Tiao G, Improgo MR, Kasar S, et al. Rare germline variants in ATM are associated with chronic lymphocytic leukemia. Leukemia. 2017;31(10):2244-2247. doi:10.1038/leu.2017.201
Publications
Taylor AR, Schaffner SF, Cerqueira GC, et al. Quantifying connectivity between local Plasmodium falciparum malaria parasite populations using identity by descent. PLoS Genet. 2017;13(10):e1007065. doi:10.1371/journal.pgen.1007065
Tang YC, Yuwen H, Wang K, et al. Aneuploid Cell Survival Relies upon Sphingolipid Homeostasis. Cancer Res. 2017;77(19):5272-5286. doi:10.1158/0008-5472.CAN-17-0049
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
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