Heritability and molecular genetic basis of antisaccade eye tracking error rate: a genome-wide association study.

ABSTRACT: Antisaccade deficits reflect abnormalities in executive function linked to various disorders including schizophrenia, externalizing psychopathology, and neurological conditions. We examined the genetic bases of antisaccade error in a sample of community-based twins and parents (N = 4,469). Biometric models showed that about half of the variance in the antisaccade response was due to genetic factors and half due to nonshared environmental factors. Molecular genetic analyses supported these results, showing that the heritability accounted for by common molecular genetic variants approximated biometric estimates. Genome-wide analyses revealed several SNPs as well as two genes-B3GNT7 and NCL-on Chromosome 2 associated with antisaccade error. SNPs and genes hypothesized to be associated with an

SUBMITTER: Vaidyanathan U 

PROVIDER: S-EPMC4238043 | biostudies-literature | 2014 Dec

REPOSITORIES: biostudies-literature