Mark Poulter
Queen Square
London, ENG, United Kingdom
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 10 publications
Rare structural genetic variation in human prion diseases.
Journal: Neurobiology of aging
Published: October 24, 2014
In vitro screen of prion disease susceptibility genes using the scrapie cell assay.
Journal: Human molecular genetics
Published: May 17, 2014
C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies.
Journal: Neurology
Published: December 24, 2013
Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale survey.
Journal: BMJ (Clinical research ed.)
Published: October 17, 2013
Validation of next-generation sequencing technologies in genetic diagnosis of dementia.
Journal: Neurobiology of aging
Published: June 03, 2013
Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia.
Journal: Acta neuropathologica
Published: May 11, 2013
Large C9orf72 hexanucleotide repeat expansions are seen in multiple neurodegenerative syndromes and are more frequent than expected in the UK population.
Journal: American journal of human genetics
Published: October 19, 2012
Overexpression of the Hspa13 (Stch) gene reduces prion disease incubation time in mice.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: August 08, 2012
Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.
Journal: Human molecular genetics
Published: January 03, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026