FACULTAD DE FARMACIA
Facultad
Washington University in St. Louis School of Medicine
San Luis, Estados UnidosPublicaciones en colaboración con investigadores/as de Washington University in St. Louis School of Medicine (31)
2024
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COQ4 is required for the oxidative decarboxylation of the C1 carbon of coenzyme Q in eukaryotic cells
Molecular Cell, Vol. 84, Núm. 5, pp. 981-989.e7
2022
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Identifying the Common Genetic Basis of Antidepressant Response
Biological Psychiatry Global Open Science, Vol. 2, Núm. 2, pp. 115-126
2021
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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
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Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders
Molecular Psychiatry, Vol. 26, Núm. 4, pp. 1286-1298
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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
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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
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Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
Autophagy, Vol. 17, Núm. 1, pp. 1-382
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Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder
Molecular Psychiatry, Vol. 26, Núm. 9, pp. 5239-5250
2020
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A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK Biobank
Nature Communications, Vol. 11, Núm. 1
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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
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Genome-wide Burden of Rare Short Deletions Is Enriched in Major Depressive Disorder in Four Cohorts
Biological Psychiatry, Vol. 85, Núm. 12, pp. 1065-1073
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Identification of common genetic risk variants for autism spectrum disorder
Nature Genetics, Vol. 51, Núm. 3, pp. 431-444
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Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns
Nature Communications, Vol. 10, Núm. 1
2018
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Analysis of shared heritability in common disorders of the brain
Science, Vol. 360, Núm. 6395
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Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder
Communications Biology, Vol. 1, Núm. 1
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Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium
Biological Psychiatry, Vol. 84, Núm. 2, pp. 138-147
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Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans
Nature Communications, Vol. 9, Núm. 1
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Improving genetic prediction by leveraging genetic correlations among human diseases and traits
Nature Communications, Vol. 9, Núm. 1
2017
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Genetic association of major depression with a typical features and obesity-related immunometabolic dysregulations
JAMA Psychiatry, Vol. 74, Núm. 12, pp. 1214-1225
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Genetic effects influencing risk for major depressive disorder in China and Europe
Translational Psychiatry, Vol. 7, Núm. 3