Evidence map›Paper›PMID 38298632›Full record

ArticleHeliyon2024

Next-generation sequencing-based analysis of homologous recombination repair gene variant in ovarian cancer.

Yaolin Song, Wenwen Ran, Huiqing Jia, Qin Yao, Guangqi Li, Yang Chen, Xiaonan Wang, Yujing Xiao, Mengqi Sun, Xiao Lu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Heliyon, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 43% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

11 authors at 1 institution in 1 country.

Yaolin SongDepartment of Pathology, The Affiliated Hospital of Qingdao University, NO.16 Jiangsu Road, Qingdao, China.
Wenwen RanDepartment of Pathology, The Affiliated Hospital of Qingdao University, NO.16 Jiangsu Road, Qingdao, China.
Huiqing JiaDepartment of Pathology, The Affiliated Hospital of Qingdao University, NO.16 Jiangsu Road, Qingdao, China.
Qin YaoDepartment of Obstetrics and Gynecology, The Affiliated Hospital of Qingdao University, NO.16 Jiangsu Road, Qingdao, China.
Guangqi LiDepartment of Pathology, The Affiliated Hospital of Qingdao University, NO.16 Jiangsu Road, Qingdao, China.
Yang ChenDepartment of Pathology, The Affiliated Hospital of Qingdao University, NO.16 Jiangsu Road, Qingdao, China.
Xiaonan WangDepartment of Pathology, The Affiliated Hospital of Qingdao University, NO.16 Jiangsu Road, Qingdao, China.
Yujing XiaoDepartment of Pathology, The Affiliated Hospital of Qingdao University, NO.16 Jiangsu Road, Qingdao, China.
Mengqi SunDepartment of Pathology, The Affiliated Hospital of Qingdao University, NO.16 Jiangsu Road, Qingdao, China.
Xiao LuDepartment of Pathology, The Affiliated Hospital of Qingdao University, NO.16 Jiangsu Road, Qingdao, China.
Xiaoming XingDepartment of Pathology, The Affiliated Hospital of Qingdao University, NO.16 Jiangsu Road, Qingdao, China.
Qingdao University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Ovarian cancer is the leading cause of death from gynecological malignancies. Investigating the HRR-related gene status, notably Methods: We collected 124 ovarian cancer cases from the Affiliated Hospital of.Qingdao University, detected the genomic alteration of 32 genes by NGS, including.19 HRR-related genes, 9 proto-oncogenes and 4 tumor suppressor genes. Clinicopathological characteristics, variants, clinical significance, and correlation with prognosis were analyzed. Results: The incidence of HRR-related gene mutation was 59.68 % and no statistical significance was found with multiple clinicopathological characteristics. Conclusions: Somatic

Indexed as

BRCA1/2 mutationGeneration sequencingHomologous recombination repairNextOvarian cancerPrognosis

Identifiers

PMID38298632
PMCPMC10827683
OpenAlexW4390611280

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.