Evidence map›Paper›PMID 33540994›Full record

ArticleLin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery2021

[Genotype and clinical phenotype analysis of 42 patients with delayed nonsyndromic hearing loss].

Wenxia Niu, Huijuan Xu, Litao Qin, Guangke Wang, Shaoguang Ding, Cuncun Xie, Xiaodong Jia, Hongjian Liu

Open access · greenAbstract read
In one paragraph

Article in Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.1field-weighted citation impact, top 64% 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

3 citing papers in PubMed, 1 citations in OpenAlex.

  1. [The study of detection and etiology of delayed sensorineural hearing loss in children].Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery · 2025
    Article
  2. [Hearing care network for early identification of delayed hearing loss in preschool children].Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery · 2023
    Article
  3. [The genotype-phenotype correlation analysis and genetic counseling of hearing loss patients with novelLin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery · 2023
    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 1 institution in 1 country.

Wenxia NiuDepartment of Otolaryngology Head and Neck Surgery,Henan University People's Hospital,Henan Provincial People's Hospital,Zhengzhou,450003,China.
Huijuan XuDepartment of Otolaryngology Head and Neck Surgery,Henan University People's Hospital,Henan Provincial People's Hospital,Zhengzhou,450003,China.
Litao QinHenan Provincial People's Hospital,Zhengzhou University People's Hospital,Medical Genetics of Henan Provincial.
Guangke WangDepartment of Otolaryngology Head and Neck Surgery,Henan Provincial People's Hospital,Zhengzhou University People's Hospital,Henan University People's Hospital.
Shaoguang DingDepartment of Otolaryngology Head and Neck Surgery,Henan Provincial People's Hospital,Zhengzhou University People's Hospital,Henan University People's Hospital.
Cuncun XieDepartment of Otolaryngology Head and Neck Surgery,Henan Provincial People's Hospital,Zhengzhou University People's Hospital,Henan University People's Hospital.
Xiaodong JiaDepartment of Otolaryngology Head and Neck Surgery,Henan Provincial People's Hospital,Zhengzhou University People's Hospital,Henan University People's Hospital.
Hongjian LiuDepartment of Otolaryngology Head and Neck Surgery,Henan Provincial People's Hospital,Zhengzhou University People's Hospital,Henan University People's Hospital.
Henan Provincial People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

ConnexinsDeafnessChildChinaDNA Mutational AnalysisGenotypeHumansInfantInfant, NewbornMutationPhenotypeSulfate TransportersConnexinsSulfate TransportersgenotypeGJB2 genenon-syndromic hearing lossSLC26A4 gene

Identifiers

PMID33540994
PMCPMC10127873
OpenAlexW3128174887

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.