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Ji, Yuan
One or more keywords matched the following items that are connected to Ji, Yuan
Item TypeName
Concept Clinical Trials, Phase I as Topic
Concept Randomized Controlled Trials as Topic
Concept Clinical Trials, Phase II as Topic
Concept Controlled Clinical Trials as Topic
Concept Clinical Trials as Topic
Academic Article Bayesian dose-finding in phase I/II clinical trials using toxicity and efficacy odds ratios.
Academic Article Adaptive randomization for multiarm comparative clinical trials based on joint efficacy/toxicity outcomes.
Academic Article Dose--schedule finding in phase I/II clinical trials using a Bayesian isotonic transformation.
Academic Article Dose-finding in phase I clinical trials based on toxicity probability intervals.
Academic Article A modified toxicity probability interval method for dose-finding trials.
Academic Article Modified toxicity probability interval design: a safer and more reliable method than the 3 + 3 design for practical phase I trials.
Academic Article An integrated dose-finding tool for phase I trials in oncology.
Academic Article Prediction of clinical phenotypes in invasive breast carcinomas from the integration of radiomics and genomics data.
Academic Article A decision-theoretic phase I-II design for ordinal outcomes in two cycles.
Academic Article TEAMS: Toxicity- and Efficacy-based Dose Insertion Design with Adaptive Model Selection for Phase I/II Dose-Escalation Trials in Oncology.
Academic Article A Bayesian Dose-finding Design for Oncology Clinical Trials of Combinational Biological Agents.
Academic Article Toxicity and Efficacy Probability Interval Design for Phase I Adoptive Cell Therapy Dose-Finding Clinical Trials.
Academic Article Structured clinical documentation in the electronic medical record to improve quality and to support practice-based research in epilepsy.
Academic Article Subgroup-Based Adaptive (SUBA) Designs for Multi-Arm Biomarker Trials.
Academic Article A Bayesian interval dose-finding design addressingOckham's razor: mTPI-2.
Academic Article Design and implementation of pragmatic clinical trials using the electronic medical record and an adaptive design.
Academic Article R-TPI: rolling toxicity probability interval design to shorten the duration and maintain safety of phase I trials.
Academic Article AAA: triple adaptive Bayesian designs for the identification of optimal dose combinations in dual-agent dose finding trials.
Academic Article The i3+3 design for phase I clinical trials.
Academic Article RoBoT: a robust Bayesian hypothesis testing method for basket trials.
Academic Article Variants in STAT4 Associated With Cure of Chronic HBV Infection in HBeAg-positive Patients Treated With Pegylated Interferon-alpha.
Academic Article Bayesian continual reassessment method for dose-finding trials infusing T cells with limited sample size.
Academic Article Monitoring late-onset toxicities in phase I trials using predicted risks.
Academic Article Discussion of "A hybrid phase I-II/III clinical trial design allowing dose re-optimization in phase III" by Andrew G. Chapple and Peter F. Thall.
Grant Bayesian Inference for Tumor Heterogeneity with Next-Generation Sequencing Data
Academic Article Bayesian Adaptive Design for Finding the Maximum Tolerated Sequence of Doses in Multicycle Dose-Finding Clinical Trials.
Academic Article Plasma metabolites with mechanistic and clinical links to the neurovascular disease cavernous angioma.
Academic Article A Multi-Arm Two-Stage (MATS) design for proof-of-concept and dose optimization in early-phase oncology trials.
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  • Clinical
  • Trials