Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Bähring, Sylvia Dr. (1) Gotthardt, Michael Prof. Dr. (5) Grossmann, Katja Dr. (1) Heuser, Arnd Dr. (3) Hübner, Norbert Prof. Dr. (2) Lee, Young-Ae Prof. Dr. (2) Luft, Friedrich Prof. Dr. (1) (-) Klaassen, Sabine Prof. Dr. med. (4) (-) Marenholz, Ingo Dr. (2) (-) Pilz, Bernhard Dr. (1) 2001 (1) 2002 (1) (-) 2003 (1) 2004 (2) 2005 (1) (-) 2006 (5) 2007 (2) 2008 (3) 2009 (4) 2010 (2) 2011 (4) 2012 (5) 2013 (9) 2014 (5) 2015 (9) 2016 (2) 2017 (4) 2018 (5) 2020 (5) 2021 (7) 2022 (14) 2023 (9) Animal Phenotyping (3) Biology of Malignant Lymphomas (5) Cardiac MRI (1) Genetics and Genomics of Cardiovascular Diseases (5) (-) Genetics of Congenital Heart Disease (4) Molecular Genetics of Chronic Inflammation and Allergic Disease (2) (-) Out-patient Clinic for Pediatric Allergology and Atopic Dermatitis (2) 6 Results: Active Filter: Klaassen, Sabine Prof. Dr. med.Marenholz, Ingo Dr.Pilz, Bernhard Dr.Genetics of Congenital Heart DiseaseOut-patient Clinic for Pediatric Allergology and Atopic Dermatitis20032006 Sort: Result score Newest to oldest Oldest to newest June 01, 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 July 04, 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 November 01, 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 October 01, 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 December 01, 2006 / Am J Hum Genet Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy A. Heuser E.R. Plovie P.T. Ellinor K.S. Grossmann J.T. Shin T. Wichter C.T. Basson B.B. Lerman S. Sasse-Klaassen L. Thierfelder C.A. MacRae B. Gerull June 01, 2003 / Am J Med Genet A Isolated noncompaction of the left ventricular myocardium in the adult is an autosomal dominant disorder in the majority of patients S. Sasse-Klaassen B. Gerull E. Oechslin R. Jenni L. Thierfelder
June 01, 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
July 04, 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
November 01, 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
October 01, 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
December 01, 2006 / Am J Hum Genet Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy A. Heuser E.R. Plovie P.T. Ellinor K.S. Grossmann J.T. Shin T. Wichter C.T. Basson B.B. Lerman S. Sasse-Klaassen L. Thierfelder C.A. MacRae B. Gerull
June 01, 2003 / Am J Med Genet A Isolated noncompaction of the left ventricular myocardium in the adult is an autosomal dominant disorder in the majority of patients S. Sasse-Klaassen B. Gerull E. Oechslin R. Jenni L. Thierfelder