Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Fischer, Cornelius Dr. (1) Rajewsky, Klaus Prof. Dr. (1) (-) Altmueller, Janine Dr.med. (50) (-) Gerhardt, Holger Prof. Dr. (2) (-) Harabula, Izabela-Cezara (1) (-) Lupianez Garcia, Dario Jesus Dr. (1) (-) Potente, Michael Prof. Dr. (6) 1999 (1) 2002 (1) 2005 (5) 2007 (1) 2008 (4) 2009 (3) 2010 (2) 2011 (2) 2012 (2) (-) 2013 (25) 2014 (16) 2015 (28) (-) 2016 (31) 2017 (36) 2018 (44) 2019 (33) 2020 (28) 2021 (54) 2022 (41) 2023 (23) 2024 (8) (-) Angiogenesis & Metabolism Laboratory (6) Cellular Neurosciences (2) Computational Regulatory Genomics (2) Experimental Ultrahigh-Field MR (5) Genetics of Metabolic and Reproductive Disorders (1) Genome Engineering & Disease Models (2) (-) Genomics (50) Immune Regulation and Cancer (4) Integrative Vascular Biology (18) Magnetic Resonance (5) Proteome Dynamics (1) RNA Biology and Posttranscriptional Regulation (1) Transgenics (2) 56 Results: Active Filter: Altmueller, Janine Dr.med.Gerhardt, Holger Prof. Dr.Harabula, Izabela-CezaraLupianez Garcia, Dario Jesus Dr.Potente, Michael Prof. Dr.Angiogenesis & Metabolism LaboratoryGenomics20132016 Sort: Result score Newest to oldest Oldest to newest February 05, 2013 / PLoS ONE Human trace amine-associated receptor TAAR5 can be activated by trimethylamine I. Wallrabenstein J. Kuklan L. Weber S. Zborala M. Werner J. Altmüller C. Becker A. Schmidt H. Hatt T. Hummel G. Gisselmann May 20, 2013 / Hum Mutat Do not trust the pedigree: reduced and sex-dependent penetrance at a novel mutation hotspot in ATL1 blurs autosomal dominant inheritance of spastic paraplegia R.E. Varga R. Schüle H. Fadel I. Valenzuela F. Speziani M. Gonzalez G. Rudenskaia G. Nürnberg H. Thiele J. Altmüller V. Alvarez J. Gamez J.Y. Garbern P. Nürnberg S. Zuchner C. Beetz May, 2013 / Nat Genet Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome M. Lemaire V. Frémeaux-Bacchi F. Schaefer M. Choi W.H. Tang M. Le Quintrec F. Fakhouri S. Taque F. Nobili F. Martinez W. Ji J.D. Overton S.M. Mane G. Nürnberg J. Altmüller H. Thiele D. Morin G. Deschenes V. Baudouin B. Llanas L. Collard M.A. Majid E. Simkova P. Nürnberg N. Rioux-Leclerc G.W. Moeckel M.C. Gubler J. Hwa C. Loirat R.P. Lifton October 03, 2013 / PLoS Comput Biol Sensitive detection of viral transcripts in human tumor transcriptomes S.E. Schelhorn M. Fischer L. Tolosi J. Altmüller P. Nürnberg H. Pfister T. Lengauer F. Berthold February, 2013 / J Hepatol Next generation sequencing of the Ago2 interacting transcriptome identified chemokine family members as novel targets of neuronal microRNAs in hepatic stellate cells A. Noetel N. Elfimova J. Altmüller C. Becker D. Becker W. Lahr P. Nürnberg H. Wasmuth A. Teufel R. Büttner H.P. Dienes M. Odenthal November 08, 2013 / PLoS ONE Comprehensive RNA-Seq expression analysis of sensory ganglia with a focus on ion channels and GPCRs in trigeminal ganglia S. Manteniotis R. Lehmann C. Flegel F. Vogel A. Hofreuter B.S.P. Schreiner J. Altmüller C. Becker N. Schöbel H. Hatt G. Gisselmann September 06, 2013 / PLoS ONE RBFOX1 and RBFOX3 mutations in rolandic epilepsy D. Lal E.M. Reinthaler J. Altmüller M.R. Toliat H. Thiele P. Nürnberg H. Lerche A. Hahn R.S. Møller H. Muhle T. Sander F. Zimprich B.A. Neubauer September 06, 2013 / PLoS ONE SOX9 duplication linked to intersex in deer R. Kropatsch G. Dekomien D.A. Akkad W.M. Gerding E. Petrasch-Parwez N.D. Young J. Altmüller P. Nürnberg R.B. Gasser J.T. Epplen October 04, 2013 / PLoS ONE A novel large in-frame deletion within the CACNA1F gene associates with a cone-rod dystrophy 3-like phenotype J. Hauke A. Schild A. Neugebauer A. Lappa J. Fricke S. Fauser S. Rösler A. Pannes D. Zarrinnam J. Altmüller S. Motameny G. Nürnberg P. Nürnberg E. Hahnen B.B. Beck February, 2013 / Neurogenetics Homozygous missense mutation of NDUFV1 as the cause of infantile bilateral striatal necrosis D. Lal K. Becker S. Motameny J. Altmüller H. Thiele P. Nürnberg U. Ahting B. Rolinski B.A. Neubauer A. Hahn Pagination Current page 1 Page 2 Page 3 Page 4 … Next page Next › Last page Last »
February 05, 2013 / PLoS ONE Human trace amine-associated receptor TAAR5 can be activated by trimethylamine I. Wallrabenstein J. Kuklan L. Weber S. Zborala M. Werner J. Altmüller C. Becker A. Schmidt H. Hatt T. Hummel G. Gisselmann
May 20, 2013 / Hum Mutat Do not trust the pedigree: reduced and sex-dependent penetrance at a novel mutation hotspot in ATL1 blurs autosomal dominant inheritance of spastic paraplegia R.E. Varga R. Schüle H. Fadel I. Valenzuela F. Speziani M. Gonzalez G. Rudenskaia G. Nürnberg H. Thiele J. Altmüller V. Alvarez J. Gamez J.Y. Garbern P. Nürnberg S. Zuchner C. Beetz
May, 2013 / Nat Genet Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome M. Lemaire V. Frémeaux-Bacchi F. Schaefer M. Choi W.H. Tang M. Le Quintrec F. Fakhouri S. Taque F. Nobili F. Martinez W. Ji J.D. Overton S.M. Mane G. Nürnberg J. Altmüller H. Thiele D. Morin G. Deschenes V. Baudouin B. Llanas L. Collard M.A. Majid E. Simkova P. Nürnberg N. Rioux-Leclerc G.W. Moeckel M.C. Gubler J. Hwa C. Loirat R.P. Lifton
October 03, 2013 / PLoS Comput Biol Sensitive detection of viral transcripts in human tumor transcriptomes S.E. Schelhorn M. Fischer L. Tolosi J. Altmüller P. Nürnberg H. Pfister T. Lengauer F. Berthold
February, 2013 / J Hepatol Next generation sequencing of the Ago2 interacting transcriptome identified chemokine family members as novel targets of neuronal microRNAs in hepatic stellate cells A. Noetel N. Elfimova J. Altmüller C. Becker D. Becker W. Lahr P. Nürnberg H. Wasmuth A. Teufel R. Büttner H.P. Dienes M. Odenthal
November 08, 2013 / PLoS ONE Comprehensive RNA-Seq expression analysis of sensory ganglia with a focus on ion channels and GPCRs in trigeminal ganglia S. Manteniotis R. Lehmann C. Flegel F. Vogel A. Hofreuter B.S.P. Schreiner J. Altmüller C. Becker N. Schöbel H. Hatt G. Gisselmann
September 06, 2013 / PLoS ONE RBFOX1 and RBFOX3 mutations in rolandic epilepsy D. Lal E.M. Reinthaler J. Altmüller M.R. Toliat H. Thiele P. Nürnberg H. Lerche A. Hahn R.S. Møller H. Muhle T. Sander F. Zimprich B.A. Neubauer
September 06, 2013 / PLoS ONE SOX9 duplication linked to intersex in deer R. Kropatsch G. Dekomien D.A. Akkad W.M. Gerding E. Petrasch-Parwez N.D. Young J. Altmüller P. Nürnberg R.B. Gasser J.T. Epplen
October 04, 2013 / PLoS ONE A novel large in-frame deletion within the CACNA1F gene associates with a cone-rod dystrophy 3-like phenotype J. Hauke A. Schild A. Neugebauer A. Lappa J. Fricke S. Fauser S. Rösler A. Pannes D. Zarrinnam J. Altmüller S. Motameny G. Nürnberg P. Nürnberg E. Hahnen B.B. Beck
February, 2013 / Neurogenetics Homozygous missense mutation of NDUFV1 as the cause of infantile bilateral striatal necrosis D. Lal K. Becker S. Motameny J. Altmüller H. Thiele P. Nürnberg U. Ahting B. Rolinski B.A. Neubauer A. Hahn
