Author: Lisa R Yanek
- ORCiD: http://orcid.org/0000-0001-7117-1075
- Most recently observed institution: GeneSTAR Research Program, Johns Hopkins University School of Medicine
Rankings
- All-time downloads: 16,845 (rank: 9,219 )
- Categories:
- genetic and genomic medicine: 1,154 (rank: 1,151 (tie) )
- genetics: 13,176 (rank: 1,020 )
- genomics: 1,852 (rank: 11,587 (tie) )
- hematology: 238 (rank: 553 (tie) )
- neuroscience: 425 (rank: 44,498 (tie) )
Downloads per author, site-wide
Preprints
Recovery of trait heritability from whole genome sequence data
genetics more details view paper- Downloaded 11,108 times
- Download rankings, all-time:
- Site-wide: 596
- In genetics: 16
- Year to date:
- Site-wide: 2,208
- Since beginning of last month:
- Site-wide: 2,513
Trans-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
genetic and genomic medicine more details view paper- Downloaded 853 times
- Download rankings, all-time:
- Site-wide: 23,324
- In genetic and genomic medicine: 61
- Year to date:
- Site-wide: 10,059
- Since beginning of last month:
- Site-wide: 5,795
Efficient variant set mixed model association tests for continuous and binary traits in large-scale whole genome sequencing studies
genetics more details view paper- Downloaded 824 times
- Download rankings, all-time:
- Site-wide: 24,518
- In genetics: 1,234
- Year to date:
- Site-wide: 50,526
- Since beginning of last month:
- Site-wide: 101,035
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 723 times
- Download rankings, all-time:
- Site-wide: 29,390
- In genomics: 2,710
- Year to date:
- Site-wide: 39,049
- Since beginning of last month:
- Site-wide: 44,822
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations
genomics more details view paper- Downloaded 654 times
- Download rankings, all-time:
- Site-wide: 33,685
- In genomics: 2,986
- Year to date:
- Site-wide: 16,812
- Since beginning of last month:
- Site-wide: 50,871
Genome Sequencing Unveils a New Regulatory Landscape of Platelet Reactivity
genomics more details view paper- Downloaded 475 times
- Download rankings, all-time:
- Site-wide: 49,938
- In genomics: 3,938
- Year to date:
- Site-wide: 84,498
- Since beginning of last month:
- Site-wide: 64,208
Rare coding variants in 35 genes associate with circulating lipid levels: a multi-ancestry analysis of 170,000 exomes
genetics more details view paper- Downloaded 462 times
- Download rankings, all-time:
- Site-wide: 51,521
- In genetics: 2,496
- Year to date:
- Site-wide: 655
- Since beginning of last month:
- Site-wide: 1,390
Common genetic variation indicates separate etiologies for periventricular and deep white matter hyperintensities
neuroscience more details view paper- Downloaded 425 times
- Download rankings, all-time:
- Site-wide: 56,228
- In neuroscience: 8,603
- Year to date:
- Site-wide: 47,602
- Since beginning of last month:
- Site-wide: 97,690
Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium
genetics more details view paper- Downloaded 263 times
- Download rankings, all-time:
- Site-wide: 84,162
- In genetics: 3,909
- Year to date:
- Site-wide: 94,260
- Since beginning of last month:
- Site-wide: 100,476
A system for phenotype harmonization in the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program
genetics more details view paper- Downloaded 260 times
- Download rankings, all-time:
- Site-wide: 84,749
- In genetics: 3,939
- Year to date:
- Site-wide: 14,820
- Since beginning of last month:
- Site-wide: 24,855
Evaluation of the causal effect of fibrinogen on incident coronary heart disease via Mendelian randomization
genetics more details view paper- Downloaded 259 times
- Download rankings, all-time:
- Site-wide: 85,019
- In genetics: 3,945
- Year to date:
- Site-wide: 90,859
- Since beginning of last month:
- Site-wide: 108,039
Whole genome sequencing association analysis of quantitative red blood cell phenotypes: the NHLBI TOPMed program
hematology more details view paper- Downloaded 238 times
- Download rankings, all-time:
- Site-wide: 89,333
- In hematology: 50
- Year to date:
- Site-wide: 3,533
- Since beginning of last month:
- Site-wide: 2,468
Rare Non-coding Variation Identified by Large Scale Whole Genome Sequencing Reveals Unexplained Heritability of Type 2 Diabetes: Trans-Omics for Precision Medicine (TOPMed) Program
genetic and genomic medicine more details view paper- Downloaded 221 times
- Download rankings, all-time:
- Site-wide: 92,791
- In genetic and genomic medicine: 305
- Year to date:
- Site-wide: 37,518
- Since beginning of last month:
- Site-wide: 8,978
Whole Genome Sequence Association Analysis of Fasting Glucose and Fasting Insulin Levels in Diverse Cohorts from the NHLBI TOPMed Program
genetic and genomic medicine more details view paper- Downloaded 80 times
- Download rankings, all-time:
- Site-wide: 119,295
- In genetic and genomic medicine: 516
- Year to date:
- Site-wide: 2,235
- Since beginning of last month:
- Site-wide: None
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News
- 27 Nov 2020: The website and API now include results pulled from medRxiv as well as bioRxiv.
- 18 Dec 2019: We're pleased to announce PanLingua, a new tool that enables you to search for machine-translated bioRxiv preprints using more than 100 different languages.
- 21 May 2019: PLOS Biology has published a community page about Rxivist.org and its design.
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- 1 Mar 2019: We now have summary statistics about bioRxiv downloads and submissions.
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- 22 Jan 2019: Nature just published an article about Rxivist and our data.
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