Evidence map›Paper›PMID 30797034›Full record

ArticleNeurobiology of learning and memory2019

Home-cage hypoactivity in mouse genetic models of autism spectrum disorder.

Christopher C Angelakos, Jennifer C Tudor, Sarah L Ferri, Thomas A Jongens, Ted Abel

Open access · bronzeAbstract read
In one paragraph

Article in Neurobiology of learning and memory, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

26 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Rescue of cone and rod photoreceptor function in a CDHR1-model of age-related retinal degeneration.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  9. Article
  10. GABAInternational journal of molecular sciences · 2023
    Article
  11. Article
  12. Deletion ofFrontiers in pharmacology · 2023
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  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

5 authors at 3 institutions in 1 country.

Christopher C AngelakosNeuroscience Graduate Group, University of Pennsylvania, Philadelphia, PA 19104, United States.
Jennifer C TudorDepartment of Biology, University of Pennsylvania, Philadelphia, PA 19104, United States; Department of Biology, Saint Joseph's University, Philadelphia, PA 19131, United States.
Sarah L FerriDepartment of Biology, University of Pennsylvania, Philadelphia, PA 19104, United States; Molecular Physiology and Biophysics, Iowa Neuroscience Institute, University of Iowa, Iowa City, IA 52242, United States.
Thomas A JongensDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, United States.
Ted AbelDepartment of Biology, University of Pennsylvania, Philadelphia, PA 19104, United States; Molecular Physiology and Biophysics, Iowa Neuroscience Institute, University of Iowa, Iowa City, IA 52242, United States. Electronic address: ted-abel@uiowa.edu.
University of Iowa · USUniversity of Pennsylvania · USSaint Joseph's University · US

Funding

Training Program in Neurodevelopmental DisabilitiesT32NS007413 · NINDS · CHILDREN'S HOSP OF PHILADELPHIA · PI AMELIA J EISCH, ERIC D MARSH · 1998 to 2026
$8.9M
The Intellectual and Developmental Disabilities Research Center at CHOP/PennU54HD086984 · NICHD · CHILDREN'S HOSP OF PHILADELPHIA · PI PUTT, MARY E. · 2016 to 2020
$6.3M
NICHD NIH HHS U54 HD086984NINDS NIH HHS T32 NS007413
6 · The paper itself

Abstract

Genome-wide association and whole exome sequencing studies from Autism Spectrum Disorder (ASD) patient populations have implicated numerous risk factor genes whose mutation or deletion results in significantly increased incidence of ASD. Behavioral studies of monogenic mutant mouse models of ASD-associated genes have been useful for identifying aberrant neural circuitry. However, behavioral results often differ from lab to lab, and studies incorporating both males and females are often not performed despite the significant sex-bias of ASD. In this study, we sought to investigate the simple, passive behavior of home-cage activity monitoring across multiple 24-h days in four different monogenic mouse models of ASD: Shank3b

Indexed as

Disease Models, AnimalAnimalsAutism Spectrum DisorderCadherinsCircadian RhythmFemaleFragile X Messenger Ribonucleoprotein 1MaleMembrane ProteinsMiceMice, KnockoutMicrofilament ProteinsMotor ActivityNerve Tissue ProteinsProtocadherinsSex FactorsCadherinsCNTNAP2 protein, mouseFmr1 protein, mouseFragile X Messenger Ribonucleoprotein 1Membrane ProteinsMicrofilament ProteinsNerve Tissue ProteinsPcdh10 protein, mouseProtocadherinsShank3 protein, mouseAutismCircadian rhythmsHome-cage activityHypoactivityMouse modelsSex differences

Identifiers

PMID30797034
PMCPMC6913530
OpenAlexW2916237377

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.