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) Conrad, Thomas Dr. (2) Diecke, Sebastian Dr. (1) Faustino Martins, Jorge Miguel (1) Fischer, Cornelius Dr. (4) Gerhardt, Holger Prof. Dr. (1) Gouti, Mina Dr. (1) Kabuss, Loreen-Claudine (1) Kunz, Severine Dr. (1) Plumbom, Izabela (1) Quedenau, Claudia (1) Rajewsky, Klaus Prof. Dr. (1) Spuler, Simone Prof. (1) Sunaga-Franze, Daniele Yumi Dr. (3) Urzi, Alessia (1) (-) Altmueller, Janine Dr.med. (25) (-) Harabula, Izabela-Cezara (1) (-) Lupianez Garcia, Dario Jesus Dr. (1) (-) Potente, Michael Prof. Dr. (5) 1999 (1) 2002 (2) 2003 (1) 2005 (5) 2007 (1) 2008 (4) 2009 (3) 2010 (2) 2011 (2) 2012 (2) 2013 (4) 2015 (6) (-) 2016 (3) 2017 (4) 2018 (6) 2019 (6) (-) 2020 (27) 2021 (50) 2022 (44) 2023 (1) (-) Angiogenesis & Metabolism Laboratory (5) Bioinformatics (1) Cellular Neurosciences (5) Computational Regulatory Genomics (2) Epigenetic Regulation and Chromatin Architecture (1) Epigenetics and Sex Development (4) Experimental Ultrahigh-Field MR (6) Genetics, Nephrology, Hypertension, and Vascular Injury (1) Genetics of Metabolic and Reproductive Disorders (1) Genome Engineering & Disease Models (3) (-) Genomics (25) Immune Regulation and Cancer (7) Integrative Vascular Biology (1) Pluripotent Stem Cells (1) Proteome Dynamics (1) Proteomics (1) Proteomics Metabolomics (1) Psychoneuroimmunology (1) RNA Biology and Posttranscriptional Regulation (4) 30 Results: Active Filter: Altmueller, Janine Dr.med.Harabula, Izabela-CezaraLupianez Garcia, Dario Jesus Dr.Potente, Michael Prof. Dr.Angiogenesis & Metabolism LaboratoryGenomics20162020 Sort: Result score Newest to oldest Oldest to newest December 31, 2020 in Sci Rep Genetic information from discordant sibling pairs points to ESRP2 as a candidate trans-acting regulator of the CF modifier gene SCNN1B T. Becker A. Pich S. Tamm S. Hedtfeld M. Ibrahim J. Altmüller N. Dalibor M.R. Toliat S. Janciauskiene B. Tümmler F. Stanke December 10, 2020 in Blood Noncanonical effector functions of the T-memory-like T-PLL cell are shaped by cooperative TCL1A and TCR signaling S. Oberbeck A. Schrader K. Warner D. Jungherz G. Crispatzu J. von Jan M. Chmielewski A. Ianevski H.H. Diebner P. Mayer A. Kondo Ados L. Wahnschaffe T. Braun T.A. Müller P. Wagle A. Bouska T. Neumann S. Pützer L. Varghese N. Pflug M. Thelen J. Makalowski N. Riet H.J.M Göx G. Rappl J. Altmüller M. Kotrová T. Persigehl G. Hopfinger M.L. Hansmann H. Schlößer S. Stilgenbauer J. Dürig D. Mougiakakos M. von Bergwelt-Baildon I. Roeder S. Hartmann M. Hallek R. Moriggl M. Brüggemann T. Aittokallio J. Iqbal S. Newrzela H. Abken M. Herling December 01, 2020 in Am J Med Genet A Evidence of pathogenicity for the leaky splice variant c.1066-6T>G in ATM S. Schröder B. Wieland A. Ohlenbusch G. Yigit J. Altmüller E. Boltshauser T. Dörk K. Brockmann November 01, 2020 in Hum Genet De novo mutations in FBRSL1 cause a novel recognizable malformation and intellectual disability syndrome R. Ufartes H. Berger K. Till G. Salinas M. Sturm J. Altmüller P. Nürnberg H. Thiele R. Funke N. Apeshiotis H. Langen B. Wollnik A. Borchers S. Pauli October 28, 2020 in Nat Commun YAP and TAZ protect against white adipocyte cell death during obesity L. Wang S.P. Wang Y. Shi R. Li S. Günther Y.T. Ong M. Potente Z. Yuan E. Liu S. Offermanns October 01, 2020 in Eur J Hum Genet A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome T.G. Drivas D. Li D. Nair J.T. Alaimo M. Alders J. Altmüller T.S. Barakat E.M. Bebin N.L. Bertsch P.R. Blackburn A. Blesson A.M. Bouman K. Brockmann P. Brunelle M. Burmeister G.M. Cooper J. Denecke A. Dieux-Coëslier H. Dubbs A. Ferrer D. Gal L.E. Bartik L.B. Gunderson L. Hasadsri M. Jain C. Karimov B. Keena E.W. Klee K. Kloth B. Lace M. Macchiaiolo J.L. Marcadier J.M. Milunsky M.P. Napier X.R. Ortiz-Gonzalez P.N. Pichurin J. Pinner Z. Powis C. Prasad F.C. Radio K.J. Rasmussen D.L. Renaud E.T. Rush C. Saunders D. Selcen A.R. Seman D.N. Shinde E.D. Smith T. Smol L. Snijders Blok J.M. Stoler S. Tang M. Tartaglia M.L. Thompson J.M. van de Kamp J. Wang D. Weise K. Weiss R. Woitschach B. Wollnik H. Yan E.H. Zackai G. Zampino P. Campeau E. Bhoj October 01, 2020 in Clin Nephrol Long-term data on two sisters with C3GN due to an identical, homozygous CFH mutation and autoantibodies A. Hackl F. Erger C. Skerka A. Wenzel N. Tschernoster R. Ehren K. Burgmaier V. Riehmer C. Licht M. Kirschfink L.T. Weber J. Altmueller P.F. Zipfel S. Habbig October 01, 2020 in J Mol Diagn Analysis of driver mutational hot spots in blood-derived cell-free DNA of patients with primary central nervous system lymphoma obtained before intracerebral biopsy M. Montesinos-Rongen A. Brunn A. Tuchscherer P. Borchmann E. Schorb B. Kasenda J. Altmüller G. Illerhaus M.I. Ruge M. Maarouf R. Büttner M.L. Hansmann M. Hallek M. Prinz R. Siebert M. Deckert September 21, 2020 in eLife Apelin signaling drives vascular endothelial cells towards a pro-angiogenic state C.S.M. Helker J. Eberlein K. Wilhelm T. Sugino J. Malchow A. Schuermann S. Baumeister H.B. Kwon H.M. Maischein M. Potente W. Herzog D.Y.R. Stainier September 15, 2020 in Circulation Intronic CRISPR repair in a preclinical model of Noonan syndrome-associated cardiomyopathy U. Hanses M. Kleinsorge L. Roos G. Yigit Y. Li B. Barbarics I. El-Battrawy H. Lan M. Tiburcy R. Hindmarsh C. Lenz G. Salinas S. Diecke C. Müller I. Adham J. Altmüller P. Nürnberg T. Paul W.H. Zimmermann G. Hasenfuss B. Wollnik L. Cyganek Pagination Current page 1 Page 2 Page 3 Next page Next › Last page Last »
December 31, 2020 in Sci Rep Genetic information from discordant sibling pairs points to ESRP2 as a candidate trans-acting regulator of the CF modifier gene SCNN1B T. Becker A. Pich S. Tamm S. Hedtfeld M. Ibrahim J. Altmüller N. Dalibor M.R. Toliat S. Janciauskiene B. Tümmler F. Stanke
December 10, 2020 in Blood Noncanonical effector functions of the T-memory-like T-PLL cell are shaped by cooperative TCL1A and TCR signaling S. Oberbeck A. Schrader K. Warner D. Jungherz G. Crispatzu J. von Jan M. Chmielewski A. Ianevski H.H. Diebner P. Mayer A. Kondo Ados L. Wahnschaffe T. Braun T.A. Müller P. Wagle A. Bouska T. Neumann S. Pützer L. Varghese N. Pflug M. Thelen J. Makalowski N. Riet H.J.M Göx G. Rappl J. Altmüller M. Kotrová T. Persigehl G. Hopfinger M.L. Hansmann H. Schlößer S. Stilgenbauer J. Dürig D. Mougiakakos M. von Bergwelt-Baildon I. Roeder S. Hartmann M. Hallek R. Moriggl M. Brüggemann T. Aittokallio J. Iqbal S. Newrzela H. Abken M. Herling
December 01, 2020 in Am J Med Genet A Evidence of pathogenicity for the leaky splice variant c.1066-6T>G in ATM S. Schröder B. Wieland A. Ohlenbusch G. Yigit J. Altmüller E. Boltshauser T. Dörk K. Brockmann
November 01, 2020 in Hum Genet De novo mutations in FBRSL1 cause a novel recognizable malformation and intellectual disability syndrome R. Ufartes H. Berger K. Till G. Salinas M. Sturm J. Altmüller P. Nürnberg H. Thiele R. Funke N. Apeshiotis H. Langen B. Wollnik A. Borchers S. Pauli
October 28, 2020 in Nat Commun YAP and TAZ protect against white adipocyte cell death during obesity L. Wang S.P. Wang Y. Shi R. Li S. Günther Y.T. Ong M. Potente Z. Yuan E. Liu S. Offermanns
October 01, 2020 in Eur J Hum Genet A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome T.G. Drivas D. Li D. Nair J.T. Alaimo M. Alders J. Altmüller T.S. Barakat E.M. Bebin N.L. Bertsch P.R. Blackburn A. Blesson A.M. Bouman K. Brockmann P. Brunelle M. Burmeister G.M. Cooper J. Denecke A. Dieux-Coëslier H. Dubbs A. Ferrer D. Gal L.E. Bartik L.B. Gunderson L. Hasadsri M. Jain C. Karimov B. Keena E.W. Klee K. Kloth B. Lace M. Macchiaiolo J.L. Marcadier J.M. Milunsky M.P. Napier X.R. Ortiz-Gonzalez P.N. Pichurin J. Pinner Z. Powis C. Prasad F.C. Radio K.J. Rasmussen D.L. Renaud E.T. Rush C. Saunders D. Selcen A.R. Seman D.N. Shinde E.D. Smith T. Smol L. Snijders Blok J.M. Stoler S. Tang M. Tartaglia M.L. Thompson J.M. van de Kamp J. Wang D. Weise K. Weiss R. Woitschach B. Wollnik H. Yan E.H. Zackai G. Zampino P. Campeau E. Bhoj
October 01, 2020 in Clin Nephrol Long-term data on two sisters with C3GN due to an identical, homozygous CFH mutation and autoantibodies A. Hackl F. Erger C. Skerka A. Wenzel N. Tschernoster R. Ehren K. Burgmaier V. Riehmer C. Licht M. Kirschfink L.T. Weber J. Altmueller P.F. Zipfel S. Habbig
October 01, 2020 in J Mol Diagn Analysis of driver mutational hot spots in blood-derived cell-free DNA of patients with primary central nervous system lymphoma obtained before intracerebral biopsy M. Montesinos-Rongen A. Brunn A. Tuchscherer P. Borchmann E. Schorb B. Kasenda J. Altmüller G. Illerhaus M.I. Ruge M. Maarouf R. Büttner M.L. Hansmann M. Hallek M. Prinz R. Siebert M. Deckert
September 21, 2020 in eLife Apelin signaling drives vascular endothelial cells towards a pro-angiogenic state C.S.M. Helker J. Eberlein K. Wilhelm T. Sugino J. Malchow A. Schuermann S. Baumeister H.B. Kwon H.M. Maischein M. Potente W. Herzog D.Y.R. Stainier
September 15, 2020 in Circulation Intronic CRISPR repair in a preclinical model of Noonan syndrome-associated cardiomyopathy U. Hanses M. Kleinsorge L. Roos G. Yigit Y. Li B. Barbarics I. El-Battrawy H. Lan M. Tiburcy R. Hindmarsh C. Lenz G. Salinas S. Diecke C. Müller I. Adham J. Altmüller P. Nürnberg T. Paul W.H. Zimmermann G. Hasenfuss B. Wollnik L. Cyganek
