ArticleImaging neuroscience (Cambridge, Mass.)2025
When no answer is better than a wrong answer: A causal perspective on batch effects.
Article in Imaging neuroscience (Cambridge, Mass.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
What it found
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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.
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Who cites it
8 citing papers in PubMed.
- Organic Chemistry as a Catalyst for AI Innovation: Challenges, Methods, and Emerging Paradigms.Chemical reviews · 2026Review
- Resting-State vs. Task-Based Functional Magnetic Resonance Imaging in Neurosurgical Planning: A Narrative Review of Clinical Applications.Biomedicines · 2026Review
- Sparse covariate-driven factorization of high-dimensional brain connectivity with application to site effect correction.Biostatistics (Oxford, England) · 2026Article
- Inflammasome-associated pyroptosis and tumor angiogenesis in prostate cancer.Iranian journal of basic medical sciences · 2026Review
- Article
- ComBatLS: A Location- and Scale-Preserving Method for Multi-Site Image Harmonization.Human brain mapping · 2025Article
- ComBatLS: A location- and scale-preserving method for multi-site image harmonization.bioRxiv : the preprint server for biology · 2024Article
- Accounting for motion in resting-state fMRI: What part of the spectrum are we characterizing in autism spectrum disorder?NeuroImage · 2022Article
Corrections and comments
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Authors and funding
11 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Batch effects, undesirable sources of variability across multiple experiments, present significant challenges for scientific and clinical discoveries. Batch effects can (i) produce spurious signals and/or (ii) obscure genuine signals, contributing to the ongoing reproducibility crisis. Because batch effects are typically modeled as classical statistical effects, they often cannot differentiate between sources of variability due to confounding biases, which may lead them to erroneously conclude batch effects are present (or not). We formalize batch effects as causal effects, and introduce algorithms leveraging causal machinery, to address these concerns. Simulations illustrate that when non-causal methods provide the wrong answer, our methods either produce more accurate answers or "no answer," meaning they assert the data are inadequate to confidently conclude on the presence of a batch effect. Applying our causal methods to 27 neuroimaging datasets yields qualitatively similar results: in situations where it is unclear whether batch effects are present, non-causal methods confidently identify (or fail to identify) batch effects, whereas our causal methods assert that it is unclear whether there are batch effects or not. In instances where batch effects should be discernable, our techniques produce different results from prior art, each of which produce results more qualitatively similar to not applying any batch effect correction to the data at all. This work, therefore, provides a causal framework for understanding the potential capabilities and limitations of analysis of multi-site data.
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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.