Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 71,071 bioRxiv papers from 310,049 authors.

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Preprints

Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism

• Downloaded 7,417 times
• Download rankings, all-time:
  • Site-wide: 234 out of 71,071
  • In genetics: 23 out of 3,937
• Year to date:
  • Site-wide: 1,002 out of 71,071
• Since beginning of last month:
  • Site-wide: 431 out of 71,071

Limited contribution of rare, noncoding variation to autism spectrum disorder from sequencing of 2,076 genomes in quartet families

• Downloaded 2,355 times
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  • Site-wide: 1,950 out of 71,071
  • In genomics: 419 out of 4,740
• Year to date:
  • Site-wide: 42,634 out of 71,071
• Since beginning of last month:
  • Site-wide: 34,758 out of 71,071

A statistical framework for mapping risk genes from de novo mutations in whole-genome sequencing studies

• Downloaded 1,628 times
• Download rankings, all-time:
  • Site-wide: 3,677 out of 71,071
  • In genetics: 312 out of 3,937
• Year to date:
  • Site-wide: 24,950 out of 71,071
• Since beginning of last month:
  • Site-wide: 33,518 out of 71,071

Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders

• Downloaded 1,267 times
• Download rankings, all-time:
  • Site-wide: 5,617 out of 71,071
  • In genomics: 949 out of 4,740
• Year to date:
  • Site-wide: 28,394 out of 71,071
• Since beginning of last month:
  • Site-wide: 31,801 out of 71,071

Mendelian randomization accounting for correlated and uncorrelated pleiotropic effects using genome-wide summary statistics.

• Downloaded 1,131 times
• Download rankings, all-time:
  • Site-wide: 6,816 out of 71,071
  • In genetics: 529 out of 3,937
• Year to date:
  • Site-wide: None out of 71,071
• Since beginning of last month:
  • Site-wide: None out of 71,071

Ultra-high throughput multiplexing and sequencing of >500 bp amplicon regions on the Illumina HiSeq 2500 platform

• Downloaded 1,085 times
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  • Site-wide: 7,297 out of 71,071
  • In microbiology: 296 out of 5,775
• Year to date:
  • Site-wide: 6,108 out of 71,071
• Since beginning of last month:
  • Site-wide: 12,558 out of 71,071

Post-transcriptionally impaired de novo mutations contribute to the genetic etiology of four neuropsychiatric disorders

• Downloaded 1,064 times
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  • Site-wide: 7,504 out of 71,071
  • In genomics: 1,194 out of 4,740
• Year to date:
  • Site-wide: 8,298 out of 71,071
• Since beginning of last month:
  • Site-wide: 12,875 out of 71,071

Primo: integration of multiple GWAS and omics QTL summary statistics for elucidation of molecular mechanisms of trait-associated SNPs and detection of pleiotropy in complex traits

• Downloaded 874 times
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  • Site-wide: 10,328 out of 71,071
  • In genomics: 1,522 out of 4,740
• Year to date:
  • Site-wide: 12,905 out of 71,071
• Since beginning of last month:
  • Site-wide: 13,780 out of 71,071

Model-based analysis of positive selection significantly expands the list of cancer driver genes, including RNA methyltransferases

• Downloaded 856 times
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  • Site-wide: 10,693 out of 71,071
  • In genomics: 1,566 out of 4,740
• Year to date:
  • Site-wide: 33,746 out of 71,071
• Since beginning of last month:
  • Site-wide: 14,929 out of 71,071

Integrative analysis of rare variants and pathway information shows convergent results between immune pathways, drug targets and epilepsy genes

• Downloaded 575 times
• Download rankings, all-time:
  • Site-wide: 19,067 out of 71,071
  • In genomics: 2,275 out of 4,740
• Year to date:
  • Site-wide: 11,370 out of 71,071
• Since beginning of last month:
  • Site-wide: 30,966 out of 71,071

Allele-specific open chromatin in human iPSC neurons elucidates functional non-coding disease variants

• Downloaded 208 times
• Download rankings, all-time:
  • Site-wide: 50,957 out of 71,071
  • In genetics: 3,025 out of 3,937
• Year to date:
  • Site-wide: 8,574 out of 71,071
• Since beginning of last month:
  • Site-wide: 15,739 out of 71,071

CCmed: cross-condition mediation analysis for identifying robust trans-eQTLs and assessing their effects on human traits

• Downloaded 205 times
• Download rankings, all-time:
  • Site-wide: 51,360 out of 71,071
  • In genetics: 3,052 out of 3,937
• Year to date:
  • Site-wide: 12,361 out of 71,071
• Since beginning of last month:
  • Site-wide: 29,032 out of 71,071

mTADA: a framework for analyzing de novo mutations in multiple traits

• Downloaded 202 times
• Download rankings, all-time:
  • Site-wide: 51,872 out of 71,071
  • In genomics: 4,103 out of 4,740
• Year to date:
  • Site-wide: 69,095 out of 71,071
• Since beginning of last month:
  • Site-wide: 66,022 out of 71,071

A Bayesian method for rare variant analysis using functional annotations and its application to Autism

• Downloaded 147 times
• Download rankings, all-time:
  • Site-wide: 60,202 out of 71,071
  • In genetics: 3,458 out of 3,937
• Year to date:
  • Site-wide: 10,382 out of 71,071
• Since beginning of last month:
  • Site-wide: 17,713 out of 71,071