Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

CNVs inform the biological network of Autism spectrum disorder.

Psychiatry research - 1 Mar 2021

Briuglia Silvana, Calabrò Marco, Capra Anna Paola, La Rosa Maria Angela, Crisafulli Concetta

Abstract excerpt

Autism spectrum disorder (ASD) is a heterogeneous condition linked to an anomalous neurodevelopment. Although the underlying causes of ASD are not well described, literature data strongly suggests a genetic component, with a complex inheritance pattern. It has recently been observed that CNVs (copy number variation) may play an important role in ASD manifestation and partially explain the complex heritability of...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Autism Spectrum Disorder
Share to DNA Copy Number Variations

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genotype

Source

Identifiers

PMID: 33524775
DOI: 10.1016/j.psychres.2021.113729

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

CNVs inform the biological network of Autism spectrum disorder.PMID 33524775Read ↗

Integrated Functional Analysis Implicates Syndromic and Rare Copy Number Variation Genes as Prominent Molecular Players in Pathogenesis of Autism Spectrum Disorders.Semantic proximity Read ↗

Genetic architecture in autism spectrum disorder.Semantic proximity Read ↗

A critical review of the impact of candidate copy number variants on autism spectrum disorder.Semantic proximity Read ↗

Genomic Copy Number Variations in the Autism Clinic—Work in ProgressSemantic proximity Read ↗

Unraveling the Genetic and Molecular Architecture of Autism Spectrum Disorder: Implications for Clinical Genetics and Genomic Diagnostics.Semantic proximity Read ↗

Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological Insights.Semantic proximity Read ↗

Current knowledge on the genetics of autism and propositions for future research.Semantic proximity Read ↗

Progress in the genetics of autism spectrum disorder.Semantic proximity Read ↗

Genetic architecture of autism spectrum disorder: Lessons from large-scale genomic studies.Semantic proximity Read ↗

Genome-wide characterization of genetic and functional dysregulation in autism spectrum disorderSemantic proximity Read ↗

Brain-Enriched Coding and Long Non-coding RNA Genes Are Overrepresented in Recurrent Neurodevelopmental Disorder CNVs.Semantic proximity Read ↗

Network topologies and convergent aetiologies arising from deletions and duplications observed in individuals with autism.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.