Evidence map›Paper›PMID 40725476›Full record

ArticleGenes2025

Clinician-Based Functional Scoring and Genomic Insights for Prognostic Stratification in Wolf-Hirschhorn Syndrome.

Julián Nevado, Raquel Blanco-Lago, Cristina Bel-Fenellós, Adolfo Hernández, María A Mori-Álvarez, Chantal Biencinto-López, Ignacio Málaga, Harry Pachajoa, Elena Mansilla, Fe A García-Santiago and 5 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. 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

15 authors.

Julián NevadoInstituto de Genética Médica y Molecular (INGEMM)-IdiPAZ, Hospital Universitario La Paz, 28046 Madrid, Spain.ORCID 0000-0001-5611-2659
Raquel Blanco-LagoServicio de Neuropediatría, Hospital Universitario Central de Asturias (HUCA), 33011 Oviedo, Spain.
Cristina Bel-FenellósDepartamento de Investigación y Psicología en Educación, Facultad de Educación, Universidad Complutense de Madrid, 28040 Madrid, Spain.ORCID 0000-0001-7397-447X
Adolfo HernándezDepartamento de Economía Financiera y Actuarial y Estadística, Facultad de Comercio y Turismo, Universidad Complutense de Madrid, 28040 Madrid, Spain.ORCID 0000-0003-1078-2328
María A Mori-ÁlvarezInstituto de Genética Médica y Molecular (INGEMM)-IdiPAZ, Hospital Universitario La Paz, 28046 Madrid, Spain.
Chantal Biencinto-LópezDepartamento de Investigación y Psicología en Educación, Facultad de Educación, Universidad Complutense de Madrid, 28040 Madrid, Spain.ORCID 0000-0002-6385-2230
Ignacio MálagaServicio de Neuropediatría, Hospital Universitario Central de Asturias (HUCA), 33011 Oviedo, Spain.ORCID 0000-0003-4074-6870
Harry PachajoaCentro de Investigaciones en Anomalías Congénitas y Enfermedades Raras, Universidad ICESI, Cali 760031, Colombia.ORCID 0000-0003-2672-0439
Elena MansillaInstituto de Genética Médica y Molecular (INGEMM)-IdiPAZ, Hospital Universitario La Paz, 28046 Madrid, Spain.ORCID 0000-0001-5601-4813
Fe A García-SantiagoInstituto de Genética Médica y Molecular (INGEMM)-IdiPAZ, Hospital Universitario La Paz, 28046 Madrid, Spain.ORCID 0000-0003-2393-7800
Pilar BarrúzInstituto de Genética Médica y Molecular (INGEMM)-IdiPAZ, Hospital Universitario La Paz, 28046 Madrid, Spain.
Jair A Tenorio-CastañoInstituto de Genética Médica y Molecular (INGEMM)-IdiPAZ, Hospital Universitario La Paz, 28046 Madrid, Spain.ORCID 0000-0002-5308-2316
Yolanda Muñoz-GªPorreroInstituto de Genética Médica y Molecular (INGEMM)-IdiPAZ, Hospital Universitario La Paz, 28046 Madrid, Spain.
Isabel VallcorbaInstituto de Genética Médica y Molecular (INGEMM)-IdiPAZ, Hospital Universitario La Paz, 28046 Madrid, Spain.ORCID 0000-0003-2110-2703
Pablo LapunzinaInstituto de Genética Médica y Molecular (INGEMM)-IdiPAZ, Hospital Universitario La Paz, 28046 Madrid, Spain.ORCID 0000-0002-6324-4825

Funding

INSTITUTO DE SALUD CARLOS III and FIBHULP FIS18/01433; PI-2734
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Wolf-Hirschhorn SyndromeAdolescentAdultChildChild, PreschoolChromosomes, Human, Pair 4EpilepsyFemaleGenomicsHumansInfantMalePhenotypePrognosisYoung Adult4p16.3COAdevelopmental delayepilepsyfunctional assessmentWolf–Hirschhorn syndrome

Identifiers

PMID40725476
PMCPMC12294571

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.