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When estimating the treatment effect in an observational study, we use a semiparametric locally efficient dimension reduction approach to assess both the treatment assignment mechanism and the average responses in both treated and nontreated groups. We then integrate all results through imputation, inverse probability weighting and doubly robust augmentation estimators. Doubly robust estimators are locally efficient while imputation estimators are super-efficient when the response models are correct. To take advantage of both procedures, we introduce a shrinkage estimator to automatically combine the two, which retains the double robustness property while improving on the variance when the response model is correct. We demonstrate the performance of these estimators through simulated experiments and a real dataset concerning the effect of maternal smoking on baby birth weight. Key words and phrases: Average Treatment Effect, Doubly Robust Estimator, Efficiency, Inverse Probability Weighting, Shrinkage Estimator.
Based on the theory of reproducing kernel Hilbert space (RKHS) and semiparametric method, we propose a new approach to nonlinear dimension reduction. The method extends the semiparametric method into a more generalized domain where both the intereste
SDRcausal is a package that implements sufficient dimension reduction methods for causal inference as proposed in Ghosh, Ma, and de Luna (2021). The package implements (augmented) inverse probability weighting and outcome regression (imputation) esti
Missing data and confounding are two problems researchers face in observational studies for comparative effectiveness. Williamson et al. (2012) recently proposed a unified approach to handle both issues concurrently using a multiply-robust (MR) metho
Causal effect estimation from observational data is an important but challenging problem. Causal effect estimation with unobserved variables in data is even more difficult. The challenges lie in (1) whether the causal effect can be estimated from obs
Standard Mendelian randomization analysis can produce biased results if the genetic variant defining the instrumental variable (IV) is confounded and/or has a horizontal pleiotropic effect on the outcome of interest not mediated by the treatment. We