Evidence map›Paper›PMID 30212237›Full record

ReviewAnnual review of genetics2018

Immunoglobulin-Like Receptors and Their Impact on Wiring of Brain Synapses.

Scott Cameron, A Kimberley McAllister

Open access · greenAbstract readReview
In one paragraph

Review in Annual review of genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

17 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Review
  3. An abundant membrane protein in the NCAM superfamily is required for epithelial organization in sea anemone embryos.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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  15. Article
  16. Neuronal immunoglobulin superfamily cell adhesion molecules in epithelial morphogenesis: insights fromPhilosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    Review
  17. Structure and Functions of Sidekicks.Frontiers in molecular neuroscience · 2020
    Review
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

2 authors at 1 institution in 1 country.

Scott CameronCenter for Neuroscience, University of California, Davis, California 95618, USA; email: sacameron@ucdavis.edu , kmcallister@ucdavis.edu.
A Kimberley McAllisterCenter for Neuroscience, University of California, Davis, California 95618, USA; email: sacameron@ucdavis.edu , kmcallister@ucdavis.edu.
University of California, Davis · US

Funding

UC Davis Conte Center: Neuroimmune Mechanisms of Psychiatric DisordersP50MH106438 · NIMH · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CARTER, CAMERON S. · 2015 to 2025
$26.1M
Immune Molecules in Early Postnatal Nervous System DevelopmentR01NS060125 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI MCALLISTER, A KIMBERLEY · 2010 to 2019
$3.3M
NIMH NIH HHS P50 MH106438NINDS NIH HHS R01 NS060125
6 · The paper itself

Abstract

Synapse formation is mediated by a surprisingly large number and wide variety of genes encoding many different protein classes. One of the families increasingly implicated in synapse wiring is the immunoglobulin superfamily (IgSF). IgSF molecules are by definition any protein containing at least one Ig-like domain, making this family one of the most common protein classes encoded by the genome. Here, we review the emerging roles for IgSF molecules in synapse formation specifically in the vertebrate brain, focusing on examples from three classes of IgSF members: ( a) cell adhesion molecules, ( b) signaling molecules, and ( c) immune molecules expressed in the brain. The critical roles for IgSF members in regulating synapse formation may explain their extensive involvement in neuropsychiatric and neurodevelopmental disorders. Solving the IgSF code for synapse formation may reveal multiple new targets for rescuing IgSF-mediated deficits in synapse formation and, eventually, new treatments for psychiatric disorders caused by altered IgSF-induced synapse wiring.

Indexed as

AnimalsBrainCell Adhesion MoleculesHumansImmunoglobulinsReceptor-Like Protein Tyrosine Phosphatases, Class 2SynapsesCell Adhesion MoleculesImmunoglobulinsReceptor-Like Protein Tyrosine Phosphatases, Class 2IgSFimmune moleculesimmunoglobulin superfamilyLAR-RPTPsMHCI moleculessynapse formationsynaptogenesis

Identifiers

PMID30212237
PMCPMC10821751
OpenAlexW2890722812

What OpenQuestion holds

Textmetadata
LicenceTDM
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.