Expression of C9orf72-related dipeptides impairs motor function in a vertebrate model
Swaminathan, Amrutha, Bouffard, Marilou, Liao, Meijiang, Ryan, Sarah, Callister, Janis Bennion, Pickering-Brown, Stuart M, Armstrong, Gary Alan Barclay, Drapeau, Pierre
Published in Human molecular genetics (15.05.2018)
Published in Human molecular genetics (15.05.2018)
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TDP-43 protein in plasma may index TDP-43 brain pathology in Alzheimer’s disease and frontotemporal lobar degeneration
Foulds, Penelope, McAuley, Erica, Gibbons, Linda, Davidson, Yvonne, Pickering-Brown, Stuart M., Neary, David, Snowden, Julie S., Allsop, David, Mann, David M. A.
Published in Acta neuropathologica (01.08.2008)
Published in Acta neuropathologica (01.08.2008)
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Analysis of the hexanucleotide repeat in C9ORF72 in Alzheimer's disease
Rollinson, Sara, Halliwell, Nicola, Young, Kate, Callister, Janis Bennion, Toulson, Greg, Gibbons, Linda, Davidson, Yvonne S, Robinson, Andrew C, Gerhard, Alex, Richardson, Anna, Neary, David, Snowden, Julie, Mann, David M.A, Pickering-Brown, Stuart M
Published in Neurobiology of aging (01.08.2012)
Published in Neurobiology of aging (01.08.2012)
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Pathogenesis/genetics of frontotemporal dementia and how it relates to ALS
Bennion Callister, Janis, Pickering-Brown, Stuart M.
Published in Experimental neurology (01.12.2014)
Published in Experimental neurology (01.12.2014)
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An immunohistochemical study of cases of sporadic and inherited frontotemporal lobar degeneration using 3R- and 4R-specific tau monoclonal antibodies
de Silva, Rohan, Lashley, Tammaryn, Strand, Catherine, Shiarli, Anna-Maria, Shi, Jing, Tian, Jinzhou, Bailey, Kathryn L, Davies, Peter, Bigio, Eileen H, Arima, Kunimasa, Iseki, Eizo, Murayama, Shigeo, Kretzschmar, Hans, Neumann, Manuela, Lippa, Carol, Halliday, Glenda, MacKenzie, James, Ravid, Rivka, Dickson, Dennis, Wszolek, Zbigniew, Iwatsubo, Takeshi, Pickering-Brown, Stuart M, Holton, Janice, Lees, Andrew, Revesz, Tamas, Mann, David M A
Published in Acta neuropathologica (01.04.2006)
Published in Acta neuropathologica (01.04.2006)
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Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degeneration
Rollinson, Sara, Rizzu, Patrizia, Sikkink, Stephen, Baker, Matthew, Halliwell, Nicola, Snowden, Julie, Traynor, Bryan J, Ruano, Dina, Cairns, Nigel, Rohrer, Jonathan D, Mead, Simon, Collinge, John, Rossor, Martin, Akay, Ela, Guerreiro, Rita, Rademakers, Rosa, Morrison, Karen E, Pastor, Pau, Alonso, Elena, Martinez-Lage, Pablo, Graff-Radford, Neil, Neary, David, Heutink, Peter, Mann, David M.A, Van Swieten, John, Pickering-Brown, Stuart M
Published in Neurobiology of aging (01.04.2009)
Published in Neurobiology of aging (01.04.2009)
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CRISPR/Cas9 does not facilitate stable expression of long C9orf72 dipeptides in mice
Ryan, Sarah, Hobbs, Eleanor, Rollinson, Sara, Pickering-Brown, Stuart M.
Published in Neurobiology of aging (01.12.2019)
Published in Neurobiology of aging (01.12.2019)
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Journal Article
Modelling C9orf72 dipeptide repeat proteins of a physiologically relevant size
Bennion Callister, Janis, Ryan, Sarah, Sim, Joan, Rollinson, Sara, Pickering-Brown, Stuart M
Published in Human molecular genetics (01.12.2016)
Published in Human molecular genetics (01.12.2016)
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Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations
SNOWDEN, Julie S, ROLLINSON, Sara, GIBBONS, Linda, QUAN HU, DUPLESSIS, Daniel, NEARY, David, MANN, David M. A, PICKERING-BROWN, Stuart M, THOMPSON, Jennifer C, HARRIS, Jennifer M, STOPFORD, Cheryl L, RICHARDSON, Anna M. T, JONES, Matthew, GERHARD, Alex, DAVIDSON, Yvonne S, ROBINSON, Andrew
Published in Brain (London, England : 1878) (01.03.2012)
Published in Brain (London, England : 1878) (01.03.2012)
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Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
Mackenzie, Ian R, Hutton, Mike, Baker, Matt, Pickering-Brown, Stuart M, Gass, Jennifer, Rademakers, Rosa, Lindholm, Caroline, Snowden, Julie, Adamson, Jennifer, Sadovnick, A. Dessa, Rollinson, Sara, Cannon, Ashley, Dwosh, Emily, Neary, David, Melquist, Stacey, Richardson, Anna, Dickson, Dennis, Berger, Zdenek, Eriksen, Jason, Robinson, Todd, Zehr, Cynthia, Dickey, Chad A, Crook, Richard, McGowan, Eileen, Mann, David, Boeve, Bradley, Feldman, Howard
Published in Nature (24.08.2006)
Published in Nature (24.08.2006)
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Extracellular Vesicles Isolated from Human Induced Pluripotent Stem Cell-Derived Neurons Contain a Transcriptional Network
Hicks, David A., Jones, Alys C., Corbett, Nicola J., Fisher, Kate, Pickering-Brown, Stuart M., Ashe, Mark P., Hooper, Nigel M.
Published in Neurochemical research (01.07.2020)
Published in Neurochemical research (01.07.2020)
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Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration
GASS, Jennifer, CANNON, Ashley, JOSEPHS, Keith, PICKERING-BROWN, Stuart M, GRAFF-RADFORD, Neill, UITTI, Ryan, DICKSON, Dennis, WSZOLEK, Zbigniew, GONZALEZ, John, BEACH, Thomas G, BIGIO, Eileen, JOHNSON, Nancy, MACKENZIE, Ian R, WEINTRAUB, Sandra, MESULAM, Marsel, WHITE, Charles L, WOODRUFF, Bryan, CASELLI, Richard, HSIUNG, Ging-Yuek, FELDMAN, Howard, KNOPMAN, Dave, HUTTON, Mike, RADEMAKERS, Rosa, BOEVE, Bradley, BAKER, Matt, ADAMSON, Jennifer, CROOK, Richard, MELQUIST, Stacey, KUNTZ, Karen, PETERSEN, Ron
Published in Human molecular genetics (15.10.2006)
Published in Human molecular genetics (15.10.2006)
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TDP-43 pathological changes in early onset familial and sporadic Alzheimer’s disease, late onset Alzheimer’s disease and Down’s Syndrome: association with age, hippocampal sclerosis and clinical phenotype
Davidson, Yvonne S., Raby, Samantha, Foulds, Penelope G., Robinson, Andrew, Thompson, Jennifer C., Sikkink, Stephen, Yusuf, Imran, Amin, Hanan, DuPlessis, Daniel, Troakes, Claire, Al-Sarraj, Safa, Sloan, Carolyn, Esiri, Margaret M., Prasher, Vee P., Allsop, David, Neary, David, Pickering-Brown, Stuart M., Snowden, Julie S., Mann, David M. A.
Published in Acta neuropathologica (01.12.2011)
Published in Acta neuropathologica (01.12.2011)
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Genetic risk factors for the posterior cortical atrophy variant of Alzheimer's disease
Schott, Jonathan M, Crutch, Sebastian J, Carrasquillo, Minerva M, Uphill, James, Shakespeare, Tim J, Ryan, Natalie S, Yong, Keir X, Lehmann, Manja, Ertekin-Taner, Nilufer, Graff-Radford, Neill R, Boeve, Bradley F, Murray, Melissa E, Khan, Qurat ul Ain, Petersen, Ronald C, Dickson, Dennis W, Knopman, David S, Rabinovici, Gil D, Miller, Bruce L, González, Aida Suárez, Gil-Néciga, Eulogio, Snowden, Julie S, Harris, Jenny, Pickering-Brown, Stuart M, Louwersheimer, Eva, van der Flier, Wiesje M, Scheltens, Philip, Pijnenburg, Yolande A, Galasko, Douglas, Sarazin, Marie, Dubois, Bruno, Magnin, Eloi, Galimberti, Daniela, Scarpini, Elio, Cappa, Stefano F, Hodges, John R, Halliday, Glenda M, Bartley, Lauren, Carrillo, Maria C, Bras, Jose T, Hardy, John, Rossor, Martin N, Collinge, John, Fox, Nick C, Mead, Simon
Published in Alzheimer's & dementia (01.08.2016)
Published in Alzheimer's & dementia (01.08.2016)
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Journal Article
FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration
Urwin, Hazel, Josephs, Keith A., Rohrer, Jonathan D., Mackenzie, Ian R., Neumann, Manuela, Authier, Astrid, Seelaar, Harro, Van Swieten, John C., Brown, Jeremy M., Johannsen, Peter, Nielsen, Jorgen E., Holm, Ida E., Dickson, Dennis W., Rademakers, Rosa, Graff-Radford, Neill R., Parisi, Joseph E., Petersen, Ronald C., Hatanpaa, Kimmo J., White III, Charles L., Weiner, Myron F., Geser, Felix, Van Deerlin, Vivianna M., Trojanowski, John Q., Miller, Bruce L., Seeley, William W., van der Zee, Julie, Kumar-Singh, Samir, Engelborghs, Sebastiaan, De Deyn, Peter P., Van Broeckhoven, Christine, Bigio, Eileen H., Deng, Han-Xiang, Halliday, Glenda M., Kril, Jillian J., Munoz, David G., Mann, David M., Pickering-Brown, Stuart M., Doodeman, Valerie, Adamson, Gary, Ghazi-Noori, Shabnam, Fisher, Elizabeth M. C., Holton, Janice L., Revesz, Tamas, Rossor, Martin N., Collinge, John, Mead, Simon, Isaacs, Adrian M.
Published in Acta neuropathologica (01.07.2010)
Published in Acta neuropathologica (01.07.2010)
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Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations
Pickering-Brown, Stuart M., Rollinson, Sara, Du Plessis, Daniel, Morrison, Karen E., Varma, Anoop, Richardson, Anna M. T., Neary, David, Snowden, Julie S., Mann, David M. A.
Published in Brain (London, England : 1878) (01.03.2008)
Published in Brain (London, England : 1878) (01.03.2008)
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The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene
Snowden, Julie S., Hu, Quan, Rollinson, Sara, Halliwell, Nicola, Robinson, Andrew, Davidson, Yvonne S., Momeni, Parastoo, Baborie, Atik, Griffiths, Timothy D., Jaros, Evelyn, Perry, Robert H., Richardson, Anna, Pickering-Brown, Stuart M., Neary, David, Mann, David M. A.
Published in Acta neuropathologica (01.07.2011)
Published in Acta neuropathologica (01.07.2011)
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