Cui, H.; Schlesinger, J.; Bansal, V.; Dunkel, I.; Meierhofer, D.; Rickert-Sperling, S.: 5Regulation of myogenesis via kinase driven activation of DPF3a, a BAF complex member and its interaction with transcription repressor HEY1. Cardiovascular Research 103 (Suppl 1), S 1 (2014)

Freiwald, A.; Weidner, C.; Witzke, A.; Huang, S.-Y.; Meierhofer, D.; Sauer, S.: Comprehensive proteomic data sets for studying adipocyte-macrophage cell-cell communication. Proteomics 13 (23-24), pp. 3424 - 3428 (2013)

Meierhofer, D.; Weidner, C.; Hartmann, L.; Mayr, J. A.; Han, C.-T.; Schroeder, F. C.; Sauer, S.: Protein sets define disease states and predict in vivo effects of drug treatment. Molecular and Cellular Proteomics 12 (7), pp. 1965 - 1979 (2013)

Weimann, M.; Grossmann, A.; Woodsmith, J.; Özkan, Z.; Birth, P.; Meierhofer, D.; Benlasfer, N.; Valovka, T.; Timmermann, B.; Wanker, E. E. et al.; Sauer, S.; Stelzl, U.: A Y2H-seq approach defines the human protein methyltransferase interactome. Nature methods 10 (4), pp. 339 - 342 (2013)

Mayr, J. A.; Zimmermann, F. A.; Fauth, C.; Bergheim, C.; Meierhofer, D.; Radmayr, D.; Zschocke, J.; Koch, J.; Sperl, W.: Lipoic acid synthetase deficiency causes neonatal-onset epilepsy, defective mitochondrial energy metabolism, and glycine elevation. The American Journal of Human Genetics 89 (6), pp. 792 - 797 (2011)

Meierhofer, D.; Wang, X.; Huang, L.; Kaiser, P.: Quantitative analysis of global ubiquitination in HeLa cells by mass spectrometry. Journal of Proteome Research 7 (10), pp. 4566 - 4576 (2008)

Mayr, J. A.; Meierhofer, D.; Zimmermann, F.; Feichtinger, R.; Kögler, C.; Ratschek, M.; Schmeller, N.; Sperl, W.; Kofler, B.: Loss of complex I due to mitochondrial DNA mutations in renal oncocytoma. Clinical Cancer Research 14 (8), pp. 2270 - 2275 (2008)

Mayr, J. A.; Zimmermann, F.; Meierhofer, D.; Schmeller, N.; Sperl, W.; Kofler, B.: Biochemical consequences of a pathogenic A3243G mtDNA mutation. Mitochondrion 6 (5), pp. 268 - 269 (2006)

Wiesbauer, M.; Meierhofer, D.; Mayr, J. A.; Sperl, W.; Paulweber, B.; Kofler, B.: Multiplex primer extension analysis for rapid detection of major European mitochondrial haplogroups. Electrophoresis 27 (19), pp. 3864 - 2868 (2006)

Meierhofer, D.; Ebner, S.; Mayr, J. A.; Jones, N. D.; Kofler, B.; Sperl, W.: Platelet transfusion can mimic somatic mtDNA mutations. Leukemia: the Journal of Normal and Malignant Hemopoiese ; Official Journal of the Leukemia Research Fund U.K. 20 (2), pp. 362 - 363 (2006)