Publicacións en colaboración con investigadores/as de Centro de Regulación Genómica (16)

2023

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

    Environment International, Vol. 173

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

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

2022

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

    Nature Communications, Vol. 13, Núm. 1

2021

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

    Environment International, Vol. 155

2016

  1. Exon-focused genome-wide association study of obsessive-compulsive disorder and shared polygenic risk with schizophrenia

    Translational Psychiatry, Vol. 6, Núm. 3

  2. PRKG1 and genetic diagnosis of early-onset thoracic aortic disease

    European Journal of Clinical Investigation, Vol. 46, Núm. 9, pp. 787-794

  3. Sequence variation between 462 human individuals fine-tunes functional sites of RNA processing

    Scientific Reports, Vol. 6

2014

  1. The human early-life exposome (HELIX): Project rationale and design

    Environmental Health Perspectives, Vol. 122, Núm. 6, pp. 535-544

2013

  1. Transcriptome and genome sequencing uncovers functional variation in humans

    Nature, Vol. 501, Núm. 7468, pp. 506-511

2012

  1. Genetic epistasis in female suicide attempters

    Progress in Neuro-Psychopharmacology and Biological Psychiatry, Vol. 38, Núm. 2, pp. 294-301

2011

  1. Deletion of LCE3C and LCE3B is a susceptibility factor for psoriatic arthritis: A study in Spanish and Italian populations and meta-analysis

    Arthritis and Rheumatism, Vol. 63, Núm. 7, pp. 1860-1865

2010

  1. Association study of 44 candidate genes with depressive and anxiety symptoms in post-partum women

    Journal of Psychiatric Research, Vol. 44, Núm. 11, pp. 717-724

  2. Nucleotide variation in central nervous system genes among male suicide attempters

    American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 153, Núm. 1, pp. 208-213

2009

  1. Identification of new putative susceptibility genes for several psychiatric disorders by association analysis of regulatory and non-synonymous SNPs of 306 genes involved in neurotransmission and neurodevelopment

    American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 150, Núm. 6, pp. 808-816

  2. Prediction of postpartum depression using multilayer perceptrons and pruning

    Methods of Information in Medicine, Vol. 48, Núm. 3, pp. 291-298

2007

  1. Association of the ARLTS1 Cys148Arg variant with sporadic and familial colorectal cancer

    Carcinogenesis, Vol. 28, Núm. 8, pp. 1687-1691