Author: Charles Laurin

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Preprints

LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis

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  • Site-wide: 1,207
  • In bioinformatics: 78
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  • Site-wide: 32,488

MR-Base: a platform for systematic causal inference across the phenome using billions of genetic associations

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  • Site-wide: 2,703
  • In epidemiology: 284
• Year to date:
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  • Site-wide: 32,565

Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases

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  • Site-wide: 2,904
  • In genetics: 113
• Year to date:
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Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

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  • Site-wide: 12,426
  • In genetics: 612
• Year to date:
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Imprinted loci may be more widespread in humans than previously appreciated and enable limited assignment of parental allelic transmissions in unrelated individuals

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  • Site-wide: 24,334
  • In genomics: 2,327
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  • Site-wide: 49,324
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Partitioning Phenotypic Variance Due To Parent-Of-Origin Effects Using Genomic Relatedness Matrices

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  • Site-wide: 72,607
  • In genetics: 3,312
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