Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Adami, Eleonora Dr. (1) Akalin, Altuna Dr. (2) Birchmeier, Walter Prof. Dr. (1) Birchmeier-Kohler, Carmen Prof. Dr. (2) Blachut, Susanne (1) Braeuning, Caroline (1) Chu, Van Trung Dr. (9) Conrad, Thomas Dr. (1) Diecke, Sebastian Dr. (1) Fischer, Cornelius Dr. (4) Gerhardt, Holger Prof. Dr. (1) Ghanbari, Mahsa Dr. (1) Graf, Robin Dr. (5) Hirsekorn, Antje (4) Hübner, Norbert Prof. Dr. (1) Hummel, Oliver (1) Janz, Martin Dr. (1) Kastelic, Nicolai (1) Kempa, Stefan Dr. (1) Kirchner, Marieluise Dr. (1) Kocks, Christine Dr. (1) Kühn, Ralf Dr. (14) Lahmann, Ines Dr. (2) Lindberg, Eric Lars-Helge (1) Lupianez Garcia, Dario Jesus Dr. (1) Maatz, Henrike Dr. (1) Mastrobuoni, Guido Dr. (1) Mertins, Philipp Dr. (1) Müller, Marion (1) Obermayer-Wasserscheid, Benedikt Dr. (2) Ohler, Uwe Prof. Dr. (14) Patone, Giannino Dr. (1) Potente, Michael Prof. Dr. (1) Preibisch, Stephan Dr. (1) Rajewsky, Klaus Prof. Dr. (21) Rajewsky, Nikolaus Prof. Dr. (2) Roßius, Jana (1) Sigal, Michael Dr. (1) Spuler, Simone Prof. (1) Sunaga-Franze, Daniele Yumi Dr. (1) Trombke, Janine (1) Vucicevic, Dubravka (1) Wolf, Jana Prof. Dr. (1) Wurmus, Ricardo (2) Wyler, Emanuel Dr. (2) Zauber, Henrik Dr. (1) (-) Altmueller, Janine Dr.med. (59) (-) Harabula, Izabela-Cezara (1) (-) Lacadie, Scott Allen Dr. (1) (-) Landthaler, Markus Prof. Dr. (4) (-) Pempe, Jenniffer (1) (-) Selbach, Matthias Prof. Dr. (3) 2002 (1) 2005 (2) 2013 (22) 2014 (17) 2015 (33) (-) 2016 (32) 2017 (35) 2018 (44) (-) 2019 (34) 2020 (25) 2021 (51) 2022 (39) 2023 (18) 2024 (5) Anchored Signalling (2) Bioinformatics and Omics Data Science (2) Bioinformatics of RNA Structure and Transcriptome Regulation (1) Biology of Malignant Lymphomas (1) Cellular Neurosciences (5) (-) Computational Regulatory Genomics (5) Developmental Biology / Signal Transduction (1) Experimental Ultrahigh-Field MR (4) Genetics and Genomics of Cardiovascular Diseases (2) Genetics of Metabolic and Reproductive Disorders (2) (-) Genome Engineering & Disease Models (1) (-) Genomics (59) (-) Immune Regulation and Cancer (2) Magnetic Resonance (4) Molecular Pathways in Cortical Development (1) Molecular Physiology of Somatic Sensation (1) Non-coding RNAs and Mechanisms of Cytoplasmic Gene Regulation (1) Pluripotent Stem Cells (1) Proteome Dynamics (14) Proteomics (2) Proteomics and Metabolomics (1) Proteomics and Molecular Mechanisms of Neurodegenerative Diseases (1) Psychoneuroimmunology (1) RNA Biology and Posttranscriptional Regulation (9) Structural Biology of Membrane-Associated Processes (3) Systems Biology of Gene Regulatory Elements (4) Transgenics (1) Translational Bioinformatics (1) 66 Results: Active Filter: Altmueller, Janine Dr.med.Harabula, Izabela-CezaraLacadie, Scott Allen Dr.Landthaler, Markus Prof. Dr.Pempe, JennifferSelbach, Matthias Prof. Dr.Computational Regulatory GenomicsGenome Engineering & Disease ModelsGenomicsImmune Regulation and Cancer20162019 Sort: Result score Newest to oldest Oldest to newest November 07, 2019 / Am J Hum Genet De novo mutations in FOXJ1 result in a motile ciliopathy with hydrocephalus and randomization of left/right body asymmetry J. Wallmeier D. Frank A. Shoemark T. Nöthe-Menchen S. Cindric H. Olbrich N.T. Loges I. Aprea G.W. Dougherty P. Pennekamp T. Kaiser H.M. Mitchison C. Hogg S.B. Carr M.A. Zariwala T. Ferkol M.W. Leigh S.D. Davis J. Atkinson S.K. Dutcher M.R. Knowles H. Thiele J. Altmüller H. Krenz M. Wöste A. Brentrup F. Ahrens C. Vogelberg D.J. Morris-Rosendahl H. Omran 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 Pagination First page « First Previous page ‹ Previous … Page 4 Page 5 Page 6 Current page 7
November 07, 2019 / Am J Hum Genet De novo mutations in FOXJ1 result in a motile ciliopathy with hydrocephalus and randomization of left/right body asymmetry J. Wallmeier D. Frank A. Shoemark T. Nöthe-Menchen S. Cindric H. Olbrich N.T. Loges I. Aprea G.W. Dougherty P. Pennekamp T. Kaiser H.M. Mitchison C. Hogg S.B. Carr M.A. Zariwala T. Ferkol M.W. Leigh S.D. Davis J. Atkinson S.K. Dutcher M.R. Knowles H. Thiele J. Altmüller H. Krenz M. Wöste A. Brentrup F. Ahrens C. Vogelberg D.J. Morris-Rosendahl H. Omran
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