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Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 70,543 bioRxiv papers from 307,989 authors.

Author: Stephan Ripke

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  • Categories:
    • bioinformatics: 3,235 (rank: 2,331 (tie) out of 26,832)
    • genetics: 72,292 (rank: 35 out of 30,526)
    • genomics: 18,949 (rank: 368 out of 34,851)

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Preprints

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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LD Score Regression Distinguishes Confounding from Polygenicity in Genome-Wide Association Studies

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Partitioning heritability by functional category using GWAS summary statistics

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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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Genetic meta-analysis identifies 9 novel loci and functional pathways for Alzheimers disease risk

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GWAS meta-analysis (N=279,930) identifies new genes and functional links to intelligence

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Regulatory variants explain much more heritability than coding variants across 11 common diseases

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Local genetic effects on gene expression across 44 human tissues

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Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions.

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Genome wide meta-analysis identifies genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders.

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Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

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Haplotypes of common SNPs can explain missing heritability of complex diseases

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Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selection

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Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

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Comparative genetic architectures of schizophrenia in East Asian and European populations

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

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Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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Using three-dimensional regulatory chromatin interactions from adult and fetal cortex to interpret genetic results for psychiatric disorders and cognitive traits

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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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Subtle stratification confounds estimates of heritability from rare variants

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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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Identifying tissues implicated in Anorexia Nervosa using Transcriptomic Imputation

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Genome-wide Association Study of Clinical Features in the Schizophrenia Psychiatric Genomics Consortium: Confirmation of Polygenic Effect on Negative Symptoms

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RICOPILI: Rapid Imputation for COnsortias PIpeLIne

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A method to exploit the structure of genetic ancestry space to enhance case-control studies

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    • In genomics: 2,874 out of 4,714
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Genomewide Analyses of Psychological Resilience in US Army Soldiers

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Genetic variation in the Major Histocompatibility Complex and association with depression

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    • In genetics: 2,264 out of 3,911
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Shared Genetic Risk between Eating Disorder- and Substance-Use-Related Phenotypes: Evidence from Genome-Wide Association Studies

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