Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Fischer, Cornelius Dr. (1) Gerhardt, Holger Prof. Dr. (1) Harabula, Izabela-Cezara (1) Hübner, Norbert Prof. Dr. (1) Janz, Martin Dr. (6) Mathas, Stephan Dr. (7) Patone, Giannino Dr. (1) Pezzutto, Antonio Prof. Dr. (1) Scheidereit, Claus Prof. Dr. (2) (-) Altmueller, Janine Dr.med. (29) (-) Lupianez Garcia, Dario Jesus Dr. (1) (-) Potente, Michael Prof. Dr. (6) (-) Rajewsky, Klaus Prof. Dr. (3) (-) 1999 (1) 2002 (1) 2005 (5) (-) 2007 (1) 2008 (4) 2009 (3) 2010 (2) 2011 (2) (-) 2012 (3) 2013 (4) 2014 (8) 2015 (27) (-) 2016 (32) 2017 (35) 2018 (44) 2019 (33) 2020 (28) 2021 (53) 2022 (41) 2023 (24) 2024 (2) (-) Angiogenesis & Metabolism Laboratory (6) (-) Biology of Malignant Lymphomas (2) Cardiac MRI (1) Cellular Neurosciences (2) Computational Regulatory Genomics (2) Developmental Biology / Signal Transduction (1) Experimental Ultrahigh-Field MR (6) Genetics of Metabolic and Reproductive Disorders (1) Genome Engineering & Disease Models (2) (-) Genomics (29) Immune Regulation and Cancer (17) Integrative Vascular Biology (1) Magnetic Resonance (6) Proteome Dynamics (2) RNA Biology and Posttranscriptional Regulation (3) Systems Biology of Gene Regulatory Elements (2) Transgenics (2) 37 Results: Active Filter: Altmueller, Janine Dr.med.Lupianez Garcia, Dario Jesus Dr.Potente, Michael Prof. Dr.Rajewsky, Klaus Prof. Dr.Angiogenesis & Metabolism LaboratoryBiology of Malignant LymphomasGenomics1999200720122016 Sort: Result score Newest to oldest Oldest to newest November 01, 2012 / Nat Immunol The cell-cycle regulator c-Myc is essential for the formation and maintenance of germinal centers D.P. Calado Y. Sasaki S.A. Godinho A. Pellerin K. Köchert B.P. Sleckman I.M. de Alboran M. Janz S. Rodig K. Rajewsky 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 14, 2016 / Nature FOXO1 couples metabolic activity and growth state in the vascular endothelium K. Wilhelm K. Happel G. Eelen S. Schoors M.F. Oellerich R. Lim B. Zimmermann I.M. Aspalter C.A. Franco T. Boettger T. Braun M. Fruttiger K. Rajewsky C. Keller J.C. Brüning H. Gerhardt P. Carmeliet M. Potente 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 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 »
November 01, 2012 / Nat Immunol The cell-cycle regulator c-Myc is essential for the formation and maintenance of germinal centers D.P. Calado Y. Sasaki S.A. Godinho A. Pellerin K. Köchert B.P. Sleckman I.M. de Alboran M. Janz S. Rodig K. Rajewsky
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 14, 2016 / Nature FOXO1 couples metabolic activity and growth state in the vascular endothelium K. Wilhelm K. Happel G. Eelen S. Schoors M.F. Oellerich R. Lim B. Zimmermann I.M. Aspalter C.A. Franco T. Boettger T. Braun M. Fruttiger K. Rajewsky C. Keller J.C. Brüning H. Gerhardt P. Carmeliet M. Potente
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
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