Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Birchmeier-Kohler, Carmen Prof. Dr. (1) Braeuning, Caroline (1) Cano Rincon, Elena Dr. (3) Chen, Wei Prof. Dr. (1) Collins, Russell Thomas Dr. (2) Conrad, Thomas Dr. (2) Daumke, Oliver Prof. Dr. (2) Diecke, Sebastian Dr. (1) Fälber, Katja Dr. (1) Fischer, Cornelius Dr. (4) Gerhardt, Holger Prof. Dr. (14) Gerlach, Kerstin (1) Giese, Wolfgang Dr. (1) Gouti, Mina Dr. (1) Hammes-Lewin, Annette Dr. (1) Hirsekorn, Antje (1) Höpken, Uta Elisabeth PD Dr. (1) Kabuss, Loreen-Claudine (1) Kammertöns, Thomas Dr. (1) Klaus-Bergmann, Alexandra Dr. (1) Klußmann, Enno PD Dr. (1) Kunz, Severine Dr. (1) Landthaler, Markus Prof. Dr. (3) Lewin, Gary Prof. Dr. (1) Meier, Katja (1) Obermayer-Wasserscheid, Benedikt Dr. (1) Ohler, Uwe Prof. Dr. (2) Panakova, Daniela Dr. (1) Plumbom, Izabela (1) Quedenau, Claudia (1) Rajewsky, Klaus Prof. Dr. (1) Rehm, Armin Dr. (1) Rocks, Oliver Dr. (2) Roske, Yvette Dr. (1) Selbach, Matthias Prof. Dr. (14) Spuler, Simone Prof. (1) Sunaga-Franze, Daniele Yumi Dr. (3) Wanker, Erich Prof. Dr. (1) Zauber, Henrik Dr. (4) Zühlke, Kerstin Dr. (1) (-) Altmueller, Janine Dr.med. (51) (-) Harabula, Izabela-Cezara (1) (-) Heinemann, Udo Prof. Dr. (1) (-) Lupianez Garcia, Dario Jesus Dr. (1) (-) Potente, Michael Prof. Dr. (5) (-) Wyler, Emanuel Dr. (1) 1999 (1) 2002 (1) 2005 (5) 2007 (1) 2008 (4) 2009 (3) 2010 (2) 2011 (2) 2012 (3) 2013 (4) 2015 (20) (-) 2016 (31) 2017 (35) 2018 (44) 2019 (33) (-) 2020 (27) 2021 (55) 2022 (42) 2023 (22) 2024 (1) Anchored Signalling (1) (-) Angiogenesis & Metabolism Laboratory (5) Bioinformatics and Omics Data Science (1) Cellular Neurosciences (5) Computational Regulatory Genomics (2) Epigenetic Regulation and Chromatin Architecture (1) Experimental Ultrahigh-Field MR (6) Genetics of Metabolic and Reproductive Disorders (1) Genome Engineering & Disease Models (3) (-) Genomics (51) Immune Regulation and Cancer (7) (-) Integrative Vascular Biology (1) Magnetic Resonance (6) Pluripotent Stem Cells (1) Protein Production and Characterization (1) (-) Proteome Dynamics (2) Proteomics (1) Proteomics and Metabolomics (1) Proteomics and Molecular Mechanisms of Neurodegenerative Diseases (1) Psychoneuroimmunology (1) RNA Biology and Posttranscriptional Regulation (4) Structural Biology of Membrane-Associated Processes (2) Transgenics (3) 58 Results: Active Filter: Altmueller, Janine Dr.med.Harabula, Izabela-CezaraHeinemann, Udo Prof. Dr.Lupianez Garcia, Dario Jesus Dr.Potente, Michael Prof. Dr.Wyler, Emanuel Dr.Angiogenesis & Metabolism LaboratoryGenomicsIntegrative Vascular BiologyProteome Dynamics20162020 Sort: Result score Newest to oldest Oldest to newest 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 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 October 20, 2016 / Nat Commun Quantitative interaction mapping reveals an extended UBX domain in ASPL that disrupts functional p97 hexamers A. Arumughan Y. Roske C. Barth L. Lleras Forero K. Bravo-Rodriguez Al. Redel S. Kostova E. McShane R. Opitz K. Faelber K. Rau T. Mielke O. Daumke M. Selbach E. Sanchez-Garcia O. Rocks D. Panáková U. Heinemann E.E. Wanker 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 July 02, 2020 / Am J Hum Genet Mutations in SREBF1, encoding sterol regulatory element binding transcription factor 1, cause autosomal-dominant IFAP syndrome H. Wang A. Humbatova Y. Liu W. Qin M. Lee N. Cesarato F. Kortüm S. Kumar M.T. Romano S. Dai R. Mo S. Sivalingam S. Motameny Y. Wu X. Wang X. Niu S. Geng D. Bornholdt P.M. Kroisel G. Tadini S.D. Walter F. Hauck K.M. Girisha A.M. Calza A. Bottani J. Altmüller A. Buness S. Yang X. Sun L. Ma K. Kutsche K.H. Grzeschik R.C. Betz Z. Lin March 01, 2020 / Hum Mutat The recurrent postzygotic pathogenic variant p.Glu47Lys in RHOA causes a novel recognizable neuroectodermal phenotype G. Yigit K. Saida D. DeMarzo N. Miyake A. Fujita T. Yang Tan S.M. White A. Wadley M.R. Toliat S. Motameny M. Franitza C.A. Stutterd P.F. Chong R. Kira T. Sengoku K. Ogata M.J. Guillen Sacoto C. Fresen B.B. Beck P. Nürnberg C. Dieterich B. Wollnik N. Matsumoto J. Altmüller May 01, 2016 / Chem Senses Transcriptome analysis of murine olfactory sensory neurons during development using single cell RNA-Seq P. Scholz B. Kalbe F. Jansen J. Altmüller C. Becker J. Mohrhardt B. Schreiner G. Gisselmann H. Hatt S. Osterloh April 01, 2016 / Fam Cancer Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis I. Spier M. Kerick D. Drichel S. Horpaopan J. Altmüller A. Laner S. Holzapfel S. Peters R. Adam B. Zhao T. Becker R.P. Lifton E. Holinski-Feder S. Perner H. Thiele M.M. Nöthen P. Hoffmann B. Timmermann M.R. Schweiger S. Aretz February 01, 2016 / Hum Genet A novel homozygous splicing mutation of CASC5 causes primary microcephaly in a large Pakistani family S. Szczepanski M.S. Hussain I. Sur J. Altmüller H. Thiele U. Abdullah S.S. Waseem A. Moawia G. Nürnberg A.A. Noegel S.M. Baig P. Nürnberg July 08, 2016 / PLoS ONE Identification of novel and recurrent disease-causing mutations in retinal dystrophies using whole exome sequencing (WES): Benefits and limitations A. Tiwari J. Lemke J. Altmüller H. Thiele E. Glaus J. Fleischhauer P. Nürnberg J. Neidhardt W. Berger Pagination Current page 1 Page 2 Page 3 Page 4 … Next page Next › Last page Last »
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 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
October 20, 2016 / Nat Commun Quantitative interaction mapping reveals an extended UBX domain in ASPL that disrupts functional p97 hexamers A. Arumughan Y. Roske C. Barth L. Lleras Forero K. Bravo-Rodriguez Al. Redel S. Kostova E. McShane R. Opitz K. Faelber K. Rau T. Mielke O. Daumke M. Selbach E. Sanchez-Garcia O. Rocks D. Panáková U. Heinemann E.E. Wanker
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
July 02, 2020 / Am J Hum Genet Mutations in SREBF1, encoding sterol regulatory element binding transcription factor 1, cause autosomal-dominant IFAP syndrome H. Wang A. Humbatova Y. Liu W. Qin M. Lee N. Cesarato F. Kortüm S. Kumar M.T. Romano S. Dai R. Mo S. Sivalingam S. Motameny Y. Wu X. Wang X. Niu S. Geng D. Bornholdt P.M. Kroisel G. Tadini S.D. Walter F. Hauck K.M. Girisha A.M. Calza A. Bottani J. Altmüller A. Buness S. Yang X. Sun L. Ma K. Kutsche K.H. Grzeschik R.C. Betz Z. Lin
March 01, 2020 / Hum Mutat The recurrent postzygotic pathogenic variant p.Glu47Lys in RHOA causes a novel recognizable neuroectodermal phenotype G. Yigit K. Saida D. DeMarzo N. Miyake A. Fujita T. Yang Tan S.M. White A. Wadley M.R. Toliat S. Motameny M. Franitza C.A. Stutterd P.F. Chong R. Kira T. Sengoku K. Ogata M.J. Guillen Sacoto C. Fresen B.B. Beck P. Nürnberg C. Dieterich B. Wollnik N. Matsumoto J. Altmüller
May 01, 2016 / Chem Senses Transcriptome analysis of murine olfactory sensory neurons during development using single cell RNA-Seq P. Scholz B. Kalbe F. Jansen J. Altmüller C. Becker J. Mohrhardt B. Schreiner G. Gisselmann H. Hatt S. Osterloh
April 01, 2016 / Fam Cancer Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis I. Spier M. Kerick D. Drichel S. Horpaopan J. Altmüller A. Laner S. Holzapfel S. Peters R. Adam B. Zhao T. Becker R.P. Lifton E. Holinski-Feder S. Perner H. Thiele M.M. Nöthen P. Hoffmann B. Timmermann M.R. Schweiger S. Aretz
February 01, 2016 / Hum Genet A novel homozygous splicing mutation of CASC5 causes primary microcephaly in a large Pakistani family S. Szczepanski M.S. Hussain I. Sur J. Altmüller H. Thiele U. Abdullah S.S. Waseem A. Moawia G. Nürnberg A.A. Noegel S.M. Baig P. Nürnberg
July 08, 2016 / PLoS ONE Identification of novel and recurrent disease-causing mutations in retinal dystrophies using whole exome sequencing (WES): Benefits and limitations A. Tiwari J. Lemke J. Altmüller H. Thiele E. Glaus J. Fleischhauer P. Nürnberg J. Neidhardt W. Berger