Clinical Insights into the Neurodevelopmental Impact of 16p CNVs in an Italian Clinical Cohort.

Ilaria La Monica, Maria Rosaria Di Iorio, Antonia Sica, Lucio Pastore, Barbara Lombardo

Abstract read

In one paragraph

Article in Genes, 2026. 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.

Contribution of Copy Number Variants and Cumulative Genetic Load to Autism Spectrum Disorders: Integrative Insights from Chromosomal Microarray Analysis.International journal of molecular sciences · 2026
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

5 authors.

Ilaria La MonicaDepartment of Molecular Medicine and Medical Biotechnologies, Federico II University, Via Sergio Pansini 5, 80131 Naples, Italy.ORCID 0009-0003-1072-3763

Maria Rosaria Di IorioCEINGE-Biotecnologie Avanzate Franco Salvatore, Via G. Salvatore 486, 80145 Naples, Italy.ORCID 0009-0004-7321-9799

Antonia SicaDepartment of Molecular Medicine and Medical Biotechnologies, Federico II University, Via Sergio Pansini 5, 80131 Naples, Italy.

Lucio PastoreDepartment of Molecular Medicine and Medical Biotechnologies, Federico II University, Via Sergio Pansini 5, 80131 Naples, Italy.ORCID 0000-0001-6894-9317

Barbara LombardoDepartment of Molecular Medicine and Medical Biotechnologies, Federico II University, Via Sergio Pansini 5, 80131 Naples, Italy.ORCID 0000-0003-3884-1043

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Chromosomes, Human, Pair 16DNA Copy Number VariationsNeurodevelopmental DisordersAdolescentAdultAutism Spectrum DisorderChildChild, PreschoolChromosome DeletionCohort StudiesComparative Genomic HybridizationDevelopmental DisabilitiesFemaleHumansIntellectual DisabilityItaly16p13.1116p13.3a-CGHchromosome 16p11.2copy number variantsgenotype–phenotype correlationItalian cohortneurodevelopmental disorders

Identifiers

PMID41751631

DOI10.3390/genes17020247

PMCPMC12940275

What OpenQuestion holds

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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.