Evidence map›Paper›PMID 36833207›Full record

ArticleGenes2023

Whole Exome Sequencing Study Suggests an Impact of

Alfiia Nurgalieva, Lilia Galliamova, Natalia Ekomasova, Maria Yankina, Dina Sakaeva, Ruslan Valiev, Darya Prokofyeva, Murat Dzhaubermezov, Yuliya Fedorova, Shamil Khusnutdinov and 1 more

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Genes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Exome sequencing points to pathogenic ATM variants in gastric cancer.European journal of human genetics : EJHG · 2026
    Article
  2. Article
  3. 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

11 authors at 2 institutions in 1 country.

Alfiia NurgalievaFederal State Budgetary Educational Institution of Higher Education, Ufa University of Science and Technology, 450076 Ufa, Russia.ORCID 0000-0001-6077-9237
Lilia GalliamovaFederal State Budgetary Educational Institution of Higher Education, Ufa University of Science and Technology, 450076 Ufa, Russia.
Natalia EkomasovaFederal State Budgetary Educational Institution of Higher Education, Ufa University of Science and Technology, 450076 Ufa, Russia.
Maria YankinaInstitute of Biochemistry and Genetics, Ufa Federal Research Center of the Russian Academy of Sciences, 450054 Ufa, Russia.
Dina SakaevaFederal State Educational Institution of Higher Education, Bashkir State Medical University, 450008 Ufa, Russia.
Ruslan ValievFederal State Budgetary Educational Institution of Higher Education, Ufa University of Science and Technology, 450076 Ufa, Russia.
Darya ProkofyevaFederal State Budgetary Educational Institution of Higher Education, Ufa University of Science and Technology, 450076 Ufa, Russia.
Murat DzhaubermezovFederal State Budgetary Educational Institution of Higher Education, Ufa University of Science and Technology, 450076 Ufa, Russia.
Yuliya FedorovaFederal State Budgetary Educational Institution of Higher Education, Ufa University of Science and Technology, 450076 Ufa, Russia.
Shamil KhusnutdinovFederal State Educational Institution of Higher Education, Bashkir State Medical University, 450008 Ufa, Russia.
Elza KhusnutdinovaFederal State Budgetary Educational Institution of Higher Education, Ufa University of Science and Technology, 450076 Ufa, Russia.ORCID 0000-0003-2987-3334
Bashkir State Medical University · RUUfa Institute of Chemistry · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gastric cancer (GC) is one of the most common cancer types in the world with a high mortality rate. Hereditary predisposition for GC is not fully elucidated so far. The aim of this study was identification of possible new candidate genes, associated with the increased risk of gastric cancer development. Whole exome sequencing (WES) was performed on 18 DNA samples from adenocarcinoma specimens and non-tumor-bearing healthy stomach tissue from the same patient. Three pathogenic variants were identified: c.1320+1G>A in the

Indexed as

Fanconi AnemiaStomach NeoplasmsAntigens, CDCadherinsExome SequencingFanconi Anemia Complementation Group A ProteinGenetic Predisposition to DiseaseGerm-Line MutationHumansVascular Endothelial Growth Factor AAntigens, CDCadherinsCDH1 protein, humanFANCA protein, humanFanconi Anemia Complementation Group A ProteinVascular Endothelial Growth Factor AVEGFA protein, humangastric cancergermline mutationspathogenic variantssomatic mutationswhole exome sequencing

Identifiers

PMID36833207
PMCPMC9956399
OpenAlexW4317930408

What OpenQuestion holds

Textmetadata
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.