Evidence map›Paper›PMID 39471229›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

Deficiency of

Weicheng Duan, Guiyang Huang, Yang Sui, Kang Wang, Yuxin Yu, Xufeng Chu, Xu Cao, Liangpei Chen, Jiahui Liu, Evan E Eichler and 1 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. 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

11 authors.

Weicheng DuanDepartment of Forensic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.ORCID 0000-0002-8183-7536
Guiyang HuangDepartment of Forensic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Yang SuiDepartment of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195.ORCID 0000-0001-7285-8733
Kang WangDepartment of Forensic Medicine, Nanjing Medical University, Nanjing 211166, China.
Yuxin YuDepartment of Endocrinology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.
Xufeng ChuDepartment of Forensic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Xu CaoDepartment of Forensic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Liangpei ChenDepartment of Forensic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Jiahui LiuDepartment of Forensic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Evan E EichlerDepartment of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195.ORCID 0000-0002-8246-4014
Bo XiongDepartment of Forensic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.ORCID 0000-0002-2695-9100

Funding

Sporadic Mutations and Autism Spectrum DisordersR01MH101221 · NIMH · UNIVERSITY OF WASHINGTON · PI EICHLER, EVAN · 2013 to 2025
$9.2M
Fundamental Research Funds for the Central Universities HUST: 5003515012HHMI (HHMI) investigator of the HHMIMOST | National Natural Science Foundation of China (NSFC) 81721005 81971084MOST | National Natural Science Foundation of China (NSFC) 82302082NIMH NIH HHS R01 MH101221the US NIH grant R01MH101221
6 · The paper itself

Abstract

The molecular mechanisms underlying the neurodevelopmental disorders (NDDs) caused by

Indexed as

DEAD-box RNA HelicasesNeurogenesisReceptors, NotchSignal TransductionZebrafishAnimalsBehavior, AnimalFemaleHumansMaleMutationNeurodevelopmental DisordersDDX3X protein, humanDEAD-box RNA HelicasesReceptors, NotchcrebbpDDX3XE/I imbalanceneurodevelopmental disorderNotch

Identifiers

PMID39471229
PMCPMC11551356

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.