Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Chekulaeva, Marina Dr. (1) Harabula, Izabela-Cezara (1) Hirsekorn, Antje (1) Landthaler, Markus Prof. Dr. (7) Lee, Young-Ae Prof. Dr. (1) Lupianez Garcia, Dario Jesus Dr. (1) Obermayer-Wasserscheid, Benedikt Dr. (1) Ohler, Uwe Prof. Dr. (2) Selbach, Matthias Prof. Dr. (2) Zauber, Henrik Dr. (1) (-) Altmueller, Janine Dr.med. (31) (-) Fischer, Cornelius Dr. (1) (-) Rajewsky, Nikolaus Prof. Dr. (1) (-) Wyler, Emanuel Dr. (1) 2002 (1) (-) 2005 (2) 2011 (1) 2012 (3) 2013 (2) 2014 (9) 2015 (28) (-) 2016 (32) 2017 (37) 2018 (42) 2019 (37) 2020 (32) 2021 (59) 2022 (52) 2023 (37) 2024 (6) Cellular Neurosciences (2) Computational Regulatory Genomics (2) Developmental Biology / Signal Transduction (1) Experimental Ultrahigh-Field MR (4) Genetics and Genomics of Cardiovascular Diseases (2) Genetics of Metabolic and Reproductive Disorders (1) Genome Engineering & Disease Models (2) (-) Genomics (32) Immune Regulation and Cancer (3) Magnetic Resonance (4) Molecular Genetics of Chronic Inflammation and Allergic Disease (1) Out-patient Clinic for Pediatric Allergology and Atopic Dermatitis (1) Proteome Dynamics (1) (-) RNA Biology and Posttranscriptional Regulation (2) Systems Biology of Gene Regulatory Elements (8) Transgenics (2) 34 Results: Active Filter: Altmueller, Janine Dr.med.Fischer, Cornelius Dr.Rajewsky, Nikolaus Prof. Dr.Wyler, Emanuel Dr.GenomicsRNA Biology and Posttranscriptional Regulation20052016 Sort: Result score Newest to oldest Oldest to newest 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 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 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 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 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 January 05, 2005 / BMC Pulm Med Phenotypic and genetic heterogeneity in a genome-wide linkage study of asthma families J. Altmüller C. Seidel Y.A. Lee S. Loesgen D. Bulle F. Friedrichs H. Jellouschek J. Kelber A. Keller A. Schuster M. Silbermann W. Wahlen P. Wolff F. Rueschendorf G. Schlenvoigt P. Nuernberg M. Wjst January 01, 2005 / Allergy A genome-wide screen on the genetics of atopy in a multiethnic European population reveals a major atopy locus on chromosome 3q21.3 T. Kurz J. Altmueller K. Strauch F. Rueschendorf A. Heinzmann M.F. Moffatt W.O.C.M. Cookson F. Inacio P. Nuernberg H.H. Stassen K.A. Deichmann February 01, 2016 / Nat Methods Detecting actively translated open reading frames in ribosome profiling data L. Calviello N. Mukherjee E. Wyler H. Zauber A. Hirsekorn M. Selbach M. Landthaler B. Obermayer U. Ohler July 07, 2016 / Mol Cell The Lupus autoantigen La prevents Mis-channeling of tRNA fragments into the human microRNA pathway D. Hasler G. Lehmann Y. Murakawa F. Klironomos L. Jakob F.A. Grässer N. Rajewsky M. Landthaler G. Meister October 07, 2016 / J Proteome Res Efficient application of de novo RNA assemblers for proteomics informed by transcriptomics T. Luge C. Fischer S. Sauer Pagination Current page 1 Page 2 Page 3 Page 4 Next page Next › Last page Last »
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
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
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
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
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
January 05, 2005 / BMC Pulm Med Phenotypic and genetic heterogeneity in a genome-wide linkage study of asthma families J. Altmüller C. Seidel Y.A. Lee S. Loesgen D. Bulle F. Friedrichs H. Jellouschek J. Kelber A. Keller A. Schuster M. Silbermann W. Wahlen P. Wolff F. Rueschendorf G. Schlenvoigt P. Nuernberg M. Wjst
January 01, 2005 / Allergy A genome-wide screen on the genetics of atopy in a multiethnic European population reveals a major atopy locus on chromosome 3q21.3 T. Kurz J. Altmueller K. Strauch F. Rueschendorf A. Heinzmann M.F. Moffatt W.O.C.M. Cookson F. Inacio P. Nuernberg H.H. Stassen K.A. Deichmann
February 01, 2016 / Nat Methods Detecting actively translated open reading frames in ribosome profiling data L. Calviello N. Mukherjee E. Wyler H. Zauber A. Hirsekorn M. Selbach M. Landthaler B. Obermayer U. Ohler
July 07, 2016 / Mol Cell The Lupus autoantigen La prevents Mis-channeling of tRNA fragments into the human microRNA pathway D. Hasler G. Lehmann Y. Murakawa F. Klironomos L. Jakob F.A. Grässer N. Rajewsky M. Landthaler G. Meister
October 07, 2016 / J Proteome Res Efficient application of de novo RNA assemblers for proteomics informed by transcriptomics T. Luge C. Fischer S. Sauer