[HTML][HTML] Biological overlap of attention-deficit/hyperactivity disorder and autism spectrum disorder: evidence from copy number variants

J Martin, M Cooper, ML Hamshere… - Journal of the American …, 2014 - Elsevier
Objective Attention-deficit/hyperactivity disorder (ADHD) and autism spectrum disorder
(ASD) often co-occur and share genetic risks. The aim of this analysis was to determine …

Microdeletions of 3q29 confer high risk for schizophrenia

JG Mulle, AF Dodd, JA McGrath, PS Wolyniec… - The American Journal of …, 2010 - cell.com
Schizophrenia (SZ) is a severe psychiatric illness that affects∼ 1% of the population and
has a strong genetic underpinning. Recently, genome-wide analysis of copy-number …

Functional impact of global rare copy number variation in autism spectrum disorders

D Pinto, AT Pagnamenta, L Klei, R Anney, D Merico… - Nature, 2010 - nature.com
The autism spectrum disorders (ASDs) are a group of conditions characterized by
impairments in reciprocal social interaction and communication, and the presence of …

[HTML][HTML] Genetic architecture of autism spectrum disorder: Lessons from large-scale genomic studies

L Choi, JY An - Neuroscience & Biobehavioral Reviews, 2021 - Elsevier
Autism spectrum disorder (ASD) is a neurodevelopmental disorder with a strong genetic
component. Recently developed genomic technologies, including microarray and next …

Genomic and genetic aspects of autism spectrum disorder

X Liu, T Takumi - Biochemical and Biophysical Research …, 2014 - Elsevier
Autism spectrum disorder (ASD) is a neurodevelopmental disorder with a strong genetic
component. The past decade has witnessed tremendous progress in the genetic studies of …

Prospective diagnostic analysis of copy number variants using SNP microarrays in individuals with autism spectrum disorders

C Nava, B Keren, C Mignot, A Rastetter… - European Journal of …, 2014 - nature.com
Copy number variants (CNVs) have repeatedly been found to cause or predispose to autism
spectrum disorders (ASDs). For diagnostic purposes, we screened 194 individuals with …

[HTML][HTML] The penetrance of copy number variations for schizophrenia and developmental delay

G Kirov, E Rees, JTR Walters, V Escott-Price… - Biological …, 2014 - Elsevier
Background Several recurrent copy number variants (CNVs) have been shown to increase
the risk of developing schizophrenia (SCZ), developmental delay (DD), autism spectrum …

A genetics-first approach to dissecting the heterogeneity of autism: phenotypic comparison of autism risk copy number variants

SJRA Chawner, JL Doherty… - American Journal of …, 2021 - Am Psychiatric Assoc
Objective: Certain copy number variants (CNVs) greatly increase the risk of autism. The
authors conducted a genetics-first study to investigate whether heterogeneity in the clinical …

Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder

RK C Yuen, D Merico, M Bookman, JL Howe… - Nature …, 2017 - nature.com
We are performing whole-genome sequencing of families with autism spectrum disorder
(ASD) to build a resource (MSSNG) for subcategorizing the phenotypes and underlying …

Genetic architecture in autism spectrum disorder

B Devlin, SW Scherer - Current opinion in genetics & development, 2012 - Elsevier
Autism spectrum disorder (ASD) is characterized by impairments in reciprocal social
interaction and communication, and by restricted and repetitive behaviors. Family studies …