Evidence map›Paper›PMID 31815120›Full record

ArticleBioMed research international2019

Gene Variant in the NF-

Pablo Coto-Segura, Eliecer Coto, Leire González-Lara, Belén Alonso, Juan Gómez, Elías Cuesta-Llavona, Rubén Queiro

Abstract read
In one paragraph

Article in BioMed research international, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Review
  6. Observational
  7. Review
  8. 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

7 authors.

Pablo Coto-SeguraDermatology Division, Hospital Alvarez Buylla-Mieres, Mieres, Spain.ORCID https://orcid.org/0000-0002-0823-4210
Eliecer CotoDepartment of Medicine, University of Oviedo, Oviedo, Spain.ORCID https://orcid.org/0000-0002-8649-9150
Leire González-LaraMolecular Genetics Unit, Hospital Universitario Central Asturias, Oviedo, Spain.
Belén AlonsoMolecular Genetics Unit, Hospital Universitario Central Asturias, Oviedo, Spain.
Juan GómezMolecular Genetics Unit, Hospital Universitario Central Asturias, Oviedo, Spain.
Elías Cuesta-LlavonaMolecular Genetics Unit, Hospital Universitario Central Asturias, Oviedo, Spain.
Rubén QueiroInstituto Investigación Sanitaria del Principado de Asturias (IISPA), Oviedo, Spain.ORCID https://orcid.org/0000-0002-8418-7145

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsThe NF- PATIENTS AND

methodsWe investigated the association between three common variants in

resultsThe rare

conclusionsOur study supports a significant effect of the

Indexed as

Adaptor Proteins, Signal TransducingAdultArthritis, PsoriaticFemaleGenetic Association StudiesGenetic Predisposition to DiseaseGenotypeHumansLogistic ModelsMaleMiddle AgedNF-kappa BNF-KappaB Inhibitor alphaNF-kappa B p50 SubunitPolymorphism, Single NucleotidePsoriasisAdaptor Proteins, Signal TransducingNF-kappa BNF-KappaB Inhibitor alphaNF-kappa B p50 SubunitNFKB1 protein, humanNFKBIA protein, humanNFKBIZ protein, human

Identifiers

PMID31815120
PMCPMC6877981

What OpenQuestion holds

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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.