Genetics of developmental dyslexia
TS Scerri, G Schulte-Körne - European child & adolescent psychiatry, 2010 - Springer
Developmental dyslexia is a highly heritable disorder with a prevalence of at least 5% in
school-aged children. Linkage studies have identified numerous loci throughout the genome …
school-aged children. Linkage studies have identified numerous loci throughout the genome …
[HTML][HTML] Neurogenetics of developmental dyslexia: from genes to behavior through brain neuroimaging and cognitive and sensorial mechanisms
Developmental dyslexia (DD) is a complex neurodevelopmental deficit characterized by
impaired reading acquisition, in spite of adequate neurological and sensorial conditions …
impaired reading acquisition, in spite of adequate neurological and sensorial conditions …
[HTML][HTML] Investigation of dyslexia and SLI risk variants in reading-and language-impaired subjects
Dyslexia (or reading disability) and specific language impairment (or SLI) are common
childhood disorders that show considerable co-morbidity and diagnostic overlaps and have …
childhood disorders that show considerable co-morbidity and diagnostic overlaps and have …
Molecular genetics of dyslexia: an overview
Dyslexia is a highly heritable learning disorder with a complex underlying genetic
architecture. Over the past decade, researchers have pinpointed a number of candidate …
architecture. Over the past decade, researchers have pinpointed a number of candidate …
[HTML][HTML] DCDC2, KIAA0319 and CMIP are associated with reading-related traits
BACKGROUND: Several susceptibility genes have been proposed for dyslexia (reading
disability; RD) and specific language impairment (SLI). RD and SLI show comorbidity, but it …
disability; RD) and specific language impairment (SLI). RD and SLI show comorbidity, but it …
Three dyslexia susceptibility genes, DYX1C1, DCDC2, and KIAA0319, affect temporo-parietal white matter structure
F Darki, M Peyrard-Janvid, H Matsson, J Kere… - Biological …, 2012 - Elsevier
BACKGROUND: Volume and integrity of white matter correlate with reading ability, but the
underlying factors contributing to this variability are unknown. METHODS: We investigated …
underlying factors contributing to this variability are unknown. METHODS: We investigated …
A theoretical molecular network for dyslexia: integrating available genetic findings
G Poelmans, JK Buitelaar, DL Pauls, B Franke - Molecular psychiatry, 2011 - nature.com
Developmental dyslexia is a common specific childhood learning disorder with a strong
heritable component. Previous studies using different genetic approaches have identified …
heritable component. Previous studies using different genetic approaches have identified …
Genetic Variance in a Component of the Language Acquisition Device: ROBO1 Polymorphisms Associated with Phonological Buffer Deficits
The region containing ROBO1 (Chromosome 3p12. 3) has been implicated as a
susceptibility gene for reading disorder and language deficit by translocation and linkage …
susceptibility gene for reading disorder and language deficit by translocation and linkage …
[HTML][HTML] Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort
Dyslexia is one of the most common childhood disorders with a prevalence of around 5–
10% in school-age children. Although an important genetic component is known to have a …
10% in school-age children. Although an important genetic component is known to have a …
[HTML][HTML] The genetics of reading disabilities: from phenotypes to candidate genes
This article provides an overview of (a) issues in definition and diagnosis of specific reading
disabilities at the behavioral level that may occur in different constellations of developmental …
disabilities at the behavioral level that may occur in different constellations of developmental …