Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 65,598 bioRxiv papers from 290,547 authors.

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Preprints

Meta-analysis of Scandinavian Schizophrenia Exomes

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Discovery Of The First Genome-Wide Significant Risk Loci For ADHD

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

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Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism

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Genomewide association study identifies 30 loci associated with bipolar disorder

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Common risk variants identified in autism spectrum disorder

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A major role for common genetic variation in anxiety disorders

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Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum

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A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

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Minimal phenotyping yields GWAS hits of reduced specificity for major depression

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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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ASD and ADHD have a similar burden of rare protein-truncating variants

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Largest genome-wide association study for PTSD identifies genetic risk loci in European and African ancestries and implicates novel biological pathways

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Genome-wide association study implicates CHRNA2 in cannabis use disorder

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A genetic investigation of sex bias in the prevalence of attention deficit hyperactivity disorder

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Genome-wide Association Study of Anxiety and Stress-related Disorders in the iPSYCH Cohort

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A genome-wide association study for shared risk across major psychiatric disorders in a nation-wide birth cohort implicates fetal neurodevelopment as a key mediator

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Mitochondrial DNA SNPs associated with Schizophrenia exhibit Highly Variable Inter-allelic Haplogroup Affiliation and Nuclear Genogeographic Affinity: Bi-Genomic Linkage Disequilibrium raises Major Concerns for Link to Disease

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Genome-wide association study of suicide attempt in psychiatric disorders identifies association with major depression polygenic risk scores

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Pharmacogenetics of antidepressant response: a polygenic approach

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The iPSYCH2012 case-cohort sample: New directions for unravelling genetic and environmental architectures of severe mental disorders

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Elevated polygenic burden for autism is associated with differential DNA methylation at birth.

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New insights on the pharmacogenomics of antidepressant response from the GENDEP and STAR*D studies: rare variant analysis and high-density imputation

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The neurobiology of BRD1 implicates sex-biased dysregulation of nuclear receptor signaling in mental disorders

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Assessing 42 inflammatory markers in 321 control subjects and 887 major depressive disorder cases: BMI and other confounders and overall predictive ability for current depression

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Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 are associated with gestational duration

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Exploring contributors to variability in estimates of SNP-heritability and genetic correlations from the iPSYCH case-cohort and published meta-studies of major psychiatric disorders.

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Genetic variation in the Major Histocompatibility Complex and association with depression

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Effect of cytochrome CYP2C19 metabolizing activity on antidepressant response and side effects: meta-analysis of data from genome-wide association studies

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Identification of risk variants and characterization of the polygenic architecture of disruptive behavior disorders in the context of ADHD

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Statin treatment and the risk of depression

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Genetic factors underlying the bidirectional relationship between autoimmune and mental disorders – findings from a Danish population-based study

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