Bullman S, Meyerson M, Kostic AD. Emerging Concepts and Technologies for the Discovery of Microorganisms Involved in Human Disease. Annu Rev Pathol. 2017;12:217-244. doi:10.1146/annurev-pathol-012615-044305
Publications
Ramkissoon SH, Bandopadhayay P, Hwang J, et al. Clinical targeted exome-based sequencing in combination with genome-wide copy number profiling: precision medicine analysis of 203 pediatric brain tumors. Neuro Oncol. 2017. doi:10.1093/neuonc/now294
Fischer M, Bittar M, Papa E, Kassam Z, Smith M. Can you cause inflammatory bowel disease with fecal transplantation? A 31-patient case-series of fecal transplantation using stool from a donor who later developed Crohn’s disease. Gut Microbes. 2017:1-3. doi:10.1080/19490976.2017.1283469
Campbell JD, Lathan C, Sholl L, et al. Comparison of Prevalence and Types of Mutations in Lung Cancers Among Black and White Populations. JAMA Oncol. 2017. doi:10.1001/jamaoncol.2016.6108
Seitz J, Rathi Y, Lyall A, et al. Alteration of gray matter microstructure in schizophrenia. Brain Imaging Behav. 2017. doi:10.1007/s11682-016-9666-7
Han PKJ, Umstead KL, Bernhardt BA, et al. A taxonomy of medical uncertainties in clinical genome sequencing. Genet Med. 2017. doi:10.1038/gim.2016.212
Woodruff LBA, Gorochowski TE, Roehner N, et al. Registry in a tube: multiplexed pools of retrievable parts for genetic design space exploration. Nucleic Acids Res. 2017. doi:10.1093/nar/gkx032
Tanay A, Regev A. Scaling single-cell genomics from phenomenology to mechanism. Nature. 2017;541(7637):331-338. doi:10.1038/nature21350
Li YY, T Y Chung G, W Y Lui V, et al. Exome and genome sequencing of nasopharynx cancer identifies NF-κB pathway activating mutations. Nat Commun. 2017;8:14121. doi:10.1038/ncomms14121
Hibar DP, Adams HHH, Jahanshad N, et al. Novel genetic loci associated with hippocampal volume. Nat Commun. 2017;8:13624. doi:10.1038/ncomms13624