Evidence map›Paper›PMID 33939317›Full record

ArticleMolecular genetics & genomic medicine2021

RNF213 variant in a patient with Legius syndrome associated with moyamoya syndrome.

Giulia Romanisio, Cristina Chelleri, Marcello Scala, Gianluca Piccolo, Barbara Carlini, Laura Gatti, Valeria Capra, Federico Zara, Anna Bersano, Marco Pavanello and 2 more

Open access · goldAbstract readCase ReportsLetter
In one paragraph

Article in Molecular genetics & genomic medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

12 authors at 2 institutions in 1 country.

Giulia RomanisioPediatric Neurology and Neuromuscular Diseases Unit, IRCCS Giannina Gaslini Institute, Genoa, Italy.
Cristina ChelleriPediatric Neurology and Neuromuscular Diseases Unit, IRCCS Giannina Gaslini Institute, Genoa, Italy.ORCID 0000-0003-2473-5282
Marcello ScalaPediatric Neurology and Neuromuscular Diseases Unit, IRCCS Giannina Gaslini Institute, Genoa, Italy.ORCID 0000-0003-2194-7239
Gianluca PiccoloPediatric Neurology and Neuromuscular Diseases Unit, IRCCS Giannina Gaslini Institute, Genoa, Italy.ORCID 0000-0003-2815-6288
Barbara CarliniMedical Genetics Unit, IRCCS Giannina Gaslini Institute, Genoa, Italy.ORCID 0000-0001-8820-4400
Laura GattiNeurobiology Laboratory, Cerebrovascular Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.ORCID 0000-0001-6751-5031
Valeria CapraMedical Genetics Unit, IRCCS Giannina Gaslini Institute, Genoa, Italy.ORCID 0000-0002-3097-0388
Federico ZaraMedical Genetics Unit, IRCCS Giannina Gaslini Institute, Genoa, Italy.ORCID 0000-0001-9744-5222
Anna BersanoCerebrovascular Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.ORCID 0000-0002-2493-628X
Marco PavanelloPediatric Neurosurgery Unit, IRCCS Giannina Gaslini Institute, Genoa, Italy.ORCID 0000-0001-7312-0204
Patrizia De MarcoMedical Genetics Unit, IRCCS Giannina Gaslini Institute, Genoa, Italy.ORCID 0000-0001-8498-3750
Maria Cristina DianaPediatric Neurology and Neuromuscular Diseases Unit, IRCCS Giannina Gaslini Institute, Genoa, Italy.ORCID 0000-0002-3594-068X
Istituto Giannina Gaslini · ITFondazione IRCCS Istituto Neurologico Carlo Besta · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Adenosine TriphosphatasesCafe-au-Lait SpotsFemaleFrameshift MutationHumansMoyamoya DiseaseSyndromeUbiquitin-Protein LigasesYoung AdultAdenosine TriphosphatasesRNF213 protein, humanUbiquitin-Protein Ligases

Identifiers

PMID33939317
PMCPMC8222830
OpenAlexW3159607557

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.