Evidence map›Paper›PMID 36142719›Full record

ReviewInternational journal of molecular sciences2022

Epilepsy Characteristics in Neurodevelopmental Disorders: Research from Patient Cohorts and Animal Models Focusing on Autism Spectrum Disorder.

Sukanya Chakraborty, Rrejusha Parayil, Shefali Mishra, Upendra Nongthomba, James P Clement

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
4.1field-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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Carvone derived cannabidiol enantiomers as novel anticonvulsants.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2025
    Article
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  8. Article
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  11. Article
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  14. Research progress inFrontiers in neurology
    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

5 authors at 2 institutions in 1 country.

Sukanya ChakrabortyNeuroscience Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bengaluru 560064, India.
Rrejusha ParayilNeuroscience Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bengaluru 560064, India.
Shefali MishraMolecular Reproduction, Development and Genetics (MRDG), Indian Institute of Science, Bengaluru 560012, India.
Upendra NongthombaMolecular Reproduction, Development and Genetics (MRDG), Indian Institute of Science, Bengaluru 560012, India.
James P ClementNeuroscience Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bengaluru 560064, India.ORCID 0000-0001-7625-6430
Jawaharlal Nehru Centre for Advanced Scientific Research · INIndian Institute of Science Bangalore · IN

Funding

Department of Biotechnology BT/PR28460/MED/122/169/2020Science and Engineering Research Board CRG/2021/000356Science and Engineering Research Board EMR/2016/004795
6 · The paper itself

Abstract

Epilepsy, a heterogeneous group of brain-related diseases, has continued to significantly burden society and families. Epilepsy comorbid with neurodevelopmental disorders (NDDs) is believed to occur due to multifaceted pathophysiological mechanisms involving disruptions in the excitation and inhibition (E/I) balance impeding widespread functional neuronal circuitry. Although the field has received much attention from the scientific community recently, the research has not yet translated into actionable therapeutics to completely cure epilepsy, particularly those comorbid with NDDs. In this review, we sought to elucidate the basic causes underlying epilepsy as well as those contributing to the association of epilepsy with NDDs. Comprehensive emphasis is put on some key neurodevelopmental genes implicated in epilepsy, such as

Indexed as

Autism Spectrum DisorderEpilepsyNeurodevelopmental DisordersAnimalsDisease Models, AnimalFragile X Messenger Ribonucleoprotein 1HumansRodentiaFMR1 protein, humanFragile X Messenger Ribonucleoprotein 1autism spectrum disorderbiomarkerselectroencephalographyepilepsyFmr1Mecp2Scna1ShankSyngap1Tsc1/2

Identifiers

PMID36142719
PMCPMC9501968
OpenAlexW4296353936

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.