ArticleJournal of the American Statistical Association2024
Statistical Inference for Maximin Effects: Identifying Stable Associations across Multiple Studies.
Article in Journal of the American Statistical Association, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Robust Inference for Federated Meta-Learning.Journal of the American Statistical Association · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
1 author.
Funding
Abstract
Integrative analysis of data from multiple sources is critical to making generalizable discoveries. Associations consistently observed across multiple source populations are more likely to be generalized to target populations with possible distributional shifts. In this paper, we model the heterogeneous multi-source data with multiple high-dimensional regressions and make inferences for the maximin effect (Meinshausen, Bühlmann, AoS, 43(4), 1801-1830). The maximin effect provides a measure of stable associations across multi-source data. A significant maximin effect indicates that a variable has commonly shared effects across multiple source populations, and these shared effects may be generalized to a broader set of target populations. There are challenges associated with inferring maximin effects because its point estimator can have a non-standard limiting distribution. We devise a novel sampling method to construct valid confidence intervals for maximin effects. The proposed confidence interval attains a parametric length. This sampling procedure and the related theoretical analysis are of independent interest for solving other non-standard inference problems. Using genetic data on yeast growth in multiple environments, we demonstrate that the genetic variants with significant maximin effects have generalizable effects under new environments. The proposed method is implemented in the
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.