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) Akalin, Altuna Dr. (2) Birchmeier, Walter Prof. Dr. (1) Birchmeier-Kohler, Carmen Prof. Dr. (2) Blachut, Susanne (1) Braeuning, Caroline (1) Chu, Van Trung Dr. (9) Conrad, Thomas Dr. (1) Diecke, Sebastian Dr. (1) Fischer, Cornelius Dr. (4) Gerhardt, Holger Prof. Dr. (1) Ghanbari, Mahsa Dr. (1) Graf, Robin Dr. (5) Hirsekorn, Antje (4) Hübner, Norbert Prof. Dr. (1) Hummel, Oliver (1) Janz, Martin Dr. (1) Kastelic, Nicolai (1) Kempa, Stefan Dr. (1) Kirchner, Marieluise Dr. (1) Kocks, Christine Dr. (1) Kühn, Ralf Dr. (14) Lahmann, Ines Dr. (2) Lindberg, Eric Lars-Helge (1) Lupianez Garcia, Dario Jesus Dr. (1) Maatz, Henrike Dr. (1) Mastrobuoni, Guido Dr. (1) Mertins, Philipp Dr. (1) Müller, Marion (1) Obermayer-Wasserscheid, Benedikt Dr. (2) Ohler, Uwe Prof. Dr. (12) Patone, Giannino Dr. (1) Potente, Michael Prof. Dr. (1) Preibisch, Stephan Dr. (1) Rajewsky, Klaus Prof. Dr. (21) Rajewsky, Nikolaus Prof. Dr. (2) Roßius, Jana (1) Sigal, Michael Dr. (1) Spuler, Simone Prof. (1) Sunaga-Franze, Daniele Yumi Dr. (1) Trombke, Janine (1) Vucicevic, Dubravka (1) Wolf, Jana Prof. Dr. (1) Wurmus, Ricardo (2) Wyler, Emanuel Dr. (2) Zauber, Henrik Dr. (1) (-) Altmueller, Janine Dr.med. (59) (-) Harabula, Izabela-Cezara (1) (-) Lacadie, Scott Allen Dr. (1) (-) Landthaler, Markus Prof. Dr. (4) (-) Pempe, Jenniffer (1) (-) Selbach, Matthias Prof. Dr. (3) 2002 (1) 2005 (2) 2013 (11) 2014 (17) 2015 (32) (-) 2016 (32) 2017 (34) 2018 (44) (-) 2019 (34) 2020 (24) 2021 (49) 2022 (39) 2023 (18) 2024 (2) Anchored Signalling (1) Bioinformatics and Omics Data Science (2) Bioinformatics of RNA Structure and Transcriptome Regulation (1) Biology of Malignant Lymphomas (1) Cellular Neurosciences (5) (-) Computational Regulatory Genomics (5) Developmental Biology / Signal Transduction (1) Experimental Ultrahigh-Field MR (4) Genetics and Genomics of Cardiovascular Diseases (2) Genetics of Metabolic and Reproductive Disorders (2) (-) Genome Engineering & Disease Models (1) (-) Genomics (59) (-) Immune Regulation and Cancer (2) Magnetic Resonance (4) Molecular Pathways in Cortical Development (1) Molecular Physiology of Somatic Sensation (1) Non-coding RNAs and Mechanisms of Cytoplasmic Gene Regulation (1) Pluripotent Stem Cells (1) Proteome Dynamics (13) Proteomics (2) Proteomics and Metabolomics (1) Proteomics and Molecular Mechanisms of Neurodegenerative Diseases (1) Psychoneuroimmunology (1) RNA Biology and Posttranscriptional Regulation (9) Structural Biology of Membrane-Associated Processes (3) Systems Biology of Gene Regulatory Elements (4) Transgenics (1) Translational Bioinformatics (1) 66 Results: Active Filter: Altmueller, Janine Dr.med.Harabula, Izabela-CezaraLacadie, Scott Allen Dr.Landthaler, Markus Prof. Dr.Pempe, JennifferSelbach, Matthias Prof. Dr.Computational Regulatory GenomicsGenome Engineering & Disease ModelsGenomicsImmune Regulation and Cancer20162019 Sort: Result score Newest to oldest Oldest to newest October 01, 2016 / Am J Med Genet A Update on the ACTG1-associated Baraitser–Winter cerebrofrontofacial syndrome N. Di Donato A. Kuechler S. Vergano W. Heinritz J. Bodurtha S.R. Merchant G. Breningstall R. Ladda S. Sell J. Altmüller N. Bögershausen A.E. Timms K. Hackmann E. Schrock S. Collins C. Olds A. Rump W.B. Dobyns June 01, 2016 / J Med Genet Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestalt N. Di Donato T. Neuhann A.K. Kahlert B. Klink K. Hackmann I. Neuhann B. Novotna J. Schallner C. Krause I.A. Glass S.E. Parnell A. Benet-Pages A.M. Nissen W. Berger J. Altmüller H. Thiele B.H.F. Weber E. Schrock W.B. Dobyns A. Bier A. Rump August 30, 2016 / Sci Rep Characterization of non-olfactory GPCRs in human sperm with a focus on GPR18 C. Flegel F. Vogel A. Hofreuter S. Wojcik C. Schoeder K. Kieć-Kononowicz N.H. Brockmeyer C.E. Müller C. Becker J. Altmüller H. Hatt G. Gisselmann March 01, 2016 / Ann Neurol Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation E. Gardella F. Becker R.S. Møller J. Schubert J.R. Lemke L.H.G. Larsen H. Eiberg M. Nothnagel H. Thiele J. Altmüller S. Syrbe A. Merkenschlager T. Bast B. Steinhoff P. Nürnberg Y. Mang L. Bakke Møller P. Gellert S.E. Heron L.M. Dibbens S. Weckhuysen H.A. Dahl S. Biskup N. Tommerup H. Hjalgrim H. Lerche S. Beniczky Y.G. Weber September 13, 2016 / Sci Data Genomic resources for wild populations of the house mouse, Mus musculus and its close relative Mus spretus B. Harr E. Karakoc R. Neme M. Teschke C. Pfeifle Ž. Pezer H. Babiker M. Linnenbrink I. Montero R. Scavetta M.R. Abai M.P. Molins M. Schlegel R.G. Ulrich J. Altmüller M. Franitza A. Büntge S. Künzel D. Tautz July 15, 2016 / eLife Tumor suppression in basal keratinocytes via dual non-cell-autonomous functions of a Na,K-ATPase beta subunit J. Hatzold F. Beleggia H. Herzig J. Altmüller P. Nürnberg W. Bloch B. Wollnik M. Hammerschmidt July 21, 2016 / Blood Complex karyotypes and KRAS and POT1 mutations impact outcome in CLL after chlorambucil-based chemotherapy or chemoimmunotherapy C.D. Herling M. Klaumünzer C.K. Rocha J. Altmüller H. Thiele J. Bahlo S. Kluth G. Crispatzu M. Herling J. Schiller A. Engelke E. Tausch H. Döhner K. Fischer V. Goede P. Nürnberg H.C. Reinhardt S. Stilgenbauer M. Hallek K.A. Kreuzer July 08, 2016 / Canine Genet Epidemiol A large deletion in RPGR causes XLPRA in Weimaraner dogs R. Kropatsch D.A. Akkad M. Frank C. Rosenhagen J. Altmüller P. Nürnberg J.T. Epplen G. Dekomien May 12, 2016 / N Engl J Med Polyhydramnios, transient antenatal Bartter's syndrome, and MAGED2 mutations K. Laghmani B.B. Beck S.S. Yang E. Seaayfan A. Wenzel B. Reusch H. Vitzthum D. Priem S. Demaretz K. Bergmann L.K. Duin H. Göbel C. Mache H. Thiele M.P. Bartram C. Dombret J. Altmüller P. Nürnberg T. Benzing E. Levtchenko H.W. Seyberth G. Klaus G. Yigit S.H. Lin A. Timmer T.J. de Koning S.A. Scherjon K.P. Schlingmann M.J.M. Bertrand M.M. Rinschen O. de Backer M. Konrad M. Kömhoff January 01, 2016 / PLoS ONE Increased probability of co-occurrence of two rare diseases in consanguineous families and resolution of a complex phenotype by next generation sequencing D. Lal B.A. Neubauer M.R. Toliat J. Altmüller H. Thiele P. Nürnberg C. Kamrath A. Schänzer T. Sander A. Hahn M. Nothnagel Pagination First page « First Previous page ‹ Previous … Page 2 Current page 3 Page 4 Page 5 … Next page Next › Last page Last »
October 01, 2016 / Am J Med Genet A Update on the ACTG1-associated Baraitser–Winter cerebrofrontofacial syndrome N. Di Donato A. Kuechler S. Vergano W. Heinritz J. Bodurtha S.R. Merchant G. Breningstall R. Ladda S. Sell J. Altmüller N. Bögershausen A.E. Timms K. Hackmann E. Schrock S. Collins C. Olds A. Rump W.B. Dobyns
June 01, 2016 / J Med Genet Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestalt N. Di Donato T. Neuhann A.K. Kahlert B. Klink K. Hackmann I. Neuhann B. Novotna J. Schallner C. Krause I.A. Glass S.E. Parnell A. Benet-Pages A.M. Nissen W. Berger J. Altmüller H. Thiele B.H.F. Weber E. Schrock W.B. Dobyns A. Bier A. Rump
August 30, 2016 / Sci Rep Characterization of non-olfactory GPCRs in human sperm with a focus on GPR18 C. Flegel F. Vogel A. Hofreuter S. Wojcik C. Schoeder K. Kieć-Kononowicz N.H. Brockmeyer C.E. Müller C. Becker J. Altmüller H. Hatt G. Gisselmann
March 01, 2016 / Ann Neurol Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation E. Gardella F. Becker R.S. Møller J. Schubert J.R. Lemke L.H.G. Larsen H. Eiberg M. Nothnagel H. Thiele J. Altmüller S. Syrbe A. Merkenschlager T. Bast B. Steinhoff P. Nürnberg Y. Mang L. Bakke Møller P. Gellert S.E. Heron L.M. Dibbens S. Weckhuysen H.A. Dahl S. Biskup N. Tommerup H. Hjalgrim H. Lerche S. Beniczky Y.G. Weber
September 13, 2016 / Sci Data Genomic resources for wild populations of the house mouse, Mus musculus and its close relative Mus spretus B. Harr E. Karakoc R. Neme M. Teschke C. Pfeifle Ž. Pezer H. Babiker M. Linnenbrink I. Montero R. Scavetta M.R. Abai M.P. Molins M. Schlegel R.G. Ulrich J. Altmüller M. Franitza A. Büntge S. Künzel D. Tautz
July 15, 2016 / eLife Tumor suppression in basal keratinocytes via dual non-cell-autonomous functions of a Na,K-ATPase beta subunit J. Hatzold F. Beleggia H. Herzig J. Altmüller P. Nürnberg W. Bloch B. Wollnik M. Hammerschmidt
July 21, 2016 / Blood Complex karyotypes and KRAS and POT1 mutations impact outcome in CLL after chlorambucil-based chemotherapy or chemoimmunotherapy C.D. Herling M. Klaumünzer C.K. Rocha J. Altmüller H. Thiele J. Bahlo S. Kluth G. Crispatzu M. Herling J. Schiller A. Engelke E. Tausch H. Döhner K. Fischer V. Goede P. Nürnberg H.C. Reinhardt S. Stilgenbauer M. Hallek K.A. Kreuzer
July 08, 2016 / Canine Genet Epidemiol A large deletion in RPGR causes XLPRA in Weimaraner dogs R. Kropatsch D.A. Akkad M. Frank C. Rosenhagen J. Altmüller P. Nürnberg J.T. Epplen G. Dekomien
May 12, 2016 / N Engl J Med Polyhydramnios, transient antenatal Bartter's syndrome, and MAGED2 mutations K. Laghmani B.B. Beck S.S. Yang E. Seaayfan A. Wenzel B. Reusch H. Vitzthum D. Priem S. Demaretz K. Bergmann L.K. Duin H. Göbel C. Mache H. Thiele M.P. Bartram C. Dombret J. Altmüller P. Nürnberg T. Benzing E. Levtchenko H.W. Seyberth G. Klaus G. Yigit S.H. Lin A. Timmer T.J. de Koning S.A. Scherjon K.P. Schlingmann M.J.M. Bertrand M.M. Rinschen O. de Backer M. Konrad M. Kömhoff
January 01, 2016 / PLoS ONE Increased probability of co-occurrence of two rare diseases in consanguineous families and resolution of a complex phenotype by next generation sequencing D. Lal B.A. Neubauer M.R. Toliat J. Altmüller H. Thiele P. Nürnberg C. Kamrath A. Schänzer T. Sander A. Hahn M. Nothnagel