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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  • In bioinformatics: 92
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MR-Base: a platform for systematic causal inference across the phenome using billions of genetic associations

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  • In epidemiology: 366
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Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases

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  • In genetics: 108
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Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

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  • In genetics: 707
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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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  • In genomics: 2,472
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Partitioning Phenotypic Variance Due To Parent-Of-Origin Effects Using Genomic Relatedness Matrices

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  • In genetics: 3,705
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