YarnallMTN, IoannidiEI, Schmitt-UlmsC, et al.Drag-and-drop genome insertion of large sequences without double-strand DNA cleavage using CRISPR-directed integrases. Nat Biotechnol, 2022; doi: 10.1038/s41587-022-01527-4.
2.
KomorAC, KimYB, PackerMS, et al.Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage. Nature, 2016; 533(7603):420–424; doi: 10.1038/nature17946
3.
AnzaloneAV, RandolphPB, DavisJR, et al.Search-and-replace genome editing without double-strand breaks or donor DNA. Nature, 2019; 576(7785):149–157; doi: 10.1038/s41586-019-1711-4
4.
NakamuraM, GaoY, DominguezAA, et al.CRISPR technologies for precise epigenome editing. Nat Cell Biol, 2021; 23(1):11–22; doi: 10.1038/s41556-020-00620-7
5.
LeibowitzML, PapathanasiouS, DoerflerPA, et al.Chromothripsis as an on-target consequence of CRISPR-Cas9 genome editing. Nat Genet, 2021; 53(6):895–905; doi: 10.1038/s41588-021-00838-7
6.
NahmadAD, ReuveniE, GoldschmidtE, et al.Frequent aneuploidy in primary human T cells after CRISPR-Cas9 cleavage. Nat Biotechnol, 2022; 40(12):1807–1813; doi: 10.1038/s41587-022-01377-0
