Evidence map›Paper›PMID 40149423›Full record

ArticleGenes2025

Exploring the Role of

Lorenzo Perilli, Simona Negro, Samanta Carbone, Michele Minerva, Maria Rosaria Curcio, Federica Lotti, Maria Antonietta Mencarelli, Francesca Ariani, Alessandra Renieri, Barbara Tomasini and 1 more

Abstract readCase Reports
In one paragraph

Article in Genes, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

11 authors.

Lorenzo PerilliClinical Pediatrics, Department of Molecular Medicine and Development, University of Siena, Azienda Ospedaliero-Universitaria Senese, 53100 Siena, Italy.ORCID 0000-0002-8630-6718
Simona NegroNeonatal Intensive Care Unit, Department of Molecular Medicine and Development, University of Siena, Azienda Ospedaliero-Universitaria Senese, 53100 Siena, Italy.ORCID 0000-0003-4249-3520
Samanta CarboneClinical Pediatrics, Department of Molecular Medicine and Development, University of Siena, Azienda Ospedaliero-Universitaria Senese, 53100 Siena, Italy.
Michele MinervaClinical Pediatrics, Department of Molecular Medicine and Development, University of Siena, Azienda Ospedaliero-Universitaria Senese, 53100 Siena, Italy.ORCID 0009-0003-4120-4878
Maria Rosaria CurcioClinical Pediatrics, Department of Molecular Medicine and Development, University of Siena, Azienda Ospedaliero-Universitaria Senese, 53100 Siena, Italy.
Federica LottiClinical Pediatrics, Department of Molecular Medicine and Development, University of Siena, Azienda Ospedaliero-Universitaria Senese, 53100 Siena, Italy.
Maria Antonietta MencarelliMedical Genetics, Department of Cellular Therapies, Hematology, and Laboratory Medicine, Azienda Ospedaliera-Universitaria Senese, 53100 Siena, Italy.
Francesca ArianiMedical Genetics, Department of Cellular Therapies, Hematology, and Laboratory Medicine, Azienda Ospedaliera-Universitaria Senese, 53100 Siena, Italy.
Alessandra RenieriMedical Genetics, Department of Cellular Therapies, Hematology, and Laboratory Medicine, Azienda Ospedaliera-Universitaria Senese, 53100 Siena, Italy.ORCID 0000-0002-0846-9220
Barbara TomasiniNeonatal Intensive Care Unit, Department of Molecular Medicine and Development, University of Siena, Azienda Ospedaliero-Universitaria Senese, 53100 Siena, Italy.
Salvatore GrossoClinical Pediatrics, Department of Molecular Medicine and Development, University of Siena, Azienda Ospedaliero-Universitaria Senese, 53100 Siena, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Craniofacial AbnormalitiesInterferon Regulatory FactorsIschemic StrokeExome SequencingFemaleHumansInfant, NewbornInterferon Regulatory FactorsIRF6 protein, humangenome wide associationIRF6ischaemic strokepediatric neurology

Identifiers

PMID40149423
PMCPMC11941822

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.