M
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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Journal ArticleDOI
Genetic variants near TIMP3 and high-density lipoprotein–associated loci influence susceptibility to age-related macular degeneration
Wei Chen,Dwight Stambolian,Albert O. Edwards,Kari Branham,Mohammad Othman,Johanna Jakobsdottir,Nirubol Tosakulwong,Margaret A. Pericak-Vance,Peter A. Campochiaro,Michael L. Klein,Perciliz L. Tan,Yvette P. Conley,Atsuhiro Kanda,Laura J. Kopplin,Yanming Li,Katherine J. Augustaitis,Athanasios J. Karoukis,William K. Scott,Anita Agarwal,Jaclyn L. Kovach,Stephen G. Schwartz,Eric A. Postel,Matthew Brooks,Keith H. Baratz,William L. Brown,Alexander J. Brucker,Anton Orlin,Gary C. Brown,Allen C. Ho,Carl D. Regillo,Larry A. Donoso,Lifeng Tian,Brian Kaderli,Dexter Hadley,Stephanie A. Hagstrom,Stephanie A. Hagstrom,Neal S. Peachey,Neal S. Peachey,Neal S. Peachey,Ronald Klein,Barbara E.K. Klein,Norimoto Gotoh,Kenji Yamashiro,Frederick L. Ferris,Jesen Fagerness,Robyn Reynolds,Lindsay A. Farrer,Ivana K. Kim,Joan W. Miller,Marta Corton,Angel Carracedo,Manuel Sánchez-Salorio,Elizabeth W. Pugh,Kimberly F. Doheny,Maria Brion,Margaret M. DeAngelis,Daniel E. Weeks,Donald J. Zack,Emily Y. Chew,John R. Heckenlively,Nagahisa Yoshimura,Sudha K. Iyengar,Peter J. Francis,Nicholas Katsanis,Johanna M. Seddon,Jonathan L. Haines,Michael B. Gorin,Gonçalo R. Abecasis,Anand Swaroop,Anand Swaroop +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.
Journal ArticleDOI
Association of the Polycystic Ovary Syndrome with Genomic Variants Related to Insulin Resistance, Type 2 Diabetes Mellitus, and Obesity
José L. San Millán,Marta Corton,Gemma Villuendas,José Sancho,Belén Peral,Héctor F. Escobar-Morreale +5 more
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.
Journal ArticleDOI
Differential Gene Expression Profile in Omental Adipose Tissue in Women with Polycystic Ovary Syndrome
Marta Corton,José I. Botella-Carretero,Alberto Benguria,Gemma Villuendas,Ángel Zaballos,José L. San Millán,Héctor F. Escobar-Morreale,Belén Peral +7 more
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.
Journal ArticleDOI
2017 update on the relationship between diabetes and colorectal cancer: epidemiology, potential molecular mechanisms and therapeutic implications.
Nieves González,Isabel Prieto,Laura del Puerto-Nevado,Sergio Portal-Núñez,Juan A. Ardura,Marta Corton,Beatriz Fernandez-Fernandez,Oscar Aguilera,Carmen Gomez-Guerrero,Sebastian Mas,Juan Antonio Moreno,Marta Ruiz-Ortega,Ana Belen Sanz,Maria Dolores Sanchez-Niño,Federico Rojo,Fernando Vivanco,Pedro Esbrit,Carmen Ayuso,Gloria Alvarez-Llamas,Jesús Egido,Jesús García-Foncillas,Alberto Ortiz +21 more
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.
Almudena Avila-Fernandez,Diego Cantalapiedra,Elena Aller,Elena Vallespín,Jana Aguirre-Lamban,Fiona Blanco-Kelly,Marta Corton,Rosa Riveiro-Alvarez,Rando Allikmets,María José Trujillo-Tiebas,José M. Millán,Frans P.M. Cremers,Carmen Ayuso +12 more
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.