Evidence map›Paper›PMID 36034301›Full record

ArticleFrontiers in neurology2022

Genetic and phenotypic spectrum of Chinese patients with epilepsy and photosensitivity.

Yue Niu, Pan Gong, Xianru Jiao, Zhao Xu, Yuehua Zhang, Zhixian Yang

Abstract read
In one paragraph

Article in Frontiers in neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. [Autosomal dominant mental retardation type 5 caused byZhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2023
    Review
  11. Article
  12. The genotype-phenotype correlations of theFrontiers in molecular neuroscience · 2023
    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

6 authors.

Yue NiuDepartment of Pediatrics, Peking University First Hospital, Beijing, China.
Pan GongDepartment of Pediatrics, Peking University First Hospital, Beijing, China.
Xianru JiaoDepartment of Pediatrics, Peking University First Hospital, Beijing, China.
Zhao XuDepartment of Pediatrics, Peking University First Hospital, Beijing, China.
Yuehua ZhangDepartment of Pediatrics, Peking University First Hospital, Beijing, China.
Zhixian YangDepartment of Pediatrics, Peking University First Hospital, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To determine the contribution of genetic etiologies in epilepsy with photosensitivity. Methods: A total of 35 epileptic patients with genetic photosensitivity from January 2019 to May 2021 were analyzed. Results: Pathogenic variants were identified in 35 patients, including Conclusion: The most common genes for epilepsy with genetic photosensitivity are

Indexed as

electroencephalographygenesphotoconvulsive responsephotoparoxysmal responsephotosensitive epilepsy

Identifiers

PMID36034301
PMCPMC9416002

What OpenQuestion holds

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Registered trials

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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.