Evidence map›Paper›PMID 38074417›Full record

ArticleGlobal medical genetics2023

Screening for Mutations in Hereditary Cancer Susceptibility Genes in a Region with High Endogamy in Brazil.

Polyanna Oliveira, Paula Correa, Angelina Acosta, Juliana Freitas, Taísa Machado-Lopes, Thais Bomfim-Palma, Ândrea Ribeiro-Dos-Santos, Sidney Santos, Roberto Nascimento, Ivana Nascimento and 1 more

Open access · diamondAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Global medical genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

11 authors at 5 institutions in 1 country.

Polyanna OliveiraDepartment of Biology, State University of Feira de Santana, Bahia, Brazil.
Paula CorreaMedical Genetics Service, University Hospital Prof. Edgard Santos, Salvador, Bahia, Brazil.
Angelina AcostaMedical Genetics Service, University Hospital Prof. Edgard Santos, Salvador, Bahia, Brazil.
Juliana FreitasDepartment of Life Sciences, State University of Bahia, Bahia, Brazil.
Taísa Machado-LopesLaboratory of Immunology and Molecular Biology, Institute of Health Sciences, Federal University of Bahia, Salvador, Brazil.
Thais Bomfim-PalmaLaboratory of Immunology and Molecular Biology, Institute of Health Sciences, Federal University of Bahia, Salvador, Brazil.
Ândrea Ribeiro-Dos-SantosLaboratory of Human and Medical Genetics, Institute of Biological Sciences, Federal University of Pará, Pará, Brazil.
Sidney SantosLaboratory of Human and Medical Genetics, Institute of Biological Sciences, Federal University of Pará, Pará, Brazil.
Roberto NascimentoLaboratory of Immunology and Molecular Biology, Institute of Health Sciences, Federal University of Bahia, Salvador, Brazil.
Ivana NascimentoLaboratory of Immunology and Molecular Biology, Institute of Health Sciences, Federal University of Bahia, Salvador, Brazil.
Kiyoko Abe-SandesDepartment of Life Sciences, State University of Bahia, Bahia, Brazil.
Universidade Federal da Bahia · BRComplexo Hospitalar Universitário Professor Edgard Santos · BRUniversidade do Estado da Bahia · BRUniversidade Federal do Pará · BRUniversidade Estadual de Feira de Santana · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

endogamyhereditary cancermultigene panelpathogenic variant

Identifiers

PMID38074417
PMCPMC10709072
OpenAlexW4389497624

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.