Publicaciones en colaboración con investigadores/as de Instituto de Salud Global de Barcelona (28)

2024

  1. Common genetic variants associated with urinary phthalate levels in children: A genome-wide study

    Environment International, Vol. 190

2023

  1. Epimutation detection in the clinical context: guidelines and a use case from a new Bioconductor package

    Epigenetics, Vol. 18, Núm. 1

  2. Epimutation detection in the clinical context: guidelines and a use case from a new Bioconductor package

    Zenodo

  3. Epimutation detection in the clinical context: guidelines and a use case from a new Bioconductor package

    Zenodo

2022

  1. Identification of autosomal cis expression quantitative trait methylation (cis eQTMs) in children's blood

    eLife, Vol. 11

  2. Multi-omics signatures of the human early life exposome

    Nature Communications, Vol. 13, Núm. 1

  3. Study of the Combined Effect of Maternal Tobacco Smoking and Polygenic Risk Scores on Birth Weight and Body Mass Index in Childhood

    Frontiers in Genetics, Vol. 13

  4. The early-life exposome modulates the effect of polymorphic inversions on DNA methylation

    Communications Biology, Vol. 5, Núm. 1

2021

  1. Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation

    Nature Genetics, Vol. 53, Núm. 9, pp. 1311-1321

  2. The early-life exposome and epigenetic age acceleration in children

    Environment International, Vol. 155

  3. Variability of multi-omics profiles in a population-based child cohort

    BMC Medicine, Vol. 19, Núm. 1

  4. eQTM catalogue in children's blood

    Dryad

2020

  1. DNA methylation and body mass index from birth to adolescence: meta-analyses of epigenome-wide association studies

    Genome Medicine, Vol. 12, Núm. 1

  2. Identifying chromosomal subpopulations based on their recombination histories advances the study of the genetic basis of phenotypic traits

    Genome Research, Vol. 31, Núm. 12, pp. 1802-1814

  3. In utero and childhood exposure to tobacco smoke and multi-layer molecular signatures in children

    BMC Medicine, Vol. 18, Núm. 1

  4. Polymorphic Inversions Underlie the Shared Genetic Susceptibility of Obesity-Related Diseases

    American Journal of Human Genetics, Vol. 106, Núm. 6, pp. 846-858

2019

  1. Common polymorphic inversions at 17q21.31 and 8p23.1 associate with cancer prognosis

    Human Genomics, Vol. 13, Núm. 1

  2. Epigenome-wide meta-analysis of DNA methylation and childhood asthma

    Journal of Allergy and Clinical Immunology, Vol. 143, Núm. 6, pp. 2062-2074

  3. Newborn DNA-methylation, childhood lung function, and the risks of asthma and COPD across the life course

    European Respiratory Journal, Vol. 53, Núm. 4

  4. scoreInvHap: Inversion genotyping for genome-wide association studies

    PLoS Genetics, Vol. 15, Núm. 7