Evidence map›Paper›PMID 35222542›Full record

ArticleFrontiers in genetics2022

Case Report: A Novel Mutation in the CRYGD Gene Causing Congenital Cataract Associated with Nystagmus in a Chinese Family.

Yunxia Gao, Xiang Ren, Xiangyu Fu, Yu Lin, Lirong Xiao, Xiaoyue Wang, Naihong Yan, Ming Zhang

Open access · goldAbstract readCase Reports
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 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 50% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Human Crystallin Variation and Cataract.Investigative ophthalmology & visual science · 2026
    Review
  2. Article
  3. Article
  4. Identification of co-segregatingFrontiers in medicine · 2025
    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

8 authors at 3 institutions in 1 country.

Yunxia GaoDepartment of Ophthalmology, Ophthalmic Laboratory, West China Hospital, Sichuan University, Chengdu, China.
Xiang RenDepartment of Ophthalmology, Ophthalmic Laboratory, West China Hospital, Sichuan University, Chengdu, China.
Xiangyu FuDepartment of Ophthalmology, Ophthalmic Laboratory, West China Hospital, Sichuan University, Chengdu, China.
Yu LinDepartment of Ophthalmology, Ophthalmic Laboratory, West China Hospital, Sichuan University, Chengdu, China.
Lirong XiaoResearch Laboratory of Ophthalmology and Vision Sciences, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, China.
Xiaoyue WangDepartment of Ophthalmology, Ophthalmic Laboratory, West China Hospital, Sichuan University, Chengdu, China.
Naihong YanResearch Laboratory of Ophthalmology and Vision Sciences, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, China.
Ming ZhangDepartment of Ophthalmology, Ophthalmic Laboratory, West China Hospital, Sichuan University, Chengdu, China.
Sichuan University · CNState Key Laboratory of BiotherapyWest China Hospital of Sichuan 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

AlphaFold2congenital cataractCRYGD genemutationnystagmus

Identifiers

PMID35222542
PMCPMC8866695
OpenAlexW4211255403

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.