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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 66,973 bioRxiv papers from 294,811 authors.

Author: Michael Boehnke

Rankings

  • All-time downloads: 68,942 (rank: 173 out of 294,953)
  • Categories:
    • bioinformatics: 2,258 (rank: 3,423 (tie) out of 25,677)
    • genetics: 29,834 (rank: 135 out of 29,418)
    • genomics: 36,850 (rank: 144 out of 33,562)

Downloads per author, site-wide

Preprints

Analysis of protein-coding genetic variation in 60,706 humans

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    • In genomics: 7 out of 4,553
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Genomewide association study identifies 30 loci associated with bipolar disorder

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    • Site-wide: 282 out of 67,014
    • In genetics: 33 out of 3,772
  • Year to date:
    • Site-wide: 315 out of 67,014
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    • Site-wide: 1,731 out of 67,014

A reference panel of 64,976 haplotypes for genotype imputation

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    • In genetics: 56 out of 3,772
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    • Site-wide: 54,351 out of 67,014

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

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    • In genomics: 164 out of 4,553
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    • Site-wide: 126 out of 67,014
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    • Site-wide: 534 out of 67,014

Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

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  • Downloaded 2,998 times
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    • In genomics: 275 out of 4,553
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Genome-wide association study of 1 million people identifies 111 loci for atrial fibrillation

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  • Downloaded 2,843 times
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    • In genetics: 123 out of 3,772
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Genetic analysis of over one million people identifies 535 novel loci for blood pressure.

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    • In genetics: 127 out of 3,772
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    • Site-wide: 24,354 out of 67,014

Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans

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    • In genomics: 589 out of 4,553
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Clustering of Type 2 Diabetes Genetic Loci by Multi-Trait Associations Identifies Disease Mechanisms and Subtypes

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  • Downloaded 1,675 times
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    • In genetics: 280 out of 3,772
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    • Site-wide: 9,089 out of 67,014
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    • Site-wide: 14,737 out of 67,014

Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

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  • Downloaded 1,673 times
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    • In genetics: 282 out of 3,772
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    • Site-wide: 40,261 out of 67,014

Genetic discovery and translational decision support from exome sequencing of 20,791 type 2 diabetes cases and 24,440 controls from five ancestries

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    • In genetics: 359 out of 3,772
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    • Site-wide: 3,825 out of 67,014
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    • Site-wide: 11,456 out of 67,014

Whole Genome Sequencing in Psychiatric Disorders: the WGSPD Consortium

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  • Downloaded 1,375 times
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    • In genomics: 815 out of 4,553
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    • Site-wide: 10,553 out of 67,014

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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    • In genomics: 880 out of 4,553
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    • Site-wide: 41,343 out of 67,014

PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION

genetics more details view paper
  • Downloaded 1,210 times
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    • In genetics: 451 out of 3,772
  • Year to date:
    • Site-wide: 3,336 out of 67,014
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    • Site-wide: 3,331 out of 67,014

Association Analysis and Meta-Analysis of Multi-allelic Variants for Large Scale Sequence Data

bioinformatics more details view paper
  • Downloaded 1,140 times
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    • Site-wide: 6,218 out of 67,014
    • In bioinformatics: 1,163 out of 6,609
  • Year to date:
    • Site-wide: 5,828 out of 67,014
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    • Site-wide: 5,453 out of 67,014

emeraLD: Rapid Linkage Disequilibrium Estimation with Massive Data Sets

bioinformatics more details view paper
  • Downloaded 1,118 times
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    • In bioinformatics: 1,198 out of 6,609
  • Year to date:
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    • Site-wide: 14,359 out of 67,014

Exome sequencing identifies high-impact trait-associated alleles enriched in Finns

genomics more details view paper
  • Downloaded 996 times
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    • In genomics: 1,234 out of 4,553
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    • Site-wide: 19,152 out of 67,014

Influence of genetic variants on gene expression in human pancreatic islets – implications for type 2 diabetes

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  • Downloaded 970 times
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    • Site-wide: 8,063 out of 67,014
    • In genomics: 1,264 out of 4,553
  • Year to date:
    • Site-wide: 2,003 out of 67,014
  • Since beginning of last month:
    • Site-wide: 5,796 out of 67,014

Genome-wide association and functional studies identify 46 novel loci for alcohol consumption and suggest common genetic mechanisms with neuropsychiatric disorders

genetics more details view paper
  • Downloaded 921 times
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    • Site-wide: 8,792 out of 67,014
    • In genetics: 657 out of 3,772
  • Year to date:
    • Site-wide: 4,365 out of 67,014
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    • Site-wide: 19,571 out of 67,014

Identification of type 2 diabetes loci in 433,540 East Asian individuals

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  • Downloaded 920 times
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    • In genetics: 659 out of 3,772
  • Year to date:
    • Site-wide: 2,203 out of 67,014
  • Since beginning of last month:
    • Site-wide: 7,482 out of 67,014

Narrow-sense heritability estimation of complex traits using identity-by-descent information.

genetics more details view paper
  • Downloaded 917 times
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    • Site-wide: 8,836 out of 67,014
    • In genetics: 661 out of 3,772
  • Year to date:
    • Site-wide: 16,917 out of 67,014
  • Since beginning of last month:
    • Site-wide: 23,165 out of 67,014

Multi-SKAT: General framework to test multiple phenotype associations of rare variants

genetics more details view paper
  • Downloaded 801 times
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    • In genetics: 793 out of 3,772
  • Year to date:
    • Site-wide: 19,198 out of 67,014
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    • Site-wide: 15,599 out of 67,014

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

genetics more details view paper
  • Downloaded 681 times
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    • Site-wide: 13,814 out of 67,014
    • In genetics: 962 out of 3,772
  • Year to date:
    • Site-wide: 12,074 out of 67,014
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    • Site-wide: 52,616 out of 67,014

Imputation aware tag SNP selection to improve power for multi-ethnic association studies

genomics more details view paper
  • Downloaded 676 times
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    • Site-wide: 13,962 out of 67,014
    • In genomics: 1,869 out of 4,553
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    • Site-wide: 52,193 out of 67,014
  • Since beginning of last month:
    • Site-wide: 45,435 out of 67,014

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

genomics more details view paper
  • Downloaded 604 times
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    • Site-wide: 16,335 out of 67,014
    • In genomics: 2,048 out of 4,553
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    • Site-wide: 35,130 out of 67,014

Sequencing and Imputation in GWAS: Cost-Effective Strategies to Increase Power and Genomic Coverage Across Diverse Populations

genetics more details view paper
  • Downloaded 597 times
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    • Site-wide: 16,573 out of 67,014
    • In genetics: 1,134 out of 3,772
  • Year to date:
    • Site-wide: 4,674 out of 67,014
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    • Site-wide: 14,615 out of 67,014

Complement component 4 genes contribute sex-specific vulnerability in diverse illnesses

genetics more details view paper
  • Downloaded 562 times
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    • Site-wide: 18,040 out of 67,014
    • In genetics: 1,211 out of 3,772
  • Year to date:
    • Site-wide: 5,203 out of 67,014
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    • Site-wide: 2,796 out of 67,014

Interactions between genetic variation and cellular environment in skeletal muscle gene expression

genetics more details view paper
  • Downloaded 485 times
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    • Site-wide: 21,676 out of 67,014
    • In genetics: 1,455 out of 3,772
  • Year to date:
    • Site-wide: 61,566 out of 67,014
  • Since beginning of last month:
    • Site-wide: 50,789 out of 67,014

Exome chip meta-analysis elucidates the genetic architecture of rare coding variants in smoking and drinking behavior

genetics more details view paper
  • Downloaded 480 times
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    • Site-wide: 22,000 out of 67,014
    • In genetics: 1,468 out of 3,772
  • Year to date:
    • Site-wide: 49,361 out of 67,014
  • Since beginning of last month:
    • Site-wide: 65,371 out of 67,014

Loss-of-function genomic variants with impact on liver-related blood traits highlight potential therapeutic targets for cardiovascular disease

genomics more details view paper
  • Downloaded 459 times
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    • Site-wide: 23,195 out of 67,014
    • In genomics: 2,556 out of 4,553
  • Year to date:
    • Site-wide: 7,250 out of 67,014
  • Since beginning of last month:
    • Site-wide: 13,901 out of 67,014

Integrating Comprehensive Functional Annotations to Boost Power and Accuracy in Gene-Based Association Analysis

genetics more details view paper
  • Downloaded 450 times
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    • Site-wide: 23,759 out of 67,014
    • In genetics: 1,568 out of 3,772
  • Year to date:
    • Site-wide: 7,512 out of 67,014
  • Since beginning of last month:
    • Site-wide: 10,534 out of 67,014

A powerful subset-based gene-set analysis method identifies novel associations and improves interpretation in UK Biobank

genetics more details view paper
  • Downloaded 212 times
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    • Site-wide: 46,399 out of 67,014
    • In genetics: 2,793 out of 3,772
  • Year to date:
    • Site-wide: 23,174 out of 67,014
  • Since beginning of last month:
    • Site-wide: 5,074 out of 67,014

Subset-Based Analysis using Gene-Environment Interactions for Discovery of Genetic Associations across Multiple Studies or Phenotypes

genetics more details view paper
  • Downloaded 211 times
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    • Site-wide: 46,486 out of 67,014
    • In genetics: 2,799 out of 3,772
  • Year to date:
    • Site-wide: 47,334 out of 67,014
  • Since beginning of last month:
    • Site-wide: 45,622 out of 67,014

Proper Conditional Analysis in the Presence of Missing Data Identified Novel Independently Associated Low Frequency Variants in Nicotine Dependence Genes

genetics more details view paper
  • Downloaded 186 times
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    • Site-wide: 49,844 out of 67,014
    • In genetics: 2,975 out of 3,772
  • Year to date:
    • Site-wide: 63,239 out of 67,014
  • Since beginning of last month:
    • Site-wide: 59,306 out of 67,014

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