Functional Genetics
About Our Group
The characterization of mutants represents a valuable instrument for functional genome analysis. Novel mouse models for metabolic diseases are in the center of our projects. By unraveling the molecular pathways and pathophysiological events leading, in particular, to diabetes we also transfer the basic research results into the development of novel strategies for diagnosis, prevention and therapy.
As a service platform we offer to interested scientific groups the ENU DNA F1 Archive with 16,800 paralleled DNA and sperm samples of ENU mutagenesis derived F1 mice for the screening of genes of interest.
Member and Spokesperson of the Executive Board (acting), Research Director Helmholtz Munich, Full Professor and Chair of Experimental Genetics Technical University Munich, Director of the Institute of Experimental Genetics Helmholtz Munich
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Selected Publications
Riedhammer, K.M. ; Nguyen, T.T. ; Koşukcu, C. ; Calzada-Wack, J. ; Li, Y. ; Batzir, N.A. ; Saygılı, S. ; Wimmers, V. ; Kim, G.J. ; Chrysanthou, M. ; Bakey, Z. ; Sofrin-Drucker, E. ; Kraiger, M. ; Sanz-Moreno, A. ; Amarie, O.V. ; Rathkolb, B. ; Klein-Rodewald, T. ; Garrett, L. ; Hölter, S.M. ; Seisenberger, C. ; Haug, S. ; Schlosser, P. ; Marschall, S. ; Wurst, W. ; Fuchs, H. ; Gailus-Durner, V. ; Wuttke, M. ; Hrabě de Angelis, M. ; Ćomić, J. ; Doğan, N. ; Özlük, Y. ; Taşdemir, M. ; Ağbaş, A. ; Canpolat, N. ; Orenstein, N. ; Çalışkan, S. ; Weber, R.G. ; Bergmann, C. ; Jeanpierre, C. ; Saunier, S. ; Lim, T.Y. ; Hildebrandt, F. ; Alhaddad, B. ; Basel-Salmon, L. ; Borovitz, Y. ; Wu, K. ; Antony, D. ; Matschkal, J. ; Schaaf, C.W. ; Renders, L. ; Schmaderer, C. ; Rogg, M. ; Schell, C. ; Meitinger, T. ; Heemann, U. ; Köttgen, A. ; Arnold, S.J. ; Ozaltin, F. ; Schmidts, M. ; Hoefele, J.
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT).Correa, D. ; Scheuber, M.I. ; Shan, H. ; Weinmann, O.W. ; Baumgartner, Y.A. ; Harten, A. ; Wahl, A.S. ; Skaar, K.L. ; Schwab, M.E.
Intranasal delivery of full-length anti-Nogo-A antibody: A potential alternative route for therapeutic antibodies to central nervous system targets.Kandaswamy, S. ; Zobel, L. ; John, B. ; Santhiya, S.T. ; Bogedein, J. ; Przemeck, G.K.H. ; Gailus-Durner, V. ; Fuchs, H. ; Biel, M. ; Hrabě de Angelis, M. ; Graw, J. ; Michalakis, S. ; Amarie, O.V.
Mutations within the cGMP-binding domain of CNGA1 causing autosomal recessive retinitis pigmentosa in human and animal model.Pawliczek, D. ; Fuchs, H. ; Gailus-Durner, V. ; Hrabě de Angelis, M. ; Quinlan, R. ; Graw, J. ; Dalke, C.
On the nature of murine radiation-induced subcapsular cataracts: Optical coherence tomography-based fine classification, in vivo dynamics and impact on visual acuity.Vidali, S. ; Gerlini, R. ; Thompson, K. ; Urquhart, J.E. ; Meisterknecht, J. ; Aguilar-Pimentel, J.A. ; Amarie, O.V. ; Becker, L. ; Breen, C. ; Calzada-Wack, J. ; Chhabra, N.F. ; Cho, Y.-L. ; da Silva Buttkus, P. ; Feichtinger, R.G. ; Gampe, K. ; Garrett, L. ; Hoefig, K.P. ; Hölter, S.M. ; Jameson, E. ; Klein-Rodewald, T. ; Leuchtenberger, S. ; Marschall, S. ; Mayer-Kuckuk, P. ; Miller, G. ; Oestereicher, M.A. ; Pfannes, K. ; Rathkolb, B. ; Rozman, J. ; Sanders, C. ; Spielmann, N. ; Stoeger, C. ; Szibor, M. ; Treise, I. ; Walter, J.H. ; Wurst, W. ; Mayr, J.A. ; Fuchs, H. ; Gärtner, U. ; Wittig, I. ; Taylor, R.W. ; Newman, W.G. ; Prokisch, H. ; Gailus-Durner, V. ; Hrabě de Angelis, M.
Characterising a homozygous two-exon deletion in UQCRH: Comparing human and mouse phenotypes.Jacobsen, H. ; Walendy-Gnirß, K. ; Tekin-Bubenheim, N. ; Kouassi, N.M. ; Ben-Batalla, I. ; Berenbrok, N. ; Wolff, M. ; dos Reis, V.P. ; Zickler, M. ; Scholl, L. ; Gries, A. ; Jania, H. ; Kloetgen, A. ; Düsedau, A. ; Pilnitz-Stolze, G. ; Jeridi, A. ; Yildirim, A.Ö. ; Fuchs, H. ; Gailus-Durner, V. ; Stoeger, C. ; Hrabě de Angelis, M. ; Manuylova, T. ; Klingel, K. ; Culley, F.J. ; Behrends, J. ; Loges, S. ; Schneider, B. ; Krauss-Etschmann, S. ; Openshaw, P.J.M. ; Gabriel, G.
Offspring born to influenza A virus infected pregnant mice have increased susceptibility to viral and bacterial infections in early life.Ehlich, H. ; Cater, H.L. ; Flenniken, A.M. ; Goncalves Da Cruz, I. ; Mura, A.M. ; Ntafis, V. ; Raess, M. ; Selloum, M. ; Stoeger, C. ; Suchanova, S. ; Vuolteenaho, R. ; Brown, S.D.M. ; Hérault, Y. ; Hinttala, R. ; Hrabě de Angelis, M. ; Kollias, G. ; Kontoyiannis, D.L. ; Malissen, B. ; McKerlie, C. ; Sedláček, R. ; Wells, S.E. ; Zarubica, A. ; Rozman, J. ; Sorg, T.
INFRAFRONTIER quality principles in systemic phenotyping.Chhabra, N.F. ; Amend, A.-L. ; Bastidas-Ponce, A. ; Sabrautzki, S. ; Tarquis Medina, M. ; Sachs, S. ; Rubey, M. ; Lorenz-Depiereux, B. ; Feuchtinger, A. ; Bakhti, M. ; Lickert, H. ; Przemeck, G.K.H. ; Hrabě de Angelis, M.
A point mutation in the Pdia6 gene results in loss of pancreatic β-cell identity causing overt diabetes.Contact