Evidence map›Paper›PMID 36246885›Full record

ArticleFrontiers in endocrinology2022

The impact of genetic variants in the

Weixing Qu, Fuzhou Zhang, Yongyi Cheng, Jing Li, Jiancheng Zhou

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 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
1.5field-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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Annals of medicine · 2025
    Article
  2. Article
  3. Article
  4. Comment on "telomerase reverse transcriptase rs2736098 and rs2736100 in bladder cancer".Reports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology · 2023
    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

5 authors at 4 institutions in 1 country.

Weixing QuDepartment of Urology, Shaanxi Provincial People's Hospital, Xi'an, China.
Fuzhou ZhangDepartment of Urology, First Hospital of Weinan City, Weinan, China.
Yongyi ChengDepartment of Urology, Shaanxi Provincial People's Hospital, Xi'an, China.
Jing LiDepartment of Urology, Shaanxi Provincial People's Hospital, Xi'an, China.
Jiancheng ZhouDepartment of Urology, Shaanxi Provincial People's Hospital, Xi'an, China.
Shaanxi Provincial People's Hospital · CNShaanxi Provincial People's Hospital · CNShanxi Medical University · CNWeinan Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Bladder cancer is the most common leading cause of mortality around the world. Previous studies have indicated that genetic factors are significantly associated with bladder cancer progression-for instance, the Methods: This study included 550 healthy subjects and 217 bladder cancer patients. The odds ratios (ORs) and 95% confidence intervals (CIs) were calculated to determine the correlation of Results: Our study showed that two SNPs were significantly associated with an increased risk of bladder cancer (rs1934951: OR 1.96, 95% CI 1.37-2.82, Conclusion: There was a significant association between

Indexed as

Urinary Bladder NeoplasmsCytochrome P-450 CYP2C8HumansOdds RatioPolymorphism, Single NucleotideCYP2C8 protein, humanCytochrome P-450 CYP2C8bladder cancercase–control studyCYP2C8genetic variantssusceptibility

Identifiers

PMID36246885
PMCPMC9554954
OpenAlexW4297493502

What OpenQuestion holds

Textmetadata
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.