In one paragraphReview in Genes, 2023. 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
0.5field-weighted citation impact, top 33% of its field
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, 2 citations in OpenAlex.
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
8 authors at 2 institutions in 2 countries.
Matheus de Mello CopelliDepartment of Translational Medicine, Area of Medical Genetics and Genomic Medicine, University of Campinas (UNICAMP), Campinas CEP 13083-887, SP, Brazil.ORCID 0000-0002-6320-1243 Eleonore PairetHuman Molecular Genetics, de Duve Institute, Université Catholique de Louvain, 1200 Brussels, Belgium.ORCID 0000-0003-0929-9101 Milena Atique-TaclaDepartment of Translational Medicine, Area of Medical Genetics and Genomic Medicine, University of Campinas (UNICAMP), Campinas CEP 13083-887, SP, Brazil.ORCID 0000-0002-0547-4913 Társis Paiva VieiraDepartment of Translational Medicine, Area of Medical Genetics and Genomic Medicine, University of Campinas (UNICAMP), Campinas CEP 13083-887, SP, Brazil.ORCID 0000-0003-4027-8341 Simone AppenzellerDepartment of Orthopedics, Rheumatology and Traumatology, School of Medical Science, University of Campinas (UNICAMP), Campinas CEP 13083-887, SP, Brazil.ORCID 0000-0001-5075-4474 Raphaël HelaersHuman Molecular Genetics, de Duve Institute, Université Catholique de Louvain, 1200 Brussels, Belgium.ORCID 0000-0002-7046-7867 Miikka VikkulaHuman Molecular Genetics, de Duve Institute, Université Catholique de Louvain, 1200 Brussels, Belgium.ORCID 0000-0002-6236-338X Vera Lúcia Gil-da-Silva-LopesDepartment of Translational Medicine, Area of Medical Genetics and Genomic Medicine, University of Campinas (UNICAMP), Campinas CEP 13083-887, SP, Brazil.ORCID 0000-0003-1288-0554 Universidade Estadual de Campinas (UNICAMP) · BRde Duve Institute · BE
Funding
No grant is acknowledged in the PubMed record.
6 · The paper itselfAbstract
PubMed holds no abstract for this paper.
Indexed as
Intellectual DisabilityMatrix Attachment Region Binding ProteinsGenetic Association StudiesHumansMalePhenotypeSyndromeTranscription FactorsMatrix Attachment Region Binding ProteinsSATB2 protein, humanTranscription Factorsbehavior problemscleft palatenatural historyosteopeniaSATB2whole-exome sequencing
Identifiers
PMID37107640
PMCPMC10137462
OpenAlexW4362733381
What OpenQuestion holds
Textmetadata
LicenceCC BY
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