Evidence map›Paper›PMID 38249294›Full record

ArticleFrontiers in molecular neuroscience2023

Yun-Yan He, Sheng Luo, Liang Jin, Peng-Yu Wang, Jie Xu, Hong-Liang Jiao, Hong-Jun Yan, Yao Wang, Qiong-Xiang Zhai, Jing-Jing Ji and 6 more

Open access · goldAbstract read
PubMed Full text at PMC Publisher
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 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
8.8field-weighted citation impact, top 2% of its field
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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Identification ofJournal of medical genetics · 2025
    Article
  4. Article
  5. Article
  6. De NovoHuman mutation · 2025
    Article
  7. Frontiers in genetics · 2025
    Article
  8. Epilepsy-associatedFrontiers in neurology · 2025
    Article
  9. Frontiers in neurology · 2025
    Article
  10. Toward precision medicine inFrontiers in neurology
    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 at 8 institutions in 1 country.

Yun-Yan He *Department of Neurology, Women and Children's Hospital, Qingdao University, Qingdao, China.
Sheng Luo *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, China.
Liang JinDepartment 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, China.
Peng-Yu 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, China.
Jie XuDepartment 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, China.
Hong-Liang JiaoDepartment of Neurosurgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Hong-Jun YanEpilepsy Center, Guangdong 999 Brain Hospital, Guangzhou, China.
Yao WangEpilepsy Center, Guangdong 999 Brain Hospital, Guangzhou, China.
Qiong-Xiang ZhaiDepartment of Pediatrics, Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
Jing-Jing JiDepartment 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, China.
Weng-Jun ZhangDepartment 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, China.
Peng ZhouDepartment 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, China.
Hua LiEpilepsy Center, Guangdong 999 Brain Hospital, Guangzhou, China.
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, China.
Song LanDepartment of Neurology, Maoming People's Hospital, Maoming, China.
Lin XuDepartment of Neurology, Women and Children's Hospital, Qingdao University, Qingdao, China.
Second Affiliated Hospital of Guangzhou Medical University · CNGuangdong 999 Brain Hospital · CNGuangzhou Medical University · CNFirst Affiliated Hospital of Zhengzhou University · CNGuangdong General Hospital · CNQingdao University · CNQingdao Women and Children's Hospital · CNUniversity of South China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The Methods: Trios-based whole-exome sequencing was performed in patients with epilepsy of unknown causes. To analyze the genotype-phenotype correlations, previously reported Results: Significance: This study suggested that

Indexed as

DLG3 geneepilepsyGenotype-phenotype correlationneurodevelopmental disordervariants

Identifiers

PMID38249294
PMCPMC10796462
OpenAlexW4390610960

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.