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Poulter, Mark
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1

Rare structural genetic variation in human prion diseases:

Lukic, Ana ; Uphill, James ; Brown, Craig A....
Neurobiology of Aging.  36 (2015)  5 - p. 2004.e1-2004.e8 , 2015
Link: https://doi.org/10.1016/..
 
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2

Screening a UK amyotrophic lateral sclerosis cohort provide..:

Fratta, Pietro ; Polke, James M. ; Newcombe, Jia...
Neurobiology of Aging.  36 (2015)  1 - p. 546.e1-546.e7 , 2015
Link: https://doi.org/10.1016/..
 
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3

Validation of next-generation sequencing technologies in ge..:

Beck, John ; Pittman, Alan ; Adamson, Gary...
Neurobiology of Aging.  35 (2014)  1 - p. 261-265 , 2014
Link: https://doi.org/10.1016/..
 
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4

C9orf72expansions are the most common genetic cause of Hunt..:

Hensman Moss, Davina J. ; Poulter, Mark ; Beck, Jon...
Neurology.  82 (2014)  4 - p. 292-299 , 2014
Link: https://doi.org/10.1212/..
 
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5

In vitro screen of prion disease susceptibility genes using..:

Brown, Craig A. ; Schmidt, Christian ; Poulter, Mark...
Human Molecular Genetics.  23 (2014)  19 - p. 5102-5108 , 2014
Link: https://doi.org/10.1093/..
 
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6

Prevalent abnormal prion protein in human appendixes after ..:

Gill, O Noel ; Spencer, Yvonne ; Richard-Loendt, Angela...
BMJ: British Medical Journal.  347 (2013)  7929 - p. 11 ff. , 2013
Link: https://www.jstor.org/st..
 
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7

P1–182: Validation of next‐generation sequencing technologi..:

Beck, Jon ; Adamson, Gary ; Campbell, Tracy...
Alzheimer's & Dementia.  9 (2013)  4S_Part_5 - p. , 2013
Link: https://doi.org/10.1016/..
 
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8

Homozygosity for the C9orf72 GGGGCC repeat expansion in fro..:

Fratta, Pietro ; Poulter, Mark ; Lashley, Tammaryn...
Acta Neuropathologica.  126 (2013)  3 - p. 401-409 , 2013
Link: https://doi.org/10.1007/..
 
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9

Overexpression of the Hspa13 (Stch) gene reduces prion dise..:

Grizenkova, Julia ; Akhtar, Shaheen ; Hummerich, Holger...
Proceedings of the National Academy of Sciences of the United States of America.  109 (2012)  34 - p. 13722-13727 , 2012
Link: https://www.jstor.org/st..
 
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10

Overexpression of theHspa13(Stch) gene reduces prion diseas..:

Grizenkova, Julia ; Akhtar, Shaheen ; Hummerich, Holger...
Proceedings of the National Academy of Sciences.  109 (2012)  34 - p. 13722-13727 , 2012
Link: https://doi.org/10.1073/..
 
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11

Duplication of amyloid precursor protein (APP), but not pri..:

McNaughton, Daniel ; Knight, William ; Guerreiro, Rita...
Neurobiology of Aging.  33 (2012)  2 - p. 426.e13-426.e21 , 2012
Link: https://doi.org/10.1016/..
 
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12

Inherited prion disease with 4-octapeptide repeat insertion..:

Kaski, Diego N. ; Pennington, Catherine ; Beck, Jon...
Brain.  134 (2011)  6 - p. 1829-1838 , 2011
Link: https://doi.org/10.1093/..
 
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13

Genome-wide association study in multiple human prion disea..:

Mead, Simon ; Uphill, James ; Beck, John...
Human Molecular Genetics.  21 (2011)  8 - p. 1897-1906 , 2011
Link: https://doi.org/10.1093/..
 
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14

PRNP allelic series from 19 years of prion protein gene seq..:

Beck, Jon A. ; Poulter, Mark ; Campbell, Tracy A....
Human Mutation.  31 (2010)  7 - p. E1551-E1563 , 2010
Link: https://doi.org/10.1002/..
 
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15

Genetic risk factors for variant Creutzfeldt–Jakob disease:..:

Mead, Simon ; Poulter, Mark ; Uphill, James...
The Lancet Neurology.  8 (2009)  1 - p. 57-66 , 2009
Link: https://doi.org/10.1016/..
 
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