Items where Author is "Rahmann, Sven"
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Markowski, Julia and Kempfer, Rieke and Kukalev, Alexander and Irastorza-Azcarate, Ibai and Loof, Gesa and Kehr, Birte and Pombo, Ana and Rahmann, Sven and Schwarz, Roland F. (2021) GAMIBHEAR: whole-genome haplotype reconstruction from Genome Architecture Mapping data. BIOINFORMATICS, 37 (19). pp. 3128-3135. ISSN 1367-4803, 1460-2059
Schroeder, Christopher and Leitao, Elsa and Wallner, Stefan and Schmitz, Gerd and Klein-Hitpass, Ludger and Sinha, Anupam and Joekel, Karl-Heinz and Heilmann-Heimbach, Stefanie and Hoffmann, Per and Noethen, Markus M. and Steffens, Michael and Ebert, Peter and Rahmann, Sven and Horsthemke, Bernhard (2017) Regions of common inter-individual DNA methylation differences in human monocytes: genetic basis and potential function. EPIGENETICS & CHROMATIN, 10: 37. ISSN 1756-8935
Wallner, Stefan and Schroeder, Christopher and Leitao, Elsa and Berulava, Tea and Haak, Claudia and Beisser, Daniela and Rahmann, Sven and Richter, Andreas S. and Manke, Thomas and Boenisch, Ulrike and Arrigoni, Laura and Froehler, Sebastian and Klironomos, Filippos and Chen, Wei and Rajewsky, Nikolaus and Mueller, Fabian and Ebert, Peter and Lengauer, Thomas and Barann, Matthias and Rosenstiel, Philip and Gasparoni, Gilles and Nordstroem, Karl and Walter, Joern and Brors, Benedikt and Zipprich, Gideon and Felder, Baerbel and Klein-Hitpass, Ludger and Attenberger, Corinna and Schmitz, Gerd and Horsthemke, Bernhard (2016) Epigenetic dynamics of monocyte-to-macrophage differentiation. EPIGENETICS & CHROMATIN, 9: 33. ISSN 1756-8935
Voigt, Claudia and Megarbane, Andre and Neveling, Kornelia and Czeschik, Johanna Christina and Albrecht, Beate and Callewaert, Bert and von Deimling, Florian and Hehr, Andreas and Smeland, Marie Falkenberg and Konig, Rainer and Kuechler, Alma and Marcelis, Carlo and Puiu, Maria and Reardon, Willie and Stensland, Hilde Monica Frostad Riise and Schweiger, Bernd and Steehouwer, Marloes and Teller, Christopher and Martin, Marcel and Rahmann, Sven and Hehr, Ute and Brunner, Han G. and Ludecke, Hermann-Josef and Wieczorek, Dagmar (2013) Oto-facial syndrome and esophageal atresia, intellectual disability and zygomatic anomalies - expanding the phenotypes associated with EFTUD2 mutations. ORPHANET JOURNAL OF RARE DISEASES, 8: 110. ISSN 1750-1172
