Extent of MGMT promoter methylation correlates with outcome in glioblastomas given temozolomide and radiotherapy von Dunn, J, Baborie, A, Alam, F, Joyce, K, Moxham, M, Sibson, R, Crooks, D, Husband, D, Shenoy, A, Brodbelt, A, Wong, H, Liloglou, T, Haylock, B, Walker, C

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Biology, genetics and imaging of glial cell tumours von Walker, C, Baborie, A, Crooks, D, Wilkins, S, Jenkinson, M D

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Nuclear carrier and RNA-binding proteins in frontotemporal lobar degeneration associated with fused in sarcoma (FUS) pathological changes von Davidson, Y. S., Robinson, A. C., Hu, Q., Mishra, M., Baborie, A., Jaros, E., Perry, R. H., Cairns, N. J., Richardson, A., Gerhard, A., Neary, D., Snowden, J. S., Bigio, E. H., Mann, D. M. A.

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G330(P) Brain biopsy in children being investigated for undiagnosed neurological conditions von Singh, A, Iyer, A, Burn, S, Malluci, C, Appleton, RE, Splinty, S, Baborie, A, Kneen, R

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What's in a name? Neuronal intermediate filament inclusion disease (NIFID), frontotemporal lobar degeneration-intermediate filament (FTLD-IF) or frontotemporal lobar degeneration-f... von Menon, R, Baborie, A, Jaros, E, Mann, D M A, Ray, P S, Larner, A J

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Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia von Swarup, Vivek, Hinz, Flora I., Rexach, Jessica E., Noguchi, Ken-ichi, Toyoshiba, Hiroyoshi, Oda, Akira, Hirai, Keisuke, Sarkar, Arjun, Seyfried, Nicholas T., Cheng, Chialin, Haggarty, Stephen J., Grossman, Murray, Van Deerlin, Vivianna M., Trojanowski, John Q., Lah, James J., Levey, Allan I., Kondou, Shinichi, Geschwind, Daniel H.

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Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies von Broce, Iris, Karch, Celeste M, Wen, Natalie, Fan, Chun C, Wang, Yunpeng, Tan, Chin Hong, Kouri, Naomi, Ross, Owen A, Höglinger, Günter U, Muller, Ulrich, Hardy, John, Momeni, Parastoo, Hess, Christopher P, Dillon, William P, Miller, Zachary A, Bonham, Luke W, Rabinovici, Gil D, Rosen, Howard J, Schellenberg, Gerard D, Franke, Andre, Karlsen, Tom H, Veldink, Jan H, Ferrari, Raffaele, Yokoyama, Jennifer S, Miller, Bruce L, Andreassen, Ole A, Dale, Anders M, Desikan, Rahul S, Sugrue, Leo P

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Significant Benefits of AIP Testing and Clinical Screening in Familial Isolated and Young-onset Pituitary Tumors von Marques, Pedro, Caimari, Francisca, Hernández-Ramírez, Laura C, Collier, David, Iacovazzo, Donato, Ronaldson, Amy, Magid, Kesson, Lim, Chung Thong, Stals, Karen, Ellard, Sian, Grossman, Ashley B, Korbonits, Márta

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Prioritization of Drug Targets for Neurodegenerative Diseases by Integrating Genetic and Proteomic Data From Brain and Blood von Ge, Yi-Jun, Zhang, Ya-Ru, Huang, Yu-Yuan, Dong, Qiang, Tan, Lan, Ferrari, Raffaele, Ramasamy, Adaikalavan, Kwok, John B.J., Dobson-Stone, Carol, Schofield, Peter R., Halliday, Glenda M., Piguet, Olivier, Bartley, Lauren, Thompson, Elizabeth, Haan, Eric, Hernández, Isabel, Ruiz, Agustín, Boada, Mercè, Cruchaga, Carlos, Benussi, Luisa, Galimberti, Daniela, Fenoglio, Chiara, Scarpini, Elio, Lleó, Alberto, Nilsson, Karin, Mackenzie, Ian R.A., Hsiung, Ging-Yuek R., Mann, David M.A., Morris, Christopher M., Attems, Johannes, Thomas, Alan J., Pietrini, P., Huey, Edward D., Tierney, Michael C., Pastor, Pau, Razquin, Cristina, Ortega-Cubero, Sara, Perneczky, Robert, Diehl-Schmid, Janine, Alexopoulos, Panagiotis, Kurz, Alexander, Rainero, Innocenzo, Rogaeva, Ekaterina, Rossi, Giacomina, Rowe, James B., Schlachetzki, Johannes C.M., Uphill, James, Collinge, John, Mead, Simon, Danek, Adrian, Van Langenhove, Tim, Cappa, Stefano F., Hannequin, Didier, Vercelletto, Martine, Brice, Alexis, Nacmias, Benedetta, Bagnoli, Silvia, Nielsen, Jørgen E., Ibach, Bernd, Gasparoni, Gilles, Gu, Wei, Warren, Jason D., Spillantini, Maria Grazia, Morris, Huw R., Snowden, Julie S., Rollinson, Sara, Richardson, Anna, Gerhard, Alexander, Bruni, Amalia C., Maletta, Raffaele, Cupidi, Chiara, Gallo, Maura, Smirne, Nicoletta, Rademakers, Rosa, Baker, Matt, Dickson, Dennis W., Petersen, Ronald C., Knopman, David, Boeve, Bradley F., Parisi, Joseph E., Seeley, William W., Miller, Bruce L., Karydas, Anna M., van Swieten, John C., Seelaar, Harro, Pijnenburg, Yolande A.L., Logroscino, Giancarlo, Capozzo, Rosa, Puca, Annibale A., Franceschi, Massimo, Postiglione, Alfredo, Sorrentino, Paolo, Kristiansen, Mark, Chiang, Huei-Hsin, Graff, Caroline, Rollin, Adeline, Lebert, Florence, Kapogiannis, Dimitrios, Ferrucci, Luigi, Hardy, John

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A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers von Zhang, Ming, Ferrari, Raffaele, Tartaglia, Maria Carmela, Keith, Julia, Surace, Ezequiel I, Wolf, Uri, Sato, Christine, Grinberg, Mark, Liang, Yan, Xi, Zhengrui, Dupont, Kyle, McGoldrick, Philip, Weichert, Anna, McKeever, Paul M, Schneider, Raphael, McCorkindale, Michael D, Manzoni, Claudia, Rademakers, Rosa, Graff-Radford, Neill R, Dickson, Dennis W, Parisi, Joseph E, Boeve, Bradley F, Petersen, Ronald C, Miller, Bruce L, Seeley, William W, van Swieten, John C, van Rooij, Jeroen, Pijnenburg, Yolande, van der Zee, Julie, Van Broeckhoven, Christine, Le Ber, Isabelle, Van Deerlin, Vivianna, Suh, EunRan, Rohrer, Jonathan D, Mead, Simon, Graff, Caroline, Öijerstedt, Linn, Pickering-Brown, Stuart, Rollinson, Sara, Rossi, Giacomina, Tagliavini, Fabrizio, Brooks, William S, Dobson-Stone, Carol, Halliday, Glenda M, Hodges, John R, Piguet, Olivier, Binetti, Giuliano, Benussi, Luisa, Ghidoni, Roberta, Nacmias, Benedetta, Sorbi, Sandro, Bruni, Amalia C, Galimberti, Daniela, Scarpini, Elio, Rainero, Innocenzo, Rubino, Elisa, Clarimon, Jordi, Lleó, Alberto, Ruiz, Agustin, Hernández, Isabel, Pastor, Pau, Diez-Fairen, Monica, Borroni, Barbara, Pasquier, Florence, Deramecourt, Vincent, Lebouvier, Thibaud, Perneczky, Robert, Diehl-Schmid, Janine, Grafman, Jordan, Huey, Edward D, Mayeux, Richard, Nalls, Michael A, Hernandez, Dena, Singleton, Andrew, Momeni, Parastoo, Zeng, Zhen, Hardy, John, Robertson, Janice, Zinman, Lorne, Rogaeva, Ekaterina

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Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes von Reus, Lianne M., Pasaniuc, Bogdan, Posthuma, Danielle, Boltz, Toni, Ferrari, Raffaele, Hernandez, Dena G., Nalls, Michael A., Rohrer, Jonathan D., Ramasamy, Adaikalavan, Brooks, William S., Halliday, Glenda M., Piguet, Olivier, Bartley, Lauren, Hernández, Isabel, Ruiz, Agustín, Boada, Mercè, Borroni, Barbara, Padovani, Alessandro, Cruchaga, Carlos, Cairns, Nigel J., Benussi, Luisa, Ghidoni, Roberta, Forloni, Gianluigi, Galimberti, Daniela, Fenoglio, Chiara, Scarpini, Elio, Blesa, Rafael, Mackenzie, Ian R.A., Hsiung, Ging-Yuek R., Mann, David M.A., Attems, Johannes, Thomas, Alan J., Huey, Edward D., Tierney, Michael C., Razquin, Cristina, Ortega-Cubero, Sara, Alonso, Elena, Perneczky, Robert, Diehl-Schmid, Janine, Alexopoulos, Panagiotis, Rubino, Elisa, Rogaeva, Ekaterina, St. George-Hyslop, Peter, Rossi, Giacomina, Rowe, James B., Schlachetzki, Johannes C.M., Uphill, James, Collinge, John, Danek, Adrian, Van Deerlin, Vivianna M., Trojanowski, John Q., van der Zee, Julie, Cappa, Stefano F., Hannequin, Didier, Brice, Alexis, Nacmias, Benedetta, Sorbi, Sandro, Bagnoli, Silvia, Piaceri, Irene, Nielsen, Jørgen E., Hjermind, Lena E., Riemenschneider, Matthias, Ibach, Bernd, Gasparoni, Gilles, Pichler, Sabrina, Warren, Jason D., Morris, Huw R., Heutink, Peter, Snowden, Julie S., Rollinson, Sara, Gerhard, Alexander, Bruni, Amalia C., Frangipane, Francesca, Cupidi, Chiara, Anfossi, Maria, Gallo, Maura, Smirne, Nicoletta, Rademakers, Rosa, Dickson, Dennis W., Graff-Radford, Neill R., Petersen, Ronald C., Josephs, Keith A., Boeve, Bradley F., Parisi, Joseph E., Seeley, William W., Pijnenburg, Yolande A.L., Scheltens, Philip, Puca, Annibale A., Postiglione, Alfredo, Milan, Graziella, Sorrentino, Paolo, Kristiansen, Mark, Chiang, Huei-Hsin, Graff, Caroline, Kapogiannis, Dimitrios, Ferrucci, Luigi, Pickering-Brown, Stuart, Singleton, Andrew B., Pijnenburg, Yolande A.L., Ophoff, Roel A.

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Corrigendum to: A novel radiological appearance of meningeal extranodal marginal-zone B-cell lymphoma [ 63 (1) 97–100] von Butteriss, D, Lewis, J, Baborie, A, Soh, C

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Frontotemporal lobar degeneration in a very young patient is associated with fused in sarcoma (FUS) pathological changes von Baborie, A., Jaros, E., Griffiths, T. D., Momeni, P., Perry, R., Mann, D. M. A.

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Gene-based association studies report genetic links for clinical subtypes of frontotemporal dementia von Mishra, Aniket, Ferrari, Raffaele, Heutink, Peter, Hardy, John, Pijnenburg, Yolande, Posthuma, Danielle

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CXCR4 involvement in neurodegenerative diseases von Bonham, Luke W., Karch, Celeste M., Fan, Chun C., Tan, Chin, Geier, Ethan G., Wang, Yunpeng, Wen, Natalie, Broce, Iris J., Li, Yi, Barkovich, Matthew J., Ferrari, Raffaele, Hardy, John, Momeni, Parastoo, Höglinger, Günter, Müller, Ulrich, Hess, Christopher P., Sugrue, Leo P., Dillon, William P., Schellenberg, Gerard D., Miller, Bruce L., Andreassen, Ole A., Dale, Anders M., Barkovich, A. James, Yokoyama, Jennifer S., Desikan, Rahul S.

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Frontotemporal dementia and its subtypes: a genome-wide association study von Hernandez, Dena G, MSc, Nalls, Michael A, PhD, Kwok, John B J, PhD, Dobson-Stone, Carol, PhD, Brooks, William S, MBBS, Schofield, Peter R, Prof, Halliday, Glenda M, Prof, Hodges, John R, Prof, Piguet, Olivier, PhD, Bartley, Lauren, MSc, Thompson, Elizabeth, MD, Haan, Eric, Prof, Ruiz, Agustín, MD, Boada, Mercè, MD, Borroni, Barbara, MD, Cruchaga, Carlos, PhD, Benussi, Luisa, PhD, Galimberti, Daniela, PhD, Fenoglio, Chiara, PhD, Serpente, Maria, PhD, Scarpini, Elio, MD, Lleó, Alberto, MD, Waldö, Maria Landqvist, MD, Nilsson, Karin, PhD, Hsiung, Ging-Yuek R, MD, Mann, David M A, Prof, Morris, Christopher M, PhD, Attems, Johannes, Prof, Griffiths, Timothy D, Prof, McKeith, Ian G, Prof, Thomas, Alan J, Prof, Huey, Edward D, MD, Jaros, Evelyn, PhD, Pastor, Pau, MD, Razquin, Cristina, PhD, Ortega-Cubero, Sara, MD, Alonso, Elena, BSc, Perneczky, Robert, MD, Alexopoulos, Panagiotis, MD, Kurz, Alexander, MD, Rubino, Elisa, MD, Pinessi, Lorenzo, Prof, St George-Hyslop, Peter, MD, Rowe, James B, PhD, Schlachetzki, Johannes C M, MD, Uphill, James, BSc, Mead, Simon, Prof, Danek, Adrian, MD, Van Deerlin, Vivianna M, PhD, van der Zee, Julie, PhD, Deschamps, William, MSc, Van Broeckhoven, Christine, Prof, Cappa, Stefano F, Prof, Le Ber, Isabelle, MD, Vercelletto, Martine, MD, Brice, Alexis, MD, Nacmias, Benedetta, PhD, Piaceri, Irene, PhD, Nielsen, Jørgen E, MD, Hjermind, Lena E, MD, Riemenschneider, Matthias, Prof, Gasparoni, Gilles, PhD, Gu, Wei, PhD, Rossor, Martin N, Prof, Fox, Nick C, Prof, Morris, Huw R, Prof, Rizzu, Patrizia, PhD, Heutink, Peter, Prof, Snowden, Julie S, Prof, Rollinson, Sara, PhD, Richardson, Anna, MB, Bruni, Amalia C, MD, Maletta, Raffaele, MD, Frangipane, Francesca, MD, Bernardi, Livia, PhD, Anfossi, Maria, PhD, Gallo, Maura, PhD, Conidi, Maria Elena, PhD, Smirne, Nicoletta, BSc, Baker, Matt, BSc, Dickson, Dennis W, Prof, Petersen, Ronald C, Prof, Boeve, Bradley F, Prof, Seeley, William W, MD, Miller, Bruce L, Prof, Karydas, Anna M, BA, Rosen, Howard, Prof, van Swieten, John C, Prof, Scheltens, Philip, Prof, Capozzo, Rosa, MD, Franceschi, Massimo, MD, Postiglione, Alfredo, Prof, Chiang, Huei-Hsin, PhD, Graff, Caroline, Prof, Rollin, Adeline, MD, Deramecourt, Vincent, MD, Lebert, Florence, MD, Kapogiannis, Dimitrios, MD, Pickering-Brown, Stuart, Prof, Hardy, John, Prof

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Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype von Mackenzie, Ian R A, Baborie, Atik, Pickering-Brown, Stuart, Du Plessis, Daniel, Jaros, Evelyn, Perry, Robert H, Neary, David, Snowden, Julie S, Mann, David M A

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Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis von Gao, Yixin, Wang, Ting, Yu, Xinghao, Zhao, Huashuo, Zeng, Ping

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Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS von Taskesen, E., Mishra, A., van der Sluis, S., Ferrari, R., Veldink, J. H., van Es, M. A., Smit, A. B., Posthuma, D., Pijnenburg, Y.

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Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia von Bonham, Luke W., Steele, Natasha Z. R., Karch, Celeste M., Broce, Iris, Geier, Ethan G., Wen, Natalie L., Momeni, Parastoo, Hardy, John, Miller, Zachary A., Gorno-Tempini, Maria Luisa, Hess, Christopher P., Lewis, Patrick, Miller, Bruce L., Seeley, William W., Manzoni, Claudia, Desikan, Rahul S., Baranzini, Sergio E., Ferrari, Raffaele, Yokoyama, Jennifer S.

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