) |
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13 Inferiority Index, Margin Functions, and Hybrid Designs for Noninferiority Trials with Binary Outcomes |
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203 | (32) |
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14 Group-Sequential Designs When Considering Two Binary Outcomes as Co-Primary Endpoints |
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235 | (28) |
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15 Issues in the Use of Existing Data: As Controls in Pre-Market Comparative Clinical Studies |
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263 | (10) |
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16 A Two-Tier Procedure for Designing and Analyzing Medical Device Trials Conducted in US and OUS Regions for Regulatory Decision Making |
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273 | (12) |
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17 Multiplicity Adjustment in Seamless Phase II/III Adaptive Trials Using Biomarkers for Dose Selection |
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285 | (18) |
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Part IV Modelling and Data Analysis |
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18 Empirical Likelihood for the AFT Model Using Kendall's Rank Estimating Equation |
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303 | (10) |
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19 Analysis of a Complex Longitudinal Health-Related Quality of Life Data by a Mixed Logistic Model |
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313 | (16) |
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20 Goodness-of-Fit Tests for Length-Biased Right-Censored Data with Application to Survival with Dementia |
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329 | (18) |
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21 Assessment of Fit in Longitudinal Data for Joint Models with Applications to Cancer Clinical Trials |
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347 | (20) |
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22 Assessing the Cumulative Exposure Response in Alzheimer's Disease Studies |
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367 | (14) |
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23 Evaluation of a Confidence Interval Approach for Relative Agreement in a Crossed Three-Way Random Effects Model |
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381 | (14) |
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Part V Personalized Medicine and Subgroup Analysis |
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24 Assessment of Methods to Identify Patient Subgroups with Enhanced Treatment Response in Randomized Clinical Trials |
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395 | (16) |
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25 A Framework of Statistical Methods for Identification of Subgroups with Differential Treatment Effects in Randomized Trials |
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411 | (16) |
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26 Biomarker Evaluation and Subgroup Identification in a Pneumonia Development Program Using SIDES |
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427 | (42) |
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Part VI Statistical Genomics and High-Dimensional Data Analysis |
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27 A Stochastic Segmentation Model for the Indentification of Histone Modification and DNase I Hypersensitive Sites in Chromatin |
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469 | (26) |
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28 Combining p Values for Gene Set Analysis |
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495 | (24) |
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29 A Simple Method for Testing Global and Individual Hypotheses Involving a Limited Number of Possibly Correlated Outcomes |
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519 | |
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Lisainfo e-raamatute kohta