Evidence map›Paper›PMID 36910266›Full record

ArticleFrontiers in molecular neuroscience2023

Xi Zhang, Neng Xiao, Yang Cao, Ying Peng, Aojie Lian, Yuanlu Chen, Pengchao Wang, Weiyue Gu, Bo Xiao, Jing Yu and 2 more

Abstract read
In one paragraph

Article in Frontiers in molecular neuroscience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. A complex of MAST1 and 14-3-3η regulates Tau phosphorylation in the developing cortex.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. Article
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  5. Article
  6. Genetic and clinical insights intoFrontiers in pediatrics · 2025
    Article
  7. Article
  8. Article
  9. Exploring the SheepAnimals : an open access journal from MDPI · 2024
    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

12 authors.

Xi ZhangDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, China.
Neng XiaoDepartment of Pediatric Neurology, Chenzhou First People's Hospital, Chenzhou, China.
Yang CaoDepartment of Radiology, Chenzhou First People's Hospital, Chenzhou, China.
Ying PengNational Health Commission Key Laboratory for Birth Defect Research and Prevention, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, China.
Aojie LianNational Health Commission Key Laboratory for Birth Defect Research and Prevention, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, China.
Yuanlu ChenDepartment of Pharmacy, Chenzhou First People's Hospital, Chenzhou, China.
Pengchao WangChigene (Beijing) Translational Medical Research Center Co., Ltd., Beijing, China.
Weiyue GuChigene (Beijing) Translational Medical Research Center Co., Ltd., Beijing, China.
Bo XiaoDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, China.
Jing YuDepartment of Neurology, Children's Hospital of Xinjiang Uygur Autonomous Region, Ürümqi, China.
Hua WangDepartment of Medical Genetics, Hunan Children's Hospital, Changsha, China.
Li ShuDepartment of Biochemistry, Molecular Biology and Medical Genetics, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: This study aims to prove that the Methods: Trio-based exome sequencing (ES) was performed on the four families enrolled in this study. We collected and systematically reviewed the four probands' clinical data, magnetic resonance images (MRI), and electroencephalography (EEG). We also carried out bioinformatics analysis by integrating published exome/genome sequencing data and human brain transcriptomic data. Results: We described four patients whose median age of seizure onset was 5 months. The primary manifestation was infantile spasms with typical hypsarrhythmia on EEG. Developmental delays or intellectual disabilities varied among the four individuals. Three Conclusion: Our results revealed that the variants of

Indexed as

epilepsygeneticinfantile spasmsMAST4neurodevelopmental delay

Identifiers

PMID36910266
PMCPMC9992645

What OpenQuestion holds

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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.