Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Hirsekorn, Antje (2) Landthaler, Markus Prof. Dr. (4) Lupianez Garcia, Dario Jesus Dr. (1) Obermayer-Wasserscheid, Benedikt Dr. (1) Ohler, Uwe Prof. Dr. (7) Rajewsky, Nikolaus Prof. Dr. (1) Selbach, Matthias Prof. Dr. (2) Vucicevic, Dubravka (1) Wyler, Emanuel Dr. (1) Zauber, Henrik Dr. (1) (-) Altmueller, Janine Dr.med. (29) (-) Chekulaeva, Marina Dr. (1) (-) Fischer, Cornelius Dr. (1) (-) Harabula, Izabela-Cezara (1) (-) Lacadie, Scott Allen Dr. (1) 2002 (1) 2005 (2) 2013 (1) 2014 (7) 2015 (27) (-) 2016 (35) 2017 (36) 2018 (48) 2019 (34) 2020 (31) 2021 (51) 2022 (47) 2023 (26) 2024 (3) Cellular Neurosciences (2) (-) Computational Regulatory Genomics (3) Experimental Ultrahigh-Field MR (4) Genome Engineering & Disease Models (2) (-) Genomics (30) Immune Regulation and Cancer (3) Magnetic Resonance (4) Non-coding RNAs and Mechanisms of Cytoplasmic Gene Regulation (1) (-) RNA Biology and Posttranscriptional Regulation (2) Transgenics (2) 35 Results: Active Filter: Altmueller, Janine Dr.med.Chekulaeva, Marina Dr.Fischer, Cornelius Dr.Harabula, Izabela-CezaraLacadie, Scott Allen Dr.Computational Regulatory GenomicsGenomicsRNA Biology and Posttranscriptional Regulation2016 Sort: Result score Newest to oldest Oldest to newest November 01, 2016 / Plant Cell Alternative splicing substantially diversifies the transcriptome during early photomorphogenesis and correlates with the energy availability in arabidopsis L. Hartmann P. Drewe-Boss T. Wiessner G. Wagner S. Geue H.C. Lee D.M. Obermueller A. Kahles J. Behr F.H. Sinz G. Raetsch A. Wachter 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 January 01, 2016 / Pac Symp Biocomput Cseq-simulator: a data simulator for CLIP-Seq experiments W. Kassuhn U. Ohler P. Drewe October 07, 2016 / J Proteome Res Efficient application of de novo RNA assemblers for proteomics informed by transcriptomics T. Luge C. Fischer S. Sauer May 07, 2016 / J Cancer TERT core promotor mutations in early-onset bladder cancer J. Giedl A. Rogler A. Wild M.O. Riener T. Filbeck M. Burger P. Ruemmele C. Hurst M. Knowles A. Hartmann U. Zinnall R. Stoehr September 15, 2016 / Mol Cell Eyes on translation M. Chekulaeva M. Landthaler December 01, 2016 / FEBS J Divergent transcription and epigenetic directionality of human promoters S.A. Lacadie M.M. Ibrahim S.A. Gokhale U. Ohler August 04, 2016 / Am J Hum Genet Exome sequencing identifies biallelic MSH3 germline mutations as a recessive subtype of colorectal adenomatous polyposis R. Adam I. Spier B. Zhao M. Kloth J. Marquez I. Hinrichsen J. Kirfel A. Tafazzoli S. Horpaopan S. Uhlhaas D. Stienen N. Friedrichs J. Altmüller A. Laner S. Holzapfel S. Peters K. Kayser H. Thiele E. Holinski-Feder G. Marra G. Kristiansen M.M. Nöthen R. Büttner G. Möslein R.C. Betz A. Brieger R.P. Lifton S. Aretz August 01, 2016 / Biol Chem A systematic comparison of two new releases of exome sequencing products: the aim of use determines the choice of product J. Altmüller S. Motameny C. Becker H. Thiele S. Chatterjee B. Wollnik P. Nürnberg February 25, 2016 / Blood Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndrome S. Ammann A. Schulz I. Krägeloh-Mann N.M.G. Dieckmann K. Niethammer S. Fuchs K.M. Eckl R. Plank R. Werner J. Altmüller H. Thiele P. Nürnberg J. Bank A. Strauss H. von Bernuth U. Zur Stadt S. Grieve G.M. Griffiths K. Lehmberg H.C. Hennies S. Ehl Pagination Current page 1 Page 2 Page 3 Page 4 Next page Next › Last page Last »
November 01, 2016 / Plant Cell Alternative splicing substantially diversifies the transcriptome during early photomorphogenesis and correlates with the energy availability in arabidopsis L. Hartmann P. Drewe-Boss T. Wiessner G. Wagner S. Geue H.C. Lee D.M. Obermueller A. Kahles J. Behr F.H. Sinz G. Raetsch A. Wachter
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
January 01, 2016 / Pac Symp Biocomput Cseq-simulator: a data simulator for CLIP-Seq experiments W. Kassuhn U. Ohler P. Drewe
October 07, 2016 / J Proteome Res Efficient application of de novo RNA assemblers for proteomics informed by transcriptomics T. Luge C. Fischer S. Sauer
May 07, 2016 / J Cancer TERT core promotor mutations in early-onset bladder cancer J. Giedl A. Rogler A. Wild M.O. Riener T. Filbeck M. Burger P. Ruemmele C. Hurst M. Knowles A. Hartmann U. Zinnall R. Stoehr
December 01, 2016 / FEBS J Divergent transcription and epigenetic directionality of human promoters S.A. Lacadie M.M. Ibrahim S.A. Gokhale U. Ohler
August 04, 2016 / Am J Hum Genet Exome sequencing identifies biallelic MSH3 germline mutations as a recessive subtype of colorectal adenomatous polyposis R. Adam I. Spier B. Zhao M. Kloth J. Marquez I. Hinrichsen J. Kirfel A. Tafazzoli S. Horpaopan S. Uhlhaas D. Stienen N. Friedrichs J. Altmüller A. Laner S. Holzapfel S. Peters K. Kayser H. Thiele E. Holinski-Feder G. Marra G. Kristiansen M.M. Nöthen R. Büttner G. Möslein R.C. Betz A. Brieger R.P. Lifton S. Aretz
August 01, 2016 / Biol Chem A systematic comparison of two new releases of exome sequencing products: the aim of use determines the choice of product J. Altmüller S. Motameny C. Becker H. Thiele S. Chatterjee B. Wollnik P. Nürnberg
February 25, 2016 / Blood Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndrome S. Ammann A. Schulz I. Krägeloh-Mann N.M.G. Dieckmann K. Niethammer S. Fuchs K.M. Eckl R. Plank R. Werner J. Altmüller H. Thiele P. Nürnberg J. Bank A. Strauss H. von Bernuth U. Zur Stadt S. Grieve G.M. Griffiths K. Lehmberg H.C. Hennies S. Ehl