Evidence map›Paper›PMID 40550696›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2025

Oddball Evoked Deviant Responses Reflect Complex Context-Dependent Expectations in Mouse V1.

Scott G Knudstrup, Catalina Martinez Reyes, Cambria M Jensen, Rachel W Schecter, Mac Kenzie Frank, Jeffrey P Gavornik

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Global context rapidly shapes sensory responses in V1.bioRxiv : the preprint server for biology · 2026
    Article
  3. Review
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

6 authors.

Scott G KnudstrupCenter for Systems Neuroscience, Department of Biology, Boston University, Boston, Massachusetts 02215.
Catalina Martinez ReyesCenter for Systems Neuroscience, Department of Biology, Boston University, Boston, Massachusetts 02215.
Cambria M JensenCenter for Systems Neuroscience, Department of Biology, Boston University, Boston, Massachusetts 02215.
Rachel W SchecterCenter for Systems Neuroscience, Department of Biology, Boston University, Boston, Massachusetts 02215.
Mac Kenzie FrankCenter for Systems Neuroscience, Department of Biology, Boston University, Boston, Massachusetts 02215.
Jeffrey P GavornikCenter for Systems Neuroscience, Department of Biology, Boston University, Boston, Massachusetts 02215 gavornik@bu.edu.

Funding

A mechanistic dissection of short and long term spatiotemporal learning in V1R01EY030200 · NEI · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI GAVORNIK, JEFFREY PETER · 2020 to 2024
$2.0M
Cortical mechanisms of learned spatial-temporal sequence codingR00MH099654 · NIMH · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI GAVORNIK, JEFFREY PETER · 2015 to 2017
$743k
NEI NIH HHS R01 EY030200NIMH NIH HHS R00 MH099654
6 · The paper itself

Abstract

Evoked responses in the mouse primary visual cortex can be modulated by the temporal context in which visual inputs are presented. Oddball stimuli embedded in a sequence of regularly repeated visual elements have been shown to drive relatively large deviant responses, a finding that is generally consistent with the theory that cortical circuits implement a form of predictive coding. These results can be confounded by short-term adaptation effects, however, that make interpretation difficult. Here we use various forms of the oddball paradigm to disentangle temporal and ordinal components of the deviant response, showing that it is a complex phenomenon affected by temporal structure, ordinal expectation, and event frequency. Specifically, we use visually evoked potentials to show that deviant responses occur over a large range of time in male and female mice, cannot be explained by a simple adaptation model, scale with predictability, and are modulated by violations of both first- and second-order sequential expectations. We also show that visual sequences can lead to long-term plasticity in some circumstances.

Indexed as

Evoked Potentials, VisualPrimary Visual CortexVisual CortexVisual PerceptionAnimalsElectroencephalographyFemaleMaleMiceMice, Inbred C57BLPhotic Stimulationmismatch negativitymouseoddball paradigmplasticitypredictive codingV1

Identifiers

PMID40550696
PMCPMC12268979

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.