Evidence map›Paper›PMID 32567430›Full record

ArticleThe Journal of international medical research2020

Association between

Meng Gao, Kuo Zeng, Ya Li, Yong-Ping Liu, Xi Xia, Feng-Ling Xu, Jun Yao, Bao-Jie Wang

Open access · goldAbstract read
In one paragraph

Article in The Journal of international medical research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 29% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. The Candidate Schizophrenia Risk GeneFrontiers in endocrinology · 2021
    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

8 authors at 1 institution in 1 country.

Meng GaoSchool of Forensic Medicine, China Medical University, Shenyang, China.
Kuo ZengSchool of Forensic Medicine, China Medical University, Shenyang, China.
Ya LiSchool of Forensic Medicine, China Medical University, Shenyang, China.
Yong-Ping LiuSchool of Forensic Medicine, China Medical University, Shenyang, China.
Xi XiaSchool of Forensic Medicine, China Medical University, Shenyang, China.
Feng-Ling XuSchool of Forensic Medicine, China Medical University, Shenyang, China.
Jun YaoSchool of Forensic Medicine, China Medical University, Shenyang, China.ORCID https://orcid.org/0000-0003-0781-5694
Bao-Jie WangSchool of Forensic Medicine, China Medical University, Shenyang, China.ORCID https://orcid.org/0000-0003-1931-423X
China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveSchizophrenia is a severe neurodevelopmental disorder with a complex genetic and environmental etiology. The gene encoding EF-hand domain-containing protein D2 (

methodsWe genotyped four

resultsThe rs2473357 genotype and allele frequency distributions differed between SCZ and controls; however, this difference disappeared after Bonferroni correction. Differences in rs2473357 genotype and allele frequency distributions between SCZ and controls were more pronounced in men than in women. The G allele increased schizophrenia risk (odds ratio = 1.807, 95% confidence interval = 1.164-2.803). Among six haplotypes (G-, A-, G-insC, A-C, G-C, and G-T), the G- haplotype frequency distribution differed between SCZ and controls in women; the A-C and G-C haplotype frequency distributions differed between SCZ and controls in men.

conclusions

Indexed as

AdultAllelesAsian PeopleCalcium-Binding ProteinsCase-Control StudiesChinaEthnicityFemaleGene FrequencyGenetic Association StudiesGenetic Predisposition to DiseaseGenotypeHaplotypesHumansMaleMiddle AgedCalcium-Binding ProteinsEFHD2 protein, humanalleleEFHD2frequency distributiongenetic polymorphismgenetic risk factorgenotypehaplotypeschizophreniasingle nucleotide polymorphism

Identifiers

PMID32567430
PMCPMC7309398
OpenAlexW3036491817

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.