Evidence map›Paper›PMID 40507980›Full record

ArticleInternational journal of molecular sciences2025

Increased

Nikolaos Settas, Adam J Bittel, Yi-Wen Chen

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. The role of mNaunyn-Schmiedeberg's archives of pharmacology · 2026
    Review
  3. 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

3 authors.

Nikolaos SettasCenter for Genetic Medicine Research, Children's National Research and Innovation Campus, Washington, DC 20012, USA.ORCID 0000-0001-7804-5303
Adam J BittelCenter for Genetic Medicine Research, Children's National Research and Innovation Campus, Washington, DC 20012, USA.ORCID 0000-0003-2134-418X
Yi-Wen ChenCenter for Genetic Medicine Research, Children's National Research and Innovation Campus, Washington, DC 20012, USA.ORCID 0000-0002-5813-1893

Funding

Mapping the non-coding RNA landscape in skeletal muscle health and diseaseR01AR081449 · NIAMS · CORNELL UNIVERSITY · PI Benjamin David Cosgrove, Iwijn De Vlaminck · 2023 to 2026
$2.1M
Investigating proteostasis in facioscapulohumeral muscular dystrophyR21AR080887 · NIAMS · CHILDREN'S RESEARCH INSTITUTE · PI CHEN, YI-WEN · 2022 to 2023
$383k
FSHD Canada Foundation 20220204- FSHDFSHD Canada Foundation FSHD-Fall2020-4060516418NIAMS NIH HHS R01 AR081449NIAMS NIH HHS R21 AR080887NIH/NIAMS 1R01AR081449-01A1NIH/NIAMS 1R21AR080887-01
6 · The paper itself

Abstract

Facioscapulohumeral muscular dystrophy (FSHD) is caused by the aberrant expression of the double homeobox 4 (

Indexed as

AdenosineMethyltransferasesMuscular Dystrophy, FacioscapulohumeralMyoblastsFemaleGene Expression RegulationHomeodomain ProteinsHumansMaleMethylationRNA, MessengerAdenosineDUX4L1 protein, humanHomeodomain ProteinsMethyltransferasesMETTL3 protein, humanRNA, MessengerferritinFSHDiron homeostasism6Amitochondrial free ironmitoferrinpost-transcriptional regulationRNA modification

Identifiers

PMID40507980
PMCPMC12155334

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.