Items where authors include "Roberts, E."

Article

Gomez, K.U., McBride, O., Roberts, E. et al. (9 more authors) (2023) The clustering of physical health conditions and associations with co-occurring mental health problems and problematic alcohol use: a cross-sectional study. BMC Psychiatry, 23. 89. ISSN 1471-244X

Wardle, H., Banks, J., Bebbington, P. et al. (45 more authors) (2020) Open letter from UK based academic scientists to the secretaries of state for digital, culture, media and sport and for health and social care regarding the need for independent funding for the prevention and treatment of gambling harms. BMJ: British Medical Journal, 370. m2613. ISSN 1759-2151

Xie, J.Y., De Felice, M., Kopruszinski, C.M. et al. (14 more authors) (2017) Kappa opioid receptor antagonists: a possible new class of therapeutics for migraine prevention. Cephalalgia, 37 (8). pp. 780-794. ISSN 0333-1024

McRae, J.F., Clayton, S., Fitzgerald, T.W. et al. (299 more authors) (2017) Prevalence and architecture of de novo mutations in developmental disorders. Nature, 542 (7642). pp. 433-438. ISSN 0028-0836

Fitzgerald, T.W., Gerety, S.S., Jones, W.D. et al. (263 more authors) (2015) Large-scale discovery of novel genetic causes of developmental disorders. Nature, 519. pp. 223-228. ISSN 0028-0836

Philip, L., Townsend, L., Roberts, E. et al. (1 more author) (2015) The Rural Digital Economy. Scottish Geographical Journal, 131 (3-4). 143 - 147. ISSN 1470-2541

Mubaidin, A., Roberts, E., Hampshire, D. et al. (7 more authors) (2003) Karak syndrome: a novel degenerative disorder of the basal ganglia and cerebellum. Journal of Medical Genetics, 40 (7). pp. 543-546. ISSN 0022-2593

Leal, G.F., Roberts, E., Silva, E.O. et al. (3 more authors) (2003) A novel locus for autosomal recessive primary microcephaly (MCPH6) maps to 13q12.2. Journal of Medical Genetics, 40 (7). pp. 540-542. ISSN 0022-2593

Roberts, E., Hampshire, D.J., Pattison, L. et al. (8 more authors) (2002) Autosomal recessive primary microcephaly: an analysis of locus heterogeneity and phenotypic variation. Journal of Medical Genetics, 39 (10). pp. 718-721. ISSN 0022-2593

Hampshire, D.J., Roberts, E., Crow, Y. et al. (5 more authors) (2001) Kufor-Rakeb syndrome, pallido-pyramidal degeneration with supranuclear upgaze paresis and dementia, maps to 1p36. Journal of Medical Genetics, 38 (10). pp. 680-682. ISSN 0022-2593