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 em 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 no Transl Psychiatry (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 em 2014