Mead S - Search Results

1

Large C9orf72 hexanucleotide repeat expansions are seen in multiple neurodegenerative syndromes and are more frequent than expected in the UK population.

Beck J, Poulter M, Hensman D, Rohrer JD, Mahoney CJ, Adamson G, Campbell T, Uphill J, Borg A, Fratta P, Orrell RW, Malaspina A, Rowe J, Brown J, Hodges J, Sidle K, Polke JM, Houlden H, Schott JM, Fox NC, Rossor MN, Tabrizi SJ, Isaacs AM, Hardy J, Warren JD, Collinge J, Mead S. Beck J, et al. Among authors: mead s. Am J Hum Genet. 2013 Mar 7;92(3):345-53. doi: 10.1016/j.ajhg.2013.01.011. Epub 2013 Feb 21. Am J Hum Genet. 2013. PMID: 23434116 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

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.

8

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

9

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

10

Prion protein (PRNP) genotypes in frontotemporal lobar degeneration syndromes.

Rohrer JD, Mead S, Omar R, Poulter M, Warren JD, Collinge J, Rossor MN. Rohrer JD, et al. Among authors: mead s. Ann Neurol. 2006 Nov;60(5):616. doi: 10.1002/ana.20931. Ann Neurol. 2006. PMID: 16969862 No abstract available.

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