Evidence map›Paper›PMID 36553517›Full record

ReviewGenes2022

Phenotypic Spectrum of

Veronica Bertini, Francesca Cambi, Alessandro Orsini, Alice Bonuccelli, Aureliano Fiorini, Andrea Santangelo, Massimo Scacciati, Maurizio Elia, Ornella Galesi, Diego Peroni and 1 more

Open access · goldAbstract readReview
In one paragraph

Review in Genes, 2022. 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
1.1field-weighted citation impact, top 19% 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. Article
  2. Article
  3. Article
  4. Frontiers in pediatrics · 2023
    Article
  5. Article
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

11 authors at 2 institutions in 1 country.

Veronica BertiniCytogenetic Unit, Department of Laboratory Medicine, Azienda Ospedaliero-Univeristaria Pisana, Via Roma 57, 56100 Pisa, Italy.
Francesca CambiCytogenetic Unit, Department of Laboratory Medicine, Azienda Ospedaliero-Univeristaria Pisana, Via Roma 57, 56100 Pisa, Italy.
Alessandro OrsiniPediatric Neurology, Pediatric Department, Santa Chiara University Hospital, Azienda Ospedaliero-Univeristaria Pisana, Via Roma 57, 56100 Pisa, Italy.
Alice BonuccelliPediatric Neurology, Pediatric Department, Santa Chiara University Hospital, Azienda Ospedaliero-Univeristaria Pisana, Via Roma 57, 56100 Pisa, Italy.
Aureliano FioriniPediatric Neurology, Pediatric Department, Santa Chiara University Hospital, Azienda Ospedaliero-Univeristaria Pisana, Via Roma 57, 56100 Pisa, Italy.
Andrea SantangeloPediatric Neurology, Pediatric Department, Santa Chiara University Hospital, Azienda Ospedaliero-Univeristaria Pisana, Via Roma 57, 56100 Pisa, Italy.ORCID 0000-0003-2668-6373
Massimo ScacciatiPediatric Neurology, Pediatric Department, Santa Chiara University Hospital, Azienda Ospedaliero-Univeristaria Pisana, Via Roma 57, 56100 Pisa, Italy.
Maurizio EliaOasi Research Institute-IRCCS, 94018 Troina, Italy.
Ornella GalesiOasi Research Institute-IRCCS, 94018 Troina, Italy.
Diego PeroniPediatric Neurology, Pediatric Department, Santa Chiara University Hospital, Azienda Ospedaliero-Univeristaria Pisana, Via Roma 57, 56100 Pisa, Italy.ORCID 0000-0002-0234-1373
Angelo ValettoCytogenetic Unit, Department of Laboratory Medicine, Azienda Ospedaliero-Univeristaria Pisana, Via Roma 57, 56100 Pisa, Italy.
Azienda Ospedaliera Universitaria Pisana · ITOasi Maria SS · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The

Indexed as

MegalencephalyUrinary TractChromosome DeletionHaploinsufficiencyHumansNFI Transcription FactorsNFIA protein, humanNFI Transcription Factorsbilateral proximally placed first fingerscorpus callosum agenesis/hypoplasiamacrocephalyNCS defectsneurodevelopmental disordersnuclearfactor I family

Identifiers

PMID36553517
PMCPMC9777632
OpenAlexW4311002101

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.