Scientific Publications Search Search Author Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Akalin, Altuna Dr. (1) Altmueller, Janine Dr.med. (62) Birchmeier, Walter Prof. Dr. (1) Birchmeier-Kohler, Carmen Prof. Dr. (21) Chekulaeva, Marina Dr. (1) Chen, Wei Prof. Dr. (1) Escobar Fernandez, Helena Dr. (1) Fischer, Cornelius Dr. (2) Franke, Vedran Dr. (1) Grosswendt, Stefanie Dr. (1) Hübner, Norbert Prof. Dr. (1) Izsvak, Zsuzsanna Dr. (1) Jüttner, Rene Dr. (3) Kocks, Christine Dr. (2) Lahmann, Ines Dr. (1) Lewin, Gary Prof. Dr. (1) Lupianez Garcia, Dario Jesus Dr. (1) Marg, Andreas Dr. (1) Müller, Thomas Dr. (6) Nazare, Marc (1) Ohler, Uwe Prof. Dr. (1) Quedenau, Claudia (1) Rajewsky, Klaus Prof. Dr. (1) Rajewsky, Nikolaus Prof. Dr. (3) Rathjen, Fritz Prof. Dr. (6) Rybak-Wolf, Agnieszka Dr. (1) Selbach, Matthias Prof. Dr. (2) Spagnoli, Francesca Dr. (1) Spuler, Simone Prof. (2) Woehler, Andrew Dr. (1) Wolf, Susanne Dr. (1) Zampieri, Niccolo Dr. (1) Zinzen, Robert Patrick Dr. (1) Zywitza, Vera Dr. (1) (-) Harabula, Izabela-Cezara (3) (-) Kühn, Ralf Dr. (2) (-) Semtner, Marcus Dr. (1) 2001 (1) 2005 (1) 2007 (1) 2009 (1) (-) 2014 (2) 2015 (1) (-) 2016 (1) (-) 2017 (3) 2018 (2) 2019 (1) 2022 (2) 2023 (1) Bioinformatics and Omics Data Science (1) Cardiac MRI (1) Cellular Neurosciences (5) Computational Regulatory Genomics (2) (-) Developmental Biology / Signal Transduction (2) (-) Developmental Neurobiology (1) Epigenetic Regulation and Chromatin Architecture (1) Experimental Ultrahigh-Field MR (9) Genetics and Genomics of Cardiovascular Diseases (3) Genetics of Metabolic and Reproductive Disorders (1) Genome Engineering & Disease Models (17) (-) Genomics (2) Immune Regulation and Cancer (4) Magnetic Resonance (9) Mobile DNA (1) Non-coding RNAs and Mechanisms of Cytoplasmic Gene Regulation (1) Proteome Dynamics (1) Proteomics and Molecular Mechanisms of Neurodegenerative Diseases (2) Psychoneuroimmunology (1) RNA Biology and Posttranscriptional Regulation (6) Systems Biology of Gene Regulatory Elements (3) Transgenics (17) 6 Results: Active Filter: Harabula, Izabela-CezaraKühn, Ralf Dr.Semtner, Marcus Dr.Developmental Biology / Signal TransductionDevelopmental NeurobiologyGenomics201420162017 Sort: Result score Newest to oldest Oldest to newest November 01, 2017 / Nat Biomed Eng Enhanced precision and efficiency S. Bashir R. Kühn 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 February 01, 2016 / Genome Res Exome sequencing and CRISPR/Cas genome editing identify mutations of ZAK as a cause of limb defects in humans and mice M. Spielmann N. Kakar N. Tayebi C. Leettola G. Nürnberg N. Sowada D.G. Lupiáñez I. Harabula R. Flöttmann D. Horn W.L. Chan L. Wittler R. Yilmaz J. Altmüller H. Thiele H. van Bokhoven C.E. Schwartz P. Nürnberg J.U. Bowie J. Ahmad C. Kubisch S. Mundlos G. Borck September 22, 2017 / Science Loss of a mammalian circular RNA locus causes miRNA deregulation and affects brain function M. Piwecka P. Glažar L.R. Hernandez-Miranda S. Memczak S.A. Wolf A. Rybak-Wolf A. Filipchyk F. Klironomos C.A. Cerda Jara P. Fenske T. Trimbuch V. Zywitza M. Plass L. Schreyer S. Ayoub C. Kocks R. Kühn C. Rosenmund C. Birchmeier N. Rajewsky November 01, 2017 / J Med Genet Mutations in MYO1H cause a recessive form of central hypoventilation with autonomic dysfunction M. Spielmann L.R. Hernandez-Miranda I. Ceccherini D.E. Weese-Mayer B.K. Kragesteen I. Harabula P. Krawitz C. Birchmeier N. Leonard S. Mundlos February 03, 2014 / J Clin Invest Changes in neural network homeostasis trigger neuropsychiatric symptoms A. Winkelmann N. Maggio J. Eller G. Caliskan M. Semtner U. Häussler R. Jüttner T. Dugladze B. Smolinsky S. Kowalczyk E. Chronowska G. Schwarz F.G. Rathjen G. Rechavi C.A. Haas A. Kulik T. Gloveli U. Heinemann J.C. Meier
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
February 01, 2016 / Genome Res Exome sequencing and CRISPR/Cas genome editing identify mutations of ZAK as a cause of limb defects in humans and mice M. Spielmann N. Kakar N. Tayebi C. Leettola G. Nürnberg N. Sowada D.G. Lupiáñez I. Harabula R. Flöttmann D. Horn W.L. Chan L. Wittler R. Yilmaz J. Altmüller H. Thiele H. van Bokhoven C.E. Schwartz P. Nürnberg J.U. Bowie J. Ahmad C. Kubisch S. Mundlos G. Borck
September 22, 2017 / Science Loss of a mammalian circular RNA locus causes miRNA deregulation and affects brain function M. Piwecka P. Glažar L.R. Hernandez-Miranda S. Memczak S.A. Wolf A. Rybak-Wolf A. Filipchyk F. Klironomos C.A. Cerda Jara P. Fenske T. Trimbuch V. Zywitza M. Plass L. Schreyer S. Ayoub C. Kocks R. Kühn C. Rosenmund C. Birchmeier N. Rajewsky
November 01, 2017 / J Med Genet Mutations in MYO1H cause a recessive form of central hypoventilation with autonomic dysfunction M. Spielmann L.R. Hernandez-Miranda I. Ceccherini D.E. Weese-Mayer B.K. Kragesteen I. Harabula P. Krawitz C. Birchmeier N. Leonard S. Mundlos
February 03, 2014 / J Clin Invest Changes in neural network homeostasis trigger neuropsychiatric symptoms A. Winkelmann N. Maggio J. Eller G. Caliskan M. Semtner U. Häussler R. Jüttner T. Dugladze B. Smolinsky S. Kowalczyk E. Chronowska G. Schwarz F.G. Rathjen G. Rechavi C.A. Haas A. Kulik T. Gloveli U. Heinemann J.C. Meier