Complejo Hospitalario Universitario de La Coruña
Centro asistencial
Helmholtz Zentrum München
Múnich, AlemaniaPublicaciones en colaboración con investigadores/as de Helmholtz Zentrum München (23)
2024
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Minimal information for studies of extracellular vesicles (MISEV2023): From basic to advanced approaches
Journal of Extracellular Vesicles, Vol. 13, Núm. 2
2023
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A second update on mapping the human genetic architecture of COVID-19
Nature
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Genetic analysis of blood molecular phenotypes reveals common properties in the regulatory networks affecting complex traits
Nature Communications, Vol. 14, Núm. 1
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Pharmacogenomics of GLP-1 receptor agonists: a genome-wide analysis of observational data and large randomised controlled trials
The Lancet Diabetes and Endocrinology, Vol. 11, Núm. 1, pp. 33-41
2020
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A reference map of potential determinants for the human serum metabolome
Nature, Vol. 588, Núm. 7836, pp. 135-140
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Dietary metabolite profiling brings new insight into the relationship between nutrition and metabolic risk: An IMI DIRECT study
EBioMedicine, Vol. 58
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Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus
Circulation: Genomic and Precision Medicine, Vol. 13, Núm. 6, pp. E002769
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Predicting and elucidating the etiology of fatty liver disease: A machine learning modeling and validation study in the IMI DIRECT cohorts
PLoS Medicine, Vol. 17, Núm. 6
2019
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Genetic studies of abdominal MRI data identify genes regulating hepcidin as major determinants of liver iron concentration
Journal of Hepatology, Vol. 71, Núm. 3, pp. 594-602
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Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
Nature Genetics, Vol. 51, Núm. 5, pp. 804-814
2018
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Pyocyanin restricts social cheating in Pseudomonas aeruginosa
Frontiers in Microbiology, Vol. 9, Núm. JUN
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Telomeres in germ line and early embryo: An overview
Reproductomics: The -Omics Revolution and Its Impact on Human Reproductive Medicine (Elsevier), pp. 77-90
2017
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The Rb1 tumour suppressor gene modifies telomeric chromatin architecture by regulating TERRA expression
Scientific Reports, Vol. 7
2016
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Genome-wide associations for birth weight and correlations with adult disease
Nature, Vol. 538, Núm. 7624, pp. 248-252
2015
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Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation
PLoS Genetics, Vol. 11, Núm. 7
2014
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A Rb1 promoter variant with reduced activity contributes to osteosarcoma susceptibility in irradiated mice
Molecular Cancer, Vol. 13, Núm. 1
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Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes
Proceedings of the National Academy of Sciences of the United States of America, Vol. 111, Núm. 36, pp. 13127-13132
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Research update for articles published in EJCI in 2012
European Journal of Clinical Investigation, Vol. 44, Núm. 10, pp. 1010-1023
2013
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Rb1 haploinsufficiency promotes telomere attrition and radiation-induced genomic instability
Cancer Research, Vol. 73, Núm. 14, pp. 4247-4255
2012
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Secondary radiation-induced bone tumours demonstrate a high degree of genomic instability predictive of a poor prognosis
Current Genomics, Vol. 13, Núm. 6, pp. 433-437