Evidence map›Paper›PMID 33732697›Full record

ArticleFrontiers in cell and developmental biology2021

Genotype-Phenotype Analysis and Mutation Spectrum in a Cohort of Chinese Patients With Congenital Nystagmus.

Xiao-Fang Wang, Hui Chen, Peng-Juan Huang, Zhuo-Kun Feng, Zi-Qi Hua, Xiang Feng, Fang Han, Xiao-Tao Xu, Ren-Juan Shen, Yang Li and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.0field-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

7 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Genes · 2023
    Article
  6. Molecular vision · 2023
    Article
  7. 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 4 institutions in 1 country.

Xiao-Fang WangSchool of Ophthalmology and Optometry, The Eye Hospital, Wenzhou Medical University, Wenzhou, China.
Hui ChenSchool of Ophthalmology and Optometry, The Eye Hospital, Wenzhou Medical University, Wenzhou, China.
Peng-Juan HuangSchool of Ophthalmology and Optometry, The Eye Hospital, Wenzhou Medical University, Wenzhou, China.
Zhuo-Kun FengSchool of Ophthalmology and Optometry, The Eye Hospital, Wenzhou Medical University, Wenzhou, China.
Zi-Qi HuaSchool of Ophthalmology and Optometry, The Eye Hospital, Wenzhou Medical University, Wenzhou, China.
Xiang FengSchool of Ophthalmology and Optometry, The Eye Hospital, Wenzhou Medical University, Wenzhou, China.
Fang HanBeijing Ophthalmology and Visual Sciences Key Laboratory, Beijing Institute of Ophthalmology, Beijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University, Beijing, China.
Xiao-Tao XuSchool of Ophthalmology and Optometry, The Eye Hospital, Wenzhou Medical University, Wenzhou, China.
Ren-Juan ShenBeijing Ophthalmology and Visual Sciences Key Laboratory, Beijing Institute of Ophthalmology, Beijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University, Beijing, China.
Yang LiBeijing Ophthalmology and Visual Sciences Key Laboratory, Beijing Institute of Ophthalmology, Beijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University, Beijing, China.
Zi-Bing JinSchool of Ophthalmology and Optometry, The Eye Hospital, Wenzhou Medical University, Wenzhou, China.
Huan-Yun YuSchool of Ophthalmology and Optometry, The Eye Hospital, Wenzhou Medical University, Wenzhou, China.
Affiliated Eye Hospital of Wenzhou Medical College · CNBeijing Tongren Hospital · CNWenzhou Medical University · CNCapital 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

congenital nystagmusFRMD7genotype-phenotypeGPR143mutation

Identifiers

PMID33732697
PMCPMC7958879
OpenAlexW3131558236

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.