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Characterization of Ubiquitinated Intraneuronal Inclusions in a Novel Belgian Frontotemporal Lobar Degeneration Family ;

Pirici, Daniel, Vandenberghe, Rik, Rademakers, Rosa, Dermaut, Bart, Cruts, Marc, Vennekens, Krist'l, Cuijt, Ivy, Lübke, Ursula, Ceuterick, Chantal, Martin, Jean-Jacques, Van Broeckhoven, Christine, Kumar-Singh, Samir
Veröffentlicht in: Journal of Neuropathology and Experimental Neurology ; volume 65, issue 3, page 289-301 ; ISSN 0022-3069;
2006

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Founder mutation p.R1441C in the leucine-rich repeat kinase 2 gene in Belgian Parkinson's disease patients

Nuytemans, Karen, Rademakers, Rosa, Theuns, Jessie, Pals, Philippe, Engelborghs, Sebastiaan, Pickut, Barbara, de Pooter, Tim, Peeters, Karin, Mattheijssens, Maria, Van den Broeck, Marleen, Cras, Patrick, De Deyn, Peter Paul, van Broeckhoven, Christine
Veröffentlicht in: European Journal of Human Genetics ; volume 16, issue 4, page 471-479 ; ISSN 1018-4813 1476-5438;
2008

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Linkage and association studies identify a novel locus for Alzheimer disease at 7q36 in a Dutch population-based sample

Rademakers, Rosa, Cruts, Marc, Sleegers, Kristel, Dermaut, Bart, Theuns, Jessie, Aulchenko, Yurii, Weckx, Stefan, de Pooter, Tim, Van den Broeck, Marleen, Corsmit, Ellen, De Rijk, Peter, Del-Favero, Jurgen, van Swieten, John, van Duijn, Cornelia M., Van Broeckhoven, Christine
2005

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Linkage and Association Studies Identify a Novel Locus for Alzheimer Disease at 7q36 in a Dutch Population-Based Sample

Rademakers, Rosa, Cruts, Marc, Sleegers, Kristel, Dermaut, Bart, Theuns, Jessie, Aulchenko, Yurii, Weckx, Stefan, De Pooter, Tim, Van den Broeck, Marleen, Corsmit, Ellen, De Rijk, Peter, Del-Favero, Jurgen, van Swieten, John, van Duijn, Cornelia M., Van Broeckhoven, Christine
Veröffentlicht in: The American Journal of Human Genetics ; volume 77, issue 4, page 643-652 ; ISSN 0002-9297;
2005

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A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD

van der Zee, Julie, Rademakers, Rosa, Engelborghs, Sebastiaan, Gijselinck, Ilse, Bogaerts, Veerle, Vandenberghe, Rik, Santens, Patrick, Caekebeke, Jo, De Pooter, Tim, Peeters, Karin, Lübke, Ursula, Van den Broeck, Marleen, Martin, Jean-Jacques, Cruts, Marc, De Deyn, Peter P., Van Broeckhoven, Christine, Dermaut, Bart
Veröffentlicht in: Brain ; volume 129, issue 4, page 841-852 ; ISSN 1460-2156 0006-8950;
2006

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EIF2AK3 variants in Dutch patients with Alzheimer's disease.

Wong, Tsz Hang, van der Lee, Sven J, Hulsman, Marc, Uitterlinden, Andre, Neumann, Manuela, Hoozemans, Jeroen J M, van Duijn, Cornelia M, Rademakers, Rosa, van Swieten, John C, van Rooij, Jeroen G J, Meeter, Lieke H H, Frick, Petra, Melhem, Shamiram, Seelaar, Harro, Ikram, M Arfan, Rozemuller, Annemieke J, Holstege, Henne
2019

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EIF2AK3 variants in Dutch patients with Alzheimer's disease

Wong, Tsz Hang, van der Lee, Sven J., van Rooij, Jeroen G.J., Meeter, Lieke H.H., Frick, Petra, Melhem, Shamiram, Seelaar, Harro, Ikram, M. Arfan, Rozemuller, Annemieke J., Holstege, Henne, Hulsman, Marc, Uitterlinden, Andre, Neumann, Manuela, Hoozemans, Jeroen J.M., van Duijn, Cornelia M., Rademakers, Rosa, van Swieten, John C.
2019

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Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of lon...

van der Lee, Sven J, Conway, Olivia J, Jansen, Iris, Carrasquillo, Minerva M, Kleineidam, Luca, van den Akker, Erik, Hernández, Isabel, van Eijk, Kristel R, Stringa, Najada, Chen, Jason A, Zettergren, Anna, Andlauer, Till FM, Diez-Fairen, Monica, Simon-Sanchez, Javier, Lleó, Alberto, Zetterberg, Henrik, Nygaard, Marianne, Blauwendraat, Cornelis, Savage, Jeanne E, Mengel-From, Jonas, Moreno-Grau, Sonia, Wagner, Michael, Fortea, Juan, Keogh, Michael J, Blennow, Kaj, Skoog, Ingmar, Friese, Manuel A, Pletnikova, Olga, Zulaica, Miren, Lage, Carmen, de Rojas, Itziar, Riedel-Heller, Steffi, Illán-Gala, Ignacio, Wei, Wei, Jeune, Bernard, Orellana, Adelina, Then Bergh, Florian, Wang, Xue, Hulsman, Marc, Beker, Nina, Tesi, Niccolo, Morris, Christopher M, Indakoetxea, Begoña, Collij, Lyduine E, Scherer, Martin, Morenas-Rodríguez, Estrella, Ironside, James W, van Berckel, Bart NM, Alcolea, Daniel, Wiendl, Heinz, Strickland, Samantha L, Pastor, Pau, Rodríguez Rodríguez, Eloy, Boeve, Bradley F, Petersen, Ronald C, Ferman, Tanis J, van Gerpen, Jay A, Reinders, Marcel JT, Uitti, Ryan J, Tárraga, Lluís, Maier, Wolfgang, Dols-Icardo, Oriol, Kawalia, Amit, Dalmasso, Maria Carolina, Boada, Mercè, Zettl, Uwe K, van Schoor, Natasja M, Beekman, Marian, Allen, Mariet, Masliah, Eliezer, de Munain, Adolfo López, Pantelyat, Alexander, Wszolek, Zbigniew K, Ross, Owen A, Dickson, Dennis W, Graff-Radford, Neill R, Knopman, David, Rademakers, Rosa, Lemstra, Afina W, Pijnenburg, Yolande AL, Scheltens, Philip, Gasser, Thomas, Chinnery, Patrick F, Hemmer, Bernhard, Huisman, Martijn A, Troncoso, Juan, Moreno, Fermin, Nohr, Ellen A, Sørensen, Thorkild IA, Heutink, Peter, Sánchez-Juan, Pascual, Posthuma, Danielle, Clarimón, Jordi, Christensen, Kaare, Ertekin-Taner, Nilüfer, Scholz, Sonja W, Ramirez, Alfredo, Ruiz, Agustín, Slagboom, Eline, van der Flier, Wiesje M
Veröffentlicht in: Acta Neuropathologica, vol 139, iss 5;
2020

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Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of lon...

van der Lee, Sven J, Conway, Olivia J, Jansen, Iris, Carrasquillo, Minerva M, Kleineidam, Luca, van den Akker, Erik, Hernández, Isabel, van Eijk, Kristel R, Stringa, Najada, Chen, Jason A, Zettergren, Anna, Andlauer, Till FM, Diez-Fairen, Monica, Simon-Sanchez, Javier, Lleó, Alberto, Zetterberg, Henrik, Nygaard, Marianne, Blauwendraat, Cornelis, Savage, Jeanne E, Mengel-From, Jonas, Moreno-Grau, Sonia, Wagner, Michael, Fortea, Juan, Keogh, Michael J, Blennow, Kaj, Skoog, Ingmar, Friese, Manuel A, Pletnikova, Olga, Zulaica, Miren, Lage, Carmen, de Rojas, Itziar, Riedel-Heller, Steffi, Illán-Gala, Ignacio, Wei, Wei, Jeune, Bernard, Orellana, Adelina, Then Bergh, Florian, Wang, Xue, Hulsman, Marc, Beker, Nina, Tesi, Niccolo, Morris, Christopher M, Indakoetxea, Begoña, Collij, Lyduine E, Scherer, Martin, Morenas-Rodríguez, Estrella, Ironside, James W, van Berckel, Bart NM, Alcolea, Daniel, Wiendl, Heinz, Strickland, Samantha L, Pastor, Pau, Rodríguez Rodríguez, Eloy, DESGESCO (Dementia Genetics Spanish Consortium), EADB (Alzheimer Disease European DNA biobank), IFGC (International FTD-Genomics Consortium), IPDGC (The International Parkinson Disease Genomics Consortium), RiMod-FTD (Risk and Modifying factors in Fronto-Temporal Dementia), Netherlands Brain Bank (NBB), Boeve, Bradley F, Petersen, Ronald C, Ferman, Tanis J, van Gerpen, Jay A, Reinders, Marcel JT, Uitti, Ryan J, Tárraga, Lluís, Maier, Wolfgang, Dols-Icardo, Oriol, Kawalia, Amit, Dalmasso, Maria Carolina, Boada, Mercè, Zettl, Uwe K, van Schoor, Natasja M, Beekman, Marian, Allen, Mariet, Masliah, Eliezer, de Munain, Adolfo López, Pantelyat, Alexander, Wszolek, Zbigniew K, Ross, Owen A, Dickson, Dennis W, Graff-Radford, Neill R, Knopman, David, Rademakers, Rosa, Lemstra, Afina W, Pijnenburg, Yolande AL, Scheltens, Philip, Gasser, Thomas, Chinnery, Patrick F, Hemmer, Bernhard, Huisman, Martijn A, Troncoso, Juan, Moreno, Fermin, Nohr, Ellen A, Sørensen, Thorkild IA, Heutink, Peter, Sánchez-Juan, Pascual, Posthuma, Danielle, GIFT (Genetic Investigation in Frontotemporal Dementia and Alzheimer’s Disease) Study Group, Clarimón, Jordi, Christensen, Kaare, Ertekin-Taner, Nilüfer, Scholz, Sonja W, Ramirez, Alfredo, Ruiz, Agustín, Slagboom, Eline, van der Flier, Wiesje M, Holstege, Henne
2021