Evidence map›Paper›PMID 37629793›Full record

ArticleMedicina (Kaunas, Lithuania)2023

Specific Learning Disorders: Variation Analysis of 15 Candidate Genes in 9 Multiplex Families.

Francesco Calì, Francesco Domenico Di Blasi, Emanuela Avola, Mirella Vinci, Antonino Musumeci, Angelo Gloria, Donatella Greco, Daniela Rita Raciti, Alessandro Zagami, Biagio Rizzo and 5 more

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

Article in Medicina (Kaunas, Lithuania), 2023. 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
2.9field-weighted citation impact, top 9% 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. Article
  3. 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

15 authors at 2 institutions in 1 country.

Francesco CalìOasi Research Institute-IRCCS, Via Conte Ruggero 73, 94018 Troina, Italy.
Francesco Domenico Di BlasiOasi Research Institute-IRCCS, Via Conte Ruggero 73, 94018 Troina, Italy.ORCID 0000-0002-2958-2927
Emanuela AvolaOasi Research Institute-IRCCS, Via Conte Ruggero 73, 94018 Troina, Italy.
Mirella VinciOasi Research Institute-IRCCS, Via Conte Ruggero 73, 94018 Troina, Italy.
Antonino MusumeciOasi Research Institute-IRCCS, Via Conte Ruggero 73, 94018 Troina, Italy.ORCID 0000-0002-8999-3365
Angelo GloriaOasi Research Institute-IRCCS, Via Conte Ruggero 73, 94018 Troina, Italy.
Donatella GrecoOasi Research Institute-IRCCS, Via Conte Ruggero 73, 94018 Troina, Italy.
Daniela Rita RacitiOasi Research Institute-IRCCS, Via Conte Ruggero 73, 94018 Troina, Italy.
Alessandro ZagamiOasi Research Institute-IRCCS, Via Conte Ruggero 73, 94018 Troina, Italy.
Biagio RizzoOasi Research Institute-IRCCS, Via Conte Ruggero 73, 94018 Troina, Italy.
Santina CittàOasi 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
Luigi VetriOasi Research Institute-IRCCS, Via Conte Ruggero 73, 94018 Troina, Italy.ORCID 0000-0002-0121-3396
Salvatore SacconeDepartment Biological, Geological and Environmental Sciences, University of Catania, Via Androne 81, 95124 Catania, Italy.ORCID 0000-0001-7568-5823
Serafino BuonoOasi Research Institute-IRCCS, Via Conte Ruggero 73, 94018 Troina, Italy.
Oasi Maria SS · 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

Specific Learning DisorderAdolescentAllelesChildHigh-Throughput Nucleotide SequencingHumansMicrotubule-Associated ProteinsNerve Tissue ProteinsReceptors, ImmunologicDCDC2 protein, humanMicrotubule-Associated ProteinsNerve Tissue ProteinsReceptors, Immunologicdyslexiamultiplex SLD familiesnext-generation sequencingsingle nucleotide polymorphismsSpecific Learning Disorder (SLD)

Identifiers

PMID37629793
PMCPMC10456226
OpenAlexW4386049636

What Socratic 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 Socratic graph.