Evidence map›Paper›PMID 40869921›Full record

ReviewGenes2025

Prenatal Rare 16q24.1 Deletion Between Genomics and Epigenetics: A Review.

Valentina Fumini, Romina Bonora, Anna Busciglio, Francesca Cartisano, Paola Celli, Ilaria Gabbiato, Nicola Guercini, Barbara Mancini, Donatella Saccilotto, Anna Zilio and 1 more

Abstract readReview
In one paragraph

Review 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

11 authors.

Valentina FuminiMedical Genetics and Genomic Unit, San Bortolo Hospital, 36100 Vicenza, Italy.
Romina BonoraMedical Genetics and Genomic Unit, San Bortolo Hospital, 36100 Vicenza, Italy.
Anna BusciglioMedical Genetics and Genomic Unit, San Bortolo Hospital, 36100 Vicenza, Italy.
Francesca CartisanoMedical Genetics and Genomic Unit, San Bortolo Hospital, 36100 Vicenza, Italy.
Paola CelliMedical Genetics and Genomic Unit, San Bortolo Hospital, 36100 Vicenza, Italy.
Ilaria GabbiatoMedical Genetics and Genomic Unit, San Bortolo Hospital, 36100 Vicenza, Italy.
Nicola GuerciniMedical Genetics and Genomic Unit, San Bortolo Hospital, 36100 Vicenza, Italy.
Barbara ManciniMedical Genetics and Genomic Unit, San Bortolo Hospital, 36100 Vicenza, Italy.ORCID 0009-0002-7000-4907
Donatella SaccilottoMedical Genetics and Genomic Unit, San Bortolo Hospital, 36100 Vicenza, Italy.
Anna ZilioMedical Genetics and Genomic Unit, San Bortolo Hospital, 36100 Vicenza, Italy.ORCID 0009-0007-9504-4514
Daniela ZuccarelloMedical Genetics and Genomic Unit, San Bortolo Hospital, 36100 Vicenza, Italy.ORCID 0000-0001-5826-6715

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alveolar capillary dysplasia with misalignment of pulmonary veins (ACDMPV) is a rare, often fatal congenital disorder characterized by severe neonatal respiratory distress and associated with complex multisystem malformations. In approximately 90% of cases, the condition is linked to deletions or mutations affecting the

Indexed as

Chromosome DeletionChromosomes, Human, Pair 16Epigenesis, GeneticForkhead Transcription FactorsPersistent Fetal Circulation SyndromeFemaleGenomicsHumansPregnancyPrenatal DiagnosisPulmonary AlveoliPulmonary VeinsUltrasonography, PrenatalForkhead Transcription FactorsFOXF1 protein, human16q24.1 microdeletionalveolar capillary dysplasia with misalignment of pulmonary veinsFOXF1

Identifiers

PMID40869921
PMCPMC12385333

What OpenQuestion holds

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Registered trials

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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.