Mead S - Search Results

1

R47H TREM2 variant increases risk of typical early-onset Alzheimer's disease but not of prion or frontotemporal dementia.

Slattery CF, Beck JA, Harper L, Adamson G, Abdi Z, Uphill J, Campbell T, Druyeh R, Mahoney CJ, Rohrer JD, Kenny J, Lowe J, Leung KK, Barnes J, Clegg SL, Blair M, Nicholas JM, Guerreiro RJ, Rowe JB, Ponto C, Zerr I, Kretzschmar H, Gambetti P, Crutch SJ, Warren JD, Rossor MN, Fox NC, Collinge J, Schott JM, Mead S. Slattery CF, et al. Among authors: mead s. Alzheimers Dement. 2014 Nov;10(6):602-608.e4. doi: 10.1016/j.jalz.2014.05.1751. Epub 2014 Aug 23. Alzheimers Dement. 2014. PMID: 25160042 Free PMC article.

2

Examination of the human prion protein-like gene doppel for genetic susceptibility to sporadic and variant Creutzfeldt-Jakob disease.

Mead S, Beck J, Dickinson A, Fisher EM, Collinge J. Mead S, et al. Neurosci Lett. 2000 Aug 25;290(2):117-20. doi: 10.1016/s0304-3940(00)01319-7. Neurosci Lett. 2000. PMID: 10936691

3

Two-octapeptide repeat deletion of prion protein associated with rapidly progressive dementia.

Beck JA, Mead S, Campbell TA, Dickinson A, Wientjens DP, Croes EA, Van Duijn CM, Collinge J. Beck JA, et al. Among authors: mead s. Neurology. 2001 Jul 24;57(2):354-6. doi: 10.1212/wnl.57.2.354. Neurology. 2001. PMID: 11468331

4

Sporadic--but not variant--Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon 1.

Mead S, Mahal SP, Beck J, Campbell T, Farrall M, Fisher E, Collinge J. Mead S, et al. Am J Hum Genet. 2001 Dec;69(6):1225-35. doi: 10.1086/324710. Epub 2001 Nov 5. Am J Hum Genet. 2001. PMID: 11704923 Free PMC article.

5

Phenotypic variability in the brains of a family with a prion disease characterized by a 144-base pair insertion in the prion protein gene.

King A, Doey L, Rossor M, Mead S, Collinge J, Lantos P. King A, et al. Among authors: mead s. Neuropathol Appl Neurobiol. 2003 Apr;29(2):98-105. doi: 10.1046/j.1365-2990.2003.00423.x. Neuropathol Appl Neurobiol. 2003. PMID: 12662318

6

Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemics.

Mead S, Stumpf MP, Whitfield J, Beck JA, Poulter M, Campbell T, Uphill JB, Goldstein D, Alpers M, Fisher EM, Collinge J. Mead S, et al. Science. 2003 Apr 25;300(5619):640-3. doi: 10.1126/science.1083320. Epub 2003 Apr 10. Science. 2003. PMID: 12690204

7

Questionnaire to reduce the risk of iatrogenic prion disease transmission.

Mead S, Prout K, Collinge J. Mead S, et al. J Hosp Infect. 2005 Aug;60(4):378-9. doi: 10.1016/j.jhin.2005.02.003. J Hosp Infect. 2005. PMID: 15939508 No abstract available.

8

Prion disease genetics.

Mead S. Mead S. Eur J Hum Genet. 2006 Mar;14(3):273-81. doi: 10.1038/sj.ejhg.5201544. Eur J Hum Genet. 2006. PMID: 16391566 Review.

9

Kuru in the 21st century--an acquired human prion disease with very long incubation periods.

Collinge J, Whitfield J, McKintosh E, Beck J, Mead S, Thomas DJ, Alpers MP. Collinge J, et al. Among authors: mead s. Lancet. 2006 Jun 24;367(9528):2068-74. doi: 10.1016/S0140-6736(06)68930-7. Lancet. 2006. PMID: 16798390

10

Inherited prion disease with six octapeptide repeat insertional mutation--molecular analysis of phenotypic heterogeneity.

Mead S, Poulter M, Beck J, Webb TE, Campbell TA, Linehan JM, Desbruslais M, Joiner S, Wadsworth JD, King A, Lantos P, Collinge J. Mead S, et al. Brain. 2006 Sep;129(Pt 9):2297-317. doi: 10.1093/brain/awl226. Brain. 2006. PMID: 16923955

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