Temporal Variant Frontotemporal Dementia Is Associated with Globular Glial Tauopathy

by Clark, Camilla N., Lashley, Tammaryn, Mahoney, Colin J., Warren, Jason D., Revesz, Tamas, Rohrer, Jonathan D.
Published 2015

Alterations in global DNA methylation and hydroxymethylation are not detected in Alzheimer's disease

by Lashley, Tammaryn, Gami, Priya, Valizadeh, Navid, Li, Abi, Revesz, Tamas, Balazs, Robert
Published 2015

C9orf72 frontotemporal lobar degeneration is characterised by frequent neuronal sense and antisense RNA foci

by Mizielinska, Sarah, Lashley, Tammaryn, Norona, Frances E., Clayton, Emma L., Ridler, Charlotte E., Fratta, Pietro, Isaacs, Adrian M.
Published 2013

Evaluating the relationship between amyloid-β and α-synuclein phosphorylated at Ser129 in dementia with Lewy bodies and Parkinson’s disease

by Swirski, Marta, Miners, J Scott, de Silva, Rohan, Lashley, Tammaryn, Ling, Helen, Holton, Janice, Revesz, Tamas, Love, Seth
Published 2014

A pathogenic progranulin mutation and C9orf72 repeat expansion in a family with frontotemporal dementia

by Lashley, Tammaryn, Rohrer, Jonathan D, Mahoney, Colin, Gordon, Elizabeth, Beck, Jon, Mead, Simon, Warren, Jason, Rossor, Martin, Revesz, Tamas
Published 2014

Neuropathological features of genetically confirmed DYT1 dystonia: investigating disease-specific inclusions

by Paudel, Reema, Kiely, Aoife, Li, Abi, Lashley, Tammaryn, Bandopadhyay, Rina, Hardy, John, Jinnah, Hyder A, Bhatia, Kailash, Houlden, Henry, Holton, Janice L
Published 2014

Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features

by Mahoney, Colin J., Beck, Jon, Rohrer, Jonathan D., Lashley, Tammaryn, Mok, Kin, Shakespeare, Tim, Yeatman, Tom, Warrington, Elizabeth K., Schott, Jonathan M., Fox, Nick C., Rossor, Martin N., Hardy, John, Collinge, John, Revesz, Tamas, Mead, Simon, Warren, Jason D.
Published 2012

The novel MAPT mutation K298E: mechanisms of mutant tau toxicity, brain pathology and tau expression in induced fibroblast-derived neurons

by Iovino, Mariangela, Pfisterer, Ulrich, Holton, Janice L., Lashley, Tammaryn, Swingler, Robert J., Calo, Laura, Treacy, Rebecca, Revesz, Tamas, Parmar, Malin, Goedert, Michel, Muqit, Miratul M. K., Spillantini, Maria Grazia
Published 2013

Widespread RNA metabolism impairment in sporadic inclusion body myositis TDP43-proteinopathy☆

by Cortese, Andrea, Plagnol, Vincent, Brady, Stefen, Simone, Roberto, Lashley, Tammaryn, Acevedo-Arozena, Abraham, de Silva, Rohan, Greensmith, Linda, Holton, Janice, Hanna, Michael G., Fisher, Elizabeth M.C., Fratta, Pietro
Published 2014

Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia

by Rohrer, Jonathan D, Beck, Jonathan, Plagnol, Vincent, Gordon, Elizabeth, Lashley, Tammaryn, Revesz, Tamas, Janssen, John C, Fox, Nick C, Warren, Jason D, Rossor, Martin N, Mead, Simon, Schott, Jonathan M
Published 2013

Qualitative changes in human γ-secretase underlie familial Alzheimer’s disease

by Szaruga, Maria, Veugelen, Sarah, Benurwar, Manasi, Lismont, Sam, Sepulveda-Falla, Diego, Lleo, Alberto, Ryan, Natalie S., Lashley, Tammaryn, Fox, Nick C., Murayama, Shigeo, Gijsen, Harrie, De Strooper, Bart, Chávez-Gutiérrez, Lucía
Published 2015

Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration

by Rohrer, Jonathan D., Lashley, Tammaryn, Schott, Jonathan M., Warren, Jane E., Mead, Simon, Isaacs, Adrian M., Beck, Jonathan, Hardy, John, de Silva, Rohan, Warrington, Elizabeth, Troakes, Claire, Al-Sarraj, Safa, King, Andrew, Borroni, Barbara, Clarkson, Matthew J., Ourselin, Sebastien, Holton, Janice L., Fox, Nick C., Revesz, Tamas, Rossor, Martin N., Warren, Jason D.
Published 2011

Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia

by 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
Published 2013

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

by 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.
Published 2015

Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseases

by Guerreiro, Rita, Escott-Price, Valentina, Darwent, Lee, Parkkinen, Laura, Ansorge, Olaf, Hernandez, Dena G., Nalls, Michael A., Clark, Lorraine, Honig, Lawrence, Marder, Karen, van der Flier, Wiesje, Holstege, Henne, Louwersheimer, Eva, Lemstra, Afina, Scheltens, Philip, Rogaeva, Ekaterina, St George-Hyslop, Peter, Londos, Elisabet, Zetterberg, Henrik, Ortega-Cubero, Sara, Pastor, Pau, Ferman, Tanis J., Graff-Radford, Neill R., Ross, Owen A., Barber, Imelda, Braae, Anne, Brown, Kristelle, Morgan, Kevin, Maetzler, Walter, Berg, Daniela, Troakes, Claire, Al-Sarraj, Safa, Lashley, Tammaryn, Compta, Yaroslau, Revesz, Tamas, Lees, Andrew, Cairns, Nigel J., Halliday, Glenda M., Mann, David, Pickering-Brown, Stuart, Powell, John, Lunnon, Katie, Lupton, Michelle K., Dickson, Dennis, Hardy, John, Singleton, Andrew, Bras, Jose
Published 2016

Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies

by Bras, Jose, Guerreiro, Rita, Darwent, Lee, Parkkinen, Laura, Ansorge, Olaf, Escott-Price, Valentina, Hernandez, Dena G., Nalls, Michael A., Clark, Lorraine N., Honig, Lawrence S., Marder, Karen, Van Der Flier, Wiesje M., Lemstra, Afina, Scheltens, Philip, Rogaeva, Ekaterina, St George-Hyslop, Peter, Londos, Elisabet, Zetterberg, Henrik, Ortega-Cubero, Sara, Pastor, Pau, Ferman, Tanis J., Graff-Radford, Neill R., Ross, Owen A., Barber, Imelda, Braae, Anne, Brown, Kristelle, Morgan, Kevin, Maetzler, Walter, Berg, Daniela, Troakes, Claire, Al-Sarraj, Safa, Lashley, Tammaryn, Compta, Yaroslau, Revesz, Tamas, Lees, Andrew, Cairns, Nigel, Halliday, Glenda M., Mann, David, Pickering-Brown, Stuart, Dickson, Dennis W., Singleton, Andrew, Hardy, John
Published 2014

Analysis of C9orf72 repeat expansions in a large international cohort of Dementia with Lewy Bodies

by Kun-Rodrigues, Celia, Ross, Owen A., Orme, Tatiana, Shepherd, Claire, Parkkinen, Laura, Darwent, Lee, Hernandez, Dena, Ansorge, Olaf, Clark, Lorraine N., Honig, Lawrence, Marder, Karen, Lemstra, Afina, Scheltens, Philip, Flier, Wiesje van der, Louwersheimer, Eva, Holstege, Henne, Rogaeva, Ekaterina, St. George-Hyslop, Peter, Londos, Elisabet, Zetterberg, Henrik, Barber, Imelda S., Braae, Anne, Brown, Kristelle, Morgan, Kevin, Maetzler, Walter, Berg, Daniela, Troakes, C., Al-Sarraj, S., Lashley, Tammaryn, Holton, Janice, Compta, Yaroslau, Van Deerlin, Vivianna, Trojanowski, John Q., Serrano, Geidy E., Beach, Thomas G., Clarimon, Jordi, Lleo, Alberto, Morenas-Rodriguez, Estrella, Lesage, Suzanne, Galasko, Douglas, Masliah, Eliezer, Santana, Isabel, Diez, Monica, Pastor, Pau, Tienari, Pentti J., Myllykangas, Liisa, Oinas, Minna, Revesz, Tamas, Lees, Andrew, Boeve, Bradley F., Petersen, Ronald C., Ferman, Tanis J., Escott-Price, Valentina, Graff-Radford, Neill R., Cairns, Nigel, Morris, John C., Stone, David, Pickering-Brown, Stuart, Mann, David, Dickson, Dennis W., Halliday, Glenda M., Singleton, Andrew, Guerreiro, Rita, Bras, Jose
Published 2016