Evidence map›Paper›PMID 33093716›Full record

ArticleRevista brasileira de ortopedia2020

Genetic Aspects in Shoulder Disorders.

Carina Cohen, Eduardo A Figueiredo, Paulo S Belangero, Carlos Vicente Andreoli, Mariana Ferreira Leal, Benno Ejnisman

Abstract read
In one paragraph

Article in Revista brasileira de ortopedia, 2020. 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
–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

4 citing papers in PubMed.

  1. Shoulder and genetics: what orthopedic surgeons need to know.JSES reviews, reports, and techniques · 2026
    Review
  2. Genetic Polymorphisms inRevista brasileira de ortopedia · 2023
    Article
  3. Article
  4. 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

6 authors.

Carina CohenDisciplina de Medicina do Esporte e Atividade Física , Centro de Traumatologia do Esporte, Universidade Federal de São Paulo, São Paulo, SP, Brasil.ORCID 0000-0002-9980-8733
Eduardo A FigueiredoDisciplina de Medicina do Esporte e Atividade Física , Centro de Traumatologia do Esporte, Universidade Federal de São Paulo, São Paulo, SP, Brasil.ORCID 0000-0003-0046-1598
Paulo S BelangeroDisciplina de Medicina do Esporte e Atividade Física , Centro de Traumatologia do Esporte, Universidade Federal de São Paulo, São Paulo, SP, Brasil.ORCID 0000-0003-4441-4742
Carlos Vicente AndreoliDisciplina de Medicina do Esporte e Atividade Física , Centro de Traumatologia do Esporte, Universidade Federal de São Paulo, São Paulo, SP, Brasil.ORCID 0000-0003-3761-0745
Mariana Ferreira LealDepartamento de Morfologia e Genética, Universidade Federal de São Paulo, São Paulo, SP, Brasil.ORCID 0000-0003-4375-2563
Benno EjnismanDisciplina de Medicina do Esporte e Atividade Física , Centro de Traumatologia do Esporte, Universidade Federal de São Paulo, São Paulo, SP, Brasil.ORCID 0000-0002-3301-1457

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The influence of genetic inheritance has been increasingly investigated in shoulder disorders, such as rotator cuff injury, instability and frozen shoulder. Although the initial findings are enlightening, it is necessary to progressively build a database of genetic markers to catalog genomic profiles that, later, may contribute for predicting the risk of the disease, as well as to the development of better diagnostic and treatment tools. The present article seeks to update what is evidence of genetic studies in the literature for these diseases, from polymorphism analyses, expression of candidate genes in tissues and broad genomic association studies (GWAS). However, it is necessary to point out that there is great difficulty in replicating and using the findings, mainly due to the lack of statistical power, the high rate of false-positive results and the large number of variables involved.

Indexed as

gene expressiongenetic polymorphismshoulder

Identifiers

PMID33093716
PMCPMC7575388

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.