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 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 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 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 2009

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 2013

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 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 2015