SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    Francesca Fontana, Kavitha Siva, Michela A. Denti, A network of RNA and protein interactions in Fronto Temporal Dementia, Frontiers in Molecular Neuroscience, 2015, 8,

    CrossRef

  2. 2
    Sara Rollinson, Janis Bennion Callister, Kate Young, Sarah J. Ryan, Ronald Druyeh, Jonathan D. Rohrer, Julie Snowden, Anna Richardson, Matt Jones, Jenny Harris, Yvonne Davidson, Andrew Robinson, John Ealing, Janel O. Johnson, Bryan Traynor, Simon Mead, David Mann, Stuart M. Pickering-Brown, A small deletion in C9orf72 hides a proportion of expansion carriers in FTLD, Neurobiology of Aging, 2015, 36, 3, 1601.e1

    CrossRef

  3. 3
    Jonathan D Rohrer, Adrian M Isaacs, Sarah Mizielinska, Simon Mead, Tammaryn Lashley, Selina Wray, Katie Sidle, Pietro Fratta, Richard W Orrell, John Hardy, Janice Holton, Tamas Revesz, Martin N Rossor, Jason D Warren, C9orf72 expansions in frontotemporal dementia and amyotrophic lateral sclerosis, The Lancet Neurology, 2015, 14, 3, 291

    CrossRef

  4. 4
    ZhanFang Sun, Hong Jiang, Bin Jiao, Xuan Hou, Lu Shen, Kun Xia, Beisha Tang, C9orf72 hexanucleotide expansion analysis in Chinese patients with multiple system atrophy, Parkinsonism & Related Disorders, 2015,

    CrossRef

  5. 5
    Serena Lattante, Sorana Ciura, Guy A. Rouleau, Edor Kabashi, Defining the genetic connection linking amyotrophic lateral sclerosis (ALS) with frontotemporal dementia (FTD), Trends in Genetics, 2015, 31, 5, 263

    CrossRef

  6. 6
    Sílvia Porta, Linda K. Kwong, John Q. Trojanowski, Virginia M.-Y. Lee, Drosha Inclusions Are New Components of Dipeptide-Repeat Protein Aggregates in FTLD-TDP and ALS C9orf72 Expansion Cases, Journal of Neuropathology & Experimental Neurology, 2015, 74, 4, 380

    CrossRef

  7. 7
    Elise Cuyvers, Julie van der Zee, Karolien Bettens, Sebastiaan Engelborghs, Mathieu Vandenbulcke, Caroline Robberecht, Lubina Dillen, Céline Merlin, Nathalie Geerts, Caroline Graff, Håkan Thonberg, Huei-Hsin Chiang, Pau Pastor, Sara Ortega-Cubero, Maria A. Pastor, Janine Diehl-Schmid, Panagiotis Alexopoulos, Luisa Benussi, Roberta Ghidoni, Giuliano Binetti, Benedetta Nacmias, Sandro Sorbi, Raquel Sanchez-Valle, Albert Lladó, Ellen Gelpi, Maria Rosário Almeida, Isabel Santana, Jordi Clarimon, Alberto Lleó, Juan Fortea, Alexandre de Mendonça, Madalena Martins, Barbara Borroni, Alessandro Padovani, Radoslav Matěj, Zdenek Rohan, Agustín Ruiz, Giovanni B. Frisoni, Gian Maria Fabrizi, Rik Vandenberghe, Peter P. De Deyn, Christine Van Broeckhoven, Kristel Sleegers, Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia: a European early-onset dementia consortium study, Neurobiology of Aging, 2015,

    CrossRef

  8. 8
    Beata Ferencz, Lotte Gerritsen, Genetics and Underlying Pathology of Dementia, Neuropsychology Review, 2015, 25, 1, 113

    CrossRef

  9. 9
    Emma Devenney, Steve Vucic, John R Hodges, Matthew C Kiernan, Motor neuron disease-frontotemporal dementia: a clinical continuum, Expert Review of Neurotherapeutics, 2015, 1

    CrossRef

  10. 10
    Johnathan Cooper-Knock, Janine Kirby, Robin Highley, Pamela J. Shaw, The Spectrum of C9orf72-mediated Neurodegeneration and Amyotrophic Lateral Sclerosis, Neurotherapeutics, 2015, 12, 2, 326

    CrossRef

  11. 11
    C. Akimoto, A. E. Volk, M. van Blitterswijk, M. Van den Broeck, C. S. Leblond, S. Lumbroso, W. Camu, B. Neitzel, O. Onodera, W. van Rheenen, S. Pinto, M. Weber, B. Smith, M. Proven, K. Talbot, P. Keagle, A. Chesi, A. Ratti, J. van der Zee, H. Alstermark, A. Birve, D. Calini, A. Nordin, D. C. Tradowsky, W. Just, H. Daoud, S. Angerbauer, M. DeJesus-Hernandez, T. Konno, A. Lloyd-Jani, M. de Carvalho, K. Mouzat, J. E. Landers, J. H. Veldink, V. Silani, A. D. Gitler, C. E. Shaw, G. A. Rouleau, L. H. van den Berg, C. Van Broeckhoven, R. Rademakers, P. M. Andersen, C. Kubisch, A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories, Journal of Medical Genetics, 2014, 51, 6, 419

    CrossRef

  12. 12
    Karen Nuytemans, Vanessa Inchausti, Gary W. Beecham, Liyong Wang, Dennis W. Dickson, John Q. Trojanowski, Virginia M.-Y. Lee, Deborah C. Mash, Matthew P. Frosch, Tatiana M. Foroud, Lawrence S. Honig, Thomas J. Montine, Ted M. Dawson, Eden R. Martin, William K. Scott, Jeffery M. Vance, Absence of C9ORF72 expanded or intermediate repeats in autopsy-confirmed Parkinson's disease, Movement Disorders, 2014, 29, 6
  13. 13
    Stephanie May, Daniel Hornburg, Martin H. Schludi, Thomas Arzberger, Kristin Rentzsch, Benjamin M. Schwenk, Friedrich A. Grässer, Kohji Mori, Elisabeth Kremmer, Julia Banzhaf-Strathmann, Matthias Mann, Felix Meissner, Dieter Edbauer, C9orf72 FTLD/ALS-associated Gly-Ala dipeptide repeat proteins cause neuronal toxicity and Unc119 sequestration, Acta Neuropathologica, 2014, 128, 4, 485

    CrossRef

  14. 14
    Ying Liu, Jin-Tai Yu, Yu Zong, Jing Zhou, Lan Tan, C9ORF72 Mutations in Neurodegenerative Diseases, Molecular Neurobiology, 2014, 49, 1, 386

    CrossRef

  15. 15
    Peter Heutink, Iris E. Jansen, Emily M. Lynes, C9orf72; abnormal RNA expression is the key, Experimental Neurology, 2014, 262, 102

    CrossRef

  16. 16
    O. Dols-Icardo, A. Garcia-Redondo, R. Rojas-Garcia, R. Sanchez-Valle, A. Noguera, E. Gomez-Tortosa, P. Pastor, I. Hernandez, J. Esteban-Perez, M. Suarez-Calvet, S. Anton-Aguirre, G. Amer, S. Ortega-Cubero, R. Blesa, J. Fortea, D. Alcolea, A. Capdevila, A. Antonell, A. Llado, J. L. Munoz-Blanco, J. S. Mora, L. Galan-Davila, F. J. Rodriguez De Rivera, A. Lleo, J. Clarimon, Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementia, Human Molecular Genetics, 2014, 23, 3, 749

    CrossRef

  17. 17
    Julie van der Zee, Christine Van Broeckhoven, Dementia in 2013: Frontotemporal lobar degeneration—building on breakthroughs, Nature Reviews Neurology, 2014, 10, 2, 70

    CrossRef

  18. 18
    Raffaele Ferrari, Dena G Hernandez, Michael A Nalls, Jonathan D Rohrer, Adaikalavan Ramasamy, John B J Kwok, Carol Dobson-Stone, William S Brooks, Peter R Schofield, Glenda M Halliday, John R Hodges, Olivier Piguet, Lauren Bartley, Elizabeth Thompson, Eric Haan, Isabel Hernández, Agustín Ruiz, Mercè Boada, Barbara Borroni, Alessandro Padovani, Carlos Cruchaga, Nigel J Cairns, Luisa Benussi, Giuliano Binetti, Roberta Ghidoni, Gianluigi Forloni, Daniela Galimberti, Chiara Fenoglio, Maria Serpente, Elio Scarpini, Jordi Clarimón, Alberto Lleó, Rafael Blesa, Maria Landqvist Waldö, Karin Nilsson, Christer Nilsson, Ian R A Mackenzie, Ging-Yuek R Hsiung, David M A Mann, Jordan Grafman, Christopher M Morris, Johannes Attems, Timothy D Griffiths, Ian G McKeith, Alan J Thomas, P Pietrini, Edward D Huey, Eric M Wassermann, Atik Baborie, Evelyn Jaros, Michael C Tierney, Pau Pastor, Cristina Razquin, Sara Ortega-Cubero, Elena Alonso, Robert Perneczky, Janine Diehl-Schmid, Panagiotis Alexopoulos, Alexander Kurz, Innocenzo Rainero, Elisa Rubino, Lorenzo Pinessi, Ekaterina Rogaeva, Peter St George-Hyslop, Giacomina Rossi, Fabrizio Tagliavini, Giorgio Giaccone, James B Rowe, Johannes C M Schlachetzki, James Uphill, John Collinge, Simon Mead, Adrian Danek, Vivianna M Van Deerlin, Murray Grossman, John Q Trojanowski, Julie van der Zee, William Deschamps, Tim Van Langenhove, Marc Cruts, Christine Van Broeckhoven, Stefano F Cappa, Isabelle Le Ber, Didier Hannequin, Véronique Golfier, Martine Vercelletto, Alexis Brice, Benedetta Nacmias, Sandro Sorbi, Silvia Bagnoli, Irene Piaceri, Jørgen E Nielsen, Lena E Hjermind, Matthias Riemenschneider, Manuel Mayhaus, Bernd Ibach, Gilles Gasparoni, Sabrina Pichler, Wei Gu, Martin N Rossor, Nick C Fox, Jason D Warren, Maria Grazia Spillantini, Huw R Morris, Patrizia Rizzu, Peter Heutink, Julie S Snowden, Sara Rollinson, Anna Richardson, Alexander Gerhard, Amalia C Bruni, Raffaele Maletta, Francesca Frangipane, Chiara Cupidi, Livia Bernardi, Maria Anfossi, Maura Gallo, Maria Elena Conidi, Nicoletta Smirne, Rosa Rademakers, Matt Baker, Dennis W Dickson, Neill R Graff-Radford, Ronald C Petersen, David Knopman, Keith A Josephs, Bradley F Boeve, Joseph E Parisi, William W Seeley, Bruce L Miller, Anna M Karydas, Howard Rosen, John C van Swieten, Elise G P Dopper, Harro Seelaar, Yolande A L Pijnenburg, Philip Scheltens, Giancarlo Logroscino, Rosa Capozzo, Valeria Novelli, Annibale A Puca, Massimo Franceschi, Alfredo Postiglione, Graziella Milan, Paolo Sorrentino, Mark Kristiansen, Huei-Hsin Chiang, Caroline Graff, Florence Pasquier, Adeline Rollin, Vincent Deramecourt, Florence Lebert, Dimitrios Kapogiannis, Luigi Ferrucci, Stuart Pickering-Brown, Andrew B Singleton, John Hardy, Parastoo Momeni, Frontotemporal dementia and its subtypes: a genome-wide association study, The Lancet Neurology, 2014, 13, 7, 686

    CrossRef

  19. 19
    Alexander M. Beer, Johnathan Cooper-Knock, Adrian Higginbottom, J. Robin Highley, Stephen B. Wharton, Paul G. Ince, Antonio Milano, Ashley A. Jones, Ammar Al-Chalabi, Janine Kirby, Pamela J. Shaw, Intermediate length C9orf72 expansion in an ALS patient without classical C9orf72 neuropathology, Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 2014, 1

    CrossRef

  20. 20
    Susan Byrne, Mark Heverin, Marwa Elamin, Cathal Walsh, Orla Hardiman, Intermediate repeat expansion length in C9orf72 may be pathological in amyotrophic lateral sclerosis, Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 2014, 15, 1-2, 148

    CrossRef

  21. 21
    M. Suarez-Calvet, O. Dols-Icardo, A. Llado, R. Sanchez-Valle, I. Hernandez, G. Amer, S. Anton-Aguirre, D. Alcolea, J. Fortea, I. Ferrer, J. van der Zee, L. Dillen, C. Van Broeckhoven, J. L. Molinuevo, R. Blesa, J. Clarimon, A. Lleo, Plasma phosphorylated TDP-43 levels are elevated in patients with frontotemporal dementia carrying a C9orf72 repeat expansion or a GRN mutation, Journal of Neurology, Neurosurgery & Psychiatry, 2014, 85, 6, 684

    CrossRef

  22. 22
    Julie van der Zee, Tim Van Langenhove, Gabor G. Kovacs, Lubina Dillen, William Deschamps, Sebastiaan Engelborghs, Radoslav Matěj, Mathieu Vandenbulcke, Anne Sieben, Bart Dermaut, Katrien Smets, Philip Van Damme, Céline Merlin, Annelies Laureys, Marleen Van Den Broeck, Maria Mattheijssens, Karin Peeters, Luisa Benussi, Giuliano Binetti, Roberta Ghidoni, Barbara Borroni, Alessandro Padovani, Silvana Archetti, Pau Pastor, Cristina Razquin, Sara Ortega-Cubero, Isabel Hernández, Mercè Boada, Agustín Ruiz, Alexandre de Mendonça, Gabriel Miltenberger-Miltényi, Frederico Simões do Couto, Sandro Sorbi, Benedetta Nacmias, Silvia Bagnoli, Caroline Graff, Huei-Hsin Chiang, Håkan Thonberg, Robert Perneczky, Janine Diehl-Schmid, Panagiotis Alexopoulos, Giovanni B. Frisoni, Christian Bonvicini, Matthis Synofzik, Walter Maetzler, Jennifer Müller vom Hagen, Ludger Schöls, Tobias B. Haack, Tim M. Strom, Holger Prokisch, Oriol Dols-Icardo, Jordi Clarimón, Alberto Lleó, Isabel Santana, Maria Rosário Almeida, Beatriz Santiago, Michael T. Heneka, Frank Jessen, Alfredo Ramirez, Raquel Sanchez-Valle, Albert Llado, Ellen Gelpi, Stayko Sarafov, Ivailo Tournev, Albena Jordanova, Eva Parobkova, Gian Maria Fabrizi, Silvia Testi, Eric Salmon, Thomas Ströbel, Patrick Santens, Wim Robberecht, Peter De Jonghe, Jean-Jacques Martin, Patrick Cras, Rik Vandenberghe, Peter Paul De Deyn, Marc Cruts, Kristel Sleegers, Christine Van Broeckhoven, Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration, Acta Neuropathologica, 2014, 128, 3, 397

    CrossRef

  23. 23
    Hannah A. Pliner, David M. Mann, Bryan J. Traynor, Searching for Grendel: origin and global spread of the C9ORF72 repeat expansion, Acta Neuropathologica, 2014, 127, 3, 391

    CrossRef

  24. 24
    E. Gelpi, J. Zee, A. Turon Estrada, C. Van Broeckhoven, R. Sanchez-Valle, TARDBP mutation p.Ile383Val associated with semantic dementia and complex proteinopathy, Neuropathology and Applied Neurobiology, 2014, 40, 2
  25. 25
    Matthis Synofzik, Christoph Born, Axel Rominger, Nina Lummel, Ludger Schöls, Saskia Biskup, Cornelius Schüle, Ute Grasshoff, Thomas Klopstock, Christopher Adamczyk, Targeted high-throughput sequencing identifies a TARDBP mutation as a cause of early-onset FTD without motor neuron disease, Neurobiology of Aging, 2014, 35, 5, 1212.e1

    CrossRef

  26. 26
    Sabina Vatovec, Anja Kovanda, Boris Rogelj, Unconventional features of C9ORF72 expanded repeat in amyotrophic lateral sclerosis and frontotemporal lobar degeneration, Neurobiology of Aging, 2014, 35, 10, 2421.e1

    CrossRef

  27. 27
    Kohji Mori, Thomas Arzberger, Friedrich A. Grässer, Ilse Gijselinck, Stephanie May, Kristin Rentzsch, Shih-Ming Weng, Martin H. Schludi, Julie van der Zee, Marc Cruts, Christine Van Broeckhoven, Elisabeth Kremmer, Hans A. Kretzschmar, Christian Haass, Dieter Edbauer, Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins, Acta Neuropathologica, 2013, 126, 6, 881

    CrossRef

  28. 28
    Rita Cacace, Caroline Van Cauwenberghe, Karolien Bettens, Ilse Gijselinck, Julie van der Zee, Sebastiaan Engelborghs, Mathieu Vandenbulcke, Jasper Van Dongen, Veerle Bäumer, Lubina Dillen, Maria Mattheijssens, Karin Peeters, Marc Cruts, Rik Vandenberghe, Peter P. De Deyn, Christine Van Broeckhoven, Kristel Sleegers, C9orf72 G4C2 repeat expansions in Alzheimer's disease and mild cognitive impairment, Neurobiology of Aging, 2013, 34, 6, 1712.e1

    CrossRef

  29. 29
    Karen Nuytemans, Güney Bademci, Martin M. Kohli, Gary W. Beecham, Liyong Wang, Juan I. Young, Fatta Nahab, Eden R. Martin, John R. Gilbert, Michael Benatar, Jonathan L. Haines, William K. Scott, Stephan Züchner, Margaret A. Pericak-Vance, Jeffery M. Vance, C9ORF72 Intermediate Repeat Copies Are a Significant Risk Factor for Parkinson Disease, Annals of Human Genetics, 2013, 77, 5
  30. 30
    Matthew B. Harms, Robert H. Baloh, Clinical Neurogenetics, Neurologic Clinics, 2013, 31, 4, 929

    CrossRef

  31. 31
    Marc Cruts, Ilse Gijselinck, Tim Van Langenhove, Julie van der Zee, Christine Van Broeckhoven, Current insights into the C9orf72 repeat expansion diseases of the FTLD/ALS spectrum, Trends in Neurosciences, 2013, 36, 8, 450

    CrossRef

  32. 32
    Barbara Borroni, Alessandro Padovani, Dementia: A new algorithm for molecular diagnostics in FTLD, Nature Reviews Neurology, 2013, 9, 5, 241

    CrossRef

  33. 33
    Ian R. Mackenzie, Thomas Arzberger, Elisabeth Kremmer, Dirk Troost, Stefan Lorenzl, Kohji Mori, Shih-Ming Weng, Christian Haass, Hans A. Kretzschmar, Dieter Edbauer, Manuela Neumann, Dipeptide repeat protein pathology in C9ORF72 mutation cases: clinico-pathological correlations, Acta Neuropathologica, 2013, 126, 6, 859

    CrossRef

  34. 34
    D. Seilhean, F. Bielle, I. Plu, C. Duyckaerts, Frontotemporal lobar degeneration: Diversity of FTLD lesions, Revue Neurologique, 2013, 169, 10, 786

    CrossRef

  35. 35
    J. Janssens, C. Van Broeckhoven, Pathological mechanisms underlying TDP-43 driven neurodegeneration in FTLD-ALS spectrum disorders, Human Molecular Genetics, 2013, 22, R1, R77

    CrossRef

  36. 36
    Julia Banzhaf-Strathmann, Rainer Claus, Oliver Mücke, Kristin Rentzsch, Julie van der Zee, Sebastiaan Engelborghs, Peter P De Deyn, Marc Cruts, Christine van Broeckhoven, Christoph Plass, Dieter Edbauer, Promoter DNA methylation regulates progranulin expression and is altered in FTLD, Acta Neuropathologica Communications, 2013, 1, 1, 16

    CrossRef

  37. 37
    Anna M. Blokhuis, Ewout J. N. Groen, Max Koppers, Leonard H. van den Berg, R. Jeroen Pasterkamp, Protein aggregation in amyotrophic lateral sclerosis, Acta Neuropathologica, 2013, 125, 6, 777

    CrossRef

  38. 38
    K. Mori, S.-M. Weng, T. Arzberger, S. May, K. Rentzsch, E. Kremmer, B. Schmid, H. A. Kretzschmar, M. Cruts, C. Van Broeckhoven, C. Haass, D. Edbauer, The C9orf72 GGGGCC Repeat Is Translated into Aggregating Dipeptide-Repeat Proteins in FTLD/ALS, Science, 2013, 339, 6125, 1335

    CrossRef

  39. 39
    Ying Liu, Jin-Tai Yu, Fu-Rong Sun, Jiang-Rong Ou, Song-Ben Qu, Lan Tan, The clinical and pathological phenotypes of frontotemporal dementia with C9ORF72 mutations, Journal of the Neurological Sciences, 2013, 335, 1-2, 26

    CrossRef

  40. 40
    Chiadi U. Onyike, Janine Diehl-Schmid, The epidemiology of frontotemporal dementia, International Review of Psychiatry, 2013, 25, 2, 130

    CrossRef