[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 …
Neural noise hypothesis of developmental dyslexia
Developmental dyslexia (decoding-based reading disorder; RD) is a complex trait with
multifactorial origins at the genetic, neural, and cognitive levels. There is evidence that low …
multifactorial origins at the genetic, neural, and cognitive levels. There is evidence that low …
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 …
Combining MeDIP-seq and MRE-seq to investigate genome-wide CpG methylation
DNA CpG methylation is a widespread epigenetic mark in high eukaryotes including
mammals. DNA methylation plays key roles in diverse biological processes such as X …
mammals. DNA methylation plays key roles in diverse biological processes such as X …
[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 …
Whole genome association scan for genetic polymorphisms influencing information processing speed
Processing speed is an important cognitive function that is compromised in psychiatric
illness (eg, schizophrenia, depression) and old age; it shares genetic background with …
illness (eg, schizophrenia, depression) and old age; it shares genetic background with …
[PDF][PDF] Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment
Reading disability (RD) and language impairment (LI) are common learning disabilities that
make acquisition and utilization of reading and verbal language skills, respectively, difficult …
make acquisition and utilization of reading and verbal language skills, respectively, difficult …
[HTML][HTML] Dyslexia risk gene relates to representation of sound in the auditory brainstem
Dyslexia is a reading disorder with strong associations with KIAA0319 and DCDC2. Both
genes play a functional role in spike time precision of neurons. Strikingly, poor readers show …
genes play a functional role in spike time precision of neurons. Strikingly, poor readers show …