Evidence map›Paper›PMID 24944800›Full record

ArticleBiomedical reports2014

WRN Cys1367Arg polymorphism is not associated with skull base chordoma.

Ke Wang, Liang Wang, Jie Feng, Shuyu Hao, Kaibing Tian, Zhen Wu, Liwei Zhang, Guijun Jia, Hong Wan, Junting Zhang

Open access · bronzeAbstract read
In one paragraph

Article in Biomedical reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 41% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. 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 2 institutions in 1 country.

Ke WangSkull Base and Brainstem Tumor Division, Department of Neurosurgery, Beijing Tian Tan Hospital, Beijing 100050, P.R. China.
Liang WangSkull Base and Brainstem Tumor Division, Department of Neurosurgery, Beijing Tian Tan Hospital, Beijing 100050, P.R. China.
Jie FengBeijing Neurosurgery Institute, Capital Medical University, Beijing 100050, P.R. China.
Shuyu HaoSkull Base and Brainstem Tumor Division, Department of Neurosurgery, Beijing Tian Tan Hospital, Beijing 100050, P.R. China.
Kaibing TianSkull Base and Brainstem Tumor Division, Department of Neurosurgery, Beijing Tian Tan Hospital, Beijing 100050, P.R. China.
Zhen WuSkull Base and Brainstem Tumor Division, Department of Neurosurgery, Beijing Tian Tan Hospital, Beijing 100050, P.R. China.
Liwei ZhangSkull Base and Brainstem Tumor Division, Department of Neurosurgery, Beijing Tian Tan Hospital, Beijing 100050, P.R. China.
Guijun JiaSkull Base and Brainstem Tumor Division, Department of Neurosurgery, Beijing Tian Tan Hospital, Beijing 100050, P.R. China.
Hong WanBeijing Neurosurgery Institute, Capital Medical University, Beijing 100050, P.R. China.
Junting ZhangSkull Base and Brainstem Tumor Division, Department of Neurosurgery, Beijing Tian Tan Hospital, Beijing 100050, P.R. China.
Beijing Tian Tan Hospital · CNCapital Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Skull base chordoma is a rare tumor with unknown risk factors. Werner syndrome, which is caused by a mutation in the WRN gene, is a disease of progeria, resembling the pathological process of aging. The present study aimed to provide data on the possible association between skull base chordoma and the single-nucleotide polymorphism (SNP) rs1346044 of the WRN gene. Between July, 2010 and September, 2012, a total of 65 patients with pathologically confirmed skull base chordoma and 65 control subjects were enrolled in this case-control study. The clinical data of the skull base chordoma patients were documented and the rs1346044 site in all the enrolled subjects was analyzed by sequencing and statistically compared using SPSS software. The A allele was the dominant allele of the rs1346044. The comparisons of genotype distributions and allele frequencies did not reveal any significant difference between the groups [P=0.383, 95% confidence interval (CI): 0.346-1.505]. The clinicopathological factors were assessed and no statistically significant difference was observed. In conclusion, the present study suggested that there is no association between rs1346044 SNP and skull base chordomas, at least in the population analyzed.

Indexed as

rs1346044single-nucleotide polymorphismskull base chordomaWRN gene

Identifiers

PMID24944800
PMCPMC4051466
OpenAlexW1993718415

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.