Evidence map›Paper›PMID 40426944›Full record

ReviewBiomedicines2025

Keep an Eye on Next Generation Sequencing (NGS) Technology: Secondary Findings and Differential Diagnosis in Inherited Retinal Dystrophies (IRDs).

Fabiana D'Esposito, Matteo Capobianco, Caterina Gagliano, Alessandro Avitabile, Giuseppe Gagliano, Gabriella Esposito, Edoardo Dammino, Antonio Carotenuto, Marco Zeppieri

Abstract readReview
In one paragraph

Review in Biomedicines, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

9 authors.

Fabiana D'EspositoImperial College Ophthalmic Research Group (ICORG) Unit, Imperial College, London NW15QH, UK.ORCID 0000-0002-7938-876X
Matteo CapobiancoDepartment of Ophthalmology, Catania University San Marco Hospital, 95121 Catania, Italy.ORCID 0009-0009-2969-8610
Caterina GaglianoDepartment of Medicine and Surgery, University of Enna "Kore", Piazza dell'Università, 94100 Enna, Italy.ORCID 0000-0001-8424-0068
Alessandro AvitabileDepartment of Ophthalmology, Catania University San Marco Hospital, 95121 Catania, Italy.ORCID 0009-0003-1051-876X
Giuseppe GaglianoDepartment of Ophthalmology, Catania University San Marco Hospital, 95121 Catania, Italy.ORCID 0009-0006-0059-5253
Gabriella EspositoDepartment of Molecular Medicine and Medical Biotechnologies, University of Naples Federico II, 80100 Naples, Italy.ORCID 0000-0002-4255-7312
Edoardo DamminoDepartment of Ophthalmology, Catania University San Marco Hospital, 95121 Catania, Italy.ORCID 0009-0008-0648-1040
Antonio CarotenutoDepartment of Neurosciences, Reproductive Sciences and Dentistry, University of Naples Federico II, 80131 Napoli, Italy.
Marco ZeppieriDepartment of Ophthalmology, University Hospital of Udine, 33100 Udine, Italy.ORCID 0000-0003-0999-5545

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

genotype–phenotype correlationinherited retinal dystrophiesmolecular diagnosisnext generation sequencing NGSNGS incidental findingsNGS secondary findings

Identifiers

PMID40426944
PMCPMC12109549

What OpenQuestion holds

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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.