Wissenschaftliche Publikationen Suche Suche Autor/in Forschungsgruppe Veröffentlichungsdatum Wirkungsfaktor Suchen Sortieren nach RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Reihenfolge AufsteigendAbsteigend Akalin, Altuna Dr. (9) Alenina, Natalia Dr. (13) Alp, Keziban Merve (1) Altmueller, Janine Dr.med. (24) Annibale, Paolo Dr. (7) Bader, Michael Prof. Dr. (49) Bähring, Sylvia Dr. (3) Bartolomaeus, Hendrik (4) Bartolomaeus, Theda (3) Bayram, Safak (1) Berruezo Llacuna, Maria (1) Beule, Dieter Dr. (17) Birchmeier, Walter Prof. Dr. (13) Birchmeier-Kohler, Carmen Prof. Dr. (9) Birol, Melissa Dr. (1) Blachut, Susanne (1) Blankenstein, Thomas Prof. Dr. (1) Blüthgen, Nils (3) Bock-Bierbaum, Tobias Dr. (2) Braeuning, Caroline (1) Bunina, Daria Dr. (2) Bunse, Mario Dr. (1) Burkert, Christian Martin (1) Castilho de Barros, Carlos Prof. Dr. (1) Chakrabarti, Sampurna Dr. (1) Chekulaeva, Marina Dr. (2) Chen, Wei Prof. Dr. (8) Chu, Van Trung Dr. (3) Cöl Arslan, Seda Dr. (1) Collins, Russell Thomas Dr. (1) Conrad, Thomas Dr. (2) Coscia, Fabian Dr. (3) Dahlmann, Mathias Dr. (3) Dang Ngoc, Tu Dr. (1) Daniel, Peter Prof. Dr. (15) Daumke, Oliver Prof. Dr. (6) Dechend, Ralf Priv. Doz. 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(11) Kempa, Stefan Dr. (8) Kettenmann, Helmut Prof. Dr. (18) Kettritz, Ralph Prof. Dr. (12) Kieback, Elisa Dr. (1) Kirchner, Marieluise Dr. (4) Kirwan, Jennifer Dr. (2) Klaassen, Sabine Prof. Dr. med. (4) Klaus-Bergmann, Alexandra Dr. (1) Klußmann, Enno PD Dr. (11) Kobelt, Dennis Dr. (7) Kocks, Christine Dr. (3) Kolesnichenko, Marina Dr. (1) Konrath, Fabian Dr. (1) Krabbe, Grietje Dr. (1) Kräker, Kristin Dr. (7) Krull, Sandra Dr. (1) Ku, Min-Chi Dr. (3) Kudryashev, Mikhail Prof. Dr. (3) Kühn, Ralf Dr. (4) Kunz, Severine Dr. (4) Kurths, Silke (1) Lacadie, Scott Allen Dr. (2) Lahmann, Ines Dr. (1) Landthaler, Markus Prof. Dr. (8) Langanki, Reika (2) Lee, Young-Ae Prof. Dr. (5) Leisegang, Matthias Prof. Dr. rer. nat. (2) Leutz, Achim Prof. Dr. (7) Lewin, Gary Prof. Dr. (10) Lindberg, Eric Lars-Helge (1) Lisewski, Ulrike Dr. (2) Löber, Ulrike Dr. (2) Lohse, Martin Prof. Dr. (14) Lopez Carballo, Jacobo (1) Ludwig, Leif S. Dr. med. Dr. rer. nat. 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Dr. (9) Schlag, Peter M. Prof. Dr. (24) Schlegel, Wolfgang-Peter (2) Schmidt, Deborah (1) Schmidt, Willi Dr. (1) Schmidt-Krüger, Vanessa Dr. (2) Schmidt-Ullrich, Ruth Dr. (5) Schmitt, Clemens Prof. Dr. (9) Schmitt, Matthias Jürgen Dr. (1) Schnögl, Sigrid (2) Schommer, Sandra (1) Schöpe, Paul Curtis (1) Schreiber, Adrian PD Dr. med. (7) Schulz-Menger, Jeanette Prof. Dr. (23) Schwarz, Roland Dr. (6) Selbach, Matthias Prof. Dr. (8) Semtner, Marcus Dr. (3) Serresi, Michela Dr. (1) Siffrin, Volker (2) Sigal, Michael Dr. (2) Simon, Katja Prof. Dr. (6) Simon, Mareike Dr. (1) Singh, Manvendra Dr. (3) Smith, Janice (2) Sommer, Thomas Prof. Dr. (8) Spagnoli, Francesca Dr. (4) Spanjaard, Bastiaan Dr. (1) Spatt, Lisa (1) Specker, Edgar Dr. (1) Sperling, Silke Prof. Dr. (5) Sporbert, Anje Dr. (1) Spuler, Simone Prof. (11) Starke, Ludger Benedikt (2) Stein, Ulrike Prof. Dr. (16) Sunaga-Franze, Daniele Yumi Dr. (3) Taube, Martin (1) Telugu, Narasimha Swamy Dr. (5) Todiras, Mihail (5) Toscano, Elisa (1) Treier, Mathias Prof. Dr. (1) Trombke, Janine (1) Tsybulskyi, Volodymyr (1) Tursun, Baris Dr. (3) Uckert, Wolfgang Prof. Dr. (4) Udhayachandran, Annapoorani Dr. (1) Uyar, Bora Dr. (1) Vidal, Marie Dr. (1) von Kries, Jens Peter Dr. (3) Waiczies, Helmar Dr. (5) Waiczies, Sonia PD Dr. (7) Wallukat, Gerd Dr. (6) Walther, Wolfgang Prof. Dr. (9) Wanker, Erich Prof. Dr. (23) Welke, Robert-William (1) Wellner, Maren Dr. (2) Wenzel, Katrin Dr. (1) Wilck, Nicola Dr. med. (8) Willnow, David (2) Willnow, Thomas Prof. Dr. (15) Winter, Lukas Dr. (4) Wolf, Jana Prof. Dr. (5) Wolf, Susanne Dr. (6) Wollert-Wulf, Brigitte (2) Wyler, Emanuel Dr. (3) Zampieri, Niccolo Dr. (5) Zauber, Henrik Dr. (1) Zenkner, Martina (1) Ziehm, Matthias Dr. (1) Zinzen, Robert Patrick Dr. (4) Zühlke, Kerstin Dr. (2) (-) Marenholz, Ingo Dr. (6) (-) Müller, Thomas Dr. (2) Entwicklungsbiologie / Signaltransduktion in Nerven und Muskelzellen (2) Genetik und Genomik von Herz- Kreislauferkrankungen (10) Hochschulambulanz für Pädiatrische Allergologie und Neurodermitis (6) Molekulare Genetik allergischer Erkrankungen (6) 2000 (3) 2002 (4) 2003 (4) 2004 (7) 2005 (9) (-) 2006 (8) 2007 (9) 2008 (6) 2010 (6) 2011 (4) 2012 (8) 2013 (5) 2014 (8) 2015 (9) 2016 (1) 2017 (7) 2018 (8) 2019 (4) (-) 2020 (8) 2021 (4) 2022 (4) 2023 (7) 2024 (1) 16 Ergebnisse: Active Filter: Marenholz, Ingo Dr.Müller, Thomas Dr.20062020 Sortieren: Treffgenauigkeit Neueste nach älteste Älteste nach neueste 28. Oktober 2020 / J Genet Genomics Phosphatidylinositol 4 kinase-β mutations cause non-syndromic sensorineural deafness and inner ear malformation X. Su Y. Feng S.A. Rahman S. Wu G. Li F. Rüschendorf L. Zhao H. Cui J. Liang L. Fang H. Hu S. Froehler Y. Yu G. Patone O. Hummel Q. Chen K. Raile F.C. Luft S. Bähring K. Hussain W. Chen J. Zhang M. Gong 01. Januar 2006 Neural development T. Mueller 01. Oktober 2006 / Am J Med Genet A Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation A. Rauch J. Hoyer S. Guth C. Zweier C. Kraus C. Becker M. Zenker U. Hueffmeier C. Thiel F. Rueschendorf P. Nuernberg A. Reis U. Trautmann 01. Oktober 2006 / Am J Hum Genet Familial chilblain lupus, a monogenic form of cutaneous lupus erythematosus, maps to chromosome 3p M.A. Lee-Kirsch M. Gong H. Schulz F. Rüschendorf A. Stein C. Pfeiffer A. Ballarini M. Gahr N. Hubner M. Linne 01. November 2006 / Biochim Biophys Acta Mol Cell Res S100A1-deficient male mice exhibit increased exploratory activity and reduced anxiety-related responses G.E. Ackermann I. Marenholz D.P. Wolfer W.Y. Chan B. Schaefer P. Erne C.W. Heizmann 01. Oktober 2006 / J Allergy Clin Immunol Filaggrin loss-of-function mutations predispose to phenotypes involved in the atopic march I. Marenholz R. Nickel F. Rueschendorf F. Schulz J. Esparza-Gordillo T. Kerscher C. Grueber S. Lau M. Worm T. Keil M. Kurek E. Zaluga U. Wahn Y.A. Lee 01. November 2006 / Nat Genet The gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, is mutated in inherited anonychia D.C. Blaydon Y. Ishii E.A. O'Toole H.C. Unsworth M.T. Teh F. Rueschendorf C. Sinclair V.K. Hopsu-Havu N. Tidman C. Moss R. Watson D. de Berker M. Wajid A.M. Christiano D.P. Kelsell 01. Februar 2006 / Hum Genet SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly M. Garshasbi M.M. Motazacker K. Kahrizi F. Behjati S.S. Abedini S.E. Nieh S.G. Firouzabadi C. Becker F. Rueschendorf P. Nuernberg A. Tzschach R. Vazifehmand F. Erdogan R. Ullmann S. Lenzner A.W. Kuss H.H. Ropers H. Najmabadi 01. Juni 2006 / Development dILA neurons in the dorsal spinal cord are the product of terminal and non-terminal asymmetric progenitor cell divisions, and require Mash1 for their development H. Wildner T. Mueller S.H. Cho D. Broehl C.L. Cepko F. Guillemot C. Birchmeier 23. April 2020 / Allergy Phenotype consensus is required to enable large-scale genetic consortium studies of food allergy Y. Asai D. Martino T. Eiwegger K. Nadeau G.H. Koppelman A.E. Clarke Y.A. Lee E.S. Chan E. Simons C. Laprise B. Mazer I. Marenholz D. Royce S.J. Elliott C. Hampson J. Gerdts A. Eslami L. Soller J. Hui M. Azad A. Sandford D. 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28. Oktober 2020 / J Genet Genomics Phosphatidylinositol 4 kinase-β mutations cause non-syndromic sensorineural deafness and inner ear malformation X. Su Y. Feng S.A. Rahman S. Wu G. Li F. Rüschendorf L. Zhao H. Cui J. Liang L. Fang H. Hu S. Froehler Y. Yu G. Patone O. Hummel Q. Chen K. Raile F.C. Luft S. Bähring K. Hussain W. Chen J. Zhang M. Gong
01. Oktober 2006 / Am J Med Genet A Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation A. Rauch J. Hoyer S. Guth C. Zweier C. Kraus C. Becker M. Zenker U. Hueffmeier C. Thiel F. Rueschendorf P. Nuernberg A. Reis U. Trautmann
01. Oktober 2006 / Am J Hum Genet Familial chilblain lupus, a monogenic form of cutaneous lupus erythematosus, maps to chromosome 3p M.A. Lee-Kirsch M. Gong H. Schulz F. Rüschendorf A. Stein C. Pfeiffer A. Ballarini M. Gahr N. Hubner M. Linne
01. November 2006 / Biochim Biophys Acta Mol Cell Res S100A1-deficient male mice exhibit increased exploratory activity and reduced anxiety-related responses G.E. Ackermann I. Marenholz D.P. Wolfer W.Y. Chan B. Schaefer P. Erne C.W. Heizmann
01. Oktober 2006 / J Allergy Clin Immunol Filaggrin loss-of-function mutations predispose to phenotypes involved in the atopic march I. Marenholz R. Nickel F. Rueschendorf F. Schulz J. Esparza-Gordillo T. Kerscher C. Grueber S. Lau M. Worm T. Keil M. Kurek E. Zaluga U. Wahn Y.A. Lee
01. November 2006 / Nat Genet The gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, is mutated in inherited anonychia D.C. Blaydon Y. Ishii E.A. O'Toole H.C. Unsworth M.T. Teh F. Rueschendorf C. Sinclair V.K. Hopsu-Havu N. Tidman C. Moss R. Watson D. de Berker M. Wajid A.M. Christiano D.P. Kelsell
01. Februar 2006 / Hum Genet SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly M. Garshasbi M.M. Motazacker K. Kahrizi F. Behjati S.S. Abedini S.E. Nieh S.G. Firouzabadi C. Becker F. Rueschendorf P. Nuernberg A. Tzschach R. Vazifehmand F. Erdogan R. Ullmann S. Lenzner A.W. Kuss H.H. Ropers H. Najmabadi
01. Juni 2006 / Development dILA neurons in the dorsal spinal cord are the product of terminal and non-terminal asymmetric progenitor cell divisions, and require Mash1 for their development H. Wildner T. Mueller S.H. Cho D. Broehl C.L. Cepko F. Guillemot C. Birchmeier
23. April 2020 / Allergy Phenotype consensus is required to enable large-scale genetic consortium studies of food allergy Y. Asai D. Martino T. Eiwegger K. Nadeau G.H. Koppelman A.E. Clarke Y.A. Lee E.S. Chan E. Simons C. Laprise B. Mazer I. Marenholz D. Royce S.J. Elliott C. Hampson J. Gerdts A. Eslami L. Soller J. Hui M. Azad A. Sandford D. Daley