Evidence map›Paper›PMID 34687857›Full record

ArticleNeuroImage2021

A visual encoding model links magnetoencephalography signals to neural synchrony in human cortex.

Eline R Kupers, Noah C Benson, Jonathan Winawer

Abstract read
In one paragraph

Article in NeuroImage, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Noninvasive Biomarkers for Assessing the Excitatory/Inhibitory Imbalance in Children with Epilepsy.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  3. Article
  4. Revisiting the role of computational neuroimaging in the era of integrative neuroscience.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Review
  5. Article
  6. Article
  7. A recurrent circuit implements normalization, simulating the dynamics of V1 activity.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
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

3 authors.

Eline R KupersDepartment of Psychology, New York University, New York, NY 10003, United States; Center for Neural Science, New York University, New York, NY 10003, United States; Department of Psychology, Stanford University, Stanford, CA 94305, United States. Electronic address: eline.kupers@nyu.edu.
Noah C BensonDepartment of Psychology, New York University, New York, NY 10003, United States; Center for Neural Science, New York University, New York, NY 10003, United States; eSciences Institute, University of Washington, Seattle, WA 98195, United States.
Jonathan WinawerDepartment of Psychology, New York University, New York, NY 10003, United States; Center for Neural Science, New York University, New York, NY 10003, United States.

Funding

Development and validation of empirical models of the neuronal population activity underlying non-invasive human brain measurementsR01MH111417 · NIMH · UNIVERSITY MEDICAL CENTER UTRECHT · PI DEVINSKY, ORRIN, DIJKHUIZEN, RICK M · 2016 to 2020
$4.4M
NIMH NIH HHS R01 MH111417
6 · The paper itself

Abstract

Synchronization of neuronal responses over large distances is hypothesized to be important for many cortical functions. However, no straightforward methods exist to estimate synchrony non-invasively in the living human brain. MEG and EEG measure the whole brain, but the sensors pool over large, overlapping cortical regions, obscuring the underlying neural synchrony. Here, we developed a model from stimulus to cortex to MEG sensors to disentangle neural synchrony from spatial pooling of the instrument. We find that synchrony across cortex has a surprisingly large and systematic effect on predicted MEG spatial topography. We then conducted visual MEG experiments and separated responses into stimulus-locked and broadband components. The stimulus-locked topography was similar to model predictions assuming synchronous neural sources, whereas the broadband topography was similar to model predictions assuming asynchronous sources. We infer that visual stimulation elicits two distinct types of neural responses, one highly synchronous and one largely asynchronous across cortex.

Indexed as

AdultBrain MappingComputer SimulationElectroencephalographyEvoked PotentialsFemaleHumansMagnetoencephalographyMalePhotic StimulationVisual CortexYoung AdultComputational modelsEvoked fieldEvoked potentialMEGStimulus-locked responseSynchronyVisual cortex

Identifiers

PMID34687857
PMCPMC8788390

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.