Evidence map›Paper›PMID 40350249›Full record

ArticleJournal of medical genetics2025

Identification of

Xiao-Yun Lei, Meng-Wen Zhang, Hui Sun, Wang Song, Xiao-Yu Liang, Cui-Shan Wang, Sheng Luo, Bing-Mei Li, Xiao-Rong Liu, Yao Wang and 6 more

Abstract read
In one paragraph

Article in Journal of medical genetics, 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. Article
  2. Article
  3. Domain specific phenotypic expansion associated with variants inmedRxiv : the preprint server for health sciences · 2025
    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

16 authors.

Xiao-Yun Lei *Department of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou 510260, Guangdong, China.
Meng-Wen Zhang *Department of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou 510260, Guangdong, China.
Hui Sun *Department of Neurology, The First Affiliated Hospital, Jinan University, 613 West Huangpu Ave, Guangzhou 510632, Guangdong, China.
Wang SongDepartment of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou 510260, Guangdong, China.
Xiao-Yu LiangDepartment of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou 510260, Guangdong, China.
Cui-Shan WangDepartment of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou 510260, Guangdong, China.
Sheng LuoDepartment of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou 510260, Guangdong, China.ORCID http://orcid.org/0000-0002-7184-1267
Bing-Mei LiDepartment of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou 510260, Guangdong, China.
Xiao-Rong LiuDepartment of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou 510260, Guangdong, China.ORCID http://orcid.org/0000-0002-7769-9564
Yao WangEpilepsy Center, Guangdong Sanjiu Brain Hospital, Guangzhou 510000, Guangdong, China.
Yang TianDepartment of Neurology, Guangzhou Women and Children's Medical Center, Guangzhou 510623, Guangdong, China.
Qian PengDepartment of pediatrics, Dongguan Maternal and Child Health Hospital, Southern Medical University Affiliated, Dongguan 523129, Guangdong, China.
Jie WangDepartment of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou 510260, Guangdong, China.
Heng MengDepartment of Neurology, The First Affiliated Hospital, Jinan University, 613 West Huangpu Ave, Guangzhou 510632, Guangdong, China henachilli@163.com memphisheng@163.com.
Na HeDepartment of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou 510260, Guangdong, China henachilli@163.com memphisheng@163.com.ORCID http://orcid.org/0000-0002-9712-7782
Wei-Ping LiaoDepartment of Neurology, Institute of Neuroscience, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou 510260, Guangdong, China.ORCID http://orcid.org/0000-0001-9929-9185

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe microtubule actin crosslinking factor 1 (

methodsTrios-based whole-exome sequencing was performed on a cohort with generalised epilepsy from the China Epilepsy Gene 1.0 project. The spatial-temporal expression, single-cell sequencing and genotype-phenotype correlation were analysed to explore the role of

resultsTwo de novo heterozygous and eight biallelic SIGNIFICANCE:

Indexed as

Epilepsy, GeneralizedGenetic Predisposition to DiseaseMicrofilament ProteinsAdolescentAdultBrainChildChild, PreschoolExome SequencingFemaleGenetic Association StudiesHumansInfantMaleMicrotubule-Associated ProteinsMutationMicrofilament ProteinsMicrotubule-Associated ProteinsEpilepsyGene ExpressionGenetic ResearchGenotypeWhole Exome Sequencing

Identifiers

PMID40350249
PMCPMC12322448

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.