Case Report of Suspected Gonadal Mosaicism in

Anna Zsigmond, Ágnes Till, Judit Bene, Márta Czakó, Alexandra Mikó, Kinga Hadzsiev

Abstract readCase Reports

In one paragraph

Article in International journal of molecular sciences, 2024. 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.

Using Whole Exome Sequencing to Identify Genetic Causes of Neurodevelopmental Disorders in a Cohort of 11 Patients: A Single Center Experience.International journal of molecular sciences · 2025
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

6 authors.

Anna ZsigmondDepartment of Medical Genetics, Medical School, University of Pécs, H-7623 Pécs, Hungary.

Ágnes TillDepartment of Medical Genetics, Medical School, University of Pécs, H-7623 Pécs, Hungary.

Judit BeneDepartment of Medical Genetics, Medical School, University of Pécs, H-7623 Pécs, Hungary.ORCID 0000-0001-5757-6244

Márta CzakóDepartment of Medical Genetics, Medical School, University of Pécs, H-7623 Pécs, Hungary.ORCID 0000-0003-3642-8028

Alexandra MikóDepartment of Medical Genetics, Medical School, University of Pécs, H-7623 Pécs, Hungary.ORCID 0000-0002-5322-4425

Kinga HadzsievDepartment of Medical Genetics, Medical School, University of Pécs, H-7623 Pécs, Hungary.ORCID 0000-0003-2303-1670

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heterozygous mutations in the

Indexed as

Forkhead Transcription FactorsMosaicismNeurodevelopmental DisordersRepressor ProteinsChild, PreschoolExome SequencingFemaleHeterozygoteHumansInfantMaleMutationForkhead Transcription FactorsFOXP1 protein, humanRepressor ProteinsFOXP1 genegonadal mosaicismneurodevelopmental disorderspeech delay

Identifiers

PMID38891897

DOI10.3390/ijms25115709

PMCPMC11171548

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.