Author: Sang Hong Lee

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Preprints

Regulatory variants explain much more heritability than coding variants across 11 common diseases

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Commentary on "Limitations of GCTA as a solution to the missing heritability problem"

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A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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A genetic investigation of sex bias in the prevalence of attention deficit hyperactivity disorder

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Estimation of genetic correlation using linkage disequilibrium score regression and genomic restricted maximum likelihood

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Mega-analysis of 31,396 individuals from 6 countries uncovers strong gene-environment interaction for human fertility

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Estimation Of Genomic Prediction Accuracy From Reference Populations With Varying Degrees Of Relationship

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Age at first birth in women is genetically associated with increased risk of schizophrenia

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Detecting genotype-population interaction effects by ancestry principal components

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A better design for stratified medicine based on genomic prediction

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CORE GREML: Estimating covariance between random effects in linear mixed models for genomic analyses of complex traits

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A Whole-Genome Approach Discovers Novel Genetic and Non-Genetic Variance Components Modulated by Lifestyle for Cardiovascular Health

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Implications of simplified linkage equilibrium SNP simulation

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GxEsum: genotype-by-environment interaction model based on summary statistics

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An integrative analysis of genomic and exposomic data for complex traits and phenotypic prediction

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Lifestyle modifies the diabetes-related metabolic risk, conditional on individual genetic differences

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