News and Publications

Recent key publications include:

Turner, S.J., Brown, A., Arpone, M., Anderson, V., Morgan, A.T., & Scheffer, I.E. (2017). Dysarthria and broader motor speech deficits in Dravet syndrome. Neurology, 88(8), 743-749.

Fedorenko, E., Morgan, A., Murray, E., Cardinaux, A., Mei, C., Tager-Flusberg, H., Fisher, S.E., & Kanwisher, N. (2016). A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2. European Journal of Human Genetics, 24, 302-306.

Liégeois, F. J., Hildebrand, M. S., Bonthrone, A., Turner, S. J., Scheffer, I. E., Bahlo, M., Connelly, A., & Morgan, A. T. (2016). Early neuroimaging markers of FOXP2 intragenic deletion. Scientific Reports, 6, 35192. 

Morgan, A.T., Mei, C., Da Costa, A., Fifer, J., Lederer, D., Benoit, V., McMillin, M.J., Buckingham, K.J., Bamshad, M.J., Pope, K., & White, S.M. (2015). Speech and language in a genotyped cohort of individuals with Kabuki syndrome. American Journal of Medical Genetics Part A, 167A, 1483–1492.

Turner, S. J., Mayes, A. K., Verhoeven, A., Mandelstam, S. A., Morgan, A. T., & Scheffer, I. E. (2015). GRIN2A: An aptly named gene for speech dysfunction. Neurology, 84(6), 586–593.

Turner, S.J., Hildebrand M.S., Block S., Damiano, J., Fahey M., Reilly S., Bahlo M., Scheffer I.E., Morgan A.T., (2013). Small Intragenic Deletion in FOXP2 associated with Childhood Apraxia of Speech and Dysarthria. American Journal of Medical Genetics, 161A(9), 2321-6.

Liégeois, F., Morgan, A.T., Connelly, A., & Vargha-Khadem, F. (2011) Endophenotypes of FOXP2: Dysfunction within the human articulatory network. European Journal of Paediatric Neurology, 15(4), 283-288.