Evidence map›Paper›PMID 41010011›Full record

ArticleGenes2025

Congenital Diaphragmatic Hernia and Joint Laxity: A Putative Link with Heritable Connective Tissue Disorders.

Alessandra Di Pede, Monia Magliozzi, Laura Valfré, Maria Lisa Dentici, Flaminia Pugnaloni, Viola Alesi, Andrea Conforti, Irma Capolupo, Annabella Braguglia, Andrea Dotta and 3 more

Abstract read
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. 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
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

13 authors.

Alessandra Di PedeMedical and Neonatal Sub-Intensive Unit, Bambino Gesù Children's Hospital IRCCS, 00165 Rome, Italy.
Monia MagliozziLaboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children's Hospital IRCCS, 00165 Rome, Italy.
Laura ValfréNeonatal and Pediatric Surgery Unit, Bambino Gesù Children's Hospital IRCCS, 00165 Rome, Italy.
Maria Lisa DenticiLaboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children's Hospital IRCCS, 00165 Rome, Italy.ORCID 0000-0002-9505-5906
Flaminia PugnaloniNeonatal Intensive Care Unit, Bambino Gesù Children's Hospital IRCCS, 00165 Rome, Italy.
Viola AlesiLaboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children's Hospital IRCCS, 00165 Rome, Italy.ORCID 0000-0001-7514-5683
Andrea ConfortiNeonatal and Pediatric Surgery Unit, Bambino Gesù Children's Hospital IRCCS, 00165 Rome, Italy.ORCID 0000-0002-0191-1880
Irma CapolupoNeonatal Intensive Care Unit, Bambino Gesù Children's Hospital IRCCS, 00165 Rome, Italy.ORCID 0000-0002-3090-2887
Annabella BragugliaMedical and Neonatal Sub-Intensive Unit, Bambino Gesù Children's Hospital IRCCS, 00165 Rome, Italy.
Andrea DottaNeonatal Intensive Care Unit, Bambino Gesù Children's Hospital IRCCS, 00165 Rome, Italy.ORCID 0000-0002-1260-6427
Pietro BagolanNeonatal and Pediatric Surgery Unit, Bambino Gesù Children's Hospital IRCCS, 00165 Rome, Italy.
Antonio NovelliLaboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children's Hospital IRCCS, 00165 Rome, Italy.ORCID 0000-0002-9037-4297
Maria Cristina DigilioMedical Genetics Unit, Translational Pediatrics and Clinical Genetics Research Area, Bambino Gesù Children's Hospital IRCCS, 00165 Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Connective Tissue DiseasesHernias, Diaphragmatic, CongenitalJoint InstabilityAdipokinesChildChild, PreschoolFemaleFibrillin-1Fibrillin-2Genetic TestingHumansInfantMaleMarfan SyndromeMutationReceptor, Notch1AdipokinesFBN1 protein, humanFBN2 protein, humanFibrillin-1Fibrillin-2Receptor, Notch1Vascular Endothelial Growth Factor AVEGFA protein, humancongenital diaphragmatic herniaconnective tissues disordersjoint laxityMarfan syndrome

Identifiers

PMID41010011
PMCPMC12469288

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.