Evidence map›Paper›PMID 40428346›Full record

ReviewGenes2025

Phenotypic Spectrum of

Maria Giovanna Tedesco, Ilaria Donati, Chiara Romeo, Sara Dal Bo, Chiara Nardini, Anna Maria Innoceta, Giulia Parmeggiani, Anna Patanè, Claudio Graziano

Abstract readCase ReportsReview
PubMed Full text at PMC Publisher
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

9 authors.

Maria Giovanna TedescoUnit of Medical Genetics, Department Maternal-Infantile, S. Maria Della Misericordia Hospital, 06129 Perugia, Italy.ORCID 0009-0006-4790-6573
Ilaria DonatiMedical Genetics Unit, MeLabeT Department, AUSL Romagna, 47521 Cesena, Italy.ORCID 0000-0002-3273-4549
Chiara RomeoDiagnostic Neuroradiology, Department of Neuroscience, AUSL Romagna, 48121 Ravenna, Italy.
Sara Dal BoDepartment of Pediatrics, Santa Maria Delle Croci Hospital, AUSL Romagna, 48121 Ravenna, Italy.
Chiara NardiniDepartment of Pediatrics, Santa Maria Delle Croci Hospital, AUSL Romagna, 48121 Ravenna, Italy.
Anna Maria InnocetaMedical Genetics Unit, MeLabeT Department, AUSL Romagna, 47521 Cesena, Italy.
Giulia ParmeggianiMedical Genetics Unit, MeLabeT Department, AUSL Romagna, 47521 Cesena, Italy.
Anna PatanèR&I Genetics SRL, 35127 Padua, Italy.
Claudio GrazianoMedical Genetics Unit, MeLabeT Department, AUSL Romagna, 47521 Cesena, Italy.ORCID 0000-0003-3875-6869

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Abnormalities, MultipleCerebellumEsophageal AtresiaEye AbnormalitiesKidney Diseases, CysticRetinaChild, PreschoolExome SequencingHumansPedigreePhenotypeesophageal atresiaJoubert syndromeKATNIPmolar tooth sign

Identifiers

PMID40428346
PMCPMC12111208

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.