Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 52,506 bioRxiv papers from 243,425 authors.

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Preprints

Intergenerational transmission of education and ADHD: Effects of parental genotypes

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The genomic architecture of blood metabolites based on a decade of genome-wide analyses

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

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Genome-wide association analysis of lifetime cannabis use (N=184,765) identifies new risk loci, genetic overlap with mental health, and a causal influence of schizophrenia on cannabis use

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The genetic architecture of the human cerebral cortex

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Genetic analysis of over one million people identifies 535 novel loci for blood pressure.

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Integrative approaches for large-scale transcriptome-wide association studies

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Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

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Trans-ancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

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Multivariate Genome-wide and integrated transcriptome and epigenome-wide analyses of the Well-being spectrum.

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Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

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Genome-wide meta-analysis of cognitive empathy: heritability, and correlates with sex, neuropsychiatric conditions and brain anatomy

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Stratified Linkage Disequilibrium Score Regression reveals enrichment of eQTL effects on complex traits is not tissue specific

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Genome-wide association study of offspring birth weight in 86,577 women highlights maternal genetic effects that are independent of fetal genetics

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Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

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Genome-wide identification of directed gene networks using large-scale population genomics data

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Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney

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Within-family studies for Mendelian randomization: avoiding dynastic, assortative mating, and population stratification biases

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Phenome-wide investigation of health outcomes associated with genetic predisposition to loneliness

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Extending Causality Tests With Genetic Instruments: An Integration Of Mendelian Randomization And The Classical Twin Design

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Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity

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Genetic overlap between schizophrenia and developmental psychopathology: a longitudinal approach applied to common childhood disorders between age 7 and 15 years

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Epigenome-wide meta-analysis of blood DNA methylation and its association with subcortical volumes: findings from the ENIGMA Epigenetics Working Group

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A role for vitamin D and omega-3 fatty acids in major depression? An exploration using genomics

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Genetic risk for major depressive disorder and loneliness in gender-specific associations with coronary artery disease

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Genetic variation in the Major Histocompatibility Complex and association with depression

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Novel DNA methylation sites of glucose and insulin homeostasis: an integrative cross-omics analysis

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EEG-based age-prediction models as stable and heritable indicators of brain maturational level in children and adolescents

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Genetic comorbidity between major depression and cardio-metabolic disease, stratified by age at onset of major depression.

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Genetics of fasting indices of glucose homeostasis using GWIS unravels tight relationships with inflammatory markers

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Predicting biological age based on the BBMRI-NL 1H-NMR metabolomics repository

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Genome-wide association study of plasma lipids

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