In one paragraphSynthesis in Genes, 2026. 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
8 authors.
Chiara GobbettoPaediatric Unit, Department of Surgical Science, Dentistry, Gynecology and Paediatrics, Azienda Ospedaliera Universitaria Integrata Verona, P.le Stefani 1, 37135 Verona, Italy.
Sofia PassarellaPaediatric Unit, Department of Surgical Science, Dentistry, Gynecology and Paediatrics, Azienda Ospedaliera Universitaria Integrata Verona, P.le Stefani 1, 37135 Verona, Italy.
Thomas ZollerPaediatric Unit, Department of Surgical Science, Dentistry, Gynecology and Paediatrics, Azienda Ospedaliera Universitaria Integrata Verona, P.le Stefani 1, 37135 Verona, Italy.ORCID 0000-0001-5429-6036 Ruggero LanzafamePaediatric Unit, Department of Surgical Science, Dentistry, Gynecology and Paediatrics, Azienda Ospedaliera Universitaria Integrata Verona, P.le Stefani 1, 37135 Verona, Italy.ORCID 0009-0009-5378-1895 Rossella GaudinoPaediatric Unit, Department of Surgical Science, Dentistry, Gynecology and Paediatrics, Azienda Ospedaliera Universitaria Integrata Verona, P.le Stefani 1, 37135 Verona, Italy.
Irene AmbrosettiClinical Genetics Unit, Azienda Ospedaliera Universitaria Integrata Verona, 37134 Verona, Italy.
Angelo PietrobelliPaediatric Unit, Department of Surgical Science, Dentistry, Gynecology and Paediatrics, Azienda Ospedaliera Universitaria Integrata Verona, P.le Stefani 1, 37135 Verona, Italy.ORCID 0000-0002-9912-3232 Franco AntoniazziPaediatric Unit, Department of Surgical Science, Dentistry, Gynecology and Paediatrics, Azienda Ospedaliera Universitaria Integrata Verona, P.le Stefani 1, 37135 Verona, Italy.ORCID 0000-0003-1405-1792 Funding
No grant is acknowledged in the PubMed record.
6 · The paper itselfAbstract
Spondylocarpotarsal synostosis syndrome (SCT) is a rare autosomal recessive skeletal dysplasia caused by biallelic loss-of-function variants in
Indexed as
FilaminsScoliosisSynostosisThoracic VertebraeAbnormalities, MultipleFemaleHumansLumbar VertebraeMusculoskeletal DiseasesFilaminsFLNB protein, humancarpal synostosiscase reportfilamin BFLNBreviewshort statureskeletal dysplasiaspondylocarpotarsal synostosis syndromevertebral fusion
Identifiers
PMID42792948
PMCPMC13606696
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