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
16 authors.
Luigi ChiriattiMolecular Genetics and Functional Genomics, Bambino Gesù Children's Hospital, IRCCS, 00143 Rome, Italy.
Roberta OnesimoCenter for Rare Diseases and Birth Defects, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli, IRCCS, 00168 Rome, Italy.ORCID 0000-0003-3128-6657 Mattia CarvettaMolecular Genetics and Functional Genomics, Bambino Gesù Children's Hospital, IRCCS, 00143 Rome, Italy.ORCID 0000-0003-4584-0663 Chiara LeoniCenter for Rare Diseases and Birth Defects, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli, IRCCS, 00168 Rome, Italy.ORCID 0000-0002-4089-637X Alessandro BrusellesDepartment of Oncology and Molecular Medicine, Istituto Superiore di Sanità, 00161 Rome, Italy.ORCID 0000-0002-1556-4998 Francesca Clementina RadioMolecular Genetics and Functional Genomics, Bambino Gesù Children's Hospital, IRCCS, 00143 Rome, Italy.ORCID 0000-0003-1993-8018 Camilla CappellettiMolecular Genetics and Functional Genomics, Bambino Gesù Children's Hospital, IRCCS, 00143 Rome, Italy.
Marco FerilliMolecular Genetics and Functional Genomics, Bambino Gesù Children's Hospital, IRCCS, 00143 Rome, Italy.
Daniela RicciNational Centre of Services and Research for Prevention of Blindness and Rehabilitation of Low Vision Patients, IAPB Italia Onlus, 00185 Rome, Italy.
Marcello NicetaMolecular Genetics and Functional Genomics, Bambino Gesù Children's Hospital, IRCCS, 00143 Rome, Italy.ORCID 0000-0003-4766-7753 Viviana CordedduDepartment of Oncology and Molecular Medicine, Istituto Superiore di Sanità, 00161 Rome, Italy.
Andrea CiolfiMolecular Genetics and Functional Genomics, Bambino Gesù Children's Hospital, IRCCS, 00143 Rome, Italy.
Cecilia ManciniMolecular Genetics and Functional Genomics, Bambino Gesù Children's Hospital, IRCCS, 00143 Rome, Italy.
Giuseppe ZampinoCenter for Rare Diseases and Birth Defects, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli, IRCCS, 00168 Rome, Italy.ORCID 0000-0002-2661-4831 Marco TartagliaMolecular Genetics and Functional Genomics, Bambino Gesù Children's Hospital, IRCCS, 00143 Rome, Italy.ORCID 0000-0001-7736-9672 Funding
Italian Ministry of Health Current Research FundsItalian Ministry of Health RF-2021-12374963
6 · The paper itselfAbstract
PubMed holds no abstract for this paper.
Indexed as
CochleaEye AbnormalitiesIntellectual DisabilityAmino Acid SubstitutionChildChild, PreschoolDevelopmental DisabilitiesFemaleGenetic Association StudiesHumansMalePhenotypeCHARGE syndromecochlear aplasiacolobomagenotype-phenotype correlationsHNRNPCmicrophthalmiaMRD74phenotypic heterogeneity
Identifiers
PMID40004505
PMCPMC11854916
What OpenQuestion holds
Textmetadata
LicenceCC BY
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