Evidence map›Paper›PMID 31762827›Full record

ArticleJournal of Cancer2019

Genetic variants in

Cheng-Yuan Gu, Sheng-Ming Jin, Xiao-Jian Qin, Yao Zhu, Dai Bo, Guo-Wen Lin, Guo-Hai Shi, Ding-Wei Ye

Abstract read
In one paragraph

Article in Journal of Cancer, 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
–field-weighted citation impact
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.

  1. Article
  2. Review
  3. Role of telomere length in human carcinogenesis (Review).International journal of oncology · 2023
    Review
  4. Article
  5. Article
  6. Article
  7. 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.

Cheng-Yuan GuDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Sheng-Ming JinDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Xiao-Jian QinDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Yao ZhuDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Dai BoDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Guo-Wen LinDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Guo-Hai ShiDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.
Ding-Wei YeDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Telomere length measured in lymphocytes has been evaluated as a potential biomarker for prostate cancer (PCa) risk. Identifying genetic variants that affect telomere length and testing their association with disease could clarify any causal role. We therefore investigated associations between genetic variants in three telomere length-related genes and PCa risk in a case-control study. The influence of these variants on the leukocyte telomere lengths was then appraised by real-time PCR.

Indexed as

polymorphismsprostate cancersusceptibilitytelomere

Identifiers

PMID31762827
PMCPMC6856594

What OpenQuestion holds

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LicenceCC BY
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.