Genetic Advances in the Study of Speech and Language Disorders

Por Newbury, D.F., Monaco, A.P.
Publicado em 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 no Mol Psychiatry (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 em 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 em 2010

FOXP2 Is Not a Major Susceptibility Gene for Autism or Specific Language Impairment

Por Newbury, D. F., Bonora, E., Lamb, J. A., Fisher, S. E., Lai, C. S. L., Baird, G., Jannoun, L., Slonims, V., Stott, C. M., Merricks, M. J., Bolton, P. F., Bailey, A. J., Monaco, A. P.
Publicado em 2002

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 em 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 no Genes Brain Behav (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 em 2014

Sixteen New Cases Contributing to the Characterization of Patients with Distal 22q11.2 Microduplications

Por Wincent, J., Bruno, D.L., van Bon, B.W.M., Bremer, A., Stewart, H., Bongers, E.M.H.F., Ockeloen, C.W., Willemsen, M.H., Keays, D.D.A., Baird, G., Newbury, D.F., Kleefstra, T., Marcelis, C., Kini, U., Stark, Z., Savarirayan, R., Sheffield, L.J., Zuffardi, O., Slater, H.R., de Vries, B.B., Knight, S.J.L., Anderlid, B.-M., Schoumans, J.
Publicado em 2011