Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Akalin, Altuna Dr. (3) Chekulaeva, Marina Dr. (1) Chen, Wei Prof. Dr. (1) Chu, Van Trung Dr. (4) Fischer, Cornelius Dr. (2) Franke, Vedran Dr. (1) Gerhardt, Holger Prof. Dr. (1) Graf, Robin Dr. (3) Harabula, Izabela-Cezara (1) Hirsekorn, Antje (4) Janz, Martin Dr. (1) Kabrani, Eleni Dr. (1) Kempa, Stefan Dr. (1) Kühn, Ralf Dr. (3) Landthaler, Markus Prof. Dr. (4) Lupianez Garcia, Dario Jesus Dr. (1) Müller, Thomas Dr. (1) Obermayer-Wasserscheid, Benedikt Dr. (1) Ohler, Uwe Prof. Dr. (20) Potente, Michael Prof. Dr. (1) Quedenau, Claudia (1) Rajewsky, Klaus Prof. Dr. (15) Rajewsky, Nikolaus Prof. Dr. (3) Selbach, Matthias Prof. Dr. (4) Uyar, Bora Dr. (1) Vucicevic, Dubravka (1) Woehler, Andrew Dr. (1) Wurmus, Ricardo (1) Zauber, Henrik Dr. (1) Zinzen, Robert Patrick Dr. (1) (-) Altmueller, Janine Dr.med. (60) (-) Birchmeier-Kohler, Carmen Prof. Dr. (1) (-) Lacadie, Scott Allen Dr. (1) (-) Wyler, Emanuel Dr. (2) 2002 (1) 2005 (2) 2013 (1) 2014 (8) 2015 (28) (-) 2016 (31) (-) 2017 (33) 2018 (42) 2019 (33) 2020 (25) 2021 (46) 2022 (38) 2023 (18) 2024 (2) Bioinformatics and Omics Data Science (2) Cardiac MRI (1) Cellular Neurosciences (4) (-) Computational Regulatory Genomics (4) Developmental Biology / Signal Transduction (15) Development and Function of Neural Circuits (1) Epigenetic Regulation and Chromatin Architecture (1) Experimental Ultrahigh-Field MR (7) From Cell States to Function (1) Genetics and Genomics of Cardiovascular Diseases (3) Genome Engineering & Disease Models (1) (-) Genomics (60) Magnetic Resonance (7) Mobile DNA (1) Myology (1) Non-coding RNAs and Mechanisms of Cytoplasmic Gene Regulation (2) Proteome Dynamics (2) Proteomics and Molecular Mechanisms of Neurodegenerative Diseases (1) Psychoneuroimmunology (1) RNA Biology and Posttranscriptional Regulation (6) Systems Biology Imaging (1) Systems Biology of Gene Regulatory Elements (5) Transgenics (1) 64 Results: Active Filter: Altmueller, Janine Dr.med.Birchmeier-Kohler, Carmen Prof. Dr.Lacadie, Scott Allen Dr.Wyler, Emanuel Dr.Computational Regulatory GenomicsGenomics20162017 Sort: Result score Newest to oldest Oldest to newest 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 19, 2017 / Nat Commun RNA localization is a key determinant of neurite-enriched proteome A. Zappulo D. van den Bruck C. Ciolli Mattioli V. Franke K. Imami E. McShane M. Moreno-Estelles L. Calviello A. Filipchyk E. Peguero-Sanchez T. Müller A. Woehler C. Birchmeier E. Merino N. Rajewsky U. Ohler E.O. Mazzoni M. Selbach A. Akalin M. Chekulaeva January 03, 2017 / BMC Bioinformatics JACUSA: site-specific identification of RNA editing events from replicate sequencing data M. Piechotta E. Wyler U. Ohler M. Landthaler C. Dieterich December 01, 2016 / FEBS J Divergent transcription and epigenetic directionality of human promoters S.A. Lacadie M.M. Ibrahim S.A. Gokhale U. Ohler December 19, 2017 / Cold Spring Harb Mol Case Stud Late diagnosis of a truncating WISP3 mutation entails a severe phenotype of progressive pseudorheumatoid dysplasia S. Alawbathani A. Kawalia M. Karakaya J. Altmüller P. Nürnberg S. Cirak July 01, 2017 / Clin Genet Genetic heterogeneity in Pakistani microcephaly families revisited I. Ahmad S.M. Baig A.R. Abdulkareem M.S. Hussain I. Sur M.R. Toliat G. Nürnberg N. Dalibor A. Moawia S.S. Waseem M. Asif H. Nagra M. Sher M.M.A. Khan I. Hassan S.U. Rehman H. Thiele J. Altmüller A.A. Noegel P. Nürnberg June 01, 2017 / Immunogenetics Mutational profiling in the peripheral blood leukocytes of patients with systemic mast cell activation syndrome using next-generation sequencing J. Altmüller B. Haenisch A. Kawalia M. Menzen M.M. Nöthen H. Fier G.J. Molderings December 01, 2017 / Nat Med A microRNA screen reveals that elevated hepatic ectodysplasin A expression contributes to obesity-induced insulin resistance in skeletal muscle M. Awazawa P. Gabel E. Tsaousidou H. Nolte M. Krüger J. Schmitz P.J. Ackermann C. Brandt J. Altmüller S. Motameny F.T. Wunderlich J.W. Kornfeld M. Blüher J.C. Brüning July 01, 2017 / Hum Genet Heterozygous HNRNPU variants cause early onset epilepsy and severe intellectual disability N.C. Bramswig H.J. Lüdecke F.F. Hamdan J. Altmüller F. Beleggia N.H. Elcioglu C. Freyer E.H. Gerkes Y.K. Demirkol K.G. Knupp A. Kuechler Y. Li D.H. Lowenstein J.L. Michaud K. Park A.P.A. Stegmann H.E. Veenstra-Knol T. Wieland B. Wollnik H. Engels T.M. Strom T. Kleefstra D. Wieczorek September 26, 2017 / Mol Ecol Copy number increases of transposable elements and protein-coding genes in an invasive fish of hybrid origin S. Dennenmoser F.J. Sedlazeck E. Iwaszkiewicz X.Y. Li J. Altmüller A.W. Nolte Pagination Current page 1 Page 2 Page 3 Page 4 … Next page Next › Last page Last »
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 19, 2017 / Nat Commun RNA localization is a key determinant of neurite-enriched proteome A. Zappulo D. van den Bruck C. Ciolli Mattioli V. Franke K. Imami E. McShane M. Moreno-Estelles L. Calviello A. Filipchyk E. Peguero-Sanchez T. Müller A. Woehler C. Birchmeier E. Merino N. Rajewsky U. Ohler E.O. Mazzoni M. Selbach A. Akalin M. Chekulaeva
January 03, 2017 / BMC Bioinformatics JACUSA: site-specific identification of RNA editing events from replicate sequencing data M. Piechotta E. Wyler U. Ohler M. Landthaler C. Dieterich
December 01, 2016 / FEBS J Divergent transcription and epigenetic directionality of human promoters S.A. Lacadie M.M. Ibrahim S.A. Gokhale U. Ohler
December 19, 2017 / Cold Spring Harb Mol Case Stud Late diagnosis of a truncating WISP3 mutation entails a severe phenotype of progressive pseudorheumatoid dysplasia S. Alawbathani A. Kawalia M. Karakaya J. Altmüller P. Nürnberg S. Cirak
July 01, 2017 / Clin Genet Genetic heterogeneity in Pakistani microcephaly families revisited I. Ahmad S.M. Baig A.R. Abdulkareem M.S. Hussain I. Sur M.R. Toliat G. Nürnberg N. Dalibor A. Moawia S.S. Waseem M. Asif H. Nagra M. Sher M.M.A. Khan I. Hassan S.U. Rehman H. Thiele J. Altmüller A.A. Noegel P. Nürnberg
June 01, 2017 / Immunogenetics Mutational profiling in the peripheral blood leukocytes of patients with systemic mast cell activation syndrome using next-generation sequencing J. Altmüller B. Haenisch A. Kawalia M. Menzen M.M. Nöthen H. Fier G.J. Molderings
December 01, 2017 / Nat Med A microRNA screen reveals that elevated hepatic ectodysplasin A expression contributes to obesity-induced insulin resistance in skeletal muscle M. Awazawa P. Gabel E. Tsaousidou H. Nolte M. Krüger J. Schmitz P.J. Ackermann C. Brandt J. Altmüller S. Motameny F.T. Wunderlich J.W. Kornfeld M. Blüher J.C. Brüning
July 01, 2017 / Hum Genet Heterozygous HNRNPU variants cause early onset epilepsy and severe intellectual disability N.C. Bramswig H.J. Lüdecke F.F. Hamdan J. Altmüller F. Beleggia N.H. Elcioglu C. Freyer E.H. Gerkes Y.K. Demirkol K.G. Knupp A. Kuechler Y. Li D.H. Lowenstein J.L. Michaud K. Park A.P.A. Stegmann H.E. Veenstra-Knol T. Wieland B. Wollnik H. Engels T.M. Strom T. Kleefstra D. Wieczorek
September 26, 2017 / Mol Ecol Copy number increases of transposable elements and protein-coding genes in an invasive fish of hybrid origin S. Dennenmoser F.J. Sedlazeck E. Iwaszkiewicz X.Y. Li J. Altmüller A.W. Nolte