Evidence map›Paper›PMID 36555772›Full record

ArticleInternational journal of molecular sciences2022

Ambra Butera, Antonio Gennaro Nicotera, Gabriella Di Rosa, Sebastiano Antonino Musumeci, Girolamo Aurelio Vitello, Antonino Musumeci, Mirella Vinci, Angelo Gloria, Concetta Federico, Salvatore Saccone and 1 more

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.3field-weighted citation impact, top 17% 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, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Neurological Diseases: A Molecular Genetic Perspective.International journal of molecular sciences · 2023
    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 3 institutions in 1 country.

Ambra ButeraDepartment of Human Pathology of the Adult and Developmental Age, "Gaetano Barresi" University of Messina, Via Consolare Valeria 1, 98125 Messina, Italy.
Antonio Gennaro NicoteraDepartment of Human Pathology of the Adult and Developmental Age, "Gaetano Barresi" University of Messina, Via Consolare Valeria 1, 98125 Messina, Italy.
Gabriella Di RosaDepartment of Human Pathology of the Adult and Developmental Age, "Gaetano Barresi" University of Messina, Via Consolare Valeria 1, 98125 Messina, Italy.
Sebastiano Antonino MusumeciOasi Research Institute-IRCCS, Via Conte Ruggero 73, 94018 Troina, Italy.
Girolamo Aurelio VitelloOasi Research Institute-IRCCS, Via Conte Ruggero 73, 94018 Troina, Italy.ORCID 0000-0002-6285-9692
Antonino MusumeciOasi Research Institute-IRCCS, Via Conte Ruggero 73, 94018 Troina, Italy.ORCID 0000-0002-8999-3365
Mirella VinciOasi Research Institute-IRCCS, Via Conte Ruggero 73, 94018 Troina, Italy.
Angelo GloriaOasi Research Institute-IRCCS, Via Conte Ruggero 73, 94018 Troina, Italy.
Concetta FedericoDepartment Biological, Geological and Environmental Sciences, University of Catania, Via Androne 81, 95124 Catania, Italy.ORCID 0000-0002-0160-9040
Salvatore SacconeDepartment Biological, Geological and Environmental Sciences, University of Catania, Via Androne 81, 95124 Catania, Italy.ORCID 0000-0001-7568-5823
Francesco CalìOasi Research Institute-IRCCS, Via Conte Ruggero 73, 94018 Troina, Italy.ORCID 0000-0001-8667-8223
Oasi Maria SS · ITUniversity of Messina · ITUniversity of Catania · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Chromosome DisordersIntellectual DisabilityChildChromosome DeletionChromosomes, Human, Pair 11Exostoses, Multiple HereditaryGene DeletionHistone DeacetylasesHumansPhenotypeHistone DeacetylasesPHF21A protein, humanBHC80contiguous gene deletionhuman chromosome 11hypotoniaintellectual disabilityPHF21A genePotocki–Shaffer syndrome

Identifiers

PMID36555772
PMCPMC9783151
OpenAlexW4312195807

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.