Evidence map›Paper›PMID 41751615›Full record

ArticleGenes2026

Reassessing Benign

Liliana Fernández-Hernández, Sergio Enríquez-Flores, Nancy L Hernández-Martínez, Melania Abreu-González, Esther Lieberman-Hernández, Gerardo Rodríguez-González, Sinuhé Reyes-Ruvalcaba, Miriam E Reyna-Fabián

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Genes, 2026. 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

8 authors.

Liliana Fernández-HernándezLaboratorio de Biología Molecular, Instituto Nacional de Pediatría, Secretaría de Salud, Mexico City C.P. 04530, Mexico.ORCID 0000-0002-4153-6966
Sergio Enríquez-FloresLaboratorio de Biomoléculas y Salud Infantil, Instituto Nacional de Pediatría, Secretaría de Salud, Mexico City C.P. 04530, Mexico.ORCID 0000-0003-2058-5707
Nancy L Hernández-MartínezLaboratorio de Biología Molecular, Instituto Nacional de Pediatría, Secretaría de Salud, Mexico City C.P. 04530, Mexico.
Melania Abreu-GonzálezLaboratorio Genos Médica, Mexico City C.P.06700, Mexico.ORCID 0000-0001-8591-0852
Esther Lieberman-HernándezDepartamento de Genética Humana, Instituto Nacional de Pediatría, Secretaría de Salud, Mexico City C.P. 04530, Mexico.
Gerardo Rodríguez-GonzálezSubdirección de Servicios Clínicos, Genética, Hospital Regional de Alta Especialidad de Zumpango, Zumpango C.P. 55600, Mexico.
Sinuhé Reyes-RuvalcabaUniversidad Cuauhtémoc, Campus Querétaro, Querétaro C.P. 76060, Mexico.
Miriam E Reyna-FabiánLaboratorio de Biología Molecular, Instituto Nacional de Pediatría, Secretaría de Salud, Mexico City C.P. 04530, Mexico.

Funding

Instituto Nacional de Pediatria Programa E022 Investigación y Desarrollo Tecnológico en Salud, Ciudad de México, México (Recursos Fiscales 2022-2024)
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

CraniosynostosesIntellectual DisabilityRepressor ProteinsAdolescentFemaleHumansModels, MolecularMutation, MissenseASXL1 protein, humanRepressor ProteinsASXL1Bohring–Opitz syndromeclonal hematopoiesis of indeterminate potential (CHIP)protein modelingVUS classification

Identifiers

PMID41751615
PMCPMC12941326

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.