Literature DB >> 8923224

Familial aggregation of spelling disability.

G Schulte-Körne1, W Deimel, K Müller, C Gutenbrunner, H Remschmidt.   

Abstract

This study examined the familial aggregation of spelling disability in a sample of 32 German school-aged children and their relatives. The influence of two different diagnostic criteria (low-achievement criterion, and regression-based IQ-discrepancy criterion) on the rate of affectedness was investigated. Results revealed that 52.3-61.9% of the sibs and 26-34% of the parents were spelling disabled. Little evidence was found for an influence of the diagnostic criterion on the rate of affectedness.

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Year:  1996        PMID： 8923224     DOI： 10.1111/j.1469-7610.1996.tb01477.x

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


  15 in total

1.  The role of phonological awareness, speech perception, and auditory temporal processing for dyslexia.

Authors:  G Schulte-Körne; W Deimel; J Bartling; H Remschmidt
Journal:  Eur Child Adolesc Psychiatry       Date:  1999       Impact factor: 4.785

2.  The influence of different diagnostic approaches on familial aggregation of spelling disability.

Authors:  H Remschmidt; K Hennighausen; G Schulte-Körne; W Deimel; A Warnke
Journal:  Eur Child Adolesc Psychiatry       Date:  1999       Impact factor: 4.785

Review 3.  Reading and spelling disorders: clinical features and causes.

Authors:  A Warnke
Journal:  Eur Child Adolesc Psychiatry       Date:  1999       Impact factor: 4.785

4.  Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.

Authors:  Johannes Schumacher; Heidi Anthoni; Faten Dahdouh; Inke R König; Axel M Hillmer; Nadine Kluck; Malou Manthey; Ellen Plume; Andreas Warnke; Helmut Remschmidt; Jutta Hülsmann; Sven Cichon; Cecilia M Lindgren; Peter Propping; Marco Zucchelli; Andreas Ziegler; Myriam Peyrard-Janvid; Gerd Schulte-Körne; Markus M Nöthen; Juha Kere
Journal:  Am J Hum Genet       Date:  2005-11-17       Impact factor: 11.025

5.  Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia.

Authors:  Natalie Cope; Denise Harold; Gary Hill; Valentina Moskvina; Jim Stevenson; Peter Holmans; Michael J Owen; Michael C O'Donovan; Julie Williams
Journal:  Am J Hum Genet       Date:  2005-02-16       Impact factor: 11.025

Review 6.  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

7.  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

8.  Altered neuronal response during rapid auditory processing and its relation to phonological processing in prereading children at familial risk for dyslexia.

Authors:  Nora M Raschle; Patrice L Stering; Sarah N Meissner; Nadine Gaab
Journal:  Cereb Cortex       Date:  2013-04-18       Impact factor: 5.357

Review 9.  Genetics of developmental dyslexia.

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

10.  Perspectives on dyslexia.

Authors:  Linda S Siegel
Journal:  Paediatr Child Health       Date:  2006-11       Impact factor: 2.253
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