A codon 129 polymorphism in the PRIP gene

Por Owen, Frank, Poulter, Mark, Collinge, John, Crow, Tim J.
Publicado em 1990

Lactase Haplotype Diversity in the Old World

Por Hollox, Edward J., Poulter, Mark, Zvarik, Marek, Ferak, Vladimir, Krause, Amanda, Jenkins, Trefor, Saha, Nilmani, Kozlov, Andrew I., Swallow, Dallas M.
Publicado em 2001

In vitro screen of prion disease susceptibility genes using the scrapie cell assay

Por Brown, Craig A., Schmidt, Christian, Poulter, Mark, Hummerich, Holger, Klöhn, Peter-C., Jat, Parmjit, Mead, Simon, Collinge, John, Lloyd, Sarah E.
Publicado em 2014

Genetic susceptibility, evolution and the kuru epidemic

Por Mead, Simon, Whitfield, Jerome, Poulter, Mark, Shah, Paresh, Uphill, James, Beck, Jonathan, Campbell, Tracy, Al-Dujaily, Huda, Hummerich, Holger, Alpers, Michael P., Collinge, John
Publicado em 2008

Duplication of amyloid precursor protein (APP), but not prion protein (PRNP) gene is a significant cause of early onset dementia in a large UK series

Por McNaughton, Daniel, Knight, William, Guerreiro, Rita, Ryan, Natalie, Lowe, Jessica, Poulter, Mark, Nicholl, David J., Hardy, John, Revesz, Tamas, Lowe, James, Rossor, Martin, Collinge, John, Mead, Simon
Publicado em 2012

Genetic risk factors for variant Creutzfeldt–Jakob disease: a genome-wide association study

Por Mead, Simon, Poulter, Mark, Uphill, James, Beck, John, Whitfield, Jerome, Webb, Thomas EF, Campbell, Tracy, Adamson, Gary, Deriziotis, Pelagia, Tabrizi, Sarah J, Hummerich, Holger, Verzilli, Claudio, Alpers, Michael P, Whittaker, John C, Collinge, John
Publicado em 2009

Overexpression of the Hspa13 (Stch) gene reduces prion disease incubation time in mice

Por Grizenkova, Julia, Akhtar, Shaheen, Hummerich, Holger, Tomlinson, Andrew, Asante, Emmanuel A., Wenborn, Adam, Fizet, Jérémie, Poulter, Mark, Wiseman, Frances K., Fisher, Elizabeth M. C., Tybulewicz, Victor L. J., Brandner, Sebastian, Collinge, John, Lloyd, Sarah E.
Publicado em 2012

C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies

Por Hensman Moss, Davina J., Poulter, Mark, Beck, Jon, Hehir, Jason, Polke, James M., Campbell, Tracy, Adamson, Garry, Mudanohwo, Ese, McColgan, Peter, Haworth, Andrea, Wild, Edward J., Sweeney, Mary G., Houlden, Henry, Mead, Simon, Tabrizi, Sarah J.
Publicado em 2014

Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale survey

Por Gill, O Noel, Spencer, Yvonne, Richard-Loendt, Angela, Kelly, Carole, Dabaghian, Reza, Boyes, Lynnette, Linehan, Jacqueline, Simmons, Marion, Webb, Paul, Bellerby, Peter, Andrews, Nick, Hilton, David A, Ironside, James W, Beck, Jon, Poulter, Mark, Mead, Simon, Brandner, Sebastian
Publicado em 2013

Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP

Por Mead, Simon, Uphill, James, Beck, John, Poulter, Mark, Campbell, Tracy, Lowe, Jessica, Adamson, Gary, Hummerich, Holger, Klopp, Norman, Rückert, Ina-Maria, Wichmann, H-Erich, Azazi, Dhoyazan, Plagnol, Vincent, Pako, Wandagi H., Whitfield, Jerome, Alpers, Michael P., Whittaker, John, Balding, David J., Zerr, Inga, Kretzschmar, Hans, Collinge, John
Publicado em 2012

Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia

Por Fratta, Pietro, Poulter, Mark, Lashley, Tammaryn, Rohrer, Jonathan D., Polke, James M., Beck, Jon, Ryan, Natalie, Hensman, Davina, Mizielinska, Sarah, Waite, Adrian J., Lai, Mang-Ching, Gendron, Tania F., Petrucelli, Leonard, Fisher, Elizabeth M. C., Revesz, Tamas, Warren, Jason D., Collinge, John, Isaacs, Adrian M., Mead, Simon
Publicado em 2013

Large C9orf72 Hexanucleotide Repeat Expansions Are Seen in Multiple Neurodegenerative Syndromes and Are More Frequent Than Expected in the UK Population

Por Beck, Jon, Poulter, Mark, Hensman, Davina, Rohrer, Jonathan D., Mahoney, Colin J., Adamson, Gary, Campbell, Tracy, Uphill, James, Borg, Aaron, Fratta, Pietro, Orrell, Richard W., Malaspina, Andrea, Rowe, James, Brown, Jeremy, Hodges, John, Sidle, Katie, Polke, James M., Houlden, Henry, Schott, Jonathan M., Fox, Nick C., Rossor, Martin N., Tabrizi, Sarah J., Isaacs, Adrian M., Hardy, John, Warren, Jason D., Collinge, John, Mead, Simon
Publicado em 2013

Screening a UK amyotrophic lateral sclerosis cohort provides evidence of multiple origins of the C9orf72 expansion()

Por Fratta, Pietro, Polke, James M., Newcombe, Jia, Mizielinska, Sarah, Lashley, Tammaryn, Poulter, Mark, Beck, Jon, Preza, Elisavet, Devoy, Anny, Sidle, Katie, Howard, Robin, Malaspina, Andrea, Orrell, Richard W., Clarke, Jan, Lu, Ching-Hua, Mok, Kin, Collins, Toby, Shoaii, Maryam, Nanji, Tina, Wray, Selina, Adamson, Gary, Pittman, Alan, Renton, Alan E., Traynor, Bryan J., Sweeney, Mary G., Revesz, Tamas, Houlden, Henry, Mead, Simon, Isaacs, Adrian M., Fisher, Elizabeth M.C.
Publicado no Neurobiol Aging (2015)