Scientific Publications Search Search Author Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Altmueller, Janine Dr.med. (62) Chen, Wei Prof. Dr. (1) Fischer, Cornelius Dr. (2) Lupianez Garcia, Dario Jesus Dr. (1) Quedenau, Claudia (1) (-) Harabula, Izabela-Cezara (2) (-) Kühn, Ralf Dr. (1) (-) 2014 (1) 2015 (1) (-) 2016 (1) (-) 2017 (1) 2022 (2) Angiogenesis & Metabolism Laboratory (1) Bioinformatics and Omics Data Science (1) Biology of Malignant Lymphomas (2) Cardiac MRI (1) Cellular Neurosciences (5) Computational Regulatory Genomics (2) Developmental Biology / Signal Transduction (3) 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 (23) Integrative Vascular Biology (1) Magnetic Resonance (9) Mobile DNA (1) Molecular Physiology of Somatic Sensation (1) Non-coding RNAs and Mechanisms of Cytoplasmic Gene Regulation (1) Proteome Dynamics (2) Proteomics and Metabolomics (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) 3 Results: Active Filter: Harabula, Izabela-CezaraKühn, Ralf Dr.Genomics201420162017 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
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