Evidence map›Paper›PMID 33096615›Full record

ArticleGenes2020

Paula Buonfiglio, Carlos D Bruque, Leonela Luce, Florencia Giliberto, Vanesa Lotersztein, Sebastián Menazzi, Bibiana Paoli, Ana Belén Elgoyhen, Viviana Dalamón

Open access · goldAbstract read
In one paragraph

Article in Genes, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. NAR genomics and bioinformatics · 2024
    Article
  2. Review
  3. Observational
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Evaluation of theIranian journal of otorhinolaryngology · 2021
    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 3 institutions in 1 country.

Paula BuonfiglioLaboratorio de Fisiología y Genética de la Audición, Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres", Consejo Nacional de Investigaciones Científicas y Técnicas-INGEBI/CONICET, C1428ADN Ciudad Autónoma de Buenos Aires, Argentina.ORCID 0000-0003-2985-4790
Carlos D BruqueCentro Nacional de Genética Médica, ANLIS-Malbrán, C1425 Ciudad Autónoma de Buenos Aires, Argentina.ORCID 0000-0003-0726-5418
Leonela LuceLaboratorio de Distrofinopatías, Cátedra de Genética, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, C1113AAD Ciudad Autónoma de Buenos Aires, Argentina.
Florencia GilibertoLaboratorio de Distrofinopatías, Cátedra de Genética, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, C1113AAD Ciudad Autónoma de Buenos Aires, Argentina.
Vanesa LoterszteinServicio de Genética, Hospital Militar Central "Dr. Cosme Argerich", C1426 Ciudad Autónoma de Buenos Aires, Argentina.
Sebastián MenazziServicio de Genética, Hospital de Clínicas "José de San Martín", C1120AAR Ciudad Autónoma de Buenos Aires, Argentina.
Bibiana PaoliServicio de Otorrinolaringología Infantil, Hospital de Clínicas "José de San Martín", C1120AAR Ciudad Autónoma de Buenos Aires, Argentina.
Ana Belén ElgoyhenLaboratorio de Fisiología y Genética de la Audición, Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres", Consejo Nacional de Investigaciones Científicas y Técnicas-INGEBI/CONICET, C1428ADN Ciudad Autónoma de Buenos Aires, Argentina.ORCID 0000-0001-9487-0311
Viviana DalamónLaboratorio de Fisiología y Genética de la Audición, Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres", Consejo Nacional de Investigaciones Científicas y Técnicas-INGEBI/CONICET, C1428ADN Ciudad Autónoma de Buenos Aires, Argentina.ORCID 0000-0001-5283-4726
Consejo Nacional de Investigaciones Científicas y Técnicas · ARHospital de Clínicas "José de San Martín" · ARArgerich Hospital · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic variants in

Indexed as

Genetic VariationGenome, HumanArgentinaCohort StudiesConnexin 26Connexin 30FemaleGenetic TestingGenomicsHearing LossHigh-Throughput Nucleotide SequencingHumansMaleConnexin 26Connexin 30GJB2 protein, humanGJB6 protein, humanargentinacurationgenetic variantsGJB2GJB6hearing loss

Identifiers

PMID33096615
PMCPMC7589744
OpenAlexW3094558604

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.