Publicacións en colaboración con investigadores/as de University of Southern California (14)

2023

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

    Nature

2022

  1. 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

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

    Nature Communications, Vol. 13, Núm. 1

2020

  1. Systematic meta-analyses, field synopsis and global assessment of the evidence of genetic association studies in colorectal cancer

    Gut, Vol. 69, Núm. 8, pp. 1460-1471

  2. 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. Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (Nature Genetics, (2019), 51, 3, (414-430), 10.1038/s41588-019-0358-2)

    Nature Genetics

  2. Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

    Nature Genetics, Vol. 51, Núm. 3, pp. 414-430

2015

  1. Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1

    Scientific Reports, Vol. 5

2013

  1. Genetic Variations in SMAD7 Are Associated with Colorectal Cancer Risk in the Colon Cancer Family Registry

    PLoS ONE, Vol. 8, Núm. 4

2012

  1. Breast feeding, parity and breast cancer subtypes in a Spanish cohort

    PLoS ONE, Vol. 7, Núm. 7

  2. Development of a panel of genome-wide ancestry informative markers to study admixture throughout the americas

    PLoS Genetics, Vol. 8, Núm. 3

  3. Family history and breast cancer hormone receptor status in a Spanish cohort

    PLoS ONE, Vol. 7, Núm. 1

  4. Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13

    Human Molecular Genetics, Vol. 21, Núm. 4, pp. 934-946

2011

  1. Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer

    PLoS Genetics, Vol. 7, Núm. 6