Evidence map›Paper›PMID 35938034›Full record

ArticleFrontiers in genetics2022

Case Report: A Novel

Xinyuan Tian, Chuan Zhang, Bingbo Zhou, Xue Chen, Xuan Feng, Lei Zheng, Yupei Wang, Shengju Hao, Ling Hui

Open access · goldAbstract readCase Reports
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. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 48% 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

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

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

9 authors at 2 institutions in 1 country.

Xinyuan TianSchool of Public Health, Gansu University of Chinese Medicine, Lanzhou, China.
Chuan ZhangCenter for Medical Genetics, Gansu Provincial Maternity and Child Health Hospital, Gansu Provincial Clinical Research Center for Birth Defects and Rare Diseases, Lanzhou, China.
Bingbo ZhouCenter for Medical Genetics, Gansu Provincial Maternity and Child Health Hospital, Gansu Provincial Clinical Research Center for Birth Defects and Rare Diseases, Lanzhou, China.
Xue ChenCenter for Medical Genetics, Gansu Provincial Maternity and Child Health Hospital, Gansu Provincial Clinical Research Center for Birth Defects and Rare Diseases, Lanzhou, China.
Xuan FengCenter for Medical Genetics, Gansu Provincial Maternity and Child Health Hospital, Gansu Provincial Clinical Research Center for Birth Defects and Rare Diseases, Lanzhou, China.
Lei ZhengCenter for Medical Genetics, Gansu Provincial Maternity and Child Health Hospital, Gansu Provincial Clinical Research Center for Birth Defects and Rare Diseases, Lanzhou, China.
Yupei WangCenter for Medical Genetics, Gansu Provincial Maternity and Child Health Hospital, Gansu Provincial Clinical Research Center for Birth Defects and Rare Diseases, Lanzhou, China.
Shengju HaoCenter for Medical Genetics, Gansu Provincial Maternity and Child Health Hospital, Gansu Provincial Clinical Research Center for Birth Defects and Rare Diseases, Lanzhou, China.
Ling HuiCenter for Medical Genetics, Gansu Provincial Maternity and Child Health Hospital, Gansu Provincial Clinical Research Center for Birth Defects and Rare Diseases, Lanzhou, China.
Gansu Provincial Maternal and Child Health Hospital · CNGansu University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dominant variants in the gap junction beta-2 (

Indexed as

dominant variantGJB2 genehearing lossmosaicismpalmoplantar keratoderma

Identifiers

PMID35938034
PMCPMC9354265
OpenAlexW4286485336

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.