Park RJ, Wang T, Koundakjian D, et al. A genome-wide CRISPR screen identifies a restricted set of HIV host dependency factors. Nat Genet. 2017;49(2):193-203. doi:10.1038/ng.3741
Publications
Lane JM, Liang J, Vlasac I, et al. Genome-wide association analyses of sleep disturbance traits identify new loci and highlight shared genetics with neuropsychiatric and metabolic traits. Nat Genet. 2017;49(2):274-281. doi:10.1038/ng.3749
Reddy HM, Cho KA, Lek M, et al. The sensitivity of exome sequencing in identifying pathogenic mutations for LGMD in the United States. J Hum Genet. 2017;62(2):243-252. doi:10.1038/jhg.2016.116
Ardlie KG, Guigo R. Data Resources for Human Functional Genomics. Curr Opin Syst Biol. 2017;1:75-79. doi:10.1016/j.coisb.2016.12.019
Takenaka MC, Quintana FJ. Tolerogenic dendritic cells. Semin Immunopathol. 2017;39(2):113-120. doi:10.1007/s00281-016-0587-8
Sandholm N, Van Zuydam N, Ahlqvist E, et al. The Genetic Landscape of Renal Complications in Type 1 Diabetes. J Am Soc Nephrol. 2017;28(2):557-574. doi:10.1681/ASN.2016020231
Spracklen CN, Smith CJ, Saftlas AF, et al. Genetic predisposition to elevated levels of C-reactive protein is associated with a decreased risk for preeclampsia. Hypertens Pregnancy. 2017;36(1):30-35. doi:10.1080/10641955.2016.1223303
Hilgendorff A, Windhorst A, Klein M, et al. Gene expression profiling at birth characterizing the preterm infant with early onset infection. J Mol Med (Berl). 2017;95(2):169-180. doi:10.1007/s00109-016-1466-4
McCaffery JM, Jablonski KA, Franks PW, et al. Replication of the Association of BDNF and MC4R Variants With Dietary Intake in the Diabetes Prevention Program. Psychosom Med. 2017;79(2):224-233. doi:10.1097/PSY.0000000000000380
Manier S, Salem KZ, Park J, Landau DA, Getz G, Ghobrial IM. Genomic complexity of multiple myeloma and its clinical implications. Nat Rev Clin Oncol. 2017;14(2):100-113. doi:10.1038/nrclinonc.2016.122