Evidence map›Paper›PMID 25180302›Full record

ReviewPhilosophical transactions of the Royal Society of London. Series B, Biological sciences2014

Perspective: network-guided pattern formation of neural dynamics.

Marc-Thorsten Hütt, Marcus Kaiser, Claus C Hilgetag

Abstract readReview
In one paragraph

Review in Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. The brainstem connectome database.Scientific data · 2022
    Article
  7. NewFrontiers in physiology · 2022
    Article
  8. Link-usage asymmetry and collective patterns emerging from rich-club organization of complex networks.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  9. Review
  10. Self-assembly of biological networks via adaptive patterning revealed by avian intradermal muscle network formation.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  11. Article
  12. What We Know About the Brain Structure-Function Relationship.Behavioral sciences (Basel, Switzerland) · 2018
    Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Is the brain really a small-world network?Brain structure & function · 2016
    Article
  18. Article
  19. Article
  20. Complex network theory and the brain.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2014
    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.

Marc-Thorsten HüttSchool of Engineering and Science, Jacobs University Bremen, Bremen, Germany m.huett@jacobs-university.de.
Marcus KaiserSchool of Computing Science, Newcastle University, Claremont Tower, Newcastle upon Tyne NE1 7RU, UK Institute of Neuroscience, Newcastle University, Framlington Place, Newcastle upon Tyne NE2 4HH, UK.ORCID http://orcid.org/0000-0002-4654-3110
Claus C HilgetagDepartment of Computational Neuroscience, University Medical Center Eppendorf, Hamburg, Germany Department of Health Sciences, Boston University, Boston, MA, USA.ORCID http://orcid.org/0000-0003-2129-8910

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The understanding of neural activity patterns is fundamentally linked to an understanding of how the brain's network architecture shapes dynamical processes. Established approaches rely mostly on deviations of a given network from certain classes of random graphs. Hypotheses about the supposed role of prominent topological features (for instance, the roles of modularity, network motifs or hierarchical network organization) are derived from these deviations. An alternative strategy could be to study deviations of network architectures from regular graphs (rings and lattices) and consider the implications of such deviations for self-organized dynamic patterns on the network. Following this strategy, we draw on the theory of spatio-temporal pattern formation and propose a novel perspective for analysing dynamics on networks, by evaluating how the self-organized dynamics are confined by network architecture to a small set of permissible collective states. In particular, we discuss the role of prominent topological features of brain connectivity, such as hubs, modules and hierarchy, in shaping activity patterns. We illustrate the notion of network-guided pattern formation with numerical simulations and outline how it can facilitate the understanding of neural dynamics.

Indexed as

Models, NeurologicalBrainComputer SimulationHumansNerve NetNeural Pathwaysbrain connectivityhierarchymodularitynetwork analysisself-organizationTuring patterns

Identifiers

PMID25180302
PMCPMC4150299

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.