Universität zu Köln

Journal Article

Bey, Katharina, Wolfsgruber, Steffen, Karaca, Ilker ORCID: 0000-0002-2139-0015, Wagner, Holger, Lardenoije, Roy, Becker, Julian, Milz, Esther, Kornhuber, Johannes ORCID: 0000-0002-8096-3987, Peters, Oliver, Froelich, Lutz, Huell, Michael, Ruether, Eckart, Wiltfang, Jens ORCID: 0000-0003-1492-5330, Riedel-Heller, Steffi, Scherer, Martin, Jessen, Frank, Maier, Wolfgang, van den Hove, Daniel L., Rutten, Bart P. F., Wagner, Michael ORCID: 0000-0003-2589-6440 and Ramirez, Alfredo ORCID: 0000-0003-4991-763X (2016). No association of the variant rs11887120 in DNMT3A with cognitive decline in individuals with mild cognitive impairment. Epigenomics, 8 (5). S. 593 - 599. LONDON: FUTURE MEDICINE LTD. ISSN 1750-192X

Karsak, Meliha, Glebov, Konstantin, Scheffold, Marina, Bajaj, Thomas, Kawalia, Amit, Karaca, Ilker, Rading, Sebastian, Kornhuber, Johannes, Peters, Oliver, Diez-Fairen, Monica ORCID: 0000-0003-1882-0309, Froelich, Lutz, Huell, Michael, Wiltfang, Jens ORCID: 0000-0003-1492-5330, Scherer, Martin, Riedel-Heller, Steffi, Schneider, Anja, Heneka, Michael T., Fliessbach, Klaus, Sharaf, Ahmed, Thiele, Holger, Lennarz, Martina, Jessen, Frank, Maier, Wolfgang, Kubisch, Christian, Ignatova, Zoya, Nuernberg, Peter, Pastor, Pau ORCID: 0000-0002-7493-8777, Walter, Jochen ORCID: 0000-0002-4678-2912 and Ramirez, Alfredo ORCID: 0000-0003-4991-763X (2020). A rare heterozygous TREM2 coding variant identified in familial clustering of dementia affects an intrinsically disordered protein region and function of TREM2. Hum. Mutat., 41 (1). S. 169 - 182. HOBOKEN: WILEY. ISSN 1098-1004

Kleineidam, Luca, Chouraki, Vincent, Prochnicki, Tomasz, van der Lee, Sven J., Madrid-Marquez, Laura, Wagner-Thelen, Holger, Karaca, Ilker, Weinhold, Leonie, Wolfsgruber, Steffen, Boland, Anne, Adami, Pamela V. Martino, Lewczuk, Piotr, Popp, Julius ORCID: 0000-0002-0068-0312, Brosseron, Frederic, Jansen, Iris E., Hulsman, Marc, Kornhuber, Johannes, Peters, Oliver, Berr, Claudine, Heun, Reinhard, Froelich, Lutz, Tzourio, Christophe, Dartigues, Jean-Francois, Huell, Michael, Espinosa, Ana, Hernandez, Isabel, de Rojas, Itziar, Orellana, Adelina, Valero, Sergi, Stringa, Najada, van Schoor, Natasja M., Huisman, Martijn, Scheltens, Philip, Ruther, Eckart, Deleuze, Jean-Francois, Wiltfan, Jens, Tarraga, Lluis, Schmid, Matthias, Scherer, Martin, Riedel-Heller, Steffi, Heneka, Michael T., Amouyel, Philippe, Jessen, Frank, Boada, Merce, Maier, Wolfgang, Schneider, Anja, Gonzalez-Perez, Antonio, van der Flier, Wiesje M., Wagner, Michael ORCID: 0000-0003-2589-6440, Lambert, Jean-Charles, Holstege, Henne, Saez, M. Eugenia, Latz, Eicke, Ruiz, Agustin and Ramirez, Alfredo ORCID: 0000-0003-4991-763X (2020). PLCG2 protective variant p.P522R modulates tau pathology and disease progression in patients with mild cognitive impairment. Acta Neuropathol., 139 (6). S. 1025 - 1045. NEW YORK: SPRINGER. ISSN 1432-0533

Lewczuk, Piotr ORCID: 0000-0002-8101-6535, Riederer, Peter, O'Bryant, Sid E., Verbeek, Marcel M., Dubois, Bruno, Visser, Pieter Jelle ORCID: 0000-0001-8008-9727, Jellinger, Kurt A., Engelborghs, Sebastiaan, Ramirez, Alfredo ORCID: 0000-0003-4991-763X, Parnetti, Lucilla ORCID: 0000-0001-5722-3967, Jack, Clifford R., Jr., Teunissen, Charlotte E., Hampel, Harald, Lleo, Alberto, Jessen, Frank, Glodzik, Lidia, de Leon, Mony J., Fagan, Anne M., Luis Molinuevo, Jose, Jansen, Willemijn J., Winblad, Bengt, Shaw, Leslie M., Andreasson, Ulf, Otto, Markus ORCID: 0000-0003-4273-4267, Mollenhauer, Brit, Wiltfang, Jens ORCID: 0000-0003-1492-5330, Turner, Martin R., Zerr, Inga, Handels, Ron ORCID: 0000-0002-8663-0630, Thompson, Alexander G., Johansson, Gunilla, Ermann, Natalia, Trojanowski, John Q., Karaca, Ilker, Wagner, Holger, Oeckl, Patrick ORCID: 0000-0002-7652-7023, van Doorn, Linda van Waalwijk, Bjerke, Maria, Kapogiannis, Dimitrios ORCID: 0000-0003-2181-3118, Kuiperij, H. Bea, Farotti, Lucia, Li, Yi, Gordon, Brian A., Epelbaum, Stephane ORCID: 0000-0003-4059-2891, Vos, Stephanie J. B., Klijn, Catharina J. M., Van Nostrand, William E., Minguillon, Carolina, Schmitz, Matthias, Gallo, Carla ORCID: 0000-0001-8348-0473, Mato, Andrea Lopez, Thibaut, Florence, Lista, Simone, Alcolea, Daniel ORCID: 0000-0002-3819-3245, Zetterberg, Henrik, Blennow, Kaj and Kornhuber, Johannes ORCID: 0000-0002-8096-3987 (2018). Cerebrospinal fluid and blood biomarkers for neurodegenerative dementias: An update of the Consensus of the Task Force on Biological Markers in Psychiatry of the World Federation of Societies of Biological Psychiatry. World J. Biol. Psychiatry, 19 (4). S. 244 - 329. ABINGDON: TAYLOR & FRANCIS LTD. ISSN 1814-1412

Minnerop, Martina, Kurzwelly, Delia, Wagner, Holger, Soehn, Anne S., Reichbauer, Jennifer, Tao, Feifei, Rattay, Tim W. ORCID: 0000-0002-5456-7761, Peitz, Michael, Rehbach, Kristina, Giorgetti, Alejandro, Pyle, Angela, Thiele, Holger, Altmueller, Janine, Timmann, Dagmar, Karaca, Ilker, Lennarz, Martina, Baets, Jonathan, Hengel, Holger, Synofzik, Matthis, Atasu, Burcu, Feely, Shawna, Kennerson, Marina, Stendel, Claudia, Lindig, Tobias, Gonzalez, Michael A., Stirnberg, Ruediger, Sturm, Marc ORCID: 0000-0002-6552-8362, Roeske, Sandra, Jung, Johanna, Bauer, Peter, Lohmann, Ebba, Herms, Stefan ORCID: 0000-0002-2786-8200, Heilmann-Heimbach, Stefanie ORCID: 0000-0003-1057-465X, Nicholson, Garth, Mahanjah, Muhammad, Sharkia, Rajech, Carloni, Paolo, Bruestle, Oliver, Klopstock, Thomas, Mathews, Katherine D., Shy, Michael E., de Jonghe, Peter, Chinnery, Patrick F., Horvath, Rita ORCID: 0000-0002-9841-170X, Kohlhase, Juergen, Schmitt, Ina, Wolf, Michael, Greschus, Susanne, Amunts, Katrin, Maier, Wolfgang, Schoels, Ludger, Nuernberg, Peter, Zuchner, Stephan, Klockgether, Thomas, Ramirez, Alfredo ORCID: 0000-0003-4991-763X and Schuele, Rebecca (2017). Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia. Brain, 140. S. 1561 - 1579. OXFORD: OXFORD UNIV PRESS. ISSN 1460-2156

Rehker, Jan, Rodhe, Johanna, Nesbitt, Ryan R., Boyle, Evan A., Martin, Beth K., Lord, Jenny, Karaca, Ilker, Naj, Adam, Jessen, Frank, Helisalmi, Seppo, Soininen, Hilkka, Hiltunen, Mikko, Ramirez, Alfredo ORCID: 0000-0003-4991-763X, Scherer, Martin, Farrer, Lindsay A., Haines, Jonathan L., Pericak-Vance, Margaret A., Raskind, Wendy H., Cruchaga, Carlos, Schellenberg, Gerard D., Joseph, Bertrand and Brkanac, Zoran (2017). Caspase-8, association with Alzheimer's Disease and functional analysis of rare variants. PLoS One, 12 (10). SAN FRANCISCO: PUBLIC LIBRARY SCIENCE. ISSN 1932-6203