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. (4) Gerhardt, Holger Prof. Dr. (14) Gerlach, Kerstin (1) Giese, Wolfgang Dr. (1) Gouti, Mina Dr. (1) Höpken, Uta Elisabeth PD Dr. (1) Kabuss, Loreen-Claudine (1) Kammertöns, Thomas Dr. (1) Kettenmann, Helmut Prof. Dr. (23) Klaus-Bergmann, Alexandra Dr. (1) Ku, Min-Chi Dr. (2) Kunz, Severine Dr. (1) Meier, Katja (1) Mertins, Philipp Dr. (1) Motta, Edyta (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) Sunaga-Franze, Daniele Yumi Dr. (3) Uckert, Wolfgang Prof. Dr. (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) 1999 (1) 2002 (1) 2005 (5) 2007 (1) 2008 (4) 2009 (3) 2010 (2) 2011 (2) 2012 (2) 2013 (14) 2014 (17) 2015 (27) (-) 2016 (33) 2017 (37) 2018 (46) 2019 (36) (-) 2020 (31) 2021 (55) 2022 (42) 2023 (24) 2024 (3) (-) 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 (54) 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 (4) Stem Cell Modeling of Development and Disease (1) Transgenics (3) 64 Results: Active Filter: Altmueller, Janine Dr.med.Harabula, Izabela-CezaraLupianez Garcia, Dario Jesus Dr.Potente, Michael Prof. Dr.Semtner, Marcus Dr.Spuler, Simone Prof.Angiogenesis & Metabolism LaboratoryCellular NeurosciencesGenomicsIntegrative Vascular Biology20162020 Sort: Result score Newest to oldest Oldest to newest 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 May 01, 2016 / Am J Med Genet A Novel IFT122 mutations in three Argentinian patients with cranioectodermal dysplasia: expanding the mutational spectrum S. Moosa M.G. Obregon J. Altmüller H. Thiele P. Nürnberg V. Fano B. Wollnik October 02, 2016 / Clin Cancer Res Heterogeneous mechanisms of primary and acquired resistance to third-generation EGFR inhibitors S. Ortiz-Cuaran M. Scheffler D. Plenker L. Dahmen A.H. Scheel L. Fernandez-Cuesta L. Meder C.M. Lovly T. Persigehl S. Merkelbach-Bruse M. Bos S. Michels R. Fischer K. Albus K. König H.U. Schildhaus Jana Fassunke M.A. Ihle H. Pasternack C. Heydt C. Becker J. Altmüller H. Ji C. Müller A. Florin J.M. Heuckmann P. Nuernberg S. Ansén L.C. Heukamp J. Berg W. Pao M. Peifer R. Buettner J. Wolf R.K. Thomas M.L. Sos 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 May 01, 2016 / Chem Senses Transcriptome analysis of murine olfactory sensory neurons during development using single cell RNA-Seq P. Scholz B. Kalbe F. Jansen J. Altmüller C. Becker J. Mohrhardt B. Schreiner G. Gisselmann H. Hatt S. Osterloh April 01, 2016 / Fam Cancer Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis I. Spier M. Kerick D. Drichel S. Horpaopan J. Altmüller A. Laner S. Holzapfel S. Peters R. Adam B. Zhao T. Becker R.P. Lifton E. Holinski-Feder S. Perner H. Thiele M.M. Nöthen P. Hoffmann B. Timmermann M.R. Schweiger S. Aretz February 01, 2016 / Hum Genet A novel homozygous splicing mutation of CASC5 causes primary microcephaly in a large Pakistani family S. Szczepanski M.S. Hussain I. Sur J. Altmüller H. Thiele U. Abdullah S.S. Waseem A. Moawia G. Nürnberg A.A. Noegel S.M. Baig P. Nürnberg 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 June 01, 2016 / PLoS Pathog The WOPR protein Ros1 is a master regulator of sporogenesis and late effector gene expression in the maize pathogen Ustilago maydis M. Tollot D. Assmann C. Becker J. Altmüller J.Y. Dutheil C.E. Wegner R. Kahmann August 01, 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 Pagination First page « First Previous page ‹ Previous … Page 2 Current page 3 Page 4 Page 5 … Next page Next › Last page Last »
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
May 01, 2016 / Am J Med Genet A Novel IFT122 mutations in three Argentinian patients with cranioectodermal dysplasia: expanding the mutational spectrum S. Moosa M.G. Obregon J. Altmüller H. Thiele P. Nürnberg V. Fano B. Wollnik
October 02, 2016 / Clin Cancer Res Heterogeneous mechanisms of primary and acquired resistance to third-generation EGFR inhibitors S. Ortiz-Cuaran M. Scheffler D. Plenker L. Dahmen A.H. Scheel L. Fernandez-Cuesta L. Meder C.M. Lovly T. Persigehl S. Merkelbach-Bruse M. Bos S. Michels R. Fischer K. Albus K. König H.U. Schildhaus Jana Fassunke M.A. Ihle H. Pasternack C. Heydt C. Becker J. Altmüller H. Ji C. Müller A. Florin J.M. Heuckmann P. Nuernberg S. Ansén L.C. Heukamp J. Berg W. Pao M. Peifer R. Buettner J. Wolf R.K. Thomas M.L. Sos
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
May 01, 2016 / Chem Senses Transcriptome analysis of murine olfactory sensory neurons during development using single cell RNA-Seq P. Scholz B. Kalbe F. Jansen J. Altmüller C. Becker J. Mohrhardt B. Schreiner G. Gisselmann H. Hatt S. Osterloh
April 01, 2016 / Fam Cancer Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis I. Spier M. Kerick D. Drichel S. Horpaopan J. Altmüller A. Laner S. Holzapfel S. Peters R. Adam B. Zhao T. Becker R.P. Lifton E. Holinski-Feder S. Perner H. Thiele M.M. Nöthen P. Hoffmann B. Timmermann M.R. Schweiger S. Aretz
February 01, 2016 / Hum Genet A novel homozygous splicing mutation of CASC5 causes primary microcephaly in a large Pakistani family S. Szczepanski M.S. Hussain I. Sur J. Altmüller H. Thiele U. Abdullah S.S. Waseem A. Moawia G. Nürnberg A.A. Noegel S.M. Baig P. Nürnberg
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
June 01, 2016 / PLoS Pathog The WOPR protein Ros1 is a master regulator of sporogenesis and late effector gene expression in the maize pathogen Ustilago maydis M. Tollot D. Assmann C. Becker J. Altmüller J.Y. Dutheil C.E. Wegner R. Kahmann
August 01, 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