Publicaciones en colaboración con investigadores/as de Wellcome Trust Sanger Institute (20)

2023

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

    Nature

2022

  1. Emergence of methicillin resistance predates the clinical use of antibiotics

    Nature, Vol. 602, Núm. 7895, pp. 135-141

  2. Mild-to-Moderate Kidney Dysfunction and Cardiovascular Disease: Observational and Mendelian Randomization Analyses

    Circulation, Vol. 146, Núm. 20, pp. 1507-1517

2021

  1. Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element

    American Journal of Human Genetics, Vol. 108, Núm. 7, pp. 1190-1203

  2. Genomic and transcriptomic analyses of breast cancer primaries and matched metastases in Aurora, the breast international group (Big) molecular screening initiative

    Cancer Discovery, Vol. 11, Núm. 11, pp. 2796-2811

  3. Spread of a SARS-CoV-2 variant through Europe in the summer of 2020

    Nature, Vol. 595, Núm. 7869, pp. 707-712

  4. The first wave of the COVID-19 epidemic in Spain was associated with early introductions and fast spread of a dominating genetic variant

    Nature Genetics, Vol. 53, Núm. 10, pp. 1405-1414

2020

  1. Reconstitution of a functional human thymus by postnatal stromal progenitor cells and natural whole-organ scaffolds

    Nature Communications, Vol. 11, Núm. 1

2019

  1. GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways

    Nature Communications, Vol. 10, Núm. 1

2018

  1. Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations

    PLoS ONE, Vol. 13, Núm. 1

2017

  1. Phylogenetic ctDNA analysis depicts early-stage lung cancer evolution

    Nature, Vol. 545, Núm. 7655, pp. 446-451

2016

  1. Summaries of plenary, symposia, and oral sessions at the XXII World Congress of Psychiatric Genetics, Copenhagen, Denmark, 12-16 October 2014

    Psychiatric Genetics, Vol. 26, Núm. 1, pp. 1-47

2015

  1. The Y-chromosome tree bursts into leaf: 13,000 high-confidence SNPs covering the majority of known clades

    Molecular Biology and Evolution, Vol. 32, Núm. 3, pp. 661-673

2014

  1. Common variant at 16p11.2 conferring risk of psychosis

    Molecular Psychiatry, Vol. 19, Núm. 1, pp. 108-114

  2. Synaptic, transcriptional and chromatin genes disrupted in autism

    Nature, Vol. 515, Núm. 7526, pp. 209-215

2011

  1. Common variants at VRK2 and TCF4 conferring risk of schizophrenia

    Human Molecular Genetics, Vol. 20, Núm. 20, pp. 4076-4081

2010

  1. Multiple common variants for celiac disease influencing immune gene expression

    Nature Genetics, Vol. 42, Núm. 4, pp. 295-302

2009

  1. Common variants conferring risk of schizophrenia

    Nature, Vol. 460, Núm. 7256, pp. 744-747

2008

  1. Identifying Genetic Traces of Historical Expansions: Phoenician Footprints in the Mediterranean

    American Journal of Human Genetics, Vol. 83, Núm. 5, pp. 633-642

2005

  1. PPARGC1A genotype (Gly482Ser) predicts exceptional endurance capacity in European men

    Journal of Applied Physiology, Vol. 99, Núm. 1, pp. 344-348