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Works
6
Balancing selection on a regulatory region exhibiting ancient variation that predates human-neandertal divergence
Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease
A second generation human haplotype map of over 3.1 million SNPs
Genevar: a database and Java application for the analysis and visualization of SNP-gene associations in eQTL studies
Chromatin marks identify critical cell types for fine mapping complex trait variants
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
