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Discovery of 42 genome-wide significant loci associated with dyslexia.
Doust C, Fontanillas P, Eising E, Gordon SD, Wang Z, Alagöz G, Molz B; 23andMe Research Team; Quantitative Trait Working Group of the GenLang Consortium; Pourcain BS, Francks C, Marioni RE, Zhao J, Paracchini S, Talcott JB, Monaco AP, Stein JF, Gruen JR, Olson RK, Willcutt EG, DeFries JC, Pennington BF, Smith SD, Wright MJ, Martin NG, Auton A, Bates TC, Fisher SE, Luciano M. Doust C, et al. Among authors: paracchini s. Nat Genet. 2022 Nov;54(11):1621-1629. doi: 10.1038/s41588-022-01192-y. Epub 2022 Oct 20. Nat Genet. 2022. PMID: 36266505 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
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.
CMIP and ATP2C2 modulate phonological short-term memory in language impairment.
Newbury DF, Winchester L, Addis L, Paracchini S, Buckingham LL, Clark A, Cohen W, Cowie H, Dworzynski K, Everitt A, Goodyer IM, Hennessy E, Kindley AD, Miller LL, Nasir J, O'Hare A, Shaw D, Simkin Z, Simonoff E, Slonims V, Watson J, Ragoussis J, Fisher SE, Seckl JR, Helms PJ, Bolton PF, Pickles A, Conti-Ramsden G, Baird G, Bishop DV, Monaco AP. Newbury DF, et al. Among authors: paracchini s. Am J Hum Genet. 2009 Aug;85(2):264-72. doi: 10.1016/j.ajhg.2009.07.004. Epub 2009 Jul 30. Am J Hum Genet. 2009. PMID: 19646677 Free PMC article.
88 results