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. (5) Blume, Alexander Dr. (1) Blüthgen, Nils (1) Borodina, Tatiana Dr. (4) Braeuning, Caroline (2) Chekulaeva, Marina Dr. (1) Chen, Wei Prof. Dr. (2) Conrad, Thomas Dr. (4) de la Rosa, Kathrin Prof. Dr. (1) Del Giudice, Simone (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) 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) Klußmann, Enno PD Dr. (1) Kocks, Christine Dr. (1) Kühn, Ralf Dr. (18) Landthaler, Markus Prof. Dr. (25) Langanki, Reika (1) Lebedin, Mikhail (1) Leutz, Achim Prof. Dr. (1) Liu, Tiannan (1) Lupianez Garcia, Dario Jesus Dr. (2) Maatz, Henrike Dr. (1) Marko, Lajos Dr. (1) Mastrobuoni, Guido Dr. (2) Minia, Igor Dr. (1) Müller, Dominik Prof. Dr. (1) Napieczynska, Hanna Dr. (1) Obermayer-Wasserscheid, Benedikt Dr. (9) 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) 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) Wyler, Emanuel Dr. (15) Zauber, Henrik Dr. (1) Zühlke, Kerstin Dr. (1) (-) Altmueller, Janine Dr.med. (81) (-) Chu, Van Trung Dr. (3) (-) Harabula, Izabela-Cezara (2) (-) Zimmermann, Karin Dr. (1) 2002 (1) 2005 (2) 2013 (10) (-) 2014 (16) 2015 (26) (-) 2016 (31) 2017 (31) 2018 (39) 2019 (34) 2020 (25) 2021 (47) (-) 2022 (38) 2023 (20) 2024 (3) Bioinformatics and Omics Data Science (1) Cellular Neurosciences (3) 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) Immune Mechanisms and Human Antibodies (1) Immune Regulation and Cancer (5) Magnetic Resonance (6) Microenvironmental Regulation in Autoimmunity and Cancer (1) Proteomics (1) (-) RNA Biology and Posttranscriptional Regulation (2) Systems Biology of Gene Regulatory Elements (1) Transgenics (3) Translational Bioinformatics (1) 85 Results: Active Filter: Altmueller, Janine Dr.med.Chu, Van Trung Dr.Harabula, Izabela-CezaraZimmermann, Karin Dr.Genome Engineering & Disease ModelsGenomicsRNA Biology and Posttranscriptional Regulation201420162022 Sort: Result score Newest to oldest Oldest to newest 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 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 March 01, 2016 / Am J Med Genet A A syndrome of microcephaly, short stature, polysyndactyly, and dental anomalies caused by a homozygous KATNB1 mutation G. Yigit D. Wieczorek N. Bögershausen F. Beleggia C. Möller-Hartmann J. Altmüller H. Thiele P. Nürnberg B. Wollnik February 01, 2014 / Biol Chem Enrichment of target sequences for next-generation sequencing applications in research and diagnostics J. Altmüller B.S. Budde P. Nürnberg January 02, 2014 / Am J Hum Genet Mutations in POGLUT1, encoding protein o-glucosyltransferase 1, cause autosomal-dominant Dowling-Degos disease F.B. Basmanav A.M. Oprisoreanu S.M. Pasternack H. Thiele G. Fritz J. Wenzel L. Größer M. Wehner S. Wolf C. Fagerberg A. Bygum J. Altmüller A. Rütten L. Parmentier L. El Shabrawi-Caelen C. Hafner P. Nürnberg R. Kruse S. Schoch S. Hanneken R.C. Betz October 01, 2014 / Hum Mutat Mutation of POC1B in a severe syndromic retinal ciliopathy B.B. Beck J.B. Phillips M.P. Bartram J. Wegner M. Thoenes A. Pannes J. Sampson R. Heller H. Göbel F. Koerber A. Neugebauer A. Hedergott G. Nürnberg P. Nürnberg H. Thiele J. Altmüller M.R. Toliat S. Staubach K.M. Boycott E.M. Valente A.R. Janecke T. Eisenberger C. Bergmann L. Tebbe Y. Wang Y. Wu A.M. Fry M. Westerfield U. Wolfrum H.J. Bolz July 01, 2014 / Neurobiol Dis Exonic microdeletions of the gephyrin gene impair GABAergic synaptic inhibition in patients with idiopathic generalized epilepsy B. Dejanovic D. Lal C.B. Catarino S. Arjune A.A. Belaidi H. Trucks C. Vollmar R. Surges W.S. Kunz S. Motameny J. Altmüller A. Köhler B.A. Neubauer P. Nürnberg S. Noachtar G. Schwarz T. Sander December 04, 2014 / Am J Hum Genet Homozygous and compound-heterozygous mutations in TGDS cause Catel-Manzke syndrome N. Ehmke A. Caliebe R. Koenig S.G. Kant Z. Stark V. Cormier-Daire D. Wieczorek G. Gillessen-Kaesbach K. Hoff A. Kawalia H. Thiele J. Altmüller B. Fischer-Zirnsak A. Knaus N. Zhu V. Heinrich C. Huber I. Harabula M. Spielmann D. Horn U. Kornak J. Hecht P.M. Krawitz P. Nürnberg R. Siebert H. Manzke S. Mundlos March 27, 2014 / Nat Commun Frequent mutations in chromatin-remodelling genes in pulmonary carcinoids L. Fernandez-Cuesta M. Peifer X. Lu R. Sun L. Ozretić D. Seidal T. Zander F. Leenders J. George C. Müller I. Dahmen B. Pinther G. Bosco K. Konrad J. Altmüller P. Nürnberg V. Achter U. Lang P.M. Schneider M. Bogus A. Soltermann O.T. Brustugun Å. Helland S. Solberg M. Lund-Iversen S. Ansén E. Stoelben G.M. Wright P. Russell Z. Wainer B. Solomon J.K. Field R. Hyde M.P. Davies L.C. Heukamp I. Petersen S. Perner C. Lovly F. Cappuzzo W.D. Travis J. Wolf M. Vingron E. Brambilla S.A. Haas R. Buettner R.K. Thomas Pagination First page « First Previous page ‹ Previous … Page 3 Current page 4 Page 5 Page 6 … Next page Next › Last page Last »
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
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
March 01, 2016 / Am J Med Genet A A syndrome of microcephaly, short stature, polysyndactyly, and dental anomalies caused by a homozygous KATNB1 mutation G. Yigit D. Wieczorek N. Bögershausen F. Beleggia C. Möller-Hartmann J. Altmüller H. Thiele P. Nürnberg B. Wollnik
February 01, 2014 / Biol Chem Enrichment of target sequences for next-generation sequencing applications in research and diagnostics J. Altmüller B.S. Budde P. Nürnberg
January 02, 2014 / Am J Hum Genet Mutations in POGLUT1, encoding protein o-glucosyltransferase 1, cause autosomal-dominant Dowling-Degos disease F.B. Basmanav A.M. Oprisoreanu S.M. Pasternack H. Thiele G. Fritz J. Wenzel L. Größer M. Wehner S. Wolf C. Fagerberg A. Bygum J. Altmüller A. Rütten L. Parmentier L. El Shabrawi-Caelen C. Hafner P. Nürnberg R. Kruse S. Schoch S. Hanneken R.C. Betz
October 01, 2014 / Hum Mutat Mutation of POC1B in a severe syndromic retinal ciliopathy B.B. Beck J.B. Phillips M.P. Bartram J. Wegner M. Thoenes A. Pannes J. Sampson R. Heller H. Göbel F. Koerber A. Neugebauer A. Hedergott G. Nürnberg P. Nürnberg H. Thiele J. Altmüller M.R. Toliat S. Staubach K.M. Boycott E.M. Valente A.R. Janecke T. Eisenberger C. Bergmann L. Tebbe Y. Wang Y. Wu A.M. Fry M. Westerfield U. Wolfrum H.J. Bolz
July 01, 2014 / Neurobiol Dis Exonic microdeletions of the gephyrin gene impair GABAergic synaptic inhibition in patients with idiopathic generalized epilepsy B. Dejanovic D. Lal C.B. Catarino S. Arjune A.A. Belaidi H. Trucks C. Vollmar R. Surges W.S. Kunz S. Motameny J. Altmüller A. Köhler B.A. Neubauer P. Nürnberg S. Noachtar G. Schwarz T. Sander
December 04, 2014 / Am J Hum Genet Homozygous and compound-heterozygous mutations in TGDS cause Catel-Manzke syndrome N. Ehmke A. Caliebe R. Koenig S.G. Kant Z. Stark V. Cormier-Daire D. Wieczorek G. Gillessen-Kaesbach K. Hoff A. Kawalia H. Thiele J. Altmüller B. Fischer-Zirnsak A. Knaus N. Zhu V. Heinrich C. Huber I. Harabula M. Spielmann D. Horn U. Kornak J. Hecht P.M. Krawitz P. Nürnberg R. Siebert H. Manzke S. Mundlos
March 27, 2014 / Nat Commun Frequent mutations in chromatin-remodelling genes in pulmonary carcinoids L. Fernandez-Cuesta M. Peifer X. Lu R. Sun L. Ozretić D. Seidal T. Zander F. Leenders J. George C. Müller I. Dahmen B. Pinther G. Bosco K. Konrad J. Altmüller P. Nürnberg V. Achter U. Lang P.M. Schneider M. Bogus A. Soltermann O.T. Brustugun Å. Helland S. Solberg M. Lund-Iversen S. Ansén E. Stoelben G.M. Wright P. Russell Z. Wainer B. Solomon J.K. Field R. Hyde M.P. Davies L.C. Heukamp I. Petersen S. Perner C. Lovly F. Cappuzzo W.D. Travis J. Wolf M. Vingron E. Brambilla S.A. Haas R. Buettner R.K. Thomas