Standout Papers

In vivo gene editing in dystrophic mouse muscle and muscle stem cells 2015 2026 2018 2022 772
  1. In vivo gene editing in dystrophic mouse muscle and muscle stem cells (2015)
    Mohammadsharif Tabebordbar, Kexian Zhu et al. Science
  2. A multifunctional AAV–CRISPR–Cas9 and its host response (2016)
    Wei Leong Chew, Mohammadsharif Tabebordbar et al. Nature Methods

Immediate Impact

19 by Nobel laureates 24 from Science/Nature 65 standout
Sub-graph 1 of 19

Citing Papers

Past, present, and future of CRISPR genome editing technologies
2024 Standout
CRISPR technologies for genome, epigenome and transcriptome editing
2024 Standout
14 intermediate papers

Works of Jason Cheng being referenced

dCas9-based gene editing for cleavage-free genomic knock-in of long sequences
2022
A multifunctional AAV–CRISPR–Cas9 and its host response
2016 Standout
and 1 more

Author Peers

Author Last Decade Papers Cites
Jason Cheng 1279 517 34 148 9 1.4k
Wei-Hsi Yeh 1616 555 13 126 11 1.8k
Michael A. Collingwood 1450 432 18 138 11 1.5k
Julian Grünewald 1520 434 16 158 11 1.6k
Nicole M. Bode 1180 414 17 126 11 1.4k
Ruth M. Castellanos Rivera 1439 668 3 127 13 1.6k
Wei Leong Chew 1756 632 9 188 22 2.0k
Joseph J. Belanto 2091 266 8 152 14 2.2k
Jean-Baptiste Renaud 1346 331 82 77 7 1.6k
Chris D. Richardson 1607 389 9 170 13 1.7k
Danny F. Xia 1953 595 52 142 7 2.1k

All Works

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2026