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 …
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 …
[图书][B] Introduction to language development
SM Kennison - 2013 - books.google.com
There are between 4,000 and 6,000 languages remaining in the world and the
characteristics of these languages vary widely. How could an infant born today master any …
characteristics of these languages vary widely. How could an infant born today master any …
A multidisciplinary approach to understanding developmental dyslexia within working-memory architecture: Genotypes, phenotypes, brain, and instruction
VW Berninger, W Raskind, T Richards… - Developmental …, 2008 - Taylor & Francis
A unifying theoretical framework of three working memory components provides a systems
perspective for discussing past and new findings in a 12-year research program that point to …
perspective for discussing past and new findings in a 12-year research program that point to …
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 …
[HTML][HTML] Brain classification reveals the right cerebellum as the best biomarker of dyslexia
Background Developmental dyslexia is a specific cognitive disorder in reading acquisition
that has genetic and neurological origins. Despite histological evidence for brain differences …
that has genetic and neurological origins. Despite histological evidence for brain differences …
[HTML][HTML] Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family …
B Peter, WH Raskind, M Matsushita, M Lisowski… - Journal of …, 2011 - Springer
Two functionally related genes, FOXP2 and CNTNAP2, influence language abilities in
families with rare syndromic and common nonsyndromic forms of impaired language …
families with rare syndromic and common nonsyndromic forms of impaired language …
Rethinking the genetic basis for comorbidity of schizophrenia and type 2 diabetes
PI Lin, AR Shuldiner - Schizophrenia research, 2010 - Elsevier
The co-occurrence of schizophrenia (SCZ) and type 2 diabetes mellitus (T2D) has been well
documented. This review article focuses on the hypothesis that the co-occurrence of SCZ …
documented. This review article focuses on the hypothesis that the co-occurrence of SCZ …