Evidence map›Paper›PMID 37240737›Full record

ArticleLife (Basel, Switzerland)2023

Felipe Rodrigues de Oliveira, Taís Nitsch Mazzola, Maricilda Palandi de Mello, Ana Paula Francese-Santos, Sofia Helena V de Lemos-Marini, Andrea Trevas Maciel-Guerra, Olaf Hiort, Ralf Werner, Gil Guerra-Junior, Helena Fabbri-Scallet

Open access · goldAbstract read
In one paragraph

Article in Life (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

20 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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  7. Coexistence ofJournal of pediatric endocrinology & metabolism : JPEM · 2025
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  12. Profile ofFrontiers in endocrinology · 2025
    Review
  13. Case Report:Frontiers in endocrinology · 2025
    Article
  14. An Infant WithJCEM case reports · 2025
    Article
  15. International journal of molecular sciences · 2024
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

10 authors at 2 institutions in 2 countries.

Felipe Rodrigues de OliveiraCenter for Molecular Biology and Genetic Engineering (CBMEG), State University of Campinas (UNICAMP), Campinas 13083-875, Brazil.ORCID 0000-0002-5624-6822
Taís Nitsch MazzolaCenter for Investigation in Paediatric, School of Medical Sciences, State University of Campinas (UNICAMP), Campinas 13083-887, Brazil.
Maricilda Palandi de MelloCenter for Molecular Biology and Genetic Engineering (CBMEG), State University of Campinas (UNICAMP), Campinas 13083-875, Brazil.ORCID 0000-0003-0521-9100
Ana Paula Francese-SantosDepartment of Translational Medicine, School of Medical Sciences, State University of Campinas (UNICAMP), Campinas 13083-887, Brazil.
Sofia Helena V de Lemos-MariniDepartment of Pediatrics, School of Medical Sciences, State University of Campinas (UNICAMP), Campinas 13083-887, Brazil.
Andrea Trevas Maciel-GuerraInterdisciplinary Group for the Study of Sex Determination and Differentiation (GIEDDS), State University of Campinas (UNICAMP), Campinas 13083-887, Brazil.ORCID 0000-0002-4850-8079
Olaf HiortDivision of Paediatric Endocrinology and Diabetes, Department of Paediatric and Adolescent Medicine, University of Lübeck, 23562 Lübeck, Germany.
Ralf WernerDivision of Paediatric Endocrinology and Diabetes, Department of Paediatric and Adolescent Medicine, University of Lübeck, 23562 Lübeck, Germany.ORCID 0000-0003-3718-3595
Gil Guerra-JuniorInterdisciplinary Group for the Study of Sex Determination and Differentiation (GIEDDS), State University of Campinas (UNICAMP), Campinas 13083-887, Brazil.
Helena Fabbri-ScalletCenter for Molecular Biology and Genetic Engineering (CBMEG), State University of Campinas (UNICAMP), Campinas 13083-875, Brazil.ORCID 0000-0002-2738-1814
Universidade Estadual de Campinas (UNICAMP) · BRUniversity of Lübeck · DE

Funding

Alexander von Humboldt Foundation HFSFundo de Apoio ao Ensino, à Pesquisa e Extensão (Faepex) 519.294National Council for Scientific and Technological Development 406605/2018-1São Paulo Research Foundation 2020/01054-0, 2018/19445-6, 2015/04763-4
6 · The paper itself

Abstract

The group of disorders known as 46,XY gonadal dysgenesis (GD) is characterized by anomalies in testis determination, including complete and partial GD (PGD) and testicular regression syndrome (TRS). Several genes are known to be involved in sex development pathways, however approximately 50% of all cases remain elusive. Recent studies have identified variants in

Indexed as

DHX37disorders of sex developmentgonadal dysgenesisNR5A1

Identifiers

PMID37240737
PMCPMC10222664
OpenAlexW4367183027

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.