Evidence map›Paper›PMID 39684352›Full record

ArticleInternational journal of molecular sciences2024

High- and Moderate-Risk Variants Among Breast Cancer Patients and Healthy Donors Enrolled in Multigene Panel Testing in a Population of Central Russia.

Syuykum Shumilova, Anastasia Danishevich, Sergey Nikolaev, George Krasnov, Anna Ikonnikova, Darya Isaeva, Sergei Surzhikov, Alexander Zasedatelev, Natalia Bodunova, Tatiana Nasedkina

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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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.

Syuykum ShumilovaEngelhardt Institute of Molecular Biology, the Russian Academy of Sciences, 119991 Moscow, Russia.ORCID 0000-0002-4124-9203
Anastasia DanishevichSBHI Moscow Clinical Scientific Center named after Loginov of Moscow Healthcare Department, 111123 Moscow, Russia.
Sergey NikolaevSBHI Moscow Clinical Scientific Center named after Loginov of Moscow Healthcare Department, 111123 Moscow, Russia.ORCID 0000-0003-0673-3590
George KrasnovEngelhardt Institute of Molecular Biology, the Russian Academy of Sciences, 119991 Moscow, Russia.ORCID 0000-0002-6493-8378
Anna IkonnikovaEngelhardt Institute of Molecular Biology, the Russian Academy of Sciences, 119991 Moscow, Russia.ORCID 0000-0002-8434-5916
Darya IsaevaSBHI Moscow Clinical Scientific Center named after Loginov of Moscow Healthcare Department, 111123 Moscow, Russia.
Sergei SurzhikovEngelhardt Institute of Molecular Biology, the Russian Academy of Sciences, 119991 Moscow, Russia.
Alexander ZasedatelevEngelhardt Institute of Molecular Biology, the Russian Academy of Sciences, 119991 Moscow, Russia.
Natalia BodunovaSBHI Moscow Clinical Scientific Center named after Loginov of Moscow Healthcare Department, 111123 Moscow, Russia.
Tatiana NasedkinaEngelhardt Institute of Molecular Biology, the Russian Academy of Sciences, 119991 Moscow, Russia.ORCID 0000-0002-2642-4202

Funding

the Russian Ministry of Science and High Education 05.604.21.0234 (RFMEFI60419X0234)
6 · The paper itself

Abstract

Assessments of breast cancer (BC) risk in carriers of pathogenic variants identified by gene panel testing in different populations are highly in demand worldwide. We performed target sequencing of 78 genes involved in DNA repair in 860 females with BC and 520 age- and family history-matched controls from Central Russia. Among BC patients, 562/860 (65.3%) were aged 50 years or less at the time of diagnosis. In total, 190/860 (22%) BC patients were carriers of 198 pathogenic/likely pathogenic (P/LP) variants in 30 genes, while among controls, 32/520 (6.2%) carriers of P/LP variants in 17 genes were identified. The odds ratio [95% confidence interval] was 16.3 [4.0-66.7] for

Indexed as

Breast NeoplasmsDNA RepairGenetic Predisposition to DiseaseGenetic TestingAdolescentAdultAgedAged, 80 and overCase-Control StudiesEarly Detection of CancerFemaleHeterozygoteHumansMiddle AgedMutationRisk AssessmentATMBRCA1/2breast cancer riskhealthy controlsmultigene panel testingpathogenic variantpatients

Identifiers

PMID39684352
PMCPMC11641773

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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.