Scientific Publications Search Search Author Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Adami, Eleonora Dr. (1) Akalin, Altuna Dr. (7) Alenina, Natalia Dr. (17) Altmueller, Janine Dr.med. (7) Bader, Michael Prof. Dr. (50) Bähring, Sylvia Dr. (2) Begay-Müller, Valerie Dr. (3) Birchmeier, Walter Prof. Dr. (10) Birchmeier-Kohler, Carmen Prof. Dr. (17) Birol, Melissa Dr. (2) Blankenstein, Thomas Prof. Dr. (9) Bunina, Daria Dr. (1) Bunse, Mario Dr. (1) Castilho de Barros, Carlos Prof. Dr. (2) Cerda Esteban, Nuria Dr. (1) Chen, Wei Prof. Dr. (26) Cöl Arslan, Seda Dr. (1) Dahlmann, Mathias Dr. (2) Daniel, Peter Prof. Dr. (5) Daumke, Oliver Prof. Dr. (8) Dechend, Ralf Priv. Doz. (34) de la Rosa, Kathrin Dr. (3) Diebolder, Christoph Dr. (3) Diecke, Sebastian Dr. (7) Edes, Inan Dr. (1) Escobar Fernandez, Helena Dr. (1) Estebanez, Luc Dr. (1) Fälber, Katja Dr. (1) Falcke, Martin Prof. Dr. (10) Fielitz, Jens Dr. (5) Fischer, Christian (2) Forslund, Sofia Dr. (5) Frahm-Barske, Silke Dr. (1) Gargiulo, Gaetano Dr. (2) Gerhardt, Holger Prof. Dr. (11) Gerlach, Kerstin (3) Gorski, Stan Dr. (2) Gotthardt, Michael Prof. Dr. (7) Gouti, Mina Dr. (1) Grossmann, Katja Dr. (1) Grosswendt, Stefanie Dr. (1) Grybowski, Andrea (1) Haas, Simon Dr. rer. nat. (3) Haase, Nadine Dr. (2) Hammes-Lewin, Annette Dr. (3) Harabula, Izabela-Cezara (1) Haseleu, Julia Dr. (1) Haucke, Volker Professor (2) Hedtrich, Sarah Prof. Dr. (1) Heinemann, Udo Prof. Dr. (12) Henssen, Anton Prof. Dr. med. (1) Herse, Florian PD Dr. (8) Herzog, Margareta (3) Heuser, Arnd Dr. (2) Hinz, Michael Dr. (3) Höpken, Uta Elisabeth PD Dr. (8) Hübner, Norbert Prof. Dr. (22) Hummel, Oliver (5) Infante Duarte, Carmen (6) Ivics, Zoltan Dr. (13) Izsvak, Zsuzsanna Dr. (16) Janke, Jürgen Dr. (2) Janz, Martin Dr. (3) Jarosch, Ernst Dr. (3) Jentsch, Thomas Prof. Dr. (12) Jouhanneau, Jean-Sebastien Dr. (1) Junker, Jan Philipp Prof. Dr. (6) Jüttner, Rene Dr. (5) Kainmüller, Dagmar Prof. Dr. (3) Kamer, Ilona (1) Kaminski, Michael Dr. (1) Kammertöns, Thomas Dr. (4) Keller, Ulrich Dr. med. (2) Kempa, Stefan Dr. (7) Kettenmann, Helmut Prof. Dr. (14) Kettritz, Ralph Prof. Dr. (18) Kieback, Elisa Dr. (2) Kirchner, Marieluise Dr. (5) Kirwan, Jennifer Dr. (3) Klaassen, Sabine Prof. Dr. med. (7) Klaus-Bergmann, Alexandra Dr. (1) Klementowicz-Skierbiszewski, Agnieszka (1) Klix, Sabrina (2) Klußmann, Enno PD Dr. (7) Kobelt, Dennis Dr. (5) Kofahl, Bente Dr. (1) Krabbe, Grietje Dr. (2) Krüger, Christina (1) Ku, Min-Chi Dr. (3) Kudryashev, Mikhail Prof. Dr. (7) Kühn, Ralf Dr. (13) Kunz, Severine Dr. (1) Lacadie, Scott Allen Dr. (2) Landthaler, Markus Prof. Dr. (12) Langnick, Claudia (2) Lee, Young-Ae Prof. Dr. (4) Leisegang, Matthias Prof. Dr. rer. nat. (4) Leutz, Achim Prof. Dr. (9) Lewin, Gary Prof. Dr. (20) Lisowski, Pawel Dr. (1) Ludwig, Leif S. Dr. med. Dr. rer. nat. (2) Luft, Friedrich Prof. Dr. (64) Lupianez Garcia, Dario Jesus Dr. (2) Maatz, Henrike Dr. (2) Maglione, Marta (1) Mahmoodzadeh, Shokoufeh PD Dr. (5) Marenholz, Ingo Dr. (2) Marg, Andreas Dr. (4) Marko, Lajos Dr. (6) Mastrobuoni, Guido Dr. (3) Mathas, Stephan Dr. (3) Mekle, Ralf (1) Mertins, Philipp Dr. (7) Metzger, Jakob Johannes Dr. (3) Meyer, Irmtraud Margret Prof. Dr. (4) Millward, Jason Dr. (4) Morano, Ingo Prof. Dr. (6) Müller, Dominik Prof. Dr. (21) Müller, Gerd Dr. (3) Müller, Marion (1) Müller, Thomas Dr. (5) Münchberg, Stefanie (1) Na, Il-Kang Dr. (2) Nguyen, Tam Hoai Dr. (4) Niendorf, Thoralf Prof. Dr. (32) Nimptsch, Katharina Dr. (7) Nolte, Christiane Dr. (1) Obermayer-Wasserscheid, Benedikt Dr. (5) Ohler, Uwe Prof. Dr. (16) Panakova, Daniela Dr. (3) Patone, Giannino Dr. (1) Paul, Friedemann Prof. Dr. med. (63) Perrot, Andreas (3) Pezzutto, Antonio Prof. Dr. (12) Piazza, Ilaria Dr. (1) Pischon, Tobias Prof. Dr. (26) Pombo, Ana Prof. Dr. (9) Popova, Elena Dr. (1) Potente, Michael Prof. Dr. (2) Poulet, James Prof. Dr. (5) Preibisch, Stephan Dr. (5) Prigione, Alessandro Prof. Dr. (6) Qadri, Fatimunnisa Dr. (6) Quedenau, Claudia (1) Rademann, Joerg Prof. Dr. (2) Radke, Michael Dr. (3) Rahn, Hans-Peter Dr. (2) Rajewsky, Klaus Prof. Dr. (12) Rajewsky, Nikolaus Prof. Dr. (18) Rathjen, Fritz Prof. Dr. (5) Rehm, Armin Dr. (4) Reimann, Henning Dr. (1) Rhein, Simone Dr. (1) Robson, Michael Dr. (2) Rocks, Oliver Dr. (1) Rosenthal, Walter Prof. Dr. (1) Roske, Yvette Dr. (3) Rother, Franziska Dr. (2) Rousselle, Anthony (1) Rybak-Wolf, Agnieszka Dr. (6) Saar, Kathrin Dr. (10) Sander, Maike Prof. Dr. (12) Sanders, Ashley Dr. (1) Sattentau, Quentin James Prof. Dr. (3) Sawamiphak, Suphansa Dr. (2) Scheidereit, Claus Prof. Dr. (4) Schiattarella, Gabriele G. Dr. (16) Schlag, Peter M. Prof. Dr. (21) Schmidt, Deborah (1) Schmidt-Krüger, Vanessa Dr. (6) Schmidt-Ullrich, Ruth Dr. (3) Schmitt, Clemens Prof. Dr. (4) Schnögl, Sigrid (1) Schreiber, Adrian PD Dr. med. (2) Schulz-Menger, Jeanette Prof. Dr. (26) Schütz, Anja Dr. (6) Schwarz, Roland Dr. (4) Selbach, Matthias Prof. Dr. (16) Semtner, Marcus Dr. (4) Serresi, Michela Dr. (2) Siffrin, Volker (6) Sigal, Michael Dr. (1) Simon, Katja Prof. Dr. (4) Singh, Manvendra Dr. (2) Smith, Janice (2) Sommer, Christian (1) Sommer, Thomas Prof. Dr. (9) Spagnoli, Francesca Dr. (4) Sperling, Silke Prof. Dr. (4) Sporbert, Anje Dr. (3) Spuler, Simone Prof. (10) Stein, Ulrike Prof. Dr. (10) Sugimoto, Yoichiro Dr. (5) Tano, Jean-Yves Dr. (4) Taube, Martin (1) Todiras, Mihail (3) Treier, Mathias Prof. Dr. (1) Tursun, Baris Dr. (3) Uckert, Wolfgang Prof. Dr. (11) von Kries, Jens Peter Dr. (2) Waiczies, Helmar Dr. (3) Waiczies, Sonia PD Dr. (7) Wallukat, Gerd Dr. (14) Walther, Wolfgang Prof. Dr. (7) Wanker, Erich Prof. Dr. (18) Wenzel, Katrin Dr. (1) Westphal, Christina Dr. (1) Wilck, Nicola Dr. med. (2) Willimsky, Gerald Dr. (1) Willnow, Thomas Prof. Dr. (15) Winter, Lukas Dr. (5) Woehler, Andrew Dr. (3) Wolf, Jana Prof. Dr. (2) Wolf, Susanne Dr. (5) Wyler, Emanuel Dr. (2) Yilmaz, Zekiye Buket Dr. (1) Zampieri, Niccolo Dr. (1) Zauber, Henrik Dr. (1) Zinzen, Robert Patrick Dr. (3) 2000 (3) 2002 (3) 2003 (2) 2004 (7) 2005 (7) 2006 (5) 2007 (7) 2008 (3) 2009 (11) 2010 (5) 2011 (1) (-) 2012 (5) 2013 (2) (-) 2014 (4) 2015 (5) 2016 (1) 2017 (5) 2018 (4) 2019 (3) 2020 (5) 2021 (2) 2022 (1) 2024 (1) Developmental Biology / Signal Transduction (1) Genetics and Genomics of Cardiovascular Diseases (9) Molecular Physiology of Somatic Sensation (1) 9 Results: Active Filter: 20122014 Sort: Result score Newest to oldest Oldest to newest June 08, 2012 / Invest Ophthalmol Vis Sci Mutations in RD3 are associated with an extremely rare and severe form of early onset retinal dystrophy M.N. Preising N. Hausotter-Will M.C. Solbach C. Friedburg F. Rueschendorf B. Lorenz May 01, 2012 / PLoS Biol A genetic basis for mechanosensory traits in humans H. Frenzel J. Bohlender K. Pinsker B. Wohlleben J. Tank S.G. Lechner D. Schiska T. Jaijo F. Rueschendorf K. Saar J. Jordan J.M. Millan M. Gross G.R. Lewin February 01, 2012 / Epilepsia Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies C. Leu C.G.F. de Kovel F. Zara P. Striano M. Pezzella A. Robbiano A. Bianchi F. Bisulli A. Coppola A.T. Giallonardo F. Beccaria D.K. Trenite D. Lindhout V. Gaus B. Schmitz D. Janz Y.G. Weber F. Becker H. Lerche A.A. Kleefuss-Lie K. Hallman W.S. Kunz C.E. Elger H. Muhle U. Stephani R.S. Moller H. Hjalgrim S. Mullen I.E. Scheffer S.F. Berkovic K.V. Everett M.R. Gardiner C. Marini R. Guerrini A.E. Lehesjoki A. Siren R. Nabbout S. Baulac E. Leguern J.M. Serratosa F. Rosenow M. Feucht I. Unterberger A. Covanis A. Suls S. Weckhuysen R. Kaneva H. Caglayan D. Turkdogan B. Baykan N. Bebek U. Ozbek A. Hempelmann H. Schulz F. Rueschendorf H. Trucks P. Nuernberg G. Avanzini B.P.C. Koeleman T. Sander December 15, 2012 / Hum Mol Genet Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32 M. Steffens C. Leu A.K. Ruppert F. Zara P. Striano A. Robbiano G. Capovilla P. Tinuper A. Gambardella A. Bianchi A. La Neve G. Crichiutti C.G.F. de Kovel D. Kasteleijn-Nolst Trenite G.J. de Haan D. Lindhout V. Gaus B. Schmitz D. Janz Y.G. Weber F. Becker H. Lerche B.J. Steinhoff A.A. Kleefuss-Lie W.S. Kunz R. Surges C.E. Elger H. Muhle S. von Spiczak P. Ostertag I. Helbig U. Stephani R.S. Moller H. Hjalgrim L.M. Dibbens S. Bellows K. Oliver S. Mullen I.E. Scheffer S.F. Berkovic K.V. Everett M.R. Gardiner C. Marini R. Guerrini A.E. Lehesjoki A. Siren M. Guipponi A. Malafosse P. Thomas R. Nabbout S. Baulac E. Leguern R. Guerrero J.M. Serratosa P.S. Reif F. Rosenow M. Mörzinger M. Feucht F. Zimprich C. Kapser C.J. Schankin A. Suls K. Smets P. De Jonghe A. Jordanova H. Caglayan Z. Yapici D.A. Yalcin B. Baykan N. Bebek U. Ozbek C. Gieger H.E. Wichmann T. Balschun D. Ellinghaus A. Franke C. Meesters T Becker T.F. Wienker A. Hempelmann H. Schulz F. Rueschendorf M. Leber S.M. Pauck H. Trucks M.R. Toliat P. Nuernberg G. Avanzini B.P. Koeleman T. Sander January 01, 2014 / Gut Cryptogenic multifocal ulcerating stenosing enteritis associated with homozygous deletion mutations in cytosolic phospholipase A2-α M.A. Brooke H.J. Longhurst V. Plagnol N.S. Kirkby J.A. Mitchell F. Rüschendorf T.D. Warner D.P. Kelsell T.T. MacDonald February 10, 2012 / Am J Hum Genet Mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss M. Baumann C. Giunta B. Krabichler F. Rueschendorf N. Zoppi M. Colombi R.E. Bittner S. Quijano-Roy F. Muntoni S. Cirak G. Schreiber Y. Zou Y. Hu N.B. Romero R.Y. Carlier A. Amberger A. Deutschmann V. Straub M. Rohrbach B. Steinmann K. Rostasy D. Karall C.G. Boennemann J. Zschocke C. Fauth May 01, 2014 / Leukemia Inherited susceptibility to pre B-ALL caused by germline transmission of PAX5 c.547G>A F. Auer F. Rueschendorf M. Gombert P. Husemann S. Ginzel S. Izraeli M. Harit M. Weintraub O.Y. Weinstein I. Lerer P. Stepensky A. Borkhardt J. Hauer October 01, 2014 / Diabetes Recessive mutations in PCBD1 cause a new type of early-onset diabetes D. Simaite J. Kofent M. Gong F. Rüschendorf S. Jia P. Arn K. Bentler C. Ellaway P. Kühnen G.F. Hoffmann N. Blau F.M. Spagnoli N. Hübner K. Raile December 01, 2014 / Nat Genet Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes J. Schubert A. Siekierska M. Langlois P. May C. Huneau F. Becker H. Muhle A. Suls J.R. Lemke C.G.F. de Kovel H. Thiele K. Konrad A. Kawalia M.R. Toliat T. Sander F. Rueschendorf A. Caliebe I. Nagel B. Kohl A. Kecskes M. Jacmin K. Hardies S. Weckhuysen E. Riesch T. Dorn E.H. Brilstra S. Baulac R.S. Moller H. Hjalgrim B.P.C. Koeleman K. Jurkat-Rott F. Lehman-Horn J.C. Roach G. Glusman L. Hood D.J. Galas B. Martin P.A.M. de Witte S. Biskup P. De Jonghe I. Helbig R. Balling P. Nuernberg A.D. Crawford C.V. Esguerra Y.G. Weber H. Lerche
June 08, 2012 / Invest Ophthalmol Vis Sci Mutations in RD3 are associated with an extremely rare and severe form of early onset retinal dystrophy M.N. Preising N. Hausotter-Will M.C. Solbach C. Friedburg F. Rueschendorf B. Lorenz
May 01, 2012 / PLoS Biol A genetic basis for mechanosensory traits in humans H. Frenzel J. Bohlender K. Pinsker B. Wohlleben J. Tank S.G. Lechner D. Schiska T. Jaijo F. Rueschendorf K. Saar J. Jordan J.M. Millan M. Gross G.R. Lewin
February 01, 2012 / Epilepsia Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies C. Leu C.G.F. de Kovel F. Zara P. Striano M. Pezzella A. Robbiano A. Bianchi F. Bisulli A. Coppola A.T. Giallonardo F. Beccaria D.K. Trenite D. Lindhout V. Gaus B. Schmitz D. Janz Y.G. Weber F. Becker H. Lerche A.A. Kleefuss-Lie K. Hallman W.S. Kunz C.E. Elger H. Muhle U. Stephani R.S. Moller H. Hjalgrim S. Mullen I.E. Scheffer S.F. Berkovic K.V. Everett M.R. Gardiner C. Marini R. Guerrini A.E. Lehesjoki A. Siren R. Nabbout S. Baulac E. Leguern J.M. Serratosa F. Rosenow M. Feucht I. Unterberger A. Covanis A. Suls S. Weckhuysen R. Kaneva H. Caglayan D. Turkdogan B. Baykan N. Bebek U. Ozbek A. Hempelmann H. Schulz F. Rueschendorf H. Trucks P. Nuernberg G. Avanzini B.P.C. Koeleman T. Sander
December 15, 2012 / Hum Mol Genet Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32 M. Steffens C. Leu A.K. Ruppert F. Zara P. Striano A. Robbiano G. Capovilla P. Tinuper A. Gambardella A. Bianchi A. La Neve G. Crichiutti C.G.F. de Kovel D. Kasteleijn-Nolst Trenite G.J. de Haan D. Lindhout V. Gaus B. Schmitz D. Janz Y.G. Weber F. Becker H. Lerche B.J. Steinhoff A.A. Kleefuss-Lie W.S. Kunz R. Surges C.E. Elger H. Muhle S. von Spiczak P. Ostertag I. Helbig U. Stephani R.S. Moller H. Hjalgrim L.M. Dibbens S. Bellows K. Oliver S. Mullen I.E. Scheffer S.F. Berkovic K.V. Everett M.R. Gardiner C. Marini R. Guerrini A.E. Lehesjoki A. Siren M. Guipponi A. Malafosse P. Thomas R. Nabbout S. Baulac E. Leguern R. Guerrero J.M. Serratosa P.S. Reif F. Rosenow M. Mörzinger M. Feucht F. Zimprich C. Kapser C.J. Schankin A. Suls K. Smets P. De Jonghe A. Jordanova H. Caglayan Z. Yapici D.A. Yalcin B. Baykan N. Bebek U. Ozbek C. Gieger H.E. Wichmann T. Balschun D. Ellinghaus A. Franke C. Meesters T Becker T.F. Wienker A. Hempelmann H. Schulz F. Rueschendorf M. Leber S.M. Pauck H. Trucks M.R. Toliat P. Nuernberg G. Avanzini B.P. Koeleman T. Sander
January 01, 2014 / Gut Cryptogenic multifocal ulcerating stenosing enteritis associated with homozygous deletion mutations in cytosolic phospholipase A2-α M.A. Brooke H.J. Longhurst V. Plagnol N.S. Kirkby J.A. Mitchell F. Rüschendorf T.D. Warner D.P. Kelsell T.T. MacDonald
February 10, 2012 / Am J Hum Genet Mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss M. Baumann C. Giunta B. Krabichler F. Rueschendorf N. Zoppi M. Colombi R.E. Bittner S. Quijano-Roy F. Muntoni S. Cirak G. Schreiber Y. Zou Y. Hu N.B. Romero R.Y. Carlier A. Amberger A. Deutschmann V. Straub M. Rohrbach B. Steinmann K. Rostasy D. Karall C.G. Boennemann J. Zschocke C. Fauth
May 01, 2014 / Leukemia Inherited susceptibility to pre B-ALL caused by germline transmission of PAX5 c.547G>A F. Auer F. Rueschendorf M. Gombert P. Husemann S. Ginzel S. Izraeli M. Harit M. Weintraub O.Y. Weinstein I. Lerer P. Stepensky A. Borkhardt J. Hauer
October 01, 2014 / Diabetes Recessive mutations in PCBD1 cause a new type of early-onset diabetes D. Simaite J. Kofent M. Gong F. Rüschendorf S. Jia P. Arn K. Bentler C. Ellaway P. Kühnen G.F. Hoffmann N. Blau F.M. Spagnoli N. Hübner K. Raile
December 01, 2014 / Nat Genet Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes J. Schubert A. Siekierska M. Langlois P. May C. Huneau F. Becker H. Muhle A. Suls J.R. Lemke C.G.F. de Kovel H. Thiele K. Konrad A. Kawalia M.R. Toliat T. Sander F. Rueschendorf A. Caliebe I. Nagel B. Kohl A. Kecskes M. Jacmin K. Hardies S. Weckhuysen E. Riesch T. Dorn E.H. Brilstra S. Baulac R.S. Moller H. Hjalgrim B.P.C. Koeleman K. Jurkat-Rott F. Lehman-Horn J.C. Roach G. Glusman L. Hood D.J. Galas B. Martin P.A.M. de Witte S. Biskup P. De Jonghe I. Helbig R. Balling P. Nuernberg A.D. Crawford C.V. Esguerra Y.G. Weber H. Lerche