Evidence map›Paper›PMID 42884048›Full record

ArticleInternational journal of molecular sciences2026

Clinical and Genetic Characterization of Russian Patients with von Hippel-Lindau Syndrome.

Dmitry S Mikhaylenko, Natalya N Vasserman, Natalya B Kuryakova, Ekaterina B Kuznetsova, Nina A Gorban, Anna A Stepanova, Olga A Shchagina, Alexander V Polyakov, Dmitry V Zaletaev, Sergey I Kutsev and 1 more

Abstract read
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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

11 authors.

Dmitry S MikhaylenkoResearch Centre for Medical Genetics, Moscow 115522, Russia.ORCID 0000-0001-9780-8708
Natalya N VassermanResearch Centre for Medical Genetics, Moscow 115522, Russia.
Natalya B KuryakovaResearch Centre for Medical Genetics, Moscow 115522, Russia.ORCID 0009-0008-8108-2824
Ekaterina B KuznetsovaResearch Centre for Medical Genetics, Moscow 115522, Russia.ORCID 0000-0001-5825-0430
Nina A GorbanResearch Centre for Medical Genetics, Moscow 115522, Russia.
Anna A StepanovaResearch Centre for Medical Genetics, Moscow 115522, Russia.ORCID 0000-0003-0416-8137
Olga A ShchaginaResearch Centre for Medical Genetics, Moscow 115522, Russia.ORCID 0000-0003-4905-1303
Alexander V PolyakovResearch Centre for Medical Genetics, Moscow 115522, Russia.
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
6 · The paper itself

Abstract

Von Hippel-Lindau syndrome (VHLS) is an autosomal dominant hereditary cancer disease caused by germline mutations in the

Indexed as

von Hippel-Lindau DiseaseVon Hippel-Lindau Tumor Suppressor ProteinAdolescentAdultAgedFemaleGenetic Association StudiesGerm-Line MutationHumansMaleMiddle AgedRussiaYoung AdultVHL protein, humanVon Hippel-Lindau Tumor Suppressor Proteingermline variantrenal cancersequencingVHL genevon Hippel–Lindau syndrome

Identifiers

PMID42884048
PMCPMC13665197

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.