Evidence map›Paper›PMID 35292975›Full record

ArticleAnnals of human genetics2022

A novel missense variant in CEACAM16 gene causes autosomal dominant nonsyndromic hearing loss.

Dejun Zhang, Jie Wu, Yongyi Yuan, Xiaohong Li, Xue Gao, Mingyu Han, Song Gao, Shasha Huang, Pu Dai

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

Article in Annals of human genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 49% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

9 authors at 4 institutions in 1 country.

Dejun ZhangCollege of Otolaryngology Head and Neck Surgery, Chinese PLA General Hospital, Beijing, China.ORCID 0000-0003-0951-9637
Jie WuCollege of Otolaryngology Head and Neck Surgery, Chinese PLA General Hospital, Beijing, China.
Yongyi YuanCollege of Otolaryngology Head and Neck Surgery, Chinese PLA General Hospital, Beijing, China.
Xiaohong LiDepartment of Otolaryngology, Head and Neck Surgery, National Children's Medical Center/Beijing Children's Hospital, Capital Medical University, Beijing, PR China.
Xue GaoDepartment of Otolaryngology, PLA Rocket Force Characteristic Medical Center, Beijing, China.
Mingyu HanCollege of Otolaryngology Head and Neck Surgery, Chinese PLA General Hospital, Beijing, China.
Song GaoDepartment of Otolaryngology, South-East Hospital Affiliated to Xiamen University, Zhangzhou, China.
Shasha HuangCollege of Otolaryngology Head and Neck Surgery, Chinese PLA General Hospital, Beijing, China.
Pu DaiCollege of Otolaryngology Head and Neck Surgery, Chinese PLA General Hospital, Beijing, China.
Chinese PLA General Hospital · CNCapital Medical University · CNPLA Academy of Military Science · CNXiamen 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

DeafnessHearing Loss, SensorineuralCell Adhesion MoleculesGenes, DominantHumansMutation, MissensePedigreeCEACAM16 protein, humanCell Adhesion Moleculesautosomal dominant nonsyndromic hearing lossCEACAM16DFNA4Bnext-generation sequencingtectorial membrane

Identifiers

PMID35292975
PMCPMC9314904
OpenAlexW4220663142

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.