Genome‐wide association study of word reading: Overlap with risk genes for neurodevelopmental disorders
KM Price, KG Wigg, Y Feng, K Blokland… - Genes, Brain and …, 2020 - Wiley Online Library
Reading disabilities (RD) are the most common neurocognitive disorder, affecting 5% to
17% of children in North America. These children often have comorbid neurodevelopmental …
17% of children in North America. These children often have comorbid neurodevelopmental …
A Common Variant Associated with Dyslexia Reduces Expression of the KIAA0319 Gene
Numerous genetic association studies have implicated the KIAA0319 gene on human
chromosome 6p22 in dyslexia susceptibility. The causative variant (s) remains unknown but …
chromosome 6p22 in dyslexia susceptibility. The causative variant (s) remains unknown but …
The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years on
LG Guidi, A Velayos‐Baeza… - European Journal of …, 2018 - Wiley Online Library
The capacity for language is one of the key features underlying the complexity of human
cognition and its evolution. However, little is known about the neurobiological mechanisms …
cognition and its evolution. However, little is known about the neurobiological mechanisms …
Lessons to be learned: How a comprehensive neurobiological framework of atypical reading development can inform educational practice
Highlights•Genetic, neural, cognitive, and environmental risks for dyslexia are
identified.•Evidence supports a multi-componential framework for dyslexia …
identified.•Evidence supports a multi-componential framework for dyslexia …
[HTML][HTML] Cellullar insights into cerebral cortical development: focusing on the locomotion mode of neuronal migration
T Kawauchi - Frontiers in cellular neuroscience, 2015 - frontiersin.org
The mammalian brain consists of numerous compartments that are closely connected with
each other via neural networks, comprising the basis of higher order brain functions. The …
each other via neural networks, comprising the basis of higher order brain functions. The …
A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia
H Anthoni, M Zucchelli, H Matsson… - Human molecular …, 2007 - academic.oup.com
DYX3, a locus for dyslexia, resides on chromosome 2p11-p15. We have refined its location
on 2p12 to a 157 kb region in two rounds of linkage disequilibrium (LD) mapping in a set of …
on 2p12 to a 157 kb region in two rounds of linkage disequilibrium (LD) mapping in a set of …
Advances in dyslexia genetics—new insights into the role of brain asymmetries
S Paracchini, R Diaz, J Stein - Advances in genetics, 2016 - Elsevier
Dyslexia is a common condition affecting up to 10% school-aged children. There is strong
evidence that genetics plays an important role in dyslexia and is expected to be complex in …
evidence that genetics plays an important role in dyslexia and is expected to be complex in …
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 …
[HTML][HTML] The evolutionary history of genes involved in spoken and written language: beyond FOXP2
Humans possess a communication system based on spoken and written language. Other
animals can learn vocalization by imitation, but this is not equivalent to human language …
animals can learn vocalization by imitation, but this is not equivalent to human language …