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) Beule, Dieter Dr. (1) Birchmeier-Kohler, Carmen Prof. Dr. (1) Braeuning, Caroline (1) Burkert, Christian Martin (1) Diecke, Sebastian Dr. (1) Fischer, Cornelius Dr. (4) Ghanbari, Mahsa Dr. (1) Gouti, Mina Dr. (1) Harabula, Izabela-Cezara (1) Henssen, Anton Dr. med. (1) Hirsekorn, Antje (3) Kabuss, Loreen-Claudine (1) Kempa, Stefan Dr. (1) Kopp, Wolfgang Dr. (1) Kunz, Severine Dr. (1) Lacadie, Scott Allen Dr. (1) Landthaler, Markus Prof. Dr. (13) Lee, Young-Ae Prof. Dr. (1) Lupianez Garcia, Dario Jesus Dr. (1) Mastrobuoni, Guido Dr. (1) Milek, Miha Dr. (2) Minia, Igor Dr. (1) Monti, Remo (1) Obermayer-Wasserscheid, Benedikt Dr. (1) Ohler, Uwe Prof. Dr. (16) Plumbom, Izabela (1) Quedenau, Claudia (1) Rajewsky, Nikolaus Prof. Dr. (1) Röefzaad, Claudia (1) Schwarz, Roland Dr. (1) Selbach, Matthias Prof. Dr. (3) Spuler, Simone Prof. (1) Sunaga-Franze, Daniele Yumi Dr. (3) Urzi, Alessia (1) Vucicevic, Dubravka (1) Zauber, Henrik Dr. (1) (-) Altmueller, Janine Dr.med. (27) (-) Chekulaeva, Marina Dr. (1) (-) Conrad, Thomas Dr. (2) (-) Wyler, Emanuel Dr. (4) 2002 (1) (-) 2005 (2) 2012 (2) 2015 (6) (-) 2016 (5) 2017 (7) 2018 (4) 2019 (7) (-) 2020 (30) 2021 (59) 2022 (56) 2023 (1) Bioinformatics (1) Cellular Neurosciences (5) (-) Computational Regulatory Genomics (4) Developmental Biology / Signal Transduction (1) Epigenetics and Sex Development (1) Experimental Ultrahigh-Field MR (6) Genetics, Nephrology, Hypertension, and Vascular Injury (1) Genetics and Genomics of Cardiovascular Diseases (2) Genetics of Metabolic and Reproductive Disorders (2) Genome Engineering & Disease Models (3) (-) Genomics (29) Immune Regulation and Cancer (6) Molecular Genetics of Chronic Inflammation and Allergic Disease (1) Non-coding RNAs and Mechanisms of Cytoplasmic Gene Regulation (2) Out-patient Clinic for Pediatric Allergology and Atopic Dermatitis (1) Pluripotent Stem Cells (1) Proteome Dynamics (1) Proteomics (1) Proteomics Metabolomics (1) Psychoneuroimmunology (1) (-) RNA Biology and Posttranscriptional Regulation (5) 37 Results: Active Filter: Altmueller, Janine Dr.med.Chekulaeva, Marina Dr.Conrad, Thomas Dr.Wyler, Emanuel Dr.Computational Regulatory GenomicsGenomicsRNA Biology and Posttranscriptional Regulation200520162020 Sort: Result score Newest to oldest Oldest to newest December 31, 2020 / 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 / 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 / Stat Methods Med Res Using gradient boosting with stability selection on health insurance claims data to identify disease trajectories in chronic obstructive pulmonary disease T. Ploner S. Heß M. Grum P. Drewe-Boss J. Walker December 01, 2020 / 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 / RNA Determination of primary microRNA processing in clinical samples by targeted pri-miR-sequencing T. Conrad E. Ntini B. Lang L. Cozzuto J.B. Andersen J.U. Marquardt J. Ponomarenko G.G. Tartaglia U.A. Vang Orom November 01, 2020 / 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 01, 2020 / 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 / 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 / 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 17, 2020 / Cell Severe COVID-19 is marked by a dysregulated myeloid cell compartment J. Schulte-Schrepping N. Reusch D. Paclik K. Baßler S. Schlickeiser B. Zhang B. Krämer T. Krammer S. Brumhard L. Bonaguro E. De Domenico Da. Wendisch M. Grasshoff T.S. Kapellos M. Beckstette T. Pecht A. Saglam O. Dietrich H.E. Mei A.R. Schulz C. Conrad D. Kunkel E. Vafadarnejad C.J. Xu A. Horne M. Herbert A. Drews C. Thibeault M. Pfeiffer S. Hippenstiel A. Hocke H. Müller-Redetzky K.M. Heim F. Machleidt A. Uhrig L. Bosquillon de Jarcy L. Jürgens M. Stegemann C.R. Glösenkamp H.D. Volk C. Goffinet M. Landthaler E. Wyler P. Georg M. Schneider C. Dang-Heine N. Neuwinger K. Kappert R. Tauber V. Corman J. Raabe K.M. Kaiser M.T. Vinh G. Rieke C. Meisel T. Ulas M. Becker R. Geffers M. Witzenrath C. Drosten N. Suttorp C. von Kalle F. Kurth K. Händler J.L. Schultze A.C. Aschenbrenner Y. Li J. Nattermann B. Sawitzki A.E. Saliba L.E. Sander Pagination Current page 1 Page 2 Page 3 Page 4 Next page Next › Last page Last »
December 31, 2020 / 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 / 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 / Stat Methods Med Res Using gradient boosting with stability selection on health insurance claims data to identify disease trajectories in chronic obstructive pulmonary disease T. Ploner S. Heß M. Grum P. Drewe-Boss J. Walker
December 01, 2020 / 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 / RNA Determination of primary microRNA processing in clinical samples by targeted pri-miR-sequencing T. Conrad E. Ntini B. Lang L. Cozzuto J.B. Andersen J.U. Marquardt J. Ponomarenko G.G. Tartaglia U.A. Vang Orom
November 01, 2020 / 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 01, 2020 / 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 / 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 / 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 17, 2020 / Cell Severe COVID-19 is marked by a dysregulated myeloid cell compartment J. Schulte-Schrepping N. Reusch D. Paclik K. Baßler S. Schlickeiser B. Zhang B. Krämer T. Krammer S. Brumhard L. Bonaguro E. De Domenico Da. Wendisch M. Grasshoff T.S. Kapellos M. Beckstette T. Pecht A. Saglam O. Dietrich H.E. Mei A.R. Schulz C. Conrad D. Kunkel E. Vafadarnejad C.J. Xu A. Horne M. Herbert A. Drews C. Thibeault M. Pfeiffer S. Hippenstiel A. Hocke H. Müller-Redetzky K.M. Heim F. Machleidt A. Uhrig L. Bosquillon de Jarcy L. Jürgens M. Stegemann C.R. Glösenkamp H.D. Volk C. Goffinet M. Landthaler E. Wyler P. Georg M. Schneider C. Dang-Heine N. Neuwinger K. Kappert R. Tauber V. Corman J. Raabe K.M. Kaiser M.T. Vinh G. Rieke C. Meisel T. Ulas M. Becker R. Geffers M. Witzenrath C. Drosten N. Suttorp C. von Kalle F. Kurth K. Händler J.L. Schultze A.C. Aschenbrenner Y. Li J. Nattermann B. Sawitzki A.E. Saliba L.E. Sander
