Publicacións en colaboración con investigadores/as de Vanderbilt University Medical Center (7)

2026

  1. Deleterious coding variation associated with autism is shared across ancestries

    Nature Medicine, Vol. 32, Núm. 4, pp. 1519-1529

2025

  1. Genome-wide analyses identify 30 loci associated with obsessive–compulsive disorder

    Nature Genetics, Vol. 57, Núm. 6, pp. 1389-1401

  2. Genome-wide association study of susceptibility to acute respiratory distress syndrome

    eBioMedicine, Vol. 120

2023

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

    Nature

2022

  1. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

    Nature Genetics, Vol. 54, Núm. 9, pp. 1320-1331

2020

  1. Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

    Cell, Vol. 180, Núm. 3, pp. 568-584.e23

2010

  1. Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration

    Proceedings of the National Academy of Sciences of the United States of America, Vol. 107, Núm. 16, pp. 7401-7406