Dyslexia is a common specific learning disability with a strong genetic basis that affects word
reading and spelling. An increasing list of loci and genes have been implicated, but …

Reading and writing are crucial life skills but roughly one in ten children are affected by
dyslexia, which can persist into adulthood. Family studies of dyslexia suggest heritability up …

Dyslexia is a common condition that impacts reading ability. Identifying affected brain
networks has been hampered by limited sample sizes of imaging case-control studies. We …

Dyslexia is a common specific learning disability with a substantive genetic component.
Several candidate genes have been proposed to be implicated in dyslexia susceptibility …

Analysis of genetic linkage to dyslexia was performed using 133,165 array‐based SNPs
genotyped in 718 persons from 101 dyslexia‐affected families. Results showed five linkage …

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 …

Genetic studies of complex traits have become increasingly successful as progress is made
in next-generation sequencing. We aimed at discovering single nucleotide variation present …

Dyslexia is a highly heritable learning disorder with a complex underlying genetic
architecture. Over the past decade, researchers have pinpointed a number of candidate …

Dyslexia, a specific reading disability, is a common (up to 10% of children) and highly
heritable (~ 70%) neurodevelopmental disorder. Behavioral and molecular genetic …

Developmental dyslexia (DD) is a learning disorder affecting the ability to read, with a
heritability of 40–60%. A notable part of this heritability remains unexplained, and large …