Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 62,734 bioRxiv papers from 278,354 authors.

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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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  • In genomics: 64 out of 4,316
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  • Site-wide: 29,619 out of 62,734

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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  • In genetics: 32 out of 3,562
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  • Site-wide: 2,111 out of 62,734

Common risk variants identified in autism spectrum disorder

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  • In genetics: 37 out of 3,562
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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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  • In genetics: 51 out of 3,562
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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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  • In genomics: 155 out of 4,316
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  • Site-wide: 21,216 out of 62,734

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

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  • In genetics: 72 out of 3,562
• Year to date:
  • Site-wide: 435 out of 62,734
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  • Site-wide: 2,681 out of 62,734

Haplotypes of common SNPs can explain missing heritability of complex diseases

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  • In genetics: 105 out of 3,562
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  • Site-wide: 36,052 out of 62,734
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  • Site-wide: 34,161 out of 62,734

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

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  • In genomics: 274 out of 4,316
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  • Site-wide: 190 out of 62,734
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  • Site-wide: 1,667 out of 62,734

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

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  • In genomics: 378 out of 4,316
• Year to date:
  • Site-wide: 38,903 out of 62,734
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  • Site-wide: 23,522 out of 62,734

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

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  • In genetics: 182 out of 3,562
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  • Site-wide: 24,130 out of 62,734

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

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  • In genetics: 286 out of 3,562
• Year to date:
  • Site-wide: 45,966 out of 62,734
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  • Site-wide: 50,304 out of 62,734

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

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  • In genetics: 303 out of 3,562
• Year to date:
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  • Site-wide: 26,854 out of 62,734

Comparative genetic architectures of schizophrenia in East Asian and European populations

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  • In genetics: 378 out of 3,562
• Year to date:
  • Site-wide: 3,156 out of 62,734
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  • Site-wide: 4,326 out of 62,734

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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  • In genomics: 838 out of 4,316
• Year to date:
  • Site-wide: 19,288 out of 62,734
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  • Site-wide: 37,147 out of 62,734

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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  • In genetics: 498 out of 3,562
• Year to date:
  • Site-wide: 2,020 out of 62,734
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  • Site-wide: 3,096 out of 62,734

Subtle stratification confounds estimates of heritability from rare variants

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  • In genetics: 595 out of 3,562
• Year to date:
  • Site-wide: 37,115 out of 62,734
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  • Site-wide: 27,396 out of 62,734

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

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  • In genetics: 932 out of 3,562
• Year to date:
  • Site-wide: 10,393 out of 62,734
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  • Site-wide: 28,994 out of 62,734

Identifying tissues implicated in Anorexia Nervosa using Transcriptomic Imputation

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  • In genetics: 1,112 out of 3,562
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  • Site-wide: 10,739 out of 62,734
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  • Site-wide: 28,491 out of 62,734

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

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  • Site-wide: 17,496 out of 62,734
  • In genetics: 1,189 out of 3,562
• Year to date:
  • Site-wide: 31,561 out of 62,734
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  • Site-wide: 40,597 out of 62,734

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

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  • In genomics: 2,606 out of 4,316
• Year to date:
  • Site-wide: 55,283 out of 62,734
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  • Site-wide: 50,689 out of 62,734

Genomewide Analyses of Psychological Resilience in US Army Soldiers

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  • In genetics: 1,724 out of 3,562
• Year to date:
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  • Site-wide: 25,890 out of 62,734

Genetic variation in the Major Histocompatibility Complex and association with depression

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  • In genetics: 2,170 out of 3,562
• Year to date:
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  • Site-wide: 51,785 out of 62,734

RICOPILI: Rapid Imputation for COnsortias PIpeLIne

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  • In genetics: 2,207 out of 3,562
• Year to date:
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  • Site-wide: 32,584 out of 62,734

Shared Genetic Risk between Eating Disorder- and Substance-Use-Related Phenotypes: Evidence from Genome-Wide Association Studies

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  • In genetics: 2,484 out of 3,562
• Year to date:
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  • Site-wide: 6,824 out of 62,734