Evidence map›Paper›PMID 34573300›Full record

ArticleGenes2021

13q Deletion Syndrome Involving

Flavia Privitera, Arianna Calonaci, Gabriella Doddato, Filomena Tiziana Papa, Margherita Baldassarri, Anna Maria Pinto, Francesca Mari, Ilaria Longo, Mauro Caini, Daniela Galimberti and 4 more

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Genes, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 31% of its field
1 · What the graph read from it

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 registry

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.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. GA4GH Phenopackets: A Practical Introduction.Advanced genetics (Hoboken, N.J.) · 2023
    Article
  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 2 institutions in 1 country.

Flavia PriviteraMedical Genetics, University of Siena, 53100 Siena, Italy.
Arianna CalonaciUnit of Pediatrics, Department of Maternal, Newborn and Child Health, Azienda Ospedaliera Universitaria Senese, Policlinico 'Santa Maria alle Scotte', 53100 Siena, Italy.
Gabriella DoddatoMedical Genetics, University of Siena, 53100 Siena, Italy.
Filomena Tiziana PapaMedical Genetics, University of Siena, 53100 Siena, Italy.
Margherita BaldassarriMedical Genetics, University of Siena, 53100 Siena, Italy.ORCID 0000-0002-0391-1980
Anna Maria PintoGenetica Medica, Azienda Ospedaliera Universitaria Senese, 53100 Siena, Italy.
Francesca MariMedical Genetics, University of Siena, 53100 Siena, Italy.
Ilaria LongoGenetica Medica, Azienda Ospedaliera Universitaria Senese, 53100 Siena, Italy.
Mauro CainiUnit of Pediatrics, Department of Maternal, Newborn and Child Health, Azienda Ospedaliera Universitaria Senese, Policlinico 'Santa Maria alle Scotte', 53100 Siena, Italy.
Daniela GalimbertiUnit of Pediatrics, Department of Maternal, Newborn and Child Health, Azienda Ospedaliera Universitaria Senese, Policlinico 'Santa Maria alle Scotte', 53100 Siena, Italy.
Theodora HadjistilianouUnit of Ophthalmology and Retinoblastoma Referral Center, Department of Surgery, University of Siena, Policlinico 'Santa Maria alle Scotte', 53100 Siena, Italy.
Sonia De FrancescoUnit of Ophthalmology and Retinoblastoma Referral Center, Department of Surgery, University of Siena, Policlinico 'Santa Maria alle Scotte', 53100 Siena, Italy.
Alessandra RenieriMedical Genetics, University of Siena, 53100 Siena, Italy.ORCID 0000-0002-0846-9220
Francesca ArianiMedical Genetics, University of Siena, 53100 Siena, Italy.
University of Siena · ITAzienda Ospedaliera Universitaria Senese · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Retinoblastoma (RB) is an ocular tumor of the pediatric age caused by biallelic inactivation of the

Indexed as

Chromosome DeletionChromosome DisordersChromosomes, Human, Pair 13Retinoblastoma Binding ProteinsChildChild, PreschoolDevelopmental DisabilitiesFemaleHumansInfantIntellectual DisabilityMalePsychomotor DisordersRetinoblastomaUbiquitin-Protein LigasesRB1 protein, humanRetinoblastoma Binding ProteinsUbiquitin-Protein Ligases13q deletion syndromearray-CGHintellectual disabilityNBEAretinoblastoma

Identifiers

PMID34573300
PMCPMC8471443
OpenAlexW3196078571

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.