Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Adami, Eleonora Dr. (4) Bader, Michael Prof. Dr. (1) Bähring, Sylvia Dr. (1) Beule, Dieter Dr. (1) Birchmeier, Walter Prof. Dr. (1) Blachut, Susanne (1) Blankenstein, Thomas Prof. Dr. (1) Gerhardt, Holger Prof. Dr. (1) Gotthardt, Michael Prof. Dr. (1) Hübner, Norbert Prof. Dr. (20) Hummel, Oliver (3) Izsvak, Zsuzsanna Dr. (1) Janke, Jürgen Dr. (1) Kammertöns, Thomas Dr. (1) Klaus-Bergmann, Alexandra Dr. (1) Kunz, Severine Dr. (1) Landthaler, Markus Prof. Dr. (2) Lee, Young-Ae Prof. Dr. (7) Leisegang, Matthias Prof. Dr. rer. nat. (1) Lewin, Gary Prof. Dr. (1) Luft, Friedrich Prof. Dr. (1) Marenholz, Ingo Dr. (4) Müller, Marion (1) Nimptsch, Katharina Dr. (1) Patone, Giannino Dr. (2) Perrot, Andreas (1) Pischon, Tobias Prof. Dr. (1) Prigione, Alessandro Prof. Dr. (1) Qadri, Fatimunnisa Dr. (1) Radke, Michael Dr. (1) Saar, Kathrin Dr. (6) Schmidt, Sabine (1) Schmidt-Krüger, Vanessa Dr. (1) Semtner, Marcus Dr. (1) Singh, Manvendra Dr. (1) Uckert, Wolfgang Prof. Dr. (1) Wanker, Erich Prof. Dr. (1) Wyler, Emanuel Dr. (1) (-) Klaassen, Sabine Prof. Dr. med. (1) (-) Maatz, Henrike Dr. (4) (-) Willnow, Thomas Prof. Dr. (1) 2000 (2) 2002 (1) 2004 (7) 2005 (8) 2006 (6) 2007 (6) 2008 (4) 2009 (11) 2010 (7) 2011 (1) (-) 2012 (7) 2013 (3) 2014 (5) 2015 (6) 2016 (2) (-) 2017 (7) 2018 (4) 2019 (4) 2020 (8) 2021 (6) 2022 (4) 2023 (4) 2024 (2) AG Müller/Dechend (ECRC) (5) Bioinformatics and Omics Data Science (1) Computational Regulatory Genomics (1) (-) Genetics and Genomics of Cardiovascular Diseases (14) Genetics of Congenital Heart Disease (5) Hypertension-caused End-Organ Damage (5) Hypertension-Mediated End-Organ Damage (5) Mathematical Modelling of Cellular Processes (1) Microenvironmental Regulation in Autoimmunity and Cancer (1) Mobile DNA (1) Molecular Biology of Peptide Hormones (1) Molecular Cardiovascular Research (13) Molecular Genetics of Chronic Inflammation and Allergic Disease (2) Molecular Pathways in Cortical Development (2) Molecular Physiology of Somatic Sensation (1) (-) Out-patient Clinic for Pediatric Allergology and Atopic Dermatitis (2) RNA Biology and Posttranscriptional Regulation (1) Systems Biology of Gene Regulatory Elements (1) Translational Cardiology and Functional Genomics (1) 14 Results: Active Filter: Klaassen, Sabine Prof. Dr. med.Maatz, Henrike Dr.Willnow, Thomas Prof. Dr.Genetics and Genomics of Cardiovascular DiseasesOut-patient Clinic for Pediatric Allergology and Atopic Dermatitis20122017 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 January 01, 2017 / Nat Genet Titin-truncating variants affect heart function in disease cohorts and the general population S. Schafer A. de Marvao E. Adami L.R. Fiedler B. Ng E. Khin O.J.L. Rackham S. van Heesch C.J. Pua M. Kui R. Walsh U. Tayal S.K. Prasad T.J.W. Dawes N.S.J. Ko D. Sim L.L.H. Chan C.W.L. Chin F. Mazzarotto P.J. Barton F. Kreuchwig D.P.V. de Kleijn T. Totman C. Biffi N. Tee D. Rueckert V. Schneider A. Faber V. Regitz-Zagrosek J.G. Seidman C.E. Seidman W.A. Linke J.P. Kovalik D. O'Regan J.S. Ware N. Hubner S.A. Cook January 01, 2017 / Methods Mol Biol Epigenetics and control of RNAs H. Maatz S. van Heesch F. Kreuchwig A. Faber E. Adami N. Hubner M. Heinig September 14, 2017 / Genome Biol Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy M. Heinig M.E. Adriaens S. Schafer H.W.M. van Deutekom E.M. Lodder J.S. Ware V. Schneider L.E. Felkin E.E. Creemers B. Meder H.A. Katus F. Rühle M. Stoll F. Cambien E. Villard P. Charron A. Varro N.H. Bishopric A.L. George C. Dos Remedios A. Moreno-Moral F. Pesce A. Bauerfeind F. Rüschendorf C. Rintisch E. Petretto P.J. Barton S.A. Cook Y.M. Pinto C.R. Bezzina N. Hubner 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 December 07, 2017 / Nature IL11 is a crucial determinant of cardiovascular fibrosis S. Schafer S. Viswanathan A.A. Widjaja W.W. Lim A. Moreno-Moral D.M. DeLaughter B. Ng G. Patone K. Chow E. Khin J. Tan S.P. Chothani L. Ye O.J. Rackham N.S. Ko N.E. Sahib C.J. Pua N.T. Zhen C. Xie M. Wang H. Maatz S. Lim K. Saar S. Blachut E. Petretto S. Schmidt T. Putoczki N. Guimarães-Camboa H. Wakimoto S. van Heesch K. Sigmundsson S.L. Lim J.L. Soon V.T. Chao Y.L. Chua T.E. Tan S.M. Evans Y.J. Loh M.H. Jamal K.K. Ong K.C. Chua B.H. Ong M.J. Chakaramakkil J.G. Seidman C.E. Seidman N. Hubner K.Y. Sin S.A. Cook April 03, 2017 / Curr Protoc Mol Biol Transcriptome-wide identification of RNA-binding protein binding sites using photoactivatable-ribonucleoside-enhanced crosslinking immunoprecipitation (PAR-CLIP) H. Maatz M. Kolinski N. Hubner M. Landthaler Pagination Current page 1 Page 2 Next page Next › Last page Last »
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
January 01, 2017 / Nat Genet Titin-truncating variants affect heart function in disease cohorts and the general population S. Schafer A. de Marvao E. Adami L.R. Fiedler B. Ng E. Khin O.J.L. Rackham S. van Heesch C.J. Pua M. Kui R. Walsh U. Tayal S.K. Prasad T.J.W. Dawes N.S.J. Ko D. Sim L.L.H. Chan C.W.L. Chin F. Mazzarotto P.J. Barton F. Kreuchwig D.P.V. de Kleijn T. Totman C. Biffi N. Tee D. Rueckert V. Schneider A. Faber V. Regitz-Zagrosek J.G. Seidman C.E. Seidman W.A. Linke J.P. Kovalik D. O'Regan J.S. Ware N. Hubner S.A. Cook
January 01, 2017 / Methods Mol Biol Epigenetics and control of RNAs H. Maatz S. van Heesch F. Kreuchwig A. Faber E. Adami N. Hubner M. Heinig
September 14, 2017 / Genome Biol Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy M. Heinig M.E. Adriaens S. Schafer H.W.M. van Deutekom E.M. Lodder J.S. Ware V. Schneider L.E. Felkin E.E. Creemers B. Meder H.A. Katus F. Rühle M. Stoll F. Cambien E. Villard P. Charron A. Varro N.H. Bishopric A.L. George C. Dos Remedios A. Moreno-Moral F. Pesce A. Bauerfeind F. Rüschendorf C. Rintisch E. Petretto P.J. Barton S.A. Cook Y.M. Pinto C.R. Bezzina N. Hubner
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
December 07, 2017 / Nature IL11 is a crucial determinant of cardiovascular fibrosis S. Schafer S. Viswanathan A.A. Widjaja W.W. Lim A. Moreno-Moral D.M. DeLaughter B. Ng G. Patone K. Chow E. Khin J. Tan S.P. Chothani L. Ye O.J. Rackham N.S. Ko N.E. Sahib C.J. Pua N.T. Zhen C. Xie M. Wang H. Maatz S. Lim K. Saar S. Blachut E. Petretto S. Schmidt T. Putoczki N. Guimarães-Camboa H. Wakimoto S. van Heesch K. Sigmundsson S.L. Lim J.L. Soon V.T. Chao Y.L. Chua T.E. Tan S.M. Evans Y.J. Loh M.H. Jamal K.K. Ong K.C. Chua B.H. Ong M.J. Chakaramakkil J.G. Seidman C.E. Seidman N. Hubner K.Y. Sin S.A. Cook
April 03, 2017 / Curr Protoc Mol Biol Transcriptome-wide identification of RNA-binding protein binding sites using photoactivatable-ribonucleoside-enhanced crosslinking immunoprecipitation (PAR-CLIP) H. Maatz M. Kolinski N. Hubner M. Landthaler