Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Akalin, Altuna Dr. (1) Bader, Michael Prof. Dr. (1) Bähring, Sylvia Dr. (1) Barke, Niclas (1) Bartolomaeus, Theda (1) Beule, Dieter Dr. (2) Blume, Alexander Dr. (1) Borodina, Tatiana Dr. (4) Braeuning, Caroline (2) Conrad, Thomas Dr. (4) de la Rosa, Kathrin Dr. (1) Deter, Aylina (1) Diecke, Sebastian Dr. (2) Escobar Fernandez, Helena Dr. (1) Faxel, Miriam (1) Fischer, Cornelius Dr. (4) Forslund, Sofia Dr. (1) Franke, Vedran Dr. (1) Freimuth, Jonas (1) Graf, Robin Dr. (3) Harabula, Izabela-Cezara (1) Heuser, Arnd Dr. (1) Hübner, Norbert Prof. Dr. (1) Jedamzick, Johanna Verena (1) Klußmann, Enno PD Dr. (1) Kühn, Ralf Dr. (14) Landthaler, Markus Prof. Dr. (2) Langanki, Reika (1) Lebedin, Mikhail (1) Leutz, Achim Prof. Dr. (1) Liu, Tiannan (1) Marko, Lajos Dr. (1) Müller, Dominik Prof. Dr. (1) Napieczynska, Hanna Dr. (1) Obermayer-Wasserscheid, Benedikt Dr. (2) Popova, Elena Dr. (1) Qadri, Fatimunnisa Dr. (1) Quedenau, Claudia (3) Rajewsky, Klaus Prof. Dr. (3) Rajewsky, Nikolaus Prof. Dr. (1) Sholokh, Anastasiia (1) Spuler, Simone Prof. (1) Sunaga-Franze, Daniele Yumi Dr. (2) Taube, Martin (1) Teixeira Alves, Luiz Gustavo Dr. (1) Uyar, Bora Dr. (1) Wendlinger, Sarah (1) Wurmus, Ricardo (1) Zimmermann, Karin Dr. (1) Zühlke, Kerstin Dr. (1) (-) Altmueller, Janine Dr.med. (65) (-) Chu, Van Trung Dr. (3) (-) Lupianez Garcia, Dario Jesus Dr. (2) (-) Wyler, Emanuel Dr. (2) 2002 (1) 2005 (2) 2014 (2) 2015 (26) (-) 2016 (31) 2017 (31) 2018 (39) 2019 (34) 2020 (25) 2021 (47) (-) 2022 (38) 2023 (20) 2024 (2) Angiogenesis & Metabolism Laboratory (7) Bioinformatics and Omics Data Science (2) Biomedical Image Analysis (1) Cellular Neurosciences (2) Computational methodologies and omic analytics (1) Computational Regulatory Genomics (3) Epigenetic Regulation and Chromatin Architecture (1) Experimental Ultrahigh-Field MR (4) (-) Genome Engineering & Disease Models (4) (-) Genomics (65) Immune Mechanisms and Human Antibodies (1) Immune Regulation and Cancer (6) Integrative Vascular Biology (2) Magnetic Resonance (4) Microenvironmental Regulation in Autoimmunity and Cancer (1) Proteome Dynamics (2) Proteomics (1) Quantitative Developmental Biology (1) RNA Biology and Posttranscriptional Regulation (14) Systems Biology of Gene Regulatory Elements (2) Transgenics (4) Translational Bioinformatics (7) 69 Results: Active Filter: Altmueller, Janine Dr.med.Chu, Van Trung Dr.Lupianez Garcia, Dario Jesus Dr.Wyler, Emanuel Dr.Genome Engineering & Disease ModelsGenomics20162022 Sort: Result score Newest to oldest Oldest to newest April 01, 2016 / Clin Genet Mutations in SEC24D cause autosomal recessive osteogenesis imperfecta S. Moosa B.H.Y. Chung J.Y.L. Tung J. Altmüller H. Thiele P. Nürnberg C. Netzer G. Nishimura B. Wollnik 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 Pagination First page « First Previous page ‹ Previous … Page 2 Current page 3 Page 4 Page 5 … Next page Next › Last page Last »
April 01, 2016 / Clin Genet Mutations in SEC24D cause autosomal recessive osteogenesis imperfecta S. Moosa B.H.Y. Chung J.Y.L. Tung J. Altmüller H. Thiele P. Nürnberg C. Netzer G. Nishimura B. Wollnik
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