Evidence map›Paper›PMID 32508883›Full record

ArticleFrontiers in genetics2020

The

Oana Kubinyecz, Pratik P Vikhe, Thomas Purnell, Steve D M Brown, Hilda Tateossian

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 55% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

5 authors at 1 institution in 1 country.

Oana KubinyeczMammalian Genetics Unit, MRC Harwell Institute, Harwell, United Kingdom.
Pratik P VikheMammalian Genetics Unit, MRC Harwell Institute, Harwell, United Kingdom.
Thomas PurnellMammalian Genetics Unit, MRC Harwell Institute, Harwell, United Kingdom.
Steve D M BrownMammalian Genetics Unit, MRC Harwell Institute, Harwell, United Kingdom.
Hilda TateossianMammalian Genetics Unit, MRC Harwell Institute, Harwell, United Kingdom.
Mary Lyon Centre at MRC Harwell · GB

Funding

Medical Research Council MC_U142684175Medical Research Council MC_UP_1503/1
6 · The paper itself

Abstract

Chronic otitis media (OM) is the most common cause of hearing loss worldwide, yet the underlying genetics and molecular pathology are poorly understood. The mouse mutant

Indexed as

chronic otitis mediaFBXO11mouse modelmutationotitis media

Identifiers

PMID32508883
PMCPMC7248398
OpenAlexW3026997255

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.