ArticleGenes2023
Prenatal Clinical Findings in
Open access · goldFull text read
In one paragraph
Article in Genes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.
0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 8% 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.
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.
Who cites it
10 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.
- A Framework for Bioinformatic Reporting in Prenatal Sequencing: Insights From a Systematic Review.Prenatal diagnosis · 2026Pooled it
- Global Recommendations for the Use of Diagnostic Genomic Sequencing in the Prenatal Setting on Behalf of the ESHG and ISPD.Prenatal diagnosis · 2026Article
- Global recommendations for the use of diagnostic genomic sequencing in the prenatal setting on behalf of the ESHG and ISPD.European journal of human genetics : EJHG · 2026Article
- The Diagnosis and Treatment Technology of Port-Wine Stain, and the Prospect of Future Treatment.Dermatology and therapy · 2026Review
- Case Report: Multidisciplinary peripartum management of diffuse capillary-malformation-like lesions with cerebrovascular malformation in pregnancy.Frontiers in medicine · 2026Article
- RAS Pathway Mutations and Therapeutics in Vascular Anomalies.Pediatric blood & cancer · 2025Review
- Molecular landscape and classification of vascular anomalies.Hematology. American Society of Hematology. Education Program · 2024Review
- Methylome analysis of endothelial cells suggests new insights on sporadic brain arteriovenous malformation.Heliyon · 2024Article
- Biomarker Landscape in RASopathies.International journal of molecular sciences · 2024Review
- Large saccular intracranial aneurysm in a child with RASA1-associated capillary malformation-arteriovenous malformation syndrome: illustrative case.Journal of neurosurgery. Case lessons · 2023Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
26 authors at 7 institutions in 1 country.
Emanuele CocciaMedical Genetics Unit, Azienda USL-IRCCS di Reggio Emilia, 42123 Reggio Emilia, Italy.
Lara ValeriMedical Genetics Unit, Azienda USL-IRCCS di Reggio Emilia, 42123 Reggio Emilia, Italy.
Roberta ZuntiniMedical Genetics Unit, Azienda USL-IRCCS di Reggio Emilia, 42123 Reggio Emilia, Italy.
Stefano Giuseppe CaraffiMedical Genetics Unit, Azienda USL-IRCCS di Reggio Emilia, 42123 Reggio Emilia, Italy.ORCID 0000-0002-5033-7854
Francesca PelusoMedical Genetics Unit, Azienda USL-IRCCS di Reggio Emilia, 42123 Reggio Emilia, Italy.ORCID 0000-0002-0976-1258
Luca PagliaiMedical Genetics Unit, Azienda USL-IRCCS di Reggio Emilia, 42123 Reggio Emilia, Italy.
Antonietta VezzaniMedical Genetics Unit, Azienda USL-IRCCS di Reggio Emilia, 42123 Reggio Emilia, Italy.
Zaira PietrangiolilloNeonatal Intensive Care Unit, Azienda USL-IRCCS di Reggio Emilia, 42123 Reggio Emilia, Italy.
Francesco LeoNeonatal Intensive Care Unit, Azienda USL-IRCCS di Reggio Emilia, 42123 Reggio Emilia, Italy.
Nives MelliNeonatal Intensive Care Unit, Azienda USL-IRCCS di Reggio Emilia, 42123 Reggio Emilia, Italy.
Valentina FioriniNeonatal Intensive Care Unit, Azienda USL-IRCCS di Reggio Emilia, 42123 Reggio Emilia, Italy.
Andrea GrecoPostgraduate School of Paediatrics, University of Modena and Reggio Emilia, 41121 Modena, Italy.
Francesca Romana LepriTranslational Cytogenomics Research Unit, Laboratory of Medical Genetics, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.
Elisa PisaneschiTranslational Cytogenomics Research Unit, Laboratory of Medical Genetics, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.
Annabella MarozzaMedical Genetics Unit, Careggi University Hospital, 50134 Florence, Italy.
Diana CarliDepartment of Public Health and Pediatric Sciences, Regina Margherita Children's Hospital, Azienda Ospedaliero-Universitaria di Torino, 10126 Turin, Italy.ORCID 0000-0001-5690-6504
Alessandro MussaDepartment of Public Health and Pediatric Sciences, Regina Margherita Children's Hospital, Azienda Ospedaliero-Universitaria di Torino, 10126 Turin, Italy.
Francesca Clementina RadioMolecular Genetics and Functional Genomics, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.ORCID 0000-0003-1993-8018
Beatrice ContiClinical Genetics Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, 20122 Milan, Italy.
Maria IasconeLaboratory of Medical Genetics, Ospedale Papa Giovanni XXIII, 24127 Bergamo, Italy.ORCID 0000-0002-4707-212X
Giancarlo GarganoNeonatal Intensive Care Unit, Azienda USL-IRCCS di Reggio Emilia, 42123 Reggio Emilia, Italy.
Antonio NovelliTranslational Cytogenomics Research Unit, Laboratory of Medical Genetics, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.ORCID 0000-0002-9037-4297
Marco TartagliaMolecular Genetics and Functional Genomics, Bambino Gesù Children's Hospital, IRCCS, 00146 Rome, Italy.ORCID 0000-0001-7736-9672
Orsetta ZuffardiUnit of Medical Genetics, Department of Molecular Medicine, University of Pavia, 27100 Pavia, Italy.
Maria Francesca BedeschiClinical Genetics Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, 20122 Milan, Italy.ORCID 0000-0002-6723-9177
Livia GaravelliMedical Genetics Unit, Azienda USL-IRCCS di Reggio Emilia, 42123 Reggio Emilia, Italy.
Azienda Sanitaria Unità Locale di Reggio Emilia · ITBambino Gesù Children's Hospital · ITFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITAzienda Ospedaliero-Universitaria Careggi · ITOspedale Papa Giovanni XXIII · ITUniversity of Modena and Reggio Emilia · ITUniversity of Pavia · IT
Funding
No grant is acknowledged in the PubMed record.
Abstract
Pathogenic variants in
Indexed as
Arteriovenous MalformationsPort-Wine StainCapillariesChildFemaleGTPase-Activating ProteinsHumansInfant, NewbornMutationp120 GTPase Activating ProteinPregnancyGTPase-Activating Proteinsp120 GTPase Activating ProteinRASA1 protein, humancapillary malformation-arteriovenous malformation (CM-AVM)chylothoraxnon-immune fetal hydropspolyhydramniosprenatal findingsRASA1
Identifiers
What OpenQuestion holds
Textfull text, public
LicenceCC BY
reference markers read2
measurements read28
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.