Evidence map›Paper›PMID 24966390›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2014

Frontal-subcortical circuits involved in reactive control and monitoring of gaze.

Katharine N Thakkar, Fiona M Z van den Heiligenberg, Rene S Kahn, Sebastiaan F W Neggers

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.5field-weighted citation impact, top 11% of its field
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

21 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Dissociation of Medial Frontal β-Bursts and Executive Control.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  6. Cognitive Control of Saccadic Selection and Inhibition from within the Core Cortical Saccadic Network.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  7. Structural Thalamofrontal Hypoconnectivity Is Related to Oculomotor Corollary Discharge Dysfunction in Schizophrenia.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  8. Article
  9. Article
  10. Article
  11. Cortical control and performance monitoring of interrupting and redirecting movements.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2017
    Review
  12. Article
  13. Article
  14. The mouse cortico-striatal projectome.Nature neuroscience · 2016
    Article
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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 at 1 institution in 1 country.

Katharine N ThakkarBrain Center Rudolf Magnus, Department of Psychiatry, University Medical Center Utrecht, 3548 CX Utrecht, The Netherlands k.n.thakkar@umcutrecht.nl.
Fiona M Z van den HeiligenbergBrain Center Rudolf Magnus, Department of Psychiatry, University Medical Center Utrecht, 3548 CX Utrecht, The Netherlands.
Rene S KahnBrain Center Rudolf Magnus, Department of Psychiatry, University Medical Center Utrecht, 3548 CX Utrecht, The Netherlands.
Sebastiaan F W NeggersBrain Center Rudolf Magnus, Department of Psychiatry, University Medical Center Utrecht, 3548 CX Utrecht, The Netherlands.
University Medical Center Utrecht · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rapid and reactive control of movement is essential in a dynamic environment and is disrupted in several neuropsychiatric disorders. Nonhuman primate neurophysiology studies have made significant contributions to our understanding of how saccadic eye movements can be rapidly inhibited, changed, and monitored. These results highlight a frontostriatal network involved in gaze control and provide a strong basis for understanding how cognitive control of action is implemented in the human brain. The goal of the present study was to bridge human and nonhuman primate studies by investigating reactive control of eye movements during fMRI using a task that has been used in neurophysiology studies: the search-step task. This task requires a speeded response to a visual target (no-step trial). On a minority (40%) of trials, the target jumps to a new location and participants are instructed to inhibit the initially planned saccade and redirect gaze toward the new location (redirect trial). Compared with no-step trials, greater activation in a frontal oculomotor network, including frontal and supplementary eye fields (SEFs), and the striatum was observed during correctly executed redirect trials. Individual differences in stopping efficiency were related to striatal activation. Further, greater activation in SEF was in a region anterior to that activated during visually guided saccades and scaled positively with error magnitude, suggesting a prominent role in response monitoring. Combined, these data lend new evidence for a role of the striatum in reactive saccade control and further clarify the role of SEF in action inhibition and performance monitoring.

Indexed as

AdultCorpus StriatumEye MovementsFemaleFrontal LobeFunctional NeuroimagingHumansImage Processing, Computer-AssistedMagnetic Resonance ImagingMaleMiddle AgedNerve NetVisual FieldsYoung Adultbasal gangliacognitive controlfunctional MRIsaccadessearch-step task

Identifiers

PMID24966390
PMCPMC6608199
OpenAlexW2025199346

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.