Croteau-Chonka DC, Rogers AJ, Raj T, et al. Expression Quantitative Trait Loci Information Improves Predictive Modeling of Disease Relevance of Non-Coding Genetic Variation. PLoS One. 2015;10(10):e0140758. doi:10.1371/journal.pone.0140758
Kogelman LJA, Zhernakova DV, Westra HJ, et al. An integrative systems genetics approach reveals potential causal genes and pathways related to obesity. Genome Med. 2015;7:105. doi:10.1186/s13073-015-0229-0
Tucker G, Loh PR, MacLeod IM, et al. Two-Variance-Component Model Improves Genetic Prediction in Family Datasets. Am J Hum Genet. 2015;97(5):677-90. doi:10.1016/j.ajhg.2015.10.002
Gutierrez-Achury J, Zorro MM, Ricaño-Ponce I, et al. Functional implications of disease-specific variants in loci jointly associated with coeliac disease and rheumatoid arthritis. Hum Mol Genet. 2016;25(1):180-90. doi:10.1093/hmg/ddv455
Gymrek M, Willems T, Guilmatre A, et al. Abundant contribution of short tandem repeats to gene expression variation in humans. Nat Genet. 2016;48(1):22-9. doi:10.1038/ng.3461
Ward LD, Kellis M. HaploReg v4: systematic mining of putative causal variants, cell types, regulators and target genes for human complex traits and disease. Nucleic Acids Res. 2016;44(D1):D877-81. doi:10.1093/nar/gkv1340
McClay JL, Shabalin AA, Dozmorov MG, et al. High density methylation QTL analysis in human blood via next-generation sequencing of the methylated genomic DNA fraction. Genome Biol. 2015;16:291. doi:10.1186/s13059-015-0842-7
Richards AL, Leonenko G, Walters JT, et al. Exome arrays capture polygenic rare variant contributions to schizophrenia. Hum Mol Genet. 2016;25(5):1001-7. doi:10.1093/hmg/ddv620
Lu Y, Day FR, Gustafsson S, et al. New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk. Nat Commun. 2016;7:10495. doi:10.1038/ncomms10495
Gusev A, Ko A, Shi H, et al. Integrative approaches for large-scale transcriptome-wide association studies. Nat Genet. 2016;48(3):245-52. doi:10.1038/ng.3506