Loley C, Alver M, Assimes TL, et al. No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis. Sci Rep. 2016;6:35278. doi:10.1038/srep35278
Publications
Schuerle S, Dudani JS, Christiansen MG, Anikeeva P, Bhatia SN. Magnetically Actuated Protease Sensors for in Vivo Tumor Profiling. Nano Lett. 2016;16(10):6303-6310. doi:10.1021/acs.nanolett.6b02670
Kim S, Cho YS, Kim HM, et al. Comparison of carnivore, omnivore, and herbivore mammalian genomes with a new leopard assembly. Genome Biol. 2016;17(1):211. doi:10.1186/s13059-016-1071-4
Izar B, Rotem A. GILA, a Replacement for the Soft-Agar Assay that Permits High-Throughput Drug and Genetic Screens for Cellular Transformation. Curr Protoc Mol Biol. 2016;116:28.8.1-28.8.12. doi:10.1002/cpmb.26
Paredes MF, James D, Gil-Perotin S, et al. Extensive migration of young neurons into the infant human frontal lobe. Science. 2016;354(6308). doi:10.1126/science.aaf7073
Yosef N, Regev A. Writ large: Genomic dissection of the effect of cellular environment on immune response. Science. 2016;354(6308):64-68. doi:10.1126/science.aaf5453
Toby IT, Levin MK, Salinas EA, et al. VDJML: a file format with tools for capturing the results of inferring immune receptor rearrangements. BMC Bioinformatics. 2016;17(Suppl 13):333. doi:10.1186/s12859-016-1214-3
Hehir-Kwa JY, Marschall T, Kloosterman WP, et al. A high-quality human reference panel reveals the complexity and distribution of genomic structural variants. Nat Commun. 2016;7:12989. doi:10.1038/ncomms12989
Shashi V, Pena LDM, Kim K, et al. De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype. Am J Hum Genet. 2016;99(4):991-999. doi:10.1016/j.ajhg.2016.08.017
Chatterjee S, Kapoor A, Akiyama JA, et al. Enhancer Variants Synergistically Drive Dysfunction of a Gene Regulatory Network In Hirschsprung Disease. Cell. 2016;167(2):355-368.e10. doi:10.1016/j.cell.2016.09.005