| Quantitative analysis of global ubiquitination in HeLa cells by mass spectrometry D Meierhofer, X Wang, L Huang, P Kaiser Journal of proteome research 7 (10), 4566-4576, 2008 | 245 | 2008 |
| Decrease of mitochondrial DNA content and energy metabolism in renal cell carcinoma D Meierhofer, JA Mayr, U Foetschl, A Berger, K Fink, N Schmeller, ... Carcinogenesis 25 (6), 1005-1010, 2004 | 178 | 2004 |
| Loss of complex I due to mitochondrial DNA mutations in renal oncocytoma JA Mayr, D Meierhofer, F Zimmermann, R Feichtinger, C Kögler, ... Clinical Cancer Research 14 (8), 2270-2275, 2008 | 159 | 2008 |
| Advantages and pitfalls of mass spectrometry based metabolome profiling in systems biology I Aretz, D Meierhofer International journal of molecular sciences 17 (5), 632, 2016 | 157 | 2016 |
| Human iPSC-derived neural progenitors are an effective drug discovery model for neurological mtDNA disorders C Lorenz, P Lesimple, R Bukowiecki, A Zink, G Inak, B Mlody, M Singh, ... Cell stem cell 20 (5), 659-674. e9, 2017 | 134 | 2017 |
| Novel real-time prediction of liver graft function during hypothermic oxygenated machine perfusion before liver transplantation X Muller, A Schlegel, P Kron, D Eshmuminov, M Würdinger, D Meierhofer, ... Annals of surgery 270 (5), 783-790, 2019 | 122 | 2019 |
| Lipoic acid synthetase deficiency causes neonatal-onset epilepsy, defective mitochondrial energy metabolism, and glycine elevation JA Mayr, FA Zimmermann, C Fauth, C Bergheim, D Meierhofer, ... The American Journal of Human Genetics 89 (6), 792-797, 2011 | 118 | 2011 |
| Serial interactome capture of the human cell nucleus T Conrad, AS Albrecht, VR de Melo Costa, S Sauer, D Meierhofer, ... Nature communications 7 (1), 11212, 2016 | 116 | 2016 |
| A Y2H-seq approach defines the human protein methyltransferase interactome M Weimann, A Grossmann, J Woodsmith, Z Özkan, P Birth, D Meierhofer, ... Nature methods 10 (4), 339-342, 2013 | 105 | 2013 |
| Severe depletion of mitochondrial DNA in spinal muscular atrophy A Berger, JA Mayr, D Meierhofer, U Fötschl, R Bittner, H Budka, C Grethen, ... Acta neuropathologica 105 (3), 245-251, 2003 | 83 | 2003 |
| Ataxin-2 (Atxn2)-knock-out mice show branched chain amino acids and fatty acids pathway alterations D Meierhofer, M Halbach, NE Şen, S Gispert, G Auburger Molecular & Cellular Proteomics 15 (5), 1728-1739, 2016 | 73 | 2016 |
| Recurrent de novo mutations affecting residue Arg138 of pyrroline-5-carboxylate synthase cause a progeroid form of autosomal-dominant cutis laxa B Fischer-Zirnsak, N Escande-Beillard, J Ganesh, YX Tan, M Al Bughaili, ... The American Journal of Human Genetics 97 (3), 483-492, 2015 | 70 | 2015 |
| Progression of pathology in PINK1-deficient mouse brain from splicing via ubiquitination, ER stress, and mitophagy changes to neuroinflammation S Torres-Odio, J Key, HH Hoepken, J Canet-Pons, L Valek, B Roller, ... Journal of neuroinflammation 14 (1), 1-26, 2017 | 65 | 2017 |
| Metabolome and proteome profiling of complex I deficiency induced by rotenone I Gielisch, D Meierhofer Journal of proteome research 14 (1), 224-235, 2015 | 65 | 2015 |
| Mitochondrial DNA mutations in renal cell carcinomas revealed no general impact on energy metabolism D Meierhofer, JA Mayr, K Fink, N Schmeller, B Kofler, W Sperl British journal of cancer 94 (2), 268-274, 2006 | 65 | 2006 |
| SON and SRRM2 are essential for nuclear speckle formation İA Ilik, M Malszycki, AK Lübke, C Schade, D Meierhofer, T Aktaş Elife 9, e60579, 2020 | 64 | 2020 |
| Hypothermic oxygenated perfusion protects from mitochondrial injury before liver transplantation A Schlegel, X Muller, M Mueller, A Stepanova, P Kron, O de Rougemont, ... EBioMedicine 60, 103014, 2020 | 60 | 2020 |
| Efficient prevention of neurodegenerative diseases by depletion of starvation response factor Ataxin-2 G Auburger, NE Sen, D Meierhofer, AN Başak, AD Gitler Trends in neurosciences 40 (8), 507-516, 2017 | 60 | 2017 |
| Glutathione metabolism in renal cell carcinoma progression and implications for therapies Y Xiao, D Meierhofer International journal of molecular sciences 20 (15), 3672, 2019 | 59 | 2019 |
| Mutations in subunits of the activating signal cointegrator 1 complex are associated with prenatal spinal muscular atrophy and congenital bone fractures E Knierim, H Hirata, NI Wolf, S Morales-Gonzalez, G Schottmann, ... The American Journal of Human Genetics 98 (3), 473-489, 2016 | 59 | 2016 |
Bernd TimmermannMax Planck Institute for Molecular Genetics, Berlin, GermanyVerified email at molgen.mpg.de
