Evidence map›Paper›PMID 33062074›Full record

ArticleDisease markers2020

Rayra Pereira Santiago, Camylla Vilas Boas Figueiredo, Luciana Magalhães Fiuza, Sétondji Cocou Modeste Alexandre Yahouédéhou, Rodrigo Mota Oliveira, Milena Magalhães Aleluia, Suellen Pinheiro Carvalho, Cleverson Alves Fonseca, Valma Maria Lopes Nascimento, Larissa Carneiro Rocha and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Disease markers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 37% 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

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 4 citations in OpenAlex.

  1. Pooled it
  2. High prevalence of molar-incisor hypomineralisation in sickle cell disease children and the association with haematologic profile: a retrospective cohort study.European archives of paediatric dentistry : official journal of the European Academy of Paediatric Dentistry · 2026
    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

12 authors at 2 institutions in 1 country.

Rayra Pereira SantiagoLaboratório de Investigação em Genética e Hematologia Translacional, Instituto Gonçalo Moniz, FIOCRUZ-BA, Salvador 40296-710, Brazil.
Camylla Vilas Boas FigueiredoLaboratório de Investigação em Genética e Hematologia Translacional, Instituto Gonçalo Moniz, FIOCRUZ-BA, Salvador 40296-710, Brazil.
Luciana Magalhães FiuzaLaboratório de Investigação em Genética e Hematologia Translacional, Instituto Gonçalo Moniz, FIOCRUZ-BA, Salvador 40296-710, Brazil.
Sétondji Cocou Modeste Alexandre YahouédéhouLaboratório de Investigação em Genética e Hematologia Translacional, Instituto Gonçalo Moniz, FIOCRUZ-BA, Salvador 40296-710, Brazil.
Rodrigo Mota OliveiraLaboratório de Investigação em Genética e Hematologia Translacional, Instituto Gonçalo Moniz, FIOCRUZ-BA, Salvador 40296-710, Brazil.
Milena Magalhães AleluiaDepartamento de Ciências Biológicas, Universidade Estadual de Santa Cruz, UESC, Ilhéus 45662-900, Brazil.
Suellen Pinheiro CarvalhoLaboratório de Investigação em Genética e Hematologia Translacional, Instituto Gonçalo Moniz, FIOCRUZ-BA, Salvador 40296-710, Brazil.
Cleverson Alves FonsecaUniversidade Federal da Bahia, UFBA, Salvador 40170-110, Brazil.
Valma Maria Lopes NascimentoFundação de Hematologia e Hemoterapia do Estado da Bahia, HEMOBA, Salvador 40286-240, Brazil.
Larissa Carneiro RochaFundação de Hematologia e Hemoterapia do Estado da Bahia, HEMOBA, Salvador 40286-240, Brazil.
Caroline Conceição GuardaLaboratório de Investigação em Genética e Hematologia Translacional, Instituto Gonçalo Moniz, FIOCRUZ-BA, Salvador 40296-710, Brazil.ORCID https://orcid.org/0000-0003-1356-8298
Marilda Souza GonçalvesLaboratório de Investigação em Genética e Hematologia Translacional, Instituto Gonçalo Moniz, FIOCRUZ-BA, Salvador 40296-710, Brazil.ORCID https://orcid.org/0000-0003-3000-1437
Universidade Federal da Bahia · BRUniversidade Estadual de Santa Cruz · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Individuals with sickle cell anemia (SCA) present chronic anemia, hemolysis, an exacerbated inflammatory response, and heterogeneous clinical complications, which may be modulated by the transforming growth factor beta (TGF-

Indexed as

Erythrocyte IndicesPolymorphism, Single NucleotideAdolescentAnemia, Sickle CellBiomarkersChildCross-Sectional StudiesFemaleFollow-Up StudiesHemolysisHumansMalePrognosisProteoglycansReceptors, Transforming Growth Factor betabetaglycanBiomarkersProteoglycansReceptors, Transforming Growth Factor beta

Identifiers

PMID33062074
PMCPMC7547350
OpenAlexW3090011837

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.