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Single-nucleotide variants and copy-number variants in ADHD (Exome)

Identifiers: SRA: SRP132527
BioProject: PRJNA433353
Study Type: 
Exome Sequencing
Abstract: The present study aimed to analyze both single-nucleotide and copy-number variants contributing to the genetic architecture of ADHD. We generated exome data from 30 Brazilian trios with sporadic ADHD. We also analyzed a Brazilian sample of 503 children/adolescent controls from a High Risk Cohort Study for the Development of Childhood Psychiatric Disorders, and also previously published results of five CNV studies and one GWAS meta-analysis of ADHD involving children/adolescents.
Center Project: Homo sapiens
External Link: /pubmed:26947246

Related SRA data

153 ( 105 samples )
153 (765.0Gbp; 364.2Gb)