Silvia Paracchini: all publications

• Publications

  • The Genetic Lexicon of Dyslexia. PubMed ID:(17444811)

  • Francks C, Paracchini S, Smith S, Richardson A, Scerri T, Cardon L, Marlow A, MacPhie I, Walter J, Pennington B, Fisher S, Olson R, DeFries J, Stein J, Monaco A. A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States. American journal of human genetics 75 (6) , 1046-58 (Epub 22 Oct 2004) PubMed ID:(15514892)

  • Paracchini S, Thomas A, Castro S, Lai C, Paramasivam M, Wang Y, Keating B, Taylor J, Hacking D, Scerri T, Francks C, Richardson A, Wade-Martins R, Stein J, Knight J, Copp A, Loturco J, Monaco A. The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration. Human molecular genetics 15 (10) , 1659-66 (Epub 06 Apr 2006) PubMed ID:(16600991)