Evidence map›Paper›PMID 30607884›Full record

ReviewWorld journal of pediatrics : WJP2019

Autism spectrum disorders: autistic phenotypes and complicated mechanisms.

Xi-Cheng Zhang, Li-Qi Shu, Xing-Sen Zhao, Xue-Kun Li

Abstract readReview
PubMed Publisher
In one paragraph

Review in World journal of pediatrics : WJP, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.9field-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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Intermittent Hypobaric Hypoxia Ameliorates Autistic-Like Phenotypes in Mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Microbiota and Autism Spectrum Disorder.Avicenna journal of medical biotechnology
    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

4 authors at 3 institutions in 2 countries.

Xi-Cheng ZhangChildren's Hospital, Zhejiang University School of Medicine, Hangzhou, 310003, China.
Li-Qi ShuSchool of Medicine and Health Sciences, George Washington University, Washington, DC, USA.
Xing-Sen ZhaoChildren's Hospital, Zhejiang University School of Medicine, Hangzhou, 310003, China.
Xue-Kun LiChildren's Hospital, Zhejiang University School of Medicine, Hangzhou, 310003, China. xuekun_li@zju.edu.cn.
Children's Hospital of Zhejiang University · CNGeorge Washington University · USZhejiang University · CN

Funding

National Key Research and Development Program of China No. 2016YFC0900400the International Collaboration Program of Science Technology Department of Zhejiang Province 2016C34004the National Natural Science Foundation of China 31571518the National Natural Science Foundation of China 31771395
6 · The paper itself

Abstract

backgroundAutism spectrum disorder (ASD), a pervasive developmental neurological disorder, is characterized by impairments in social interaction and communication, and stereotyped, repetitive patterns of interests or behaviors. The mechanism of ASDs is complex, and genetic components and epigenetic modifications play important roles. In this review, we summarized the recent progresses of ASDs focusing on the genetic and epigenetic mechanisms. We also briefly discussed current animal models of ASD and the application of high-throughput sequencing technologies in studying ASD. DATA SOURCES: Original research articles and literature reviews published in PubMed-indexed journals.

resultsIndividuals with ASDs exhibit a set of phenotypes including neurological alteration. Genetic components including gene mutation, copy-number variations, and epigenetic modifications play important and diverse roles in ASDs. The establishment of animal models and development of new-generation sequencing technologies have contributed to reveal the complicated mechanisms underlying autistic phenotypes.

conclusionsDramatic progress has been made for understanding the roles of genetic and epigenetic components in ASD. Future basic and translational studies should be carried out towards those candidate therapeutic targets.

Indexed as

AnimalsAutism Spectrum DisorderDisease Models, AnimalDNA Copy Number VariationsDNA MethylationEpigenesis, GeneticGenetic VariationGenome-Wide Association StudyHigh-Throughput Nucleotide SequencingHumansMutationPhenotypeAutism spectrum disordersCNVEpigeneticsGeneticsNext-generation sequencing

Identifiers

PMID30607884
OpenAlexW2907975609

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.