Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Akalin, Altuna Dr. (1) Birchmeier, Walter Prof. Dr. (1) Blüthgen, Nils (1) Chen, Wei Prof. Dr. (1) Di Virgilio, Michela Prof. Dr. (1) Gerhardt, Holger Prof. Dr. (1) Graf, Robin Dr. (3) Harabula, Izabela-Cezara (1) Heinemann, Udo Prof. Dr. (1) Henssen, Anton Prof. Dr. med. (1) Hinz, Michael Dr. (1) Hirsekorn, Antje (3) Hübner, Norbert Prof. Dr. (1) Janz, Martin Dr. (1) Kempa, Stefan Dr. (2) Kühn, Ralf Dr. (10) Lacadie, Scott Allen Dr. (4) Landthaler, Markus Prof. Dr. (11) Lupianez Garcia, Dario Jesus Dr. (1) Mastrobuoni, Guido Dr. (2) Obermayer-Wasserscheid, Benedikt Dr. (2) Ohler, Uwe Prof. Dr. (12) Potente, Michael Prof. Dr. (1) Rajewsky, Klaus Prof. Dr. (23) Rajewsky, Nikolaus Prof. Dr. (4) Scheidereit, Claus Prof. Dr. (1) Schütz, Anja Dr. (1) Selbach, Matthias Prof. Dr. (6) Vucicevic, Dubravka (1) Wanker, Erich Prof. Dr. (1) Wolf, Jana Prof. Dr. (1) Wurmus, Ricardo (1) Zauber, Henrik Dr. (2) Zinzen, Robert Patrick Dr. (1) (-) Altmueller, Janine Dr.med. (53) (-) Chekulaeva, Marina Dr. (1) (-) Chu, Van Trung Dr. (6) (-) Fischer, Cornelius Dr. (1) (-) Semtner, Marcus Dr. (1) (-) Wyler, Emanuel Dr. (4) 2002 (1) 2005 (2) 2012 (2) 2013 (10) 2014 (16) (-) 2015 (30) (-) 2016 (35) 2017 (39) 2018 (43) 2019 (42) 2020 (35) 2021 (59) 2022 (55) 2023 (38) 2024 (8) Cardiac MRI (2) Cellular Neurosciences (2) (-) Computational Regulatory Genomics (1) Experimental Ultrahigh-Field MR (7) Genetics and Genomics of Cardiovascular Diseases (2) Genetics of Metabolic and Reproductive Disorders (2) Genome Diversification & Integrity (1) (-) Genome Engineering & Disease Models (4) (-) Genomics (54) (-) Immune Regulation and Cancer (7) Magnetic Resonance (7) Mathematical Modelling of Cellular Processes (1) Non-coding RNAs and Mechanisms of Cytoplasmic Gene Regulation (1) Protein Production and Characterization (1) Proteome Dynamics (3) Proteomics and Metabolomics (1) Proteomics and Molecular Mechanisms of Neurodegenerative Diseases (1) (-) RNA Biology and Posttranscriptional Regulation (5) Systems Biology of Gene Regulatory Elements (1) Transgenics (4) 65 Results: Active Filter: Altmueller, Janine Dr.med.Chekulaeva, Marina Dr.Chu, Van Trung Dr.Fischer, Cornelius Dr.Semtner, Marcus Dr.Wyler, Emanuel Dr.Computational Regulatory GenomicsGenome Engineering & Disease ModelsGenomicsImmune Regulation and CancerRNA Biology and Posttranscriptional Regulation20152016 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 January 01, 2015 / Front Mol Biosci Characterization of the olfactory receptors expressed in human spermatozoa C. Flegel F. Vogel A. Hofreuter B.S.P. Schreiner S. Osthold S. Veitinger C. Becker N.H. Brockmeyer M. Muschol G. Wennemuth J. Altmüller H. Hatt G. Gisselmann 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 Pagination First page « First Previous page ‹ Previous Page 1 Current page 2 Page 3 Page 4 … 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
January 01, 2015 / Front Mol Biosci Characterization of the olfactory receptors expressed in human spermatozoa C. Flegel F. Vogel A. Hofreuter B.S.P. Schreiner S. Osthold S. Veitinger C. Becker N.H. Brockmeyer M. Muschol G. Wennemuth J. Altmüller H. Hatt G. Gisselmann
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