An influence function projection approach exploits graph-implied conditional independences to improve the efficiency of semiparametric estimators for upper and lower bounds on average causal effects under sensitivity models for unmeasured confounding.
Journal of the Royal Statistical Society: Series B (Methodological) , volume=
4 Pith papers cite this work. Polarity classification is still indexing.
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2026 4verdicts
UNVERDICTED 4representative citing papers
Introduces Bayesian Sensitivity Value (BSV) for causal inference sensitivity analysis based on evidence-derived priors and Monte Carlo estimation, applied to diabetes treatment effects.
A new adaptive variance estimator for relative sparsity coefficients is introduced that fully utilizes the prior asymptotic normality theorem and incorporates variable selection effects.
CAFE assesses the fit of observational CATE estimates by partitioning RCT data via propensity scores and comparing to experimental group averages, with theory and extensions for confounders.
citing papers explorer
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Exploiting independence constraints for efficient estimation of bounds on causal effects in the presence of unmeasured confounding
An influence function projection approach exploits graph-implied conditional independences to improve the efficiency of semiparametric estimators for upper and lower bounds on average causal effects under sensitivity models for unmeasured confounding.
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Bayesian Sensitivity of Causal Inference Estimators under Evidence-Based Priors
Introduces Bayesian Sensitivity Value (BSV) for causal inference sensitivity analysis based on evidence-derived priors and Monte Carlo estimation, applied to diabetes treatment effects.
-
An adaptive variance estimator for relative sparsity
A new adaptive variance estimator for relative sparsity coefficients is introduced that fully utilizes the prior asymptotic normality theorem and incorporates variable selection effects.
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Assessing Estimate of CATE from Observational Data via an RCT Study
CAFE assesses the fit of observational CATE estimates by partitioning RCT data via propensity scores and comparing to experimental group averages, with theory and extensions for confounders.