Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects

por Newbury, D. F., Paracchini, S., Scerri, T. S., Winchester, L., Addis, L., Richardson, Alex J., Walter, J., Stein, J. F., Talcott, J. B., Monaco, A. P.
Publicado 2010

The DCDC2 deletion is not a risk factor for dyslexia

por Scerri, T S, Macpherson, E, Martinelli, A, Wa, W C, Monaco, A P, Stein, J, Zheng, M, Suk-Han Ho, C, McBride, C, Snowling, M, Hulme, C, Hayiou-Thomas, M E, Waye, M M Y, Talcott, J B, Paracchini, S
Publicado 2017

Genome-wide screening for DNA variants associated with reading and language traits

por Gialluisi, A, Newbury, D F, Wilcutt, E G, Olson, R K, DeFries, J C, Brandler, W M, Pennington, B F, Smith, S D, Scerri, T S, Simpson, N H, Luciano, M, Evans, D M, Bates, T C, Stein, J F, Talcott, J B, Monaco, A P, Paracchini, S, Francks, C, Fisher, S E
Publicado 2014