Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Bader, Michael Prof. Dr. (1) Bähring, Sylvia Dr. (1) Gösele, Claudia Dr. (4) Gotthardt, Michael Prof. Dr. (1) Hübner, Norbert Prof. Dr. (25) Hummel, Oliver (8) Infante Duarte, Carmen (1) Klaassen, Sabine Prof. Dr. med. (1) Klaus-Bergmann, Alexandra Dr. (1) Lee, Young-Ae Prof. Dr. (8) Lewin, Gary Prof. Dr. (1) Luft, Friedrich Prof. Dr. (3) Maatz, Henrike Dr. (1) Marenholz, Ingo Dr. (3) Millward, Jason Dr. (1) Müller, Dominik Prof. Dr. (1) Müller, Marion (1) Niendorf, Thoralf Prof. Dr. (22) Patone, Giannino Dr. (1) Paul, Friedemann Prof. Dr. med. (2) Perrot, Andreas (1) Radke, Michael Dr. (1) Saar, Kathrin Dr. (8) Schmidt-Krüger, Vanessa Dr. (1) Schulz-Menger, Jeanette Prof. Dr. (7) Waiczies, Helmar Dr. (3) Waiczies, Sonia PD Dr. (3) Willnow, Thomas Prof. Dr. (1) Winter, Lukas Dr. (3) (-) Birchmeier, Walter Prof. Dr. (1) 2001 (1) (-) 2004 (7) 2005 (7) 2006 (6) 2007 (8) 2008 (4) (-) 2009 (13) 2010 (5) 2011 (1) (-) 2012 (9) 2013 (11) 2014 (7) 2015 (15) 2016 (8) 2017 (12) 2018 (9) 2019 (9) 2020 (16) 2021 (25) 2022 (3) 2023 (1) 2024 (2) Animal Phenotyping (1) Cardiac MRI (1) Developmental Biology / Signal Transduction (2) Developmental Neurobiology (1) (-) Experimental Ultrahigh-Field MR (5) (-) Genetics and Genomics of Cardiovascular Diseases (24) Genetics of Congenital Heart Disease (1) Innate Immunity & Neuroinflammation (1) Magnetic Resonance (5) Mobile DNA (1) Molecular Genetics of Chronic Inflammation and Allergic Disease (3) Molecular Physiology of Somatic Sensation (1) Out-patient Clinic for Pediatric Allergology and Atopic Dermatitis (3) Proteome Dynamics (1) Translational Oncology of Solid Tumors (2) 29 Results: Active Filter: Birchmeier, Walter Prof. Dr.Experimental Ultrahigh-Field MRGenetics and Genomics of Cardiovascular Diseases200420092012 Sort: Result score Newest to oldest Oldest to newest August 01, 2004 / Am J Hum Genet Mutations in the gene encoding gap junction protein alpha 12 (connexin 46.6) cause Pelizaeus-Merzbacher-like disease B. Uhlenberg M. Schuelke F. Rueschendorf N. Ruf A.M. Kaindl M. Henneke H. Thiele G. Stoltenburg-Didinger F. Aksu H. Topaloglu P. Nuernberg C. Huebner B. Weschke J. Gaertner January 01, 2004 / Nat Genet Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophy A.R. Janecke D.A. Thompson G. Utermann C. Becker C.A. Huebner E. Schmid C.L. McHenry A.R. Nair F. Rueschendorf J. Heckenlively B. Wissinger P. Nuernberg A. Gal January 01, 2004 / J Clin Endocrinol Metab Genome-wide linkage analysis reveals evidence for four new susceptibility loci for familial euthyroid goiter Y. Bayer S. Neumann B. Meyer F. Rueschendorf A. Reske T. Brix L. Hegedues P. Langer P. Nuernberg R. Paschke January 01, 2004 / J Med Genet Missense mutations of ACTA1 cause dominant congenital myopathy with cores A.M. Kaindl F. Rueschendorf S. Krause H.H. Goebel K. Koehler C. Becker D. Pongratz J. Mueller-Hoecker P. Nuernberg G. Stoltenburg-Didinger H. Lochmueller A. Huebner January 01, 2004 / J Med Genet Molecular karyotyping using an SNP array for genomewide genotyping A. Rauch F. Rueschendorf J. Huang U. Trautmann C. Becker C. Thiel K.W. Jones A. Reis P. Nuernberg January 01, 2004 / Endocr Res Mutations in a novel gene, encoding a single transmembrane domain protein are associated with familial glucocorticoid deficiency type 2 L.A. Metherell S. Cooray A. Huebner F. Rueschendorf D. Naville M. Begeot A.J.L. Clark May 01, 2009 / J Hypertens A novel locus for arterial hypertension on chromosome 1p36 maps to a metabolic syndrome trait cluster in the Sorbs, a Slavic population isolate in Germany* K. Hoffmann C. Planitz F. Rueschendorf B. Mueller-Myhsok H.H. Stassen B. Lucke M. Mattheisen M. Stumvoll R. Bochmann M. Zschornack T.F. Wienker P. Nuernberg A. Reis F.C. Luft T.H. Lindner May 01, 2009 / J Clin Invest Girls homozygous for an IL-2-inducible T cell kinase mutation that leads to protein deficiency develop fatal EBV-associated lymphoproliferation K. Huck O. Feyen T. Niehues F. Rueschendorf N. Huebner H.J. Laws T. Telieps S. Knapp H.H. Wacker A. Meindl H. Jumaa A. Borkhardt July 01, 2009 / Nat Genet RNASET2-deficient cystic leukoencephalopathy resembles congenital cytomegalovirus brain infection M. Henneke S. Diekmann A. Ohlenbusch J. Kaiser V. Engelbrecht A. Kohlschuetter R. Kraetzner M. Madruga-Garrido M. Mayer L. Opitz D. Rodriguez F. Rueschendorf J. Schumacher H. Thiele S. Thoms R. Steinfeld P. Nuernberg J. Gaertner February 13, 2009 / Am J Hum Genet Mutations in SPINT2 cause a syndromic form of congenital sodium diarrhea P. Heinz-Erian T. Mueller B. Krabichler M. Schranz C. Becker F. Rueschendorf P. Nuernberg B. Rossier M. Vujic I.W. Booth C. Holmberg C. Wijmenga G. Grigelioniene C.M. Kneepkens S. Rosipal M. Mistrik M. Kappler L. Michaud L.C. Doczy V.M. Siu M. Krantz H. Zoller G. Utermann A.R. Janecke Pagination Current page 1 Page 2 Page 3 Next page Next › Last page Last »
August 01, 2004 / Am J Hum Genet Mutations in the gene encoding gap junction protein alpha 12 (connexin 46.6) cause Pelizaeus-Merzbacher-like disease B. Uhlenberg M. Schuelke F. Rueschendorf N. Ruf A.M. Kaindl M. Henneke H. Thiele G. Stoltenburg-Didinger F. Aksu H. Topaloglu P. Nuernberg C. Huebner B. Weschke J. Gaertner
January 01, 2004 / Nat Genet Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophy A.R. Janecke D.A. Thompson G. Utermann C. Becker C.A. Huebner E. Schmid C.L. McHenry A.R. Nair F. Rueschendorf J. Heckenlively B. Wissinger P. Nuernberg A. Gal
January 01, 2004 / J Clin Endocrinol Metab Genome-wide linkage analysis reveals evidence for four new susceptibility loci for familial euthyroid goiter Y. Bayer S. Neumann B. Meyer F. Rueschendorf A. Reske T. Brix L. Hegedues P. Langer P. Nuernberg R. Paschke
January 01, 2004 / J Med Genet Missense mutations of ACTA1 cause dominant congenital myopathy with cores A.M. Kaindl F. Rueschendorf S. Krause H.H. Goebel K. Koehler C. Becker D. Pongratz J. Mueller-Hoecker P. Nuernberg G. Stoltenburg-Didinger H. Lochmueller A. Huebner
January 01, 2004 / J Med Genet Molecular karyotyping using an SNP array for genomewide genotyping A. Rauch F. Rueschendorf J. Huang U. Trautmann C. Becker C. Thiel K.W. Jones A. Reis P. Nuernberg
January 01, 2004 / Endocr Res Mutations in a novel gene, encoding a single transmembrane domain protein are associated with familial glucocorticoid deficiency type 2 L.A. Metherell S. Cooray A. Huebner F. Rueschendorf D. Naville M. Begeot A.J.L. Clark
May 01, 2009 / J Hypertens A novel locus for arterial hypertension on chromosome 1p36 maps to a metabolic syndrome trait cluster in the Sorbs, a Slavic population isolate in Germany* K. Hoffmann C. Planitz F. Rueschendorf B. Mueller-Myhsok H.H. Stassen B. Lucke M. Mattheisen M. Stumvoll R. Bochmann M. Zschornack T.F. Wienker P. Nuernberg A. Reis F.C. Luft T.H. Lindner
May 01, 2009 / J Clin Invest Girls homozygous for an IL-2-inducible T cell kinase mutation that leads to protein deficiency develop fatal EBV-associated lymphoproliferation K. Huck O. Feyen T. Niehues F. Rueschendorf N. Huebner H.J. Laws T. Telieps S. Knapp H.H. Wacker A. Meindl H. Jumaa A. Borkhardt
July 01, 2009 / Nat Genet RNASET2-deficient cystic leukoencephalopathy resembles congenital cytomegalovirus brain infection M. Henneke S. Diekmann A. Ohlenbusch J. Kaiser V. Engelbrecht A. Kohlschuetter R. Kraetzner M. Madruga-Garrido M. Mayer L. Opitz D. Rodriguez F. Rueschendorf J. Schumacher H. Thiele S. Thoms R. Steinfeld P. Nuernberg J. Gaertner
February 13, 2009 / Am J Hum Genet Mutations in SPINT2 cause a syndromic form of congenital sodium diarrhea P. Heinz-Erian T. Mueller B. Krabichler M. Schranz C. Becker F. Rueschendorf P. Nuernberg B. Rossier M. Vujic I.W. Booth C. Holmberg C. Wijmenga G. Grigelioniene C.M. Kneepkens S. Rosipal M. Mistrik M. Kappler L. Michaud L.C. Doczy V.M. Siu M. Krantz H. Zoller G. Utermann A.R. Janecke