Evidence map›Paper›PMID 41103616›Full record

ArticleBiological psychiatry global open science2025

Exploration of a DDX3X Gene Supplementation Therapy Including Expanded Characterization and Novel Findings of Sleep Disturbances in

Andrea Boitnott, Anjala Jiji, Erik J Plautz, Yuhui Hu, Xin Chen, Steven J Gray

Abstract read
In one paragraph

Article in Biological psychiatry global open science, 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. DDX3X overexpression in mice can cause rapid tissue-specific toxicity and mortality.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
  2. Article
  3. 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

6 authors.

Andrea BoitnottDepartment of Pediatrics, UT Southwestern Medical Center, Dallas, Texas.
Anjala JijiDepartment of Pediatrics, UT Southwestern Medical Center, Dallas, Texas.
Erik J PlautzDepartment of Neurology, UT Southwestern Medical Center, Dallas, Texas.
Yuhui HuDepartment of Pediatrics, UT Southwestern Medical Center, Dallas, Texas.
Xin ChenDepartment of Pediatrics, UT Southwestern Medical Center, Dallas, Texas.
Steven J GrayDepartment of Pediatrics, UT Southwestern Medical Center, Dallas, Texas.

Funding

UT Southwestern NORCP30DK127984 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI JAY D. HORTON · 2022 to 2026
$7.4M
NIDDK NIH HHS P30 DK127984
6 · The paper itself

Abstract

Background: DDX3X syndrome is a neurodevelopmental disorder caused by mutations in the Methods: An AAV9 (adeno-associated virus serotype 9)-mediated gene supplementation therapy was designed and tested for efficacy and safety in a mouse model of DDX3X syndrome. A total of 182 female Results: There was no effect of treatment on early postnatal developmental milestones. At 3 months, a dose-dependent amelioration in anxiety-like behavior was observed in treated Conclusions: While the gene therapy design used in this study was not effective, the data suggest that behavior can be modified by altering

Indexed as

AAV9AnxietyDDX3XGene therapyNeurodevelopmental disorderSleep

Identifiers

PMID41103616
PMCPMC12524031

What OpenQuestion holds

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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.