Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Bader, Michael Prof. Dr. (2) Birchmeier-Kohler, Carmen Prof. Dr. (1) Braeuning, Caroline (1) Conrad, Thomas Dr. (2) Diecke, Sebastian Dr. (1) Edes, Inan Dr. (1) Fischer, Cornelius Dr. (5) Gerhardt, Holger Prof. Dr. (1) Gouti, Mina Dr. (1) Hodge, Russell (1) Infante Duarte, Carmen (2) Ittermann, Bernd Dr. (1) Kettenmann, Helmut Prof. Dr. (2) Klix, Sabrina (1) Ku, Min-Chi Dr. (4) Kunz, Severine Dr. (1) Landthaler, Markus Prof. Dr. (1) Millward, Jason Dr. (3) Münchberg, Stefanie (1) Niendorf, Thoralf Prof. Dr. (38) Paul, Friedemann Prof. Dr. med. (7) Popova, Elena Dr. (1) Qadri, Fatimunnisa Dr. (1) Quedenau, Claudia (1) Rajewsky, Klaus Prof. Dr. (1) Reimann, Henning Dr. (3) Sai, Somesh (1) Schulz-Menger, Jeanette Prof. Dr. (2) Sohn, Madlen (1) Spuler, Simone Prof. (1) Starke, Ludger Benedikt (2) Sunaga-Franze, Daniele Yumi Dr. (2) Todiras, Mihail (1) Uckert, Wolfgang Prof. Dr. (1) Vitcetz, Sarah Nathalie (1) Waiczies, Sonia PD Dr. (13) Winter, Lukas Dr. (9) Wolf, Susanne Dr. (2) (-) Altmueller, Janine Dr.med. (53) (-) Harabula, Izabela-Cezara (1) (-) Lupianez Garcia, Dario Jesus Dr. (1) (-) Plumbom, Izabela (1) (-) Potente, Michael Prof. Dr. (5) (-) Wyler, Emanuel Dr. (1) 1999 (1) 2002 (1) 2005 (5) 2007 (1) 2008 (6) 2009 (4) 2010 (2) 2011 (7) 2012 (6) 2013 (33) 2014 (19) 2015 (36) (-) 2016 (36) 2017 (43) 2018 (48) 2019 (35) (-) 2020 (34) 2021 (58) 2022 (42) 2023 (24) 2024 (6) (-) Angiogenesis & Metabolism Laboratory (5) Bioinformatics and Omics Data Science (1) Cellular Neurosciences (6) Computational Regulatory Genomics (2) Epigenetic Regulation and Chromatin Architecture (1) (-) Experimental Ultrahigh-Field MR (10) Genetics of Metabolic and Reproductive Disorders (1) Genome Engineering & Disease Models (3) (-) Genomics (55) Immune Regulation and Cancer (7) Innate Immunity & Neuroinflammation (1) Integrative Vascular Biology (1) Magnetic Resonance (10) Out-patient Clinic for Neuroimmunology (1) Pluripotent Stem Cells (1) Proteome Dynamics (1) Proteomics (1) Proteomics and Metabolomics (1) Psychoneuroimmunology (1) RNA Biology and Posttranscriptional Regulation (5) Transgenics (3) 70 Results: Active Filter: Altmueller, Janine Dr.med.Harabula, Izabela-CezaraLupianez Garcia, Dario Jesus Dr.Plumbom, IzabelaPotente, Michael Prof. Dr.Wyler, Emanuel Dr.Angiogenesis & Metabolism LaboratoryExperimental Ultrahigh-Field MRGenomics20162020 Sort: Result score Newest to oldest Oldest to newest 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 August, 2016 / Acta Neuropathol Neuropathological signs of inflammation correlate with mitochondrial DNA deletions in mesial temporal lobe epilepsy E. Volmering P. Niehusmann V. Peeva A. Grote G. Zsurka J. Altmüller P. Nürnberg A.J. Becker S. Schoch C.E. Elger W.S. Kunz June, 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 May 05, 2020 / bioRxiv Single cell RNA-sequencing-based analysis of CD4(+) T-cell subset-specific susceptibility to transcriptional modulation by HIV-1 latency-reversing agents J. Kazmierski D. Postmus E. Wyler C. Fischer J. Jansen K. Meixenberger S.N. Vitcetz M. Sohn S. Sauer N. Bannert M. Landthaler C. Goffinet January, 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 08, 2016 / PLoS ONE Identification of novel and recurrent disease-causing mutations in retinal dystrophies using whole exome sequencing (WES): Benefits and limitations A. Tiwari J. Lemke J. Altmüller H. Thiele E. Glaus J. Fleischhauer P. Nürnberg J. Neidhardt W. Berger 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 September, 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 December 13, 2016 / Breast Cancer-Targets Ther Expression and functionality of TRPV1 in breast cancer cells L.V. Weber K. Al-Refae G. Wölk G. Bonatz J. Altmüller C. Becker G. Gisselmann H. Hatt September, 2016 / NMR Biomed W(h)ither human cardiac and body magnetic resonance at ultrahigh fields? technical advances, practical considerations, applications, and clinical opportunities T. Niendorf K. Paul C. Oezerdem A. Graessl S. Klix T. Huelnhagen F. Hezel J. Rieger H. Waiczies J. Frahm A.M. Nagel E. Oberacker L. Winter Pagination First page « First Previous page ‹ Previous … Page 2 Current page 3 Page 4 Page 5 … Next page Next › Last page Last »
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
August, 2016 / Acta Neuropathol Neuropathological signs of inflammation correlate with mitochondrial DNA deletions in mesial temporal lobe epilepsy E. Volmering P. Niehusmann V. Peeva A. Grote G. Zsurka J. Altmüller P. Nürnberg A.J. Becker S. Schoch C.E. Elger W.S. Kunz
June, 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
May 05, 2020 / bioRxiv Single cell RNA-sequencing-based analysis of CD4(+) T-cell subset-specific susceptibility to transcriptional modulation by HIV-1 latency-reversing agents J. Kazmierski D. Postmus E. Wyler C. Fischer J. Jansen K. Meixenberger S.N. Vitcetz M. Sohn S. Sauer N. Bannert M. Landthaler C. Goffinet
January, 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 08, 2016 / PLoS ONE Identification of novel and recurrent disease-causing mutations in retinal dystrophies using whole exome sequencing (WES): Benefits and limitations A. Tiwari J. Lemke J. Altmüller H. Thiele E. Glaus J. Fleischhauer P. Nürnberg J. Neidhardt W. Berger
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
September, 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
December 13, 2016 / Breast Cancer-Targets Ther Expression and functionality of TRPV1 in breast cancer cells L.V. Weber K. Al-Refae G. Wölk G. Bonatz J. Altmüller C. Becker G. Gisselmann H. Hatt
September, 2016 / NMR Biomed W(h)ither human cardiac and body magnetic resonance at ultrahigh fields? technical advances, practical considerations, applications, and clinical opportunities T. Niendorf K. Paul C. Oezerdem A. Graessl S. Klix T. Huelnhagen F. Hezel J. Rieger H. Waiczies J. Frahm A.M. Nagel E. Oberacker L. Winter