Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia von Cuyvers, Elise, Bettens, Karolien, Philtjens, Stéphanie, Van Langenhove, Tim, Gijselinck, Ilse, van der Zee, Julie, Engelborghs, Sebastiaan, Vandenbulcke, Mathieu, Van Dongen, Jasper, Geerts, Nathalie, Maes, Githa, Mattheijssens, Maria, Peeters, Karin, Cras, Patrick, Vandenberghe, Rik, De Deyn, Peter P, Van Broeckhoven, Christine, Cruts, Marc, Sleegers, Kristel

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An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer’s disease von 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

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NEK1 genetic variability in a Belgian cohort of ALS and ALS-FTD patients von Nguyen, Hung Phuoc, Van Mossevelde, Sara, Dillen, Lubina, De Bleecker, Jan L., Moisse, Matthieu, Van Damme, Philip, Van Broeckhoven, Christine, van der Zee, Julie, Engelborghs, Sebastiaan, Crols, Roeland, De Deyn, Peter P., De Jonghe, Peter, Baets, Jonathan, Cras, Patrick, Mercelis, Rudy, Vandenberghe, Rik, Sieben, Anne, Santens, Patrick, Ivanoiu, Adrian, Deryck, Olivier, Vanopdenbosch, Ludo, Delbeck, Jean

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MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study von Valentino, Rebecca R, Heckman, Michael G, Shoai, Maryam, Martinez-Carrasco, Alejandro, Tamvaka, Nicole, Walton, Ronald L, Real, Raquel, Mok, Kin, Christopher, Elizabeth A, Lee, Edward B, Frosch, Matthew P, Molina-Porcel, Laura, Gefen, Tamar, Robinson, Andrew C, Kobylecki, Christopher, Rowe, James B, Beach, Thomas G, Teich, Andrew F, Keith, Julia L, Bodi, Istvan, Gearing, Marla, Arzberger, Thomas, Morris, Christopher M, White, Charles L, Mechawar, Naguib, MacKenzie, Ian R, McLean, Catriona, Wang, Shih-Hsiu J, Nagra, Rashed M, Kovacs, Gabor G, Giaccone, Giorgio, Ang, Lee-Cyn, Morris, Huw R, Hardy, John A, Dickson, Dennis W, Ross, Owen A, Warner, Thomas T, Boeve, Bradley F, Duara, Ranjan, Josephs, Keith A, Murray, Melissa E, Lyons, Kelly E, Whitwell, Jennifer L, Miller, Bruce, Schlereth, Athena, Van Deerlin, Vivianna M, Wolk, David A, Connors, Theresa R, Dooley, Patrick M, Aldecoa, Iban, Gelpi, Ellen, Sánchez-Valle, Raquel, Sanz-Cartagena, Pilar, Bigio, Eileen H, Weintraub, Sandra, Schneider, Julie A, Chang, Koping, Troncoso, Juan C, Jones, Matthew, Richardson, Anna, Roncaroli, Federico, Snowden, Julie, Serrano, Geidy E, Goldman, James E, Leskinen, Sandra P, Masellis, Mario, King, Andrew, Al-Sarraj, Safa, Troakes, Claire, Hodges, John R, Kril, Jillian J, Kwok, John B, Roeber, Sigrun, Attems, Johannes, Thomas, Alan J, Evers, Bret M., Bieniek, Kevin F, Sieben, Anne A, Cras, Patrick P, De Vil, Bart B, Castellani, Rudolph J, Chaffee, Ann, Franklin, Erin, Jacobsen, Max, Keene, Dirk, Latimer, Caitlin S, Purohit, Dushyant P, Schantz, Aimee, Walker, Jamie, De Deyn, Peter P, Duyckaerts, Charles, Seilhean, Danielle, Turbant-Leclere, Sabrina, Nennesmo, Inger, Riehl, James, Nacmias, Benedetta, Finger, Elizabeth C, Blauwendraat, Cornelis, Nalls, Mike A, Singleton, Andrew B

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No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients von 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, Goeman, Johan, Nuytten, Dirk, Sieben, Anne, De Bleecker, Jan L., Santens, Patrick, Versijpt, Jan, Michotte, Alex, Ivanoiu, Adrian, Deryck, Olivier, Bergmans, Bruno, Willems, Christiana, De Klippel, Nina, Peeters, Dirk, Archettim, Silvana, Bonomi, Elisa, Piaceri, Irene, Ferrari, Camilla, Simões do Couto, Frederico, Verdelho, Ana, Miltenberger-Miltényi, Gabriel

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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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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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CSF proteome profiling reveals biomarkers to discriminate dementia with Lewy bodies from Alzheimer´s disease von del Campo, Marta, Vermunt, Lisa, Peeters, Carel F. W., Sieben, Anne, Hok-A-Hin, Yanaika S., Lleó, Alberto, Alcolea, Daniel, van Nee, Mirrelijn, Engelborghs, Sebastiaan, van Alphen, Juliette L., Arezoumandan, Sanaz, Chen-Plotkin, Alice, Irwin, David J., van der Flier, Wiesje M., Lemstra, Afina W., Teunissen, Charlotte E.

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Rare exonic variant affects GRN splicing and contributes to frontotemporal lobar degeneration von Wauters, Eline, Gossye, Helena, Frydas, Alexandros, Sieben, Anne, Van Broeckhoven, Christine

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Activation of Mitochondrial Protein Phosphatase SLP2 by MIA40 Regulates Seed Germination von Uhrig, R. Glen, Labandera, Anne-Marie, Tang, Lay-Yin, Sieben, Nicolas A., Goudreault, Marilyn, Yeung, Edward, Gingras, Anne-Claude, Samuel, Marcus A., Moorhead, Greg B.G.

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Bilingualism delays clinical manifestation of Alzheimer's disease von WOUMANS, EVY, SANTENS, PATRICK, SIEBEN, ANNE, VERSIJPT, JAN, STEVENS, MICHAËL, DUYCK, WOUTER

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Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patients von Perrone, Federica, Nguyen, Hung Phuoc, Van Mossevelde, Sara, Moisse, Matthieu, Sieben, Anne, Santens, Patrick, De Bleecker, Jan, Vandenbulcke, Mathieu, Engelborghs, Sebastiaan, Baets, Jonathan, Cras, Patrick, Vandenberghe, Rik, De Jonghe, Peter, De Deyn, Peter P, Martin, Jean-Jacques, Van Damme, Philip, Van Broeckhoven, Christine, van der Zee, Julie

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Biomarker A+T−: is this Alzheimer’s disease or not? A combined CSF and pathology study von Vromen, Eleonora M, de Boer, Sterre C M, Teunissen, Charlotte E, Rozemuller, Annemieke, Sieben, Anne, Bjerke, Maria, Visser, Pieter Jelle, Bouwman, Femke H, Engelborghs, Sebastiaan, Tijms, Betty M

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The Electrophysiological Correlates of Phoneme Perception in Primary Progressive Aphasia: A Preliminary Case Series von Stalpaert, Jara, Miatton, Marijke, Sieben, Anne, Van Langenhove, Tim, van Mierlo, Pieter, De Letter, Miet

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Pooled analysis of patients with inherited prion disease caused by two- to twelve-octapeptide repeat insertions in the prion protein gene (PRNP) von Van den Broecke, Astrid, Decruyenaere, Alexander, Schuermans, Nika, Verdin, Hannah, Ghijsels, Jody, Sieben, Anne, Dermaut, Bart, Hemelsoet, Dimitri

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Suprasternal Bronchogenic Cyst in an 8-Year-Old Girl von Asena Altun, Giada Bilotta, Gilles Van Haesendonck, Callum Farris, Olivier M Vanderveken, Anne Sieben, An Boudewyns

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Associating Alzheimer's disease pathology with its cerebrospinal fluid biomarkers von Bridel, Claire, Somers, Charisse, Sieben, Anne, Rozemuller, Annemieke, Niemantsverdriet, Ellis, Struyfs, Hanne, Vermeiren, Yannick, Van Broeckhoven, Christine, De Deyn, Peter P, Bjerke, Maria, Nagels, Guy, Teunissen, Charlotte E, Engelborghs, Sebastiaan

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Family-based exome sequencing identifies RBM45 as a possible candidate gene for frontotemporal dementia and amyotrophic lateral sclerosis von van der Zee, Julie, Dillen, Lubina, Baradaran-Heravi, Yalda, Gossye, Helena, Koçoğlu, Cemile, Cuyt, Ivy, Dermaut, Bart, Sieben, Anne, Baets, Jonathan, De Jonghe, Peter, Vandenberghe, Rik, De Deyn, Peter, Cras, Patrick, Engelborghs, Sebastiaan, Van Broeckhoven, Christine

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