A systematic review of associations between genetic polymorphism and dyslexia in the Indian population
DR Rahul, RJ Ponniah - Journal of Biosciences, 2022 - Springer
There is growing interest in understanding the genetic mechanisms underlying dyslexia.
Accordingly, the literature on dyslexia is replete with shreds of evidence linking genes and …
Accordingly, the literature on dyslexia is replete with shreds of evidence linking genes and …
[HTML][HTML] Allelic variants of DYX1C1 are not associated with dyslexia in India
P Saviour, S Kumar, U Kiran, RR Ravuri… - Indian Journal of …, 2008 - ncbi.nlm.nih.gov
Dyslexia is a hereditary neurological disorder that manifests as an unexpected difficulty in
learning to read despite adequate intelligence, education, and normal senses. The …
learning to read despite adequate intelligence, education, and normal senses. The …
An examination of candidate gene SNPs for dyslexia in an Indian sample
Developmental dyslexia (DD) is a complex neuro-genetic disorder associated with difficulty
in learning to read despite adequate intelligence and educational opportunities. Studies in …
in learning to read despite adequate intelligence and educational opportunities. Studies in …
Analysis of genetic variants of dyslexia candidate genes KIAA0319 and DCDC2 in Indian population
Developmental dyslexia (DD) is a heritable, complex genetic disorder associated with
impairment in reading and writing skills despite having normal intellectual ability and …
impairment in reading and writing skills despite having normal intellectual ability and …
Genetic variant in KIAA0319, but not in DYX1C1, is associated with risk of dyslexia: An integrated meta‐analysis
L Zou, W Chen, S Shao, Z Sun, R Zhong… - American Journal of …, 2012 - Wiley Online Library
Abstract DYX1C1 and KIAA0319 have been two of the most extensively studied candidate
genes for dyslexia given their important roles in the neuronal migration and neurite growth …
genes for dyslexia given their important roles in the neuronal migration and neurite growth …
Dyslexia risk variant rs600753 is linked with dyslexia-specific differential allelic expression of DYX1C1
B Müller, J Boltze, I Czepezauer, V Hesse… - … and molecular biology, 2018 - SciELO Brasil
An increasing number of genetic variants involved in dyslexia development were discovered
during the last years, yet little is known about the molecular functional mechanisms of these …
during the last years, yet little is known about the molecular functional mechanisms of these …
Association of the rs3743205 variant of DYX1C1 with dyslexia in Chinese children
Background Dyslexia is a learning disability that is characterized by difficulties in the
acquisition of reading and spelling skills independent of intelligence, motivation or …
acquisition of reading and spelling skills independent of intelligence, motivation or …
Unfolding the genetic pathways of dyslexia in Asian population: A review
Dyslexia also known as specific reading disorder is a complex heritable disorder with
unexpected difficulty in learning to read and spell despite adequate intelligence, education …
unexpected difficulty in learning to read and spell despite adequate intelligence, education …
Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia
Z Brkanac, NH Chapman… - American Journal of …, 2007 - Wiley Online Library
Dyslexia is a common heterogeneous disorder with a significant genetic component.
Multiple studies have replicated the evidence for linkage between variously defined …
Multiple studies have replicated the evidence for linkage between variously defined …
Opposite Associations between Individual KIAA0319 Polymorphisms and Developmental Dyslexia Risk across Populations: A Stratified Meta-Analysis by the Study …
S Shao, Y Niu, X Zhang, R Kong, J Wang, L Liu… - Scientific Reports, 2016 - nature.com
KIAA0319 at the DYX2 locus is one of the most extensively studied candidate genes for
developmental dyslexia (DD) owing to its important role in neuronal migration. Previous …
developmental dyslexia (DD) owing to its important role in neuronal migration. Previous …