Evidence map›Paper›PMID 40677923›Full record

ArticleHuman mutation2025

De Novo

Hong-Jun Yan, Peng-Yu Wang, Wen-Hui Liu, Yu-Jie Gu, Jia-Cheng Pan, Hua Li, Sheng Luo

Abstract readCase Reports
In one paragraph

Article in Human mutation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Epilepsy-associatedFrontiers in neurology · 2025
    Article
  4. 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

7 authors.

Hong-Jun YanEpilepsy Center, Guangdong Sanjiu Brain Hospital, Guangzhou, Guangdong, China.
Peng-Yu WangInstitute 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, Guangdong, China.ORCID 0009-0001-6848-2021
Wen-Hui LiuInstitute 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, Guangdong, China.ORCID 0009-0006-7261-3107
Yu-Jie GuInstitute 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, Guangdong, China.
Jia-Cheng PanSchool of Computer and Information Engineering, Nanjing University of Technology, Nanjing, China.
Hua LiEpilepsy Center, Guangdong Sanjiu Brain Hospital, Guangzhou, Guangdong, China.
Sheng LuoInstitute 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, Guangdong, China.ORCID 0000-0002-7184-1267

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic factors are estimated to contribute to 80% of people with epilepsy. However, only four genes were reported to be associated with temporal lobe epilepsy (TLE). This study is aimed at investigating the association between

Indexed as

ActinsEpilepsy, Temporal LobeGenetic Predisposition to DiseaseAge of OnsetExome SequencingGenetic Association StudiesHumansPhenotypeActinsACTBcorrelation between spatiotemporal expression and phenotypeshippocampal sclerosisphenotypic spectrumtemporal lobe epilepsy

Identifiers

PMID40677923
PMCPMC12267973

What Socratic 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 Socratic graph.