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. (19) Akalin, Altuna Dr. (4) Altmueller, Janine Dr.med. (3) Arnau Soler, Aleix Dr. (2) Bader, Michael Prof. Dr. (7) Bähring, Sylvia Dr. (8) Bartels-Klein, Eireen (1) Bartolomaeus, Theda (2) Bernert, Carola (2) Beule, Dieter Dr. (2) Birchmeier, Walter Prof. Dr. (1) Birchmeier-Kohler, Carmen Prof. Dr. (2) Blachut, Susanne (6) Blankenstein, Thomas Prof. Dr. (1) Bock-Bierbaum, Tobias Dr. (5) Born, Gabriele (1) Borodina, Tatiana Dr. (1) Chekulaeva, Marina Dr. (1) Chen, Wei Prof. Dr. (7) Coralluzzo, Violeta (1) Costanza, Mariantonia Dr. (2) Dartsch, Josephine (1) Daumke, Oliver Prof. Dr. (91) Dechend, Ralf Priv. Doz. 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Prof. Dr. (1) Schlegel, Jeanette (2) Schmidt, Sabine (3) Schmidt-Krüger, Vanessa Dr. (2) Schulz-Menger, Jeanette Prof. Dr. (2) Schütz, Anja Dr. (1) Selbach, Matthias Prof. Dr. (10) Semtner, Marcus Dr. (1) Sholokh, Anastasiia (1) Shvetsov, Nikolay (1) Simon, Katja Prof. Dr. (1) Singh, Manvendra Dr. (1) Spagnoli, Francesca Dr. (2) Sporbert, Anje Dr. (1) Sprink, Thiemo Dr. (2) Spuler, Simone Prof. (6) Sunaga-Franze, Daniele Yumi Dr. (1) Taube, Martin (2) Telugu, Narasimha Swamy Dr. (1) Todiras, Mihail (1) Uckert, Wolfgang Prof. Dr. (1) Uyar, Bora Dr. (1) Vazquez Sarandeses, Elena (2) Vidal, Marie Dr. (1) von Kries, Jens Peter Dr. (2) Wallukat, Gerd Dr. (4) Wanker, Erich Prof. Dr. (5) Weismehl, Marius (1) Wenzel, Katrin Dr. (6) Willnow, Thomas Prof. Dr. (4) Witt, Marie Dr. (2) Woehler, Andrew Dr. (1) Wollert-Wulf, Brigitte (1) Wyler, Emanuel Dr. (3) Yilmaz, Zekiye Buket Dr. (1) Zauber, Henrik Dr. (2) Zenkner, Martina (1) Ziehm, Matthias Dr. (1) Zühlke, Kerstin Dr. (5) Zywitza, Vera Dr. (1) (-) Hummel, Oliver (35) (-) Rajewsky, Nikolaus Prof. Dr. (4) 2004 (10) 2005 (9) 2006 (5) 2007 (9) 2008 (6) 2009 (15) 2010 (8) 2011 (2) 2012 (6) 2013 (5) 2014 (9) 2015 (6) 2016 (4) 2017 (4) 2018 (3) 2019 (4) 2020 (6) 2021 (3) 2022 (2) 2024 (1) AG Müller/Dechend (ECRC) (1) Anchored Signalling (2) Animal Phenotyping (2) Bioinformatics and Omics Data Science (8) Clinic of Psychiatry / Modul Psychiatry of Aging (1) Computational methodologies and omic analytics (1) Computational Regulatory Genomics (5) Developmental Biology / Signal Transduction (8) Development and Function of Neural Circuits (1) Epigenetic Modifications in Neuroblastoma (1) Epigenetic Regulation and Chromatin Architecture (2) Flow Cytometry (1) From Cell States to Function (4) Gastrointestinal Barrier, Regeneration and Carcinogenesis (1) (-) Genetics and Genomics of Cardiovascular Diseases (115) Genome Diversification & Integrity (1) Genome Engineering & Disease Models (3) Genomics (6) Hypertension-caused End-Organ Damage (1) Hypertension-Mediated End-Organ Damage (1) Immune Regulation and Cancer (2) Integrative Vascular Biology (1) Mathematical Cell Physiology (2) Mobile DNA (15) Molecular Biology of Peptide Hormones (2) Molecular Cardiovascular Research (1) Molecular Genetics of Chronic Inflammation and Allergic Disease (29) Molecular Pathways in Cortical Development (1) Molecular Physiology of Somatic Sensation (2) Myology (2) Non-coding RNAs and Mechanisms of Cytoplasmic Gene Regulation (4) Organoids (8) Out-patient Clinic for Pediatric Allergology and Atopic Dermatitis (29) Pluripotent Stem Cells (3) Protein Production and Characterization (1) Proteome Dynamics (13) Proteomics (3) Proteomics and Metabolomics (7) Proteomics and Molecular Mechanisms of Neurodegenerative Diseases (6) Psychoneuroimmunology (1) Quantitative Developmental Biology (2) Quantitative Stem Cell Biology (1) RNA Biology and Posttranscriptional Regulation (19) (-) Structural Biology of Membrane-Associated Processes (2) Systems Biology Imaging (5) Systems Biology of Gene Regulatory Elements (160) Transgenics (3) Translational Bioinformatics (3) Translational Cardiology and Functional Genomics (2) Translational Oncology of Solid Tumors (1) 117 Results: Active Filter: Hummel, OliverRajewsky, Nikolaus Prof. Dr.Genetics and Genomics of Cardiovascular DiseasesStructural Biology of Membrane-Associated Processes Sort: Result score Newest to oldest Oldest to newest October 28, 2020 / J Genet Genomics Phosphatidylinositol 4 kinase-β mutations cause non-syndromic sensorineural deafness and inner ear malformation X. Su Y. Feng S.A. Rahman S. Wu G. Li F. Rüschendorf L. Zhao H. Cui J. Liang L. Fang H. Hu S. Froehler Y. Yu G. Patone O. Hummel Q. Chen K. Raile F.C. Luft S. Bähring K. Hussain W. Chen J. Zhang M. Gong April 01, 2004 / Genome Res Integrated and sequence-ordered BAC- and YAC-based physical maps for the rat genome M. Krzywinski J. Wallis C. Gösele I. Bosdet R. Chiu T. Graves O. Hummel D. Layman C. Mathewson N. Wye B. Zhu D. Albracht J. Asano S. Barber M. Brown-John S. Chan S. Chand A. Cloutier J. Davito C. Fjell T. Gaige D. Ganten N. Girn K. Guggenheimer H. Himmelbauer T. Kreitler S. Leach D. Lee H. Lehrach M. Mayo K. Mead T. Olson P. Pandoh A.L. Prabhu H. Shin S. Taenzer J. Thompson M. Tsai J. Walker G. Yang M. Sekhon L. Hillier H. Zimdahl A. Marziali K. Osoegawa S. Zhao A. Siddiqui P.J. de Jong W. Warren E. Mardis J.D. McPherson R. Wilson N. Hübner S. Jones M. Marra J. Schein 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 / Science A SNP map of the rat genome generated from cDNA sequences H. Zimdahl G. Nyakatura P. Brandt H. Schulz O. Hummel B. Fartmann D. Brett M. Droege J. Monti Y.A. Lee Y.Y. Sun S.Y. Zhao E.E. Winter C.P. Ponting Y. Chen A. Kasprzyk E. Birney D. Ganten N. Hubner January 01, 2004 / J Evol Biol Divergent genetic and epigenetic post-zygotic isolation mechanisms in Mus and Peromyscus U. Zechner W. Shi M. Hemberger H. Himmelbauer S. Otto A. Orth V. Kalscheuer U. Fischer R. Elango A. Reis W. Vogel H. Ropers F. Rueschendorf R. Fundele October 01, 2006 / J Allergy Clin Immunol Filaggrin loss-of-function mutations predispose to phenotypes involved in the atopic march I. Marenholz R. Nickel F. Rueschendorf F. Schulz J. Esparza-Gordillo T. Kerscher C. Grueber S. Lau M. Worm T. Keil M. Kurek E. Zaluga U. Wahn Y.A. Lee November 01, 2006 / Nat Genet The gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, is mutated in inherited anonychia D.C. Blaydon Y. Ishii E.A. O'Toole H.C. Unsworth M.T. Teh F. Rueschendorf C. Sinclair V.K. Hopsu-Havu N. Tidman C. Moss R. Watson D. de Berker M. Wajid A.M. Christiano D.P. Kelsell January 01, 2007 / Bioinformatics Linkage analysis using sex-specific recombination fractions with GENEHUNTER-MODSCORE J. Dietter M. Mattheisen R. Fuerst F. Rueschendorf T.F. Wienker K. Strauch Pagination Current page 1 Page 2 Page 3 Page 4 … Next page Next › Last page Last »
October 28, 2020 / J Genet Genomics Phosphatidylinositol 4 kinase-β mutations cause non-syndromic sensorineural deafness and inner ear malformation X. Su Y. Feng S.A. Rahman S. Wu G. Li F. Rüschendorf L. Zhao H. Cui J. Liang L. Fang H. Hu S. Froehler Y. Yu G. Patone O. Hummel Q. Chen K. Raile F.C. Luft S. Bähring K. Hussain W. Chen J. Zhang M. Gong
April 01, 2004 / Genome Res Integrated and sequence-ordered BAC- and YAC-based physical maps for the rat genome M. Krzywinski J. Wallis C. Gösele I. Bosdet R. Chiu T. Graves O. Hummel D. Layman C. Mathewson N. Wye B. Zhu D. Albracht J. Asano S. Barber M. Brown-John S. Chan S. Chand A. Cloutier J. Davito C. Fjell T. Gaige D. Ganten N. Girn K. Guggenheimer H. Himmelbauer T. Kreitler S. Leach D. Lee H. Lehrach M. Mayo K. Mead T. Olson P. Pandoh A.L. Prabhu H. Shin S. Taenzer J. Thompson M. Tsai J. Walker G. Yang M. Sekhon L. Hillier H. Zimdahl A. Marziali K. Osoegawa S. Zhao A. Siddiqui P.J. de Jong W. Warren E. Mardis J.D. McPherson R. Wilson N. Hübner S. Jones M. Marra J. Schein
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 / Science A SNP map of the rat genome generated from cDNA sequences H. Zimdahl G. Nyakatura P. Brandt H. Schulz O. Hummel B. Fartmann D. Brett M. Droege J. Monti Y.A. Lee Y.Y. Sun S.Y. Zhao E.E. Winter C.P. Ponting Y. Chen A. Kasprzyk E. Birney D. Ganten N. Hubner
January 01, 2004 / J Evol Biol Divergent genetic and epigenetic post-zygotic isolation mechanisms in Mus and Peromyscus U. Zechner W. Shi M. Hemberger H. Himmelbauer S. Otto A. Orth V. Kalscheuer U. Fischer R. Elango A. Reis W. Vogel H. Ropers F. Rueschendorf R. Fundele
October 01, 2006 / J Allergy Clin Immunol Filaggrin loss-of-function mutations predispose to phenotypes involved in the atopic march I. Marenholz R. Nickel F. Rueschendorf F. Schulz J. Esparza-Gordillo T. Kerscher C. Grueber S. Lau M. Worm T. Keil M. Kurek E. Zaluga U. Wahn Y.A. Lee
November 01, 2006 / Nat Genet The gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, is mutated in inherited anonychia D.C. Blaydon Y. Ishii E.A. O'Toole H.C. Unsworth M.T. Teh F. Rueschendorf C. Sinclair V.K. Hopsu-Havu N. Tidman C. Moss R. Watson D. de Berker M. Wajid A.M. Christiano D.P. Kelsell
January 01, 2007 / Bioinformatics Linkage analysis using sex-specific recombination fractions with GENEHUNTER-MODSCORE J. Dietter M. Mattheisen R. Fuerst F. Rueschendorf T.F. Wienker K. Strauch