AAFE - Almer,G.; Hainfellner,J.A.; Brücke,T.; Jellinger,K.A.; Kleinert,R.; Bayer,G.; Windl,O.; Kretzschmar,H.A.; Hill,A.F.; Sidle,K.; Collinge,J.; Budka,H. - Fatal familial insomnia: a new Austrian family. - Brain: A Journal of Neurology 1999 Jan; 122(1): 5-16
AOOR - Collinge,J.; Palmer,M.S.; Sidle,K.C.L.; Hill,A.F.; Gowland,I.; Meads,J.; Asante,E.A.; Bradley,R.; Doey,L.J.; Lantos,P.L. - Unaltered susceptibility to BSE in transgenic mice expressing human prion protein - Nature 1997 Oct 2; 389(6650): 526
ACTR - Collinge,J.; Sidle,K.C.L.; Meads,J.; Ironside,J.; Hill,A.F. - Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD - Nature 1996 Oct 24; 383(6602): 685-90
ACTV - Collinge,J.; Palmer,M.S.; Sidle,K.C.L.; Hill,A.F.; Gowland,I.; Meads,J.; Asante,E.A.; Bradley,R.; Doey,L.J.; Lantos,P.L. - Unaltered susceptibility to BSE in transgenic mice expressing human prion protein - Nature 1995 Dec 21-28; 378(6559): 779-83
ACTW - Collinge,J.; Palmer,M.S.; Sidle,K.C.L.; Gowland,I.; Medori,R.; Ironside,J.; Lantos,P. - Transmission of fatal familial insomnia to laboratory animals - Lancet 1995 Aug 26; 346(8974): 569-70
ACTY - Collinge,J.; Whittington,M.A.; Sidle,K.C.L.; Smith,C.J.; Palmer,M.S.; Clarke,A.R.; Jefferys,J.G.R. - Prion protein is necessary for normal synaptic function - Nature 1994 Jul 28; 370(6487): 295-7
ACTZ - Collinge,J.; Palmer,M.S.; Sidle,K.C.L.; Mahal,S.P.; Campbell,T.A.; Brown,J.; Hardy,J.; Brun,A.E.; Gustafson,L.; Bakker,E.; Roos,R.; Groen,J.J. - Familial Pick's disease and dementia in frontal lobe degeneration of non-Alzheimer type are not variants of prion disease - Journal of Neurology, Neurosurgery and Psychiatry 1994 Jun; 57(6): 762
ACUD - Collinge,J.; Palmer,M.S.; Campbell,T.A.; Sidle,K.C.L.; Carroll,D.; Harding,A. - Inherited prion disease (PrP lysine 200) in Britain: two case reports. - British Medical Journal 1993 Jan 30; 306(6873): 301-2
ANYD - Hill,A.F.; Joiner,S.; Wadsworth,J.D.F.; Sidle,K.C.L.; Bell,J.E.; Budka,H.; Ironside,J.W.; Collinge,J. - Molecular classification of sporadic Creutzfeldt-Jakob disease - Brain: A Journal of Neurology 2003 Jun; 126(6): 1333-46
AFJN - Hill,A.F.; Sidle,K.C.L.; Joiner,S.; Keyes,P.; Martin,T.C.; Dawson,M.; Collinge,J. - Molecular screening of sheep for bovine spongiform encephalopathy - Neuroscience Letters 1998 Oct 23; 255(3): 159-62
AFJO - Hill,A.F.; Desbruslais,M.; Joiner,S.; Sidle,K.C.L.; Gowland,I.; Collinge,J.; Doey,L.J.; Lantos,P. - The same prion strain causes vCJD and BSE - Nature 1997 Oct 2; 389(6650): 448-50, 526
AJDV - Palmer,M.S.; Mahal,S.P.; Campbell,T.A.; Hill,A.F.; Sidle,K.C.L.; Laplanche,J.L.; Collinge,J. - Deletions in the prion protein gene are not associated with CJD - Human Molecular Genetics 1993 May; 2(5): 541-4
ALPM - Telling,G.C.; Scott,M.R.D.; Hsiao,K.K.; Foster,D.B.; Yang,S.L.; Torchia,M.; Sidle,K.C.L.; Collinge,J.; DeArmond,S.J.; Prusiner,S.B. - Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein - Proceedings of the National Academy of Sciences of the United States of America 1994 Oct 11; 91(21): 9936-40
AUMI - Whittington,M.A.; Sidle,K.C.L.; Gowland,I.; Meads,J.; Hill,A.F.; Palmer,M.S.; Jefferys,J.G.R.; Collinge,J. - Rescue of neurophysiological phenotype seen in PRP null mice by transgene encoding human prion protein, (vol 9, pg 197, 1995) - Nature Genetics 1995 Apr; 9(4): 451
AMLA - Whittington,M.A.; Sidle,K.C.L.; Gowland,I.; Meads,J.; Hill,A.F.; Palmer,M.S.; Jefferys,J.G.R.; Collinge,J. - Rescue of neurophysiological phenotype seen in PrP null mice by transgene encoding human prion protein - Nature Genetics 1995 Feb; 9(2): 197-201
AMQK - Windl,O.; Dempster,M.; Estibeiro,J.P.; Lathe,R.; de Silva,R.N.; Esmonde,T.F.G.; Will,R.; Springbett,A.; Campbell,T.A.; Sidle,K.C.L.; Palmer,M.S.; Collinge,J. - Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene. - Human Genetics 1996 Sep; 98(3): 259-64