Publicaciones en colaboración con investigadores/as de Brigham and Women's Hospital (19)

2023

  1. Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations

    Nature genetics, Vol. 55, Núm. 3, pp. 369-376

2022

  1. Identifying the Common Genetic Basis of Antidepressant Response

    Biological Psychiatry Global Open Science, Vol. 2, Núm. 2, pp. 115-126

2021

  1. Association of polygenic score for major depression with response to lithium in patients with bipolar disorder

    Molecular Psychiatry, Vol. 26, Núm. 6, pp. 2457-2470

  2. Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders

    Molecular Psychiatry, Vol. 26, Núm. 4, pp. 1286-1298

  3. Correction: Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank (Molecular Psychiatry, (2020), 25, 7, (1430-1446), 10.1038/s41380-019-0546-6)

    Molecular Psychiatry

  4. Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder (Molecular Psychiatry, (2021), 26, 9, (5239-5250), 10.1038/s41380-020-01006-9)

    Molecular Psychiatry

  5. Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder

    Molecular Psychiatry, Vol. 26, Núm. 9, pp. 5239-5250

2020

  1. A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK Biobank

    Nature Communications, Vol. 11, Núm. 1

  2. Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank

    Molecular Psychiatry, Vol. 25, Núm. 7, pp. 1430-1446

2019

  1. Assessment of bidirectional relationships between physical activity and depression among adults a 2-sample Mendelian randomization study

    JAMA Psychiatry, Vol. 76, Núm. 4, pp. 399-408

  2. Genome-wide association study identifies 30 loci associated with bipolar disorder

    Nature Genetics, Vol. 51, Núm. 5, pp. 793-803

  3. Identification of common genetic risk variants for autism spectrum disorder

    Nature Genetics, Vol. 51, Núm. 3, pp. 431-444

  4. Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns

    Nature Communications, Vol. 10, Núm. 1

2018

  1. Analysis of shared heritability in common disorders of the brain

    Science, Vol. 360, Núm. 6395

  2. Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder

    Communications Biology, Vol. 1, Núm. 1

  3. Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

    Nature Genetics, Vol. 50, Núm. 5, pp. 668-681

  4. Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder

    PLoS ONE, Vol. 13, Núm. 12

2017

  1. An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype

    Biological Psychiatry, Vol. 82, Núm. 5, pp. 322-329

  2. Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes

    Scientific Reports, Vol. 7, Núm. 1