Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Cano Rincon, Elena Dr. (3) Chen, Wei Prof. Dr. (1) Collins, Russell Thomas Dr. (1) Daumke, Oliver Prof. Dr. (2) Fälber, Katja Dr. (1) Fischer, Cornelius Dr. (1) Hammes-Lewin, Annette Dr. (1) Heinemann, Udo Prof. Dr. (1) Hirsekorn, Antje (1) Klußmann, Enno PD Dr. (1) Landthaler, Markus Prof. Dr. (2) Lewin, Gary Prof. Dr. (1) Obermayer-Wasserscheid, Benedikt Dr. (1) Ohler, Uwe Prof. Dr. (2) Panakova, Daniela Dr. (1) Rajewsky, Klaus Prof. Dr. (1) Rocks, Oliver Dr. (2) Roske, Yvette Dr. (1) Selbach, Matthias Prof. Dr. (8) Wanker, Erich Prof. Dr. (1) Zauber, Henrik Dr. (3) Zühlke, Kerstin Dr. (1) (-) Altmueller, Janine Dr.med. (29) (-) Gerhardt, Holger Prof. Dr. (10) (-) Harabula, Izabela-Cezara (1) (-) Lupianez Garcia, Dario Jesus Dr. (1) (-) Potente, Michael Prof. Dr. (2) (-) Wyler, Emanuel Dr. (1) 1996 (1) 1997 (1) 1999 (5) 2000 (6) 2001 (1) 2002 (5) 2003 (4) 2004 (2) 2005 (7) 2006 (3) 2007 (5) 2008 (13) 2009 (10) 2010 (4) 2011 (11) 2012 (6) 2013 (11) 2014 (15) 2015 (37) (-) 2016 (41) 2017 (43) 2018 (52) 2019 (40) 2020 (31) 2021 (62) 2022 (50) 2023 (26) 2024 (3) (-) Angiogenesis & Metabolism Laboratory (2) Cellular Neurosciences (2) Computational Regulatory Genomics (2) Experimental Ultrahigh-Field MR (4) Genome Engineering & Disease Models (2) (-) Genomics (29) Immune Regulation and Cancer (4) (-) Integrative Vascular Biology (10) Magnetic Resonance (4) (-) Proteome Dynamics (1) RNA Biology and Posttranscriptional Regulation (1) Transgenics (2) 41 Results: Active Filter: Altmueller, Janine Dr.med.Gerhardt, Holger Prof. Dr.Harabula, Izabela-CezaraLupianez Garcia, Dario Jesus Dr.Potente, Michael Prof. Dr.Wyler, Emanuel Dr.Angiogenesis & Metabolism LaboratoryGenomicsIntegrative Vascular BiologyProteome Dynamics2016 Sort: Result score Newest to oldest Oldest to newest 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 July 26, 2016 / Oncotarget The activation of OR51E1 causes growth suppression of human prostate cancer cells D. Maßberg N. Jovancevic A. Offermann A. Simon A. Baniahmad S. Perner T. Pungsrinont K. Luko S. Philippou B. Ubrig M. Heiland L. Weber J. Altmüller C. Becker G. Gisselmann L. Gelis H. Hatt April 01, 2016 / Clin Genet Mutations in SEC24D cause autosomal recessive osteogenesis imperfecta S. Moosa B.H.Y. Chung J.Y.L. Tung J. Altmüller H. Thiele P. Nürnberg C. Netzer G. Nishimura B. Wollnik September 01, 2016 / Am J Med Genet A A novel homozygous PAM16 mutation in a patient with a milder phenotype and longer survival S. Moosa V. Fano M.G. Obregon J. Altmüller H. Thiele P. Nürnberg G. Nishimura B. Wollnik May 01, 2016 / Am J Med Genet A Novel IFT122 mutations in three Argentinian patients with cranioectodermal dysplasia: expanding the mutational spectrum S. Moosa M.G. Obregon J. Altmüller H. Thiele P. Nürnberg V. Fano B. Wollnik October 02, 2016 / Clin Cancer Res Heterogeneous mechanisms of primary and acquired resistance to third-generation EGFR inhibitors S. Ortiz-Cuaran M. Scheffler D. Plenker L. Dahmen A.H. Scheel L. Fernandez-Cuesta L. Meder C.M. Lovly T. Persigehl S. Merkelbach-Bruse M. Bos S. Michels R. Fischer K. Albus K. König H.U. Schildhaus Jana Fassunke M.A. Ihle H. Pasternack C. Heydt C. Becker J. Altmüller H. Ji C. Müller A. Florin J.M. Heuckmann P. Nuernberg S. Ansén L.C. Heukamp J. Berg W. Pao M. Peifer R. Buettner J. Wolf R.K. Thomas M.L. Sos November 04, 2016 / Sci Rep The mutation p.E113K in the Schiff base counterion of rhodopsin is associated with two distinct retinal phenotypes within the same family C. Reiff M. Owczarek-Lipska G. Spital C. Röger H. Hinz C. Jüschke H. Thiele J. Altmüller P. Nürnberg R. Da Costa J. Neidhardt Pagination First page « First Previous page ‹ Previous Page 1 Current page 2 Page 3 Page 4 … Next page Next › Last page Last »
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
July 26, 2016 / Oncotarget The activation of OR51E1 causes growth suppression of human prostate cancer cells D. Maßberg N. Jovancevic A. Offermann A. Simon A. Baniahmad S. Perner T. Pungsrinont K. Luko S. Philippou B. Ubrig M. Heiland L. Weber J. Altmüller C. Becker G. Gisselmann L. Gelis H. Hatt
April 01, 2016 / Clin Genet Mutations in SEC24D cause autosomal recessive osteogenesis imperfecta S. Moosa B.H.Y. Chung J.Y.L. Tung J. Altmüller H. Thiele P. Nürnberg C. Netzer G. Nishimura B. Wollnik
September 01, 2016 / Am J Med Genet A A novel homozygous PAM16 mutation in a patient with a milder phenotype and longer survival S. Moosa V. Fano M.G. Obregon J. Altmüller H. Thiele P. Nürnberg G. Nishimura B. Wollnik
May 01, 2016 / Am J Med Genet A Novel IFT122 mutations in three Argentinian patients with cranioectodermal dysplasia: expanding the mutational spectrum S. Moosa M.G. Obregon J. Altmüller H. Thiele P. Nürnberg V. Fano B. Wollnik
October 02, 2016 / Clin Cancer Res Heterogeneous mechanisms of primary and acquired resistance to third-generation EGFR inhibitors S. Ortiz-Cuaran M. Scheffler D. Plenker L. Dahmen A.H. Scheel L. Fernandez-Cuesta L. Meder C.M. Lovly T. Persigehl S. Merkelbach-Bruse M. Bos S. Michels R. Fischer K. Albus K. König H.U. Schildhaus Jana Fassunke M.A. Ihle H. Pasternack C. Heydt C. Becker J. Altmüller H. Ji C. Müller A. Florin J.M. Heuckmann P. Nuernberg S. Ansén L.C. Heukamp J. Berg W. Pao M. Peifer R. Buettner J. Wolf R.K. Thomas M.L. Sos
November 04, 2016 / Sci Rep The mutation p.E113K in the Schiff base counterion of rhodopsin is associated with two distinct retinal phenotypes within the same family C. Reiff M. Owczarek-Lipska G. Spital C. Röger H. Hinz C. Jüschke H. Thiele J. Altmüller P. Nürnberg R. Da Costa J. Neidhardt