Literature DB >> 17038000

Interrelationship and familiality of dyslexia related quantitative measures.

G Schulte-Körne1, A Ziegler, W Deimel, J Schumacher, E Plume, C Bachmann, A Kleensang, P Propping, M M Nöthen, A Warnke, H Remschmidt, I R König.   

Abstract

Dyslexia is a complex gene-environment disorder with poorly understood etiology that affects about 5% of school-age children. Dyslexia occurs in all languages and is associated with a high level of social and psychological morbidity for the individual and their family; approximately 40-50% have persistent disability into adulthood. The core symptoms are word reading and spelling deficits, but several other cognitive components influence the core phenotype. A broad spectrum of dyslexia related phenotypes, including phonological decoding, phoneme awareness, orthographic processing, short-term memory, rapid naming and basic mathematical abilities, were investigated in large sample of 287 German dyslexia families. We explored the interrelationship between the component phenotypes using correlation and principal component analyses (PCA). In addition, we estimated familiality for phenotypes as well as for the factors suggested by PCA. The correlation between the component phenotypes varied between -0.1 and 0.7. The PCA resulted in three factors: a general dyslexia factor, a speed of processing factor and a mathematical abilities factor. The familiality estimates of single components and factors ranged between 0.25 and 0.63. Instead of analyzing single dyslexia-related components, multivariate analyses including factor analytic approaches may help in the identification of susceptibility genes.

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Year:  2006        PMID: 17038000     DOI: 10.1111/j.1469-1809.2006.00312.x

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN: 0003-4800            Impact factor:   1.670


  13 in total

1.  Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort.

Authors:  Jessica Becker; Darina Czamara; Tom S Scerri; Franck Ramus; Valéria Csépe; Joel B Talcott; John Stein; Andrew Morris; Kerstin U Ludwig; Per Hoffmann; Ferenc Honbolygó; Dénes Tóth; Fabien Fauchereau; Caroline Bogliotti; Stéphanie Iannuzzi; Yves Chaix; Sylviane Valdois; Catherine Billard; Florence George; Isabelle Soares-Boucaud; Christophe-Loïc Gérard; Sanne van der Mark; Enrico Schulz; Anniek Vaessen; Urs Maurer; Kaisa Lohvansuu; Heikki Lyytinen; Marco Zucchelli; Daniel Brandeis; Leo Blomert; Paavo H T Leppänen; Jennifer Bruder; Anthony P Monaco; Bertram Müller-Myhsok; Juha Kere; Karin Landerl; Markus M Nöthen; Gerd Schulte-Körne; Silvia Paracchini; Myriam Peyrard-Janvid; Johannes Schumacher
Journal:  Eur J Hum Genet       Date:  2013-09-11       Impact factor: 4.246

2.  Oral and hand movement speeds are associated with expressive language ability in children with speech sound disorder.

Authors:  Beate Peter
Journal:  J Psycholinguist Res       Date:  2012-12

3.  Genome scan for spelling deficits: effects of verbal IQ on models of transmission and trait gene localization.

Authors:  Kevin Rubenstein; Mark Matsushita; Virginia W Berninger; Wendy H Raskind; Ellen M Wijsman
Journal:  Behav Genet       Date:  2010-09-18       Impact factor: 2.805

Review 4.  Genetics of dyslexia: the evolving landscape.

Authors:  Johannes Schumacher; Per Hoffmann; Christine Schmäl; Gerd Schulte-Körne; Markus M Nöthen
Journal:  J Med Genet       Date:  2007-02-16       Impact factor: 6.318

5.  Global processing speed in children with low reading ability and in children and adults with typical reading ability: exploratory factor analytic models.

Authors:  Beate Peter; Mark Matsushita; Wendy H Raskind
Journal:  J Speech Lang Hear Res       Date:  2010-11-16       Impact factor: 2.297

6.  Genome scan for cognitive trait loci of dyslexia: Rapid naming and rapid switching of letters, numbers, and colors.

Authors:  Kevin B Rubenstein; Wendy H Raskind; Virginia W Berninger; Mark M Matsushita; Ellen M Wijsman
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2014-05-08       Impact factor: 3.568

7.  Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample.

Authors:  Kerstin U Ludwig; Darina Roeske; Johannes Schumacher; Gerd Schulte-Körne; Inke R König; Andreas Warnke; Ellen Plume; Andreas Ziegler; Helmut Remschmidt; Bertram Müller-Myhsok; Markus M Nöthen; Per Hoffmann
Journal:  J Neural Transm (Vienna)       Date:  2008-09-23       Impact factor: 3.575

8.  Evidence for the late MMN as a neurophysiological endophenotype for dyslexia.

Authors:  Nina Neuhoff; Jennifer Bruder; Jürgen Bartling; Andreas Warnke; Helmut Remschmidt; Bertram Müller-Myhsok; Gerd Schulte-Körne
Journal:  PLoS One       Date:  2012-05-14       Impact factor: 3.240

9.  The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language.

Authors:  Heidi Anthoni; Lara E Sucheston; Barbara A Lewis; Isabel Tapia-Páez; Xiaotang Fan; Marco Zucchelli; Mikko Taipale; Catherine M Stein; Marie-Estelle Hokkanen; Eero Castrén; Bruce F Pennington; Shelley D Smith; Richard K Olson; J Bruce Tomblin; Gerd Schulte-Körne; Markus Nöthen; Johannes Schumacher; Bertram Müller-Myhsok; Per Hoffmann; Jeffrey W Gilger; George W Hynd; Jaana Nopola-Hemmi; Paavo H T Leppanen; Heikki Lyytinen; Jacqueline Schoumans; Magnus Nordenskjöld; Jason Spencer; Davor Stanic; Wah Chin Boon; Evan Simpson; Sari Mäkelä; Jan-Åke Gustafsson; Myriam Peyrard-Janvid; Sudha Iyengar; Juha Kere
Journal:  Behav Genet       Date:  2012-03-17       Impact factor: 2.805

10.  A common variant in myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults.

Authors:  K U Ludwig; P Sämann; M Alexander; J Becker; J Bruder; K Moll; D Spieler; M Czisch; A Warnke; S J Docherty; O S P Davis; R Plomin; M M Nöthen; K Landerl; B Müller-Myhsok; P Hoffmann; J Schumacher; G Schulte-Körne; D Czamara
Journal:  Transl Psychiatry       Date:  2013-02-19       Impact factor: 6.222

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