2011
Humangenetik, Publikationen 2011
- Müller U: Discovery of MSX2 mutation in craniosynostosis: A retrospective view. Monographs in Human Genetics, 19: 8-12 (2011)
- Müller U: Pathological mechanisms and parent-of-origin effects in hereditary paraganglioma/pheochromocytoma (PGL/PCC). Neurogenetics, 12:175-181 (2011) DOI 10.1007s10048-011-0280-y
- Müller U, Winter P, Graeber MB: Alois Alzheimer's case, Auguste D., did not carry the N141I mutation in PSEN2 characteristic of Alzheimer disease in Volga Germans. Arch Neurol 68:1210-1211 (2011)
- Höglinger GU, Müller U: Durchbruch bei der Erforschung der PSP. DNP 12:19 (2011)
- Höglinger GU, Melhem NM, Dickson DW, Sleiman PMA, Wang L-S, Klei L, Rademakers R, de Silva R, Litvan I, Riley DE, van Swieten JC, Heutink P, Wszolek ZK, Uitti RJ, Vandrovcova J, Hurtig HI, Gross RG, Maetzler W, Goldwurm S, Tolosa E, Borroni B, Pastor P, PSP Genetics Study Group, Cantwell LB, Han MR, Dillman A, van der Brug MP, Gibbs JR, Cookson MR, Hernandez DG, Singleton AB, Farrer MJ, Yu C-E, Golbe LI, Revesz T, Hardy J, Lees AJ, Devlin B, Hakonarson H, Müller U, Schellenberg GD: Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. (corresponding authors: Ulrich Müller, Gerald Schellenberg.) Nat Genet 43: 699-705 (2011)
s.a. Pressemitteilung der Deutschen Gesellschaft für Neurologie - Gu H, Wei X, Chen S, Kurz A, Müller U, Gasser T, Dodel RC, Farlow MR, Du Y: Association of Clusterin Gene Polymorphisms with Late-Onset Alzheimer's Disease. Dement Geriatr Cogn Disorder 32: 198-201 (2011)
- Weber A, Taube S, Starke S, Bergmann E, Christiansen NM, Christiansen H. Detection of tumor cells by amplicon-fusion-site polymerase chain reaction (AFS-PCR). J Clin Invest., 2011;121(2):545-553.