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Marc Cruts

1991–2022 年に発表

77
論文数
21,408
被引用数
73
h 指数
77
i10 指数

被引用数

Marc Cruts の年別被引用数1991 年: 被引用 3 件1992 年: 被引用 15 件1993 年: 被引用 23 件1994 年: 被引用 43 件1995 年: 被引用 49 件1996 年: 被引用 50 件1997 年: 被引用 60 件1998 年: 被引用 65 件1999 年: 被引用 33 件2000 年: 被引用 79 件2001 年: 被引用 74 件2002 年: 被引用 49 件2003 年: 被引用 53 件2004 年: 被引用 49 件2005 年: 被引用 66 件2006 年: 被引用 181 件2007 年: 被引用 201 件2008 年: 被引用 238 件2009 年: 被引用 188 件2010 年: 被引用 200 件2011 年: 被引用 231 件2012 年: 被引用 296 件2013 年: 被引用 311 件2014 年: 被引用 302 件2015 年: 被引用 306 件2016 年: 被引用 334 件2017 年: 被引用 293 件2018 年: 被引用 233 件2019 年: 被引用 622 件2020 年: 被引用 587 件2021 年: 被引用 549 件2022 年: 被引用 351 件2023 年: 被引用 272 件2024 年: 被引用 373 件2025 年: 被引用 179 件2026 年: 被引用 3 件

引用元

国・地域

この著者を引用した国・地域の世界地図アメリカ合衆国: 引用元論文 2,447 件、この内訳の 29.8%イギリス: 引用元論文 758 件、この内訳の 9.2%ドイツ: 引用元論文 494 件、この内訳の 6%カナダ: 引用元論文 382 件、この内訳の 4.7%イタリア: 引用元論文 359 件、この内訳の 4.4%ベルギー: 引用元論文 345 件、この内訳の 4.2%オランダ: 引用元論文 323 件、この内訳の 3.9%中国: 引用元論文 312 件、この内訳の 3.8%フランス: 引用元論文 297 件、この内訳の 3.6%オーストラリア: 引用元論文 294 件、この内訳の 3.6%スペイン: 引用元論文 225 件、この内訳の 2.8%日本: 引用元論文 225 件、この内訳の 2.7%
0%29.8%その他 21.3%

機関

分野

  • Medicine70.5%
  • Biochemistry, Genetics and Molecular Biology18.2%
  • Neuroscience8.8%
  • Immunology and Microbiology0.9%
  • Computer Science0.4%
  • Environmental Science0.3%
  • その他0.9%

トピック

  • 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%
  • その他58.9%

共著者

全論文

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

    著者: 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 被引用: 1,297

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

    著者: 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 被引用: 1,542

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

    著者: 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 ほか 58 名 - The Lancet Neurology 2014 被引用: 402

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

    著者: 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 被引用: 497

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

    著者: Karen Nuytemans, Jessie Theuns, Marc Cruts, Christine Van Broeckhoven - Human Mutation 2010 被引用: 555

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

    著者: 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 被引用: 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

    著者: 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 被引用: 346

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

    著者: 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 ほか 69 名 - Biological Psychiatry 2022 被引用: 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

    著者: 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 被引用: 628

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

    著者: 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 被引用: 247

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

    著者: 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 被引用: 232

  12. Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia

    著者: 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 ほか 74 名 - Nature Medicine 2018 被引用: 156

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

    著者: 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 被引用: 129

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

    著者: 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 被引用: 177

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

    著者: 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 被引用: 153

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

    著者: 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 被引用: 492

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

    著者: 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 被引用: 325

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

    著者: 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 被引用: 280

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

    著者: 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 ほか 70 名 - Human Mutation 2012 被引用: 269

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

    著者: 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 被引用: 188

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

    著者: Rosa Rademakers, Marc Cruts, Christine Van Broeckhoven - Human Mutation 2004 被引用: 363

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

    著者: 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 被引用: 173

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

    著者: 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 被引用: 117

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

    著者: 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 被引用: 735