Author: Nicholette D Palmer

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Preprints

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

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  • Site-wide: 990
  • In genomics: 93
• Year to date:
  • Site-wide: 1,366
• Since beginning of last month:
  • Site-wide: 1,263

Inherited Causes of Clonal Hematopoiesis of Indeterminate Potential in TOPMed Whole Genomes

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  • Site-wide: 4,294
  • In genomics: 494
• Year to date:
  • Site-wide: 6,966
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  • Site-wide: 7,105

Population sequencing data reveal a compendium of mutational processes in human germline

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  • Site-wide: 14,323
  • In genetics: 735
• Year to date:
  • Site-wide: 19,386
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  • Site-wide: 10,155

A high-resolution HLA reference panel capturing global population diversity enables multi-ethnic fine-mapping in HIV host response

• Downloaded 973 times
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  • Site-wide: 20,419
  • In hiv aids: 8
• Year to date:
  • Site-wide: 10,926
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  • Site-wide: 8,055

rs641738C>T near MBOAT7 promotes steatosis, NASH, fibrosis and hepatocellular carcinoma in non-alcoholic fatty liver disease: a meta-analysis

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  • Site-wide: 28,628
  • In gastroenterology: 20
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  • Site-wide: 24,124
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  • Site-wide: 15,638

Loss-of-function genomic variants with impact on liver-related blood traits highlight potential therapeutic targets for cardiovascular disease

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  • Site-wide: 30,097
  • In genomics: 2,748
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  • Site-wide: 50,587
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  • Site-wide: 59,076

The Trans-Ancestral Genomic Architecture of Glycaemic Traits

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  • Site-wide: 31,796
  • In genetics: 1,585
• Year to date:
  • Site-wide: 14,696
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  • Site-wide: 10,647

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

• Downloaded 660 times
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  • Site-wide: 35,185
  • In genomics: 3,083
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  • Site-wide: 65,623

Rare coding variants in 35 genes associate with circulating lipid levels: a multi-ancestry analysis of 170,000 exomes

• Downloaded 504 times
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  • Site-wide: 49,207
  • In genetics: 2,353
• Year to date:
  • Site-wide: 3,660
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  • Site-wide: None

Multi-ancestry analysis of gene-sleep interactions in 126,926 individuals identifies multiple novel blood lipid loci that contribute to our understanding of sleep-associated adverse blood lipid profile

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  • In genomics: 3,920
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  • Site-wide: 92,591

Genetic variants for head size share genes and pathways with cancer

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  • Site-wide: 73,930
  • In genomics: 5,035
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  • Site-wide: 44,004
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  • Site-wide: 56,808

Robust, flexible, and scalable tests for Hardy-Weinberg Equilibrium across diverse ancestries

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  • Site-wide: 85,368
  • In bioinformatics: 7,666
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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

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  • Site-wide: 86,422
  • In genetic and genomic medicine: 290
• Year to date:
  • Site-wide: 21,253
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  • Site-wide: 18,746

Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure

• Downloaded 199 times
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  • Site-wide: 102,026
  • In genomics: 6,016
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  • Site-wide: 96,692
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  • Site-wide: 101,609

Whole Genome Sequence Association Analysis of Fasting Glucose and Fasting Insulin Levels in Diverse Cohorts from the NHLBI TOPMed Program

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  • Site-wide: 112,411
  • In genetic and genomic medicine: 487
• Year to date:
  • Site-wide: 6,907
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  • Site-wide: 13,027