References

• 1998Functional disruption in the organization of the brain for reading in dyslexia873 cited
• 1994Quantitative Trait Locus for Reading Disability on Chromosome 6532 cited
• 2008Relations Among Speech, Language, and Reading Disorders524 cited
• 2005DCDC2 is associated with reading disability and modulates neuronal development in the brain383 cited
• 2001Disrupted neural responses to phonological and orthographic processing in dyslexic children: an fMRI study374 cited
• 1987Evidence for a genetic aetiology in reading disability of twins312 cited
• 2006The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319 , a novel gene involved in neuronal migration270 cited
• 1999Quantitative-Trait Locus for Specific Language and Reading Deficits on Chromosome 6p249 cited
• 2005Strong Genetic Evidence of DCDC2 as a Susceptibility Gene for Dyslexia236 cited
• 2004A 77-Kilobase Region of Chromosome 6p22.2 Is Associated with Dyslexia in Families From the United Kingdom and From the United States234 cited
• 2010Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects224 cited
• 2013The NIH Toolbox Cognition Battery: Results from a large normative developmental sample (PING).208 cited
• 2007Developmental dyslexia: Gray matter abnormalities in the occipitotemporal cortex201 cited
• 1999