Evidence map›Paper›PMID 36330437›Full record

ArticleFrontiers in genetics2022

Case report:

Laura Alías, Miguel López de Heredia, Sabina Luna, Núria Clivillé, Lídia González-Quereda, Pía Gallano, Júlia de Juan, Albert Pujol, Santiago Diez, Susana Boronat and 3 more

Abstract 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. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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.

  1. Article
  2. Review
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

13 authors.

Laura AlíasGenetics Department, IIB Sant Pau, Hospital de la Santa Creu I Sant Pau, Barcelona, Spain.
Miguel López de HerediaCentre for Biomedical Network Research on Rare Diseases (CIBERER), Instituto de Salud Carlos III, Madrid, Spain.
Sabina LunaOphthalmology Department, Hospital de la Santa Creu I Sant Pau, Barcelona, Spain.
Núria ClivilléGenetics Department, IIB Sant Pau, Hospital de la Santa Creu I Sant Pau, Barcelona, Spain.
Lídia González-QueredaGenetics Department, IIB Sant Pau, Hospital de la Santa Creu I Sant Pau, Barcelona, Spain.
Pía GallanoGenetics Department, IIB Sant Pau, Hospital de la Santa Creu I Sant Pau, Barcelona, Spain.
Júlia de JuanOtorhinolaringologyst Department, Hospital de la Santa Creu I Sant Pau, Barcelona, Spain.
Albert PujolOtorhinolaringologyst Department, Hospital de la Santa Creu I Sant Pau, Barcelona, Spain.
Santiago DiezOtorhinolaringology Department, Hospital Esperit Sant, Santa Coloma de Gramenet, Spain.
Susana BoronatChild Neurology Unit, Hospital de la Santa Creu I Sant Pau, Barcelona, Spain.
César OrúsOtorhinolaringologyst Department, Hospital de la Santa Creu I Sant Pau, Barcelona, Spain.
Adriana LasaGenetics Department, IIB Sant Pau, Hospital de la Santa Creu I Sant Pau, Barcelona, Spain.
María Del Prado VenegasOtorhinolaringologyst Department, Hospital de la Santa Creu I Sant Pau, Barcelona, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

congenital hearing lossNGSoptic atrophyWFS1 geneWolfram-like syndrome

Identifiers

PMID36330437
PMCPMC9623256

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.