Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Gotthardt, Michael Prof. Dr. (1) Heuser, Arnd Dr. (1) Hummel, Oliver (2) Janke, Jürgen Dr. (1) Lee, Young-Ae Prof. Dr. (9) Marenholz, Ingo Dr. (4) Nimptsch, Katharina Dr. (1) Patone, Giannino Dr. (1) Perrot, Andreas (1) Pischon, Tobias Prof. Dr. (1) Radke, Michael Dr. (1) (-) Hübner, Norbert Prof. Dr. (4) (-) Klaassen, Sabine Prof. Dr. med. (7) (-) Maatz, Henrike Dr. (1) (-) Saar, Kathrin Dr. (2) 1995 (2) 1997 (2) 1999 (1) 2001 (1) 2002 (1) 2003 (2) 2004 (3) 2006 (3) 2007 (3) (-) 2008 (3) 2009 (2) 2010 (1) 2011 (2) (-) 2012 (4) 2013 (7) 2014 (3) 2015 (9) 2016 (3) (-) 2017 (3) 2018 (4) 2019 (6) 2020 (3) 2021 (7) 2022 (12) 2023 (8) AG Müller/Dechend (ECRC) (6) Animal Phenotyping (2) Bioinformatics and Omics Data Science (1) Computational Regulatory Genomics (1) Genetics and Genomics of Cardiovascular Diseases (36) (-) Genetics of Congenital Heart Disease (7) Hypertension-caused End-Organ Damage (6) Hypertension-Mediated End-Organ Damage (6) Integrative Vascular Biology (1) Mobile DNA (3) Molecular Biology of Peptide Hormones (2) Molecular Cardiovascular Research (1) Molecular Genetics of Chronic Inflammation and Allergic Disease (3) Molecular Immunology and Gene Therapy (1) Molecular Physiology of Somatic Sensation (1) Nephrology and Inflammatory Vascular Diseases (1) (-) Out-patient Clinic for Pediatric Allergology and Atopic Dermatitis (3) Proteomics and Molecular Mechanisms of Neurodegenerative Diseases (1) RNA Biology and Posttranscriptional Regulation (2) Systems Biology of Gene Regulatory Elements (1) Translational Bioinformatics (1) Translational Cardiology and Functional Genomics (1) 10 Results: Active Filter: Hübner, Norbert Prof. Dr.Klaassen, Sabine Prof. Dr. med.Maatz, Henrike Dr.Saar, Kathrin Dr.Genetics of Congenital Heart DiseaseOut-patient Clinic for Pediatric Allergology and Atopic Dermatitis200820122017 Sort: Result score Newest to oldest Oldest to newest May 01, 2008 / Nat Genet SNP and haplotype mapping for genetic analysis in the rat K. Saar A. Beck M.T. Bihoreau E. Birney D. Brocklebank Y. Chen E. Cuppen S. Demonchy J. Dopazo P. Flicek M. Foglio A. Fujiyama I.G. Gut D. Gauguier R. Guigo V. Guryev M. Heinig O. Hummel N. Jahn S. Klages V. Kren M. Kube H. Kuhl T. Kuramoto Y. Kuroki D. Lechner Y.A. Lee N. Lopez-Bigas G.M. Lathrop T. Mashimo I. Medina R. Mott G. Patone J.A. Perrier-Cornet M. Platzer M. Pravenec R. Reinhardt Y. Sakaki M. Schilhabel H. Schulz T. Serikawa M. Shikhagaie S. Tatsumoto S. Taudien A. Toyoda B. Voigt D. Zelenika H. Zimdahl N. Huebner June 03, 2008 / Circulation Mutations in sarcomere protein genes in left ventricular noncompaction S. Klaassen S. Probst E. Oechslin B. Gerull G. Krings P. Schuler M. Greutmann D. Huerlimann M. Yegitbasi L. Pons M. Gramlich J.D. Drenckhahn A. Heuser F. Berger R. Jenni L. Thierfelder January 01, 2008 Focused Review: Ventricular noncompaction: an update S. Klaassen October 20, 2017 / Nat Commun Genome-wide association study identifies the SERPINB gene cluster as a susceptibility locus for food allergy I. Marenholz S. Grosche B. Kalb F. Rüschendorf K. Blümchen R. Schlags N. Harandi M. Price G. Hansen J. Seidenberg H. Röblitz S. Yürek S. Tschirner X. Hong X. Wang G. Homuth C.O. Schmidt M.M. Nöthen N. Hübner B. Niggemann K. Beyer Y.A. Lee December 01, 2017 / Nat Genet Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology M.A. Ferreira J.M. Vonk H. Baurecht I. Marenholz C. Tian J.D. Hoffman Q. Helmer A. Tillander V. Ullemar J. van Dongen Yi Lu F. Rueschendorf J. Esparza-Gordillo C.W. Medway E. Mountjoy K. Burrows O. Hummel S. Grosche B.M. Brumpton J.S. Witte J.J. Hottenga G. Willemsen J. Zheng E. Rodriguez M. Hotze A. Franke J.A. Revez J. Beesley M.C. Matheson S.C. Dharmage L.M. Bain L.G. Fritsche M.E. Gabrielsen B. Balliu J.B. Nielsen W. Zhou K. Hveem A. Langhammer O.L. Holmen M. Løset G.R. Abecasis C.J. Willer A. Arnold G. Homuth C.O. Schmidt P.J. Thompson N.G. Martin D.L. Duffy N. Novak H. Schulz S. Karrasch C. Gieger K. Strauch R.B. Melles D.A. Hinds N. Hübner S. Weidinger P.K.E. Magnusson R. Jansen E. Jorgenson Y.A. Lee D.I. Boomsma C. Almqvist R. Karlsson G.H. Koppelman L. Paternoster May 01, 2012 / Nat Med RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing W. Guo S. Schafer M.L. Greaser M.H. Radke M. Liss T. Govindarajan H. Maatz H. Schulz S.E. Lincoln A.M. Parrish V. Dauksaite P. Vakeel S. Klaassen B. Gerull L. Thierfelder V. Regitz-Zagrosek T.A. Hacker K.W. Saupe G.W. Dec P.T. Ellinor C.A. MacRae B. Spallek R. Fischer A. Perrot C. Ozcelik K. Saar N. Hubner M. Gotthardt January 15, 2012 / Am J Cardiol Predictors of adverse outcome in adolescents and adults with isolated left ventricular noncompaction M. Greutmann M.L. Mah C.K. Silversides S. Klaassen C.H. Attenhofer Jost R. Jenni E.N. Oechslin December 01, 2012 / Eur Radiol Value of cardiovascular MR in diagnosing left ventricular non-compaction cardiomyopathy and in discriminating between other cardiomyopathies M. Grothoff M. Pachowsky J. Hoffmann M. Posch S. Klaassen L. Lehmkuhl M. Gutberlet January 01, 2017 / Kardiologie up2date Myokarditis im Kindes- und Jugendalter S. Schubert D. Messroghli S. Klaassen F. Berger September 06, 2012 / PLoS Genet Rare copy number variants contribute to congenital left-sided heart disease M.P. Hitz L.P. Lemieux-Perreault C. Marshall Y. Feroz-Zada R. Davies S.W. Yang A.C. Lionel G. D'Amours E. Lemyre R. Cullum J.L. Bigras M. Thibeault P. Chetaille A. Montpetit P. Khairy B. Overduin S. Klaassen P. Hoodless P. Awadalla J. Hussin Y. Idaghdour M. Nemer A.F. Stewart C. Boerkoel S.W. Scherer A. Richter M.P. Dube G. Andelfinger
May 01, 2008 / Nat Genet SNP and haplotype mapping for genetic analysis in the rat K. Saar A. Beck M.T. Bihoreau E. Birney D. Brocklebank Y. Chen E. Cuppen S. Demonchy J. Dopazo P. Flicek M. Foglio A. Fujiyama I.G. Gut D. Gauguier R. Guigo V. Guryev M. Heinig O. Hummel N. Jahn S. Klages V. Kren M. Kube H. Kuhl T. Kuramoto Y. Kuroki D. Lechner Y.A. Lee N. Lopez-Bigas G.M. Lathrop T. Mashimo I. Medina R. Mott G. Patone J.A. Perrier-Cornet M. Platzer M. Pravenec R. Reinhardt Y. Sakaki M. Schilhabel H. Schulz T. Serikawa M. Shikhagaie S. Tatsumoto S. Taudien A. Toyoda B. Voigt D. Zelenika H. Zimdahl N. Huebner
June 03, 2008 / Circulation Mutations in sarcomere protein genes in left ventricular noncompaction S. Klaassen S. Probst E. Oechslin B. Gerull G. Krings P. Schuler M. Greutmann D. Huerlimann M. Yegitbasi L. Pons M. Gramlich J.D. Drenckhahn A. Heuser F. Berger R. Jenni L. Thierfelder
October 20, 2017 / Nat Commun Genome-wide association study identifies the SERPINB gene cluster as a susceptibility locus for food allergy I. Marenholz S. Grosche B. Kalb F. Rüschendorf K. Blümchen R. Schlags N. Harandi M. Price G. Hansen J. Seidenberg H. Röblitz S. Yürek S. Tschirner X. Hong X. Wang G. Homuth C.O. Schmidt M.M. Nöthen N. Hübner B. Niggemann K. Beyer Y.A. Lee
December 01, 2017 / Nat Genet Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology M.A. Ferreira J.M. Vonk H. Baurecht I. Marenholz C. Tian J.D. Hoffman Q. Helmer A. Tillander V. Ullemar J. van Dongen Yi Lu F. Rueschendorf J. Esparza-Gordillo C.W. Medway E. Mountjoy K. Burrows O. Hummel S. Grosche B.M. Brumpton J.S. Witte J.J. Hottenga G. Willemsen J. Zheng E. Rodriguez M. Hotze A. Franke J.A. Revez J. Beesley M.C. Matheson S.C. Dharmage L.M. Bain L.G. Fritsche M.E. Gabrielsen B. Balliu J.B. Nielsen W. Zhou K. Hveem A. Langhammer O.L. Holmen M. Løset G.R. Abecasis C.J. Willer A. Arnold G. Homuth C.O. Schmidt P.J. Thompson N.G. Martin D.L. Duffy N. Novak H. Schulz S. Karrasch C. Gieger K. Strauch R.B. Melles D.A. Hinds N. Hübner S. Weidinger P.K.E. Magnusson R. Jansen E. Jorgenson Y.A. Lee D.I. Boomsma C. Almqvist R. Karlsson G.H. Koppelman L. Paternoster
May 01, 2012 / Nat Med RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing W. Guo S. Schafer M.L. Greaser M.H. Radke M. Liss T. Govindarajan H. Maatz H. Schulz S.E. Lincoln A.M. Parrish V. Dauksaite P. Vakeel S. Klaassen B. Gerull L. Thierfelder V. Regitz-Zagrosek T.A. Hacker K.W. Saupe G.W. Dec P.T. Ellinor C.A. MacRae B. Spallek R. Fischer A. Perrot C. Ozcelik K. Saar N. Hubner M. Gotthardt
January 15, 2012 / Am J Cardiol Predictors of adverse outcome in adolescents and adults with isolated left ventricular noncompaction M. Greutmann M.L. Mah C.K. Silversides S. Klaassen C.H. Attenhofer Jost R. Jenni E.N. Oechslin
December 01, 2012 / Eur Radiol Value of cardiovascular MR in diagnosing left ventricular non-compaction cardiomyopathy and in discriminating between other cardiomyopathies M. Grothoff M. Pachowsky J. Hoffmann M. Posch S. Klaassen L. Lehmkuhl M. Gutberlet
January 01, 2017 / Kardiologie up2date Myokarditis im Kindes- und Jugendalter S. Schubert D. Messroghli S. Klaassen F. Berger
September 06, 2012 / PLoS Genet Rare copy number variants contribute to congenital left-sided heart disease M.P. Hitz L.P. Lemieux-Perreault C. Marshall Y. Feroz-Zada R. Davies S.W. Yang A.C. Lionel G. D'Amours E. Lemyre R. Cullum J.L. Bigras M. Thibeault P. Chetaille A. Montpetit P. Khairy B. Overduin S. Klaassen P. Hoodless P. Awadalla J. Hussin Y. Idaghdour M. Nemer A.F. Stewart C. Boerkoel S.W. Scherer A. Richter M.P. Dube G. Andelfinger