Leyton-Mange JS, Hucker WJ, Mihatov N, et al. Experience With Wearable Cardioverter-Defibrillators at 2 Academic Medical Centers. JACC Clin Electrophysiol. 2018;4(2):231-239. doi:10.1016/j.jacep.2017.09.180
Publications
Filbin MG, Sturm D. Gliomas in Children. Semin Neurol. 2018;38(1):121-130. doi:10.1055/s-0038-1635106
Wang G, Chow RD, Ye L, et al. Mapping a functional cancer genome atlas of tumor suppressors in mouse liver using AAV-CRISPR-mediated direct in vivo screening. Sci Adv. 2018;4(2):eaao5508. doi:10.1126/sciadv.aao5508
Pérez-Palma E, Saarentaus E, Ravoet M, et al. Duplications at 19q13.33 in patients with neurodevelopmental disorders. Neurol Genet. 2018;4(1):e210. doi:10.1212/NXG.0000000000000210
Attar M, Sharma E, Li S, et al. A practical solution for preserving single cells for RNA sequencing. Sci Rep. 2018;8(1):2151. doi:10.1038/s41598-018-20372-7
Li N, Lagier-Tourenne C. Nuclear pores: the gate to neurodegeneration. Nat Neurosci. 2018;21(2):156-158. doi:10.1038/s41593-017-0066-0
Bobbili DR, Lal D, May P, et al. Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy. Eur J Hum Genet. 2018;26(2):258-264. doi:10.1038/s41431-017-0034-x
Donaghey J, Thakurela S, Charlton J, et al. Genetic determinants and epigenetic effects of pioneer-factor occupancy. Nat Genet. 2018;50(2):250-258. doi:10.1038/s41588-017-0034-3
Maass PG, Barutcu R, Shechner DM, Weiner CL, Melé M, Rinn JL. Spatiotemporal allele organization by allele-specific CRISPR live-cell imaging (SNP-CLING). Nat Struct Mol Biol. 2018;25(2):176-184. doi:10.1038/s41594-017-0015-3
Crawford KM, Gallego-Fabrega C, Kourkoulis C, et al. Cerebrovascular Disease Knowledge Portal: An Open-Access Data Resource to Accelerate Genomic Discoveries in Stroke. Stroke. 2018;49(2):470-475. doi:10.1161/STROKEAHA.117.018922