Evidence map›Paper›PMID 31810366›Full record

ReviewGenes2019

Stability and Lability of Parental Methylation Imprints in Development and Disease.

Sabina Farhadova, Melisa Gomez-Velazquez, Robert Feil

Open access · goldAbstract readReview
In one paragraph

Review in Genes, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 20% of its field
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

15 citing papers in PubMed, 41 citations in OpenAlex.

  1. Precision epigenetic therapies in oncology.Cancer metastasis reviews · 2025
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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

3 authors at 1 institution in 1 country.

Sabina FarhadovaInstitute of Molecular Genetics (IGMM), CNRS, University of Montpellier, 1919 route de Mende, 34293 Montpellier, France.
Melisa Gomez-VelazquezInstitute of Molecular Genetics (IGMM), CNRS, University of Montpellier, 1919 route de Mende, 34293 Montpellier, France.
Robert FeilInstitute of Molecular Genetics (IGMM), CNRS, University of Montpellier, 1919 route de Mende, 34293 Montpellier, France.
Centre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA methylation plays essential roles in mammals. Of particular interest are parental methylation marks that originate from the oocyte or the sperm, and bring about mono-allelic gene expression at defined chromosomal regions. The remarkable somatic stability of these parental imprints in the pre-implantation embryo-where they resist global waves of DNA demethylation-is not fully understood despite the importance of this phenomenon. After implantation, some methylation imprints persist in the placenta only, a tissue in which many genes are imprinted. Again here, the underlying epigenetic mechanisms are not clear. Mouse studies have pinpointed the involvement of transcription factors, covalent histone modifications, and histone variants. These and other features linked to the stability of methylation imprints are instructive as concerns their conservation in humans, in which different congenital disorders are caused by perturbed parental imprints. Here, we discuss DNA and histone methylation imprints, and why unravelling maintenance mechanisms is important for understanding imprinting disorders in humans.

Indexed as

AllelesDNA MethylationGene Expression Regulation, DevelopmentalGenetic Diseases, InbornGenomic ImprintingAnimalsHistonesHumansMiceProtein Processing, Post-TranslationalHistonesDMRDNA methylationevolutiongenomic imprintinghistone methylationICRimprinting disordersPolycomb

Identifiers

PMID31810366
PMCPMC6947649
OpenAlexW2990330256

What OpenQuestion holds

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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.