Evidence map›Paper›PMID 41962546›Full record

ArticleStem cell reports2026

Cranial placode differentiation defect in individuals born without a nose.

Vanitha Venkoba Rao, Xinran Ji, Jasmine Yi Ying Heng, Frederique Magdinier, Bruno Reversade, Shifeng Xue

Abstract read
In one paragraph

Article in Stem cell reports, 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

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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

6 authors.

Vanitha Venkoba RaoDepartment of Biological Sciences, National University of Singapore, Singapore, Singapore.
Xinran JiDepartment of Biological Sciences, National University of Singapore, Singapore, Singapore.
Jasmine Yi Ying HengDepartment of Biological Sciences, National University of Singapore, Singapore, Singapore.
Frederique MagdinierAix Marseille University, INSERM, Marseille Medical Genetics, Marseille, France.
Bruno ReversadeLaboratory of Human Genetics & Therapeutics, Biomedical Sciences Division, KAUST, Thuwal, Kingdom of Saudi Arabia.
Shifeng XueDepartment of Biological Sciences, National University of Singapore, Singapore, Singapore. Electronic address: shifengxue@nus.edu.sg.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bosma arhinia microphthalmia syndrome (BAMS) is a rare congenital disorder characterized by the absence of a nose, along with eye and reproductive anomalies. BAMS is caused by heterozygous missense variants in SMCHD1, an epigenetic regulator. Despite uncovering its genetic basis, the cellular basis of the disease has remained elusive. The embryonic development of the nose involves direct contributions from both the neural crest and cranial placodes. Here, we differentiated patient-derived induced pluripotent stem cells toward the cranial placode lineage and found that they exhibited significant differentiation defects. Combined transcriptome and DNA methylome analyses further revealed dysregulation in cell adhesion but without overt apoptosis. Together our research suggests that BAMS is caused by impaired differentiation to cranial placode cells and changes in cell adhesion, offering new insights into the cellular pathology of this enigmatic syndrome.

Indexed as

Cell DifferentiationChoanal AtresiaEctodermal PlacodesMicrophthalmosNoseCell AdhesionDNA MethylationHumansInduced Pluripotent Stem CellsNeural CrestarhiniaBAMScranial placodecraniofacialFSHDnosestem cell

Identifiers

PMID41962546
PMCPMC13163215

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Registered trials

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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.