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) Bader, Michael Prof. Dr. (1) Bähring, Sylvia Dr. (1) Barke, Niclas (1) Bartolomaeus, Theda (1) Beule, Dieter Dr. (4) Blume, Alexander Dr. (1) Blüthgen, Nils (1) Borodina, Tatiana Dr. (4) Braeuning, Caroline (1) Brüning, Ulrike Dr. (1) Chekulaeva, Marina Dr. (1) Chen, Wei Prof. Dr. (2) Conrad, Thomas Dr. (3) de la Rosa, Kathrin Prof. Dr. (1) Del Giudice, Simone (1) Deter, Aylina (1) Diecke, Sebastian Dr. (2) Escobar Fernandez, Helena Dr. (1) Essex, Morgan (1) Faxel, Miriam (1) Fischer, Cornelius Dr. (4) Forslund, Sofia Dr. (2) Franke, Vedran Dr. (1) Freimuth, Jonas (1) Fritsche, Raphaela Dr. (1) Gotthardt, Michael Prof. Dr. (1) Graf, Robin Dr. (3) Haghverdi, Laleh Dr. (1) Heinemann, Udo Prof. Dr. (1) Herzog, Margareta (1) Heuser, Arnd Dr. (1) Hinze, Christian Dr. med. Dipl.-Math. (2) Hirsekorn, Antje (1) Hübner, Norbert Prof. Dr. (2) Jedamzick, Johanna Verena (1) Kempa, Stefan Dr. (2) Kirchner, Marieluise Dr. (1) Kirwan, Jennifer Dr. (1) Klußmann, Enno PD Dr. (1) Kocks, Christine Dr. (1) Kühn, Ralf Dr. (18) Landthaler, Markus Prof. Dr. (26) Langanki, Reika (1) Lebedin, Mikhail (1) Leutz, Achim Prof. Dr. (1) Liu, Tiannan (1) Löber, Ulrike Dr. (1) Lupianez Garcia, Dario Jesus Dr. (2) Maatz, Henrike Dr. (1) Marko, Lajos Dr. (2) Mastrobuoni, Guido Dr. (2) Minia, Igor Dr. (1) Müller, Dominik Prof. Dr. (1) Napieczynska, Hanna Dr. (1) Obermayer-Wasserscheid, Benedikt Dr. (8) Ohler, Uwe Prof. Dr. (3) Popova, Elena Dr. (1) Qadri, Fatimunnisa Dr. (1) Quedenau, Claudia (3) Radke, Michael Dr. (1) Rajewsky, Klaus Prof. Dr. (3) Rajewsky, Nikolaus Prof. Dr. (5) Rybak-Wolf, Agnieszka Dr. (1) Sai, Somesh (1) Sander, Maike Prof. Dr. (1) Schütz, Anja Dr. (1) Selbach, Matthias Prof. Dr. (6) Sholokh, Anastasiia (1) Spuler, Simone Prof. (1) Sunaga-Franze, Daniele Yumi Dr. (2) Taube, Martin (1) Teixeira Alves, Luiz Gustavo Dr. (4) Uyar, Bora Dr. (1) Villamil, Gabriel (1) Wendlinger, Sarah (1) Wurmus, Ricardo (1) Zauber, Henrik Dr. (1) Zühlke, Kerstin Dr. (1) (-) Altmueller, Janine Dr.med. (81) (-) Chu, Van Trung Dr. (3) (-) Harabula, Izabela-Cezara (2) (-) Wyler, Emanuel Dr. (16) (-) Zimmermann, Karin Dr. (1) 2002 (1) 2005 (2) 2012 (2) 2013 (21) (-) 2014 (16) 2015 (30) (-) 2016 (32) 2017 (37) 2018 (39) 2019 (37) 2020 (29) 2021 (63) (-) 2022 (51) 2023 (30) 2024 (14) Bioinformatics and Omics Data Science (1) Biomedical Image Analysis (1) Cellular Neurosciences (3) Computational methodologies and omic analytics (1) Computational Regulatory Genomics (1) Developmental Neurobiology (1) Experimental Ultrahigh-Field MR (6) Genetics of Congenital Heart Disease (1) Genetics of Metabolic and Reproductive Disorders (1) (-) Genome Engineering & Disease Models (3) (-) Genomics (82) Host-microbiome factors in cardiovascular disease (1) Immune Mechanisms and Human Antibodies (1) Immune Regulation and Cancer (5) Magnetic Resonance (6) Microenvironmental Regulation in Autoimmunity and Cancer (1) Proteome Dynamics (2) (-) RNA Biology and Posttranscriptional Regulation (16) Systems Biology of Gene Regulatory Elements (2) Transgenics (3) Translational Bioinformatics (8) 99 Results: Active Filter: Altmueller, Janine Dr.med.Chu, Van Trung Dr.Harabula, Izabela-CezaraWyler, Emanuel Dr.Zimmermann, Karin Dr.Genome Engineering & Disease ModelsGenomicsRNA Biology and Posttranscriptional Regulation201420162022 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 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 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 February 07, 2022 / Curr Biol Inflammation and convergent placenta gene co-option contributed to a novel reproductive tissue L. Hilgers O. Roth A.W. Nolte A. Schüller T. Spanke J.M. Flury I.V. Utama J. Altmüller D. Wowor B. Misof F. Herder A. Böhne J. Schwarzer February 03, 2022 / Cell Complement activation induces excessive T cell cytotoxicity in severe COVID-19 P. Georg R. Astaburuaga-García L. Bonaguro S. Brumhard L. Michalick L.J. Lippert T. Kostevc C. Gäbel M. Schneider M. Streitz V. Demichev I. Gemünd M. Barone P. Tober-Lau E.T. Helbig D. Hillus L. Petrov J. Stein H.P. Dey D. Paclik C. Iwert M. Mülleder S.K. Aulakh S. Djudjaj R.D. Bülow H.E. Mei A.R. Schulz A. Thiel S. Hippenstiel A.E. Saliba R. Eils I. Lehmann M.A. Mall S. Stricker J. Röhmel V.M. Corman D. Beule E. Wyler M. Landthaler B. Obermayer S. von Stillfried P. Boor M. Demir H. Wesselmann N. Suttorp A. Uhrig H. Müller-Redetzky J. Nattermann W.M. Kuebler C. Meisel M. Ralser J.L. Schultze A.C. Aschenbrenner C. Thibeault F. Kurth L.E. Sander N. Blüthgen B. Sawitzki March, 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 January 04, 2022 / PLoS Pathog Engineering, decoding and systems-level characterization of chimpanzee cytomegalovirus Q.V. Phan B. Bogdanow E. Wyler M. Landthaler F. Liu C. Hagemeier L. 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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
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
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
February 07, 2022 / Curr Biol Inflammation and convergent placenta gene co-option contributed to a novel reproductive tissue L. Hilgers O. Roth A.W. Nolte A. Schüller T. Spanke J.M. Flury I.V. Utama J. Altmüller D. Wowor B. Misof F. Herder A. Böhne J. Schwarzer
February 03, 2022 / Cell Complement activation induces excessive T cell cytotoxicity in severe COVID-19 P. Georg R. Astaburuaga-García L. Bonaguro S. Brumhard L. Michalick L.J. Lippert T. Kostevc C. Gäbel M. Schneider M. Streitz V. Demichev I. Gemünd M. Barone P. Tober-Lau E.T. Helbig D. Hillus L. Petrov J. Stein H.P. Dey D. Paclik C. Iwert M. Mülleder S.K. Aulakh S. Djudjaj R.D. Bülow H.E. Mei A.R. Schulz A. Thiel S. Hippenstiel A.E. Saliba R. Eils I. Lehmann M.A. Mall S. Stricker J. Röhmel V.M. Corman D. Beule E. Wyler M. Landthaler B. Obermayer S. von Stillfried P. Boor M. Demir H. Wesselmann N. Suttorp A. Uhrig H. Müller-Redetzky J. Nattermann W.M. Kuebler C. Meisel M. Ralser J.L. Schultze A.C. Aschenbrenner C. Thibeault F. Kurth L.E. Sander N. Blüthgen B. Sawitzki
March, 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
January 04, 2022 / PLoS Pathog Engineering, decoding and systems-level characterization of chimpanzee cytomegalovirus Q.V. Phan B. Bogdanow E. Wyler M. Landthaler F. Liu C. Hagemeier L. Wiebusch