Identification of biomarker‐by‐treatment interactions in randomized clinical trials with survival outcomes and high‐dimensional spaces
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Publication:5280185
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Cites work
- scientific article; zbMATH DE number 720689 (Why is no real title available?)
- scientific article; zbMATH DE number 845714 (Why is no real title available?)
- scientific article; zbMATH DE number 6123298 (Why is no real title available?)
- scientific article; zbMATH DE number 3385132 (Why is no real title available?)
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- Adaptive Lasso for Cox's proportional hazards model
- Boosting With theL2Loss
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- Model Selection and Estimation in Regression with Grouped Variables
- Operating Characteristics and Extensions of the False Discovery Rate Procedure
- Regularization and Variable Selection Via the Elastic Net
- Ridge Regression: Biased Estimation for Nonorthogonal Problems
- The Adaptive Lasso and Its Oracle Properties
Cited in
(11)- Identifying optimal biomarker combinations for treatment selection via a robust kernel method
- Ranked sparsity: a cogent regularization framework for selecting and estimating feature interactions and polynomials
- Two‐stage penalized regression screening to detect biomarker–treatment interactions in randomized clinical trials
- Two-step hypothesis testing to detect gene-environment interactions in a genome-wide scan with a survival endpoint
- A Scalable Hierarchical Lasso for Gene–Environment Interactions
- Efficient screening of predictive biomarkers for individual treatment selection
- A simulation study comparing different statistical approaches for the identification of predictive biomarkers
- A three-stage approach to identify biomarker signatures for cancer genetic data with survival endpoints
- Oblique random survival forests
- IPF-LASSO: integrative \(L_1\)-penalized regression with penalty factors for prediction based on multi-omics data
- Sparse classification with paired covariates
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