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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 57,793 bioRxiv papers from 266,023 authors.

Author: Michael Boehnke

Rankings

  • All-time downloads: 53,426 (rank: 223 out of 266,023)
  • Categories:
    • bioinformatics: 2,346 (rank: 2,820 (tie) out of 23,180)
    • genetics: 16,028 (rank: 412 out of 25,343)
    • genomics: 35,052 (rank: 141 out of 30,373)

Downloads per author, site-wide

Preprints

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

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

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    • In genomics: 5 out of 4,057
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    • Site-wide: 3,530 out of 57,793
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    • Site-wide: 4,753 out of 57,793

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

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    • In genomics: 225 out of 4,057
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    • Site-wide: 116 out of 57,793
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    • Site-wide: 297 out of 57,793

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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    • In genomics: 252 out of 4,057
  • Year to date:
    • Site-wide: 9,741 out of 57,793
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    • Site-wide: 14,291 out of 57,793

Genome-wide association study of 1 million people identifies 111 loci for atrial fibrillation

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    • In genetics: 115 out of 3,318
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    • Site-wide: 4,472 out of 57,793
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    • Site-wide: 8,496 out of 57,793

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

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    • In genetics: 116 out of 3,318
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    • Site-wide: 10,124 out of 57,793

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

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

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  • Downloaded 1,637 times
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Clustering of Type 2 Diabetes Genetic Loci by Multi-Trait Associations Identifies Disease Mechanisms and Subtypes

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    • In genetics: 269 out of 3,318
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    • Site-wide: 11,930 out of 57,793

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: 345 out of 3,318
  • Year to date:
    • Site-wide: 2,768 out of 57,793
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    • Site-wide: 7,497 out of 57,793

Whole Genome Sequencing in Psychiatric Disorders: the WGSPD Consortium

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    • In genomics: 780 out of 4,057
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    • Site-wide: 22,139 out of 57,793
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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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    • In genomics: 798 out of 4,057
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PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION

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    • In genetics: 477 out of 3,318
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emeraLD: Rapid Linkage Disequilibrium Estimation with Massive Data Sets

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  • Downloaded 989 times
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    • In bioinformatics: 1,208 out of 5,897
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Association Analysis and Meta-Analysis of Multi-allelic Variants for Large Scale Sequence Data

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  • Downloaded 961 times
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    • In bioinformatics: 1,265 out of 5,897
  • Year to date:
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    • Site-wide: 6,235 out of 57,793

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

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    • In genomics: 1,201 out of 4,057
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  • Since beginning of last month:
    • Site-wide: 9,111 out of 57,793

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

genetics more details view paper
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    • In genetics: 630 out of 3,318
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    • Site-wide: 13,616 out of 57,793
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    • Site-wide: 19,701 out of 57,793

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

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    • In genetics: 654 out of 3,318
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    • Site-wide: 5,099 out of 57,793

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

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    • In genomics: 1,422 out of 4,057
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    • Site-wide: 2,581 out of 57,793

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

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  • Downloaded 733 times
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    • In genetics: 764 out of 3,318
  • Year to date:
    • Site-wide: 18,008 out of 57,793
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    • Site-wide: 16,968 out of 57,793

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

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  • Downloaded 730 times
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    • Site-wide: 10,583 out of 57,793
    • In genetics: 770 out of 3,318
  • Year to date:
    • Site-wide: 1,901 out of 57,793
  • Since beginning of last month:
    • Site-wide: 444 out of 57,793

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

genomics more details view paper
  • Downloaded 653 times
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    • In genomics: 1,716 out of 4,057
  • Year to date:
    • Site-wide: 44,641 out of 57,793
  • Since beginning of last month:
    • Site-wide: 46,317 out of 57,793

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

genomics more details view paper
  • Downloaded 577 times
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    • Site-wide: 14,682 out of 57,793
    • In genomics: 1,893 out of 4,057
  • Year to date:
    • Site-wide: 37,249 out of 57,793
  • Since beginning of last month:
    • Site-wide: 39,380 out of 57,793

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

genetics more details view paper
  • Downloaded 470 times
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    • Site-wide: 18,976 out of 57,793
    • In genetics: 1,297 out of 3,318
  • Year to date:
    • Site-wide: 52,034 out of 57,793
  • Since beginning of last month:
    • Site-wide: 53,919 out of 57,793

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

genetics more details view paper
  • Downloaded 461 times
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    • Site-wide: 19,387 out of 57,793
    • In genetics: 1,331 out of 3,318
  • Year to date:
    • Site-wide: 39,824 out of 57,793
  • Since beginning of last month:
    • Site-wide: 33,101 out of 57,793

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

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  • Downloaded 454 times
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    • In genetics: 1,347 out of 3,318
  • Year to date:
    • Site-wide: 4,292 out of 57,793
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    • Site-wide: 6,008 out of 57,793

Ancestry-agnostic estimation of DNA sample contamination from sequence reads

bioinformatics more details view paper
  • Downloaded 396 times
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    • In bioinformatics: 3,242 out of 5,897
  • Year to date:
    • Site-wide: 7,965 out of 57,793
  • Since beginning of last month:
    • Site-wide: 7,312 out of 57,793

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 356 times
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    • In genomics: 2,682 out of 4,057
  • Year to date:
    • Site-wide: 6,391 out of 57,793
  • Since beginning of last month:
    • Site-wide: 14,796 out of 57,793

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

genetics more details view paper
  • Downloaded 186 times
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    • Site-wide: 42,003 out of 57,793
    • In genetics: 2,584 out of 3,318
  • Year to date:
    • Site-wide: 40,005 out of 57,793
  • Since beginning of last month:
    • Site-wide: 25,262 out of 57,793

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 172 times
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    • In genetics: 2,671 out of 3,318
  • Year to date:
    • Site-wide: 53,792 out of 57,793
  • Since beginning of last month:
    • Site-wide: 54,516 out of 57,793

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