Entries of Horsthemke, Bernhard on the publication server

Schröder, Christopher, Leitão, Elsa, Wallner, Stefan, Schmitz, Gerd, Klein-Hitpass, Ludger, Sinha, Anupam, Jöckel, Karl-Heinz, Heilmann-Heimbach, Stefanie , Hoffmann, Per, Nöthen, Markus M., Steffens, Michael, Ebert, Peter , 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 (1). Fulltext not available.

Wallner, Stefan, Schröder, Christopher, Leitão, Elsa, Berulava, Tea, Haak, Claudia, Beißer, Daniela, Rahmann, Sven, Richter, Andreas S. , Manke, Thomas , Bönisch, Ulrike, Arrigoni, Laura , Fröhler, Sebastian, Klironomos, Filippos, Chen, Wei, Rajewsky, Nikolaus, Müller, Fabian, Ebert, Peter , Lengauer, Thomas, Barann, Matthias, Rosenstiel, Philip , Gasparoni, Gilles, Nordström, Karl, Walter, Jörn, Brors, Benedikt , Zipprich, Gideon, Felder, Bärbel, Klein-Hitpass, Ludger, Attenberger, Corinna, Schmitz, Gerd and Horsthemke, Bernhard (2016) Epigenetic dynamics of monocyte-to-macrophage differentiation. Epigenetics & Chromatin 9 (1). Fulltext not available.

Wieczorek, Dagmar, Newman, William G. , Wieland, Thomas, Berulava, Tea, Kaffe, Maria, Falkenstein, Daniela, Beetz, Christian , Graf, Elisabeth, Schwarzmayr, Thomas, Douzgou, Sofia, Clayton-Smith, Jill, Daly, Sarah B., Williams, Simon G. , Bhaskar, Sanjeev S., Urquhart, Jill E. , Anderson, Beverley, O’Sullivan, James, Boute, Odile, Gundlach, Jasmin, Czeschik, Johanna Christina, van Essen, Anthonie J., Hazan, Filiz, Park, Sarah, Hing, Anne, Kuechler, Alma, Lohmann, Dietmar R. , Ludwig, Kerstin U., Mangold, Elisabeth, Steenpaß, Laura, Zeschnigk, Michael, Lemke, Johannes R., Lourenco, Charles Marques, Hehr, Ute, Prott, Eva-Christina, Waldenberger, Melanie, Böhmer, Anne C., Horsthemke, Bernhard, O’Keefe, Raymond T., Meitinger, Thomas , Burn, John, Lüdecke, Hermann-Josef and Strom, Tim M. (2014) Compound Heterozygosity of Low-Frequency Promoter Deletions and Rare Loss-of-Function Mutations in TXNL4A Causes Burn-McKeown Syndrome. The American Journal of Human Genetics 95 (6), pp. 698-707. Fulltext not available.

Rademacher, Katrin, Schröder, Christopher, Kanber, Deniz, Klein-Hitpass, Ludger, Wallner, Stefan, Zeschnigk, Michael and Horsthemke, Bernhard (2014) Evolutionary Origin and Methylation Status of Human Intronic CpG Islands that Are Not Present in Mouse. Genome Biology and Evolution 6 (7), pp. 1579-1588. Fulltext not available.