Evidence map›Paper›PMID 34064479›Full record

ArticleBiomedicines2021

Role of RNA in Molecular Diagnosis of MADD Patients.

Célia Nogueira, Lisbeth Silva, Ana Marcão, Carmen Sousa, Helena Fonseca, Hugo Rocha, Teresa Campos, Elisa Leão Teles, Esmeralda Rodrigues, Patrícia Janeiro and 2 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Biomedicines, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
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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

12 authors at 3 institutions in 1 country.

Célia NogueiraResearch & Development Unit, Human Genetics Department, National Institute of Health Doutor Ricardo Jorge, 4000-055 Porto, Portugal.
Lisbeth SilvaResearch & Development Unit, Human Genetics Department, National Institute of Health Doutor Ricardo Jorge, 4000-055 Porto, Portugal.ORCID 0000-0001-7125-8488
Ana MarcãoNewborn Screening, Metabolism & Genetics Unit, Human Genetics Department, National Institute of Health Doutor Ricardo Jorge, 4000-055 Porto, Portugal.ORCID 0000-0001-8549-166X
Carmen SousaNewborn Screening, Metabolism & Genetics Unit, Human Genetics Department, National Institute of Health Doutor Ricardo Jorge, 4000-055 Porto, Portugal.
Helena FonsecaNewborn Screening, Metabolism & Genetics Unit, Human Genetics Department, National Institute of Health Doutor Ricardo Jorge, 4000-055 Porto, Portugal.
Hugo RochaNewborn Screening, Metabolism & Genetics Unit, Human Genetics Department, National Institute of Health Doutor Ricardo Jorge, 4000-055 Porto, Portugal.
Teresa CamposInherited Metabolic Diseases Reference Centre, São João Hospital University Centre, EPE, 4200-319 Porto, Portugal.ORCID 0000-0002-0314-5622
Elisa Leão TelesInherited Metabolic Diseases Reference Centre, São João Hospital University Centre, EPE, 4200-319 Porto, Portugal.ORCID 0000-0002-3011-0249
Esmeralda RodriguesInherited Metabolic Diseases Reference Centre, São João Hospital University Centre, EPE, 4200-319 Porto, Portugal.
Patrícia JaneiroInherited Metabolic Diseases Reference Centre, Lisboa Norte University Centre, EPE, 1649-028 Lisboa, Portugal.
Ana GasparInherited Metabolic Diseases Reference Centre, Lisboa Norte University Centre, EPE, 1649-028 Lisboa, Portugal.
Laura VilarinhoResearch & Development Unit, Human Genetics Department, National Institute of Health Doutor Ricardo Jorge, 4000-055 Porto, Portugal.ORCID 0000-0001-6186-779X
National Institute of Health Dr. Ricardo Jorge · PTHospital de São João · PTCentro Hospitalar Lisboa Norte · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The electron-transfer flavoprotein dehydrogenase gene (

Indexed as

ETFDHglutaric aciduria type IIMADDNBSRNAβ-oxidation

Identifiers

PMID34064479
PMCPMC8147995
OpenAlexW3159634693

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.