Evidence map›Paper›PMID 31122238›Full record

ArticleBMC psychiatry2019

Family-based association study of ZNF804A polymorphisms and autism in a Han Chinese population.

Ziqi Wang, Tian Zhang, Jing Liu, Han Wang, Tianlan Lu, Meixiang Jia, Dai Zhang, Lifang Wang, Jun Li

Open access · goldAbstract read
In one paragraph

Article in BMC psychiatry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Genetic polymorphism and neuroanatomical changes in schizophrenia.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    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

9 authors at 2 institutions in 1 country.

Ziqi WangPeking University Sixth Hospital, No. 51, Hua Yuan Bei Road, Beijing, 100191, China.
Tian ZhangPeking University Sixth Hospital, No. 51, Hua Yuan Bei Road, Beijing, 100191, China.
Jing LiuPeking University Sixth Hospital, No. 51, Hua Yuan Bei Road, Beijing, 100191, China.
Han WangPeking University Sixth Hospital, No. 51, Hua Yuan Bei Road, Beijing, 100191, China.
Tianlan LuPeking University Sixth Hospital, No. 51, Hua Yuan Bei Road, Beijing, 100191, China.
Meixiang JiaPeking University Sixth Hospital, No. 51, Hua Yuan Bei Road, Beijing, 100191, China.
Dai ZhangPeking University Sixth Hospital, No. 51, Hua Yuan Bei Road, Beijing, 100191, China. daizhang@bjmu.edu.cn.
Lifang WangPeking University Sixth Hospital, No. 51, Hua Yuan Bei Road, Beijing, 100191, China. lifangwang@bjmu.edu.cn.
Jun LiPeking University Sixth Hospital, No. 51, Hua Yuan Bei Road, Beijing, 100191, China. junli1985@bjmu.edu.cn.
Peking University Sixth Hospital · CNPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAutism is a complex neurodevelopmental disorder with high heritability. Zinc finger protein 804A (ZNF804A) was suggested to play important roles in neurodevelopment. Previous studies indicated that single-nucleotide polymorphism (SNP) rs1344706 in ZNF804A was strongly associated with schizophrenia and might influence social interaction. Only one study explored the significance of ZNF804A polymorphisms in autism, which discovered that rs7603001 was nominally associated with autism. Moreover, no previous study investigated the association between ZNF804A and autism in a Han Chinese population. Here, we investigated whether these two SNPs (rs1344706 and rs7603001) in ZNF804A contribute to the risk of autism in a Han Chinese population.

methodsWe performed a family-based association study in 640 Han Chinese autism trios. Sanger sequencing was used for sample genotyping. Then, single marker association analyses were conducted using the family-based association test (FBAT) program.

resultsNo significant association was found between the two SNPs (rs1344706 and rs7603001) in ZNF804A and autism (P > 0.05).

conclusionsOur findings suggested that rs1344706 and rs7603001 in ZNF804A might not be associated with autism in a Han Chinese population.

Indexed as

Population SurveillanceAdolescentAsian PeopleAutistic DisorderChildChild, PreschoolFamily RelationsFemaleGenetic Association StudiesGenetic Predisposition to DiseaseHumansKruppel-Like Transcription FactorsMalePolymorphism, Single NucleotideKruppel-Like Transcription FactorsZNF804A protein, humanAutismFamily-based association studySingle-nucleotide polymorphismZNF804A

Identifiers

PMID31122238
PMCPMC6533675
OpenAlexW2947346054

What OpenQuestion holds

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LicenceCC BY
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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.