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 …
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 …
DYX1C1 is required for axonemal dynein assembly and ciliary motility
DYX1C1 has been associated with dyslexia and neuronal migration in the developing
neocortex. Unexpectedly, we found that deleting exons 2–4 of Dyx1c1 in mice caused a …
neocortex. Unexpectedly, we found that deleting exons 2–4 of Dyx1c1 in mice caused a …
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 …
The Axon Guidance Receptor Gene ROBO1 Is a Candidate Gene for Developmental Dyslexia
K Hannula-Jouppi, N Kaminen-Ahola, M Taipale… - PLoS …, 2005 - journals.plos.org
Dyslexia, or specific reading disability, is the most common learning disorder with a
complex, partially genetic basis, but its biochemical mechanisms remain poorly understood …
complex, partially genetic basis, but its biochemical mechanisms remain poorly understood …
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 …
Genetics of dyslexia: the evolving landscape
J Schumacher, P Hoffmann, C Schmäl… - Journal of medical …, 2007 - jmg.bmj.com
Dyslexia is among the most common neurodevelopmental disorders, with a prevalence of 5–
12%. At the phenotypic level, various cognitive components that enable reading and …
12%. At the phenotypic level, various cognitive components that enable reading and …
A 77-kilobase region of chromosome 6p22. 2 is associated with dyslexia in families from the United Kingdom and from the United States
C Francks, S Paracchini, SD Smith… - The American Journal of …, 2004 - cell.com
Several quantitative trait loci (QTLs) that influence developmental dyslexia (reading
disability [RD]) have been mapped to chromosome regions by linkage analysis. The most …
disability [RD]) have been mapped to chromosome regions by linkage analysis. The most …
The eloquent ape: genes, brains and the evolution of language
SE Fisher, GF Marcus - Nature Reviews Genetics, 2006 - nature.com
The human capacity to acquire complex language seems to be without parallel in the natural
world. The origins of this remarkable trait have long resisted adequate explanation, but …
world. The origins of this remarkable trait have long resisted adequate explanation, but …