In one paragraphArticle in Genes, 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
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
9 authors.
Agnieszka Madej-PilarczykDepartment of Medical Genetics, The Children's Memorial Health Institute, Member of the European Reference Network ITHACA, 04-730 Warsaw, Poland.ORCID 0009-0003-7671-2848 Marzena GawlikDepartment of Medical Genetics, The Children's Memorial Health Institute, Member of the European Reference Network ITHACA, 04-730 Warsaw, Poland.
Beata ChałupczyńskaDepartment of Medical Genetics, The Children's Memorial Health Institute, Member of the European Reference Network ITHACA, 04-730 Warsaw, Poland.ORCID 0009-0004-1782-8127 Jagoda BłaszkiewiczDepartment of Medical Genetics, The Children's Memorial Health Institute, Member of the European Reference Network ITHACA, 04-730 Warsaw, Poland.
Dorota WicherDepartment of Medical Genetics, The Children's Memorial Health Institute, Member of the European Reference Network ITHACA, 04-730 Warsaw, Poland.ORCID 0000-0002-8360-0006 Agata CieślikowskaDepartment of Medical Genetics, The Children's Memorial Health Institute, Member of the European Reference Network ITHACA, 04-730 Warsaw, Poland.ORCID 0000-0003-0603-7763 Anila Babameto-LakuService of Genetics Laboratory, Faculty of Medicine, University Hospital Center "Mother Teresa", 1000 Tirana, Albania.
Krystyna ChrzanowskaDepartment of Medical Genetics, The Children's Memorial Health Institute, Member of the European Reference Network ITHACA, 04-730 Warsaw, Poland.ORCID 0000-0003-3888-0624 Elżbieta CiaraDepartment of Medical Genetics, The Children's Memorial Health Institute, Member of the European Reference Network ITHACA, 04-730 Warsaw, Poland.ORCID 0000-0002-1065-7968 Funding
CMHI projects S205/2024, MEiN 7071/IB/SN/2020, MEiN 7088/II-KDM/SN/2020
6 · The paper itselfAbstract
PubMed holds no abstract for this paper.
Indexed as
DNA-Binding ProteinsNeurodevelopmental DisordersTranscription FactorsAdolescentChildChild, PreschoolFemaleHumansInfantMaleMutationPhenotypeDNA-Binding ProteinsPURA protein, humanTranscription Factorsepileptic encephalopathyhypotoniamolecular geneticsPURA gene variantsPURA-NDDPURA-related neurodevelopmental disorderrare disorder
Identifiers
PMID42510805
PMCPMC13409535
What OpenQuestion holds
Textmetadata
LicenceCC BY
Read underepoch 390