Evidence map›Paper›PMID 26595880›Full record

ArticleBehavioral neuroscience2015

Heterozygous deletion of α-neurexin I or α-neurexin II results in behaviors relevant to autism and schizophrenia.

James Dachtler, Jose L Ivorra, Tessa E Rowland, Colin Lever, R John Rodgers, Steven J Clapcote

Open access · hybridAbstract read
In one paragraph

Article in Behavioral neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 2 pooled it
3.8field-weighted citation impact, top 6% 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

59 citing papers in PubMed, 2 syntheses or guidelines pooled it, 87 citations in OpenAlex.

  1. Pooled it
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  14. Alpha-neurexins in health and disease.Frontiers in molecular neuroscience · 2025
    Review
  15. Review
  16. Article
  17. Landscape ofJournal of clinical medicine · 2024
    Review
  18. Article
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  20. 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

6 authors at 2 institutions in 1 country.

James DachtlerSchool of Biomedical Sciences, University of Leeds.
Jose L IvorraSchool of Biomedical Sciences, University of Leeds.
Tessa E RowlandSchool of Biomedical Sciences, University of Leeds.
Colin LeverDepartment of Psychology, Durham University.
R John RodgersInstitute of Psychological Sciences, University of Leeds.
Steven J ClapcoteSchool of Biomedical Sciences, University of Leeds.
University of Leeds · GBDurham University · GB

Funding

Medical Research Council G0900625
6 · The paper itself

Abstract

The neurexins are a family of presynaptic cell adhesion molecules. Human genetic studies have found heterozygous deletions affecting NRXN1 and NRXN2, encoding α-neurexin I (Nrxn1α) and α-neurexin II (Nrxn2α), in individuals with autism spectrum disorders and schizophrenia. However, the link between α-neurexin deficiency and the manifestation of psychiatric disorders remain unclear. To assess whether the heterozygous loss of neurexins results in behaviors relevant to autism or schizophrenia, we used mice with heterozygous (HET) deletion of Nrxn1α or Nrxn2α. We found that in a test of social approach, Nrxn1α HET mice show no social memory for familiar versus novel conspecifics. In a passive avoidance test, female Nrxn1α HET mice cross to the conditioned chamber sooner than female wild-type and Nrxn2α HET mice. Nrxn2α HET mice also express a lack of long-term object discrimination, indicating a deficit in cognition. The observed Nrxn1α and Nrxn2α genotypic effects were specific, as neither HET deletion had effects on a wide range of other behavioral measures, including several measures of anxiety. Our findings demonstrate that the heterozygous loss of α-neurexin I and α-neurexin II in mice leads to phenotypes relevant to autism and schizophrenia.

Indexed as

Social BehaviorAnimalsAnxietyAutistic DisorderCalcium-Binding ProteinsCognitionDiscrimination, PsychologicalFemaleLearningMaleMemoryMice, Inbred C57BLMice, KnockoutMotor ActivityNerve Tissue ProteinsNeural Cell Adhesion MoleculesCalcium-Binding ProteinsNerve Tissue ProteinsNeural Cell Adhesion Moleculesneurexin IINrxn1 protein, mouse

Identifiers

PMID26595880
PMCPMC4655861
OpenAlexW2157320870

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.