Publicacións en colaboración con investigadores/as de Helmholtz Zentrum München (23)

2024

  1. Minimal information for studies of extracellular vesicles (MISEV2023): From basic to advanced approaches

    Journal of Extracellular Vesicles, Vol. 13, Núm. 2

2023

  1. A second update on mapping the human genetic architecture of COVID-19

    Nature

  2. Genetic analysis of blood molecular phenotypes reveals common properties in the regulatory networks affecting complex traits

    Nature Communications, Vol. 14, Núm. 1

  3. 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

  1. A reference map of potential determinants for the human serum metabolome

    Nature, Vol. 588, Núm. 7836, pp. 135-140

  2. Dietary metabolite profiling brings new insight into the relationship between nutrition and metabolic risk: An IMI DIRECT study

    EBioMedicine, Vol. 58

  3. Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus

    Circulation: Genomic and Precision Medicine, Vol. 13, Núm. 6, pp. E002769

  4. 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

  1. 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

  2. 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

  1. Pyocyanin restricts social cheating in Pseudomonas aeruginosa

    Frontiers in Microbiology, Vol. 9, Núm. JUN

  2. 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

  1. The Rb1 tumour suppressor gene modifies telomeric chromatin architecture by regulating TERRA expression

    Scientific Reports, Vol. 7

2016

  1. Genome-wide associations for birth weight and correlations with adult disease

    Nature, Vol. 538, Núm. 7624, pp. 248-252

2015

  1. Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation

    PLoS Genetics, Vol. 11, Núm. 7

2014

  1. A Rb1 promoter variant with reduced activity contributes to osteosarcoma susceptibility in irradiated mice

    Molecular Cancer, Vol. 13, Núm. 1

  2. 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

  3. Research update for articles published in EJCI in 2012

    European Journal of Clinical Investigation, Vol. 44, Núm. 10, pp. 1010-1023

2013

  1. Rb1 haploinsufficiency promotes telomere attrition and radiation-induced genomic instability

    Cancer Research, Vol. 73, Núm. 14, pp. 4247-4255

2012

  1. 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