Discover Community Create You

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

Distribution of disease-associated copy number variants across distinct disorders of cognitive development.

Journal of the American Academy of Child and Adolescent Psychiatry - 1 Apr 2013

Pescosolido Matthew F, Gamsiz Ece D, Nagpal Shailender, Morrow Eric M

Abstract excerpt

OBJECTIVE: The purpose of the present study was to discover the extent to which distinct DSM disorders share large, highly recurrent copy number variants (CNVs) as susceptibility factors. We also sought to identify gene mechanisms common to groups of diagnoses and/or specific to a given diagnosis based on associations with CNVs. METHOD: Systematic review of 820 PubMed articles on autism spectrum disorder (ASD),...

Read the complete abstract on PubMed

Topics

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

Share to DNA Copy Number Variations
Share to Epilepsy research and treatment

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Fetal and Pediatric Neurological Disorders

Share to Genetic Predisposition to Disease

Share to Genomic variations and chromosomal abnormalities

Share to Intellectual Disability

Share to Mental Disorders

Source

Open in PubMed Open full text

Identifiers

PMID: 23582872
DOI: 10.1016/j.jaac.2013.01.003
PMCID: PMC3774163

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Distribution of disease-associated copy number variants across distinct disorders of cognitive development.PMID 23582872Read ↗

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

Synaptic and Gene Regulatory Mechanisms in Schizophrenia, Autism, and 22q11.2 CNV Mediated Risk for Neuropsychiatric DisordersSemantic proximity Read ↗

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

Recurrent copy number variations as risk factors for neurodevelopmental disorders: critical overview and analysis of clinical implications.Semantic proximity Read ↗

Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.Semantic proximity Read ↗

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

Identification of novel driver risk genes in CNV loci associated with neurodevelopmental disorders.Semantic proximity Read ↗

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

Neuroimaging Findings in Neurodevelopmental Copy Number Variants: Identifying Molecular Pathways to Convergent Phenotypes.Semantic proximity Read ↗

Converging pathways found in copy number variation syndromes with high schizophrenia riskSemantic proximity Read ↗

Copy number variation and neuropsychiatric illness.Semantic proximity Read ↗

Genomic copy number variation in disorders of cognitive development.Semantic proximity Read ↗

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