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

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

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