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The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration.
Paracchini S, Thomas A, Castro S, Lai C, Paramasivam M, Wang Y, Keating BJ, Taylor JM, Hacking DF, Scerri T, Francks C, Richardson AJ, Wade-Martins R, Stein JF, Knight JC, Copp AJ, Loturco J, Monaco AP. Paracchini S, et al. Among authors: scerri t. Hum Mol Genet. 2006 May 15;15(10):1659-66. doi: 10.1093/hmg/ddl089. Epub 2006 Apr 6. Hum Mol Genet. 2006. PMID: 16600991
PCSK6 is associated with handedness in individuals with dyslexia.
Scerri TS, Brandler WM, Paracchini S, Morris AP, Ring SM, Richardson AJ, Talcott JB, Stein J, Monaco AP. Scerri TS, et al. Hum Mol Genet. 2011 Feb 1;20(3):608-14. doi: 10.1093/hmg/ddq475. Epub 2010 Nov 4. Hum Mol Genet. 2011. PMID: 21051773 Free PMC article.
Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia.
Harold D, Paracchini S, Scerri T, Dennis M, Cope N, Hill G, Moskvina V, Walter J, Richardson AJ, Owen MJ, Stein JF, Green ED, O'Donovan MC, Williams J, Monaco AP. Harold D, et al. Among authors: scerri t. Mol Psychiatry. 2006 Dec;11(12):1085-91, 1061. doi: 10.1038/sj.mp.4001904. Epub 2006 Oct 10. Mol Psychiatry. 2006. PMID: 17033633 Clinical Trial.
The genetic lexicon of dyslexia.
Paracchini S, Scerri T, Monaco AP. Paracchini S, et al. Among authors: scerri t. Annu Rev Genomics Hum Genet. 2007;8:57-79. doi: 10.1146/annurev.genom.8.080706.092312. Annu Rev Genomics Hum Genet. 2007. PMID: 17444811 Review.
A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.
Francks C, Paracchini S, Smith SD, Richardson AJ, Scerri TS, Cardon LR, Marlow AJ, MacPhie IL, Walter J, Pennington BF, Fisher SE, Olson RK, DeFries JC, Stein JF, Monaco AP. Francks C, et al. Am J Hum Genet. 2004 Dec;75(6):1046-58. doi: 10.1086/426404. Epub 2004 Oct 22. Am J Hum Genet. 2004. PMID: 15514892 Free PMC article.
39 results