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Shi Bo

Publications and source records attributed to Shi Bo.

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MediEncoder: Nonlinear Representation Learning for High-Dimensional Causal Mediation Analysis

Causal mediation analysis decomposes a treatment effect into indirect pathways through mediators and direct pathways not operating through them. Modern biomedical studies often involve high-dimensional covariates and mediators that are noisy proxies for lower-dimensional latent biological processes. Existing methods typically rely on sparsity, linear factor models, or ignore the connection among variables in the learned representations, which can be restrictive when measurements are nonlinear and covariate and mediator factors are structurally dependent. We propose MediEncoder, a representation-learning framework for nonlinear high-dimensional mediation analysis. MediEncoder jointly learns low-dimensional covariate and mediator representations using a coupled encoder-decoder architecture with a cross-factor network that links treatment and covariate representations to mediator representations. The learned features are then used in a cross-fitted efficient influence function-based estimator of natural direct and indirect effects. The resulting estimator is multiply robust and asymptotically normal under suitable regularity conditions. Simulations show that MediEncoder improves estimation accuracy over competing dimension-reduction approaches, and an application to Alzheimer's Disease Neuroimaging Initiative data illustrates its utility in high-dimensional biomedical causal mediation analysis.

stat.ME

Causal Imitation Learning Under Measurement Error and Distribution Shift

We study offline imitation learning (IL) when part of the decision-relevant state is observed only through noisy measurements and the distribution may change between training and deployment. Such settings induce spurious state-action correlations, so standard behavioral cloning (BC) -- whether conditioning on raw measurements or ignoring them -- can converge to systematically biased policies under distribution shift. We propose a general framework for IL under measurement error, inspired by explicitly modeling the causal relationships among the variables, yielding a target that retains a causal interpretation and is robust to distribution shift. Building on ideas from proximal causal inference, we introduce \texttt{CausIL}, which treats noisy state observations as proxy variables, and we provide identification conditions under which the target policy is recoverable from demonstrations without rewards or interactive expert queries. We develop estimators for both discrete and continuous state spaces; for continuous settings, we use an adversarial procedure over RKHS function classes to learn the required parameters. We evaluate \texttt{CausIL} on semi-simulated longitudinal data from the PhysioNet/Computing in Cardiology Challenge 2019 cohort and demonstrate improved robustness to distribution shift compared to BC baselines.

cs.LG

Debiased Causal Mediation Analysis in Ultra-High-Dimensional Settings in the Presence of Interaction Effects

Mediation analysis is a crucial tool for uncovering the mechanisms through which a treatment affects an outcome, providing deeper causal insights and guiding effective interventions. Despite substantial advances in mediation analysis with fixed- or low-dimensional mediators and covariates, estimation and inference for mediation functionals remain limited when both mediators and covariates are ultra-high-dimensional. In this paper, we propose an estimator for the mediation functional in a high-dimensional setting that accommodates the treatment--covariate interactions in the mediator model, as well as treatment--covariate and treatment--mediator interactions in the outcome model. As the parameter of interest involves high-dimensional components from different treatment arms and regression equations, existing debiasing approaches are not directly applicable, motivating our multi-step debiasing technique for handling such structurally complex functionals. We establish that the proposed estimator is $\sqrt{n}$-consistent and asymptotically normal, enabling valid inference for natural direct and indirect effects. We evaluate our proposed methodology through extensive simulation studies and apply it to the TCGA lung cancer dataset to estimate the effect of smoking, mediated by DNA methylation, on the survival time of lung cancer patients.

stat.ME