Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Birchmeier-Kohler, Carmen Prof. Dr. (1) Braeuning, Caroline (1) Cano Rincon, Elena Dr. (3) Collins, Russell Thomas Dr. (2) Conrad, Thomas Dr. (2) Diecke, Sebastian Dr. (1) Edes, Inan Dr. (1) Fischer, Cornelius Dr. (5) Gerhardt, Holger Prof. Dr. (14) Gerlach, Kerstin (1) Giese, Wolfgang Dr. (1) Gouti, Mina Dr. (1) Höpken, Uta Elisabeth PD Dr. (1) Kammertöns, Thomas Dr. (1) Kettenmann, Helmut Prof. Dr. (23) Klaus-Bergmann, Alexandra Dr. (1) Ku, Min-Chi Dr. (2) Kunz, Severine Dr. (1) Landthaler, Markus Prof. Dr. (1) Meier, Katja (1) Mertins, Philipp Dr. (1) Motta, Edyta Maria (1) Niendorf, Thoralf Prof. Dr. (1) Nolte, Christiane Dr. (1) Plumbom, Izabela (1) Quedenau, Claudia (1) Rajewsky, Klaus Prof. Dr. (1) Rehm, Armin Dr. (1) Sai, Somesh (1) Sohn, Madlen (1) Sunaga-Franze, Daniele Yumi Dr. (2) Uckert, Wolfgang Prof. Dr. (1) Vitcetz, Sarah Nathalie (1) Waiczies, Sonia PD Dr. (2) Wolf, Susanne Dr. (8) (-) Altmueller, Janine Dr.med. (53) (-) Harabula, Izabela-Cezara (1) (-) Lupianez Garcia, Dario Jesus Dr. (1) (-) Potente, Michael Prof. Dr. (5) (-) Semtner, Marcus Dr. (5) (-) Spuler, Simone Prof. (1) (-) Wyler, Emanuel Dr. (1) 1999 (1) 2002 (1) 2005 (5) 2007 (1) 2008 (4) 2009 (3) 2010 (2) 2011 (2) 2012 (2) 2013 (25) 2014 (17) 2015 (28) (-) 2016 (33) 2017 (38) 2018 (46) 2019 (36) (-) 2020 (32) 2021 (56) 2022 (42) 2023 (24) 2024 (7) (-) Angiogenesis & Metabolism Laboratory (5) Bioinformatics and Omics Data Science (2) Cardiac MRI (1) (-) Cellular Neurosciences (5) Computational Regulatory Genomics (2) Developmental Biology / Signal Transduction (2) Epigenetic Regulation and Chromatin Architecture (1) Experimental Ultrahigh-Field MR (6) Genetics and Genomics of Cardiovascular Diseases (1) Genetics of Metabolic and Reproductive Disorders (1) Genome Engineering & Disease Models (3) (-) Genomics (55) Immune Regulation and Cancer (7) (-) Integrative Vascular Biology (1) Magnetic Resonance (6) Mobile DNA (1) Molecular Physiology of Somatic Sensation (1) Myology (14) Pluripotent Stem Cells (3) Proteome Dynamics (1) Proteomics (1) Proteomics and Metabolomics (2) Psychoneuroimmunology (1) RNA Biology and Posttranscriptional Regulation (5) Stem Cell Modeling of Development and Disease (1) Transgenics (3) 65 Results: Active Filter: Altmueller, Janine Dr.med.Harabula, Izabela-CezaraLupianez Garcia, Dario Jesus Dr.Potente, Michael Prof. Dr.Semtner, Marcus Dr.Spuler, Simone Prof.Wyler, Emanuel Dr.Angiogenesis & Metabolism LaboratoryCellular NeurosciencesGenomicsIntegrative Vascular Biology20162020 Sort: Result score Newest to oldest Oldest to newest 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
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