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Marc Cruts

Active 1991–2022

77
Papers
21,408
Citations
73
h-index
77
i10-index

Citations

Citations per year for Marc Cruts1991: 3 citations1992: 15 citations1993: 23 citations1994: 43 citations1995: 49 citations1996: 50 citations1997: 60 citations1998: 65 citations1999: 33 citations2000: 79 citations2001: 74 citations2002: 49 citations2003: 53 citations2004: 49 citations2005: 66 citations2006: 181 citations2007: 201 citations2008: 238 citations2009: 188 citations2010: 200 citations2011: 231 citations2012: 296 citations2013: 311 citations2014: 302 citations2015: 306 citations2016: 334 citations2017: 293 citations2018: 233 citations2019: 622 citations2020: 587 citations2021: 549 citations2022: 351 citations2023: 272 citations2024: 373 citations2025: 179 citations2026: 3 citations

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 2,447 citing papers, 29.8% of this breakdownUnited Kingdom: 758 citing papers, 9.2% of this breakdownGermany: 494 citing papers, 6% of this breakdownCanada: 382 citing papers, 4.7% of this breakdownItaly: 359 citing papers, 4.4% of this breakdownBelgium: 345 citing papers, 4.2% of this breakdownNetherlands: 323 citing papers, 3.9% of this breakdownChina: 312 citing papers, 3.8% of this breakdownFrance: 297 citing papers, 3.6% of this breakdownAustralia: 294 citing papers, 3.6% of this breakdownSpain: 225 citing papers, 2.8% of this breakdownJapan: 225 citing papers, 2.7% of this breakdown
0%29.8%Other 21.3%

Institutions

Fields

  • Medicine70.5%
  • Biochemistry, Genetics and Molecular Biology18.2%
  • Neuroscience8.8%
  • Immunology and Microbiology0.9%
  • Computer Science0.4%
  • Environmental Science0.3%
  • Other0.9%

Topics

  • Alzheimer's disease research and treatments14.1%
  • Amyotrophic Lateral Sclerosis Research11.3%
  • Parkinson's Disease Mechanisms and Treatments4.7%
  • Neurogenetic and Muscular Disorders Research4.6%
  • Dementia and Cognitive Impairment Research3.5%
  • Neuroinflammation and Neurodegeneration Mechanisms2.9%
  • Other58.9%

Coauthors

All papers

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  1. The C9orf72 GGGGCC Repeat Is Translated into Aggregating Dipeptide-Repeat Proteins in FTLD/ALS

    Authors: Kohji Mori, Shih‐Ming Weng, Thomas Arzberger, Stephanie May, Kristin Rentzsch, Elisabeth Kremmer, Bettina Schmid, Hans A. Kretzschmar, Marc Cruts, Christine Van Broeckhoven, Christian Haass, Dieter Edbauer - Science 2013 cited by 1,297

  2. Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

    Authors: Marc Cruts, Ilse Gijselinck, Julie van der Zee, Sebastiaan Engelborghs, Hans Wils, Daniel Pirici, Rosa Rademakers, Rik Vandenberghe, Bart Dermaut, Jean‐Jacques Martin, Cornelia M. van Duijn, Karin Peeters, Raf Sciot, Patrick Santens, Tim De Pooter, Maria Mattheijssens, Marleen Van den Broeck, Ivy Cuijt, Krist’l Vennekens, Peter Paul De Deyn, Samir Kumar‐Singh, Christine Van Broeckhoven - Nature 2006 cited by 1,542

  3. Frontotemporal dementia and its subtypes: a genome-wide association study

    Authors: Raffaele Ferrari, Dena G. Hernandez, Michael A. Nalls, Jonathan D. Rohrer, Adaikalavan Ramasamy, John B. 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, Agustı́n Ruiz, Merçé Boada, Barbara Borroni, Alessandro Padovani, Carlos Cruchaga, Nigel J. Cairns, Luisa Benussi, Giuliano Binetti, Roberta Ghidoni, Gianluigi Forloni, Daniela Galimberti, Chiara Fenoglio, María Serpente, Elio Scarpini, Jordi Clarimón, Alberto Lleó, Rafael Blesa, Maria Landqvist Waldö, Karin Nilsson, Christer Nilsson, Ian R. Mackenzie, Ging‐Yuek Robin Hsiung, David Mann, Jordan Grafman, Christopher M. Morris, Johannes Attems, Timothy D. Griffiths, Ian G. McKeith, Alan Thomas, Pietro Pietrini, Edward D. Huey, Eric M. Wassermann, Atik Baborie, Evelyn Jaros, Michael C Tierney, Pau Pástor, Cristina Razquín, 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 and 58 more - The Lancet Neurology 2014 cited by 402

  4. Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins

    Authors: 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 - Acta Neuropathologica 2013 cited by 497

  5. Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update

    Authors: Karen Nuytemans, Jessie Theuns, Marc Cruts, Christine Van Broeckhoven - Human Mutation 2010 cited by 555

  6. APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy

    Authors: Kristel Sleegers, Nathalie Brouwers, Ilse Gijselinck, Jessie Theuns, D. Goossens, J. Wauters, Jurgen Del‐Favero, Marc Cruts, Cornelia M. van Duijn, Christine Van Broeckhoven - Brain 2006 cited by 418

  7. hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutations

    Authors: Kohji Mori, Sven Lammich, Ian R. Mackenzie, Ignasi Forné, Sonja Zilow, Hans A. Kretzschmar, Dieter Edbauer, Jonathan Janssens, Gernot Kleinberger, Marc Cruts, Jochen Herms, Manuela Neumann, Christine Van Broeckhoven, Thomas Arzberger, Christian Haass - Acta Neuropathologica 2013 cited by 346

  8. Prioritization of Drug Targets for Neurodegenerative Diseases by Integrating Genetic and Proteomic Data From Brain and Blood

    Authors: Yi‐Jun Ge, Ya‐Nan Ou, Yue‐Ting Deng, Bang‐Sheng Wu, Yang Liu, Ya-Ru Zhang, Shi-Dong Chen, Yuyuan Huang, Qiang Dong, Lan Tan, Jin‐Tai Yu, Raffaele Ferrari, Dena Hernandez, Michael A. Nalls, Jonathan D. Rohrer, Adaikalavan Ramasamy, John B. 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, Agustı́n Ruiz, Merçé Boada, Barbara Borroni, Alessandro Padovani, Carlos Cruchaga, Nigel J. Cairns, Luisa Benussi, Giuliano Binetti, Roberta Ghidoni, Gianluigi Forloni, Daniela Galimberti, Chiara Fenoglio, María Serpente, Elio Scarpini, Jordi Clarimón, Alberto Lleó, Rafael Blesa, Maria Landqvist Waldö, Karin Nilsson, Christer Nilsson, Ian R. Mackenzie, Ging‐Yuek Robin Hsiung, David Mann, Jordan Grafman, Christopher M. Morris, Johannes Attems, Timothy D. Griffiths, Ian G. McKeith, Alan Thomas, Pietro Pietrini, Edward D. Huey, Eric M. Wassermann, Atik Baborie, Evelyn Jaros, Michael C. Tierney, Pau Pástor, Cristina Razquín, 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 and 69 more - Biological Psychiatry 2022 cited by 50

  9. A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study

    Authors: Ilse Gijselinck, Tim Van Langenhove, Julie van der Zee, Kristel Sleegers, Stéphanie Philtjens, Gernot Kleinberger, Jonathan Janssens, Karolien Bettens, Caroline Van Cauwenberghe, Sandra Pereson, Sebastiaan Engelborghs, Anne Sieben, Peter De Jonghe, Rik Vandenberghe, Patrick Santens, Jan De Bleecker, Githa Maes, Veerle Bäumer, Lubina Dillen, Geert Joris, Ivy Cuijt, Ellen Corsmit, Ellen Elinck, Jasper Van Dongen, Steven Vermeulen, Marleen Van den Broeck, C Vaerenberg, Maria Mattheijssens, Karin Peeters, Wim Robberecht, Patrick Cras, Jean‐Jacques Martin, Peter P. De Deyn, Marc Cruts, Christine Van Broeckhoven - The Lancet Neurology 2011 cited by 628

  10. The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter

    Authors: Ilse Gijselinck, Sara Van Mossevelde, Julie van der Zee, Anne Sieben, Sebastiaan Engelborghs, Jan De Bleecker, Adrian Ivanoiu, Olivier Deryck, Dieter Edbauer, M. Zhang, Bavo Heeman, Veerle Bäumer, Marleen Van den Broeck, Maria Mattheijssens, Karin Peeters, Ekaterina Rogaeva, Peter De Jonghe, Patrick Cras, J-J Martin, Peter P. De Deyn, Marc Cruts, Christine Van Broeckhoven - Molecular Psychiatry 2015 cited by 247

  11. Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b/C4b binding sites

    Authors: Nathalie Brouwers, Caroline Van Cauwenberghe, Sebastiaan Engelborghs, J-C Lambert, Karolien Bettens, Nathalie Le Bastard, Florence Pasquier, Ana Gil Montoya, Karin Peeters, Maria Mattheijssens, Rik Vandenberghe, Peter Paul De Deyn, Marc Cruts, Philippe Amouyel, Kristel Sleegers, Christine Van Broeckhoven - Molecular Psychiatry 2011 cited by 232

  12. Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia

    Authors: Vivek Swarup, Flora I. Hinz, Jessica E. Rexach, K Noguchi, Hiroyoshi Toyoshiba, Akira Oda, Keisuke Hirai, Arjun Sarkar, Nicholas T. Seyfried, Chialin Cheng, Stephen J. Haggarty, Raffaele Ferrari, Jonathan D. Rohrer, Adaikalavan Ramasamy, John Hardy, Dena Hernandez, Michael A. Nalls, Andrew Singleton, John B. 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, Agustı́n Ruiz, Merçé Boada, Barbara Borroni, Alessandro Padovani, Nigel J. Cairns, Carlos Cruchaga, Giuliano Binetti, Roberta Ghidoni, Luisa Benussi, Gianluigi Forloni, Diego Albani, Daniela Galimberti, Chiara Fenoglio, María Serpente, Elio Scarpini, Jordi Clarimón, Alberto Lleó, Rafael Blesa, Maria Landqvist Waldö, Karin Nilsson, Christer Nilsson, Ian R. Mackenzie, Ging‐Yuek Robin Hsiung, David M. A. Mann, Jordan Grafman, Christopher M. Morris, Johannes Attems, Timothy D. Griffiths, Ian G. McKeith, Alan Thomas, Evelyn Jaros, Pietro Pietrini, Edward D. Huey, Eric M. Wassermann, Michael C. Tierney, Atik Baborie, Pau Pástor, Sara Ortega‐Cubero, Cristina Razquín, 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, Stuart Pickering‐Brown, Parastoo Momeni, Julie van der Zee, Marc Cruts, Christine Van Broeckhoven, Stefano F. Cappa, Isabelle Leber, Alexis Brice, Didier Hannequin, Véronique Golfier and 74 more - Nature Medicine 2018 cited by 156

  13. TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort

    Authors: Julie van der Zee, Tim Van Langenhove, Gernot Kleinberger, Kristel Sleegers, Sebastiaan Engelborghs, Rik Vandenberghe, Patrick Santens, Marleen Van den Broeck, Geert Joris, J Bryś, Maria Mattheijssens, Karin Peeters, Patrick Cras, Peter P. De Deyn, Marc Cruts, Christine Van Broeckhoven - Brain 2011 cited by 129

  14. Loss of ALS-associated TDP-43 in zebrafish causes muscle degeneration, vascular dysfunction, and reduced motor neuron axon outgrowth

    Authors: Bettina Schmid, Alexander Hruscha, Sebastian Hogl, Julia Banzhaf‐Strathmann, Katrin Strecker, Julie van der Zee, Mathias Teucke, Stefan Eimer, Jan Hegermann, Maike Kittelmann, Elisabeth Kremmer, Marc Cruts, Barbara Solchenberger, Laura Hasenkamp, Frauke van Bebber, Christine Van Broeckhoven, Dieter Edbauer, Stefan F. Lichtenthaler, Christian Haass - National Academy of Sciences, Proceedings of the National Academy of Sciences 2013 cited by 177

  15. TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions

    Authors: Michael D. Gallagher, EunRan Suh, Murray Grossman, Lauren Elman, Leo McCluskey, John C. van Swieten, Safa Al‐Sarraj, Manuela Neumann, Ellen Gelpí, Bernardino Ghetti, Jonathan D. Rohrer, Glenda M. Halliday, Christine Van Broeckhoven, Danielle Seilhean, Pamela J. Shaw, Matthew P. Frosch, Irina Alafuzoff, Anna Antonell, Nenad Bogdanović, William S. Brooks, Nigel J. Cairns, Johnathan Cooper‐Knock, Carl W. Cotman, Patrick Cras, Marc Cruts, Peter Paul De Deyn, Charles DeCarli, Carol Dobson‐Stone, Sebastiaan Engelborghs, Nick C. Fox, Douglas Galasko, Marla Gearing, Ilse Gijselinck, Jordan Grafman, Päivi Hartikainen, Kimmo J. Hatanpaa, J. Robin Highley, John R. Hodges, Christine Hulette, Paul G. Ince, Lee‐Way Jin, Janine Kirby, Julia Kofler, Jillian J. Kril, John B. Kwok, Allan I. Levey, Andrew P. Lieberman, Albert Lladó, Jean‐Jacques Martin, Eliezer Masliah, Christopher McDermott, Ann C. McKee, Catriona McLean, Simon Mead, Carol A. Miller, Josh Miller, David G. Muñoz, Jill R. Murrell, Henry L. Paulson, Olivier Piguet, Martin N. Rossor, Raquel Sánchez‐Valle, Mary Sano, Julie A. Schneider, Lisa C. Silbert, Salvatore Spina, Julie van der Zee, Tim Van Langenhove, Jason D. Warren, Stephen B. Wharton, Charles L. White, Randall L. Woltjer, John Q. Trojanowski, Virginia M.‐Y. Lee, Vivianna M. Van Deerlin, Alice Chen‐Plotkin - Acta Neuropathologica 2014 cited by 153

  16. Genetic Association of Apolipoprotein E with Age-Related Macular Degeneration

    Authors: Caroline C. W. Klaver, Mike Kliffen, Cornelia M. van Duijn, Albert Hofman, Marc Cruts, Diederick E. Grobbee, Christine Van Broeckhoven, Paulus T.V.M. de Jong - The American Journal of Human Genetics 1998 cited by 492

  17. Mean age-of-onset of familial alzheimer disease caused by presenilin mutations correlates with both increased Aβ42 and decreased Aβ40

    Authors: Samir Kumar‐Singh, Jessie Theuns, Bianca Van Broeck, Daniel Pirici, Krist’l Vennekens, Ellen Corsmit, Marc Cruts, Bart Dermaut, Rong Wang, Christine Van Broeckhoven - Human Mutation 2006 cited by 325

  18. Drosophila screen connects nuclear transport genes to DPR pathology in c9ALS/FTD

    Authors: Steven Boeynaems, Elke Bogaert, Emiel Michiels, Ilse Gijselinck, Anne Sieben, Ana Jovičić, Greet De Baets, Wendy Scheveneels, Jolien Steyaert, Ivy Cuijt, Kevin J. Verstrepen, Patrick Callaerts, Frédéric Rousseau, Joost Schymkowitz, Marc Cruts, Christine Van Broeckhoven, Philip Van Damme, Aaron D. Gitler, Wim Robberecht, Ludo Van Den Bosch - Scientific Reports 2016 cited by 280

  19. A Pan‐European Study of theC9orf72Repeat Associated withFTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats

    Authors: Julie van der Zee, Ilse Gijselinck, Lubina Dillen, Tim Van Langenhove, Jessie Theuns, Sebastiaan Engelborghs, Stéphanie Philtjens, Mathieu Vandenbulcke, Kristel Sleegers, Anne Sieben, Veerle Bäumer, Githa Maes, Ellen Corsmit, Barbara Borroni, Alessandro Padovani, Silvana Archetti, Robert Perneczky, Janine Diehl‐Schmid, Alexandre de Mendonça, Gábriel Miltenberger-Miltényi, Sónia Pereira, José Pimentel, Benedetta Nacmias, Silvia Bagnoli, Sandro Sorbi, Caroline Graff, Huei‐Hsin Chiang, Marie Westerlund, Raquel Sánchez‐Valle, Albert Lladó, Ellen Gelpí, Isabel Santana, Maria Rosário Almeida, Beatriz Santiago, Giovanni B. Frisoni, Orazio Zanetti, Cristian Bonvicini, Matthis Synofzik, Walter Maetzler, Jennifer Müller vom Hagen, Lüdger Schöls, Michael T. Heneka, Frank Jessen, Radoslav Matěj, Eva Parobková, Gábor G. Kovács, Thomas Ströbel, Stayko Sarafov, Ivailo Tournev, Albena Jordanova, Adrian Danek, Thomas Arzberger, Gian Maria Fabrizi, Silvia Testi, Éric Salmon, Patrick Santens, Jean‐Jacques Martin, Patrick Cras, Rik Vandenberghe, Peter Paul De Deyn, Marc Cruts, Christine Van Broeckhoven, Julie van der Zee, Ilse Gijselinck, Lubina Dillen, Tim Van Langenhove, Jessie Theuns, Stéphanie Philtjens, Kristel Sleegers, Veerle Bäumer, Githa Maes, Ellen Corsmit, Marc Cruts, Christine Van Broeckhoven, Julie van der Zee, Ilse Gijselinck, Lubina Dillen, Tim Van Langenhove, Stéphanie Philtjens, Jessie Theuns, Kristel Sleegers, Veerle Bäumer, Githa Maes, Marc Cruts, Christine Van Broeckhoven, Sebastiaan Engelborghs, Peter P. De Deyn, Patrick Cras, Sebastiaan Engelborghs, Peter P. De Deyn, Mathieu Vandenbulcke, Mathieu Vandenbulcke, Barbara Borroni, Alessandro Padovani, Silvana Archetti, Robert Perneczky, Janine Diehl‐Schmid, Matthis Synofzik, Walter Maetzler, Jennifer Müller vom Hagen and 70 more - Human Mutation 2012 cited by 269

  20. Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia

    Authors: Elise Cuyvers, Karolien Bettens, Stéphanie Philtjens, Tim Van Langenhove, Ilse Gijselinck, Julie van der Zee, Sebastiaan Engelborghs, Mathieu Vandenbulcke, Jasper Van Dongen, Nathalie Geerts, Githa Maes, Maria Mattheijssens, Karin Peeters, Patrick Cras, Rik Vandenberghe, Peter P. De Deyn, Christine Van Broeckhoven, Marc Cruts, Kristel Sleegers - Neurobiology of Aging 2013 cited by 188

  21. The role of tau (MAPT) in frontotemporal dementia and related tauopathies

    Authors: Rosa Rademakers, Marc Cruts, Christine Van Broeckhoven - Human Mutation 2004 cited by 363

  22. Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort

    Authors: Ilse Gijselinck, Sara Van Mossevelde, Julie van der Zee, Anne Sieben, Stéphanie Philtjens, Bavo Heeman, Sebastiaan Engelborghs, Mathieu Vandenbulcke, Greet De Baets, Veerle Bäumer, Ivy Cuijt, Marleen Van den Broeck, Karin Peeters, Maria Mattheijssens, Frédéric Rousseau, Rik Vandenberghe, Peter De Jonghe, Patrick Cras, Peter P. De Deyn, Jean‐Jacques Martin, Marc Cruts, Christine Van Broeckhoven, Dirk Nuytten, Tim Van Langenhove, Katrien Smets, Jonathan Baets, Wim Robberecht, Philip Van Damme, Jan De Bleecker, Patrick Santens, Bart Dermaut, Olivier Deryck, Bruno Bergmans, Jean Delbeck, Jan Versijpt, Alex Michotte, Christiana Willems, Adrian Ivanoiu, Éric Salmon - Neurology 2015 cited by 173

  23. Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

    Authors: Julie van der Zee, Tim Van Langenhove, Gábor G. Kovács, 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 Pástor, Cristina Razquín, Sara Ortega‐Cubero, Isabel Hernández, Merçé Boada, Agustı́n Ruiz, Alexandre de Mendonça, Gábriel 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, Cristian Bonvicini, Matthis Synofzik, Walter Maetzler, Jennifer Müller vom Hagen, Lüdger 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 Ramı́rez, Raquel Sánchez‐Valle, Albert Lladó, Ellen Gelpí, Stayko Sarafov, Ivailo Tournev, Albena Jordanova, Eva Parobková, Gian Maria Fabrizi, Silvia Testi, Éric 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 - Acta Neuropathologica 2014 cited by 117

  24. Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the β–amyloid precursor protein gene

    Authors: Lydia Hendriks, Cornelia M. van Duijn, Patrick Cras, Marc Cruts, Wim Van Hul, F. van Harskamp, Andrew Warren, Melvin G. McInnis, Stylianos E. Antonarakis, Jean‐Jacques Martin, Albert Hofman, Christine Van Broeckhoven - Nature Genetics 1992 cited by 735