Evidence map›Paper›PMID 36360163›Full record

ArticleGenes2022

Dyslexia and Attention Deficit Hyperactivity Disorder Associated to a De Novo 1p34.3 Microdeletion.

Ornella Galesi, Francesco Domenico Di Blasi, Lucia Grillo, Flaviana Elia, Maria Concetta Giambirtone, Maria Grazia Figura, Biagio Rizzo, Serafino Buono, Corrado Romano

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

Article in Genes, 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 31% 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, 2 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

9 authors at 2 institutions in 1 country.

Ornella GalesiLaboratory of Medical Genetics, Oasi Research Institute-IRCCS, 94018 Troina, Italy.
Francesco Domenico Di BlasiUnit of Psychology, Oasi Research Institute-IRCCS, 94018 Troina, Italy.ORCID 0000-0002-2958-2927
Lucia GrilloLaboratory of Medical Genetics, Oasi Research Institute-IRCCS, 94018 Troina, Italy.
Flaviana EliaUnit of Psychology, Oasi Research Institute-IRCCS, 94018 Troina, Italy.
Maria Concetta GiambirtoneLaboratory of Medical Genetics, Oasi Research Institute-IRCCS, 94018 Troina, Italy.
Maria Grazia FiguraUnit of Neurology and Clinical Neurophysiopathology, Oasi Research Institute-IRCCS, 94018 Troina, Italy.
Biagio RizzoUnit of Otorhinolaryngology, Oasi Research Institute-IRCCS, 94018 Troina, Italy.
Serafino BuonoUnit of Psychology, Oasi Research Institute-IRCCS, 94018 Troina, Italy.
Corrado RomanoResearch Unit of Rare Diseases and Neurodevelopmental Disorders, Oasi Research Institute-IRCCS, 94018 Troina, Italy.ORCID 0000-0003-1049-0683
Oasi Maria SS · ITUniversity of Catania · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The authors report on a boy with dyslexia and attention deficit hyperactivity disorder. A protocol of standardized tests assessed the neuroadaptive profile, allowing deep neuropsychiatric phenotyping. In addition to the diagnosis of dyslexia and attention deficit hyperactivity disorder, such methodology led to endeavor cognitive, adaptive, and academic skills. Chromosomal microarray analysis detected a 452.4 Kb de novo heterozygous microdeletion in chromosomal region 1p34.3, including seven OMIM genes. The authors took a thorough evaluation of the association to the phenotype of the deleted genes. Further reports could strengthen such association.

Indexed as

Attention Deficit Disorder with HyperactivityDyslexiaHeterozygoteHumansPhenotype1p34.3 microdeletionAGO1 geneattention deficit hyperactivity disorderdyslexiaKIAA0319L gene

Identifiers

PMID36360163
PMCPMC9689888
OpenAlexW4307264334

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.