Gymrek M, Willems T, Reich D, Erlich Y iv. Interpreting short tandem repeat variations in humans using mutational constraint. Nat Genet. 2017;49(10):1495-1501. doi:10.1038/ng.3952
Publications
Landry L, Nielsen DE, Carere DA, Roberts S, Green RC, PGen Study Group. Racial minority group interest in direct-to-consumer genetic testing: findings from the PGen study. J Community Genet. 2017;8(4):293-301. doi:10.1007/s12687-017-0325-5
Ng B, White CC, Klein HU, et al. An xQTL map integrates the genetic architecture of the human brain’s transcriptome and epigenome. Nat Neurosci. 2017;20(10):1418-1426. doi:10.1038/nn.4632
de la Fuente-Núñez C, Silva ON, Lu TK, Franco OL. Antimicrobial peptides: Role in human disease and potential as immunotherapies. Pharmacol Ther. 2017;178:132-140. doi:10.1016/j.pharmthera.2017.04.002
Vardarajan BN, Tosto G, Lefort R, et al. Ultra-rare mutations in segregate in Caribbean Hispanic families with Alzheimer disease. Neurol Genet. 2017;3(5):e178. doi:10.1212/NXG.0000000000000178
Habib N, Avraham-Davidi I, Basu A, et al. Massively parallel single-nucleus RNA-seq with DroNc-seq. Nat Methods. 2017;14(10):955-958. doi:10.1038/nmeth.4407
Hellwege JN, Jeff JM, Wise LA, et al. A multi-stage genome-wide association study of uterine fibroids in African Americans. Hum Genet. 2017;136(10):1363-1373. doi:10.1007/s00439-017-1836-1
May-Wilson S, Sud A, Law PJ, et al. Pro-inflammatory fatty acid profile and colorectal cancer risk: A Mendelian randomisation analysis. Eur J Cancer. 2017;84:228-238. doi:10.1016/j.ejca.2017.07.034
Schep AN, Wu B, Buenrostro JD, Greenleaf WJ. chromVAR: inferring transcription-factor-associated accessibility from single-cell epigenomic data. Nat Methods. 2017;14(10):975-978. doi:10.1038/nmeth.4401
Toledo E, Wang DD, Ruiz-Canela M, et al. Plasma lipidomic profiles and cardiovascular events in a randomized intervention trial with the Mediterranean diet. Am J Clin Nutr. 2017;106(4):973-983. doi:10.3945/ajcn.116.151159