Evidence map›Paper›PMID 42278264›Full record

ArticleInternational journal of molecular sciences2026

Experience in Molecular Genetic Diagnostics of Birt-Hogg-Dubé Syndrome: Characteristics of Identified Mutations and Evolution of the Methodological Approach.

Irina G Sermyagina, Dmitry S Mikhaylenko, Natalya B Kuryakova, Viktoria V Musatova, Olga A Solovova, Anait E Voskanyan, Ludmila A Bessonova, Yulia L Melyanovskaya, Elena I Kondratyeva, Alexander V Polyakov and 4 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2026. 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
–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

0 citing papers in PubMed.

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

14 authors.

Irina G SermyaginaResearch Centre for Medical Genetics, Moscow 115522, Russia.
Dmitry S MikhaylenkoResearch Centre for Medical Genetics, Moscow 115522, Russia.ORCID 0000-0001-9780-8708
Natalya B KuryakovaResearch Centre for Medical Genetics, Moscow 115522, Russia.ORCID 0009-0008-8108-2824
Viktoria V MusatovaResearch Centre for Medical Genetics, Moscow 115522, Russia.
Olga A SolovovaResearch Centre for Medical Genetics, Moscow 115522, Russia.ORCID 0000-0002-1389-4731
Anait E VoskanyanResearch Centre for Medical Genetics, Moscow 115522, Russia.
Ludmila A BessonovaResearch Centre for Medical Genetics, Moscow 115522, Russia.
Yulia L MelyanovskayaResearch Centre for Medical Genetics, Moscow 115522, Russia.ORCID 0000-0002-8814-5532
Elena I KondratyevaResearch Centre for Medical Genetics, Moscow 115522, Russia.ORCID 0000-0001-6395-0407
Alexander V PolyakovResearch Centre for Medical Genetics, Moscow 115522, Russia.
Olga A ShchaginaResearch Centre for Medical Genetics, Moscow 115522, Russia.ORCID 0000-0003-4905-1303
Dmitry V ZaletaevResearch Centre for Medical Genetics, Moscow 115522, Russia.ORCID 0000-0002-9323-2673
Sergey I KutsevResearch Centre for Medical Genetics, Moscow 115522, Russia.
Vladimir V StrelnikovResearch Centre for Medical Genetics, Moscow 115522, Russia.ORCID 0000-0001-9283-902X

Funding

Ministry of Science and Higher Education of the Russian Federation Federal Scientific-technical program for genetic technologies development for 2019-2030, agreement No. 075-15-2025-481
6 · The paper itself

Abstract

Birt-Hogg-Dubé syndrome (BHDS) is a hereditary cancer syndrome caused by pathogenic variants in the

Indexed as

Birt-Hogg-Dube SyndromeMutationProto-Oncogene ProteinsTumor Suppressor ProteinsAdultFemaleGerm-Line MutationHumansMaleMiddle AgedYoung AdultFLCN protein, humanProto-Oncogene ProteinsTumor Suppressor ProteinsBirt–Hogg–Dubé syndromeFLCN genegermline variantsequencing

Identifiers

PMID42278264
PMCPMC13256909

What OpenQuestion holds

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Registered trials

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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.