Rose H. Reader

Next-generation sequencing identifies novel gene variants and pathways involved in specific language impairment

A. Hoischen, C. Francks, J. Veltman, 2016, bioRxiv.

Advances in the Production and Batch Reformatting of Phage Antibody Libraries

Rose H. Reader, B. Maddison, K. Gough, 2019, Molecular Biotechnology.

Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment

A. Hoischen, C. Francks, J. Veltman, 2017, Scientific Reports.

Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment

A. Hoischen, C. Francks, G. Baird, 2015, PLoS genetics.

Genome-wide analysis identifies a role for common copy number variants in specific language impairment

William W. Cohen, Gillian Baird, A Pickles, 2015, European Journal of Human Genetics.

Genome-wide analysis identi fi es a role for common copy number variants in speci fi c language impairment

G. Baird, P. Bolton, J. Knight, 2015 .

Genome-Wide Studies of Specific Language Impairment

D. Newbury, R. Nudel, Rose H. Reader, 2014, Current Behavioral Neuroscience Reports.

Next-generation sequencing identifies novel gene variants and pathways involved in specific language impairment

A. Hoischen, C. Francks, J. Veltman, 2016, bioRxiv.