ArticleDiagnostics (Basel, Switzerland)2025
A Specific Haplotype of the
Ana Djuranovic Uklein, Natasa Cerovac, Dijana Perovic, Nela Maksimovic, Biljana Jekic, Milka Grk, Marija Dusanovic Pjevic, Milica Rasic, Natasa Stojanovski, Milica Pesic and 2 more
Abstract read
In one paragraphArticle in Diagnostics (Basel, Switzerland), 2025. 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
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 registryThe 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 literatureWho cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
4 · The recordCorrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
5 · Who and what moneyAuthors and funding
12 authors.
Ana Djuranovic UkleinInstitute of Human Genetics, Faculty of Medicine, University of Belgrade, 11000 Belgrade, Serbia.ORCID 0000-0002-8144-4433 Dijana PerovicInstitute of Human Genetics, Faculty of Medicine, University of Belgrade, 11000 Belgrade, Serbia.ORCID 0000-0003-1077-2373 Nela MaksimovicInstitute of Human Genetics, Faculty of Medicine, University of Belgrade, 11000 Belgrade, Serbia.ORCID 0000-0002-5815-573X Biljana JekicInstitute of Human Genetics, Faculty of Medicine, University of Belgrade, 11000 Belgrade, Serbia.
Milka GrkInstitute of Human Genetics, Faculty of Medicine, University of Belgrade, 11000 Belgrade, Serbia.ORCID 0000-0002-7534-9608 Marija Dusanovic PjevicInstitute of Human Genetics, Faculty of Medicine, University of Belgrade, 11000 Belgrade, Serbia.ORCID 0000-0002-3564-2623 Milica RasicInstitute of Human Genetics, Faculty of Medicine, University of Belgrade, 11000 Belgrade, Serbia.ORCID 0000-0002-3269-7872 Natasa StojanovskiInstitute of Human Genetics, Faculty of Medicine, University of Belgrade, 11000 Belgrade, Serbia.ORCID 0009-0005-2582-9557 Milica PesicInstitute of Human Genetics, Faculty of Medicine, University of Belgrade, 11000 Belgrade, Serbia.
Ivana NovakovicInstitute of Human Genetics, Faculty of Medicine, University of Belgrade, 11000 Belgrade, Serbia.
Tatjana DamnjanovicInstitute of Human Genetics, Faculty of Medicine, University of Belgrade, 11000 Belgrade, Serbia.
Funding
Ministry of Science, Technological Development, and Innovation of the Republic of Serbia 451-03-66/2024-03/200110
6 · The paper itselfAbstract
PubMed holds no abstract for this paper.
Indexed as
cerebral palsyhypoxic–ischemic encephalopathyMMP2MRIpromoter polymorphisms
Identifiers
PMID41464177
PMCPMC12731818
What OpenQuestion holds
Textmetadata
LicenceCC BY
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