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 …
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia
A Gialluisi, TFM Andlauer, N Mirza-Schreiber… - Molecular …, 2021 - nature.com
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 …
heritability of 40–60%. A notable part of this heritability remains unexplained, and large …
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 …
Insights into dyslexia genetics research from the last two decades
Dyslexia, a specific reading disability, is a common (up to 10% of children) and highly
heritable (~ 70%) neurodevelopmental disorder. Behavioral and molecular genetic …
heritable (~ 70%) neurodevelopmental disorder. Behavioral and molecular genetic …
The roles of genes in the neuronal migration and neurite outgrowth network in developmental dyslexia: single-and multiple-risk genetic variants
S Shao, R Kong, L Zou, R Zhong, J Lou, J Zhou… - Molecular …, 2016 - Springer
Abnormal regulation of neural migration and neurite growth is thought to be an important
feature of developmental dyslexia (DD). We investigated 16 genetic variants, selected by …
feature of developmental dyslexia (DD). We investigated 16 genetic variants, selected by …
Dense‐map genome scan for dyslexia supports loci at 4q13, 16p12, 17q22; suggests novel locus at 7q36
LL Field, K Shumansky, J Ryan… - Genes, Brain and …, 2013 - Wiley Online Library
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 …
genotyped in 718 persons from 101 dyslexia‐affected families. Results showed five linkage …
Genes, cognition and dyslexia: learning to read the genome
Studies of dyslexia provide vital insights into the cognitive architecture underpinning both
disordered and normal reading. It is well established that inherited factors contribute to …
disordered and normal reading. It is well established that inherited factors contribute to …
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 …
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 …
Identification of candidate genes for dyslexia susceptibility on chromosome 18
Background Six independent studies have identified linkage to chromosome 18 for
developmental dyslexia or general reading ability. Until now, no candidate genes have been …
developmental dyslexia or general reading ability. Until now, no candidate genes have been …