In one paragraphArticle in Genes, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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 registryThe 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 literatureWho cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
4 · The recordCorrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
5 · Who and what moneyAuthors and funding
15 authors.
Rossana Santiago de Sousa AzulayService of Endocrinology, University Hospital of the Federal University of Maranhão (HUUFMA/EBSERH), São Luis 65020-070, Brazil.ORCID 0000-0002-6097-8145 Alexandre Nogueira FacundoService of Endocrinology, University Hospital of the Federal University of Maranhão (HUUFMA/EBSERH), São Luis 65020-070, Brazil.ORCID 0000-0002-1465-860X Sarah Sousa E SousaResearch Group in Endocrinology and Clinical and Molecular Metabolism (ENDOCLIM), São Luis 65020-040, Brazil.
Gilvan Cortes NascimentoService of Endocrinology, University Hospital of the Federal University of Maranhão (HUUFMA/EBSERH), São Luis 65020-070, Brazil.
Marcelo MagalhãesResearch Group in Endocrinology and Clinical and Molecular Metabolism (ENDOCLIM), São Luis 65020-040, Brazil.ORCID 0000-0002-0464-4343 Clariano Pires de Oliveira NetoService of Endocrinology, University Hospital of the Federal University of Maranhão (HUUFMA/EBSERH), São Luis 65020-070, Brazil.ORCID 0000-0002-6726-4786 Joana D'arc Matos França de AbreuService of Endocrinology, University Hospital of the Federal University of Maranhão (HUUFMA/EBSERH), São Luis 65020-070, Brazil.ORCID 0000-0001-5124-7394 Débora Cristina Ferreira LagoService of Endocrinology, University Hospital of the Federal University of Maranhão (HUUFMA/EBSERH), São Luis 65020-070, Brazil.ORCID 0000-0002-9311-5047 Sabrina da Silva Pereira DamianseService of Endocrinology, University Hospital of the Federal University of Maranhão (HUUFMA/EBSERH), São Luis 65020-070, Brazil.
Viviane Chaves de CarvalhoService of Endocrinology, University Hospital of the Federal University of Maranhão (HUUFMA/EBSERH), São Luis 65020-070, Brazil.
Caio Andrade NascimentoResearch Group in Endocrinology and Clinical and Molecular Metabolism (ENDOCLIM), São Luis 65020-040, Brazil.
Vandilson Pinheiro RodriguesResearch Group in Endocrinology and Clinical and Molecular Metabolism (ENDOCLIM), São Luis 65020-040, Brazil.ORCID 0000-0002-6785-7864 Fernanda Borchers Coeli-LacchiniDepartment of Medicine, Ribeirao Preto Medical School, University of Sao Paulo, Sao Paulo 14048-900, Brazil.
Margaret de CastroDepartment of Medicine, Ribeirao Preto Medical School, University of Sao Paulo, Sao Paulo 14048-900, Brazil.ORCID 0000-0003-4932-4623 Manuel Dos Santos FariaService of Endocrinology, University Hospital of the Federal University of Maranhão (HUUFMA/EBSERH), São Luis 65020-070, Brazil.
Funding
No grant is acknowledged in the PubMed record.
6 · The paper itselfAbstract
PubMed holds no abstract for this paper.
Indexed as
Adrenal Hyperplasia, CongenitalSex Chromosome DisordersSteroid 21-HydroxylaseTrisomyAdultChromosomes, Human, XFemaleHumansSex Chromosome AberrationsSex Chromosome Disorders of Sex DevelopmentSteroid 21-Hydroxylase21-hydroxylase deficiencycongenital adrenal hyperplasiaprimary ovarian failuretriple x karyotype
Identifiers
PMID40149505
PMCPMC11942218
What OpenQuestion holds
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