Evidence map›Paper›PMID 31426718›Full record

ArticleThyroid : official journal of the American Thyroid Association2019

Interaction of Genetic Variations in

Liliana R Santos, Cecília Durães, Panos G Ziros, Ana Pestana, César Esteves, Celestino Neves, Davide Carvalho, Massimo Bongiovanni, Cédric O Renaud, Dionysios V Chartoumpekis and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Thyroid : official journal of the American Thyroid Association, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

17 citing papers in PubMed, 18 citations in OpenAlex.

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  16. The Keap1/Nrf2 Signaling Pathway in the Thyroid-2020 Update.Antioxidants (Basel, Switzerland) · 2020
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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

14 authors at 3 institutions in 3 countries.

Liliana R SantosDepartment of Internal Medicine, Hospital de Santa Maria, Lisbon, Portugal.
Cecília DurãesInstitute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Porto, Portugal.
Panos G ZirosService of Endocrinology, Diabetology and Metabolism, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Ana PestanaInstitute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Porto, Portugal.
César EstevesFaculty of Medicine, University of Porto, Porto, Portugal.
Celestino NevesFaculty of Medicine, University of Porto, Porto, Portugal.
Davide CarvalhoFaculty of Medicine, University of Porto, Porto, Portugal.
Massimo BongiovanniService of Clinical Pathology, Institute of Pathology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Cédric O RenaudService of Endocrinology, Diabetology and Metabolism, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Dionysios V ChartoumpekisDepartment of Internal Medicine, Division of Endocrinology, School of Medicine, University of Patras, Patras, Greece.
Ioannis G HabeosDepartment of Internal Medicine, Division of Endocrinology, School of Medicine, University of Patras, Patras, Greece.
Manuel Sobrinho SimõesInstitute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Porto, Portugal.
Paula SoaresInstitute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Porto, Portugal.
Gerasimos P SykiotisService of Endocrinology, Diabetology and Metabolism, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Universidade do Porto · PTUniversity of Lausanne · CHUniversity of Patras · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Genetic Predisposition to DiseasePolymorphism, Single NucleotideAnimalsCells, CulturedHaplotypesHashimoto DiseaseHumansMembrane ProteinsMiceMice, Inbred C57BLNF-E2-Related Factor 2Promoter Regions, GeneticRiskSelenoproteinsMembrane ProteinsNFE2L2 protein, humanNF-E2-Related Factor 2SelenoproteinsSELENOS protein, humanNFE2L2Nrf2oxidative stressseleniumselenoprotein SSELENOS

Identifiers

PMID31426718
PMCPMC6760180
OpenAlexW2969731171

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.