Associated Papers
Association between KIAA0319 SNPs and risk of dyslexia: a meta-analysis.
Deng KG et al.
Journal of Genetics, 2019
XomAnnotate: Analysis of Heterogeneous and Complex Exome- A Step towards Translational Medicine.
Talukder AK et al.
Plos One, 2015
Association of SNPs of DYX1C1 with developmental dyslexia in an Indian population.
Venkatesh SK et al.
Psychiatric Genetics, 2014
Genome-wide copy number scan identifies disruption of PCDH11X in developmental dyslexia.
Veerappa AM et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2013
An examination of candidate gene SNPs for dyslexia in an Indian sample.
Venkatesh SK et al.
Behavior Genetics, 2011
Exome sequencing reveals comprehensive genomic alterations across eight cancer cell lines.
Chang H et al.
Plos One, 2011
Allelic variants of DYX1C1 are not associated with dyslexia in India.
Saviour P et al.
Indian Journal of Human Genetics, 2008
Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia.
Brkanac Z et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2007
A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia.
Marino C et al.
European Journal of Human Genetics : Ejhg, 2005
A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain.
Taipale M et al.
Proceedings of the National Academy of Sciences of the United States of America, 2003