Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Akalin, Altuna Dr. (1) Bader, Michael Prof. Dr. (2) Badillo Lisakowski, Victor Christian Dr. (1) Bähring, Sylvia Dr. (2) Barke, Niclas (1) Bartels-Klein, Eireen (1) Bartolomaeus, Theda (2) Beule, Dieter Dr. (5) Birchmeier, Walter Prof. Dr. (1) Birchmeier-Kohler, Carmen Prof. Dr. (1) Blume, Alexander Dr. (1) Blüthgen, Nils (1) Borodina, Tatiana Dr. (8) Braeuning, Caroline (5) Chen, Wei Prof. Dr. (2) Conrad, Thomas Dr. (15) Dechend, Ralf Priv. Doz. (1) Deter, Aylina (1) Diecke, Sebastian Dr. (4) Escobar Fernandez, Helena Dr. (1) Faxel, Miriam (1) Fischer, Cornelius Dr. (16) Forslund, Sofia Dr. (2) Franke, Vedran Dr. (1) Freimuth, Jonas (1) Geisberger, Sabrina Yasmin Dr. (1) Gerhardt, Holger Prof. Dr. (8) Gotthardt, Michael Prof. Dr. (1) Gouti, Mina Dr. (1) Haas, Simon Dr. rer. nat. (1) Hartl, Kimberly (1) Henssen, Anton Prof. Dr. med. (2) Herse, Florian PD Dr. (1) Heuser, Arnd Dr. (2) Hinze, Christian Dr. med. Dipl.-Math. (1) Hollfinger, Irene (1) Höpken, Uta Elisabeth PD Dr. (1) Hübner, Norbert Prof. Dr. (1) Junker, Jan Philipp Prof. Dr. (1) Kabuss, Loreen-Claudine (1) Kalnytska, Oleksandra (1) Kettenmann, Helmut Prof. Dr. (1) Klaus-Bergmann, Alexandra Dr. (1) Klußmann, Enno PD Dr. (2) Kocks, Christine Dr. (1) Kühn, Ralf Dr. (1) Kunz, Severine Dr. (2) Landthaler, Markus Prof. Dr. (2) Langanki, Reika (2) Lee, Young-Ae Prof. Dr. (2) Leutz, Achim Prof. Dr. (1) Liu, Tiannan (1) Marenholz, Ingo Dr. (1) Marko, Lajos Dr. (2) Müller, Dominik Prof. Dr. (1) Müller, Marion (1) Müllerke, Stefanie (1) Na, Il-Kang Dr. (1) Napieczynska, Hanna Dr. (1) Neuschulz, Anika (1) Obermayer-Wasserscheid, Benedikt Dr. (4) Olivares Chauvet, Pedro Dr. (1) Paul, Friedemann Prof. Dr. med. (1) Plumbom, Izabela (1) Popova, Elena Dr. (1) Qadri, Fatimunnisa Dr. (2) Quedenau, Claudia (7) Rajewsky, Nikolaus Prof. Dr. (3) Sai, Somesh (1) Schmidt-Krüger, Vanessa Dr. (1) Schmitt, Clemens Prof. Dr. (1) Schwarz, Roland Dr. (1) Secener, Ali Kerim (1) Siffrin, Volker (1) Sigal, Michael Dr. (2) Spuler, Simone Prof. (2) Sunaga-Franze, Daniele Yumi Dr. (9) Taube, Martin (1) Teixeira Alves, Luiz Gustavo Dr. (1) Uyar, Bora Dr. (1) Wendlinger, Sarah (1) Willnow, Thomas Prof. Dr. (1) Woehler, Andrew Dr. (1) Wurmus, Ricardo (1) Zimmermann, Karin Dr. (1) Zühlke, Kerstin Dr. (1) (-) Altmueller, Janine Dr.med. (289) (-) Harabula, Izabela-Cezara (2) (-) Lupianez Garcia, Dario Jesus Dr. (1) (-) Potente, Michael Prof. Dr. (58) (-) Rajewsky, Klaus Prof. Dr. (1) (-) Semtner, Marcus Dr. (1) (-) Sholokh, Anastasiia (2) (-) Wyler, Emanuel Dr. (2) 1999 (1) 2002 (1) 2005 (5) 2007 (1) 2008 (4) 2009 (3) 2010 (2) 2011 (2) 2012 (2) 2013 (4) 2014 (7) 2015 (27) 2016 (31) 2017 (35) 2018 (44) 2019 (33) 2020 (27) 2021 (53) 2022 (42) 2023 (23) 2024 (2) Advanced Light Microscopy (1) AG Müller/Dechend (ECRC) (1) Anchored Signalling (4) (-) Angiogenesis & Metabolism Laboratory (58) Animal Phenotyping (4) Bioinformatics and Omics Data Science (9) Biology of Malignant Lymphomas (6) Biomedical Image Analysis (1) Cancer Genetics and Cellular Stress Responses (2) Cardiac MRI (4) Cellular Neurosciences (17) Clinical Research Unit (2) Computational methodologies and omic analytics (1) Computational Regulatory Genomics (6) Developmental Biology / Signal Transduction (7) Developmental Neurobiology (1) Epigenetic Regulation and Chromatin Architecture (7) Experimental Ultrahigh-Field MR (20) Gastrointestinal Barrier, Regeneration and Carcinogenesis (1) Genetics and Genomics of Cardiovascular Diseases (9) Genetics of Metabolic and Reproductive Disorders (19) Genome Diversification & Integrity (2) Genome Engineering & Disease Models (38) (-) Genomics (291) Host-microbiome factors in cardiovascular disease (2) Hypertension-caused End-Organ Damage (1) Hypertension-Mediated End-Organ Damage (1) Immune Mechanisms and Human Antibodies (4) Immune Regulation and Cancer (84) Integrative Vascular Biology (8) Magnetic Resonance (20) Mathematical Modelling of Cellular Processes (1) Microenvironmental Regulation in Autoimmunity and Cancer (1) Mobile DNA (1) Molecular Biology of Peptide Hormones (2) Molecular Genetics of Chronic Inflammation and Allergic Disease (2) Molecular Physiology of Somatic Sensation (1) Myology (1) Non-coding RNAs and Mechanisms of Cytoplasmic Gene Regulation (1) Organoids (1) Out-patient Clinic for Neuroimmunology (1) Out-patient Clinic for Pediatric Allergology and Atopic Dermatitis (2) Pluripotent Stem Cells (5) Protein Production and Characterization (1) Proteome Dynamics (9) Proteomics (8) Proteomics and Metabolomics (5) Proteomics and Molecular Mechanisms of Neurodegenerative Diseases (3) Psychoneuroimmunology (4) Quantitative Developmental Biology (1) RNA Biology and Posttranscriptional Regulation (56) Structural Biology of Membrane-Associated Processes (1) Systems Biology Imaging (1) Systems Biology of Gene Regulatory Elements (16) Transgenics (38) Translational Bioinformatics (12) Translational Tumorimmunology (1) 349 Results: Active Filter: Altmueller, Janine Dr.med.Harabula, Izabela-CezaraLupianez Garcia, Dario Jesus Dr.Potente, Michael Prof. Dr.Rajewsky, Klaus Prof. Dr.Semtner, Marcus Dr.Sholokh, AnastasiiaWyler, Emanuel Dr.Angiogenesis & Metabolism LaboratoryGenomics Sort: Result score Newest to oldest Oldest to newest January 01, 2002 / Hum Mol Genet STAT6 as an asthma candidate gene: polymorphism-screening, association and haplotype analysis in a Caucasian sib-pair study G. Duetsch T. Illig S. Loesgen K. Rohde N. Klopp N. Herbon H. Gohlke J. Altmueller M. Wjst February 01, 2022 / Am J Med Genet A Genomic basis of syndromic short stature in an Algerian patient cohort S. Moosa F. Chentli J. Altmüller N. Bögershausen P. Nürnberg G. Yigit Y. Li B. Wollnik April 01, 2021 / Nat Cell Biol Control of endothelial quiescence by FOXO-regulated metabolites J. Andrade C. Shi A.S.H. Costa J. Choi J. Kim A. Doddaballapur T. Sugino Y.T. Ong M. Castro B. Zimmermann M. Kaulich S. Guenther K. Wilhelm Y. Kubota T. Braun G.Y. Koh A.R. Grosso C. Frezza M. Potente June 10, 2021 / Nature PIK3CA and CCM mutations fuel cavernomas through a cancer-like mechanism A.A. Ren D.A. Snellings Y.S. Su C.C. Hong M. Castro A.T. Tang M.R. Detter N. Hobson R. Girard S. Romanos R. Lightle T. Moore R. Shenkar C. Benavides M.M. Beaman H. Mueller-Fielitz M. Chen P. Mericko J. Yang D.C. Sung M.T. Lawton M. Ruppert M. Schwaninger J. Körbelin M. Potente I.A. Awad D.A. Marchuk M.L. Kahn January 01, 2022 / Am J Med Genet A A novel homozygous synonymous variant further expands the phenotypic spectrum of POLR3A-related pathologies D. Lessel K. Rading S.E. Campbell H. Thiele J. Altmüller L.B. Gordon C. Kubisch December 01, 2021 / Hum Genet Biallelic variants in YRDC cause a developmental disorder with progeroid features J. Schmidt J. Goergens T. Pochechueva A. Kotter N. Schwenzer M. Sitte G. Werner J. Altmueller H. Thiele P. Nürnberg J. Isensee Y. Li C. Müller B. Leube H.C. Reinhardt T. Hucho G. Salinas M. Helm R.D. Jachimowicz D. Wieczorek T. Kohl S.E. Lehnart G. Yigit B. Wollnik May 16, 2022 / EMBO J Human UPF3A and UPF3B enable fault-tolerant activation of nonsense-mediated mRNA decay D. Wallmeroth J.W. Lackmann S. Kueckelmann J. Altmüller C. Dieterich V. Boehm N.H. Gehring November 01, 2021 / J Am Soc Nephrol mTOR-activating mutations in RRAGD are causative for kidney tubulopathy and cardiomyopathy K.P. Schlingmann F. Jouret K. Shen A. Nigam F. Arjona C. Dafinger P. Houillier D. Jones F. Kleinerüschkamp J. Oh N. Godefroid M. Eltan T. Güran S. Burtey M.C. Parotte J. König A. Braun C. Bos M.I. Serra H. Rehmann F. Zwartkruis K. Renkema K. Klingel E. Schulze-Bahr B. Schermer C. Bergmann J. Altmüller H. Thiele B. Beck K. Dahan D. Sabatini M. Liebau R. Vargas-Poussou N. Knoers M. Konrad J. de Baaij October 01, 2021 / Genes A homozygous AKNA frameshift variant is associated with microcephaly in a Pakistani family S.S. Waseem A. Moawia B. Budde M. Tariq A. Khan Z. Ali S. Khan M. Iqbal N.A. Malik S.U. Haque J. Altmüller H. Thiele M.S. Hussain S. Cirak S.M. Baig P. Nürnberg February 01, 2022 / Eur J Hum Genet Familial cleft tongue caused by a unique translation initiation codon variant in TP63 J. Schmidt G. Schreiber J. Altmüller H. Thiele P. Nürnberg Y. Li S. Kaulfuß R. Funke B. Wilken G. Yigit B. Wollnik Pagination Current page 1 Page 2 Page 3 Page 4 … Next page Next › Last page Last »
January 01, 2002 / Hum Mol Genet STAT6 as an asthma candidate gene: polymorphism-screening, association and haplotype analysis in a Caucasian sib-pair study G. Duetsch T. Illig S. Loesgen K. Rohde N. Klopp N. Herbon H. Gohlke J. Altmueller M. Wjst
February 01, 2022 / Am J Med Genet A Genomic basis of syndromic short stature in an Algerian patient cohort S. Moosa F. Chentli J. Altmüller N. Bögershausen P. Nürnberg G. Yigit Y. Li B. Wollnik
April 01, 2021 / Nat Cell Biol Control of endothelial quiescence by FOXO-regulated metabolites J. Andrade C. Shi A.S.H. Costa J. Choi J. Kim A. Doddaballapur T. Sugino Y.T. Ong M. Castro B. Zimmermann M. Kaulich S. Guenther K. Wilhelm Y. Kubota T. Braun G.Y. Koh A.R. Grosso C. Frezza M. Potente
June 10, 2021 / Nature PIK3CA and CCM mutations fuel cavernomas through a cancer-like mechanism A.A. Ren D.A. Snellings Y.S. Su C.C. Hong M. Castro A.T. Tang M.R. Detter N. Hobson R. Girard S. Romanos R. Lightle T. Moore R. Shenkar C. Benavides M.M. Beaman H. Mueller-Fielitz M. Chen P. Mericko J. Yang D.C. Sung M.T. Lawton M. Ruppert M. Schwaninger J. Körbelin M. Potente I.A. Awad D.A. Marchuk M.L. Kahn
January 01, 2022 / Am J Med Genet A A novel homozygous synonymous variant further expands the phenotypic spectrum of POLR3A-related pathologies D. Lessel K. Rading S.E. Campbell H. Thiele J. Altmüller L.B. Gordon C. Kubisch
December 01, 2021 / Hum Genet Biallelic variants in YRDC cause a developmental disorder with progeroid features J. Schmidt J. Goergens T. Pochechueva A. Kotter N. Schwenzer M. Sitte G. Werner J. Altmueller H. Thiele P. Nürnberg J. Isensee Y. Li C. Müller B. Leube H.C. Reinhardt T. Hucho G. Salinas M. Helm R.D. Jachimowicz D. Wieczorek T. Kohl S.E. Lehnart G. Yigit B. Wollnik
May 16, 2022 / EMBO J Human UPF3A and UPF3B enable fault-tolerant activation of nonsense-mediated mRNA decay D. Wallmeroth J.W. Lackmann S. Kueckelmann J. Altmüller C. Dieterich V. Boehm N.H. Gehring
November 01, 2021 / J Am Soc Nephrol mTOR-activating mutations in RRAGD are causative for kidney tubulopathy and cardiomyopathy K.P. Schlingmann F. Jouret K. Shen A. Nigam F. Arjona C. Dafinger P. Houillier D. Jones F. Kleinerüschkamp J. Oh N. Godefroid M. Eltan T. Güran S. Burtey M.C. Parotte J. König A. Braun C. Bos M.I. Serra H. Rehmann F. Zwartkruis K. Renkema K. Klingel E. Schulze-Bahr B. Schermer C. Bergmann J. Altmüller H. Thiele B. Beck K. Dahan D. Sabatini M. Liebau R. Vargas-Poussou N. Knoers M. Konrad J. de Baaij
October 01, 2021 / Genes A homozygous AKNA frameshift variant is associated with microcephaly in a Pakistani family S.S. Waseem A. Moawia B. Budde M. Tariq A. Khan Z. Ali S. Khan M. Iqbal N.A. Malik S.U. Haque J. Altmüller H. Thiele M.S. Hussain S. Cirak S.M. Baig P. Nürnberg
February 01, 2022 / Eur J Hum Genet Familial cleft tongue caused by a unique translation initiation codon variant in TP63 J. Schmidt G. Schreiber J. Altmüller H. Thiele P. Nürnberg Y. Li S. Kaulfuß R. Funke B. Wilken G. Yigit B. Wollnik