Literature DB >> 17931436

Exploring interactive effects of genes and environments in etiology of individual differences in reading comprehension.

Elena L Grigorenko1, Colin G Deyoung, Marya Getchell, Gerald J Haeffel, Britt A F Klinteberg, Roman A Koposov, Lars Oreland, Andrew J Pakstis, Vladislav V Ruchkin, Carolyn M Yrigollen.   

Abstract

It is established that reading and reading-related processes are heritable; genes thus play an important role in the foundation of individual differences in reading. In this article, we focus on one facet of reading-comprehension. Comprehension is a higher order cognitive skill that requires many other cognitive processes for it to unfold completely and successfully. One such process is executive functioning, which has been associated with genetic variation in the catechol-O-methyltransferase (COMT) gene. Genotypes and haplotypes of four single nucleotide polymorphisms in COMT were investigated in 179 incarcerated adolescent delinquents. Four hierarchical logistic regression models predicting the presence/absence of comprehension difficulties were fitted to the data; genetic variation in COMT and the presence/absence of maternal rejection were investigated as main effects and as effects acting interactively. Three out of four interaction terms were found to be important predictors of individual differences in comprehension. These findings were supported by the results of the haplotype analyses, in which the four investigated polymorphisms were considered simultaneously.

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Year:  2007        PMID: 17931436     DOI: 10.1017/S0954579407000557

Source DB:  PubMed          Journal:  Dev Psychopathol        ISSN: 0954-5794


  7 in total

1.  Lexical decision as an endophenotype for reading comprehension: an exploration of an association.

Authors:  Adam Naples; Len Katz; Elena L Grigorenko
Journal:  Dev Psychopathol       Date:  2012-11

2.  The COMT Val/Met polymorphism is associated with reading-related skills and consistent patterns of functional neural activation.

Authors:  Nicole Landi; Stephen J Frost; W Einar Mencl; Jonathan L Preston; Leslie K Jacobsen; Maria Lee; Carolyn Yrigollen; Kenneth R Pugh; Elena L Grigorenko
Journal:  Dev Sci       Date:  2012-10-03

3.  Reading and a diffusion model analysis of reaction time.

Authors:  Adam Naples; Leonard Katz; Elena L Grigorenko
Journal:  Dev Neuropsychol       Date:  2012       Impact factor: 2.253

Review 4.  In search of the perfect phenotype: an analysis of linkage and association studies of reading and reading-related processes.

Authors:  Thomas Skiba; Nicole Landi; Richard Wagner; Elena L Grigorenko
Journal:  Behav Genet       Date:  2011-01-19       Impact factor: 2.805

5.  Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African-American youth.

Authors:  Dongnhu Thuy Truong; Andrew Kenneth Adams; Steven Paniagua; Jan C Frijters; Richard Boada; Dina E Hill; Maureen W Lovett; E Mark Mahone; Erik G Willcutt; Maryanne Wolf; John C Defries; Alessandro Gialluisi; Clyde Francks; Simon E Fisher; Richard K Olson; Bruce F Pennington; Shelley D Smith; Joan Bosson-Heenan; Jeffrey R Gruen
Journal:  J Med Genet       Date:  2019-04-17       Impact factor: 6.318

6.  Enrichment of putatively damaging rare variants in the DYX2 locus and the reading-related genes CCDC136 and FLNC.

Authors:  Andrew K Adams; Shelley D Smith; Dongnhu T Truong; Erik G Willcutt; Richard K Olson; John C DeFries; Bruce F Pennington; Jeffrey R Gruen
Journal:  Hum Genet       Date:  2017-09-02       Impact factor: 4.132

7.  Genetic association study of dyslexia and ADHD candidate genes in a Spanish cohort: Implications of comorbid samples.

Authors:  Mirian Sánchez-Morán; Juan Andrés Hernández; Jon Andoni Duñabeitia; Adelina Estévez; Laura Bárcena; Aintzane González-Lahera; María Teresa Bajo; Luis J Fuentes; Ana M Aransay; Manuel Carreiras
Journal:  PLoS One       Date:  2018-10-31       Impact factor: 3.240

  7 in total

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