ArXiv TLDR

Nonparametric Point Identification of Treatment Effect Distributions via Rank Stickiness

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2604.21548

Tengyuan Liang

econ.EMstat.ME

TLDR

This paper introduces rank stickiness for nonparametric point identification of treatment effect distributions, allowing rank violations and yielding tighter variance estimates.

Key contributions

  • Nonparametrically identifies treatment effect distributions using a novel "rank stickiness" parameter.
  • Introduces the Bregman-Sinkhorn copula, uniquely determined by marginals and rank stickiness.
  • Derives a variance estimator for ATE that is tighter than Fréchet–Hoeffding and Neyman bounds.
  • Empirical copula converges at the parametric √n-rate, despite infinite-dimensional parameter space.

Why it matters

This paper addresses a critical challenge in causal inference by providing a method for full identification of treatment effect distributions without strong assumptions. It offers a more precise understanding of treatment heterogeneity and improves the accuracy of policy evaluations.

Original Abstract

Treatment effect distributions are not identified without restrictions on the joint distribution of potential outcomes. Existing approaches either impose rank preservation -- a strong assumption -- or derive partial identification bounds that are often wide. We show that a single scalar parameter, rank stickiness, suffices for nonparametric point identification while permitting rank violations. The identified joint distribution -- the coupling that maximizes average rank correlation subject to a relative entropy constraint, which we call the Bregman-Sinkhorn copula -- is uniquely determined by the marginals and rank stickiness. Its conditional distribution is an exponential tilt of the marginal with a Bregman divergence as the exponent, yielding closed-form conditional moments and rank violation probabilities; the copula nests the comonotonic and Gaussian copulas as special cases. The empirical Bregman-Sinkhorn copula converges at the parametric $\sqrt{n}$-rate with a Gaussian process limit, despite the infinite-dimensional parameter space. We apply the framework to estimate the full treatment effect distribution, derive a variance estimator for the average treatment effect tighter than the Fréchet--Hoeffding and Neyman bounds, and extend to observational studies under unconfoundedness.

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