Evidence map›Paper›PMID 39273284›Full record

ReviewInternational journal of molecular sciences2024

The Spectrum of Disease-Associated Alleles in Countries with a Predominantly Slavic Population.

Grigoriy A Yanus, Evgeny N Suspitsin, Evgeny N Imyanitov

Abstract readReview
In one paragraph

Review 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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Breast-Ovarian Hereditary Cancer Syndrome: BeyondCurrent oncology (Toronto, Ont.) · 2026
    Review
  2. 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

3 authors.

Grigoriy A YanusLaboratory of Molecular Diagnostics, St. Petersburg State Pediatric Medical University, 194100 St. Petersburg, Russia.ORCID 0000-0002-9844-4536
Evgeny N SuspitsinDepartment of Medical Genetics, St. Petersburg State Pediatric Medical University, 194100 St. Petersburg, Russia.ORCID 0000-0001-9764-2090
Evgeny N ImyanitovDepartment of Medical Genetics, St. Petersburg State Pediatric Medical University, 194100 St. Petersburg, Russia.ORCID 0000-0003-4529-7891

Funding

Russian Science Foundation 24-45-00067
6 · The paper itself

Abstract

There are more than 260 million people of Slavic descent worldwide, who reside mainly in Eastern Europe but also represent a noticeable share of the population in the USA and Canada. Slavic populations, particularly Eastern Slavs and some Western Slavs, demonstrate a surprisingly high degree of genetic homogeneity, and, consequently, remarkable contribution of recurrent alleles associated with hereditary diseases. Along with pan-European pathogenic variants with clearly elevated occurrence in Slavic people (e.g.,

Indexed as

AllelesGenetic Predisposition to DiseaseEastern European PeopleGene FrequencyGenetic Diseases, InbornGenetics, PopulationGerm-Line MutationHumansfounder effectfounder mutationgenetic burdengermline mutationinherited diseasemedical geneticsnext-generation sequencingpathogenic variantsSlavs

Identifiers

PMID39273284
PMCPMC11394759

What OpenQuestion holds

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LicenceCC BY
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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.