Dr Justin Davies is a Consultant in Paediatric Endocrinology and Honorary Senior Lecturer at University Hospital Southampton, where he has worked since 2005. He graduated from the University of Wales College of Medicine. He trained in paediatric endocrinology and diabetes in Cardiff with attachments at Great Ormond Street Hospital London and St Bartholomew's Hospital, London, and was a Lecturer in Paediatric Endocrinology at Cardiff University. In 2004 he was awarded an MD for his thesis on the effects of chemotherapy on osteoblast function. He is a member of the Society for Endocrinology Study Interest Group for Late Effects of Cancer Treatment. At Southampton he is the lead clinician for paediatric endocrinology. Dr Davies was the secretary of the British Paediatric and Adolescent Bone Group and his research interest is in bone disorders and body composition in childhood. He is currently an Executive Committe member and Treasurer of the British Society of Paediatric Endocrinology and Diabetes.A

Secondary Osteoporosis in Children Dr Davies research interest is into the impact of childhood disease on bone mass acquisition and body composition.

Diagnosis and management of Silver-Russell syndrome: first international consensus statement - Wakeling, E., Brioude, F., Lokulo-Sodipe, K., O'Connell, S.M., Salem, J., Bliek, J., Canton, A., Chrzanowska, K.H., Davies, J.H., Dias, R., Dubern, B., Elbracht, M., Giabicani, E., Grimberg, A., Groenskov, K., Hokken-Koelega, A., Jorge, A.A., Kagami, M., Linglart, A., Maghnie, M., Mohnike, K., Monk, D., Moore, G., Murray, P.G., Ogata, T., Oliver Petit, I., Russo, S., Said, E., Toumba, M., Tumer, Z., Binder, G., Eggermann, T., Harbison, M.D., Temple, I.K., Mackay, D.J.G. and Netchine, I. Published:2016Publication:Nature Reviews EndocrinologyVolume:13, (2)Page Range:105-124doi:10.1038/nrendo.2016.138 Comprehensive screening of eight known causative genes in congenital hypothyroidism with gland-in-situ - Nicholas, A.K., Serra, E.G., Cangul, H., Alyaarubi, S., Ullah, I., Schoenmakers, E., Deeb, A., Habeb, A.M., AlMaghamsi, M., Peters, C., Nathwani, N., Aycan, Z., Saglam, H., Bober, E., Dattani, M., Shenoy, S., Murray, P.G., Babiker, A., Willemsen, R., Thankamony, A., Lyons, G., Irwin, R., Padidela, R., Tharian, K., Davies, J.H., Puthi, V., Park, S.-M., Massoud, A.F., Gregory, J.W., Albanese, A., Pease-Gevers, E., Martin, H., Brugger, K., Maher, E.R., Chatterjee, K., Anderson, C.A. and Schoenmakers, N. Published:2016Publication:The Journal of Clinical Endocrinology & MetabolismVolume:101, (12)Page Range:4521-4531doi:10.1210/jc.2016-1879 Further defining the phenotypic spectrum of B4GALT7 mutations - Salter, Claire G., Davies, Justin H., Moon, Rebecca J., Fairhurst, Joanna, Bunyan, David and Foulds, Nicola Published:2016Publication:American Journal of Medical Genetics Part AVolume:170, (6)Page Range:1556-1563doi:10.1002/ajmg.a.37604PMID:26940150