In staggered difference-in-differences (DiD) designs, units enter treatment at different calendar times, so the treatment effect is not a single number but a set of Cohort-Average Treatment effects on the Treated (CATTs), one per cohort-time cell. Estimating every CATT as its own parameter, as the standard fully flexible estimator does, is unbiased but inefficient when some of these effects are in fact equal, whereas pooling them all into a single two-way fixed effects (TWFE) coefficient is efficient but, whenever the heterogeneity is genuine, biased for the individual effects. We frame the choice between these extremes as a partition-selection problem on the cohort-time cells and address it with a Dirichlet Process (DP) mixture prior on the CATTs. The model favors parsimonious groupings without fixing their number, and a collapsed Gibbs sampler delivers point estimates, credible intervals that marginalize the unknown partition, and co-clustering probabilities for every pair of CATTs. With the error variance held fixed and a pairwise penalty placed on the partition, a maximum a posteriori (MAP) partition reduces to an $\ell_0$-penalized regression, connecting the Bayesian formulation to the homogeneity-pursuit literature. In a calibrated simulation, the model cuts the sampling variance of the cohort-time effects by 26--52\% relative to the fully flexible estimator, without the pooled estimator's bias, provided the distinct effects are separated enough to be recovered, and the posterior delivers near-nominal confidence-interval coverage by averaging over the unknown partition. In two applications the method recovers a precision-improving partial-homogeneity structure in one, where the cohort-time effects are genuinely heterogeneous, and reports that full pooling is adequate in the other, where they are not.
In difference-in-differences (DiD), researchers may use pre-treatment trends to select a control group for which the parallel-trends assumption appears plausible, with the aim of estimating the average treatment effect on the treated (ATT). Our earlier paper,Nakano and Hoshino (2016), and the present paper jointly prov...
When parallel trends fails for some treated cohorts but not others, the average treatment effect on the treated (ATT), an average over all of them, is exactly the target that becomes hard to recover. We propose changing the estimand rather than defending it. The credible-subpopulation local ATT (LATT) is the effect for...
This paper studies difference-in-differences with staggered adoption and a continuous, time-invariant dose. Each cohort-time comparison contains two margins. The level margin is the average treatment effect at realized doses. Under level parallel trends it equals the level contrast between the treated cohort and not-ye...
Panel conditioning, the causal effect of prior survey participation on responses, can vary with tenure. Under an additive model of cell means in period, entry cohort, and tenure, we characterize which features of the conditioning path a staggered panel identifies on its observed support, and how the unidentified compon...
Staggered distributional difference-in-differences produces cohort-specific potential-outcome distributions, but applied work typically wants one overall quantile treatment effect. Two natural summaries---averaging cohort quantile treatment effects (QTTs) and mixing cohort distributions before inversion---use the same...
Researchers often summarize mediation in clustered data with a single-level product-of-coefficients estimator. We show what this pooled analysis estimates and why the target depends on the design. The pooled a-path is weighted by the within-between variance composition of the treatment. The pooled b-path uses a differe...
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