Scientific Publications Search Search Author Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Akalin, Altuna Dr. (4) Alenina, Natalia Dr. (9) Altmueller, Janine Dr.med. (1) Bader, Michael Prof. Dr. (53) Bähring, Sylvia Dr. (4) Begay-Müller, Valerie Dr. (2) Birchmeier, Walter Prof. Dr. (11) Birchmeier-Kohler, Carmen Prof. Dr. (15) Blankenstein, Thomas Prof. Dr. (11) Castilho de Barros, Carlos Prof. Dr. (1) Chen, Wei Prof. Dr. (10) Cöl Arslan, Seda Dr. (1) Dahlmann, Mathias Dr. (1) Daniel, Peter Prof. Dr. (11) Daumke, Oliver Prof. Dr. (6) Dechend, Ralf Priv. Doz. (25) Diebolder, Christoph Dr. (2) Di Virgilio, Michela Prof. Dr. (1) Edes, Inan Dr. (1) Fälber, Katja Dr. (1) Falcke, Martin Prof. Dr. (7) Falk, Kirsten Dr. (3) Fielitz, Jens Dr. (4) Forslund, Sofia Dr. (2) Gerhardt, Holger Prof. Dr. (7) Gerlach, Kerstin (1) Gorski, Stan Dr. (1) Gösele, Claudia Dr. (1) Gotthardt, Michael Prof. Dr. (4) Hammes-Lewin, Annette Dr. (5) Haucke, Volker Professor (1) Heinemann, Udo Prof. Dr. (14) Herse, Florian PD Dr. (7) Heuser, Arnd Dr. (1) Hinz, Michael Dr. (5) Hofstätter, Maria (1) Höpken, Uta Elisabeth PD Dr. (9) Hübner, Norbert Prof. Dr. (11) Hummel, Oliver (1) Infante Duarte, Carmen (4) Ivics, Zoltan Dr. (8) Izsvak, Zsuzsanna Dr. (8) Janke, Jürgen Dr. (4) Janz, Martin Dr. (3) Jarosch, Ernst Dr. (2) Jentsch, Thomas Prof. Dr. (10) Junker, Jan Philipp Prof. Dr. (3) Jüttner, Rene Dr. (3) Kainmüller, Dagmar Prof. Dr. (1) Kaminski, Michael Dr. (1) Kammertöns, Thomas Dr. (3) Kempa, Stefan Dr. (5) Kettenmann, Helmut Prof. Dr. (12) Kettritz, Ralph Prof. Dr. (19) Kirchner, Marieluise Dr. (2) Kirwan, Jennifer Dr. (2) Klaassen, Sabine Prof. Dr. med. (5) Klaus-Bergmann, Alexandra Dr. (1) Klußmann, Enno PD Dr. (5) Kobelt, Dennis Dr. (4) Krabbe, Grietje Dr. (1) Krüger, Christina (1) Kudryashev, Mikhail Prof. Dr. (5) Kühn, Ralf Dr. (13) Kunz, Severine Dr. (1) Lacadie, Scott Allen Dr. (2) Landthaler, Markus Prof. Dr. (6) Lee, Young-Ae Prof. Dr. (3) Leisegang, Matthias Prof. Dr. rer. nat. (3) Leutz, Achim Prof. Dr. (8) Lewin, Gary Prof. Dr. (15) Ludwig, Leif S. Dr. med. Dr. rer. nat. (1) Luft, Friedrich Prof. Dr. (98) Lupianez Garcia, Dario Jesus Dr. (2) Maatz, Henrike Dr. (1) Maglione, Marta (1) Mahmoodzadeh, Shokoufeh PD Dr. (1) Marenholz, Ingo Dr. (1) Marg, Andreas Dr. (3) Marko, Lajos Dr. (2) Mastrobuoni, Guido Dr. (2) Mathas, Stephan Dr. (6) Mertins, Philipp Dr. (3) Metzger, Jakob Johannes Dr. (2) Meyer, Irmtraud Margret Prof. Dr. (4) Millward, Jason Dr. (3) Morano, Ingo Prof. Dr. (7) Müller, Dominik Prof. Dr. (18) Müller, Gerd Dr. (2) Müller, Marion (1) Müller, Thomas Dr. (3) Na, Il-Kang Dr. (1) Nguyen, Tam Hoai Dr. (4) Niendorf, Thoralf Prof. Dr. (15) Nimptsch, Katharina Dr. (3) Nolte, Christiane Dr. (1) Ohler, Uwe Prof. Dr. (11) Paul, Friedemann Prof. Dr. med. (26) Perrot, Andreas (6) Pezzutto, Antonio Prof. Dr. (7) Pilz, Bernhard Dr. (4) Pischon, Tobias Prof. Dr. (14) Pombo, Ana Prof. Dr. (5) Popova, Elena Dr. (2) Potente, Michael Prof. Dr. (2) Poulet, James Prof. Dr. (3) Preibisch, Stephan Dr. (3) Prigione, Alessandro Prof. Dr. (2) Qadri, Fatimunnisa Dr. (2) Quedenau, Claudia (1) Quensel, Christina Dr. (2) Rademann, Joerg Prof. Dr. (1) Radke, Michael Dr. (1) Rahn, Hans-Peter Dr. (2) Rajewsky, Klaus Prof. Dr. (5) Rajewsky, Nikolaus Prof. Dr. (8) Rathjen, Fritz Prof. Dr. (4) Rehm, Armin Dr. (4) Rocks, Oliver Dr. (1) Rosenthal, Walter Prof. Dr. (1) Roske, Yvette Dr. (2) Rother, Franziska Dr. (1) Rybak-Wolf, Agnieszka Dr. (3) Saar, Kathrin Dr. (7) Sander, Maike Prof. Dr. (6) Sanders, Ashley Dr. (1) Scheidereit, Claus Prof. Dr. (5) Schiattarella, Gabriele G. Dr. (5) Schlag, Peter M. Prof. Dr. (74) Schmidt-Krüger, Vanessa Dr. (4) Schmidt-Ullrich, Ruth Dr. (2) Schmitt, Clemens Prof. Dr. (5) Schnögl, Sigrid (1) Schreiber, Adrian PD Dr. med. (2) Schulz-Menger, Jeanette Prof. Dr. (15) Schütz, Anja Dr. (5) Schwarz, Roland Dr. (2) Selbach, Matthias Prof. Dr. (7) Siffrin, Volker (1) Sigal, Michael Dr. (1) Smith, Janice (1) Sommer, Thomas Prof. Dr. (7) Spagnoli, Francesca Dr. (2) Sperling, Silke Prof. Dr. (1) Sporbert, Anje Dr. (3) Spuler, Simone Prof. (4) Stein, Ulrike Prof. Dr. (18) Sugimoto, Yoichiro Dr. (3) Tursun, Baris Dr. (3) Uckert, Wolfgang Prof. Dr. (4) Volkwein, Corinna (1) von Kries, Jens Peter Dr. (1) Waiczies, Helmar Dr. (2) Waiczies, Sonia PD Dr. (7) Wallukat, Gerd Dr. (15) Walther, Wolfgang Prof. Dr. (11) Wanker, Erich Prof. Dr. (14) Wellner, Maren Dr. (2) Wenzel, Katrin Dr. (1) Willimsky, Gerald Dr. (2) Willnow, Thomas Prof. Dr. (16) Winter, Lukas Dr. (3) Woehler, Andrew Dr. (2) Wolf, Jana Prof. Dr. (1) Wyler, Emanuel Dr. (2) Zinzen, Robert Patrick Dr. (2) 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) Genetics and Genomics of Cardiovascular Diseases (5) Molecular Physiology of Somatic Sensation (1) 8 Results: Active Filter: 20022012 Sort: Result score Newest to oldest Oldest to newest 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 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 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 October 01, 2002 / Hum Genet Periodic catatonia: confirmation of linkage to chromosome 15 and further evidence for genetic heterogeneity G. Stoeber D. Seelow F. Rueschendorf A. Ekici H. Beckmann A. Reis October 01, 2002 / Epilepsy Res Association of the 867Asp variant of the human anion exchanger 3 gene with common subtypes of idiopathic generalized epilepsy T. Sander M.R. Toliat A. Heils G. Leschik C. Becker F. Rueschendorf K. Rohde S. Mundlos P. Nuernberg May 01, 2002 / Am J Hum Genet Mapping of gene loci for nephronophthisis type 4 and Senior-Loken syndrome, to chromosome 1p36 M.J. Schuermann E. Otto A. Becker K. Saar F. Rueschendorf B.C. Polak S. Ala-Mello J. Hoefele A. Wiedensohler M. Haller H. Omran P. Nuernberg F. Hildebrandt
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
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
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
October 01, 2002 / Hum Genet Periodic catatonia: confirmation of linkage to chromosome 15 and further evidence for genetic heterogeneity G. Stoeber D. Seelow F. Rueschendorf A. Ekici H. Beckmann A. Reis
October 01, 2002 / Epilepsy Res Association of the 867Asp variant of the human anion exchanger 3 gene with common subtypes of idiopathic generalized epilepsy T. Sander M.R. Toliat A. Heils G. Leschik C. Becker F. Rueschendorf K. Rohde S. Mundlos P. Nuernberg
May 01, 2002 / Am J Hum Genet Mapping of gene loci for nephronophthisis type 4 and Senior-Loken syndrome, to chromosome 1p36 M.J. Schuermann E. Otto A. Becker K. Saar F. Rueschendorf B.C. Polak S. Ala-Mello J. Hoefele A. Wiedensohler M. Haller H. Omran P. Nuernberg F. Hildebrandt