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

A brief report: de novo copy number variants in children with attention deficit hyperactivity disorder.

Translational psychiatry - 12 May 2020

Martin Joanna, Hosking Grace, Wadon Megan, Agha Sharifah Shameem, Langley Kate, Rees Elliott, Owen Michael J, O'Donovan Michael, Kirov George, Thapar Anita

Abstract excerpt

Recent case-control genetic studies of attention deficit hyperactivity disorder (ADHD) have implicated common and rare genetic risk alleles, highlighting the polygenic and complex aetiology of this neurodevelopmental disorder. Studies of other neurodevelopmental disorders, such as autism spectrum disorder (ASD), Tourette disorder, developmental delay/intellectual disability and schizophrenia indicate that...

Read the complete abstract on PubMed

Topics

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

Share to Attention Deficit Disorder with Hyperactivity
Share to Autism Spectrum Disorder

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Copy Number Variations

Share to Genetic Predisposition to Disease

Share to Schizophrenia

Source

Open in PubMed Open full text

Identifiers

PMID: 32398668
DOI: 10.1038/s41398-020-0821-y
PMCID: PMC7217839

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A brief report: de novo copy number variants in children with attention deficit hyperactivity disorder.PMID 32398668Read ↗

Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorderSemantic proximity Read ↗

Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis.Semantic proximity Read ↗

Genome-wide copy number variation analysis in adult attention-deficit and hyperactivity disorder.Semantic proximity Read ↗

Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.Semantic proximity Read ↗

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes.Semantic proximity Read ↗

Clinical and cognitive characteristics of children with attention-deficit hyperactivity disorder, with and without copy number variants.Semantic proximity Read ↗

Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD.Semantic proximity Read ↗

Rare genomic deletions and duplications and their role in neurodevelopmental disorders.Semantic proximity Read ↗

An integrative approach to investigate the respective roles of single-nucleotide variants and copy-number variants in Attention-Deficit/Hyperactivity Disorder.Semantic proximity Read ↗

Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree.Semantic proximity Read ↗

From Rare Copy Number Variants to Biological Processes in ADHD.Semantic proximity Read ↗

Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder.Semantic proximity Read ↗

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