Evidence map›Paper›PMID 30744987›Full record

ArticleNeuron2019

Neural Competitive Queuing of Ordinal Structure Underlies Skilled Sequential Action.

Katja Kornysheva, Daniel Bush, Sofie S Meyer, Anna Sadnicka, Gareth Barnes, Neil Burgess

Abstract read
In one paragraph

Article in Neuron, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

  1. Article
  2. Article
  3. Micro-offline gains do not reflect offline learning during early motor skill acquisition in humans.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Cortical Areas for Planning Sequences before and during Movement.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  10. Article
  11. The Hippocampus Preorders Movements for Skilled Action Sequences.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

6 authors.

Katja KornyshevaSchool of Psychology and Bangor Imaging Unit, Bangor University, Bangor, Wales LL57 2AS, UK; Institute of Cognitive Neuroscience, University College London, London WC1N 3AZ, UK. Electronic address: e.kornysheva@bangor.ac.uk.
Daniel BushInstitute of Cognitive Neuroscience, University College London, London WC1N 3AZ, UK; Queen Square Institute of Neurology, University College London, London WC1N 3BG, UK.
Sofie S MeyerInstitute of Cognitive Neuroscience, University College London, London WC1N 3AZ, UK; Queen Square Institute of Neurology, University College London, London WC1N 3BG, UK.
Anna SadnickaMotor Control and Disorders Group, St George's University of London, London SW17 0RE, UK; Sobell Department for Motor Neuroscience and Movement Disorders, University College London, London WC1N 3BG, UK.
Gareth BarnesWellcome Trust Centre for Human Neuroimaging, University College London, London WC1N 3AR, UK.
Neil BurgessInstitute of Cognitive Neuroscience, University College London, London WC1N 3AZ, UK; Queen Square Institute of Neurology, University College London, London WC1N 3BG, UK; Wellcome Trust Centre for Human Neuroimaging, University College London, London WC1N 3AR, UK.

Funding

Wellcome Trust 202805/Z/16/Z
6 · The paper itself

Abstract

Fluent retrieval and execution of movement sequences is essential for daily activities, but the neural mechanisms underlying sequence planning remain elusive. Here participants learned finger press sequences with different orders and timings and reproduced them in a magneto-encephalography (MEG) scanner. We classified the MEG patterns for each press in the sequence and examined pattern dynamics during preparation and production. Our results demonstrate the "competitive queuing" (CQ) of upcoming action representations, extending previous computational and non-human primate recording studies to non-invasive measures in humans. In addition, we show that CQ reflects an ordinal template that generalizes across specific motor actions at each position. Finally, we demonstrate that CQ predicts participants' production accuracy and originates from parahippocampal and cerebellar sources. These results suggest that the brain learns and controls multiple sequences by flexibly combining representations of specific actions and interval timing with high-level, parallel representations of sequence position.

Indexed as

AdultApraxiasBrainCerebellumFemaleHealthy VolunteersHumansLearningMagnetoencephalographyMaleMemoryMotor ActivityMovementParahippocampal GyrusPsychomotor PerformanceYoung Adult

Identifiers

PMID30744987
PMCPMC6436939

What OpenQuestion holds

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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.