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J C DeFries

Publications and source records attributed to J C DeFries.

115 records · Page 7Linked to original sources
PubMedDate not supplied

Evidence for a genetic aetiology in reading disability of twins.

Reading disability (dyslexia) is a major social, educational, and mental health problem. Although estimates of prevalence vary, up to 10-15% of school-age children have severe reading deficits in spite of average intelligence and adequate educational opportunity. That reading disability may have a constitutional basis has long been recognized, and results of twin and family studies suggest that one or more of its forms may be heritable; however, definitive evidence for a genetic aetiology has not been reported. Establishing a heritable basis for reading disability could suggest possible causes, give improved risk estimates, facilitate early diagnosis, and provide validity tests for ostensible subtypes. In this report, we apply a recently developed multiple regression analysis to data collected from a sample of 64 pairs of identical twins and 55 pairs of fraternal twins, in which at least one member of the pairs is reading disabled, and present evidence for a significant genetic aetiology.

Dyslexia↗
PubMedDate not supplied

Genetic influence on general mental ability increases between infancy and middle childhood.

Adoption studies can provide direct evidence for the independent effects of family environment and heredity that are always confounded in intact nuclear families. When children are separated from their biological mothers shortly after birth and placed nonselectively in adoptive homes, adoptive-parent/adopted-child resemblance can be ascribed to cultural transmission, whereas biological-parent/adopted-child similarities are due to heritable factors. Furthermore, a longitudinal adoption study facilitates examination of changes in these two main sources of variation during development. The Colorado Adoption Project is the first large-scale longitudinal adoption study of behavioural development and was initiated in 1975. Data were collected from biological parents of 245 adopted children, the adoptive parents and parents of 245 matched nonadopted children. The children have subsequently been tested at 1, 2, 3 and 4 years of age, and at the end of their first year in primary school (average age, 7.4 years). The number of subjects tested is now adequate for analysis of data over 7 years. The results provide conclusive evidence for increasing heritable variation of general mental ability, ranging from 9% at 1 year of age to 36% at 7 years.

Adoption↗
PubMedDate not supplied

Differential genetic etiology of reading disability as a function of IQ.

To test the hypothesis that the genetic etiology of reading disability differs as a function of IQ, composite reading performance data from 223 pairs of identical twins and 169 pairs of same-gender fraternal twins in which at least one member of each pair was classified with reading disability were subjected to multiple regression analysis (DeFries & Fulker, 1985, 1988). In the total sample, heritability of the group deficit in reading performance (h(g)2) was .58 (+/- .08). However, when the basic regression model was fitted separately to data from twin pairs with average Wechsler (1974, 1981) full scale IQ scores below 100 or 100 and above, resulting estimates of h(g)2 were .43 and .72, respectively, a significant difference (p < or = .03, one-tailed). The results of fitting extended regression models to reading performance and continuous IQ data provide evidence that the genetic etiology of reading disability differs as a linear function of IQ (p < or = .007, one-tailed). These results suggest that IQ is relevant for the diagnosis of reading disability and that environmental influences may be more salient as a cause of reading difficulties in children with lower IQ scores.

Adolescent↗
PubMedDate not supplied

A twin study of mathematics disability.

Although results obtained from recent twin and adoption studies suggest that individual differences in mathematics performance are due in part to heritable influences, no genetic analysis of mathematics disability (MD) has been previously reported. In this article we present data from the first twin sample ascertained for mathematics deficits (40 identical and 23 same-sex fraternal twin pairs in which at least one member had MD). When mathematics performance data from these twin pairs were subjected to a multiple regression analysis, evidence for a significant genetic etiology was obtained. However, tests for the differential etiology of MD as a function of reading performance level were nonsignificant. Results of this first twin study of MD indicate that the condition is significantly heritable, but data from additional twin pairs will be required to test hypotheses of differential etiology more rigorously.

Achievement↗