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Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia.
Gialluisi A, Andlauer TFM, Mirza-Schreiber N, Moll K, Becker J, Hoffmann P, Ludwig KU, Czamara D, St Pourcain B, Brandler W, Honbolygó F, Tóth D, Csépe V, Huguet G, Morris AP, Hulslander J, Willcutt EG, DeFries JC, Olson RK, Smith SD, Pennington BF, Vaessen A, Maurer U, Lyytinen H, Peyrard-Janvid M, Leppänen PHT, Brandeis D, Bonte M, Stein JF, Talcott JB, Fauchereau F, Wilcke A, Francks C, Bourgeron T, Monaco AP, Ramus F, Landerl K, Kere J, Scerri TS, Paracchini S, Fisher SE, Schumacher J, Nöthen MM, Müller-Myhsok B, Schulte-Körne G. Gialluisi A, et al. Among authors: paracchini s. Transl Psychiatry. 2019 Feb 11;9(1):77. doi: 10.1038/s41398-019-0402-0. Transl Psychiatry. 2019. PMID: 30741946 Free PMC article.
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. Among authors: paracchini s. 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.
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. 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
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: paracchini s. 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. 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.
Alternative splicing in the dyslexia-associated gene KIAA0319.
Velayos-Baeza A, Toma C, da Roza S, Paracchini S, Monaco AP. Velayos-Baeza A, et al. Among authors: paracchini s. Mamm Genome. 2007 Sep;18(9):627-34. doi: 10.1007/s00335-007-9051-3. Epub 2007 Sep 11. Mamm Genome. 2007. PMID: 17846832
A common variant associated with dyslexia reduces expression of the KIAA0319 gene.
Dennis MY, Paracchini S, Scerri TS, Prokunina-Olsson L, Knight JC, Wade-Martins R, Coggill P, Beck S, Green ED, Monaco AP. Dennis MY, et al. Among authors: paracchini s. PLoS Genet. 2009 Mar;5(3):e1000436. doi: 10.1371/journal.pgen.1000436. Epub 2009 Mar 27. PLoS Genet. 2009. PMID: 19325871 Free PMC article.
88 results