Evidence map›Paper›PMID 36583017›Full record

ArticleFrontiers in genetics2022

Phenotype and genotype analyses of Chinese patients with autosomal dominant mental retardation type 5 caused by

Yanxin Wang, Yuqiang Lv, Zilong Li, Min Gao, Xiaomeng Yang, Yue Li, Jianguo Shi, Zaifen Gao, Yi Liu, Zhongtao Gai

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

Article in Frontiers in genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Epilepsy associated withFrontiers in pediatrics · 2026
    Article
  2. Article
  3. Frontiers in pediatrics · 2025
    Article
  4. NovelMolecular syndromology · 2023
    Article
  5. [Autosomal dominant mental retardation type 5 caused byZhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2023
    Review
  6. Roadmap to advance therapeutics forTherapeutic advances in rare disease
    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

10 authors at 2 institutions in 1 country.

Yanxin WangDepartment of Pediatrics, Children's Hospital Affiliated to Shandong University, Ji'nan, China.
Yuqiang LvPediatric Research Institute, Children's Hospital Affiliated to Shandong University, Ji'nan, China.
Zilong LiPediatric Research Institute, Children's Hospital Affiliated to Shandong University, Ji'nan, China.
Min GaoPediatric Research Institute, Children's Hospital Affiliated to Shandong University, Ji'nan, China.
Xiaomeng YangPediatric Research Institute, Children's Hospital Affiliated to Shandong University, Ji'nan, China.
Yue LiPediatric Research Institute, Children's Hospital Affiliated to Shandong University, Ji'nan, China.
Jianguo ShiEpilepsy Center, Children's Hospital Affiliated to Shandong University, Ji'nan, China.
Zaifen GaoEpilepsy Center, Children's Hospital Affiliated to Shandong University, Ji'nan, China.
Yi LiuPediatric Research Institute, Children's Hospital Affiliated to Shandong University, Ji'nan, China.
Zhongtao GaiPediatric Research Institute, Children's Hospital Affiliated to Shandong University, Ji'nan, China.
Shandong Center for Disease Control and Prevention · CNShandong 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

autosomal dominant mental retardation type 5developmental delayepilepsyintellectual disabilitymutationnext-generation sequencingSYNGAP1

Identifiers

PMID36583017
PMCPMC9792850
OpenAlexW4312138097

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.