Hector, R. D. et al. (2017) CDKL5 variants: improving our understanding of a rare neurological disorder. Neurology Genetics, 3(6), e200. (doi: 10.1212/NXG.0000000000000200) (PMID:29264392) (PMCID:PMC5732004)

Hector, R. D. , Dando, O., Ritakari, T. E., Kind, P. C., Bailey, M. E.S. and Cobb, S. R. (2017) Characterisation of Cdkl5 transcript isoforms in rat. Gene, 603, pp. 21-26. (doi: 10.1016/j.gene.2016.12.001) (PMID:27940108)

Ross, P. D. et al. (2016) Exclusive expression of MeCP2 in the nervous system distinguishes between brain and peripheral Rett syndrome-like phenotypes. Human Molecular Genetics, 25(20), pp. 4389-4404. (doi: 10.1093/hmg/ddw269) (PMID:28173151) (PMCID:PMC5886038)

Hector, R. D. , Dando, O., Landsberger, N., Kilstrup-Nielsen, C., Kind, P. C., Bailey, M. E.S. and Cobb, S. R. (2016) Characterisation of CDKL5 transcript isoforms in human and mouse. PLoS ONE, 11(6), e0157758. (doi: 10.1371/journal.pone.0157758) (PMID:27315173) (PMCID:PMC4912119)

Gadalla, K. K. E. , Ross, P. D., Hector, R. D. , Bahey, N. G., Bailey, M. E.S. and Cobb, S. R. (2015) Gene therapy for Rett syndrome: prospects and challenges. Future Neurology, 10(5), pp. 467-484. (doi: 10.2217/fnl.15.29)