NanoPack: visualizing and processing long-read sequencing data von De Coster, Wouter, D'Hert, Svenn, Schultz, Darrin T, Cruts, Marc, Van Broeckhoven, Christine

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Locus-specific mutation databases for neurodegenerative brain diseases von Cruts, Marc, Theuns, Jessie, Van Broeckhoven, Christine

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Relationship between C9orf72 repeat size and clinical phenotype von Van Mossevelde, Sara, van der Zee, Julie, Cruts, Marc, Van Broeckhoven, Christine

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Drosophila screen connects nuclear transport genes to DPR pathology in c9ALS/FTD von Boeynaems, Steven, Bogaert, Elke, Michiels, Emiel, Gijselinck, Ilse, Sieben, Anne, Jovičić, Ana, De Baets, Greet, Scheveneels, Wendy, Steyaert, Jolien, Cuijt, Ivy, Verstrepen, Kevin J., Callaerts, Patrick, Rousseau, Frederic, Schymkowitz, Joost, Cruts, Marc, Van Broeckhoven, Christine, Van Damme, Philip, Gitler, Aaron D., Robberecht, Wim, Van Den Bosch, Ludo

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The genetics and neuropathology of frontotemporal lobar degeneration von Sieben, Anne, Van Langenhove, Tim, Engelborghs, Sebastiaan, Martin, Jean-Jacques, Boon, Paul, Cras, Patrick, De Deyn, Peter-Paul, Santens, Patrick, Van Broeckhoven, Christine, Cruts, Marc

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A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identificati... von Gijselinck, Ilse, PhD, Van Langenhove, Tim, MD, van der Zee, Julie, PhD, Sleegers, Kristel, PhD, Philtjens, Stéphanie, MSc, Kleinberger, Gernot, MSc, Janssens, Jonathan, MSc, Bettens, Karolien, PhD, Van Cauwenberghe, Caroline, MSc, Pereson, Sandra, MSc, Engelborghs, Sebastiaan, Prof, Sieben, Anne, MD, De Jonghe, Peter, Prof, Vandenberghe, Rik, Prof, Santens, Patrick, Prof, De Bleecker, Jan, Prof, Maes, Githa, MSc, Bäumer, Veerle, BSc, Dillen, Lubina, PhD, Joris, Geert, BSc, Cuijt, Ivy, MSc, Corsmit, Ellen, BSc, Elinck, Ellen, MSc, Van Dongen, Jasper, BSc, Vermeulen, Steven, MSc, Van den Broeck, Marleen, BSc, Vaerenberg, Carolien, MSc, Mattheijssens, Maria, BSc, Peeters, Karin, BSc, Robberecht, Wim, Prof, Cras, Patrick, Prof, Martin, Jean-Jacques, Prof, De Deyn, Peter P, Prof, Cruts, Marc, Prof, Van Broeckhoven, Christine, Prof

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Loss of progranulin function in frontotemporal lobar degeneration von Cruts, Marc, Van Broeckhoven, Christine

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Loss of ALS-associated TDP-43 in zebrafish causes muscle degeneration, vascular dysfunction, and reduced motor neuron axon outgrowth von Schmid, Bettina, Hruscha, Alexander, Hogl, Sebastian, Banzhaf-Strathmann, Julia, Strecker, Katrin, van der Zee, Julie, Teucke, Mathias, Eimer, Stefan, Hegermann, Jan, Kittelmann, Maike, Kremmer, Elisabeth, Cruts, Marc, Solchenberger, Barbara, Hasenkamp, Laura, van Bebber, Frauke, Van Broeckhoven, Christine, Edbauer, Dieter, Lichtenthaler, Stefan F., Haass, Christian

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Serum biomarker for progranulin-associated frontotemporal lobar degeneration von Sleegers, Kristel, Brouwers, Nathalie, Van Damme, Philip, Engelborghs, Sebastiaan, Gijselinck, Ilse, van der Zee, Julie, Peeters, Karin, Mattheijssens, Maria, Cruts, Marc, Vandenberghe, Rik, De Deyn, Peter P., Robberecht, Wim, Van Broeckhoven, Christine

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novoSNP, a novel computational tool for sequence variation discovery von Weckx, Stefan, Del-Favero, Jurgen, Rademakers, Rosa, Claes, Lieve, Cruts, Marc, De Jonghe, Peter, Van Broeckhoven, Christine, De Rijk, Peter

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Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort von 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, Goeman, Johan, Nuytten, Dirk, Vandenbulcke, Mathieu, Santens, Patrick, De Bleecker, Jan, Sieben, Anne, Dermaut, Bart, Versijpt, Jan, Michotte, Alex, Deryck, Olivier, Bergmans, Bruno, Willems, Christiana, Ivanoiu, Adrian, Salmon, Eric, Alexopoulos, Panagiotis, Sorbi, Sandro, Bessi, Valentina, Bagnoli, Silvia, Santana, Isabel, Simões do Couto, Frederico, Martins, Madalena, Thonberg, Håkan, Fratiglioni, Laura, Padovani, Alessandro, Rohan, Zdenek, Razquin, Cristina, Lorenzo, Elena, Iglesias, Elena, Seijo-Martínez, Manuel, Rene, Ramon, Gascon, Jordi, Campdelacreu, Jaume, Koutroumani, Maria, Lleó, Alberto, Fortea, Juan, Blesa, Rafael

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Explorative genetic study of UBQLN2 and PFN1 in an extended Flanders-Belgian cohort of frontotemporal lobar degeneration patients von Dillen, Lubina, Van Langenhove, Tim, Engelborghs, Sebastiaan, Vandenbulcke, Mathieu, Sarafov, Stayko, Tournev, Ivailo, Merlin, Celine, Cras, Patrick, Vandenberghe, Rik, De Deyn, Peter P, Jordanova, Albena, Cruts, Marc, Van Broeckhoven, Christine, van der Zee, Julie

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Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update von Nuytemans, Karen, Theuns, Jessie, Cruts, Marc, Van Broeckhoven, Christine

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Ataxin-2 polyQ expansions in FTLD-ALS spectrum disorders in Flanders-Belgian cohorts von Van Langenhove, Tim, van der Zee, Julie, Engelborghs, Sebastiaan, Vandenberghe, Rik, Santens, Patrick, Van den Broeck, Marleen, Mattheijssens, Maria, Peeters, Karin, Nuytten, Dirk, Cras, Patrick, De Deyn, Peter P, De Jonghe, Peter, Cruts, Marc, Van Broeckhoven, Christine

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Presenilin mutations in Alzheimer's disease von Cruts, Marc, Van Broeckhoven, Christine

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Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia von van der Zee, Julie, Le Ber, Isabelle, Maurer-Stroh, Sebastian, Engelborghs, Sebastiaan, Gijselinck, Ilse, Camuzat, Agnès, Brouwers, Nathalie, Vandenberghe, Rik, Sleegers, Kristel, Hannequin, Didier, Dermaut, Bart, Schymkowitz, Joost, Campion, Dominique, Santens, Patrick, Martin, Jean-Jacques, Lacomblez, Lucette, De Pooter, Tim, Peeters, Karin, Mattheijssens, Maria, Vercelletto, Martine, Van den Broeck, Marleen, Cruts, Marc, De Deyn, Peter P., Rousseau, Frederic, Brice, Alexis, Van Broeckhoven, Christine

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Extended FTLD pedigree segregating a Belgian GRN-null mutation: neuropathological heterogeneity in one family von Sieben, Anne, Van Mossevelde, Sara, Wauters, Eline, Engelborghs, Sebastiaan, van der Zee, Julie, Van Langenhove, Tim, Santens, Patrick, Praet, Marleen, Boon, Paul, Miatton, Marijke, Van Hoecke, Sofie, Vandenbulcke, Mathieu, Vandenberghe, Rik, Cras, Patrick, Cruts, Marc, De Deyn, Peter Paul, Van Broeckhoven, Christine, Martin, Jean-Jacques

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Data Mining: Applying the AD&FTD Mutation Database to Progranulin von Cruts, Marc, Van Broeckhoven, Christine

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

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The C9orf72 GGGGCC Repeat Is Translated into Aggregating Dipeptide-Repeat Proteins in FTLD/ALS von Mori, Kohji, Weng, Shih-Ming, Arzberger, Thomas, May, Stephanie, Rentzsch, Kristin, Kremmer, Elisabeth, Schmid, Bettina, Kretzschmar, Hans A., Cruts, Marc, Van Broeckhoven, Christine, Haass, Christian, Edbauer, Dieter

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