Author: Jee-Young Moon
- ORCiD: http://orcid.org/0000-0001-9218-8335
- Most recently observed institution: Department of Epidemiology and Population Health, Albert Einstein College of Medicine
Rankings
- All-time downloads: 6,940 (rank: 28,334 (tie) )
- Categories:
- genetics: 2,770 (rank: 6,483 (tie) )
- genomics: 3,703 (rank: 6,486 (tie) )
- hematology: 467 (rank: 441 (tie) )
Downloads per author, site-wide
Preprints
Inherited Causes of Clonal Hematopoiesis of Indeterminate Potential in TOPMed Whole Genomes
genomics more details view paper- Downloaded 2,882 times
- Download rankings, all-time:
- Site-wide: 4,344
- In genomics: 488
- Year to date:
- Site-wide: 7,523
- Since beginning of last month:
- Site-wide: 9,299
Large-scale association analyses identify host factors influencing human gut microbiome composition
genetics more details view paper- Downloaded 2,153 times
- Download rankings, all-time:
- Site-wide: 6,682
- In genetics: 324
- Year to date:
- Site-wide: 3,010
- Since beginning of last month:
- Site-wide: 9,093
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 667 times
- Download rankings, all-time:
- Site-wide: 36,862
- In genomics: 3,144
- Year to date:
- Site-wide: 74,919
- Since beginning of last month:
- Site-wide: 101,408
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 617 times
- Download rankings, all-time:
- Site-wide: 40,775
- In genetics: 1,942
- Year to date:
- Site-wide: 4,854
- Since beginning of last month:
- Site-wide: 14,419
Whole genome sequencing association analysis of quantitative red blood cell phenotypes: the NHLBI TOPMed program
hematology more details view paper- Downloaded 467 times
- Download rankings, all-time:
- Site-wide: 56,853
- In hematology: 34
- Year to date:
- Site-wide: 6,336
- Since beginning of last month:
- Site-wide: 11,234
find-tfbs: a tool to identify functional non-coding variants associated with complex human traits using open chromatin maps and phased whole-genome sequences
genomics more details view paper- Downloaded 154 times
- Download rankings, all-time:
- Site-wide: 116,623
- In genomics: 6,472
- Year to date:
- Site-wide: 55,463
- Since beginning of last month:
- Site-wide: 53,865
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