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Biorxiv : the Preprint Server for Biology|April 1, 2024
CROPseq-multi: a versatile solution for multiplexed perturbation and decoding in pooled CRISPR screensRussell T Walton, Yue Qin, Paul C BlaineyMolecular Systems Biology|November 11, 2022
Pooled genetic screens with image-based profilingRussell T Walton, Avtar Singh, Paul C BlaineyNature Protocols|February 6, 2021
Scalable characterization of the PAM requirements of CRISPR-Cas enzymes using HT-PAMDARussell T Walton, Jonathan Y Hsu, J Keith Joung, et al.Science (New York, N.Y.)|March 29, 2020
Unconstrained genome targeting with near-PAMless engineered CRISPR-Cas9 variantsRussell T Walton, Kathleen A Christie, Madelynn N Whittaker, et al.Nature Biotechnology|October 6, 2022
Precise DNA cleavage using CRISPR-SpRYgestsKathleen A Christie, Jimmy A Guo, Rachel A Silverstein, et al.Science (New York, N.Y.)|September 8, 2018
Discovery of widespread type I and type V CRISPR-Cas inhibitorsNicole D Marino, Jenny Y Zhang, Adair L Borges, et al.Nature Biotechnology|February 12, 2019
Engineered CRISPR-Cas12a variants with increased activities and improved targeting ranges for gene, epigenetic and base editingBenjamin P Kleinstiver, Alexander A Sousa, Russell T Walton, et al.Nature Biotechnology|June 17, 2020
Publisher Correction: Engineered CRISPR-Cas12a variants with increased activities and improved targeting ranges for gene, epigenetic and base editingBenjamin P Kleinstiver, Alexander A Sousa, Russell T Walton, et al.Nature|April 22, 2025
Custom CRISPR-Cas9 PAM variants via scalable engineering and machine learningRachel A Silverstein, Nahye Kim, Ann-Sophie Kroell, et al.American Journal of Human Genetics|April 22, 2021
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed programYao Hu, Adrienne M Stilp, Caitlin P McHugh, et al.Pageof 1