| OPA1 mutations induce mitochondrial DNA instability and optic atrophy ‘plus’ phenotypes P Amati-Bonneau, ML Valentino, P Reynier, ME Gallardo, B Bornstein, ... Brain 131 (2), 338-351, 2008 | 562 | 2008 |
| Differences in reactive oxygen species production explain the phenotypes associated with common mouse mitochondrial DNA variants R Moreno-Loshuertos, R Acín-Pérez, P Fernández-Silva, N Movilla, ... Nature genetics 38 (11), 1261-1268, 2006 | 377 | 2006 |
| Clustering of missense mutations in the C-terminal region of factor H in atypical hemolytic uremic syndrome D Pérez-Caballero, C González-Rubio, ME Gallardo, M Vera, ... The American Journal of Human Genetics 68 (2), 478-484, 2001 | 354 | 2001 |
| A novel protein tyrosine phosphatase gene is mutated in progressive myoclonus epilepsy of the Lafora type (EPM2) JM Serratosa, P Gómez-Garre, ME Gallardo, B Anta, DBV de Bernabé, ... Human molecular genetics 8 (2), 345-352, 1999 | 260 | 1999 |
| Prenatal detection of a cystic fibrosis mutation in fetal DNA from maternal plasma RC González-González MC1, García-Hoyos M, Trujillo MJ, Rodríguez de Alba M ... Prenat. Diagn. 22 (10), 946-8, 2002 | 224 | 2002 |
| Genomic cloning and characterization of the human homeobox gene SIX6 reveals a cluster of SIX genes in chromosome 14 and associates SIX6 hemizygosity with bilateral … ME Gallardo, J Lopez-Rios, I Fernaud-Espinosa, B Granadino, R Sanz, ... Genomics 61 (1), 82-91, 1999 | 189 | 1999 |
| Designing recombinant Pseudomonas strains to enhance biodesulfurization ME Gallardo, A Ferrandez, V De Lorenzo, JL García, E Diaz Journal of bacteriology 179 (22), 7156-7160, 1997 | 157 | 1997 |
| The molecular basis of 3-methylcrotonylglycinuria, a disorder of leucine catabolism ME Gallardo, LR Desviat, JM Rodríguez, J Esparza-Gordillo, ... The American Journal of Human Genetics 68 (2), 334-346, 2001 | 98 | 2001 |
| Six9 (Optx2), a new member of the six gene family of transcription factors, is expressed at early stages of vertebrate ocular and pituitary development J López-Rı́os, ME Gallardo, SR de Córdoba, P Bovolenta Mechanisms of development 83 (1-2), 155-159, 1999 | 94 | 1999 |
| The thyroid hormone receptor β induces DNA damage and premature senescence A Zambrano, V García-Carpizo, ME Gallardo, R Villamuera, ... Journal of Cell Biology 204 (1), 129-146, 2014 | 83 | 2014 |
| m. 6267G> A: a recurrent mutation in the human mitochondrial DNA that reduces cytochrome c oxidase activity and is associated with tumors ME Gallardo, R Moreno‐Loshuertos, C López, M Casqueiro, J Silva, ... Human mutation 27 (6), 575-582, 2006 | 81 | 2006 |
| Analysis of the developmental SIX6 homeobox gene in patients with anophthalmia/microphthalmia ME Gallardo, S Rodríguez de Córdoba, AS Schneider, MA Dwyer, ... American Journal of Medical Genetics Part A 129 (1), 92-94, 2004 | 79 | 2004 |
| Genetic basis of end‐stage hypertrophic cardiomyopathy P Garcia‐Pavia, ME Vázquez, J Segovia, C Salas, P Avellana, ... European journal of heart failure 13 (11), 1193-1201, 2011 | 78 | 2011 |
| MidA is a putative methyltransferase that is required for mitochondrial complex I function S Carilla-Latorre, ME Gallardo, SJ Annesley, J Calvo-Garrido, O Graña, ... Journal of Cell Science 123 (10), 1674-1683, 2010 | 71 | 2010 |
| Enhanced tumorigenicity by mitochondrial DNA mild mutations A Cruz-Bermúdez, CG Vallejo, RJ Vicente-Blanco, ME Gallardo, ... Oncotarget 6 (15), 13628, 2015 | 63 | 2015 |
| Evolution Meets Disease: Penetrance and Functional Epistasis of Mitochondrial tRNA Mutations R Moreno-Loshuertos, G Ferrin, R Acin-Perez, ME Gallardo, C Viscomi, ... PLoS genetics 7 (4), e1001379, 2011 | 63 | 2011 |
| iPSC s: A powerful tool for skeletal muscle tissue engineering M del Carmen Ortuño‐Costela, M García‐López, V Cerrada, ME Gallardo Journal of cellular and molecular medicine 23 (6), 3784-3794, 2019 | 55 | 2019 |
| Genomic Cloning, Structure, Expression Pattern, and Chromosomal Location of the HumanSIX3Gene B Granadino, ME Gallardo, J López-Rı́os, R Sanz, C Ramos, C Ayuso, ... Genomics 55 (1), 100-105, 1999 | 52 | 1999 |
| The challenge of bringing iPSCs to the patient MC Ortuño-Costela, V Cerrada, M García-López, ME Gallardo International journal of molecular sciences 20 (24), 6305, 2019 | 50 | 2019 |
| Alkaptonuria in the Dominican Republic: identification of the founder AKU mutation and further evidence of mutation hot spots in the HGO gene EG De Jorge, I Lorda, ME Gallardo, B Pérez, CP De Ferrán, H Mendoza, ... Journal of Medical Genetics 39 (7), e40-e40, 2002 | 50 | 2002 |
