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Publications by Weber, Bernhard H. F.

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Jump to: 2016 | 2015 | 2014 | 2012 | 2010 | 2006
Number of items: 12.

2016

Weber, Bernhard H. F. and Grassmann, Felix and Cantsilieris, Stuart and Schulz-Kuhnt, Anja-Sabrina and White, Stefan J. and Richardson, Andrea J. and Hewitt, Alex W. and Vote, Brendan J. and Schmied, Denise and Guymer, Robyn H. and Baird, Paul N. (2016) Multiallelic copy number variation in the complement component 4A (C4A) gene is associated with late-stage age-related macular degeneration (AMD). Jornal of Neuroinflammation 13 (81), pp. 1-9.
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2015

Heid, Iris M. and Stark, Klaus and Olden, Matthias and Brandl, Caroline and Dietl, Alexander and Zimmermann, Martina E. and Schelter, Sabine C. and Loss, Julika and Leitzmann, Michael F. and Böger, Carsten A. and Luchner, Andreas and Kronenberg, Florian and Helbig, Horst and Weber, Bernhard H. F. (2015) The German AugUR study: study protocol of a prospective study to investigate chronic diseases in the elderly. BMC Geriatrics 15 (130), pp. 1-8.
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Weber, Bernhard H. F. and Grassmann, Felix and Fleckenstein, Monika and Chew, Emmily Y. and Strunz, Tobias and Schmitz-Valkenberg, Steffen and Göbel, Arno P. and Klein, Michael L. and Ratnapariya, Rinki and Swaroop, Anand and Holz, Frank G. (2015) Clinical and Genetic Factors Associated with Progression of Geographic Atrophy Lesions in Age-Related Macular Degeneration. PLoS ONE 10 (5), pp. 1-13.
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Weber, Bernhard H. F. and Bergholz, Richard and Mändl, Julia and Jägle, Herbert and Ruether, Klaus and Grassmann, Felix (2015) Common synonymous variants in ABCA4 are protective for chloroquine induced maculopathy (toxic maculopathy). BMC Ophthalmology 15 (18), pp. 1-7.
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Hebel, Udo and Weber, Bernhard H. F., eds. (2015) Forschungsbericht 2006–2014/ Universität Regensburg. Forschungsberichte der Universität, Universität Regensburg, Regensburg.
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2014

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.
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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.
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2012

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.
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2010

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.
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2006

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. Fulltext restricted.
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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. Fulltext restricted.
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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. Fulltext restricted.
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