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Marta Corton

Researcher at Autonomous University of Madrid

Publications -  121
Citations -  3316

Marta Corton is an academic researcher from Autonomous University of Madrid. The author has contributed to research in topics: Retinitis pigmentosa & Medicine. The author has an hindex of 26, co-authored 88 publications receiving 2548 citations. Previous affiliations of Marta Corton include University of Santiago de Compostela & Spanish National Research Council.

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Genetic variants near TIMP3 and high-density lipoprotein–associated loci influence susceptibility to age-related macular degeneration

Wei Chen, +69 more
TL;DR: A genome-wide association scan for age-related macular degeneration (AMD) showed that 329 of 331 individuals with the highest-risk genotypes were cases, and 85% of these had advanced AMD, consistent with the hypothesis that HDL metabolism is associated with AMD pathogenesis.
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Association of the Polycystic Ovary Syndrome with Genomic Variants Related to Insulin Resistance, Type 2 Diabetes Mellitus, and Obesity

TL;DR: The paraoxonase -108 C-->T variant and the ApaI polymorphism in the IGF2 gene are associated with PCOS and might contribute to increased oxidative stress, insulin resistance, and hyperandrogenism in this prevalent disorder.
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Differential Gene Expression Profile in Omental Adipose Tissue in Women with Polycystic Ovary Syndrome

TL;DR: The differences in the gene expression profiles in visceral adipose tissue of PCos patients compared with nonhyperandrogenic women involve multiple genes related to several biological pathways, suggesting that the involvement of abdominal obesity in the pathogenesis of PCOS is more ample than previously thought and is not restricted to the induction of insulin resistance.
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2017 update on the relationship between diabetes and colorectal cancer: epidemiology, potential molecular mechanisms and therapeutic implications.

TL;DR: The epidemiological evidence, potential pathophysiological mechanisms and therapeutic implications of the association between DM and colorectal cancer, and the biological plausibility of a cause-and-effect relationship through characterization of the molecular pathways involved are reviewed.
Journal Article

Mutation analysis of 272 Spanish families affected by autosomal recessive retinitis pigmentosa using a genotyping microarray.

TL;DR: The genotyping microarray combined with segregation and sequence analysis allowed us to identify the causative mutations in 11% of the families, and Retinol Dehydrogenase 12 was the most frequently mutated gene in the juvenile RP group, and Usher Syndrome 2A and Ceramide Kinase-Like were the mostrequently mutated genes in the typical RP group.