Evidence map›Paper›PMID 34739555›Full record

ArticleExperimental brain research2022

Pharmacological intervention in young adolescents rescues synaptic physiology and behavioural deficits in Syngap1

Vijaya Verma, M J Vijay Kumar, Kavita Sharma, Sridhar Rajaram, Ravi Muddashetty, Ravi Manjithaya, Thomas Behnisch, James P Clement

Abstract read
PubMed Publisher
In one paragraph

Article in Experimental brain research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 16% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. SYNGAP-1 Mutation And Catatonia: A Case Series and Systematic Review.Journal of child and adolescent psychopharmacology · 2024
    Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Adult Phenotype ofNeurology. Genetics · 2023
    Article
  7. AdultiScience · 2022
    Article
  8. Review
  9. 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

8 authors at 3 institutions in 2 countries.

Vijaya VermaNeuroscience Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore, 560064, India.
M J Vijay KumarNeuroscience Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore, 560064, India.
Kavita SharmaInternational Centre for Material Sciences, Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore, 560064, India.
Sridhar RajaramInternational Centre for Material Sciences, Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore, 560064, India.
Ravi MuddashettyInstitute for Stem Cell Biology and Regenerative Medicine, Bangalore, 560065, India.
Ravi ManjithayaNeuroscience Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore, 560064, India.
Thomas BehnischInstitutes of Brain Sciences, Fudan University, Shanghai, 200032, China.
James P ClementNeuroscience Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore, 560064, India. clement@jncasr.ac.in.ORCID http://orcid.org/0000-0001-7625-6430
Jawaharlal Nehru Centre for Advanced Scientific Research · INFudan University · CNInstitute for Stem Cell Biology and Regenerative Medicine · IN

Funding

science and engineering research board EMR/2016/004795science and engineering research board SB/YS/LS-215/2013
6 · The paper itself

Abstract

Haploinsufficiency in SYNGAP1 is implicated in intellectual disability (ID) and autism spectrum disorder (ASD) and affects the maturation of dendritic spines. The abnormal spine development has been suggested to cause a disbalance of excitatory and inhibitory (E/I) neurotransmission at distinct developmental periods. In addition, E/I imbalances in Syngap1

Indexed as

Autism Spectrum Disorderras GTPase-Activating ProteinsAnimalsGlycogen Synthase Kinase 3 betaMiceSynapsesSynaptic TransmissionGlycogen Synthase Kinase 3 betaras GTPase-Activating ProteinsSyngap1 protein, mouseAutism spectrum disorderGABAGSK-3βIntellectual disabilityKCC2NKCC1Syngap1 heterozygous mutation

Identifiers

PMID34739555
OpenAlexW3209737468

What OpenQuestion holds

Textmetadata
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.