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. (2) Altmueller, Janine Dr.med. (1) Bähring, Sylvia Dr. (1) Bartels-Klein, Eireen (1) Dechend, Ralf Priv. Doz. (1) Diecke, Sebastian Dr. (1) Gösele, Claudia Dr. (1) Gotthardt, Michael Prof. Dr. (1) Hammes-Lewin, Annette Dr. (1) Hodge, Russell (1) Hollfinger, Irene (1) Hübner, Norbert Prof. Dr. (30) Klußmann, Enno PD Dr. (1) Landthaler, Markus Prof. Dr. (1) Lee, Young-Ae Prof. Dr. (8) Luft, Friedrich Prof. Dr. (1) Maatz, Henrike Dr. (1) Marenholz, Ingo Dr. (5) Müller, Dominik Prof. Dr. (1) Perrot, Andreas (1) Qadri, Fatimunnisa Dr. (1) Radke, Michael Dr. (1) Rajewsky, Nikolaus Prof. Dr. (1) Saar, Kathrin Dr. (1) Schmidt-Krüger, Vanessa Dr. (1) Selbach, Matthias Prof. Dr. (1) Siffrin, Volker (1) Wanker, Erich Prof. Dr. (1) Willnow, Thomas Prof. Dr. (9) Wyler, Emanuel Dr. (1) (-) 1992 (1) 1994 (8) (-) 1995 (10) 1996 (7) 1997 (7) 1998 (3) 1999 (9) 2000 (4) 2001 (8) 2002 (14) 2003 (13) 2004 (17) 2005 (28) 2006 (53) 2007 (33) 2008 (32) 2009 (35) 2010 (32) 2011 (16) 2012 (28) 2013 (32) 2014 (28) (-) 2015 (33) 2016 (26) 2017 (23) 2018 (17) 2019 (16) 2020 (25) 2021 (29) 2022 (24) 2023 (20) 2024 (8) Advanced Light Microscopy (1) AG Müller/Dechend (ECRC) (24) AG Schreiber [ECRC] (6) Anchored Signalling (9) Angiogenesis & Metabolism Laboratory (3) Animal Phenotyping (1) Biobank (21) Bioinformatics and Omics Data Science (4) Bioinformatics of RNA Structure and Transcriptome Regulation (2) Biology of Malignant Lymphomas (5) Biomedical Image Analysis (2) Cancer Genetics and Cellular Stress Responses (1) Cardiac MRI (16) Cell Biology of Immunity (6) Cellular Neurosciences (59) Chromatin (dys)function in disease (1) Clinic of Psychiatry / Modul Psychiatry of Aging (13) Computational methodologies and omic analytics (3) Computational Regulatory Genomics (8) Cryo-Electron Microscopy (2) Developmental Biology / Signal Transduction (12) Developmental Neurobiology (7) Endocrinology, Diabetes and Nutritional Medicine (8) Epigenetic Modifications in Neuroblastoma (2) Epigenetic Regulation and Chromatin Architecture (5) Experimental Ultrahigh-Field MR (27) Gastrointestinal Barrier, Regeneration and Carcinogenesis (3) (-) Genetics and Genomics of Cardiovascular Diseases (32) Genetics of Congenital Heart Disease (3) Genetics of Metabolic and Reproductive Disorders (4) Genome Diversification & Integrity (3) Genome Engineering & Disease Models (14) Genome instability and somatic mosaicism (1) Genomics (16) Host-microbiome factors in cardiovascular disease (3) Hypertension-caused End-Organ Damage (24) Hypertension-Mediated End-Organ Damage (24) immune Cell Function in Health and Disease (1) Immune Dysregulations in Oncology (6) Immune Mechanisms and Human Antibodies (1) Immune Regulation and Cancer (15) Innate Immunity & Neuroinflammation (6) In Situ Structural Biology (5) Integrative Vascular Biology (9) Interdisciplinary Retina Research (6) Intracellular Proteolysis (14) Kidney Cell Engineering (1) Magnetic Resonance (27) Mathematical Cell Physiology (10) Mathematical Modelling of Cellular Processes (4) Mechanism-based Cancer Therapies (2) Microenvironmental Regulation in Autoimmunity and Cancer (4) Mobile DNA (8) Molecular Biology of Peptide Hormones (49) (-) Molecular Cardiovascular Research (12) Molecular Epidemiology (21) Molecular Genetics of Chronic Inflammation and Allergic Disease (14) Molecular Immunology and Gene Therapy (23) Molecular mechanisms of environment sensing (1) (-) Molecular Pathways in Cortical Development (1) Molecular Physiology of Somatic Sensation (10) Myology (5) Nephrology and Inflammatory Vascular Diseases (9) Neural Circuits and Behaviour (3) Neuroimmunology Laboratory (6) Out-patient Clinic for Neuroimmunology (42) Out-patient Clinic for Pediatric Allergology and Atopic Dermatitis (14) Pancreatic Organoid Research and Disease Modeling (14) Pathogenesis of ANCAinduced Glomerulonephritis (6) Pluripotent Stem Cells (4) Protein Production and Characterization (2) Proteome Dynamics (12) Proteomics (6) Proteomics and Metabolomics (10) Proteomics and Molecular Mechanisms of Neurodegenerative Diseases (21) Psychoneuroimmunology (7) Quantitative Developmental Biology (5) RNA Biology and Posttranscriptional Regulation (7) Stem Cell Dynamics and Mitochondrial Genomics (2) Stem Cell Modeling of Development and Disease (1) Structural Biology of Membrane-Associated Processes (5) Synaptic Transmission and Plasticity (15) Systems Biology Imaging (1) Systems Biology of Gene Regulatory Elements (14) Systems Hematology, Stem Cells & Precision Medicine (2) Transgenics (14) Translational Approaches in Heart Failure and Cardiometabolic Disease (8) Translational Cardiology and Functional Genomics (3) Translational Oncology of Solid Tumors (88) Translational Organ Models (5) 44 Results: Active Filter: Genetics and Genomics of Cardiovascular DiseasesMolecular Cardiovascular ResearchMolecular Pathways in Cortical Development199219952015 Sort: Result score Newest to oldest Oldest to newest July 01, 2015 / Hum Genet Skeletal dysplasia in a consanguineous clan from the island of Nias/Indonesia is caused by a novel mutation in B3GAT3 B.S. Budde S. Mizumoto R. Kogawa C. Becker J. Altmüller H. Thiele F. Rueschendorf M.R. Toliat G. Kaleschke J.M. Haemmerle W. Hoehne K. Sugahara P. Nuernberg I. Kennerknecht May 06, 2015 / BMC Genomics Genomic landscape of rat strain and substrain variation R. Hermsen J. de Ligt W. Spee F. Blokzijl S. Schäfer E. Adami S. Boymans S Flink R. van Boxtel R.H. van der Weide T. Aitman N. Hübner M. Simonis B. Tabakoff V. Guryev E. Cuppen June 01, 2015 / Genome Res Genomic redistribution of GR monomers and dimers mediates transcriptional response to exogenous glucocorticoid in vivo H.W. Lim N.H. Uhlenhaut A. Rauch J. Weiner S. Hübner N. Hübner K.J. Won M.A. Lazar J. Tuckermann D.J. Steger June 01, 2015 / Nat Genet PDE3A mutations cause autosomal dominant hypertension with brachydactyly P.G. Maass A. Aydin F.C. Luft C. Schächterle A. Weise S. Stricker C. Lindschau M. Vaegler F. Qadri H.R. Toka H. Schulz P.M. Krawitz D. Parkhomchuk J. Hecht I. Hollfinger Y. Wefeld-Neuenfeld E. Bartels-Klein A. Mühl M. Kann H. Schuster D. Chitayat M.G. Bialer T.F. Wienker J. Ott K. Rittscher T. Liehr J. Jordan G. Plessis J. Tank K. Mai R. Naraghi R. Hodge M. Hopp L.O. Hattenbach A. Busjahn A. Rauch F. Vandeput M. Gong F. Rüschendorf N. Hübner H. Haller S. Mundlos N. Bilginturan M.A. Movsesian E. Klussmann O. Toka S. Bähring May 19, 2015 / Cell Rep Quantitative interaction proteomics of neurodegenerative disease proteins F. Hosp H. Vossfeldt M. Heinig D. Vasiljevic A. Arumughan E. Wyler M. Landthaler N. Hubner E.E. Wanker L. Lannfelt M. Ingelsson M. Lalowski A. Voigt M. Selbach December 15, 2015 / J Immunol Role of sortilin in models of autoimmune neuroinflammation E. Reuter J. Weber M. Paterka R. Ploen T. Breiderhoff J. van Horssen T.E. Willnow V. Siffrin F. Zipp February 01, 2015 / BIOspektrum Alternatives Spleißen im Herzen [Alternative splicing in the heart] H. Maatz M. Heinig N. Hübner December 01, 2015 / Nat Genet Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis L. Paternoster M. Standl J. Waage H. Baurecht M. Hotze D.P. Strachan J.A. Curtin K. Bønnelykke C. Tian A. Takahashi J. Esparza-Gordillo A.C. Alves J.P. Thyssen H.T. den Dekker M.A. Ferreira E. Altmaier P.M.A. Sleiman F.L. Xiao J.R. Gonzalez I. Marenholz B. Kalb M. Pino-Yanes C.J. Xu L. Carstensen M.M. Groen-Blokhuis C. Venturini C.E. Pennell S.J. Barton A.M. Levin I. Curjuric M. Bustamante E. Kreiner-Møller G.A. Lockett J. Bacelis S. Bunyavanich R.A. Myers A. Matanovic A. Kumar J.Y. Tung T. Hirota M. Kubo W.L. McArdle A.J. Henderson J.P. Kemp J. Zheng G.D. Smith F. Rüschendorf A. Bauerfeind M.A. Lee-Kirsch A. Arnold G. Homuth C.O. Schmidt E. Mangold S. Cichon T. Keil E. Rodríguez A. Peters A. Franke W. Lieb N. Novak R. Fölster-Holst M. Horikoshi J. Pekkanen S. Sebert L.L. Husemoen N. Grarup J.C. de Jongste F. Rivadeneira A. Hofman V.W.V. Jaddoe S.G.M.A. Pasmans N.J. Elbert A.G. Uitterlinden G.B. Marks P.J. Thompson M.C. Matheson C.F. Robertson J.S. Ried J. Li X.B. Zuo X.D. Zheng X.Y. Yin L.D. Sun M.A. McAleer G.M. O'Regan C.M.R. Fahy L.E. Campbell M. Macek M. Kurek D. Hu C. Eng D.S. Postma B. Feenstra F. Geller J.J. Hottenga C.M. Middeldorp P. Hysi V. Bataille T. Spector C.M.T. Tiesler E. Thiering B. Pahukasahasram J.J. Yang M. Imboden S. Huntsman N. Vilor-Tejedor C.L. Relton R. Myhre W. Nystad A. Custovic S.T. Weiss D.A. Meyers C. Söderhäll E. Melén C. Ober B.A. Raby A. Simpson B. Jacobsson J.W. Holloway H. Bisgaard J. Sunyer N.M. Probst-Hensch L.K. Williams K.M. Godfrey C.A. Wang D.I. Boomsma M. Melbye G.H. Koppelman D. Jarvis W.H.I. McLean A.D. Irvine X.J. Zhang H. Hakonarson C. Gieger E.G. Burchard N.G. Martin L. Duijts A. Linneberg M.R. Jarvelin M.M. Noethen S. Lau N. Hübner Y.A. Lee M. Tamari D.A. Hinds D. Glass S.J. Brown J. Heinrich D.M. Evans S. Weidinger October 01, 2015 / Clin Exp Pharmacol Physiol Novel candidate genes for impaired nephron development in a rat model with inherited nephron deficit and albuminuria L. Herlan A. Schulz L. Schulte H. Schulz N. Hübner R. Kreutz August 28, 2015 / Science Titin mutations in iPS cells define sarcomere insufficiency as a cause of dilated cardiomyopathy J.T. Hinson A. Chopra N. Nafissi W.J. Polacheck C.C. Benson S. Swist J. Gorham L. Yang S. Schafer C.C. Sheng A. Haghighi J. Homsy N. Hubner G. Church S.A. Cook W.A. Linke C.S. Chen J.G. Seidman C.E. Seidman Pagination Current page 1 Page 2 Page 3 Page 4 … Next page Next › Last page Last »
July 01, 2015 / Hum Genet Skeletal dysplasia in a consanguineous clan from the island of Nias/Indonesia is caused by a novel mutation in B3GAT3 B.S. Budde S. Mizumoto R. Kogawa C. Becker J. Altmüller H. Thiele F. Rueschendorf M.R. Toliat G. Kaleschke J.M. Haemmerle W. Hoehne K. Sugahara P. Nuernberg I. Kennerknecht
May 06, 2015 / BMC Genomics Genomic landscape of rat strain and substrain variation R. Hermsen J. de Ligt W. Spee F. Blokzijl S. Schäfer E. Adami S. Boymans S Flink R. van Boxtel R.H. van der Weide T. Aitman N. Hübner M. Simonis B. Tabakoff V. Guryev E. Cuppen
June 01, 2015 / Genome Res Genomic redistribution of GR monomers and dimers mediates transcriptional response to exogenous glucocorticoid in vivo H.W. Lim N.H. Uhlenhaut A. Rauch J. Weiner S. Hübner N. Hübner K.J. Won M.A. Lazar J. Tuckermann D.J. Steger
June 01, 2015 / Nat Genet PDE3A mutations cause autosomal dominant hypertension with brachydactyly P.G. Maass A. Aydin F.C. Luft C. Schächterle A. Weise S. Stricker C. Lindschau M. Vaegler F. Qadri H.R. Toka H. Schulz P.M. Krawitz D. Parkhomchuk J. Hecht I. Hollfinger Y. Wefeld-Neuenfeld E. Bartels-Klein A. Mühl M. Kann H. Schuster D. Chitayat M.G. Bialer T.F. Wienker J. Ott K. Rittscher T. Liehr J. Jordan G. Plessis J. Tank K. Mai R. Naraghi R. Hodge M. Hopp L.O. Hattenbach A. Busjahn A. Rauch F. Vandeput M. Gong F. Rüschendorf N. Hübner H. Haller S. Mundlos N. Bilginturan M.A. Movsesian E. Klussmann O. Toka S. Bähring
May 19, 2015 / Cell Rep Quantitative interaction proteomics of neurodegenerative disease proteins F. Hosp H. Vossfeldt M. Heinig D. Vasiljevic A. Arumughan E. Wyler M. Landthaler N. Hubner E.E. Wanker L. Lannfelt M. Ingelsson M. Lalowski A. Voigt M. Selbach
December 15, 2015 / J Immunol Role of sortilin in models of autoimmune neuroinflammation E. Reuter J. Weber M. Paterka R. Ploen T. Breiderhoff J. van Horssen T.E. Willnow V. Siffrin F. Zipp
February 01, 2015 / BIOspektrum Alternatives Spleißen im Herzen [Alternative splicing in the heart] H. Maatz M. Heinig N. Hübner
December 01, 2015 / Nat Genet Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis L. Paternoster M. Standl J. Waage H. Baurecht M. Hotze D.P. Strachan J.A. Curtin K. Bønnelykke C. Tian A. Takahashi J. Esparza-Gordillo A.C. Alves J.P. Thyssen H.T. den Dekker M.A. Ferreira E. Altmaier P.M.A. Sleiman F.L. Xiao J.R. Gonzalez I. Marenholz B. Kalb M. Pino-Yanes C.J. Xu L. Carstensen M.M. Groen-Blokhuis C. Venturini C.E. Pennell S.J. Barton A.M. Levin I. Curjuric M. Bustamante E. Kreiner-Møller G.A. Lockett J. Bacelis S. Bunyavanich R.A. Myers A. Matanovic A. Kumar J.Y. Tung T. Hirota M. Kubo W.L. McArdle A.J. Henderson J.P. Kemp J. Zheng G.D. Smith F. Rüschendorf A. Bauerfeind M.A. Lee-Kirsch A. Arnold G. Homuth C.O. Schmidt E. Mangold S. Cichon T. Keil E. Rodríguez A. Peters A. Franke W. Lieb N. Novak R. Fölster-Holst M. Horikoshi J. Pekkanen S. Sebert L.L. Husemoen N. Grarup J.C. de Jongste F. Rivadeneira A. Hofman V.W.V. Jaddoe S.G.M.A. Pasmans N.J. Elbert A.G. Uitterlinden G.B. Marks P.J. Thompson M.C. Matheson C.F. Robertson J.S. Ried J. Li X.B. Zuo X.D. Zheng X.Y. Yin L.D. Sun M.A. McAleer G.M. O'Regan C.M.R. Fahy L.E. Campbell M. Macek M. Kurek D. Hu C. Eng D.S. Postma B. Feenstra F. Geller J.J. Hottenga C.M. Middeldorp P. Hysi V. Bataille T. Spector C.M.T. Tiesler E. Thiering B. Pahukasahasram J.J. Yang M. Imboden S. Huntsman N. Vilor-Tejedor C.L. Relton R. Myhre W. Nystad A. Custovic S.T. Weiss D.A. Meyers C. Söderhäll E. Melén C. Ober B.A. Raby A. Simpson B. Jacobsson J.W. Holloway H. Bisgaard J. Sunyer N.M. Probst-Hensch L.K. Williams K.M. Godfrey C.A. Wang D.I. Boomsma M. Melbye G.H. Koppelman D. Jarvis W.H.I. McLean A.D. Irvine X.J. Zhang H. Hakonarson C. Gieger E.G. Burchard N.G. Martin L. Duijts A. Linneberg M.R. Jarvelin M.M. Noethen S. Lau N. Hübner Y.A. Lee M. Tamari D.A. Hinds D. Glass S.J. Brown J. Heinrich D.M. Evans S. Weidinger
October 01, 2015 / Clin Exp Pharmacol Physiol Novel candidate genes for impaired nephron development in a rat model with inherited nephron deficit and albuminuria L. Herlan A. Schulz L. Schulte H. Schulz N. Hübner R. Kreutz
August 28, 2015 / Science Titin mutations in iPS cells define sarcomere insufficiency as a cause of dilated cardiomyopathy J.T. Hinson A. Chopra N. Nafissi W.J. Polacheck C.C. Benson S. Swist J. Gorham L. Yang S. Schafer C.C. Sheng A. Haghighi J. Homsy N. Hubner G. Church S.A. Cook W.A. Linke C.S. Chen J.G. Seidman C.E. Seidman