Literature DB >> 11806692

Annotation: Genetics of reading and spelling disorder.

G Schulte-Körne1.   

Abstract

Recent advances in understanding the genetics of reading and spelling disorder are reviewed and, based on theoretical models of reading development, different related phenotypes such as phonological and orthographic processing are examined. Family and twin studies show a moderate to high familiality and heritability. Segregation analyses suggest a major gene effect, with reduced penetrance in females, as well as a polygenic model. Linkage analyses and an association study have identified possible loci on chromosomes 6 and 15. These results suggest that reading and spelling disorder should be regarded as a complex disorder, strongly influenced by genetic factors. However, the role of environmental factors should also be considered as the clinical implications of the genetic findings in terms of aetiology and intervention still require far more exploration.

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Mesh:

Year:  2001        PMID: 11806692     DOI: 10.1111/1469-7610.00797

Source DB:  PubMed          Journal:  J Child Psychol Psychiatry        ISSN: 0021-9630            Impact factor:   8.982


  7 in total

1.  Focus on words: a twin study of reading and inattention.

Authors:  Allison Zumberge; Laura A Baker; Franklin R Manis
Journal:  Behav Genet       Date:  2007-01-30       Impact factor: 2.805

Review 2.  Neuropsychology of Learning Disabilities: The Past and the Future.

Authors:  Jack M Fletcher; Elena L Grigorenko
Journal:  J Int Neuropsychol Soc       Date:  2017-10       Impact factor: 2.892

3.  No evidence for association between dyslexia and DYX1C1 functional variants in a group of children and adolescents from Southern Italy.

Authors:  Giulia Bellini; Carmela Bravaccio; Filippo Calamoneri; Maria Donatella Cocuzza; Pasquale Fiorillo; Antonella Gagliano; Domenico Mazzone; Emanuele Miraglia del Giudice; Geoffredo Scuccimarra; Roberto Militerni; Antonio Pascotto
Journal:  J Mol Neurosci       Date:  2005       Impact factor: 3.444

4.  A combined fMRI study of typed spelling and reading.

Authors:  Jeremy J Purcell; Eileen M Napoliello; Guinevere F Eden
Journal:  Neuroimage       Date:  2010-11-23       Impact factor: 6.556

5.  Linkage analyses of chromosomal region 18p11-q12 in dyslexia.

Authors:  J Schumacher; I R König; E Plume; P Propping; A Warnke; M Manthey; M Duell; A Kleensang; D Repsilber; M Preis; H Remschmidt; A Ziegler; M M Nöthen; G Schulte-Körne
Journal:  J Neural Transm (Vienna)       Date:  2005-08-03       Impact factor: 3.575

Review 6.  Genetics of developmental dyslexia.

Authors:  Thomas S Scerri; Gerd Schulte-Körne
Journal:  Eur Child Adolesc Psychiatry       Date:  2009-11-29       Impact factor: 4.785

7.  Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family.

Authors:  C G F de Kovel; F A Hol; J G A M Heister; J J H T Willemen; L A Sandkuijl; B Franke; G W Padberg
Journal:  J Med Genet       Date:  2004-09       Impact factor: 6.318

  7 in total

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