![Foto de Marta](/img/nophoto.png)
Marta
Cortón Pérez
Publicacións nas que colabora con Marta Cortón Pérez (9)
2023
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A crowdsourcing database for the copy-number variation of the Spanish population
Human Genomics, Vol. 17, Núm. 1
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A second update on mapping the human genetic architecture of COVID-19
Nature
2022
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Novel genes and sex differences in COVID-19 severity
Human molecular genetics, Vol. 31, Núm. 22, pp. 3789-3806
2021
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CSVS, a crowdsourcing database of the Spanish population genetic variability
Nucleic acids research, Vol. 49, Núm. D1, pp. D1130-D1137
2014
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Involvement of LCA5 in leber congenital amaurosis and retinitis pigmentosa in the Spanish population
Ophthalmology, Vol. 121, Núm. 1, pp. 399-407
2011
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A pharmacogenetics study of TPMT and ITPA genes detects a relationship with side effects and clinical response in patients with inflammatory bowel disease receiving azathioprine
Journal of Gastrointestinal and Liver Diseases, Vol. 20, Núm. 3, pp. 247-253
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Genetic association study of age-related macular degeneration in the Spanish population
Acta Ophthalmologica, Vol. 89, Núm. 1
2010
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Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration
Proceedings of the National Academy of Sciences of the United States of America, Vol. 107, Núm. 16, pp. 7401-7406
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Identification of a novel mutation in the human PDE6A gene in autosomal recessive retinitis pigmentosa: Homology with the nmf28/nmf28 mice model
Clinical Genetics