Menotti M, Ambrogio C, Cheong T-C, et al. Wiskott-Aldrich syndrome protein (WASP) is a tumor suppressor in T cell lymphoma. Nat Med. 2019;25(1):130-140. doi:10.1038/s41591-018-0262-9.

Li J, Zhang W, Yang H, et al. Spatiotemporal profile of postsynaptic interactomes integrates components of complex brain disorders. Nat Neurosci. 2017;20(8):1150-1161. doi:10.1038/nn.4594.

Rohban MH, Singh S, Wu X, et al. Systematic morphological profiling of human gene and allele function via Cell Painting. Elife. 2017;6. doi:10.7554/eLife.24060.

Gu X, Orozco JM, Saxton RA, et al. SAMTOR is an -adenosylmethionine sensor for the mTORC1 pathway. Science. 2017;358(6364):813-818. doi:10.1126/science.aao3265.

Du Z, Brewster R, Merrill PH, et al. Meningioma transcription factors link cell lineage with systemic metabolic cues. Neuro Oncol. 2018;20(10):1331-1343. doi:10.1093/neuonc/noy057.

Chao MJ, Kim K-H, Shin JW, et al. Population-specific genetic modification of Huntington’s disease in Venezuela. PLoS Genet. 2018;14(5):e1007274. doi:10.1371/journal.pgen.1007274.

Jayaraman D, Bae B-I, Walsh CA. The Genetics of Primary Microcephaly. Annu Rev Genomics Hum Genet. 2018;19:177-200. doi:10.1146/annurev-genom-083117-021441.

Kanneganti A, Malireddi RKS, Saavedra PHV, et al. GSDMD is critical for autoinflammatory pathology in a mouse model of Familial Mediterranean Fever. J Exp Med. 2018;215(6):1519-1529. doi:10.1084/jem.20172060.

Bick AG, Weinstock JS, Nandakumar SK, et al. Inherited causes of clonal haematopoiesis in 97,691 whole genomes. Nature. 2020;586(7831):763-768. doi:10.1038/s41586-020-2819-2.

Garvie CW, Wu X, Papanastasiou M, et al. Structure of PDE3A-SLFN12 complex reveals requirements for activation of SLFN12 RNase. Nat Commun. 2021;12(1):4375. doi:10.1038/s41467-021-24495-w.