Association of a null allele of SPRN with variant Creutzfeldt–Jakob disease

por Beck, J A, Campbell, T A, Adamson, G, Poulter, M, Uphill, J B, Molou, E, Collinge, J, Mead, S
Publicado 2008

Genome-wide association study of behavioural and psychiatric features in human prion disease

por Thompson, A G B, Uphill, J, Lowe, J, Porter, M-C, Lukic, A, Carswell, C, Rudge, P, MacKay, A, Collinge, J, Mead, S
Publicado 2015

Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series

por Webb, T. E. F., Poulter, M., Beck, J., Uphill, J., Adamson, G., Campbell, T., Linehan, J., Powell, C., Brandner, S., Pal, S., Siddique, D., Wadsworth, J. D., Joiner, S., Alner, K., Petersen, C., Hampson, S., Rhymes, C., Treacy, C., Storey, E., Geschwind, M. D., Nemeth, A. H., Wroe, S., Collinge, J., Mead, S.
Publicado 2008