Evidence map›Paper›PMID 37347056›Full record

ArticleFrontiers in genetics2023

Case report: Sex-specific characteristics of epilepsy phenotypes associated with Xp22.31 deletion: a case report and review.

Yi Wu, Dan Wu, Yulong Lan, Shaocong Lan, Duo Li, Zexin Zheng, Hongwu Wang, Lian Ma

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Frontiers in genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 30% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
  2. 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

8 authors at 5 institutions in 2 countries.

Yi WuDepartment of Pediatrics, Second Affiliated Hospital of Shantou University Medical College, Shantou, China.
Dan WuDepartment of Pediatrics, Second Affiliated Hospital of Shantou University Medical College, Shantou, China.
Yulong LanCentre for Precision Health, School of Medical and Health Sciences, Edith Cowan University, Joondalup, WA, Australia.
Shaocong LanDepartment of clinical Medicine, Guangdong Medical University, Zhanjiang, China.
Duo LiDepartment of Pediatrics, Second Affiliated Hospital of Shantou University Medical College, Shantou, China.
Zexin ZhengDepartment of Pediatrics, Second Affiliated Hospital of Shantou University Medical College, Shantou, China.
Hongwu WangDepartment of Pediatrics, Second Affiliated Hospital of Shantou University Medical College, Shantou, China.
Lian MaDepartment of Pediatrics, Second Affiliated Hospital of Shantou University Medical College, Shantou, China.
Second Affiliated Hospital of Shantou University Medical College · CNShantou University · CNEdith Cowan University · AUGuangdong Medical College · CNShenzhen Children's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Deletion in the Xp22.31 region is increasingly suggested to be involved in the etiology of epilepsy. Little is known regarding the genomic and clinical delineations of X-linked epilepsy in the Chinese population or the sex-stratified difference in epilepsy characteristics associated with deletions in the Xp22.31 region. In this study, we reported two siblings with a 1.69 Mb maternally inherited microdeletion at Xp22.31 involving the genes

Indexed as

copy number variationsepilepsymicrodeletionsex-specificX-linked ichthyosisXp22.31

Identifiers

PMID37347056
PMCPMC10280017
OpenAlexW4379534339

What OpenQuestion 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 OpenQuestion graph.