Evidence map›Paper›PMID 32606704›Full record

ArticleNeuropsychiatric disease and treatment2020

Association Between Polymorphisms in the 5' Region of the

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

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Neuropsychiatric disease and treatment, 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
0.2field-weighted citation impact, top 54% 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. Review
  2. Article
  3. Involvement of Scratch2 in GalR1-mediated depression-like behaviors in the rat ventral periaqueductal gray.Proceedings of the National Academy of Sciences of the United States of America · 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

10 authors at 1 institution in 1 country.

Ya LiSchool of Forensic Medicine, China Medical University, Shenyang 110122, People's Republic of China.
Meng GaoSchool of Forensic Medicine, China Medical University, Shenyang 110122, People's Republic of China.
Kuo ZengSchool of Forensic Medicine, China Medical University, Shenyang 110122, People's Republic of China.
Jia-Xin XingSchool of Forensic Medicine, China Medical University, Shenyang 110122, People's Republic of China.
Feng-Ling XuSchool of Forensic Medicine, China Medical University, Shenyang 110122, People's Republic of China.
Jin-Feng XuanSchool of Forensic Medicine, China Medical University, Shenyang 110122, People's Republic of China.
Xi XiaSchool of Forensic Medicine, China Medical University, Shenyang 110122, People's Republic of China.
Yong-Ping LiuSchool of Forensic Medicine, China Medical University, Shenyang 110122, People's Republic of China.
Jun YaoSchool of Forensic Medicine, China Medical University, Shenyang 110122, People's Republic of China.ORCID 0000-0003-0781-5694
Bao-Jie WangSchool of Forensic Medicine, China Medical University, Shenyang 110122, People's Republic of China.
China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEpidemiological studies have shown that genetic factors are among the causes of schizophrenia. Galanin receptor 1 is an inhibitory receptor of galanin that is widely distributed in the central nervous system. This study mainly explored the relationship between polymorphisms of the 5' region of the

methodsA 1545 bp fragment of the 5' regulatory region of the

resultsAmong the haplotypes composed of the 16 detected SNPs, the haplotype H3 was identified as conferring a risk of schizophrenia (

conclusionThis study identified an association between polymorphisms in the 5' region of the

Indexed as

galanin receptor 1genetic polymorphismnorthern Chinese Han populationschizophreniasingle-nucleotide variant

Identifiers

PMID32606704
PMCPMC7306470
OpenAlexW3034328709

What OpenQuestion holds

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LicenceCC BY-NC
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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.