Analysis of exome data in a UK cohort of 603 patients with syndromic orofacial clefting identifies causal molecular pathways by Wilson, K, Newbury, DF, Kini, U

Stage 2 registered report: variation in neurodevelopmental outcomes in children with sex chromosome trisomies: testing the double hit hypothesis by Newbury, DF, Simpson, NH, Thompson, PA, Bishop, DVM

Generalized Structured Component Analysis in candidate gene association studies: applications and limitations by Thompson, PA, Bishop, DVM, Eising, E, Fisher, SE, Newbury, DF

Copy number variation burden does not predict severity of neurodevelopmental phenotype in children with a sex chromosome trisomy. by Mountford, HS, Bishop, DVM, Thompson, PA, Simpson, NH, Newbury, DF

Logical and methodological issues affecting genetic studies of humans reported in top neuroscience journals by Grabitz, CR, Button, KS, Munafò, MR, Newbury, DF, Pernet, CR, Thompson, PA, Bishop, DVM

Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment by Chen, XS, Reader, RH, Hoischen, A, Veltman, JA, Simpson, NH, Francks, C, Newbury, DF, Fisher, SE

Multi-level evidence of an allelic hierarchy of USH2A variants in hearing, auditory processing and speech/language outcomes by Perrino, PA, Talbot, L, Kirkland, R, Hill, A, Rendall, AR, Mountford, HS, Taylor, J, WGS500 Consortium, Buscarello, AN, Lahiri, N, Saggar, A, Fitch, RH, Newbury, DF