Fundación Pública Galega de Medicina Xenómica
Centro de investigación
Hospital Universitario de Valladolid
Valladolid, EspañaPublicacións en colaboración con investigadores/as de Hospital Universitario de Valladolid (12)
2024
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Evaluation of Genetic Variants Associated with the Risk of Thiopurine-Related Pancreatitis: A Case Control Study from ENEIDA Registry
Digestive Diseases, Vol. 42, Núm. 3, pp. 257-264
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Novel risk loci for COVID-19 hospitalization among admixed American populations
eLife, Vol. 13
2022
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A genome-wide association study of survival in patients with sepsis
Critical Care, Vol. 26, Núm. 1
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Genetic landscape of Segawa disease in Spain. Long-term treatment outcomes
Parkinsonism and Related Disorders, Vol. 94, pp. 67-78
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Novel genes and sex differences in COVID-19 severity
Human molecular genetics, Vol. 31, Núm. 22, pp. 3789-3806
2017
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The genetic component of bicuspid aortic valve and aortic dilation. An exome-wide association study
Journal of Molecular and Cellular Cardiology, Vol. 102, pp. 3-9
2015
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Association between SNPs of metalloproteinases and prostaglandin f2α receptor genes and latanoprost response in open-angle glaucoma
Ophthalmology, Vol. 122, Núm. 5, pp. 1040-1048.e4
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No major host genetic risk factor contributed to A(H1N1)2009 influenza severity
PLoS ONE, Vol. 10, Núm. 9
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Predicting proliferative vitreoretinopathy: Temporal and external validation of models based on genetic and clinical variables
British Journal of Ophthalmology, Vol. 99, Núm. 1, pp. 41-48
2013
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A genetic case-control study confirms the implication of SMAD7 and TNF locus in the development of proliferative vitreoretinopathy
Investigative Ophthalmology and Visual Science, Vol. 54, Núm. 3, pp. 1665-1678
2009
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Development of predictive models of proliferative vitreoretinopathy based on genetic variables: The retina 4 project
Investigative Ophthalmology and Visual Science, Vol. 50, Núm. 5, pp. 2384-2390