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Displaying 18 results.
    • Journal article
    Premature termination codon mutations in ABCA7 contribute to Alzheimer's disease risk in Belgian patients.
    Bossaerts, Liene Hens, Elisabeth Hanseeuw, Bernard[UCL] Vandenberghe, Rik Cras, Patrick De Deyn, Peter P Engelborghs, Sebastiaan Van Broeckhoven, Christine BELNEU Consortium (2021) Neurobiology of aging — Vol. 106, p. 307.e1-307.e7 (2021)
    • Journal article
    Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort
    Van Mossevelde, Sara van der Zee, Julie Gijselinck, Ilse Engelborghs, Sebastiaan Sieben, Anne Van Langenhove, Tim De Bleecker, Jan Baets, Jonathan Vandenbulcke, Mathieu Van Laere, Koen Ceyssens, Sarah Van den Broeck, Marleen Peeters, Karin Mattheijssens, Maria Cras, Patrick Vandenberghe, Rik De Jonghe, Peter Martin, Jean-Jacques De Deyn, Peter P Cruts, Marc Van Broeckhoven, Christine Belgian Neurology consortium Ivanoiu, Adrian[UCL] (2016) Brain : a journal of neurology — Vol. 139, no.2, p. 452-467 (2016)
    • Journal article
    Frontotemporal Lobar Degeneration Case with an N-Terminal TUBA4A Mutation Exhibits Reduced TUBA4A Levels in the Brain and TDP-43 Pathology
    Van Schoor, Evelien Vandenbulcke, Mathieu Bercier, Valérie Vandenberghe, Rik van der Zee, Julie Van Broeckhoven, Christine Otto, Markus Hanseeuw, Bernard[UCL] Van Damme, Philip Van Den Bosch, Ludo Thal, Dietmar Rudolf (2022) Biomolecules — Vol. 12, no. 3, p. 440 [1-13] (2022)
    • Journal article
    Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort.
    Verheijen, Jan van der Zee, Julie Gijselinck, Ilse Van den Bossche, Tobi Dillen, Lubina Heeman, Bavo Gómez-Tortosa, Estrella Lladó, Albert Sanchez-Valle, Raquel Graff, Caroline Pastor, Pau Pastor, Maria A Benussi, Luisa Ghidoni, Roberta Binetti, Giuliano Clarimon, Jordi de Mendonça, Alexandre Gelpi, Ellen Tsolaki, Magda Diehl-Schmid, Janine Nacmias, Benedetta Almeida, Maria Rosário Borroni, Barbara Matej, Radoslav Ruiz, Agustín Engelborghs, Sebastiaan Vandenberghe, Rik De Deyn, Peter P Cruts, Marc Van Broeckhoven, Christine Sleegers, Kristel BELNEU Consortium EU EOD Consortium Ivanoiu, Adrian[UCL] (2018) Neurobiology of aging — Vol. 62, p. 245.e1-245.e7 (2018)
    • Journal article
    TBK1Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis
    van der Zee, Julie Gijselinck, Ilse Van Mossevelde, Sara Perrone, Federica Dillen, Lubina Heeman, Bavo Bâumer, Veerle Engelborghs, Sebastiaan De Bleecker, Jan Baets, Jonathan Gelpi, Ellen Rojas-García, Ricardo Clarimón, Jordi Lleó, Alberto Diehl-Schmid, Janine Alexopoulos, Panagiotis Perneczky, Robert Synofzik, Matthis Just, Jennifer Schöls, Ludger Graff, Caroline Thonberg, Hakan Borroni, Barbara Padovani, Alessandro Jordanova, Albena Sarafov, Stayko Tournev, Ivailo de Mendonça, Alexandre Miltenberger-Miltényi, Gabriel Simões do Couto, Frederico Ramirez, Alfredo Jessen, Frank Heneka, Michael T. Gómez-Tortosa, Estrella Danek, Adrian Cras, Patrick Vandenberghe, Rik De Jonghe, Peter De Deyn, Peter P. Sleegers, Kristel Cruts, Marc Van Broeckhoven, Christine Goeman, Johan Nuytten, Dirk Smets, Katrien Robberecht, Wim Damme, Philip Van Bleecker, Jan De Santens, Patrick Dermaut, Bart Versijpt, Jan Michotte, Alex Ivanoiu, Adrian[UCL] Deryck, Olivier Bergmans, Bruno Delbeck, Jean Bruyland, Marc Willems, Christiana Salmon, Eric Pastor, Pau Ortega-Cubero, Sara Benussi, Luisa Ghidoni, Roberta Binetti, Giuliano Hernàndez, Isabel Boada, Mercè Ruiz, Agustín Sorbi, Sandro Nacmias, Benedetta Bagnoli, Silvia Sorbi, Sandro Sanchez-Valle, Raquel Llado, Albert Santana, Isabel Rosàrio Almeida, Maria Frisoni, Giovanni B Maetzler, Walter Matej, Radoslav Fraidakis, Matthew J. Kovacs, Gabor G. Fabrizi, Gian Maria Testi, Silvia (2017) Human Mutation — Vol. 38, no. 3, p. 297-309 (2017)
    • Journal article
    No evidence for the involvement of CAG/CTG repeats from within 18q21.33-q23 in bipolar disorder.
    Goossens, Dirk Villafuerte, Sandra Tissir, Fadel[UCL] Van Gestel, Sofie Claes, Stephan Souery, Daniel Massat, Isabelle Van den Bossche, Dirk Van Zand, Karel Mendlewicz, Julien Van Broeckhoven, Christine Del-Favero, Jurgen (2000) European Journal of Human Genetics — Vol. 8, no.5, p. 385-8 (2000)
    • Journal article
    The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter
    Gijselinck, Ilse Van Mossevelde, Sara van der Zee, Julie Sieben, Anne Engelborghs, Sebastiaan De Bleecker, Jan Ivanoiu, Adrian[UCL] Deryck, Olivier Edbauer, Dieter Zhang, Ming Heeman, Bavo Bäumer, Veerle Van den Broeck, Marleen Mattheijssens, Maria Peeters, Karin Rogaeva, Ekaterina De Jonghe, Peter Cras, Patrick Martin, Jean-Jacques de Deyn, Peter Paul Cruts, Marc Van Broeckhoven, Christine (2016) Molecular Psychiatry — Vol. 21, no. 8, p. 1112-1124 (2016)
    • Journal article
    Phenotypical characterization of α-galactosidase A gene mutations identified in a large Fabry disease screening program in stroke in the young.
    De Brabander, Isabel Yperzeele, Laetitia Ceuterick-De Groote, Chantal Brouns, Raf Baker, Robert Belachew, Shibeshih Delbecq, Jean De Keulenaer, Gilles Dethy, Sophie Eyskens, François Fumal, Arnaud Hemelsoet, Dimitri Hughes, Derralynn Jeangette, Sandrine Nuytten, Dirk Redondo, Patricia Sadzot, Bernard Sindic, Christian[UCL] Sheorajpanday, Rishi Thijs, Vincent Van Broeckhoven, Christine De Deyn, Peter P (2013) Clinical Neurology and Neurosurgery — Vol. 115, no.7, p. 1088-1093 (2013)
    • Journal article
    Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia.
    Philtjens, Stéphanie Van Mossevelde, Sara van der Zee, Julie Wauters, Eline Dillen, Lubina Vandenbulcke, Mathieu Vandenberghe, Rik Ivanoiu, Adrian[UCL] Sieben, Anne Willems, Christiana Benussi, Luisa Ghidoni, Roberta Binetti, Giuliano Borroni, Barbara Padovani, Alessandro Pastor, Pau Diez-Fairen, Monica Aguilar, Miquel de Mendonça, Alexandre Miltenberger-Miltényi, Gabriel Hernández, Isabel Boada, Merce Ruiz, Agustín Nacmias, Benedetta Sorbi, Sandro Almeida, Maria Rosário Santana, Isabel Clarimón, Jordi Lleó, Alberto Frisoni, Giovanni B Sanchez-Valle, Raquel Lladó, Albert Gómez-Tortosa, Estrella Gelpi, Ellen Van den Broeck, Marleen Peeters, Karin Cras, Patrick De Deyn, Peter P Engelborghs, Sebastiaan Cruts, Marc Van Broeckhoven, Christine BELNEU Consortium EU EOD Consortium (2018) Neurobiology of Aging — Vol. 66, no. 181, p. e3-181.e10 (2018)
    • Journal article
    An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer's disease.
    De Roeck, Arne Duchateau, Lena Van Dongen, Jasper Cacace, Rita Bjerke, Maria Van den Bossche, Tobi Cras, Patrick Vandenberghe, Rik De Deyn, Peter P Engelborghs, Sebastiaan Van Broeckhoven, Christine Sleegers, Kristel BELNEU Consortium Ivanoiu, Adrian[UCL] (2018) Acta neuropathologica — Vol. 135, no. 6, p. 827-837 (2018)
    • Journal article
    Clinical Evidence of Disease Anticipation in Families Segregating aC9orf72Repeat Expansion
    Van Mossevelde, Sara van der Zee, Julie Gijselinck, Ilse Sleegers, Kristel De Bleecker, Jan Sieben, Anne Vandenberghe, Rik Van Langenhove, Tim Baets, Jonathan Deryck, Olivier Santens, Patrick Ivanoiu, Adrian[UCL] Willems, Christiana Bäumer, Veerle Van den Broeck, Marleen Peeters, Karin Mattheijssens, Maria De Jonghe, Peter Cras, Patrick Martin, Jean-Jacques Cruts, Marc De Deyn, Peter P. Engelborghs, Sebastiaan Van Broeckhoven, Christine (2017) JAMA Neurology — Vol. 74, no. 4, p. 445-452 (2017)
    • Journal article
    NEK1 genetic variability in a Belgian cohort of ALS and ALS-FTD patients.
    Nguyen, Hung Phuoc Van Mossevelde, Sara Dillen, Lubina De Bleecker, Jan L Moisse, Matthieu Van Damme, Philip Van Broeckhoven, Christine van der Zee, Julie BELNEU Consortium Ivanoiu, Adrian[UCL] (2018) Neurobiology of aging — Vol. 61, p. 255.e1-255.e7 (2018)
    • Journal article
    Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains
    Janssens, Jonathan Philtjens, Stéphanie Kleinberger, Gernot Van Mossevelde, Sara van der Zee, Julie Cacace, Rita Engelborghs, Sebastiaan Sieben, Anne Banzhaf-Strathmann, Julia Dillen, Lubina Merlin, Céline Cuijt, Ivy Robberecht, Caroline Schmid, Bettina Santens, Patrick Ivanoiu, Adrian[UCL] Vandenbulcke, Mathieu Vandenberghe, Rik Cras, Patrick De Deyn, Peter P. Martin, Jean-Jacques Maudsley, Stuart Haass, Christian Cruts, Marc Van Broeckhoven, Christine (2015) Acta Neuropathologica Communications — Vol. 3, no.1, p. 68 (2015)
    • Journal article
    Distinct Clinical Characteristics of C9orf72 Expansion Carriers Compared With GRN, MAPT, and Nonmutation Carriers in a Flanders-Belgian FTLD Cohort.
    Van Langenhove, Tim van der Zee, Julie Gijselinck, Ilse Engelborghs, Sebastiaan Vandenberghe, Rik Vandenbulcke, Mathieu De Bleecker, Jan Sieben, Anne Versijpt, Jan Ivanoiu, Adrian[UCL] Deryck, Olivier Willems, Christiana Dillen, Lubina Philtjens, Stéphanie Maes, Githa Bäumer, Veerle Van Den Broeck, Marleen Mattheijssens, Maria Peeters, Karin Martin, Jean-Jacques Michotte, Alex Santens, Patrick De Jonghe, Peter Cras, Patrick De Deyn, Peter P Cruts, Marc Van Broeckhoven, Christine (2013) JAMA Neurology — Vol. 70, no.3, p. 365-73 (2013)
    • Journal article
    Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability.
    Cacace, Rita Heeman, Bavo Van Mossevelde, Sara De Roeck, Arne Hoogmartens, Julie De Rijk, Peter Gossye, Helena De Vos, Kristof De Coster, Wouter Strazisar, Mojca De Baets, Greet Angèle[UCL] Schymkowitz, Joost Rousseau, Frederic Geerts, Nathalie De Pooter, Tim Peeters, Karin Sieben, Anne Martin, Jean-Jacques Engelborghs, Sebastiaan Salmon, Eric Santens, Patrick Vandenberghe, Rik Cras, Patrick P De Deyn, Peter C van Swieten, John M van Duijn, Cornelia van der Zee, Julie Sleegers, Kristel Van Broeckhoven, Christine BELNEU Consortium (2019) Acta neuropathologica — Vol. 137, no.6, p. 901-918 (2019)
    • Journal article
    No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients.
    Baradaran-Heravi, Yalda Dillen, Lubina Nguyen, Hung Phuoc Van Mossevelde, Sara Baets, Jonathan De Jonghe, Peter Engelborghs, Sebastiaan De Deyn, Peter P Vandenbulcke, Mathieu Vandenberghe, Rik Van Damme, Philip Cras, Patrick Salmon, Eric Synofzik, Matthis Heutink, Peter Wilke, Carlo Simon-Sanchez, Javier Rojas-Garcia, Ricard Turon-Sans, Janina Lleó, Alberto Illán-Gala, Ignacio Clarimón, Jordi Borroni, Barbara Padovani, Alessandro Pastor, Pau Diez-Fairen, Monica Aguilar, Miquel Gelpi, Ellen Sanchez-Valle, Raquel Borrego-Ecija, Sergi Matej, Radoslav Parobkova, Eva Nacmias, Benedetta Sorbi, Sandro Bagnoli, Silvia de Mendonça, Alexandre Ferreira, Catarina Fraidakis, Matthew J Diehl-Schmid, Janine Alexopoulos, Panagiotis Almeida, Maria Rosário Santana, Isabel Van Broeckhoven, Christine van der Zee, Julie BELNEU Consortium EU EOD Consortium Ivanoiu, Adrian[UCL] (2018) Neurobiology of aging — Vol. 69, p. 293.e9-293.e11 (2018)
    • Journal article
    Clinical variability and onset age modifiers in an extended Belgian GRN founder family.
    Wauters, Eline Van Mossevelde, Sara Sleegers, Kristel van der Zee, Julie Engelborghs, Sebastiaan Sieben, Anne Vandenberghe, Rik Philtjens, Stéphanie Van den Broeck, Marleen Peeters, Karin Cuijt, Ivy De Coster, Wouter Van Langenhove, Tim Santens, Patrick Ivanoiu, Adrian[UCL] Cras, Patrick De Bleecker, Jan L Versijpt, Jan Crols, Roeland De Klippel, Nina Martin, Jean-Jacques De Deyn, Peter P Cruts, Marc Van Broeckhoven, Christine Belgian Neurology (BELNEU) Consortium (2018) Neurobiology of Aging — Vol. 67, p. 84-94 (2018)
    • Journal article
    CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro
    van der Zee, Julie Urwin, Hazel Engelborghs, Sebastiaan Bruyland, Marc Vandenberghe, Rik[UCL] Dermaut, Bart De Pooter, Tim Peeters, Karin Santens, Patrick De Deyn, Peter P. Fisher, Elizabeth M.[UCL] Collinge, John Isaacs, Adrian M. Van Broeckhoven, Christine (2008) Human Molecular Genetics — Vol. 17, no. 2, p. 313-322 (2008)