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Author: Jeffrey C Barrett

Rankings

  • All-time downloads: 70,603 (rank: 2,227 )
  • Categories:
    • bioinformatics: 571 (rank: 25,273 (tie) )
    • epidemiology: 1,605 (rank: 7,541 (tie) )
    • genetic and genomic medicine: 874 (rank: 3,932 (tie) )
    • genetics: 38,542 (rank: 143 )
    • genomics: 12,073 (rank: 1,654 )
    • infectious diseases: 16,938 (rank: 3,247 (tie) )

Downloads per author, site-wide

Preprints

Transmission of SARS-CoV-2 Lineage B.1.1.7 in England: Insights from linking epidemiological and genetic data

infectious diseases more details view paper
  • Downloaded 16,938 times
  • Download rankings, all-time:
    • Site-wide: 471
    • In infectious diseases: 166
  • Year to date:
    • Site-wide: 96
  • Since beginning of last month:
    • Site-wide: 3,085

Exploring the genetic architecture of inflammatory bowel disease by whole genome sequencing identifies association at ADCY7

genetics more details view paper
  • Downloaded 8,353 times
  • Download rankings, all-time:
    • Site-wide: 1,190
    • In genetics: 31
  • Year to date:
    • Site-wide: 124,187
  • Since beginning of last month:
    • Site-wide: 62,542

Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation

genetics more details view paper
  • Downloaded 7,565 times
  • Download rankings, all-time:
    • Site-wide: 1,346
    • In genetics: 36
  • Year to date:
    • Site-wide: 30,793
  • Since beginning of last month:
    • Site-wide: 73,311

New mutations, old statistical challenges

genetics more details view paper
  • Downloaded 7,183 times
  • Download rankings, all-time:
    • Site-wide: 1,436
    • In genetics: 44
  • Year to date:
    • Site-wide: 71,300
  • Since beginning of last month:
    • Site-wide: 73,202

Integrating healthcare and research genetic data empowers the discovery of 28 novel developmental disorders

genomics more details view paper
  • Downloaded 4,108 times
  • Download rankings, all-time:
    • Site-wide: 3,116
    • In genomics: 322
  • Year to date:
    • Site-wide: 12,537
  • Since beginning of last month:
    • Site-wide: 20,812

Association mapping of inflammatory bowel disease loci to single variant resolution

genetics more details view paper
  • Downloaded 3,646 times
  • Download rankings, all-time:
    • Site-wide: 3,673
    • In genetics: 127
  • Year to date:
    • Site-wide: 72,382
  • Since beginning of last month:
    • Site-wide: 73,396

De novo mutations in regulatory elements cause neurodevelopmental disorders

genetics more details view paper
  • Downloaded 2,139 times
  • Download rankings, all-time:
    • Site-wide: 7,920
    • In genetics: 348
  • Year to date:
    • Site-wide: 103,920
  • Since beginning of last month:
    • Site-wide: None

Common genetic variants contribute to risk of rare severe neurodevelopmental disorders

genetics more details view paper
  • Downloaded 1,942 times
  • Download rankings, all-time:
    • Site-wide: 9,128
    • In genetics: 390
  • Year to date:
    • Site-wide: 72,572
  • Since beginning of last month:
    • Site-wide: 72,978

Quantifying the contribution of recessive coding variation to developmental disorders

genetics more details view paper
  • Downloaded 1,914 times
  • Download rankings, all-time:
    • Site-wide: 9,332
    • In genetics: 403
  • Year to date:
    • Site-wide: 96,893
  • Since beginning of last month:
    • Site-wide: 73,147

HLA-DQA1*05 is associated with the development of antibodies to anti-TNF therapy

genomics more details view paper
  • Downloaded 1,882 times
  • Download rankings, all-time:
    • Site-wide: 9,577
    • In genomics: 979
  • Year to date:
    • Site-wide: 46,684
  • Since beginning of last month:
    • Site-wide: 80,593

Patterns of within-host genetic diversity in SARS-CoV-2

genomics more details view paper
  • Downloaded 1,845 times
  • Download rankings, all-time:
    • Site-wide: 9,844
    • In genomics: 1,006
  • Year to date:
    • Site-wide: 2,617
  • Since beginning of last month:
    • Site-wide: 27,032

Open Targets Genetics: An open approach to systematically prioritize causal variants and genes at all published human GWAS trait-associated loci

genetics more details view paper
  • Downloaded 1,700 times
  • Download rankings, all-time:
    • Site-wide: 11,113
    • In genetics: 494
  • Year to date:
    • Site-wide: 8,294
  • Since beginning of last month:
    • Site-wide: 18,633

Genomic reconstruction of the SARS-CoV-2 epidemic in England

epidemiology more details view paper
  • Downloaded 1,605 times
  • Download rankings, all-time:
    • Site-wide: 12,094
    • In epidemiology: 867
  • Year to date:
    • Site-wide: 1,636
  • Since beginning of last month:
    • Site-wide: 5,985

Pathogenicity and selective constraint on variation near splice sites

genetics more details view paper
  • Downloaded 1,565 times
  • Download rankings, all-time:
    • Site-wide: 12,507
    • In genetics: 568
  • Year to date:
    • Site-wide: 75,493
  • Since beginning of last month:
    • Site-wide: 61,346

Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease

genomics more details view paper
  • Downloaded 1,478 times
  • Download rankings, all-time:
    • Site-wide: 13,633
    • In genomics: 1,394
  • Year to date:
    • Site-wide: 105,066
  • Since beginning of last month:
    • Site-wide: None

Integrating healthcare and research genetic data empowers the discovery of 49 novel developmental disorders

genomics more details view paper
  • Downloaded 1,198 times
  • Download rankings, all-time:
    • Site-wide: 18,695
    • In genomics: 1,823
  • Year to date:
    • Site-wide: 84,386
  • Since beginning of last month:
    • Site-wide: 71,076

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

genetics more details view paper
  • Downloaded 1,164 times
  • Download rankings, all-time:
    • Site-wide: 19,514
    • In genetics: 903
  • Year to date:
    • Site-wide: 96,909
  • Since beginning of last month:
    • Site-wide: 61,869

Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders

genomics more details view paper
  • Downloaded 1,049 times
  • Download rankings, all-time:
    • Site-wide: 22,778
    • In genomics: 2,161
  • Year to date:
    • Site-wide: 106,995
  • Since beginning of last month:
    • Site-wide: 59,815

Rare schizophrenia risk variants are enriched in genes shared with neurodevelopmental disorders

genetics more details view paper
  • Downloaded 1,042 times
  • Download rankings, all-time:
    • Site-wide: 22,997
    • In genetics: 1,055
  • Year to date:
    • Site-wide: 91,477
  • Since beginning of last month:
    • Site-wide: 73,298

Sequencing of over 100,000 individuals identifies multiple genes and rare variants associated with Crohns disease susceptibility

genetic and genomic medicine more details view paper
  • Downloaded 874 times
  • Download rankings, all-time:
    • Site-wide: 29,606
    • In genetic and genomic medicine: 115
  • Year to date:
    • Site-wide: 3,765
  • Since beginning of last month:
    • Site-wide: 13,569

Designing an intuitive web application for drug discovery scientists

bioinformatics more details view paper
  • Downloaded 571 times
  • Download rankings, all-time:
    • Site-wide: 52,238
    • In bioinformatics: 5,330
  • Year to date:
    • Site-wide: 138,657
  • Since beginning of last month:
    • Site-wide: None

Joint sequencing of human and pathogen genomes reveals the genetics of pneumococcal meningitis

genomics more details view paper
  • Downloaded 513 times
  • Download rankings, all-time:
    • Site-wide: 59,334
    • In genomics: 4,351
  • Year to date:
    • Site-wide: 144,591
  • Since beginning of last month:
    • Site-wide: 72,340

Exome sequencing and genotyping identify a rare variant in NLRP7 gene associated with ulcerative colitis.

genetics more details view paper
  • Downloaded 329 times
  • Download rankings, all-time:
    • Site-wide: 91,126
    • In genetics: 3,944
  • Year to date:
    • Site-wide: 144,419
  • Since beginning of last month:
    • Site-wide: None

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