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. Author manuscript; available in PMC: 2014 Jul 1.
Published in final edited form as: Cogn Neuropsychiatry. 2012 Oct 3;18(4):10.1080/13546805.2012.698100. doi: 10.1080/13546805.2012.698100

Table 1.

Demographic Data and Genotype Sample for All Diagnostic Groups

Mean Standard deviation

Patients Siblings Controls Patients Siblings Controls
n 20 15 66
Age (in years) 21.7 21.5 20.8 3.3 2.9 3.5
Sex (% male) 95 53 44
Parent’s edu. (years) 14.8 14.8 14.5 2.4 2.2 1.9
Education (years) 11.5 13.3 13.1 2.0 2.9 2.6
Handedness (% right) 80 93 81
Valine Homozygotes 10 6 21
Methionine Carriers 10 9 45

Note: The proportion of males and females differed significantly between the patient and sibling groups (χ2 (1) = 8.44, p < .01) and between the patient and control groups (χ2 (1) = 16.2, p < .001). No gender differences were observed between the siblings and control groups. No differences in our results were observed when gender was entered as a covariate. The three diagnostic groups differed in years of education (F (2, 98) = 3.87, p = 0.02), with both siblings and controls having more personal education than patients. However, the groups did not differ in parental socioeconomic status (F (2, 98) = 0.26, p > 0.50), or age (F (2, 98) = 0.64, p > 0.50).