Evidence map›Paper›PMID 41920867›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2026

Distinct laminar origins of sensory-evoked high-gamma and low-frequency ECoG signals revealed by optogenetics.

Pierre-Marie Garderes, Daniel E Feldman, Kristofer E Bouchard

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

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.

2 · The registry

The trial behind it

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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

1 citing paper in PubMed.

  1. Distinct laminar origins of sensory-evoked high-gamma and low-frequency ECoG signals revealed by optogenetics.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Pierre-Marie GarderesDepartment of Neuroscience, University of California, Berkeley, CA 94720.ORCID 0000-0003-2451-894X
Daniel E FeldmanDepartment of Neuroscience, University of California, Berkeley, CA 94720.ORCID 0000-0003-4646-8170
Kristofer E BouchardHelen Wills Neuroscience Institute, University of California, Berkeley, CA 94720.ORCID 0000-0002-1974-4603

Funding

Origins of ECoGR01NS118648 · NINDS · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI BOUCHARD, KRISTOFER E. · 2020 to 2024
$1.9M
HHS | NIH | National Institute of Neurological Disorders and Stroke (NINDS) NS092367HHS | NIH | National Institute of Neurological Disorders and Stroke (NINDS) NS118648LBNL LDRD Neural Systems and Machine Learning LabNINDS NIH HHS R01 NS118648
6 · The paper itself

Abstract

Electrocorticography (ECoG) provides a high-spatiotemporal-resolution measure of cortical activity (cortical surface electrical potentials, CSEPs) in humans and animals. The CSEP high-gamma band (Hγ, 65 to 170 Hz) correlates with neuronal firing rates at the columnar spatial scale and is widely used as a biomarker of local activity. Whether Hγ reports all stages of columnar processing, intermediate processing in L2/3 (close to the ECoG electrode), or the main columnar output in L5, is unknown. We disentangled the laminar origins of Hγ and other ECoG bands by optogenetically suppressing L2/3 or L5 pyramidal cells during micro-ECoG recording in the mouse somatosensory cortex. Whisker deflections evoked transient, topographically localized CSEPs. L5 optogenetic suppression most strongly reduced 65 to 450 Hz (Hγ-uHγ) bands in sensory-evoked ECoG signals, whereas L2/3 suppression most strongly reduced 4 to 27 Hz (θ-β) bands. Thus, different CSEP frequency bands reflect layer-specific activity and are biomarkers of distinct stages of sensory-evoked columnar processing.

Indexed as

Evoked Potentials, SomatosensoryGamma RhythmOptogeneticsSomatosensory CortexAnimalsElectroencephalographyMicePyramidal CellsVibrissaeelectrocorticographyhigh-gammainverse problemlaminar originoptogenetics

Identifiers

PMID41920867
PMCPMC13056151

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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.