Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Chu, Van Trung Dr. (3) Fischer, Cornelius Dr. (1) Gerhardt, Holger Prof. Dr. (1) Graf, Robin Dr. (2) Harabula, Izabela-Cezara (1) Kühn, Ralf Dr. (2) Landthaler, Markus Prof. Dr. (2) Lupianez Garcia, Dario Jesus Dr. (1) Ohler, Uwe Prof. Dr. (7) Potente, Michael Prof. Dr. (1) Rajewsky, Klaus Prof. Dr. (11) Selbach, Matthias Prof. Dr. (2) Vucicevic, Dubravka (1) (-) Altmueller, Janine Dr.med. (29) (-) Hirsekorn, Antje (2) (-) Janz, Martin Dr. (1) (-) Lacadie, Scott Allen Dr. (1) (-) Obermayer-Wasserscheid, Benedikt Dr. (1) (-) Wyler, Emanuel Dr. (1) (-) Zauber, Henrik Dr. (1) 2002 (1) 2005 (2) 2012 (1) 2013 (1) 2014 (8) 2015 (30) (-) 2016 (33) 2017 (34) 2018 (42) 2019 (34) 2020 (25) 2021 (47) 2022 (40) 2023 (22) 2024 (2) Biology of Malignant Lymphomas (1) Cellular Neurosciences (2) (-) Computational Regulatory Genomics (3) Experimental Ultrahigh-Field MR (4) (-) Genomics (29) (-) Immune Regulation and Cancer (1) Magnetic Resonance (4) Proteome Dynamics (3) RNA Biology and Posttranscriptional Regulation (1) 33 Results: Active Filter: Altmueller, Janine Dr.med.Hirsekorn, AntjeJanz, Martin Dr.Lacadie, Scott Allen Dr.Obermayer-Wasserscheid, Benedikt Dr.Wyler, Emanuel Dr.Zauber, Henrik Dr.Computational Regulatory GenomicsGenomicsImmune Regulation and Cancer2016 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 February 01, 2016 / Nat Methods Detecting actively translated open reading frames in ribosome profiling data L. Calviello N. Mukherjee E. Wyler H. Zauber A. Hirsekorn M. Selbach M. Landthaler B. Obermayer U. Ohler January 01, 2016 / Methods Mol Biol Identifying RBP targets with RIP-seq H.H. Wessels A. Hirsekorn U. Ohler N. Mukherjee May 03, 2016 / Proc Natl Acad Sci U S A Canonical NF-κB signaling is uniquely required for the long-term persistence of functional mature B cells E. Derudder S. Herzog V. Labi T. Yasuda K. Köchert M. Janz A. Villunger M. Schmidt-Supprian K. Rajewsky 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 March 15, 2016 / Hum Mol Genet Three-layered proteomic characterization of a novel ACTN4 mutation unravels its pathogenic potential in FSGS M.P. Bartram S. Habbig C. Pahmeyer M. Höhne L.T. Weber H. Thiele J. Altmüller N. Kottoor A. Wenzel M. Krueger B. Schermer T. Benzing M.M. Rinschen B.B. Beck October 01, 2016 / Am J Med Genet A Update on the ACTG1-associated Baraitser–Winter cerebrofrontofacial syndrome N. Di Donato A. Kuechler S. Vergano W. Heinritz J. Bodurtha S.R. Merchant G. Breningstall R. Ladda S. Sell J. Altmüller N. Bögershausen A.E. Timms K. Hackmann E. Schrock S. Collins C. Olds A. Rump W.B. Dobyns 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
February 01, 2016 / Nat Methods Detecting actively translated open reading frames in ribosome profiling data L. Calviello N. Mukherjee E. Wyler H. Zauber A. Hirsekorn M. Selbach M. Landthaler B. Obermayer U. Ohler
January 01, 2016 / Methods Mol Biol Identifying RBP targets with RIP-seq H.H. Wessels A. Hirsekorn U. Ohler N. Mukherjee
May 03, 2016 / Proc Natl Acad Sci U S A Canonical NF-κB signaling is uniquely required for the long-term persistence of functional mature B cells E. Derudder S. Herzog V. Labi T. Yasuda K. Köchert M. Janz A. Villunger M. Schmidt-Supprian K. Rajewsky
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
March 15, 2016 / Hum Mol Genet Three-layered proteomic characterization of a novel ACTN4 mutation unravels its pathogenic potential in FSGS M.P. Bartram S. Habbig C. Pahmeyer M. Höhne L.T. Weber H. Thiele J. Altmüller N. Kottoor A. Wenzel M. Krueger B. Schermer T. Benzing M.M. Rinschen B.B. Beck
October 01, 2016 / Am J Med Genet A Update on the ACTG1-associated Baraitser–Winter cerebrofrontofacial syndrome N. Di Donato A. Kuechler S. Vergano W. Heinritz J. Bodurtha S.R. Merchant G. Breningstall R. Ladda S. Sell J. Altmüller N. Bögershausen A.E. Timms K. Hackmann E. Schrock S. Collins C. Olds A. Rump W.B. Dobyns