Ji Z, He L, Rotem A, et al. Genome-scale identification of transcription factors that mediate an inflammatory network during breast cellular transformation. Nat Commun. 2018;9(1):2068. doi:10.1038/s41467-018-04406-2
Boycott KM, Rath A, Chong JX, et al. International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases. Am J Hum Genet. 2017;100(5):695-705. doi:10.1016/j.ajhg.2017.04.003
Xue Y, Mezzavilla M, Haber M, et al. Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations. Nat Commun. 2017;8:15927. doi:10.1038/ncomms15927
Zepeda-Mendoza CJ, Menon S, Morton CC. Computational Prediction of Position Effects of Human Chromosome Rearrangements. Curr Protoc Hum Genet. 2018;97(1). doi:10.1002/cphg.57
Ni G, Moser G, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Wray NR, Lee H. Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood. Am J Hum Genet. 2018;102(6):1185-1194. doi:10.1016/j.ajhg.2018.03.021
Mathieson I, Alpaslan-Roodenberg S, Posth C, et al. The genomic history of southeastern Europe. Nature. 2018;555(7695):197-203. doi:10.1038/nature25778
ENCODE Project Consortium, Snyder MP, Gingeras TR, et al. Perspectives on ENCODE. Nature. 2020;583(7818):693-698. doi:10.1038/s41586-020-2449-8
Sandoval GJ, Hahn WC. Going beyond genetics to discover cancer targets. Genome Biol. 2017;18(1):95. doi:10.1186/s13059-017-1238-7
Mashl J, Scott AD, Huang K lin, et al. GenomeVIP: a cloud platform for genomic variant discovery and interpretation. Genome Res. 2017;27(8):1450-1459. doi:10.1101/gr.211656.116
Waage J, Standl M, Curtin JA, et al. Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis. Nat Genet. 2018;50(8):1072-1080. doi:10.1038/s41588-018-0157-1