학술논문

Sequencing of sporadic Attention‐Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum disorder
Document Type
article
Source
American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 174(4)
Subject
Biological Sciences
Bioinformatics and Computational Biology
Genetics
Prevention
Neurosciences
Attention Deficit Hyperactivity Disorder (ADHD)
Intellectual and Developmental Disabilities (IDD)
Brain Disorders
Pediatric
Human Genome
Mental Health
Autism
Clinical Research
Aetiology
2.1 Biological and endogenous factors
Mental health
Adult
Attention Deficit Disorder with Hyperactivity
Autism Spectrum Disorder
Biomarkers
Child
Exome
Female
Genetic Predisposition to Disease
High-Throughput Nucleotide Sequencing
Humans
Male
Mutation
Missense
Phenotype
attention deficit hyperactivity disorder
exome sequencing
molecular inversion probe (MIP) sequencing
sporadic ADHD
autism spectrum disorder
intellectual disability
University of Washington Center for Mendelian Genomics
Clinical Sciences
Clinical sciences
Language
Abstract
Attention-Deficit Hyperactivity Disorder (ADHD) has high heritability; however, studies of common variation account for