Entries of Heim, Katharina on the publication server

Ellinghaus, David, Baurecht, Hansjörg , Esparza-Gordillo, Jorge, Rodríguez, Elke, Matanovic, Anja, Marenholz, Ingo, Hübner, Norbert, Schaarschmidt, Heidi, Novak, Natalija, Michel, Sven, Maintz, Laura, Werfel, Thomas, Meyer-Hoffert, Ulf, Hotze, Melanie, Prokisch, Holger , Heim, Katharina, Herder, Christian, Hirota, Tomomitsu, Tamari, Mayumi, Kubo, Michiaki, Takahashi, Atsushi, Nakamura, Yusuke, Tsoi, Lam C , Stuart, Philip, Elder, James T, Sun, Liangdan, Zuo, Xianbo, Yang, Sen, Zhang, Xuejun, Hoffmann, Per, Nöthen, Markus M, Fölster-Holst, Regina, Winkelmann, Juliane , Illig, Thomas, Boehm, Bernhard O, Duerr, Richard H , Büning, Carsten, Brand, Stephan, Glas, Jürgen, McAleer, Maeve A, Fahy, Caoimhe M, Kabesch, Michael, Brown, Sara , McLean, W H Irwin , Irvine, Alan D , Schreiber, Stefan , Lee, Young-Ae, Franke, Andre and Weidinger, Stephan (2013) High-density genotyping study identifies four new susceptibility loci for atopic dermatitis. Nature Genetics 45 (7), pp. 808-812. Fulltext not available.

Hartig, Monika B., Iuso, Arcangela, Haack, Tobias, Kmiec, Tomasz , Jurkiewicz, Elzbieta , Heim, Katharina, Roeber, Sigrun, Tarabin, Victoria, Dusi, Sabrina , Krajewska-Walasek, Malgorzata , Jozwiak, Sergiusz , Hempel, Maja, Winkelmann, Juliane , Elstner, Matthias, Oexle, Konrad, Klopstock, Thomas, Mueller-Felber, Wolfgang, Gasser, Thomas, Trenkwalder, Claudia, Tiranti, Valeria , Kretzschmar, Hans, Schmitz, Gerd , Strom, Tim M., Meitinger, Thomas and Prokisch, Holger (2011) Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation. The American Journal of Human Genetics 89 (4), pp. 543-550. Fulltext not available.

Linsel-Nitschke, Patrick, Heeren, Jörg, Aherrahrou, Zouhair, Bruse, Petra, Gieger, Christian , Illig, Thomas, Prokisch, Holger , Heim, Katharina, Doering, Angela, Peters, Annette , Meitinger, Thomas , Wichmann, H.-Erich, Hinney, Anke , Reinehr, Thomas, Roth, Christian, Ortlepp, Jan. R., Soufi, Mouhidien, Sattler, Alexander M., Schaefer, Jürgen, Stark, Klaus , Hengstenberg, Christian, Schaefer, Arne, Schreiber, Stefan , Kronenberg, Florian , Samani, Nilesh J., Schunkert, Heribert and Erdmann, Jeanette (2010) Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease. Atherosclerosis 208 (1), pp. 183-189. Fulltext not available.