Word reading fluency: role of genome-wide single-nucleotide polymorphisms in developmental stability and correlations with print exposure

Child Dev. 2014 May-Jun;85(3):1190-1205. doi: 10.1111/cdev.12207. Epub 2014 Jan 6.

Abstract

The genetic effects on individual differences in reading development were examined using genome-wide complex trait analysis (GCTA) in a twin sample. In unrelated individuals (one twin per pair, n = 2,942), the GCTA-based heritability of reading fluency was ~20%-29% at ages 7 and 12. GCTA bivariate results showed that the phenotypic stability of reading fluency from 7 to 12 years (r = 0.69) is largely driven by genetic stability (genetic r = 0.69). Genetic effects on print exposure at age 12 were moderate (~26%) and correlated with those influencing reading fluency at 12 (genetic r = 0.89), indicative of a gene-environment correlation. These findings were largely consistent with quantitative genetic twin analyses that used both twins in each pair (n = 1,066-1,409).

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Twin Study

MeSH terms

  • Child
  • Child Development / physiology*
  • Female
  • Gene-Environment Interaction*
  • Genome-Wide Association Study*
  • Humans
  • Individuality*
  • Male
  • Polymorphism, Single Nucleotide / genetics
  • Reading*