Evidence map›Paper›PMID 33801843›Full record

ArticleInternational journal of molecular sciences2021

Toward the Pathogenicity of the

Chin-Ju Hu, Ying-Chang Lu, Ting-Hua Yang, Yen-Hui Chan, Cheng-Yu Tsai, I-Shing Yu, Shu-Wha Lin, Tien-Chen Liu, Yen-Fu Cheng, Chen-Chi Wu and 1 more

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

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 35% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Molecular Features of SLC26A4 Common Variant p.L117F.Journal of clinical medicine · 2022
    Article
  3. Review
  4. Article
  5. 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

11 authors at 6 institutions in 2 countries.

Chin-Ju HuDepartment of Otolaryngology, National Taiwan University Hospital, Taipei 100, Taiwan.
Ying-Chang LuDepartment of Otolaryngology, National Taiwan University Hospital, Taipei 100, Taiwan.
Ting-Hua YangDepartment of Otolaryngology, National Taiwan University Hospital, Taipei 100, Taiwan.
Yen-Hui ChanDepartment of Otolaryngology, National Taiwan University Hospital, Taipei 100, Taiwan.
Cheng-Yu TsaiDepartment of Otolaryngology, National Taiwan University Hospital, Taipei 100, Taiwan.
I-Shing YuTransgenic Mouse Models Core (TMMC), Division of Genomic Medicine, Research Center for Medical Excellence, National Taiwan University, Taipei 100, Taiwan.
Shu-Wha LinTransgenic Mouse Models Core (TMMC), Division of Genomic Medicine, Research Center for Medical Excellence, National Taiwan University, Taipei 100, Taiwan.ORCID 0000-0001-6748-5581
Tien-Chen LiuDepartment of Otolaryngology, National Taiwan University Hospital, Taipei 100, Taiwan.ORCID 0000-0001-6771-5025
Yen-Fu ChengDepartment of Medical Research, Taipei Veteran General Hospital, Taipei 112, Taiwan.ORCID 0000-0003-1995-5854
Chen-Chi WuDepartment of Otolaryngology, National Taiwan University Hospital, Taipei 100, Taiwan.
Chuan-Jen HsuDepartment of Otolaryngology, National Taiwan University Hospital, Taipei 100, Taiwan.ORCID 0000-0002-7548-7736
National Taiwan University · TWNational Taiwan University Hospital · TWTaipei Tzu Chi Hospital · TWHarvard University · USNational Yang Ming Chiao Tung University · TWTaipei Veterans General Hospital · TW

Funding

National Taiwan University Hospital NHRI-EX109-10914PINational Taiwan University Hospital NTUH.108-T14National Taiwan University Hospital VN108-09Taipei Veterans General Hospital VN109-15
6 · The paper itself

Abstract

Recessive variants of the

Indexed as

Disease Models, AnimalMutationAnimalsGenetic Association StudiesGenetic Predisposition to DiseaseGenotypeHearing Loss, SensorineuralHumansMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicPhenotypeSulfate TransportersVestibular AqueductSlc26a4 protein, mouseSulfate Transportershumanmicep.C565Y variantPendred syndromeSLC26A4

Identifiers

PMID33801843
PMCPMC8001573
OpenAlexW3135013920

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.