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. (1) Chen, Wei Prof. Dr. (1) Daumke, Oliver Prof. Dr. (3) Fielitz, Jens Dr. (1) Gotthardt, Michael Prof. Dr. (2) Haucke, Volker Professor (1) Heinemann, Udo Prof. Dr. (1) Hübner, Norbert Prof. Dr. (15) Kirchner, Marieluise Dr. (1) Landthaler, Markus Prof. Dr. (2) Maatz, Henrike Dr. (1) Patone, Giannino Dr. (1) Radke, Michael Dr. (1) Rajewsky, Nikolaus Prof. Dr. (1) Saar, Kathrin Dr. (5) Schütz, Anja Dr. (1) Selbach, Matthias Prof. Dr. (1) Spagnoli, Francesca Dr. (1) Spuler, Simone Prof. (1) (-) Hummel, Oliver (4) 2004 (10) 2005 (9) 2006 (5) 2007 (9) 2008 (6) 2009 (15) 2011 (2) 2012 (6) 2013 (5) (-) 2014 (8) 2015 (5) 2016 (4) 2017 (4) 2018 (3) 2019 (4) 2020 (5) 2021 (3) 2022 (2) 2024 (1) Developmental Biology / Signal Transduction (1) (-) Genetics and Genomics of Cardiovascular Diseases (8) Mobile DNA (2) Molecular Genetics of Chronic Inflammation and Allergic Disease (1) Out-patient Clinic for Pediatric Allergology and Atopic Dermatitis (1) Proteome Dynamics (1) Proteomics and Molecular Mechanisms of Neurodegenerative Diseases (1) 8 Results: Active Filter: Hummel, OliverGenetics and Genomics of Cardiovascular Diseases2014 Sort: Result score Newest to oldest Oldest to newest June 10, 2014 / Sci Data Genomes and phenomes of a population of outbred rats and its progenitors A. Baud V. Guryev O. Hummel M. Johannesson J. Flint January 01, 2014 / Gut Cryptogenic multifocal ulcerating stenosing enteritis associated with homozygous deletion mutations in cytosolic phospholipase A2-α M.A. Brooke H.J. Longhurst V. Plagnol N.S. Kirkby J.A. Mitchell F. Rüschendorf T.D. Warner D.P. Kelsell T.T. MacDonald December 01, 2014 / Nat Genet Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes J. Schubert A. Siekierska M. Langlois P. May C. Huneau F. Becker H. Muhle A. Suls J.R. Lemke C.G.F. de Kovel H. Thiele K. Konrad A. Kawalia M.R. Toliat T. Sander F. Rueschendorf A. Caliebe I. Nagel B. Kohl A. Kecskes M. Jacmin K. Hardies S. Weckhuysen E. Riesch T. Dorn E.H. Brilstra S. Baulac R.S. Moller H. Hjalgrim B.P.C. Koeleman K. Jurkat-Rott F. Lehman-Horn J.C. Roach G. Glusman L. Hood D.J. Galas B. Martin P.A.M. de Witte S. Biskup P. De Jonghe I. Helbig R. Balling P. Nuernberg A.D. Crawford C.V. Esguerra Y.G. Weber H. Lerche May 01, 2014 / Leukemia Inherited susceptibility to pre B-ALL caused by germline transmission of PAX5 c.547G>A F. Auer F. Rueschendorf M. Gombert P. Husemann S. Ginzel S. Izraeli M. Harit M. Weintraub O.Y. Weinstein I. Lerer P. Stepensky A. Borkhardt J. Hauer April 28, 2014 / Nat Commun Klf4 and Klf5 differentially inhibit mesoderm and endoderm differentiation in embryonic stem cells I. Aksoy V. Giudice E. Delahaye F. Wianny M. Aubry M. Mure J. Chen R. Jauch G.K. Bogu T. Nolden H. Himmelbauer M.X. Doss A. Sachinidis H. Schulz O. Hummel P. Martinelli N. Hübner L.W. Stanton F.X. Real P.Y. Bourillot P. Savatier June 15, 2014 / Physiol Genomics Protease inhibitor 15, a candidate gene for abdominal aortic internal elastic lamina ruptures in the rat S. Falak S. Schafer A. Baud O. Hummel H. Schulz D. Gauguier N. Hubner M. Osborne-Pellegrin June 01, 2014 / Genome Res Natural variation of histone modification and its impact on gene expression in the rat genome C. Rintisch M. Heinig A. Bauerfeind S. Schafer C. Mieth G. Patone O. Hummel W. Chen S. Cook E. Cuppen M. Colomé-Tatché F. Johannes R.C. Jansen H. Neil M. Werner M. Pravenec M. Vingron N. Hubner October 01, 2014 / Diabetes Recessive mutations in PCBD1 cause a new type of early-onset diabetes D. Simaite J. Kofent M. Gong F. Rüschendorf S. Jia P. Arn K. Bentler C. Ellaway P. Kühnen G.F. Hoffmann N. Blau F.M. Spagnoli N. Hübner K. Raile
June 10, 2014 / Sci Data Genomes and phenomes of a population of outbred rats and its progenitors A. Baud V. Guryev O. Hummel M. Johannesson J. Flint
January 01, 2014 / Gut Cryptogenic multifocal ulcerating stenosing enteritis associated with homozygous deletion mutations in cytosolic phospholipase A2-α M.A. Brooke H.J. Longhurst V. Plagnol N.S. Kirkby J.A. Mitchell F. Rüschendorf T.D. Warner D.P. Kelsell T.T. MacDonald
December 01, 2014 / Nat Genet Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes J. Schubert A. Siekierska M. Langlois P. May C. Huneau F. Becker H. Muhle A. Suls J.R. Lemke C.G.F. de Kovel H. Thiele K. Konrad A. Kawalia M.R. Toliat T. Sander F. Rueschendorf A. Caliebe I. Nagel B. Kohl A. Kecskes M. Jacmin K. Hardies S. Weckhuysen E. Riesch T. Dorn E.H. Brilstra S. Baulac R.S. Moller H. Hjalgrim B.P.C. Koeleman K. Jurkat-Rott F. Lehman-Horn J.C. Roach G. Glusman L. Hood D.J. Galas B. Martin P.A.M. de Witte S. Biskup P. De Jonghe I. Helbig R. Balling P. Nuernberg A.D. Crawford C.V. Esguerra Y.G. Weber H. Lerche
May 01, 2014 / Leukemia Inherited susceptibility to pre B-ALL caused by germline transmission of PAX5 c.547G>A F. Auer F. Rueschendorf M. Gombert P. Husemann S. Ginzel S. Izraeli M. Harit M. Weintraub O.Y. Weinstein I. Lerer P. Stepensky A. Borkhardt J. Hauer
April 28, 2014 / Nat Commun Klf4 and Klf5 differentially inhibit mesoderm and endoderm differentiation in embryonic stem cells I. Aksoy V. Giudice E. Delahaye F. Wianny M. Aubry M. Mure J. Chen R. Jauch G.K. Bogu T. Nolden H. Himmelbauer M.X. Doss A. Sachinidis H. Schulz O. Hummel P. Martinelli N. Hübner L.W. Stanton F.X. Real P.Y. Bourillot P. Savatier
June 15, 2014 / Physiol Genomics Protease inhibitor 15, a candidate gene for abdominal aortic internal elastic lamina ruptures in the rat S. Falak S. Schafer A. Baud O. Hummel H. Schulz D. Gauguier N. Hubner M. Osborne-Pellegrin
June 01, 2014 / Genome Res Natural variation of histone modification and its impact on gene expression in the rat genome C. Rintisch M. Heinig A. Bauerfeind S. Schafer C. Mieth G. Patone O. Hummel W. Chen S. Cook E. Cuppen M. Colomé-Tatché F. Johannes R.C. Jansen H. Neil M. Werner M. Pravenec M. Vingron N. Hubner
October 01, 2014 / Diabetes Recessive mutations in PCBD1 cause a new type of early-onset diabetes D. Simaite J. Kofent M. Gong F. Rüschendorf S. Jia P. Arn K. Bentler C. Ellaway P. Kühnen G.F. Hoffmann N. Blau F.M. Spagnoli N. Hübner K. Raile