Dutta AK, Alberge JB, Sklavenitis-Pistofidis R, Lightbody ED, Getz G, Ghobrial IM. Single-cell profiling of tumour evolution in multiple myeloma - opportunities for precision medicine. Nat Rev Clin Oncol. 2022. doi:10.1038/s41571-021-00593-y
Publications
Voorhies M, Cohen S, Shea TP, et al. Chromosome-Level Genome Assembly of a Human Fungal Pathogen Reveals Synteny among Geographically Distinct Species. mBio. 2022:e0257421. doi:10.1128/mbio.02574-21
Pages M, Rotem D, Gydush G, et al. Liquid biopsy detection of genomic alterations in pediatric brain tumors from cell-free DNA in peripheral blood, CSF, and urine. Neuro Oncol. 2022. doi:10.1093/neuonc/noab299
Ma Y, Yu L, Olah M, et al. Epigenomic features related to microglia are associated with attenuated effect of APOE ε4 on Alzheimer’s disease risk in humans. Alzheimer’s & dementia : the journal of the Alzheimer’s Association. 2022;18(4):688-699. doi:10.1002/alz.12425
PMCID
PMC9475136
Veitch DP, Weiner MW, Aisen PS, et al. Using the Alzheimer’s Disease Neuroimaging Initiative to improve early detection, diagnosis, and treatment of Alzheimer’s disease. Alzheimer’s & dementia : the journal of the Alzheimer’s Association. 2022;18(4):824-857. doi:10.1002/alz.12422
PMCID
PMC9158456
Gao Y, Felsky D, Reyes-Dumeyer D, et al. Integration of GWAS and brain transcriptomic analyses in a multiethnic sample of 35,245 older adults identifies DCDC2 gene as predictor of episodic memory maintenance. Alzheimer’s & dementia : the journal of the Alzheimer’s Association. 2022;18(10):1797-1811. doi:10.1002/alz.12524
PMCID
PMC9170841
Ming C, Wang M, Wang Q, et al. Whole genome sequencing-based copy number variations reveal novel pathways and targets in Alzheimer’s disease. Alzheimer’s & dementia : the journal of the Alzheimer’s Association. 2022;18(10):1846-1867. doi:10.1002/alz.12507
PMCID
PMC9264340
Rebbeck TR, Bridges JFP, Mack JW, et al. A Framework for Promoting Diversity, Equity, and Inclusion in Genetics and Genomics Research. JAMA health forum. 2022;3(4). doi:10.1001/jamahealthforum.2022.0603
Halford JL, Morrill VN, Choi SH, et al. Publisher Correction: Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes. Nature communications. 2022;13(1):5767. doi:10.1038/s41467-022-33534-z
Nauffal V, Morrill VN, Jurgens SJ, et al. Monogenic and Polygenic Contributions to QTc Prolongation in the Population. Circulation. 2022;145(20):1524-1533. doi:10.1161/CIRCULATIONAHA.121.057261