Publicaciones en colaboración con investigadores/as de University of Tartu (22)

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. Distinct whole-blood transcriptome profile of children with metabolic healthy overweight/obesity compared to metabolic unhealthy overweight/obesity

    Pediatric Research, Vol. 89, Núm. 7, pp. 1687-1694

  5. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1

    Autophagy, Vol. 17, Núm. 1, pp. 1-382

  6. The Gut Microbiome in Polycystic Ovary Syndrome and Its Association with Metabolic Traits

    Journal of Clinical Endocrinology and Metabolism, Vol. 106, Núm. 3, pp. 858-871

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

  3. Inflammatory markers and bone mass in children with overweight/obesity: the role of muscular fitness

    Pediatric Research, Vol. 87, Núm. 1, pp. 42-47

2019

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

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

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

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

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

    Nature Communications, Vol. 10, Núm. 1

2018

  1. A review of exposure assessment methods for epidemiological studies of health effects related to industrially contaminated sites

    Epidemiologia e Prevenzione, Vol. 42, Núm. 5-6, pp. 21-36

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

    Science, Vol. 360, Núm. 6395

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

    Communications Biology, Vol. 1, Núm. 1

  4. 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

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

    PLoS ONE, Vol. 13, Núm. 12

  6. Improving genetic prediction by leveraging genetic correlations among human diseases and traits

    Nature Communications, Vol. 9, Núm. 1

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