Evidence map›Paper›PMID 36120649›Full record

ArticleFrontiers in pediatrics2022

Neurodevelopmental disorders and anti-epileptic treatment in a patient with a

Ying Yu, Cuiyun Li, Wei Li, Liting Chen, Dan Wang, Jie Wang, Jian Wang, Ruen Yao

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

Article in Frontiers in pediatrics, 2022. 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
0.9field-weighted citation impact, top 22% 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, 5 citations in OpenAlex.

  1. Article
  2. NovelFrontiers in pediatrics · 2026
    Article
  3. Article
  4. Article
  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

8 authors at 2 institutions in 1 country.

Ying YuAntenatal Diagnostic Center, Sanya Women and Children's Hospital Managed by Shanghai Children's Medical Center, Sanya, China.
Cuiyun LiAntenatal Diagnostic Center, Sanya Women and Children's Hospital Managed by Shanghai Children's Medical Center, Sanya, China.
Wei LiAntenatal Diagnostic Center, Sanya Women and Children's Hospital Managed by Shanghai Children's Medical Center, Sanya, China.
Liting ChenAntenatal Diagnostic Center, Sanya Women and Children's Hospital Managed by Shanghai Children's Medical Center, Sanya, China.
Dan WangDepartment of Science and Education, Sanya Women and Children's Hospital Managed by Shanghai Children's Medical Center, Sanya, China.
Jie WangAntenatal Diagnostic Center, Sanya Women and Children's Hospital Managed by Shanghai Children's Medical Center, Sanya, China.
Jian WangMolecular Genetic Diagnosis Center, Sanya Women and Children's Hospital Managed by Shanghai Children's Medical Center, Sanya, China.
Ruen YaoMolecular Genetic Diagnosis Center, Sanya Women and Children's Hospital Managed by Shanghai Children's Medical Center, Sanya, China.
Shanghai Children's Medical Center · CNShanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

SATB1 variants causing developmental delay with dysmorphic facies and dental anomalies have been reported in a small cohort. Most patients present epilepsy as a main clinical feature in neurodevelopmental disorders; however, its treatment is unknown. Here, we present a Chinese patient with a

Indexed as

anti-epileptic drugsepilepsyneurodevelopmental delayprotein-truncating variantsSATB1

Identifiers

PMID36120649
PMCPMC9479181
OpenAlexW4294243406

What OpenQuestion holds

Textmetadata
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.