Ester López‐Gallardo

Unmasking the causes of multifactorial disorders: OXPHOS differences between mitochondrial haplogroups

Aurora Gómez-Durán, David Pacheu‐Grau, Ester López‐Gallardo et al. · Human Molecular Genetics · 2010 · 288 citations

Life Sciences, Genetics, Molecular Genetics +17

Cerebral folate deficiency and leukoencephalopathy caused by a mitochondrial DNA deletion

Merçè Pineda, Aída Ormazábal, Ester López‐Gallardo et al. · Annals of Neurology · 2005 · 158 citations

Life Sciences, Neurology, Neuroscience +17

Transcriptomic profiling of TK2 deficient human skeletal muscle suggests a role for the p53 signalling pathway and identifies growth and differentiation factor-15 as a potential novel biomarker for mitochondrial myopathies

Susana G. Kalko, Sonia Paco, Cristina Jou et al. · BMC Genomics · 2014 · 126 citations · Full text

Life Sciences, Genetics, Molecular Biology +17

Oxidative phosphorylation differences between mitochondrial DNA haplogroups modify the risk of Leber's hereditary optic neuropathy

Aurora Gómez-Durán, David Pacheu‐Grau, Íñigo Martínez‐Romero et al. · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 2012 · 107 citations

Medicine, Genetics, Molecular Genetics +16

Secondary coenzyme Q 10 deficiencies in oxidative phosphorylation (OXPHOS) and non-OXPHOS disorders

Dèlia Yubero, Raquel Montero, Miguel Á. Martín et al. · Mitochondrion · 2016 · 78 citations

Life Sciences, Biochemistry, Physiology +15