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(30) de la Rosa, Kathrin Dr. (3) Diebolder, Christoph Dr. (1) Diecke, Sebastian Dr. (7) Escobar Fernandez, Helena Dr. (1) Estebanez, Luc Dr. (1) Falcke, Martin Prof. Dr. (6) Falk, Kirsten Dr. (3) Fielitz, Jens Dr. (6) Fischer, Christian (2) Forslund, Sofia Dr. (3) Frahm-Barske, Silke Dr. (1) Gargiulo, Gaetano Dr. (2) Gerlach, Kerstin (2) Gorski, Stan Dr. (3) Gotthardt, Michael Prof. Dr. (10) Gouti, Mina Dr. (2) Grossmann, Katja Dr. (3) Grosswendt, Stefanie Dr. (1) Grybowski, Andrea (1) Haas, Simon Dr. rer. nat. (3) Haase, Nadine Dr. (2) Hammes-Lewin, Annette Dr. (3) Hänig, Christian (1) Harabula, Izabela-Cezara (1) Haseleu, Julia Dr. (1) Haucke, Volker Professor (1) Heinemann, Udo Prof. Dr. (20) Henssen, Anton Prof. Dr. med. 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(1) Luft, Friedrich Prof. Dr. (186) Luganskaja, Tatjana (1) Lusatis, Simone (1) Lutter, Steffen (1) Maatz, Henrike Dr. (2) Mahmoodzadeh, Shokoufeh PD Dr. (4) Marenholz, Ingo Dr. (3) Marg, Andreas Dr. (1) Marko, Lajos Dr. (4) Mastrobuoni, Guido Dr. (1) Mathas, Stephan Dr. (7) Mekle, Ralf (1) Mertins, Philipp Dr. (5) Metzger, Jakob Johannes Dr. (1) Meyer, Irmtraud Margret Prof. Dr. (1) Millward, Jason Dr. (1) Morano, Ingo Prof. Dr. (19) Müller, Dominik Prof. Dr. (27) Müller, Gerd Dr. (3) Müller, Thomas Dr. (5) Münchberg, Stefanie (1) Na, Il-Kang Dr. (6) Neuendorf, Nancy (1) Nguyen, Tam Hoai Dr. (1) Niendorf, Thoralf Prof. Dr. (26) Nimptsch, Katharina Dr. (4) Nolte, Christiane Dr. (3) Obermayer-Wasserscheid, Benedikt Dr. (5) Ohler, Uwe Prof. Dr. (14) Panakova, Daniela Dr. (3) Patone, Giannino Dr. (1) Paul, Friedemann Prof. Dr. med. (37) Perrot, Andreas (11) Pezzutto, Antonio Prof. Dr. (10) Piazza, Ilaria Dr. (1) Pilz, Bernhard Dr. (3) Pischon, Tobias Prof. Dr. (31) Pombo, Ana Prof. Dr. (8) Popova, Elena Dr. (3) Poulet, James Prof. Dr. (5) Preibisch, Stephan Dr. (3) Prigione, Alessandro Prof. Dr. (5) Qadri, Fatimunnisa Dr. (4) Quensel, Christina Dr. (1) Rademann, Joerg Prof. Dr. (1) Radke, Michael Dr. (2) Rahn, Hans-Peter Dr. (3) Rajewsky, Klaus Prof. Dr. (9) Rajewsky, Nikolaus Prof. Dr. (21) Rathjen, Fritz Prof. Dr. (6) Rehm, Armin Dr. (3) Reimann, Henning Dr. (1) Rhein, Simone Dr. (1) Robson, Michael Dr. (2) Rocks, Oliver Dr. (11) Rosenthal, Walter Prof. Dr. (3) Roske, Yvette Dr. (4) Rother, Franziska Dr. (1) Rousselle, Anthony (1) Rybak-Wolf, Agnieszka Dr. (3) Saar, Kathrin Dr. (8) Sander, Maike Prof. Dr. (9) Sattentau, Quentin James Prof. Dr. (1) Sawamiphak, Suphansa Dr. (2) Scheidereit, Claus Prof. Dr. (17) Schiattarella, Gabriele G. Dr. (11) Schlag, Peter M. Prof. Dr. (66) Schlegel, Wolfgang-Peter (2) Schmidt, Deborah (1) Schmidt, Willi Dr. (1) Schmidt-Krüger, Vanessa Dr. (3) Schmidt-Ullrich, Ruth Dr. (3) Schmitt, Clemens Prof. Dr. (5) Schreiber, Adrian PD Dr. med. (2) Schulz-Menger, Jeanette Prof. Dr. (21) Schütz, Anja Dr. (1) Schwarz, Roland Dr. (3) Selbach, Matthias Prof. Dr. (17) Semtner, Marcus Dr. (4) Serresi, Michela Dr. (2) Siffrin, Volker (5) Simon, Katja Prof. Dr. (2) Singh, Manvendra Dr. (2) Smith, Janice (2) Sommer, Christian (1) Sommer, Thomas Prof. Dr. (12) Spagnoli, Francesca Dr. (4) Sporbert, Anje Dr. (1) Spuler, Simone Prof. (12) Stein, Ulrike Prof. Dr. (17) Sugimoto, Yoichiro Dr. (2) Tano, Jean-Yves Dr. (4) Taube, Martin (1) Todiras, Mihail (3) Treier, Mathias Prof. Dr. (2) Tursun, Baris Dr. (2) Uckert, Wolfgang Prof. Dr. (9) von Kries, Jens Peter Dr. (1) Waiczies, Helmar Dr. (1) Waiczies, Sonia PD Dr. (5) Wallukat, Gerd Dr. (8) Walther, Wolfgang Prof. Dr. (16) Wanker, Erich Prof. Dr. (32) Wellner, Maren Dr. (2) Wenzel, Katrin Dr. (1) Westphal, Christina Dr. (1) Wilck, Nicola Dr. med. (2) Willimsky, Gerald Dr. (1) Willnow, Thomas Prof. Dr. (23) Winter, Lukas Dr. (2) Woehler, Andrew Dr. (1) Wolf, Jana Prof. Dr. (4) Wolf, Susanne Dr. (9) Wollert-Wulf, Brigitte (2) Zampieri, Niccolo Dr. (3) Zauber, Henrik Dr. (1) Zinzen, Robert Patrick Dr. (4) (-) Gerhardt, Holger Prof. Dr. (13) (-) Klaassen, Sabine Prof. Dr. med. (6) (-) Sperling, Silke Prof. Dr. (6) (-) Yilmaz, Zekiye Buket Dr. (1) Animal Phenotyping (3) Genetik von Angeborenen Herzerkrankungen (6) Integrative Vaskuläre Biologie (13) Mathematische Modellierung zellulärer Prozesse (1) 1996 (1) (-) 1997 (1) 1999 (4) 2000 (6) (-) 2001 (2) 2002 (5) 2003 (6) 2004 (8) 2005 (7) (-) 2006 (8) 2007 (7) 2008 (17) 2009 (9) 2010 (6) 2011 (15) 2012 (8) 2013 (13) (-) 2014 (14) 2015 (16) 2016 (24) 2017 (13) 2018 (13) 2019 (18) 2020 (9) 2021 (15) 2022 (21) 2023 (13) 2024 (1) 25 Ergebnisse: Active Filter: Gerhardt, Holger Prof. Dr.Klaassen, Sabine Prof. Dr. med.Sperling, Silke Prof. Dr.Yilmaz, Zekiye Buket Dr.1997200120062014 Sortieren: Treffgenauigkeit Neueste nach älteste Älteste nach neueste 02. Januar 2014 / Am J Hum Genet Reponse to De Leeuw and Houge A.K. Arndt C.A. Macrae S. Klaassen 01. Juni 2006 / J Mol Med Identification of a novel frameshift mutation in the giant muscle filament titin in a large Australian family with dilated cardiomyopathy B. Gerull J. Atherton A. Geupel S. Sasse-Klaassen A. Heuser M. Frenneaux M. McNabb H. Granzier S. Labeit L. Thierfelder 04. Juli 2006 / J Am Coll Cardiol A novel locus for dilated cardiomyopathy, diffuse myocardial fibrosis, and sudden death on chromosome 10q25-26 P.T. Ellinor S. Sasse-Klaassen S. Probst B. Gerull J.T. Shin A. Toeppel A. Heuser B. Michely D.M. Yoerger B.S. Song B. Pilz G. Krings B. Coplin P.E. Lange G.W. Dec H.C. Hennies L. Thierfelder C.A. MacRae 06. Januar 2014 / PLoS ONE Outlier-based identification of copy number variations using targeted resequencing in a small cohort of patients with tetralogy of fallot V. Bansal C. Dorn M. Grunert S. Klaassen R. Hetzer F. Berger S.R. Sperling 15. Juni 2014 / Hum Mol Genet Rare and private variations in neural crest, apoptosis and sarcomere genes define the polygenic background of isolated Tetralogy of Fallot M. Grunert C. Dorn M. Schueler I. Dunkel J. Schlesinger S. Mebus V. Alexi-Meskishvili A. Perrot K. Wassilew B. Timmermann R. Hetzer F. Berger S.R. Sperling 03. April 2014 / Am J Hum Genet Rare variants in NR2F2 cause congenital heart defects in humans S. Al Turki A.K. Manickaraj C.L. Mercer S.S. Gerety M.P. Hitz S. Lindsay L.C.A. D'Alessandro G.J. Swaminathan J. Bentham A.K. Arndt J. Low J. Breckpot M. Gewillig B. Thienpont H. Abdul-Khaliq C. Harnack K. Hoff H.H. Kramer S. Schubert R. Siebert O. Toka C. Cosgrove H. Watkins A.M. Lucassen I.M. O'Kelly A.P. Salmon F.A. Bu'Lock J. Granados-Riveron K. Setchfield C. Thornborough J.D. Brook B. Mulder S. Klaassen S. Bhattacharya K. Devriendt D.F. Fitzpatrick D.I. Wilson S. Mital M.E. Hurles 11. Dezember 2014 / Cell Rep Quantitative dissection and modeling of the NF-κB p100-p105 module reveals interdependent precursor proteolysis Z.B. Yilmaz B. Kofahl P. Beaudette K. Baum I. Ipenberg F. Weih J. Wolf G. Dittmar C. Scheidereit 01. Januar 2006 / Genome Inform A new statistical model to select target sequences bound by transcription factors U.J. Pape S. Grossmann S. Hammer S. Sperling M. Vingron 01. Januar 2006 / Methods Mol Med Array analysis applied to malformed hearts: Molecular dissection of tetralogy of Fallot S. Sperling 01. Februar 2001 / Hum Mol Genet Triple A syndrome is caused by mutations in AAAS, a new WD-repeat protein gene K. Handschug S. Sperling S.J. Yoon S. Hennig A.J. Clark A. Huebner Seitennummerierung Aktuelle Seite 1 Seite 2 Seite 3 Nächste Seite Next › Letzte Seite Last »
01. Juni 2006 / J Mol Med Identification of a novel frameshift mutation in the giant muscle filament titin in a large Australian family with dilated cardiomyopathy B. Gerull J. Atherton A. Geupel S. Sasse-Klaassen A. Heuser M. Frenneaux M. McNabb H. Granzier S. Labeit L. Thierfelder
04. Juli 2006 / J Am Coll Cardiol A novel locus for dilated cardiomyopathy, diffuse myocardial fibrosis, and sudden death on chromosome 10q25-26 P.T. Ellinor S. Sasse-Klaassen S. Probst B. Gerull J.T. Shin A. Toeppel A. Heuser B. Michely D.M. Yoerger B.S. Song B. Pilz G. Krings B. Coplin P.E. Lange G.W. Dec H.C. Hennies L. Thierfelder C.A. MacRae
06. Januar 2014 / PLoS ONE Outlier-based identification of copy number variations using targeted resequencing in a small cohort of patients with tetralogy of fallot V. Bansal C. Dorn M. Grunert S. Klaassen R. Hetzer F. Berger S.R. Sperling
15. Juni 2014 / Hum Mol Genet Rare and private variations in neural crest, apoptosis and sarcomere genes define the polygenic background of isolated Tetralogy of Fallot M. Grunert C. Dorn M. Schueler I. Dunkel J. Schlesinger S. Mebus V. Alexi-Meskishvili A. Perrot K. Wassilew B. Timmermann R. Hetzer F. Berger S.R. Sperling
03. April 2014 / Am J Hum Genet Rare variants in NR2F2 cause congenital heart defects in humans S. Al Turki A.K. Manickaraj C.L. Mercer S.S. Gerety M.P. Hitz S. Lindsay L.C.A. D'Alessandro G.J. Swaminathan J. Bentham A.K. Arndt J. Low J. Breckpot M. Gewillig B. Thienpont H. Abdul-Khaliq C. Harnack K. Hoff H.H. Kramer S. Schubert R. Siebert O. Toka C. Cosgrove H. Watkins A.M. Lucassen I.M. O'Kelly A.P. Salmon F.A. Bu'Lock J. Granados-Riveron K. Setchfield C. Thornborough J.D. Brook B. Mulder S. Klaassen S. Bhattacharya K. Devriendt D.F. Fitzpatrick D.I. Wilson S. Mital M.E. Hurles
11. Dezember 2014 / Cell Rep Quantitative dissection and modeling of the NF-κB p100-p105 module reveals interdependent precursor proteolysis Z.B. Yilmaz B. Kofahl P. Beaudette K. Baum I. Ipenberg F. Weih J. Wolf G. Dittmar C. Scheidereit
01. Januar 2006 / Genome Inform A new statistical model to select target sequences bound by transcription factors U.J. Pape S. Grossmann S. Hammer S. Sperling M. Vingron
01. Januar 2006 / Methods Mol Med Array analysis applied to malformed hearts: Molecular dissection of tetralogy of Fallot S. Sperling
01. Februar 2001 / Hum Mol Genet Triple A syndrome is caused by mutations in AAAS, a new WD-repeat protein gene K. Handschug S. Sperling S.J. Yoon S. Hennig A.J. Clark A. Huebner