| Unmasking the causes of multifactorial disorders: OXPHOS differences between mitochondrial haplogroups A Gómez-Durán, D Pacheu-Grau, E López-Gallardo, C Díez-Sánchez, ... Human molecular genetics 19 (17), 3343-3353, 2010 | 306 | 2010 |
| Mitochondrial DNA background modulates the assembly kinetics of OXPHOS complexes in a cellular model of mitochondrial disease R Pello, MA Martín, V Carelli, LG Nijtmans, A Achilli, M Pala, A Torroni, ... Human molecular genetics 17 (24), 4001-4011, 2008 | 178 | 2008 |
| Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseases G Hudson, A Gomez-Duran, IJ Wilson, PF Chinnery PLoS genetics 10 (5), e1004369, 2014 | 170 | 2014 |
| Oxidative phosphorylation differences between mitochondrial DNA haplogroups modify the risk of Leber's hereditary optic neuropathy A Gómez-Durán, D Pacheu-Grau, Í Martínez-Romero, E López-Gallardo, ... Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1822 (8 …, 2012 | 110 | 2012 |
| Soy lecithin interferes with mitochondrial function in frozen‐thawed ram spermatozoa I Del Valle, A Gómez‐Durán, WV Holt, T Muiño‐Blanco, ... Journal of andrology 33 (4), 717-725, 2012 | 87 | 2012 |
| An atlas of mitochondrial DNA genotype–phenotype associations in the UK Biobank E Yonova-Doing, C Calabrese, A Gomez-Duran, K Schon, W Wei, ... Nature genetics 53 (7), 982-993, 2021 | 71 | 2021 |
| Mutations in mitochondrial DNA causing tubulointerstitial kidney disease TM Connor, S Hoer, A Mallett, DP Gale, A Gomez-Duran, V Posse, ... PLoS genetics 13 (3), e1006620, 2017 | 66 | 2017 |
| Oldies but goldies mtDNA population variants and neurodegenerative diseases PF Chinnery, A Gomez-Duran Frontiers in neuroscience 12, 399639, 2018 | 65 | 2018 |
| Exposure of monocytic cells to lipopolysaccharide induces coordinated endotoxin tolerance, mitochondrial biogenesis, mitophagy, and antioxidant defenses JD Widdrington, A Gomez-Duran, A Pyle, MH Ruchaud-Sparagano, ... Frontiers in immunology 9, 2217, 2018 | 65 | 2018 |
| Altered 2-thiouridylation impairs mitochondrial translation in reversible infantile respiratory chain deficiency V Boczonadi, PM Smith, A Pyle, A Gomez-Duran, U Schara, M Tulinius, ... Human molecular genetics 22 (22), 4602-4615, 2013 | 60 | 2013 |
| Mitochondrial pharmacogenomics: barcode for antibiotic therapy D Pacheu-Grau, A Gómez-Durán, MJ López-Pérez, J Montoya, ... Drug discovery today 15 (1-2), 33-39, 2010 | 59 | 2010 |
| Metabolic effects of bezafibrate in mitochondrial disease H Steele, A Gomez‐Duran, A Pyle, S Hopton, J Newman, RJ Stefanetti, ... EMBO molecular medicine 12 (3), e11589, 2020 | 57 | 2020 |
| Association of mitochondrial haplogroup J and mtDNA oxidative damage in two different North Spain elderly populations E Dominguez-Garrido, D Martinez-Redondo, C Martin-Ruiz, ... Biogerontology 10, 435-442, 2009 | 53 | 2009 |
| Mitochondrial antibiograms in personalized medicine D Pacheu-Grau, A Gomez-Durán, E Iglesias, E Lopez-Gallardo, ... Human molecular genetics 22 (6), 1132-1139, 2013 | 51 | 2013 |
| The mitochondrial protein CHCHD2 primes the differentiation potential of human induced pluripotent stem cells to neuroectodermal lineages L Zhu, A Gomez-Duran, G Saretzki, S Jin, K Tilgner, D Melguizo-Sanchis, ... Journal of Cell Biology 215 (2), 187-202, 2016 | 49 | 2016 |
| Background sequence characteristics influence the occurrence and severity of disease-causing mtDNA mutations W Wei, A Gomez-Duran, G Hudson, PF Chinnery PLoS genetics 13 (12), e1007126, 2017 | 48 | 2017 |
| Altered RNA metabolism due to a homozygous RBM7 mutation in a patient with spinal motor neuropathy M Giunta, S Edvardson, Y Xu, M Schuelke, A Gomez-Duran, V Boczonadi, ... Human molecular genetics 25 (14), 2985-2996, 2016 | 48 | 2016 |
| Metabolic shift underlies recovery in reversible infantile respiratory chain deficiency D Hathazi, H Griffin, MJ Jennings, M Giunta, C Powell, SF Pearce, ... The EMBO journal 39 (23), e105364, 2020 | 37 | 2020 |
| Mitochondrial dysfunction in liver failure requiring transplantation M Lane, V Boczonadi, S Bachtari, A Gomez-Duran, T Langer, A Griffiths, ... Journal of inherited metabolic disease 39, 427-436, 2016 | 35 | 2016 |
| Clinical and functional characterisation of the combined respiratory chain defect in two sisters due to autosomal recessive mutations in MTFMT VCM Neeve, A Pyle, V Boczonadi, A Gomez-Duran, H Griffin, ... Mitochondrion 13 (6), 743-748, 2013 | 34 | 2013 |
