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Chunk #0 — Method — Subjects and Clinical Measures

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Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD.
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The ADHD patient sample consisted of 799 Caucasian children from Cardiff, Wales (N=559); St. Andrews, Scotland (N=44); and Dublin, Ireland (N=196). All children were recruited from community clinics and met DSM-IV or ICD-10 criteria for ADHD or hyperkinetic disorder. To be comparable with other GWAS, we excluded children with a major medical or neurological condition (including epilepsy), autism, bipolar disorder, or intellectual disability (IQ <70).