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 …

[HTML][HTML] Opposite Associations between Individual KIAA0319 Polymorphisms and Developmental Dyslexia Risk across Populations: A Stratified Meta-Analysis by the …

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 …

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 …

Further evidence for DYX1C1 as a susceptibility factor for dyslexia

F Dahdouh, H Anthoni, I Tapia-Páez… - Psychiatric …, 2009 - journals.lww.com
Objective Dyslexia-susceptibility-1-candidate-1 (DYX1C1) was the first gene associated with
dyslexia. Since the original report of 2003, eight replication attempts have been published …

[HTML][HTML] A family-based association study does not support DYX1C1 on 15q21. 3 as a candidate gene in developmental dyslexia

C Marino, R Giorda, M Luisa Lorusso… - European Journal of …, 2005 - nature.com
We applied a family-based association approach to investigate the role of the DYX1C1 gene
on chromosome 15q as a candidate gene for developmental dyslexia (DD) to 158 families …

The KIAA0319-Like (KIAA0319L) Gene on Chromosome 1p34 as a Candidate for Reading Disabilities

JM Couto, L Gomez, K Wigg, T Cate-Carter… - Journal of …, 2008 - Taylor & Francis
A locus on chromosome 1p34-36 (DYX8) has been linked to developmental dyslexia or
reading disabilities (RD) in three independent samples. In the current study, we investigated …

A family‐based association analysis and meta‐analysis of the reading disabilities candidate gene DYX1C1

C Tran, F Gagnon, KG Wigg, Y Feng… - American Journal of …, 2013 - Wiley Online Library
Reading disabilities (RD) have a significant genetic basis and have shown linkage to
multiple regions including chromosome 15q. Dyslexia susceptibility 1 candidate gene 1 …

[HTML][HTML] Association of the rs3743205 variant of DYX1C1 with dyslexia in Chinese children

CKP Lim, CSH Ho, CHN Chou, MMY Waye - Behavioral and Brain …, 2011 - Springer
Background Dyslexia is a learning disability that is characterized by difficulties in the
acquisition of reading and spelling skills independent of intelligence, motivation or …

Association of SNPs of DYX1C1 with developmental dyslexia in an Indian population

SK Venkatesh, A Siddaiah, P Padakannaya… - Psychiatric …, 2014 - journals.lww.com
Objective DYX1C1 has been identified as a susceptible candidate gene for developmental
dyslexia (DD); studies in various populations have yielded inconclusive results and the …

Association of short‐term memory with a variant within DYX1C1 in developmental dyslexia

C Marino, A Citterio, R Giorda, A Facoetti… - Genes, Brain and …, 2007 - Wiley Online Library
A substantial genetic contribution in the etiology of developmental dyslexia (DD) has been
well documented with independent groups reporting a susceptibility locus on chromosome …