Evidence map›Paper›PMID 27492494›Full record

ArticleAutism research : official journal of the International Society for Autism Research2017

Novel Shank3 mutant exhibits behaviors with face validity for autism and altered striatal and hippocampal function.

Thomas C Jaramillo, Haley E Speed, Zhong Xuan, Jeremy M Reimers, Christine Ochoa Escamilla, Travis P Weaver, Shunan Liu, Irina Filonova, Craig M Powell

Abstract read
In one paragraph

Article in Autism research : official journal of the International Society for Autism Research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed, 1 pooled it
5.5field-weighted citation impact, top 4% 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

78 citing papers in PubMed, 1 synthesis or guideline pooled it, 125 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Behavioral decline in Shank3Molecular autism · 2024
    Article
  14. Article
  15. Article
  16. Behavioral regression in shank3Research square · 2024
    Article
  17. Article
  18. Article
  19. HeterozygousHeliyon · 2024
    Article
  20. Article

18 more citing papers are in PubMed but not listed here.

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

9 authors at 1 institution in 1 country.

Thomas C JaramilloDepartment of Neurology and Neurotherapeutics, University of Texas Southwestern Medical Center, Dallas, Texas.
Haley E SpeedDepartment of Neurology and Neurotherapeutics, University of Texas Southwestern Medical Center, Dallas, Texas.
Zhong XuanDepartment of Neurology and Neurotherapeutics, University of Texas Southwestern Medical Center, Dallas, Texas.
Jeremy M ReimersDepartment of Neurology and Neurotherapeutics, University of Texas Southwestern Medical Center, Dallas, Texas.
Christine Ochoa EscamillaDepartment of Neurology and Neurotherapeutics, University of Texas Southwestern Medical Center, Dallas, Texas.
Travis P WeaverDepartment of Neurology and Neurotherapeutics, University of Texas Southwestern Medical Center, Dallas, Texas.
Shunan LiuDepartment of Neurology and Neurotherapeutics, University of Texas Southwestern Medical Center, Dallas, Texas.
Irina FilonovaDepartment of Neurology and Neurotherapeutics, University of Texas Southwestern Medical Center, Dallas, Texas.
Craig M PowellDepartment of Psychiatry and Neuroscience Graduate Program, University of Texas Southwestern Medical Center, Dallas, Texas.
The University of Texas Southwestern Medical Center · US

Funding

NOVEL GENETIC MODELS OF AUTISMR01HD069560 · NICHD · UT SOUTHWESTERN MEDICAL CENTER · PI POWELL, CRAIG M · 2011 to 2020
$4.8M
Novel Genetic Animal Models of AutismR21HD065290 · NICHD · UT SOUTHWESTERN MEDICAL CENTER · PI POWELL, CRAIG M · 2009 to 2010
$550k
NICHD NIH HHS R01 HD069560NICHD NIH HHS R21 HD065290
6 · The paper itself

Abstract

Mutations/deletions in the SHANK3 gene are associated with autism spectrum disorders and intellectual disability. Here, we present electrophysiological and behavioral consequences in novel heterozygous and homozygous mice with a transcriptional stop cassette inserted upstream of the PDZ domain-coding exons in Shank3 (Shank3

Indexed as

AnimalsAutistic DisorderBehavior, AnimalBlotting, WesternCorpus StriatumDisease Models, AnimalExonsFemaleHippocampusMaleMiceMice, KnockoutMicrofilament ProteinsMutationNerve Tissue ProteinsReproducibility of ResultsMicrofilament ProteinsNerve Tissue ProteinsShank3 protein, mouseautism spectrum disordergroomingmouse modelPhelan-McDermid syndromeShank3social interaction

Identifiers

PMID27492494
PMCPMC5274551
OpenAlexW2497572150

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.