Evidence map›Paper›PMID 37303953›Full record

ArticleFrontiers in genetics2023

A syndrome featuring developmental disorder of the nervous system induced by a novel mutation in the

Si Huang, Jiaxin Xu, Yiyang Li, Wenhui Mo, Xiuwen Lin, Yajun Wang, Fujian Liang, Yan Bai, Guochun Huang, Jing Chen and 2 more

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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. A Boy with a Novel Variant inChildren (Basel, Switzerland) · 2025
    Article
  4. Review
  5. Review
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

12 authors at 2 institutions in 1 country.

Si HuangDepartment of Pediatrics, Foshan Fosun Chancheng Hospital, Foshan, China.
Jiaxin XuDepartment of Pediatrics, Foshan Fosun Chancheng Hospital, Foshan, China.
Yiyang LiDepartment of Pediatrics, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Wenhui MoDepartment of Pediatrics, Foshan Fosun Chancheng Hospital, Foshan, China.
Xiuwen LinDepartment of Pediatrics, Foshan Fosun Chancheng Hospital, Foshan, China.
Yajun WangDepartment of Pediatrics, Shunde Women and Children's Hospital of Guangdong Medical University, Foshan, China.
Fujian LiangDepartment of Pediatrics, Foshan Fosun Chancheng Hospital, Foshan, China.
Yan BaiDepartment of Pediatrics, Foshan Fosun Chancheng Hospital, Foshan, China.
Guochun HuangDepartment of Pediatrics, Shunde Women and Children's Hospital of Guangdong Medical University, Foshan, China.
Jing ChenDepartment of Pediatrics, Shunde Women and Children's Hospital of Guangdong Medical University, Foshan, China.
Jing XinDepartment of Pediatrics, Foshan Fosun Chancheng Hospital, Foshan, China.
Guoda MaDepartment of Pediatrics, Shunde Women and Children's Hospital of Guangdong Medical University, Foshan, China.
Guangdong Medical College · CNGuangzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

central nervous systemframeshift mutationimmune system diseasesmultisystemTCF20

Identifiers

PMID37303953
PMCPMC10248432
OpenAlexW4378231985

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.