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. (4) Heinemann, Udo Prof. Dr. (1) Ivics, Zoltan Dr. (3) Izsvak, Zsuzsanna Dr. (3) Jentsch, Thomas Prof. Dr. (1) Lee, Young-Ae Prof. Dr. (5) Luft, Friedrich Prof. Dr. (1) (-) Hübner, Norbert Prof. Dr. (4) (-) Saar, Kathrin Dr. (1) (-) 1995 (2) 1997 (2) 1999 (1) (-) 2001 (1) (-) 2003 (2) 2004 (1) 2008 (3) 2009 (3) 2010 (3) 2011 (2) 2012 (1) 2013 (3) 2014 (4) 2015 (8) 2016 (1) 2018 (3) 2019 (4) 2020 (2) 2021 (2) 2022 (1) 2023 (3) Genetics and Genomics of Cardiovascular Diseases (13) Genetics of Congenital Heart Disease (1) (-) Molecular Genetics of Chronic Inflammation and Allergic Disease (4) (-) Out-patient Clinic for Pediatric Allergology and Atopic Dermatitis (4) (-) Translational Cardiology and Functional Genomics (1) 5 Results: Active Filter: Hübner, Norbert Prof. Dr.Saar, Kathrin Dr.Molecular Genetics of Chronic Inflammation and Allergic DiseaseOut-patient Clinic for Pediatric Allergology and Atopic DermatitisTranslational Cardiology and Functional Genomics199520012003 Sort: Result score Newest to oldest Oldest to newest June 01, 2003 / Hum Mol Genet Genome-wide linkage reveals a locus for human essential (primary) hypertension on chromosome 12p M. Gong H.Y. Zhang H. Schulz Y.A. Lee K. Sun S. Bähring F.C. Luft P. Nürnberg A. Reis K. Rohde D. Ganten R.T. Hui N. Hübner February 21, 2003 / J Biol Chem Conditional expression of mutant M-line titins results in cardiomyopathy with altered sarcomere structure M. Gotthardt R.E. Hammer N. Hübner J. Monti C.C. Witt M. McNabb J.A. Richardson H. Granzier S. Labeit J. Herz January 01, 2001 / J Med Genet Localisation of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia, and distinctive facies to chromosome 15q26 R. Bayoumi K. Saar Y.A. Lee G. Nuernberg A. Reis M. Nur-E-Kamal L.I. Al Gazali January 01, 1995 / Mamm Genome The gene encoding endothelial nitric oxide synthase, Nos3, maps to rat chromosome 4 N. Hübner R. Kreutz S. Rubattu Y.A. Lee D. Ganten P.D. Allen K. Lindpaintner January 01, 1995 Genetische Analyse des Bluthochdrucks Y.A. Lee N. Hübner D. Ganten
June 01, 2003 / Hum Mol Genet Genome-wide linkage reveals a locus for human essential (primary) hypertension on chromosome 12p M. Gong H.Y. Zhang H. Schulz Y.A. Lee K. Sun S. Bähring F.C. Luft P. Nürnberg A. Reis K. Rohde D. Ganten R.T. Hui N. Hübner
February 21, 2003 / J Biol Chem Conditional expression of mutant M-line titins results in cardiomyopathy with altered sarcomere structure M. Gotthardt R.E. Hammer N. Hübner J. Monti C.C. Witt M. McNabb J.A. Richardson H. Granzier S. Labeit J. Herz
January 01, 2001 / J Med Genet Localisation of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia, and distinctive facies to chromosome 15q26 R. Bayoumi K. Saar Y.A. Lee G. Nuernberg A. Reis M. Nur-E-Kamal L.I. Al Gazali
January 01, 1995 / Mamm Genome The gene encoding endothelial nitric oxide synthase, Nos3, maps to rat chromosome 4 N. Hübner R. Kreutz S. Rubattu Y.A. Lee D. Ganten P.D. Allen K. Lindpaintner