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Cousens, S; Smith, PG; Ward, H; Everington, D; Knight, RS; Zeidler, M; Stewart, G; Smith-Bathgate, EA; MacLeod, MA; MacKenzie, J; +1 more... Will, RG; (2001) Geographical distribution of variant Creutzfeldt-Jakob disease in Great Britain, 1994-2000. Lancet, 357 (9261). pp. 1002-7. ISSN 0140-6736 DOI: https://doi.org/10.1016/S0140-6736(00)04236-7 Full text not available from this repository.

D'Aignaux, JH; Cousens, SN; Delasnerie-Laupretre, N; Brandel, JP; Salomon, D; Laplanche, JL; Hauw, JJ; Alperovitch, A; (2002) Analysis of the geographical distribution of sporadic Creutzfeldt-Jakob disease in France between 1992 and 1998. International journal of epidemiology, 31 (2). pp. 490-5. ISSN 0300-5771 DOI: https://doi.org/10.1093/ije/31.2.490 Full text not available from this repository.

D'Aignaux, JN; Cousens, SN; Smith, PG; (2001) Predictability of the UK variant Creutzfeldt-Jakob disease epidemic. Science (New York, NY), 294 (5547). pp. 1729-31. ISSN 0036-8075 DOI: https://doi.org/10.1126/science.1064748 Full text not available from this repository.

Llewelyn, CA; Hewitt, PE; Knight, RSG; Amar, K; Cousens, S; MacKenzie, J; Will, RG; (2004) Possible transmission of variant Creutzfeldt-Jakob disease by blood transfusion. Lancet, 363 (9407). pp. 417-421. ISSN 0140-6736 DOI: https://doi.org/10.1016/S0140-6736(04)15486-X Full text not available from this repository.

Mead, S; Poulter, M; Uphill, J; Beck, J; Whitfield, J; Webb, TEF; Campbell, T; Adamson, G; Deriziotis, P; Tabrizi, SJ; +5 more... Hummerich, H; Verzilli, C; Alpers, MP; Whittaker, JC; Collinge, J; (2009) Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study. Lancet neurology, 8 (1). pp. 57-66. ISSN 1474-4422 DOI: https://doi.org/10.1016/S1474-4422(08)70265-5

Mead, S; Uphill, J; Beck, J; Poulter, M; Campbell, T; Lowe, J; Adamson, G; Hummerich, H; Klopp, N; Ruckert, IM; +11 more... Wichmann, HE; Azazi, D; Plagnol, V; Pako, WH; Whitfield, J; Alpers, MP; Whittaker, J; Balding, DJ; Zerr, I; Kretzschmar, H; Collinge, J; (2012) Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP. Human molecular genetics, 21 (8). pp. 1897-1906. ISSN 0964-6906 DOI: https://doi.org/10.1093/hmg/ddr607 Full text not available from this repository.

Smith, PG; (2003) The epidemics of bovine spongiform encephalopathy and variant Creutzfeldt-Jakob disease: current status and future prospects. Bulletin of the World Health Organization, 81 (2). pp. 123-30. ISSN 0042-9686 https://researchonline.lshtm.ac.uk/id/eprint/16381

Ward, HJT; Everington, D; Cousens, SN; Smith-Bathgate, B; Gillies, M; Murray, K; Knight, RSG; Smith, PG; Will, RG; (2008) Risk factors for sporadic Creutzfeldt-Jakob disease. Annals of neurology, 63 (3). pp. 347-354. ISSN 0364-5134 DOI: https://doi.org/10.1002/ana.21294 Full text not available from this repository.