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Journal Article
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
Vollersen, Nele, Zhao, Wenbo ORCID: 0000-0002-3418-9433, Rolvien, Tim, Lange, Fabiola, Schmidt, Felix Nikolai, Sonntag, Stephan, Shmerling, Doron, von Kroge, Simon, Stockhausen, Kilian Elia, Sharaf, Ahmed, Schweizer, Michaela, Karsak, Meliha, Busse, Bjoern, Bockamp, Ernesto, Semler, Oliver, Amling, Michael, Oheim, Ralf, Schinke, Thorsten and Yorgan, Timur Alexander
(2021).
The WNT1(G177C) mutation specifically affects skeletal integrity in a mouse model of osteogenesis imperfecta type XV.
Bone Res., 9 (1).
LONDON:
SPRINGERNATURE.
ISSN 2095-6231