Evidence map›Paper›PMID 36756634›Full record

ArticleFrontiers in psychiatry2022

The association between gene polymorphisms in voltage-gated potassium channels Kv2.1 and Kv4.2 and susceptibility to autism spectrum disorder.

Zehui Liu, Xiaolei Yang, Peiwen Guo, Feng Wang, Wei Xia, Yuxin Chen, Mingyang Zou, Caihong Sun

Open access · goldAbstract read
In one paragraph

Article in Frontiers in psychiatry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

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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

8 authors at 3 institutions in 2 countries.

Zehui LiuDepartment of Children's and Adolescent Health, Public Health College, Harbin Medical University, Harbin, China.
Xiaolei YangDepartment of Preventive Medicine, School of Public Health, Qiqihar Medical University, Qiqihar, China.
Peiwen GuoDepartment of Children's and Adolescent Health, Public Health College, Harbin Medical University, Harbin, China.
Feng WangDepartment of Children's and Adolescent Health, Public Health College, Harbin Medical University, Harbin, China.
Wei XiaDepartment of Children's and Adolescent Health, Public Health College, Harbin Medical University, Harbin, China.
Yuxin ChenFaculty of Arts and Science, University of Toronto, Toronto, ON, Canada.
Mingyang ZouDepartment of Children's and Adolescent Health, Public Health College, Harbin Medical University, Harbin, China.
Caihong SunDepartment of Children's and Adolescent Health, Public Health College, Harbin Medical University, Harbin, China.
Harbin Medical University · CNQiqihar Medical University · CNUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Autism spectrum disorder (ASD) is a heritable form of neurodevelopmental disorder that arises through synaptic dysfunction. Given the involvement of voltage-gated potassium (Kv) channels in the regulation of synaptic plasticity, we aimed to explore the relationship between the genetic variants in the Methods: A total of 243 patients with ASD and 243 healthy controls were included in the present study. Sixty single nucleotide polymorphisms (SNPs) (35 in Results: There were no significant differences in the distribution of allele frequencies and genotype frequencies in Conclusion: Our results provide evidence that

Indexed as

autism spectrum disorderKv2.1Kv4.2single nucleotide polymorphismssusceptibility

Identifiers

PMID36756634
PMCPMC9900626
OpenAlexW4317745740

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.