Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Cano Rincon, Elena Dr. (3) Chen, Wei Prof. Dr. (1) Collins, Russell Thomas Dr. (1) Daumke, Oliver Prof. Dr. (2) Fälber, Katja Dr. (1) Fischer, Cornelius Dr. (1) Gerhardt, Holger Prof. Dr. (14) Hammes-Lewin, Annette Dr. (1) Heinemann, Udo Prof. Dr. (1) Hirsekorn, Antje (1) Klußmann, Enno PD Dr. (1) Landthaler, Markus Prof. Dr. (2) Lewin, Gary Prof. Dr. (1) Obermayer-Wasserscheid, Benedikt Dr. (1) Ohler, Uwe Prof. Dr. (2) Panakova, Daniela Dr. (1) Potente, Michael Prof. Dr. (3) Rajewsky, Klaus Prof. Dr. (1) Rocks, Oliver Dr. (2) Roske, Yvette Dr. (1) Selbach, Matthias Prof. Dr. (10) Wanker, Erich Prof. Dr. (1) Zühlke, Kerstin Dr. (1) (-) Altmueller, Janine Dr.med. (29) (-) Harabula, Izabela-Cezara (1) (-) Lupianez Garcia, Dario Jesus Dr. (1) (-) Wyler, Emanuel Dr. (1) (-) Zauber, Henrik Dr. (3) 2002 (1) 2005 (2) 2012 (1) 2014 (8) 2015 (29) (-) 2016 (32) 2018 (42) 2019 (30) 2020 (25) 2021 (50) 2022 (37) 2023 (18) 2024 (3) Cellular Neurosciences (2) Computational Regulatory Genomics (2) Experimental Ultrahigh-Field MR (4) Genome Engineering & Disease Models (2) (-) Genomics (29) Immune Regulation and Cancer (3) Magnetic Resonance (4) (-) Proteome Dynamics (3) RNA Biology and Posttranscriptional Regulation (1) Transgenics (2) 32 Results: Active Filter: Altmueller, Janine Dr.med.Harabula, Izabela-CezaraLupianez Garcia, Dario Jesus Dr.Wyler, Emanuel Dr.Zauber, Henrik Dr.GenomicsProteome Dynamics2016 Sort: Result score Newest to oldest Oldest to newest October 20, 2016 / Cell Kinetic analysis of protein stability reveals age-dependent degradation E. McShane C. Sin H. Zauber J.N. Wells N. Donnelly X. Wang J. Hou W. Chen Z. Storchova J.A. Marsh A. Valleriani M. Selbach 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 August 01, 2016 / Mol Cell Proteomics Systematic errors in peptide and protein identification and quantification by modified peptides B. Bogdanow H. Zauber M. Selbach 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 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 June 01, 2016 / J Med Genet Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestalt N. Di Donato T. Neuhann A.K. Kahlert B. Klink K. Hackmann I. Neuhann B. Novotna J. Schallner C. Krause I.A. Glass S.E. Parnell A. Benet-Pages A.M. Nissen W. Berger J. Altmüller H. Thiele B.H.F. Weber E. Schrock W.B. Dobyns A. Bier A. Rump Pagination Current page 1 Page 2 Page 3 Page 4 Next page Next › Last page Last »
October 20, 2016 / Cell Kinetic analysis of protein stability reveals age-dependent degradation E. McShane C. Sin H. Zauber J.N. Wells N. Donnelly X. Wang J. Hou W. Chen Z. Storchova J.A. Marsh A. Valleriani M. Selbach
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
August 01, 2016 / Mol Cell Proteomics Systematic errors in peptide and protein identification and quantification by modified peptides B. Bogdanow H. Zauber M. Selbach
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
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
June 01, 2016 / J Med Genet Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestalt N. Di Donato T. Neuhann A.K. Kahlert B. Klink K. Hackmann I. Neuhann B. Novotna J. Schallner C. Krause I.A. Glass S.E. Parnell A. Benet-Pages A.M. Nissen W. Berger J. Altmüller H. Thiele B.H.F. Weber E. Schrock W.B. Dobyns A. Bier A. Rump