Evidence map›Paper›PMID 30127996›Full record

ArticleOncology letters2018

Genetic variations in the

Efthimios Dardiotis, Vasileios Siokas, Antonios Garas, Evangelos Paraskevaidis, Maria Kyrgiou, Georgia Xiromerisiou, Efthimios Deligeoroglou, Georgios Galazios, Emmanuel N Kontomanolis, Demetrios A Spandidos and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Does SCFD1 rs10139154 Polymorphism Decrease Alzheimer's Disease Risk?Journal of molecular neuroscience : MN · 2019
    Article
  8. Article
  9. Lack of Association of the rs11655081 ARSG Gene with Blepharospasm.Journal of molecular neuroscience : MN · 2019
    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

12 authors at 7 institutions in 2 countries.

Efthimios DardiotisDepartment of Neurology, Laboratory of Neurogenetics, University of Thessaly, University Hospital of Larissa, 41100 Larissa, Greece.
Vasileios SiokasDepartment of Neurology, Laboratory of Neurogenetics, University of Thessaly, University Hospital of Larissa, 41100 Larissa, Greece.
Antonios GarasDepartment of Obstetrics and Gynecology, University Hospital of Larissa, 41100 Larissa, Greece.
Evangelos ParaskevaidisDivision of Obstetrics-Gynaecology, University Hospital of Ioannina, 45501 Ioannina, Greece.
Maria KyrgiouDepartment of Surgery and Cancer, IRDB, Imperial College London, London W120NN, UK.
Georgia XiromerisiouDepartment of Neurology, Laboratory of Neurogenetics, University of Thessaly, University Hospital of Larissa, 41100 Larissa, Greece.
Efthimios DeligeoroglouDivision of Pediatric-Adolescent Gynecology and Reconstructive Surgery, 2nd Department of Obstetrics and Gynecology, National and Kapodistrian University of Athens, Medical School, 'Aretaieion' Hospital, 11528 Athens, Greece.
Georgios GalaziosDepartment of Obstetrics/Gynecology, Democritus University of Thrace, 68100 Alexandroupolis, Greece.
Emmanuel N KontomanolisDepartment of Obstetrics/Gynecology, Democritus University of Thrace, 68100 Alexandroupolis, Greece.
Demetrios A SpandidosLaboratory of Clinical Virology, Medical School, University of Crete, 71003 Heraklion, Greece.
Aristidis TsatsakisLaboratory of Toxicology, Medical School, University of Crete, 71003 Heraklion, Greece.
Alexandros DaponteDepartment of Obstetrics and Gynecology, University Hospital of Larissa, 41100 Larissa, Greece.
University Hospital of Larissa · GRDemocritus University of Thrace · GRUniversity of Crete · GRImperial College London · GBNational and Kapodistrian University of Athens · GRUniversity Hospital of Ioannina · GRUniversity of Thessaly · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human papillomavirus (HPV) infection alone is not sufficient to explain the development of cervical cancer. Genetic variants have been linked to the development of precancerous lesions and cervical cancer. In this study, we aimed to evaluate the association of 10 single nucleotide polymorphisms (SNPs) of the Fas cell surface death receptor (

Indexed as

cell entry genescervical cancerDNA repairsulfatase 1viral infection

Identifiers

PMID30127996
PMCPMC6096185
OpenAlexW2846350463

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.