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Author: Daniel E. Weeks

  • ORCiD: http://orcid.org/0000-0001-9410-7228
  • Most recently observed institution: Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA

Rankings

  • All-time downloads: 20,705 (rank: 11,259 )
  • Categories:
    • bioinformatics: 409 (rank: 33,981 (tie) )
    • genetic and genomic medicine: 1,836 (rank: 2,371 )
    • genetics: 3,799 (rank: 5,091 (tie) )
    • genomics: 12,101 (rank: 1,753 )
    • obstetrics and gynecology: 625 (rank: 583 (tie) )
    • ophthalmology: 1,935 (rank: 38 (tie) )

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Preprints

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

genomics more details view paper
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Inherited Causes of Clonal Hematopoiesis of Indeterminate Potential in TOPMed Whole Genomes

genomics more details view paper
  • Downloaded 3,235 times
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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 1,277 times
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Deep-learning-based Prediction of Late Age-Related Macular Degeneration Progression

ophthalmology more details view paper
  • Downloaded 1,176 times
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    • In ophthalmology: 8
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GWAS-based Machine Learning for Prediction of Age-Related Macular Degeneration Risk

ophthalmology more details view paper
  • Downloaded 759 times
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    • In ophthalmology: 19
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Genome-wide association studies in Samoans give insight into the genetic architecture of fasting serum lipid levels

genetics more details view paper
  • Downloaded 745 times
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    • In genetics: 1,899
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Discordant association of the CREBRF rs373863828 minor allele with increased body mass index and protection from type 2 diabetes in Māori and Pacific (Polynesian) people living in Aotearoa New Zealand

genetics more details view paper
  • Downloaded 687 times
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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 597 times
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A system for phenotype harmonization in the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program

genetics more details view paper
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    • In genetics: 2,663
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A missense variant in CREBRF is associated with taller stature in Samoans

genetics more details view paper
  • Downloaded 519 times
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    • In genetics: 2,973
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Bidirectional Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of intermediate potential

genetic and genomic medicine more details view paper
  • Downloaded 490 times
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    • In genetic and genomic medicine: 368
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Robust, flexible, and scalable tests for Hardy-Weinberg Equilibrium across diverse ancestries

bioinformatics more details view paper
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    • In bioinformatics: 7,995
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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 371 times
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    • In genetic and genomic medicine: 527
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Racial Differences in DNA Methylation-Based Age Acceleration in Preeclamptic and Normotensive Pregnancy

obstetrics and gynecology more details view paper
  • Downloaded 314 times
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Utilization of Epigenome-wide DNA Methylation for Longitudinal Comparison of White Blood Cell Proportions Across Preeclamptic and Normotensive Pregnancy by Self-Reported Race

obstetrics and gynecology more details view paper
  • Downloaded 311 times
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A population-specific missense variant rs1597000001 in CETP promotes a favorable lipid profile and reduces CETP activity.

genetic and genomic medicine more details view paper
  • Downloaded 198 times
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CREBRF missense variant rs373863828 has both direct and indirect effects on type 2 diabetes and fasting glucose in Polynesians living in Samoa and Aotearoa New Zealand.

genetic and genomic medicine more details view paper
  • Downloaded 180 times
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Methylation Data Processing Protocol & Comparison of Blood and Cerebral Spinal Fluid Following Aneurysmal Subarachnoid Hemorrhage

genomics more details view paper
  • Downloaded 165 times
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