Publicaciones en colaboración con investigadores/as de Universitat Pompeu Fabra (19)

2024

  1. Integrating Multi-Omics with environmental data for precision health: A novel analytic framework and case study on prenatal mercury induced childhood fatty liver disease

    Environment International, Vol. 190

  2. Proceedings of the 5th Meeting of Translational Hepatology, organized by the Spanish Association for the Study of the Liver (AEEH)

    Gastroenterologia y Hepatologia

2023

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

    Nature

  2. Erratum to: Mapping the human genetic architecture of COVID-19 (Nature, (2021), 600, 7889, (472-477), 10.1038/s41586-021-03767-x)

    Nature

2022

  1. Association of Prenatal Exposure to Endocrine-Disrupting Chemicals with Liver Injury in Children

    JAMA Network Open, Vol. 5, Núm. 7, pp. E2220176

  2. Detailed stratified GWAS analysis for severe COVID-19 in four European populations

    Human Molecular Genetics, Vol. 31, Núm. 23, pp. 3945-3966

2021

  1. In Utero Exposure to Mercury Is Associated With Increased Susceptibility to Liver Injury and Inflammation in Childhood

    Hepatology, Vol. 74, Núm. 3, pp. 1546-1559

  2. Mapping the human genetic architecture of COVID-19

    Nature, Vol. 600, Núm. 7889, pp. 472-477

  3. Prenatal and childhood exposure to air pollution and traffic and the risk of liver injury in European children

    Environmental Epidemiology, Vol. 5, Núm. 3

2020

  1. Prenatal Exposure to Perfluoroalkyl Substances Associated With Increased Susceptibility to Liver Injury in Children

    Hepatology, Vol. 72, Núm. 5, pp. 1758-1770

  2. Smelling the Dark Proteome: Functional Characterization of PITH Domain-Containing Protein 1 (C1orf128) in Olfactory Metabolism

    Journal of Proteome Research, Vol. 19, Núm. 12, pp. 4826-4843

2017

  1. Stem cell-like transcriptional reprogramming mediates metastatic resistance to mTOR inhibition

    Oncogene, Vol. 36, Núm. 19, pp. 2737-2749

2016

  1. Fatty acid amide hydrolase inhibition for the symptomatic relief of Parkinson's disease

    Brain, Behavior, and Immunity, Vol. 57, pp. 94-105

  2. Karyotypic complexity rather than chromosome 8 abnormalities aggravates the outcome of chronic lymphocytic leukemia patients with TP53 aberrations

    Oncotarget, Vol. 7, Núm. 49, pp. 80916-80924

2014

  1. Interstitial 13q14 deletions detected in the karyotype and translocations with concomitant deletion at 13q14 in chronic lymphocytic leukemia: Different genetic mechanisms but equivalent poorer clinical outcome

    Genes Chromosomes and Cancer, Vol. 53, Núm. 9, pp. 788-797

2013

  1. Landscape of somatic mutations and clonal evolution in mantle cell lymphoma

    Proceedings of the National Academy of Sciences of the United States of America, Vol. 110, Núm. 45, pp. 18250-18255

2011

  1. Modeling the effector - Regulatory T cell cross-regulation reveals the intrinsic character of relapses in Multiple Sclerosis

    BMC Systems Biology, Vol. 5

2010

  1. Switcher-random-walks: A cognitive-inspired mechanism for network exploration

    International Journal of Bifurcation and Chaos

2008

  1. Genomic regulation of CTLA4 and Multiple Sclerosis

    Journal of Neuroimmunology, Vol. 203, Núm. 1, pp. 108-115