ArticleNature communications2026
Local graph estimation with pathwise false discovery control.
Article in Nature communications, 2026. 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.
- Local graph estimation with pathwise false discovery control.Nature communications · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
Abstract
Many datasets include a small set of variables, such as biomarkers or clinical outcomes, whose relationships to the broader system are of primary scientific interest. Estimating the full network of inter-variable relationships in such settings often obscures local structures around these targets, limiting interpretability. To address this fundamental problem, we introduce local graph estimation, a statistical framework for inferring substructures around target variables. We show that traditional graph estimation methods often fail to recover local structure, and present pathwise feature selection (PFS) as an effective alternative. PFS estimates local subgraphs by iteratively applying feature selection and propagating uncertainty along network paths, providing rigorous finite-sample false discovery control even in settings with mixed variable types and nonlinear dependencies. In four distinct applications spanning environmental and public health, multiomics, brain connectomics, and single-nucleus RNA sequencing, PFS recovers interpretable networks consistent with domain knowledge, highlighting its ability to uncover established mechanisms and generate novel hypotheses.
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What OpenQuestion holds
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.