Evidence map›Paper›PMID 27567313›Full record

ArticleBiological psychiatry2017

Sociability Deficits and Altered Amygdala Circuits in Mice Lacking Pcdh10, an Autism Associated Gene.

Hannah Schoch, Arati S Kreibich, Sarah L Ferri, Rachel S White, Dominique Bohorquez, Anamika Banerjee, Russell G Port, Holly C Dow, Lucero Cordero, Ashley A Pallathra and 11 more

Abstract read
In one paragraph

Article in Biological psychiatry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

37 citing papers in PubMed, 94 citations in OpenAlex.

  1. Article
  2. Long-read whole-genome sequencing of SHR rat substrains with distinct substance use phenotypes.Mammalian genome : official journal of the International Mammalian Genome Society · 2025
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  3. Article
  4. Review
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  6. Article
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  8. Article
  9. The role of Pcdh10 in neurological disease and cancer.Journal of cancer research and clinical oncology · 2023
    Review
  10. Genes · 2023
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Krüppel-like Transcription Factor 7 Is a Causal Gene in Autism Development.International journal of molecular sciences · 2022
    Article
  16. Article
  17. Article
  18. Article
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  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 3 institutions in 3 countries.

Hannah SchochCell and Molecular Biology Graduate Group, Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Arati S KreibichCenter for Neurobiology and Behavior, Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Sarah L FerriDepartment of Biology, University of Pennsylvania, Philadelphia.
Rachel S WhiteCenter for Neurobiology and Behavior, Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Dominique BohorquezCenter for Neurobiology and Behavior, Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Anamika BanerjeeCenter for Neurobiology and Behavior, Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Russell G PortCenter for Neurobiology and Behavior, Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Holly C DowCenter for Neurobiology and Behavior, Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Lucero CorderoCenter for Neurobiology and Behavior, Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Ashley A PallathraCenter for Neurobiology and Behavior, Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Hyong KimCenter for Neurobiology and Behavior, Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Hongzhe LiDepartment of Biostatistics and Epidemiology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Warren B BilkerDepartment of Biostatistics and Epidemiology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Shinji HiranoDepartment of Cell Biology, Kansai Medical University, Osaka, Japan.
Robert T SchultzDepartment of Psychiatry,Perelman School of Medicine at the University of Pennsylvania, Philadelphia; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia; Center for Autism Research, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Karin Borgmann-WinterCenter for Neurobiology and Behavior, Perelman School of Medicine at the University of Pennsylvania, Philadelphia; Department of Child and Adolescent Psychiatry, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Chang-Gyu HahnCenter for Neurobiology and Behavior, Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Dirk FeldmeyerInstitute of Neuroscience and Medicine, Forschungzentrum Julich, Julich; Department of Psychiatry, Psychotherapy and Psychosomatics, Medical School, RWTH Aachen University, Aachen, Germany.
Gregory C CarlsonCenter for Neurobiology and Behavior, Perelman School of Medicine at the University of Pennsylvania, Philadelphia.
Ted AbelDepartment of Biology, University of Pennsylvania, Philadelphia.
Edward S BrodkinCenter for Neurobiology and Behavior, Perelman School of Medicine at the University of Pennsylvania, Philadelphia. Electronic address: ebrodkin@mail.med.upenn.edu.
University of Pennsylvania · USForschungszentrum Jülich · DEKansai Medical University · JP

Funding

NMDA Receptor Hypofunction in the Amygdala of Schizophrenia PatientsP50MH096891 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI BILKER, WARREN B. · 2012 to 2016
$10.6M
Training Program in Neurodevelopmental DisabilitiesT32NS007413 · NINDS · CHILDREN'S HOSP OF PHILADELPHIA · PI AMELIA J EISCH, ERIC D MARSH · 1998 to 2026
$8.9M
TRAINING PROGRAM IN BEHAVIORAL/COGNITIVE NEUROSCIENCET32MH017168 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI KABLE, JOSEPH W · 1985 to 2018
$4.2M
Neurobiology of sociability in a mouse model system relevant to autismR01MH080718 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI BRODKIN, EDWARD S · 2007 to 2011
$1.9M
ARRA NIH HHSNIMH NIH HHS P50 MH096891NIMH NIH HHS R01 MH080718NIMH NIH HHS T32 MH017168NINDS NIH HHS T32 NS007413
6 · The paper itself

Abstract

backgroundBehavioral symptoms in individuals with autism spectrum disorder (ASD) have been attributed to abnormal neuronal connectivity, but the molecular bases of these behavioral and brain phenotypes are largely unknown. Human genetic studies have implicated PCDH10, a member of the δ2 subfamily of nonclustered protocadherin genes, in ASD. PCDH10 expression is enriched in the basolateral amygdala, a brain region implicated in the social deficits of ASD. Previous reports indicate that Pcdh10 plays a role in axon outgrowth and glutamatergic synapse elimination, but its roles in social behaviors and amygdala neuronal connectivity are unknown. We hypothesized that haploinsufficiency of Pcdh10 would reduce social approach behavior and alter the structure and function of amygdala circuits.

methodsMice lacking one copy of Pcdh10 (Pcdh10

resultsMale Pcdh10

conclusionsOur studies reveal that male Pcdh10

Indexed as

Social BehaviorAmygdalaAnimalsAutism Spectrum DisorderBehavior, AnimalCadherinsDendritic SpinesDisease Models, AnimalElectric StimulationFemaleGamma RhythmHaploinsufficiencyMaleMiceMice, Inbred C57BLMice, Mutant StrainsCadherinsGprin1 protein, mouseNerve Tissue ProteinsPcdh10 protein, mouseProtocadherinsReceptors, N-Methyl-D-AspartateAmygdalaAutismGeneNMDAProtocadherinSynapse

Identifiers

PMID27567313
PMCPMC5161717
OpenAlexW2433184682

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.