Bounds on Distributional Treatment Effect Parameters using Panel Data with an Application on Job Displacement
利用面板数据界定分布处理效应:岗位流失应用AI 解读 ↓
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利用面板数据界定分布处理效应:岗位流失应用AI 解读 ↓
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This paper develops new techniques to bound distributional treatment effect parameters that depend on the joint distribution of potential outcomes -- an object not identified by standard identifying assumptions such as selection on observables or even when treatment is randomly assigned. I show that panel data and an additional assumption on the dependence between untreated potential outcomes for the treated group over time (i) provide more identifying power for distributional treatment effect parameters than existing bounds and (ii) provide a more plausible set of conditions than existing methods that obtain point identification. I apply these bounds to study heterogeneity in the effect of job displacement during the Great Recession. Using standard techniques, I find that workers who were displaced during the Great Recession lost on average 34\% of their earnings relative to their counterfactual earnings had they not been displaced. Using the methods developed in the current paper, I also show that the average effect masks substantial heterogeneity across workers.
测地线双重差分
Summary Difference-in-differences (DID) is a widely used quasi-experimental design for causal inference, traditionally applied to scalar or Euclidean outcomes, while extensions to outcomes residing in non-Euclidean spaces remain limited. Existing methods for such outcomes have primarily focused on univariate distributions, leveraging linear operations in the space of quantile functions, but these approaches cannot be directly extended to outcomes in general metric spaces. In…
可能非连续结局下处理组的分位数与分布处理效应
Applied Difference-in-Differences studies often involve outcomes that are discrete, mixed, censored, or otherwise non-continuously distributed, while policy questions frequently concern distributional effects rather than mean effects alone. This paper develops a distributional DiD framework for identifying and conducting uniform inference on distribution and quantile treatment effects on the treated in such settings under stated identifying and regularity conditions.…
面板数据中集约边际效应的估计
Many policies operate through two different channels: the extensive margin (e.g., the decision to participate) and the intensive margin (e.g., the intensity of the response among participants). This paper develops a novel identification strategy to estimate the intensive margin effect in panel data settings. I adapt the Horowitz-Manski-Lee bounds to the Changes-in-Changes framework to partially identify both the average and quantile intensive margin treatment effects.…
基于分位数的非加性固定效应模型
I propose a quantile-based nonadditive fixed effects panel model to study heterogeneous causal effects. Similar to standard fixed effects (FE) model, my model allows arbitrary dependence between regressors and unobserved heterogeneity, but it generalizes the additive separability of standard FE to allow the unobserved heterogeneity to enter nonseparably. Similar to structural quantile models, my model's random coefficient vector depends on an unobserved, scalar ''rank''…
去偏且具有半参数效率的变化中变化估计量
We present a novel extension of the influential changes-in-changes (CiC) framework of Athey and Imbens (2006) for estimating the average treatment effect on the treated (ATT) and distributional causal effects in panel data with unmeasured confounding. While CiC relaxes the parallel trends assumption in difference-in-differences (DiD), existing methods typically assume a scalar unobserved confounder and monotonic outcome relationships, and lack inference tools that…
利用 Copula 相等假设部分识别面板数据中的分布处理效应
This paper aims to partially identify the distributional treatment effects (DTEs) that depend on the unknown joint distribution of treated and untreated potential outcomes. We construct the DTE bounds using panel data and allow individuals to switch between the treated and untreated states more than once over time. Individuals are grouped based on their past treatment history, and DTEs are allowed to be heterogeneous across different groups. We provide two alternative…