Evidence map›Paper›PMID 36466804›Full record

ReviewFrontiers in molecular neuroscience2022

Alterations of presynaptic proteins in autism spectrum disorder.

Xin Yi Yeo, Yi Tang Lim, Woo Ri Chae, Chungwon Park, Hyokeun Park, Sangyong Jung

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in molecular neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

12 citing papers in PubMed, 13 citations in OpenAlex.

  1. Fully Automated Azeotropic Drying-Free Synthesis of [Molecules (Basel, Switzerland) · 2026
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  4. Membrane Merger Dynamics in Exocytosis and Endocytosis.Advances in experimental medicine and biology · 2026
    Review
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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

6 authors at 2 institutions in 3 countries.

Xin Yi YeoInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research, Singapore, Singapore.
Yi Tang LimInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research, Singapore, Singapore.
Woo Ri ChaeInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research, Singapore, Singapore.
Chungwon ParkDivision of Life Science, The Hong Kong University of Science and Technology, Kowloon, Hong Kong SAR, China.
Hyokeun ParkDivision of Life Science, The Hong Kong University of Science and Technology, Kowloon, Hong Kong SAR, China.
Sangyong JungInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research, Singapore, Singapore.
Agency for Science, Technology and Research · SGHong Kong University of Science and Technology · HK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The expanded use of hypothesis-free gene analysis methods in autism research has significantly increased the number of genetic risk factors associated with the pathogenesis of autism. A further examination of the implicated genes directly revealed the involvement in processes pertinent to neuronal differentiation, development, and function, with a predominant contribution from the regulators of synaptic function. Despite the importance of presynaptic function in synaptic transmission, the regulation of neuronal network activity, and the final behavioral output, there is a relative lack of understanding of the presynaptic contribution to the pathology of autism. Here, we will review the close association among autism-related mutations, autism spectrum disorders (ASD) phenotypes, and the altered presynaptic protein functions through a systematic examination of the presynaptic risk genes relating to the critical stages of synaptogenesis and neurotransmission.

Indexed as

autism spectrum disorders (ASD)presynaptic proteinspresynaptic vesicle dynamicssynaptogenesissynaptopathyvesicle release machinery

Identifiers

PMID36466804
PMCPMC9715400
OpenAlexW4309606058

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.