… 1 of KIAA0319. Here, we test the hypothesis that variant(s) responsible for reduced KIAA0319
expression resides on the risk haplotype close to the gene's transcription start site. We …

… We hypothesized that causal risk variants in KIAA0319 function by altering transcription,
and are located in the region of open chromatin identified by Couto et al. (2010). In the current …

… gene KIAA0319-Like (KIAA0319L) within DYX8, as it is homologous to KIAA0319, a strong
RD candidate gene … the supporting evidence for its homolog KIAA0319 on chromosome 6p. …

… found evidence that variation in the KIAA0319 gene confers susceptibility to DD, we sought
to refine this genetic association by genotyping 36 additional SNPs in the gene. Nine SNPs, …

… KIAA0319. Phylogenetically similar READ1 variants showed synergistic effects with the
KIAA0319 … different allele classes in READ1, the KIAA0319 risk haplotype and reading-related …

… In conclusion, our results suggested that the 931C > T variant in KIAA0319, but not the −3G
> A in DYX1C1, was significantly associated with the risk of dyslexia. © 2012 Wiley …

… This analysis suggests that the KIAA0319, DCDC2, and CMIP genes contribute specifically
to reading abilities and in particular to single-word reading and single-word spelling tests. …

… valuable for the functional characterization of this gene and the analysis in animal models. …
, mouse, and rat KIAA0319 genes. We detected several variants and defined their expression …

… including a SNP (rs4504469) in exon 4 of the KIAA0319 gene that changes an amino acid
(P=.002; … Our data strongly implicate KIAA0319 as a susceptibility gene for dyslexia. The gene …

… To the best of our knowledge, this is the first genetic study that demonstrated KIAA0319 as
a potential candidate gene for DD in Indian population. More studies with larger sample size …