Evidence map›Paper›PMID 31686851›Full record

ArticleOncoTargets and therapy2019

Contribution of interaction between genetic variants of interleukin-11 and

Chuanwen Liao, Shuqin Hu, Zihan Zheng, Huazhang Tong

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

Article in OncoTargets and therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Identification of Hub Genes in Type 2 Diabetes Mellitus Using Bioinformatics Analysis.Diabetes, metabolic syndrome and obesity : targets and therapy · 2020
    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

4 authors at 1 institution in 1 country.

Chuanwen LiaoDepartment of Gastrointestinal Surgery, People's Hospital of Jiangxi Province, Nanchang, Jiangxi Province 330006, People's Republic of China.
Shuqin HuMedical Department, People's Hospital of Jiangxi Province, Nanchang, Jiangxi Province 330006, People's Republic of China.
Zihan ZhengDepartment of Gastrointestinal Surgery, People's Hospital of Jiangxi Province, Nanchang, Jiangxi Province 330006, People's Republic of China.
Huazhang TongDepartment of Radiotherapy, People's Hospital of Jiangxi Province, Nanchang, Jiangxi Province 330006, People's Republic of China.
Jiangxi Provincial People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGastric cancer (GC) ranks the second leading cause of cancer-related mortality worldwide. We aimed to clarify the relevance of genetic variants of

methodsA case-control study with 880 GC cases and 900 healthy controls was conducted in a Chinese population. Six tagSNPs were detected by Taqman Allelic Discrimination assay, while

resultsWe found that rs1126760 (C vs T: OR=1.39, 95% CIs=1.13-1.70,

conclusionOur study provides strong evidence that genetic variants of the

Indexed as

gastric cancerHelicobacter pyloriIL-11polymorphism

Identifiers

PMID31686851
PMCPMC6751226
OpenAlexW2973140693

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.