Wertz MH, Pineda S, Lee H, Kulicke R, Kellis M, Heiman M. Interleukin-6 deficiency exacerbates Huntington’s disease model phenotypes. Mol Neurodegener. 2020;15(1):29. doi:10.1186/s13024-020-00379-3
Publications
Wills JW, Robertson J, Summers HD, et al. Image-Based Cell Profiling Enables Quantitative Tissue Microscopy in Gastroenterology. Cytometry A. 2020. doi:10.1002/cyto.a.24042
Song M, Nguyen LH, Emilsson L, Chan AT, Ludvigsson JF. Antibiotic Use Associated With Risk of Colorectal Polyps in a Nationwide Study. Clin Gastroenterol Hepatol. 2020. doi:10.1016/j.cgh.2020.05.036
Ray J, Boydston EA, Shortt E, et al. A PEROXO-Tag Enables Rapid Isolation of Peroxisomes from Human Cells. iScience. 2020;23(5):101109. doi:10.1016/j.isci.2020.101109
Chen ZZ, Gerszten RE. Metabolomics and Proteomics in Type 2 Diabetes. Circ Res. 2020;126(11):1613-1627. doi:10.1161/CIRCRESAHA.120.315898
Bustoros M, Sklavenitis-Pistofidis R, Park J, et al. Genomic Profiling of Smoldering Multiple Myeloma Identifies Patients at a High Risk of Disease Progression. J Clin Oncol. 2020:JCO2000437. doi:10.1200/JCO.20.00437
Ollila HM. Narcolepsy Type 1: What have we learned from genetics? Sleep. 2020. doi:10.1093/sleep/zsaa099
Xiang J, Peng J, Baxter S, Peng Z. AutoPVS1: An automatic classification tool for PVS1 interpretation of null variants. Hum Mutat. 2020. doi:10.1002/humu.24051
Kabitzke P, Morales D, He D, et al. Mouse Model Systems of Autism Spectrum Disorder: Replicability and Informatics Signature. Genes Brain Behav. 2020:e12676. doi:10.1111/gbb.12676
Olinger E, Hofmann P, Kidd K, et al. Clinical and Genetic Spectra of Autosomal Dominant Tubulointerstitial Kidney Disease due to Mutations in UMOD and MUC1. Kidney Int. 2020. doi:10.1016/j.kint.2020.04.038