Literature DB >> 19347574

Genetic covariance structure of reading, intelligence and memory in children.

Marieke van Leeuwen1, Stéphanie M van den Berg, Jiska S Peper, Hilleke E Hulshoff Pol, Dorret I Boomsma.   

Abstract

This study investigates the genetic relationship among reading performance, IQ, verbal and visuospatial working memory (WM) and short-term memory (STM) in a sample of 112, 9-year-old twin pairs and their older siblings. The relationship between reading performance and the other traits was explained by a common genetic factor for reading performance, IQ, WM and STM and a genetic factor that only influenced reading performance and verbal memory. Genetic variation explained 83% of the variation in reading performance; most of this genetic variance was explained by variation in IQ and memory performance. We hypothesize, based on these results, that children with reading problems possibly can be divided into three groups: (1) children low in IQ and with reading problems; (2) children with average IQ but a STM deficit and with reading problems; (3) children with low IQ and STM deficits; this group may experience more reading problems than the other two.

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Mesh:

Year:  2009        PMID: 19347574     DOI: 10.1007/s10519-009-9264-1

Source DB:  PubMed          Journal:  Behav Genet        ISSN: 0001-8244            Impact factor:   2.805


  6 in total

Review 1.  Cross-Study Differences in the Etiology of Reading Comprehension: a Meta-Analytical Review of Twin Studies.

Authors:  Callie W Little; Rasheda Haughbrook; Sara A Hart
Journal:  Behav Genet       Date:  2016-09-14       Impact factor: 2.805

2.  DCDC2 genetic variants and susceptibility to developmental dyslexia.

Authors:  Cecilia Marino; Haiying Meng; Sara Mascheretti; Marianna Rusconi; Natalie Cope; Roberto Giorda; Massimo Molteni; Jeffrey R Gruen
Journal:  Psychiatr Genet       Date:  2012-02       Impact factor: 2.458

3.  Smoking outcome expectancies in young adult female smokers: individual differences and associations with nicotine dependence in a genetically informative sample.

Authors:  Sean D Kristjansson; Michele L Pergadia; Arpana Agrawal; Christina N Lessov-Schlaggar; Denis M McCarthy; Thomas M Piasecki; Alexis E Duncan; Kathleen K Bucholz; Pamela A F Madden; Kenneth J Sher; Andrew C Heath
Journal:  Drug Alcohol Depend       Date:  2010-12-30       Impact factor: 4.492

4.  An assessment of gene-by-gene interactions as a tool to unfold missing heritability in dyslexia.

Authors:  S Mascheretti; A Bureau; V Trezzi; R Giorda; C Marino
Journal:  Hum Genet       Date:  2015-04-28       Impact factor: 4.132

5.  Common variation within the SETBP1 gene is associated with reading-related skills and patterns of functional neural activation.

Authors:  Meaghan V Perdue; Sara Mascheretti; Sergey A Kornilov; Kaja K Jasińska; Kayleigh Ryherd; W Einar Mencl; Stephen J Frost; Elena L Grigorenko; Kenneth R Pugh; Nicole Landi
Journal:  Neuropsychologia       Date:  2018-08-23       Impact factor: 3.139

6.  Shared cognitive impairments and aetiology in ADHD symptoms and reading difficulties.

Authors:  Celeste H M Cheung; Alexis C Frazier-Wood; Alexis C Fazier-Wood; Philip Asherson; Fruhling Rijsdijk; Jonna Kuntsi
Journal:  PLoS One       Date:  2014-06-02       Impact factor: 3.240

  6 in total

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