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Page 1
The genetic basis of dyslexia.
Francks C, MacPhie IL, Monaco AP. Francks C, et al. Among authors: monaco ap. Lancet Neurol. 2002 Dec;1(8):483-90. doi: 10.1016/s1474-4422(02)00221-1. Lancet Neurol. 2002. PMID: 12849333 Review.
Chorein detection for the diagnosis of chorea-acanthocytosis.
Dobson-Stone C, Velayos-Baeza A, Filippone LA, Westbury S, Storch A, Erdmann T, Wroe SJ, Leenders KL, Lang AE, Dotti MT, Federico A, Mohiddin SA, Fananapazir L, Daniels G, Danek A, Monaco AP. Dobson-Stone C, et al. Among authors: monaco ap. Ann Neurol. 2004 Aug;56(2):299-302. doi: 10.1002/ana.20200. Ann Neurol. 2004. PMID: 15293285
Analysis of the human VPS13 gene family.
Velayos-Baeza A, Vettori A, Copley RR, Dobson-Stone C, Monaco AP. Velayos-Baeza A, et al. Among authors: monaco ap. Genomics. 2004 Sep;84(3):536-49. doi: 10.1016/j.ygeno.2004.04.012. Genomics. 2004. PMID: 15498460
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: monaco ap. 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. Among authors: monaco ap. 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
706 results