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. (1) Annibale, Paolo Dr. (1) Bader, Michael Prof. Dr. (1) Bähring, Sylvia Dr. (1) Barke, Niclas (1) Bartolomaeus, Theda (1) Beule, Dieter Dr. (2) Birchmeier, Walter Prof. Dr. (1) Birchmeier-Kohler, Carmen Prof. Dr. (1) Blachut, Susanne (1) Blume, Alexander Dr. (1) Borodina, Tatiana Dr. (4) Braeuning, Caroline (3) Conrad, Thomas Dr. (5) de la Rosa, Kathrin Dr. (1) Deter, Aylina (1) Diecke, Sebastian Dr. (19) Escobar Fernandez, Helena Dr. (1) Faxel, Miriam (1) Fischer, Cornelius Dr. (7) Forslund, Sofia Dr. (1) Frahm-Barske, Silke Dr. (3) Franke, Vedran Dr. (1) Freimuth, Jonas (1) Genehr, Carolin (1) Graf, Robin Dr. (4) Harabula, Izabela-Cezara (1) Heuser, Arnd Dr. (1) Hinze, Christian Dr. med. Dipl.-Math. (1) Hübner, Norbert Prof. Dr. (2) Hummel, Oliver (1) Izsvak, Zsuzsanna Dr. (1) Jedamzick, Johanna Verena (1) Kirchner, Marieluise Dr. (1) Klußmann, Enno PD Dr. (2) Krüger, Norman (1) Kühn, Ralf Dr. (22) Lahmann, Ines Dr. (1) Landthaler, Markus Prof. Dr. (3) Langanki, Reika (1) Lebedin, Mikhail (1) Leutz, Achim Prof. Dr. (1) Lindberg, Eric Lars-Helge (1) Lisowski, Pawel Dr. (2) Liu, Tiannan (1) Maatz, Henrike Dr. (1) Marko, Lajos Dr. (1) Mertins, Philipp Dr. (1) Müller, Dominik Prof. Dr. (1) Müller, Marion (1) Napieczynska, Hanna Dr. (1) Obermayer-Wasserscheid, Benedikt Dr. (3) Ohler, Uwe Prof. Dr. (1) Patone, Giannino Dr. (1) Popova, Elena Dr. (1) Preibisch, Stephan Dr. (1) Prigione, Alessandro Prof. Dr. (3) Qadri, Fatimunnisa Dr. (1) Quedenau, Claudia (3) Rajewsky, Klaus Prof. Dr. (7) Rajewsky, Nikolaus Prof. Dr. (2) Roßius, Jana (1) Ruiz Orera, Jorge Dr. (1) Sholokh, Anastasiia (1) Sigal, Michael Dr. (1) Spuler, Simone Prof. (2) Sunaga-Franze, Daniele Yumi Dr. (3) Taube, Martin (1) Teixeira Alves, Luiz Gustavo Dr. (1) Telugu, Narasimha Swamy Dr. (5) Trombke, Janine (1) Uyar, Bora Dr. (1) von Kries, Jens Peter Dr. (1) Wanker, Erich Prof. Dr. (1) Wendlinger, Sarah (1) Wolf, Jana Prof. Dr. (1) Wurmus, Ricardo (1) Zimmermann, Karin Dr. (1) Zühlke, Kerstin Dr. (1) Zywitza, Vera Dr. (3) (-) Altmueller, Janine Dr.med. (95) (-) Chu, Van Trung Dr. (7) (-) Lupianez Garcia, Dario Jesus Dr. (2) (-) Pempe, Jenniffer (1) (-) Wyler, Emanuel Dr. (3) 2002 (1) 2005 (2) 2014 (7) 2015 (26) (-) 2016 (31) 2017 (31) 2018 (40) (-) 2019 (35) 2020 (25) 2021 (47) (-) 2022 (38) 2023 (21) 2024 (3) Angiogenesis & Metabolism Laboratory (10) Bioinformatics and Omics Data Science (3) Biomedical Image Analysis (1) Cellular Neurosciences (5) Computational methodologies and omic analytics (1) Computational Regulatory Genomics (4) Epigenetic Regulation and Chromatin Architecture (1) Experimental Ultrahigh-Field MR (4) Genetics and Genomics of Cardiovascular Diseases (1) Genetics of Metabolic and Reproductive Disorders (2) (-) Genome Engineering & Disease Models (8) (-) Genomics (95) Immune Mechanisms and Human Antibodies (1) Immune Regulation and Cancer (12) Integrative Vascular Biology (2) Magnetic Resonance (4) Microenvironmental Regulation in Autoimmunity and Cancer (1) (-) Pluripotent Stem Cells (1) Proteome Dynamics (2) Proteomics (3) Psychoneuroimmunology (1) Quantitative Developmental Biology (1) RNA Biology and Posttranscriptional Regulation (17) Systems Biology of Gene Regulatory Elements (5) Transgenics (8) Translational Bioinformatics (8) 104 Results: Active Filter: Altmueller, Janine Dr.med.Chu, Van Trung Dr.Lupianez Garcia, Dario Jesus Dr.Pempe, JennifferWyler, Emanuel Dr.Genome Engineering & Disease ModelsGenomicsPluripotent Stem Cells201620192022 Sort: Result score Newest to oldest Oldest to newest February 01, 2022 / Am J Med Genet A Genomic basis of syndromic short stature in an Algerian patient cohort S. Moosa F. Chentli J. Altmüller N. Bögershausen P. Nürnberg G. Yigit Y. Li B. Wollnik January 01, 2022 / Am J Med Genet A A novel homozygous synonymous variant further expands the phenotypic spectrum of POLR3A-related pathologies D. Lessel K. Rading S.E. Campbell H. Thiele J. Altmüller L.B. Gordon C. Kubisch May 16, 2022 / EMBO J Human UPF3A and UPF3B enable fault-tolerant activation of nonsense-mediated mRNA decay D. Wallmeroth J.W. Lackmann S. Kueckelmann J. Altmüller C. Dieterich V. Boehm N.H. Gehring February 01, 2022 / Eur J Hum Genet Familial cleft tongue caused by a unique translation initiation codon variant in TP63 J. Schmidt G. Schreiber J. Altmüller H. Thiele P. Nürnberg Y. Li S. Kaulfuß R. Funke B. Wilken G. Yigit B. Wollnik April 01, 2022 / J Am Soc Nephrol Claudin-10a deficiency shifts proximal tubular Cl(-) permeability to cation selectivity via claudin-2 redistribution T. Breiderhoff N. Himmerkus L. Meoli A. Fromm S. Sewerin N. Kriuchkova O. Nagel Y. Ladilov S. Krug C. Quintanova M. Stumpp D. Garbe-Schönberg U. Westernströer C. Merkel M. Brinkhus J. Altmüller M. Schweiger D. Mueller K. Mutig M. Morawski J. Halbritter S. Milatz M. Bleich D. Günzel March 01, 2022 / Hum Mutat Genomic variants reducing expression of two endocytic receptors in 46,XY differences of sex development H.L. Marko N.C. Hornig R.C. Betz P.M. Holterhus J. Altmüller H. Thiele M. Fabiano H.U. Schweikert D. Braun U. Schweizer February 10, 2022 / J Proteomics MAGED2 controls vasopressin-induced aquaporin-2 expression in collecting duct cells B. Reusch M.P. Bartram C. Dafinger N. Palacio-Escat A. Wenzel R.A. Fenton J. Saez-Rodriguez B. Schermer T. Benzing J. Altmüller B.B. Beck M.M. Rinschen April 01, 2022 / Am J Med Genet A A novel missense variant of SCN4A co-segregates with congenital essential tremor in a consanguineous Kurdish family M. Asif I.D. Mocanu U. Abdullah W. Höhne J. Altmüller E.U.H. Makhdoom H. Thiele S.M. Baig P. Nürnberg L. Graul-Neumann M.S. Hussain May 20, 2022 / J Med Genet Loss-of-function variants in DNM1 cause a specific form of developmental and epileptic encephalopathy only in biallelic state G. Yigit R. Sheffer M. Daana Y. Li E. Kaygusuz H. Mor-Shakad J. Altmüller P. Nürnberg L. Douiev S. Kaulfuss P. Burfeind B. Wollnik K. Brockmann January 01, 2022 / Haematologica Micro-RNA networks in T-cell prolymphocytic leukemia reflect T-cell activation and shape DNA damage response and survival pathways T. Braun M. Glass L. Wahnschaffe M. Otte P. Mayer M. Franitza J. Altmüller M. Hallek S. Hüttelmaier A. Schrader M. Herling Pagination Current page 1 Page 2 Page 3 Page 4 … Next page Next › Last page Last »
February 01, 2022 / Am J Med Genet A Genomic basis of syndromic short stature in an Algerian patient cohort S. Moosa F. Chentli J. Altmüller N. Bögershausen P. Nürnberg G. Yigit Y. Li B. Wollnik
January 01, 2022 / Am J Med Genet A A novel homozygous synonymous variant further expands the phenotypic spectrum of POLR3A-related pathologies D. Lessel K. Rading S.E. Campbell H. Thiele J. Altmüller L.B. Gordon C. Kubisch
May 16, 2022 / EMBO J Human UPF3A and UPF3B enable fault-tolerant activation of nonsense-mediated mRNA decay D. Wallmeroth J.W. Lackmann S. Kueckelmann J. Altmüller C. Dieterich V. Boehm N.H. Gehring
February 01, 2022 / Eur J Hum Genet Familial cleft tongue caused by a unique translation initiation codon variant in TP63 J. Schmidt G. Schreiber J. Altmüller H. Thiele P. Nürnberg Y. Li S. Kaulfuß R. Funke B. Wilken G. Yigit B. Wollnik
April 01, 2022 / J Am Soc Nephrol Claudin-10a deficiency shifts proximal tubular Cl(-) permeability to cation selectivity via claudin-2 redistribution T. Breiderhoff N. Himmerkus L. Meoli A. Fromm S. Sewerin N. Kriuchkova O. Nagel Y. Ladilov S. Krug C. Quintanova M. Stumpp D. Garbe-Schönberg U. Westernströer C. Merkel M. Brinkhus J. Altmüller M. Schweiger D. Mueller K. Mutig M. Morawski J. Halbritter S. Milatz M. Bleich D. Günzel
March 01, 2022 / Hum Mutat Genomic variants reducing expression of two endocytic receptors in 46,XY differences of sex development H.L. Marko N.C. Hornig R.C. Betz P.M. Holterhus J. Altmüller H. Thiele M. Fabiano H.U. Schweikert D. Braun U. Schweizer
February 10, 2022 / J Proteomics MAGED2 controls vasopressin-induced aquaporin-2 expression in collecting duct cells B. Reusch M.P. Bartram C. Dafinger N. Palacio-Escat A. Wenzel R.A. Fenton J. Saez-Rodriguez B. Schermer T. Benzing J. Altmüller B.B. Beck M.M. Rinschen
April 01, 2022 / Am J Med Genet A A novel missense variant of SCN4A co-segregates with congenital essential tremor in a consanguineous Kurdish family M. Asif I.D. Mocanu U. Abdullah W. Höhne J. Altmüller E.U.H. Makhdoom H. Thiele S.M. Baig P. Nürnberg L. Graul-Neumann M.S. Hussain
May 20, 2022 / J Med Genet Loss-of-function variants in DNM1 cause a specific form of developmental and epileptic encephalopathy only in biallelic state G. Yigit R. Sheffer M. Daana Y. Li E. Kaygusuz H. Mor-Shakad J. Altmüller P. Nürnberg L. Douiev S. Kaulfuss P. Burfeind B. Wollnik K. Brockmann
January 01, 2022 / Haematologica Micro-RNA networks in T-cell prolymphocytic leukemia reflect T-cell activation and shape DNA damage response and survival pathways T. Braun M. Glass L. Wahnschaffe M. Otte P. Mayer M. Franitza J. Altmüller M. Hallek S. Hüttelmaier A. Schrader M. Herling