| Loss of VPS13C function in autosomal-recessive parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-dependent mitophagy S Lesage, V Drouet, E Majounie, V Deramecourt, M Jacoupy, A Nicolas, ... The American Journal of Human Genetics 98 (3), 500-513, 2016 | 414 | 2016 |
| The CoQH2/CoQ ratio serves as a sensor of respiratory chain efficiency A Guaras, E Perales-Clemente, E Calvo, R Acín-Pérez, M Loureiro-Lopez, ... Cell reports 15 (1), 197-209, 2016 | 261 | 2016 |
| Tissue-specific loss of DARS2 activates stress responses independently of respiratory chain deficiency in the heart SA Dogan, C Pujol, P Maiti, A Kukat, S Wang, S Hermans, K Senft, ... Cell metabolism 19 (3), 458-469, 2014 | 214 | 2014 |
| Import of tRNAs and aminoacyl-tRNA synthetases into mitochondria AM Duchêne, C Pujol, L Maréchal-Drouard Current genetics 55, 1-18, 2009 | 146 | 2009 |
| How can organellar protein N-terminal sequences be dual targeting signals? In silico analysis and mutagenesis approach C Pujol, L Maréchal-Drouard, AM Duchêne Journal of molecular biology 369 (2), 356-367, 2007 | 76 | 2007 |
| Inhibition of lysosome membrane recycling causes accumulation of gangliosides that contribute to neurodegeneration M Boutry, J Branchu, C Lustremant, C Pujol, J Pernelle, R Matusiak, ... Cell reports 23 (13), 3813-3826, 2018 | 72 | 2018 |
| Dual-targeted tRNA-dependent amidotransferase ensures both mitochondrial and chloroplastic Gln-tRNAGln synthesis in plants C Pujol, M Bailly, D Kern, L Maréchal-Drouard, H Becker, AM Duchêne Proceedings of the National Academy of Sciences 105 (17), 6481-6485, 2008 | 71 | 2008 |
| Characterization of Arabidopsis thaliana genes encoding functional homologues of the yeast metal chaperone Cox19p, involved in cytochrome c oxidase biogenesis CV Attallah, E Welchen, C Pujol, G Bonnard, DH Gonzalez Plant molecular biology 65, 343-355, 2007 | 54 | 2007 |
| Defining the determinants for dual targeting of amino acyl-tRNA synthetases to mitochondria and chloroplasts AK Berglund, C Pujol, AM Duchene, E Glaser Journal of molecular biology 393 (4), 803-814, 2009 | 49 | 2009 |
| Succinate Dehydrogenase Upregulation Destabilize Complex I and Limits the Lifespan of gas-1 Mutant C Pujol, I Bratic-Hench, M Sumakovic, J Hench, A Mourier, L Baumann, ... PloS one 8 (3), e59493, 2013 | 39 | 2013 |
| French Parkinson’s Disease Genetics Study (PDG), International Parkinson’s Disease Genomics Consortium (IPDGC). 2016. Loss of VPS13C Function in Autosomal-Recessive … S Lesage, V Drouet, E Majounie, V Deramecourt, M Jacoupy, A Nicolas, ... Am J Hum Genet 98, 500-513, 0 | 37 | |
| CYP2U1 activity is altered by missense mutations in hereditary spastic paraplegia 56 CM Durand, L Dhers, C Tesson, A Tessa, L Fouillen, S Jacqueré, ... Human Mutation 39 (1), 140-151, 2018 | 27 | 2018 |
| FGF21 modulates mitochondrial stress response in cardiomyocytes only under mild mitochondrial dysfunction M Croon, K Szczepanowska, M Popovic, C Lienkamp, K Senft, ... Science Advances 8 (14), eabn7105, 2022 | 26 | 2022 |
| A Tissue-Specific Approach to the Analysis of Metabolic Changes in Caenorhabditis elegans J Hench, I Bratić Hench, C Pujol, S Ipsen, S Brodesser, A Mourier, ... PLoS One 6 (12), e28417, 2011 | 22 | 2011 |
| S. French Parkinson’s Disease Genetics, and C. International Parkinson’s Disease Genomics. 2016. Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes … S Lesage, V Drouet, E Majounie, V Deramecourt, M Jacoupy, A Nicolas, ... Am J Hum Genet 98 (3), 500-513, 0 | 18 | |
| Implication of folate deficiency in CYP2U1 loss of function C Pujol, A Legrand, L Parodi, P Thomas, F Mochel, D Saracino, G Coarelli, ... Journal of Experimental Medicine 218 (11), e20210846, 2021 | 16 | 2021 |
| Pseudoxanthoma elasticum overlaps hereditary spastic paraplegia type 56 A Legrand, C Pujol, CM Durand, A Mesnil, I Rubera, C Duranton, S Zuily, ... Journal of Internal Medicine 289 (5), 709-725, 2021 | 9 | 2021 |
| French Parkinson’s Disease Genetics, S, International Parkinson’s Disease Genomics, C, International Parkinson’s Disease Genomics Consortium, I, 2016. Loss of VPS13C function … S Lesage, V Drouet, E Majounie, V Deramecourt, M Jacoupy, A Nicolas, ... American journal of human genetics 98, 500-513, 0 | 5 | |
| MPC2 variants disrupt mitochondrial pyruvate metabolism and cause an early-onset mitochondriopathy C Pujol, E Lebigot, P Gaignard, S Galai, I Kraoua, JP Bault, R Dard, ... Brain 146 (3), 858-864, 2023 | 3 | 2023 |
| Mitochondrial aspartyl-tRNA synthetase (DARS2) deficiency in mice SA Dogan, C Pujol, A Trifunovic Experimental Gerontology 7 (48), 696, 2013 | 1 | 2013 |
