Evidence map›Paper›PMID 40474964›Full record

ArticleNeuroscience insights2025

Rare Copy Number Variants Intersecting Parkinson's-associated Genes in a Cohort of children With Autism Spectrum Disorders.

Alina Erbescu, Sorina Mihaela Papuc, Magdalena Budișteanu, Maria Dobre, Catrinel Iliescu, Mihail Eugen Hinescu, Aurora Arghir, Monica Neagu

Abstract read
In one paragraph

Article in Neuroscience insights, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

8 authors.

Alina ErbescuVictor Babes National Institute of Pathology, Bucharest, Romania.
Sorina Mihaela PapucVictor Babes National Institute of Pathology, Bucharest, Romania.ORCID https://orcid.org/0000-0002-1352-3535
Magdalena BudișteanuVictor Babes National Institute of Pathology, Bucharest, Romania.
Maria DobreVictor Babes National Institute of Pathology, Bucharest, Romania.
Catrinel IliescuProf. Dr. Alex. Obregia Clinical Hospital of Psychiatry, Bucharest, Romania.
Mihail Eugen HinescuVictor Babes National Institute of Pathology, Bucharest, Romania.
Aurora ArghirVictor Babes National Institute of Pathology, Bucharest, Romania.
Monica NeaguVictor Babes National Institute of Pathology, Bucharest, Romania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autism spectrum disorders (ASDs) are neurodevelopmental conditions characterized by important clinical and genetic heterogeneity. Recent studies suggested an overlap between ASD and Parkinson's disease (PD) in terms of clinical manifestation and underlying genetic defects. Our aim was to assess using a chromosomal microarray assay the frequency of rare exonic deletions that overlap with PD associated genes in a pediatric ASD group. Three hundred and five children diagnosed with ASD were enrolled in a study focused on deep phenotyping and genomic profiling by chromosomal microarrays. In the investigated group, four children with ASD harbored deletions encompassing genes involved in Mendelian forms of PD or contributing to PD risk. Deletions of Parkin RBR E3 ubiquitin protein ligase (

Indexed as

Autistic behaviorcopy number variantsmonogenic Parkinson’s diseasemovement disorders

Identifiers

PMID40474964
PMCPMC12138218

What OpenQuestion holds

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Registered trials

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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.