AAWY - Baker,H.F.; Poulter,M.; Crow,T.J.; Frith,C.D.; Lofthouse,R.; Ridley,R.M. - Aminoacid polymorphism in human prion protein and age at death in inherited prion disease - Lancet 1991 May 25; 337(8752): 1286
AOQF - Beck,J.A.; Poulter,M.; Campbell,T.A.; Uphill,J.B.; Adamson,G.; Mead,S.; Collinge,J. - PRNP haplotype analysis in PNG populations - International Conference - Prion diseases: from basic research to intervention concepts - TSE-Forum, 08.10.-10.10.2003, Gasteig, München - Poster session - DG-64
ACUG - Collinge,J.; Brown,J.; Hardy,J.; Mullan,M.; Rossor,M.N.; Baker,H.F.; Crow,T.J.; Lofthouse,R.; Poulter,M.; Ridley,R.; Owen,F.; Bennett,C.; Dunn,G.; Harding,A.E.; Quinn,N.; Doshi,B.; Roberts,G.W.; Honavar,M.; Janota,I.; Lantos,P.L. - Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features. - Brain: A Journal of Neurology 1992 Jun; 115(3): 687-710
ACUH - Collinge,J.; Poulter,M.; Davis,M.B.; Baraitser,M.; Owen,F.; Crow,T.J.; Harding,A.E. - Presymptomatic detection or exclusion of prion protein gene defects in families with inherited prion diseases - American Journal of Human Genetics 1991 Dec; 49(6): 1351-4
ACUJ - Collinge,J.; Owen,F.; Poulter,M.; Leach,M.; Crow,T.J.; Rossor,M.N.; Hardy,J.; Mullan,M.J.; Janota,I.; Lantos,P.L. - Prion dementia without characteristic pathology - Lancet 1990 Jul 7; 336(8706): 7-9
ACUK - Collinge,J.; Harding,A.E.; Owen,F.; Poulter,M.; Lofthouse,R.; Boughey,A.M.; Shah,T.; Crow,T.J. - Diagnosis of Gerstmann-Sträussler syndrome in familial dementia with prion protein gene analysis - Lancet 1989 Jul 1; 2(8653): 15-7
ADQG - Duchen,L.W.; Poulter,M.; Harding,A.E. - Dementia associated with a 216 base pair insertion in the prion protein gene. Clinical and neuropathological features. - Brain: A Journal of Neurology 1993 Jun; 116(3): 555-67
AUAS - Hill,A.F.; Joiner,S.; Beck,J.A.; Campbell,T.A.; Dickinson,A.; Poulter,M.; Wadsworth,J.D.F.; Collinge,J. - Distinct glycoform ratios of protease resistant prion protein associated with PRNP point mutations - Brain: A Journal of Neurology 2006 Mar; 129(3): 676-85
AFQH - Hsiao,K.K.; Baker,H.F.; Crow,T.J.; Poulter,M.; Owen,F.; Terwilliger,J.D.; Westaway,D.; Ott,J.; Prusiner,S.B. - Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome - Nature 1989 Mar 23; 338(6213): 342-5
AVGE - Mead,S.; Poulter,M.; Beck,J.; Webb,T.E.F.; Campbell,T.A.; Linehan,J.M.; Desbruslais,M.; Joiner,S.; Wadsworth,J.D.F.; King,A.; Lantos,P.; Collinge,J. - Inherited prion disease with six octapeptide repeat insertional mutation - molecular analysis of phenotypic heterogeneity - Brain: A Journal of Neurology 2006 Sep; 129(9): 2297-317
ANUX - Mead,S.; Stumpf,M.P.; Whitfield,J.; Beck,J.A.; Poulter,M.; Campbell,T.A.; Uphill,J.B.; Goldstein,D.; Alpers,M.P.; Fisher,E.M.C.; Collinge,J. - Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemics - Science 2003 Apr 25; 300(5619): 640-3
AJCX - Owen,F.; Poulter,M.; Collinge,J.; Leach,M.; Lofthouse,R.; Crow,T.J.; Harding,A.E. - A dementing illness associated with a novel insertion in the prion protein gene - Brain Research. Molecular Brain Research 1992 Mar; 13(1-2): 155-7
AJCY - Owen,F.; Poulter,M.; Collinge,J.; Leach,M.; Shah,T.; Lofthouse,R.; Chen,Y.F.; Crow,T.J.; Harding,A.E.; Hardy,J.; Rossor,M.N. - Insertions in the prion protein gene in atypical dementias - Experimental Neurology 1991 May; 112(2): 240-2
AJCZ - Owen,F.; Poulter,M.; Collinge,J.; Crow,T.J. - Codon 129 changes in the prion protein gene in Caucasians - American Journal of Human Genetics 1990 Jun; 46(6): 1215-6
AJDA - Owen,F.; Poulter,M.; Collinge,J.; Crow,T.J. - A codon 129 polymorphism in the PRIP gene - Nucleic Acids Research 1990 May 25; 18(10): 3103
AJDB - Owen,F.; Poulter,M.; Shah,T.; Collinge,J.; Lofthouse,R.; Baker,H.F.; Ridley,R.; McVey,J.; Crow,T.J. - An in-frame insertion in the prion protein gene in familial Creutzfeldt-Jakob disease - Brain Research. Molecular Brain Research 1990 Apr; 7(3): 273-6
AJDC - Owen,F.; Poulter,M.; Lofthouse,R.; Collinge,J.; Crow,T.J.; Risby,D.; Baker,H.F.; Ridley,R.M.; Hsiao,K.; Prusiner,S.B. - Insertion in prion protein gene in familial Creutzfeldt-Jakob disease - Lancet 1989 Jan 7; 1(8628): 51-2
AOXZ - Poulter,M.; Beck,J.A.; Campbell,T.A.; Uphill,J.B.; Adamson,G.; Mead,S.; Collinge,J. - Small Pool PCR to test for somatic octapeptide repeat variation in sporadic CJD patients - International Conference - Prion diseases: from basic research to intervention concepts - TSE-Forum, 08.10.-10.10.2003, Gasteig, München - Poster session - DG-65
AJOM - Poulter,M.; Baker,H.F.; Frith,C.D.; Leach,M.; Lofthouse,R.; Ridley,R.M.; Shah,T.; Owen,F.; Collinge,J.; Brown,J.; Hardy,J.; Mullan,M.J.; Harding,A.E.; Bennett,C.; Doshi,R.; Crow,T.J. - Inherited prion disease with 144 base pair gene insertion. 1. Genealogical and molecular studies. - Brain: A Journal of Neurology 1992 Jun; 115(3): 675-85
ARVI - Ridley,R.M.; Baker,H.F.; Poulter,M.; Lofthouse,R.; Owen,F.; Collinge,J.; Crow,T.J. - Genetics of human transmissible dementia - Sub-Acute Spongiform Encephalopathies, edited by Ray Bradley, Marc Savey and Brian Marchant - Proceedings of a Seminar in the CEC Agricultural Research Programme, held in Brussels, 12-14 November 1990, 1991; 55: 203-18
AVRL - Rohrer,J.D.; Mead,S.; Omar,R.; Poulter,M.; Warren,J.D.; Collinge,J.; Rossor,M.N. - Prion protein (PRNP) genotypes in frontotemporal lobar degeneration syndromes - Annals of Neurology 2006 Nov; 60(5): 616; author reply 617