Evidence map›Paper›PMID 36077416›Full record

ArticleInternational journal of molecular sciences2022

Characterization of 22q12 Microdeletions Causing Position Effect in Rare NF2 Patients with Complex Phenotypes.

Viviana Tritto, Marica Eoli, Rosina Paterra, Serena Redaelli, Marco Moscatelli, Francesco Rusconi, Paola Riva

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

7 authors at 3 institutions in 1 country.

Viviana TrittoDipartimento di Biotecnologie Mediche e Medicina Traslazionale, Università degli Studi di Milano, 20054 Segrate, Italy.ORCID 0000-0002-4558-8376
Marica EoliUnità di Neuro-Oncologia Molecolare, Fondazione IRCCS, Istituto Neurologico Carlo Besta, 20133 Milan, Italy.ORCID 0000-0003-4744-9377
Rosina PaterraUnità di Neuro-Oncologia Molecolare, Fondazione IRCCS, Istituto Neurologico Carlo Besta, 20133 Milan, Italy.
Serena RedaelliDipartimento di Medicina e Chirurgia, University of Milano-Bicocca, 20900 Monza, Italy.ORCID 0000-0003-0415-4085
Marco MoscatelliUnità di Neuroradiologia, Fondazione IRCCS, Istituto Neurologico Carlo Besta, 20133 Milan, Italy.ORCID 0000-0002-6745-474X
Francesco RusconiDipartimento di Biotecnologie Mediche e Medicina Traslazionale, Università degli Studi di Milano, 20054 Segrate, Italy.ORCID 0000-0003-0500-7845
Paola RivaDipartimento di Biotecnologie Mediche e Medicina Traslazionale, Università degli Studi di Milano, 20054 Segrate, Italy.ORCID 0000-0001-6481-8467
Fondazione IRCCS Istituto Neurologico Carlo Besta · ITUniversity of Milan · ITUniversity of Milano-Bicocca · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurofibromatosis type 2 is an autosomal dominant tumor-prone disorder mainly caused by

Indexed as

Intellectual DisabilityNeurofibromatosis 2Adaptor Protein Complex 1Adaptor Protein Complex beta SubunitsHumansPhenotypeAdaptor Protein Complex 1Adaptor Protein Complex beta SubunitsAP1B1 protein, human22q12 microdeletiongenotype-phenotype correlationhaploinsufficiencyNF2non-allelic homologous recombinationposition effect

Identifiers

PMID36077416
PMCPMC9456353
OpenAlexW4294739491

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.