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Chunk #63 — Methods — Discovery Cohort

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A genome-wide investigation of SNPs and CNVs in schizophrenia.
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Healthy volunteers were randomly selected from the general population both for the Munich and Aberdeen cohorts (ascertained by mail for Munich, and by general practitioners for Aberdeen). In the Aberdeen study volunteers were screened for absence of psychiatric disorders and only those with no major psychiatric episodes or major mental illness in a first degree relative were included in the study. In the Munich cohort several screenings were conducted before the volunteers were enrolled in the study in order to exclude subjects with central neurological diseases and psychotic disorders or subjects who had first-degree relatives with psychotic disorders. First, subjects who responded were screened by phone for the absence of neuropsychiatric disorders. Second, detailed medical and psychiatric histories were assessed for the volunteers and their first-degree relatives using systematic forms. Third, if no exclusion criteria were fulfilled, they were invited to a comprehensive interview including the SCID [52] to validate the absence of psychotic disorders. Finally, a neurological examination was conducted to exclude subjects with current CNS impairment. In the case that the volunteers were older than 60 years, the