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Marta Corton (ORCID 0000-0003-0087-1626)
Marta Corton (ORCID 0000-0003-0087-1626)
Researcher IIS-Fundacion Jimenez Diaz, Madrid, Spain
Email verificata su fjd.es
Titolo
Citata da
Citata da
Anno
Genetic variants near TIMP3 and high-density lipoprotein–associated loci influence susceptibility to age-related macular degeneration
W Chen, D Stambolian, AO Edwards, KE Branham, M Othman, ...
Proceedings of the National Academy of Sciences 107 (16), 7401-7406, 2010
6182010
Association of the polycystic ovary syndrome with genomic variants related to insulin resistance, type 2 diabetes mellitus, and obesity
JL San Millán, M Cortón, G Villuendas, J Sancho, B Peral, ...
The Journal of Clinical Endocrinology & Metabolism 89 (6), 2640-2646, 2004
2292004
Differential gene expression profile in omental adipose tissue in women with polycystic ovary syndrome
M Cortón, JI Botella-Carretero, A Benguria, G Villuendas, A Zaballos, ...
The Journal of Clinical Endocrinology & Metabolism 92 (1), 328-337, 2007
2052007
The Spectrum of PAX6 Mutations and Genotype-Phenotype Correlations in the Eye
D Lima Cunha, G Arno, M Corton, M Moosajee
Genes 10 (12), 1050, 2019
1542019
2017 update on the relationship between diabetes and colorectal cancer: epidemiology, potential molecular mechanisms and therapeutic implications
N Gonzalez, I Prieto, L del Puerto-Nevado, S Portal-Nunez, JA Ardura, ...
Oncotarget 8 (11), 18456, 2017
1362017
Proteomic analysis of human omental adipose tissue in the polycystic ovary syndrome using two-dimensional difference gel electrophoresis and mass spectrometry
M Cortón, JI Botella-Carretero, JA López, E Camafeita, JL San Millán, ...
Human Reproduction 23 (3), 651-661, 2008
1352008
Mutation analysis of 272 Spanish families affected by autosomal recessive retinitis pigmentosa using a genotyping microarray
A Ávila-Fernández, D Cantalapiedra, E Aller, E Vallespín, ...
Molecular vision 16, 2550, 2010
1242010
GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19
E Pairo-Castineira, K Rawlik, AD Bretherick, T Qi, Y Wu, I Nassiri, ...
Nature 617 (7962), 764-768, 2023
1072023
Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications
I Perea-Romero, G Gordo, IF Iancu, M Del Pozo-Valero, B Almoguera, ...
Scientific reports 11 (1), 1526, 2021
1052021
Searching urinary tumor markers for bladder cancer using a two-dimensional differential gel electrophoresis (2D-DIGE) approach
E Orenes-Piñero, M Cortón, P González-Peramato, F Algaba, I Casal, ...
Journal of proteome research 6 (11), 4440-4448, 2007
942007
Exome sequencing of index patients with retinal dystrophies as a tool for molecular diagnosis
M Corton, KM Nishiguchi, A Avila-Fernández, K Nikopoulos, ...
PloS one 8 (6), e65574, 2013
922013
Improved resolution of the human adipose tissue proteome at alkaline and wide range pH by the addition of hydroxyethyl disulfide
M Cortón, G Villuendas, JI Botella, JL San Millán, HF Escobar‐Morreale, ...
Proteomics 4 (2), 438-441, 2004
852004
NHEJ-mediated repair of CRISPR-Cas9-induced DNA breaks efficiently corrects mutations in HSPCs from patients with fanconi anemia
FJ Román-Rodríguez, L Ugalde, L Álvarez, B Díez, MJ Ramírez, ...
Cell Stem Cell 25 (5), 607-621. e7, 2019
842019
Mutations in IMPG1 cause vitelliform macular dystrophies
G Manes, I Meunier, A Avila-Fernández, S Banfi, G Le Meur, X Zanlonghi, ...
The American Journal of Human Genetics 93 (3), 571-578, 2013
832013
Outcome of ABCA4 disease-associated alleles in autosomal recessive retinal dystrophies: retrospective analysis in 420 Spanish families
R Riveiro-Alvarez, MA Lopez-Martinez, J Zernant, J Aguirre-Lamban, ...
Ophthalmology 120 (11), 2332-2337, 2013
822013
High frequency of CRB1 mutations as cause of Early-Onset Retinal Dystrophies in the Spanish population
M Corton, SD Tatu, A Avila-Fernandez, E Vallespín, I Tapias, ...
Orphanet journal of rare diseases 8, 1-12, 2013
742013
Genomic landscape of sporadic retinitis pigmentosa: findings from 877 Spanish cases
I Martin-Merida, A Avila-Fernandez, M Del Pozo-Valero, F Blanco-Kelly, ...
Ophthalmology 126 (8), 1181-1188, 2019
692019
Toward the mutational landscape of autosomal dominant retinitis pigmentosa: a comprehensive analysis of 258 Spanish families
I Martin-Merida, D Aguilera-Garcia, P Fernandez-San Jose, ...
Investigative ophthalmology & visual science 59 (6), 2345-2354, 2018
662018
Panel-based NGS reveals novel pathogenic mutations in autosomal recessive retinitis pigmentosa
R Perez-Carro, M Corton, I Sánchez-Navarro, O Zurita, N Sanchez-Bolivar, ...
Scientific reports 6 (1), 19531, 2016
632016
Genetic association study of age‐related macular degeneration in the Spanish population
M Brión, M Sanchez‐Salorio, M Cortón, M de la Fuente, B Pazos, ...
Acta ophthalmologica 89 (1), e12-e22, 2011
632011
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
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