Evidence map›Paper›PMID 42531143›Full record

ArticleEpigenetics2026

Culture-dependent decoupling of

Céline Selenou, Frédéric Brioude, Laure Sudre, Aurélie Pham, Irène Netchine, Marie-Laure Sobrier, Éloïse Giabicani

Abstract read
In one paragraph

Article in Epigenetics, 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

7 authors.

Céline SelenouSorbonne Université, INSERM, Centre de Recherche Saint-Antoine, Paris, France.ORCID 0000-0002-3986-1671
Frédéric BrioudeSorbonne Université, INSERM, Centre de Recherche Saint-Antoine, APHP, Hôpital Armand Trousseau, Endocrinologie Moléculaire et Pathologies d'Empreinte, Paris, France.ORCID 0000-0001-8122-760X
Laure SudreSorbonne Université, INSERM, Centre de Recherche Saint-Antoine, Paris, France.ORCID 0000-0001-6238-8395
Aurélie PhamSorbonne Université, INSERM, Centre de Recherche Saint-Antoine, APHP, Hôpital Armand Trousseau, Service de Néonatologie, Paris, France.
Irène NetchineSorbonne Université, INSERM, Centre de Recherche Saint-Antoine, APHP, Hôpital Armand Trousseau, Endocrinologie Moléculaire et Pathologies d'Empreinte, Paris, France.ORCID 0000-0003-1324-3389
Marie-Laure SobrierSorbonne Université, INSERM, Centre de Recherche Saint-Antoine, Paris, France.ORCID 0000-0001-6396-100X
Éloïse GiabicaniSorbonne Université, INSERM, Centre de Recherche Saint-Antoine, APHP, Hôpital Armand Trousseau, Endocrinologie Moléculaire et Pathologies d'Empreinte, Paris, France.ORCID 0000-0001-5360-8616

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genomic imprinting is an epigenetic mechanism leading to the monoallelic expression of a subset of genes, mainly regulated by DNA methylation at imprinting control regions (ICRs). Silver-Russell syndrome (SRS) is a paradigmatic imprinting disorder in which loss of methylation at the 11p15.5

Indexed as

DNA MethylationGenomic ImprintingInsulin-Like Growth Factor IIRNA, Long NoncodingSilver-Russell SyndromeAllelesCells, CulturedDental PulpFibroblastsHumansInduced Pluripotent Stem CellsH19 long non-coding RNAIGF2 protein, humanInsulin-Like Growth Factor IIRNA, Long NoncodingAllele-specific expressiongenomic imprintingH19ICRmethylationSilver-Russell syndrome

Identifiers

PMID42531143
PMCPMC13432853

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.