Evidence map›Paper›PMID 42353617›Full record

ArticleCurrent issues in molecular biology2026

In Silico Systems Biology Approach for Prioritization of Candidate Genes Linked to Lipid Metabolism in the Context of Cardiovascular Disease Susceptibility in a Serbian Cohort.

Tamara Drljača, Vladimir Perović, Nevena Veljković, Branislava Gemović

Abstract read
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Article in Current issues in molecular biology, 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
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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

4 authors.

Tamara DrljačaLaboratory for Bioinformatics and Computational Chemistry, Institute of Nuclear Sciences Vinča, National Institute of the Republic of Serbia, University of Belgrade, 11000 Belgrade, Serbia.ORCID 0000-0002-1644-2538
Vladimir PerovićLaboratory for Bioinformatics and Computational Chemistry, Institute of Nuclear Sciences Vinča, National Institute of the Republic of Serbia, University of Belgrade, 11000 Belgrade, Serbia.ORCID 0000-0002-3700-6452
Nevena VeljkovićLaboratory for Bioinformatics and Computational Chemistry, Institute of Nuclear Sciences Vinča, National Institute of the Republic of Serbia, University of Belgrade, 11000 Belgrade, Serbia.
Branislava GemovićLaboratory for Bioinformatics and Computational Chemistry, Institute of Nuclear Sciences Vinča, National Institute of the Republic of Serbia, University of Belgrade, 11000 Belgrade, Serbia.ORCID 0000-0002-8987-020X

Funding

Ministry of Science, Technological Development, and Innovation 451-03-66/2024-03/200017
6 · The paper itself

Abstract

backgroundThe population of Serbia faces a significant burden from cardiovascular diseases (CVDs). This study aimed to computationally investigate genetic factors that contribute to the prevalence of these diseases by examining the possible involvement of common variants on lipid metabolism.

methodsWe examined how a variant prevalent in the Serbian population, chr7:g.56019730G>A in the

resultsThe PSP interactions affected by the R49W variant, such as SHMT1/2, were primarily in pathways associated with serine, glycine, and sphingolipid metabolism, highly relevant for CVD etiology. Further, we identified frequent variant combinations within the

conclusionsThis study underscores the importance of investigating genetic variant combinations in complex diseases, and provides a hypothesis generating foundation for future research into the relationship between these genes and cardiovascular diseases.

Indexed as

cardiovascular diseasescomputational biologylipid metabolismPSPHvariant combinations

Identifiers

PMID42353617
PMCPMC13298024

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