Publicacións en colaboración con investigadores/as de Universitat Pompeu Fabra (54)

2024

  1. Clonal chromosomal mosaicism and loss of chromosome Y in elderly men increase vulnerability for SARS-CoV-2

    Communications biology, Vol. 7, Núm. 1, pp. 202

2023

  1. A crowdsourcing database for the copy-number variation of the Spanish population

    Human Genomics, Vol. 17, Núm. 1

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

    Nature

  3. Childhood exposure to non-persistent endocrine disrupting chemicals and multi-omic profiles: A panel study

    Environment International, Vol. 173

  4. Prenatal environmental exposures associated with sex differences in childhood obesity and neurodevelopment

    BMC medicine, Vol. 21, Núm. 1, pp. 142

2022

  1. CIBERER: Spanish national network for research on rare diseases: A highly productive collaborative initiative

    Clinical genetics, Vol. 101, Núm. 5-6, pp. 481-493

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

    eLife, Vol. 11

  3. Meta-analysis of epigenome-wide association studies in newborns and children show widespread sex differences in blood DNA methylation

    Mutation Research - Reviews in Mutation Research, Vol. 789

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

    Nature Communications, Vol. 13, Núm. 1

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

    Communications Biology, Vol. 5, Núm. 1

2021

  1. Schuurs-Hoeijmakers Syndrome (PACS1 Neurodevelopmental Disorder): Seven Novel Patients and a Review

    Genes, Vol. 12, Núm. 5

  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

2020

  1. Association between DNA methylation and ADHD symptoms from birth to school age: a prospective meta-analysis

    Translational Psychiatry, Vol. 10, Núm. 1

  2. Corrigendum to `Exploring Genetic Variants in Obsessive Compulsive Disorder Severity: A GWAS Approach.' Journal of Affective Disorders 267 (2020) 23-32. (Journal of Affective Disorders (2020) 267 (23–32), (S0165032719316714), (10.1016/j.jad.2020.01.161))

    Journal of Affective Disorders

  3. Exploring genetic variants in obsessive compulsive disorder severity: A GWAS approach

    Journal of Affective Disorders, Vol. 267, pp. 23-32

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

    BMC Medicine, Vol. 18, Núm. 1

  5. Using methylome data to inform exposome-health association studies: An application to the identification of environmental drivers of child body mass index

    Environment International, Vol. 138

2019

  1. Do polygenic risk and stressful life events predict pharmacological treatment response in obsessive compulsive disorder? A gene–environment interaction approach

    Translational Psychiatry, Vol. 9, Núm. 1

  2. Erratum to: Germline variation at 8q24 and prostate cancer risk in men of European ancestry (Nature Communications, (2018), 9, 1, (4616), 10.1038/s41467-018-06863-1)

    Nature Communications