Genetic Advances in the Study of Speech and Language Disorders

por Newbury, D.F., Monaco, A.P.
Publicado 2010

Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders

por Devanna, P, Chen, X S, Ho, J, Gajewski, D, Smith, S D, Gialluisi, A, Francks, C, Fisher, S E, Newbury, D F, Vernes, S C
Publicado 2018

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

A locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31-q14.3

por Addis, L, Friederici, A D, Kotz, S A, Sabisch, B, Barry, J, Richter, N, Ludwig, A A, Rübsamen, R, Albert, F W, Pääbo, S, Newbury, D F, Monaco, A P
Publicado 2010

Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment

por Nudel, R, Simpson, N H, Baird, G, O’Hare, A, Conti-Ramsden, G, Bolton, P F, Hennessy, E R, Ring, S M, Davey Smith, G, Francks, C, Paracchini, S, Monaco, A P, Fisher, S E, Newbury, D F
Publicado 2014

Lack of replication for the myosin-18B association with mathematical ability in independent cohorts

por Pettigrew, K A, Fajutrao Valles, S F, Moll, K, Northstone, K, Ring, S, Pennell, C, Wang, C, Leavett, R, Hayiou-Thomas, M E, Thompson, P, Simpson, N H, Fisher, S E, Whitehouse, A J O, Snowling, M J, Newbury, D F, Paracchini, S
Publicado 2015

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