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) Chekulaeva, Marina Dr. (1) Deubzer, Hedwig PD Dr. med. (1) Diecke, Sebastian Dr. (1) Faustino Martins, Jorge Miguel (1) 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. (10) Mastrobuoni, Guido Dr. (1) Milek, Miha Dr. (2) Minia, Igor Dr. (1) Monti, Remo (1) Obermayer-Wasserscheid, Benedikt Dr. (1) Ohler, Uwe Prof. Dr. (15) 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) Worsley Hunt, Christine Rebecca Dr. (1) Wyler, Emanuel Dr. (4) Zauber, Henrik Dr. (1) (-) Altmueller, Janine Dr.med. (25) (-) Conrad, Thomas Dr. (2) (-) Fischer, Cornelius Dr. (4) (-) Lupianez Garcia, Dario Jesus Dr. (1) 2002 (1) 2005 (2) 2015 (3) (-) 2016 (2) 2017 (1) 2018 (4) 2019 (6) (-) 2020 (29) 2021 (46) 2022 (45) Bioinformatics (1) Cellular Neurosciences (5) Developmental Biology / Signal Transduction (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 (31) Immune Regulation and Cancer (6) Myology (1) Pluripotent Stem Cells (1) Proteomics (1) Psychoneuroimmunology (1) Stem Cell Modeling of Development and Disease (1) 31 Results: Active Filter: Altmueller, Janine Dr.med.Conrad, Thomas Dr.Fischer, Cornelius Dr.Lupianez Garcia, Dario Jesus Dr.Genomics20162020 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 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 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 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 18, 2020 in Sci Adv Viral cGAMP nuclease reveals the essential role of DNA sensing in protection against acute lethal virus infection B. Hernáez G. Alonso I. Georgana M. El-Jesr R. Martín K.H.Y. Shair C. Fischer S. Sauer C. Maluquer de Motes A. Alcamí 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 Page 4 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 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 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 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 18, 2020 in Sci Adv Viral cGAMP nuclease reveals the essential role of DNA sensing in protection against acute lethal virus infection B. Hernáez G. Alonso I. Georgana M. El-Jesr R. Martín K.H.Y. Shair C. Fischer S. Sauer C. Maluquer de Motes A. Alcamí
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
