M. Esther Gallardo - Concepedia

Author

M. Esther Gallardo

Also Known As

Gallardo M, M E Gallardo, M Esther Gallardo, M Gallardo, M. E. Gallardo, M. Esther Gallardo, M. Gallardo, M.E. Gallardo, M.Esther Gallardo, Maria Esther Gallardo

Publications

2.6K

Citations

H-Index

Concepts

All Affiliations

Universidad Autónoma de Madrid Instituto de Investigaciones Biomédicas Sols-Morreale Centre for Biomedical Network Research on Rare Diseases Centro de Investigación Biomédica en Red Research Institute Hospital 12 de Octubre

About

M. Esther Gallardo is an author at Universidad Autónoma de Madrid specializing in medicine, genetics, and genomics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	12	1.7K
2	Engineering	2	2	143
3	Natural Sciences	2	2	43
4	Biochemistry	2	2	116
5	Biology	2	2	338

M. Esther Gallardo

Publications

2.3K

Citations

H-Index

Page 1

	Year	Citations
OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes Patrizia Amati‐Bonneau, Maria Lucia Valentino, Pascal Reynier, Brain Opa1 GeneGenome InstabilityMitochondrial BiogenesisOphthalmologyMitochondrial Function	2007	510
Differences in reactive oxygen species production explain the phenotypes associated with common mouse mitochondrial DNA variants Raquel Moreno‐Loshuertos, Rebeca Acín‐Pérez, Patricio Fernández‐Silva, Nature Genetics BiologyRedox SignalingMitochondrial FunctionGeneticsMolecular Genetics	2006	326
Clustering of Missense Mutations in the C-Terminal Region of Factor H in Atypical Hemolytic Uremic Syndrome David Pérez-Caballero, Carolina González-Rubio, M. Esther Gallardo, The American Journal of Human Genetics Missense MutationsUrologyC-terminal RegionHaplotype DeterminationGenetic Disorder	2001	289
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 Anophthalmia and Pituitary Anomalies M. Esther Gallardo, Javier López-Rı́os, Isabel Fernaud-Espinosa, Genomics Allelic VariantSix GenesDevelopmental BiologyGenetic DisorderMedicine	1999	176
Designing recombinant Pseudomonas strains to enhance biodesulfurization M. Esther Gallardo, Abel Ferrández, Vı́ctor de Lorenzo Journal of Bacteriology EngineeringEnvironmental BiotechnologyDesulfurizationBiosynthesisBioenergetics	1997	123
The Molecular Basis of 3-Methylcrotonylglycinuria, a Disorder of Leucine Catabolism M. Esther Gallardo, Lourdes R. Desviat, José Manuel Rodríguez Rodríguez, The American Journal of Human Genetics UrologyBiochemistryCatabolismGlycobiologyLeucine Catabolism	2001	85
Genetic Basis of End-Stage Hypertrophic Cardiomyopathy Pablo García‐Pavía, María Eugenia Vázquez, Javier Segovia, European Journal of Heart Failure	2011	67
The thyroid hormone receptor β induces DNA damage and premature senescence Alberto Zambrano, Verónica García-Carpizo, M. Esther Gallardo, The Journal of Cell Biology	2014	66
m.6267G>A: a recurrent mutation in the human mitochondrial DNA that reduces cytochrome c oxidase activity and is associated with tumors M. Esther Gallardo, Raquel Moreno‐Loshuertos, Celia López‐Menéndez, Human Mutation	2006	59
Evolution Meets Disease: Penetrance and Functional Epistasis of Mitochondrial tRNA Mutations Raquel Moreno‐Loshuertos, Gustavo Ferrín, Rebeca Acín‐Pérez, PLoS Genetics	2011	58

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