Evidence map›Paper›PMID 41657455›Full record

ReviewTranslational pediatrics2026

Advances and challenges of precision epigenetic therapy in treating genomic imprinting diseases.

Ying Lv, Mingyan Li, Chai Ji

Abstract readReview
In one paragraph

Review in Translational pediatrics, 2026. 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.

  1. Review
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.

Ying LvDepartment of Child Health Care, National Clinical Research Center for Child and Adolescents' Health, The Children's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Mingyan LiDepartment of Child Health Care, National Clinical Research Center for Child and Adolescents' Health, The Children's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Chai JiDepartment of Child Health Care, National Clinical Research Center for Child and Adolescents' Health, The Children's Hospital, Zhejiang University School of Medicine, Hangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genomic imprinting disorders (IDs) arise from the disruption of parent-of-origin-specific gene expression, a process governed by heritable epigenetic marks. Conventional therapies are largely symptomatic and fail to correct the underlying defect in dynamic gene regulation. Epigenome editing, using programmable DNA-targeting tools to rewrite epigenetic information, has emerged as a powerful therapeutic strategy that directly addresses this molecular pathology. This review synthesizes the transformative progress of the past decade, arguing that epigenome editing is poised to revolutionize the treatment of these conditions. We detail key breakthroughs in both editor design and

Indexed as

Angelman syndrome (AS)delivery systemepigenome editingImprinting disorders (IDs)Prader-Willi syndrome (PWS)

Identifiers

PMID41657455
PMCPMC12877898

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.