Behavior genetics association abstracts.
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In the fire ant, the number of queens per colony is determined by the workers' Gp-9 genotype. This gene has been found to encode an odorant binding protein, which probably influences workers' abilities to recognize queens and regulate their numbers. Remarkably, the same gene seems to control social organization in three other closely related species.
A meta-analysis of family and twin studies on gambling and problem gambling was initiated in an effort to determine the probable role of genetic factors in high risk wagering. Two twin studies and 17 investigations employing the family history or family study method were included in this meta-analysis. A summation of the 19 studies produced a small but significant overall effect size (weighted phi = .10, unweighted phi = .13), with both family (weighted phi = .12, unweighted phi = .14) and twin (weighted phi = .06, unweighted phi = .05) studies achieving significant individual mean effects. Given the paucity of twin data, further analysis was confined to family studies and revealed a stronger familial effect for the sons of problem gambling fathers than for the daughters of problem gambling mothers and for more severe forms of problem gambling than for less severe forms of problem wagering, and was strongest for high severity problem gambling in males. The implications of these results are discussed.
The current article presents results from a twin study of genetic and environmental components of maternal sensitivity and infant attachment and their association. The sample consisted of 136 twin pairs from 2 sites: Leiden, the Netherlands, and London, UK. Maternal sensitivity was assessed in the home at 9-10 months, and infant attachment security was observed in the laboratory at 12 months. The study yielded little evidence that genetic factors are involved in variations between twins in maternal sensitivity ratings but did find that shared variance in maternal sensitivity was able to account for some of the similarity between twins in attachment security. Weak nonshared associations between sensitivity and attachment appeared to suppress the magnitude of the correlation between attachment and sensitivity in twin children. The results could indicate that the attachment security of one twin may depend on the relationship the parent has with the other twin. The results are brought to bear on the validity of attachment theory as a theory of primarily shared environmental effects in children's development and the continuing challenge posed to attachment theory by within-family differences in socioemotional processes.
In a sample of 157 monozygotic and dizygotic twins, genetic and environmental influences on infant attachment and temperament were quantified. Only unique environmental or error components could explain the variance in disorganized versus organized attachment as assessed in the Ainsworth Strange Situation Procedure. For secure versus nonsecure attachment, 52% of the variance in attachment security was explained by shared environment, and 48% of the variance was explained by unique environmental factors and measurement error. The role of genetic factors in attachment disorganization and attachment security was negligible. Genetic factors explained 77% of the variance in temperamental reactivity, and unique environmental factors and measurement error explained 23%. Differences in temperamental reactivity were not associated with attachment concordance.
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A meta-analysis was performed on 50 family, twin, and adoption studies in which problem drinking and alcohol dependence served as the primary criterion measure. The results showed that far from being an established "fact," the genetic foundations of alcohol misuse are modest and heterogeneous. A weighted mean phi effect size of 0.12 (95% Confidence Interval = 0.11-0.12) was obtained for the total sample of 72 effect sizes. Four potential moderator variables (proband gender, sample nationality, pattern severity, year of publication) were examined with outcomes confirming that the heritability of alcohol misuse is stronger in males and in studies employing more severe definitions of abuse (alcoholism, alcohol dependence). When the effect size measure was restricted to studies using male subjects with more severe diagnoses of alcohol misuse, the unweighted mean phi effect size was only 0.18 (95% Confidence Interval = 0.15-0.21), with an even smaller weighted mean phi effect size of 0.15 (95% Confidence Interval = 0.12-0.18); results which indicate an upper limit of 30-36% for the heritability of alcohol misuse.
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