| Obesity-induced CerS6-dependent C16: 0 ceramide production promotes weight gain and glucose intolerance SM Turpin, HT Nicholls, DM Willmes, A Mourier, S Brodesser, ... Cell metabolism 20 (4), 678-686, 2014 | 615 | 2014 |
| Germline mitochondrial DNA mutations aggravate ageing and can impair brain development JM Ross, JB Stewart, E Hagström, S Brené, A Mourier, G Coppotelli, ... Nature 501 (7467), 412-415, 2013 | 291 | 2013 |
| MICOS coordinates with respiratory complexes and lipids to establish mitochondrial inner membrane architecture JR Friedman, A Mourier, J Yamada, JM McCaffery, J Nunnari Elife 4, e07739, 2015 | 262 | 2015 |
| Adipose-specific deletion of TFAM increases mitochondrial oxidation and protects mice against obesity and insulin resistance C Vernochet, A Mourier, O Bezy, Y Macotela, J Boucher, MJ Rardin, D An, ... Cell metabolism 16 (6), 765-776, 2012 | 255 | 2012 |
| Mitofusin 2 is required to maintain mitochondrial coenzyme Q levels A Mourier, E Motori, T Brandt, M Lagouge, I Atanassov, A Galinier, ... Journal of Cell Biology 208 (4), 429-442, 2015 | 228 | 2015 |
| Transcriptomic and proteomic landscape of mitochondrial dysfunction reveals secondary coenzyme Q deficiency in mammals I Kühl, M Miranda, I Atanassov, I Kuznetsova, Y Hinze, A Mourier, ... elife 6, e30952, 2017 | 181 | 2017 |
| Mitofusin 2 is necessary for striatal axonal projections of midbrain dopamine neurons S Lee, FH Sterky, A Mourier, M Terzioglu, S Cullheim, L Olson, ... Human molecular genetics 21 (22), 4827-4835, 2012 | 179 | 2012 |
| Adipose tissue mitochondrial dysfunction triggers a lipodystrophic syndrome with insulin resistance, hepatosteatosis, and cardiovascular complications C Vernochet, F Damilano, A Mourier, O Bezy, MA Mori, G Smyth, ... The FASEB Journal 28 (10), 4408, 2014 | 162 | 2014 |
| MTERF1 binds mtDNA to prevent transcriptional interference at the light-strand promoter but is dispensable for rRNA gene transcription regulation M Terzioglu, B Ruzzenente, J Harmel, A Mourier, E Jemt, MD Lopez, ... Cell metabolism 17 (4), 618-626, 2013 | 154 | 2013 |
| Variation in germline mtDNA heteroplasmy is determined prenatally but modified during subsequent transmission C Freyer, LM Cree, A Mourier, JB Stewart, C Koolmeister, D Milenkovic, ... Nature genetics 44 (11), 1282-1285, 2012 | 139 | 2012 |
| Mitochondrial fusion is required for regulation of mitochondrial DNA replication E Silva Ramos, E Motori, C Brüser, I Kühl, A Yeroslaviz, B Ruzzenente, ... PLoS genetics 15 (6), e1008085, 2019 | 138 | 2019 |
| Hierarchical RNA processing is required for mitochondrial ribosome assembly O Rackham, JD Busch, S Matic, SJ Siira, I Kuznetsova, I Atanassov, ... Cell reports 16 (7), 1874-1890, 2016 | 135 | 2016 |
| Changes of mitochondrial ultrastructure and function during ageing in mice and Drosophila T Brandt, A Mourier, LS Tain, L Partridge, NG Larsson, W Kühlbrandt Elife 6, e24662, 2017 | 130 | 2017 |
| POLRMT regulates the switch between replication primer formation and gene expression of mammalian mtDNA I Kühl, M Miranda, V Posse, D Milenkovic, A Mourier, SJ Siira, ... Science advances 2 (8), e1600963, 2016 | 125 | 2016 |
| MTERF3 regulates mitochondrial ribosome biogenesis in invertebrates and mammals A Wredenberg, M Lagouge, A Bratic, MD Metodiev, H Spåhr, A Mourier, ... PLoS genetics 9 (1), e1003178, 2013 | 124 | 2013 |
| The respiratory chain supercomplex organization is independent of COX7a2l isoforms A Mourier, S Matic, B Ruzzenente, NG Larsson, D Milenkovic Cell metabolism 20 (6), 1069-1075, 2014 | 123 | 2014 |
| Loss of LRPPRC causes ATP synthase deficiency A Mourier, B Ruzzenente, T Brandt, W Kühlbrandt, NG Larsson Human molecular genetics 23 (10), 2580-2592, 2014 | 119 | 2014 |
| A phenotype-driven approach to generate mouse models with pathogenic mtDNA mutations causing mitochondrial disease JHK Kauppila, HL Baines, A Bratic, ML Simard, C Freyer, A Mourier, ... Cell reports 16 (11), 2980-2990, 2016 | 114 | 2016 |
| COX7A2L is a mitochondrial complex III binding protein that stabilizes the III2+ IV supercomplex without affecting respirasome formation R Pérez-Pérez, T Lobo-Jarne, D Milenkovic, A Mourier, A Bratic, ... Cell reports 16 (9), 2387-2398, 2016 | 111 | 2016 |
| Rescue of primary ubiquinone deficiency due to a novel COQ7 defect using 2, 4–dihydroxybensoic acid C Freyer, H Stranneheim, K Naess, A Mourier, A Felser, C Maffezzini, ... Journal of medical genetics 52 (11), 779-783, 2015 | 110 | 2015 |
