Evidence map›Paper›PMID 41807068›Full record

RevieweNeuro2026

Representation Biases: Variance Is Not Always a Good Proxy for Importance.

Andrew Kyle Lampinen, Stephanie C Y Chan, Yuxuan Li, Katherine Hermann

Abstract readReview
In one paragraph

Review in eNeuro, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Andrew Kyle LampinenGoogle DeepMind, Mountain View, California 94043 lampinen@google.com.ORCID 0000-0002-6988-8437
Stephanie C Y ChanGoogle DeepMind, Mountain View, California 94043.ORCID 0000-0003-2590-7832
Yuxuan LiGoogle DeepMind, Mountain View, California 94043.
Katherine HermannGoogle DeepMind, Mountain View, California 94043.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A central approach in neuroscience is to analyze neural representations as a means to understand a system's function, through the use of methods like principal component analysis, regression, and representational similarity analysis. These analyses often rest on a tacit "linking assumption": that the features explaining the most variance in neural activity are the most important for the system's computation. Here, we challenge this assumption. We review recent work in machine learning demonstrating "representation biases"-the fact that learned representations can be biased toward certain features over others. For example, learned representations heavily overrepresent simple (linear) features while representing complex (nonlinear) features much more weakly, even when both are equally critical for the system's computations. We review the origins of these biases in learning dynamics and patterns of computation. We then discuss their consequences for neuroscience. We show that if a subset of features dominates the representations, standard analytic techniques can yield highly biased inferences-for example, resulting in the mistaken conclusion that a system is simpler than it really is or that two systems are more similar than they really are. We discuss some connections between these findings and recent empirical developments in neuroscience. Finally, we present homomorphic encryption as a conceptual case study of the potential for a total dissociation between representational geometry and computation. We conclude that achieving a complete understanding of neural systems requires moving beyond high-variance signals, as critical computational mechanisms may be hidden in low-variance components.

Indexed as

Machine LearningModels, NeurologicalNeurosciencesAnimalsHumansartificial neural networkscomputational neurosciencedeep learningrepresentation analysisstatistical methods

Identifiers

PMID41807068
PMCPMC12983188

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Registered trials

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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.