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Grassmann, Felix and Schoenberger, Peter G. A. and Brandl, Caroline and Schick, Tina and Hasler, Daniele and Meister, Gunter and Fleckenstein, Monika and Lindner, Moritz and Helbig, Horst and Fauser, Schascha and Weber, Bernhard H. F. (2014) A circulating microRNA profile is associated with late-stage neovascular age-related macular degeneration. PLoS ONE 9 (9), e107461.
Pauly, Diana and Nagel, Benedik M. and Reinders, Jörg and Kilian, Tobias and Wulf, Matthias and Ackermann, Susanne and Ehrenstein, Boris and Zipfel, Peter F. and Skerka, Christine and Weber, Bernhard H. F. (2014) A Novel Antibody against Human Properdin Inhibits the Alternative Complement System and Specifically Detects Properdin from Blood Samples. PLos ONE 9 (5), e96371.
Grassmann, Felix and Fritsche, Lars G. and Keilhauer, Claudia N. and Heid, Iris M. and Weber, Bernhard H. F. (2012) Modelling the Genetic Risk in Age-Related Macular Degeneration. PloS ONE 7, e37979.
Milenkovic, Vladimir M. and Brockmann, Marisa and Stöhr, Heidi and Weber, Bernhard H. F. and Strauss, Olaf (2010) Evolution and functional divergence of the anoctamin family of membrane proteins. BMC evolutionary biology 10, p. 319.
Wirtenberger, Michael and Tchatchou, Sandrine and Hemminki, Kari and Schmutzhard, Julia and Sutter, Christian and Schmutzler, Rita K. and Meindl, Alfons and Wappenschmidt, Barbara and Kiechle, Marion and Arnold, Norbert and Weber, Bernhard H. F. and Niederacher, Dieter and Bartram, Claus R. and Burwinkel, Barbara (2006) Associations of genetic variants in the estrogen receptor coactivators PPARGC1A, PPARGC1B and EP300 with familial breast cancer. Carcinogenesis 27 (11), pp. 2201-2208.
Wirtenberger, Michael and Frank, Bernd and Hemminki, Kari and Klaes, Rüdiger and Schmutzler, Rita K. and Wappenschmidt, Barbara and Meindl, Alfons and Kiechle, Marion and Arnold, Norbert and Weber, Bernhard H. F. and Niederacher, Dieter and Bartram, Claus R. and Burwinkel, Barbara (2006) Interaction of Werner and Bloom syndrome genes with p53 in familial breast cancer. Carcinogenesis 27 (8), pp. 1655-1660.
Metzger, Silke and Bauer, Peter and Tomiuk, Juergen and Laccone, Franco and Didonato, Stefano and Gellera, Cinzia and Soliveri, Paola and Lange, Herwig W. and Weirich-Schwaiger, Helga and Wenning, Gregor K. and Melegh, Bela and Havasi, Victoria and Balikó, Lazlo and Wieczorek, Stefan and Arning, Larissa and Zaremba, Jacek and Sulek, Anna and Hoffman-Zacharska, Dorota and Basak, A. Nazli and Ersoy, Nagehan and Zidovska, Jana and Kebrdlova, Vera and Pandolfo, Massimo and Ribaï, Pascale and Kadasi, Ludovit and Kvasnicova, Marta and Weber, Bernhard H. F. and Kreuz, Friedmar and Dose, Matthias and Stuhrmann, Manfred and Riess, Olaf (2006) The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington's disease. Neurogenetics 7 (1), pp. 27-30.