Standout Papers
- Conversion of 5-Methylcytosine to 5-Hydroxymethylcytosine in Mammalian DNA by MLL Partner TET1 (2009)
- Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage (2016)
- Search-and-replace genome editing without double-strand breaks or donor DNA (2019)
- Programmable base editing of A•T to G•C in genomic DNA without DNA cleavage (2017)
- Genome editing with CRISPR–Cas nucleases, base editors, transposases and prime editors (2020)
- Cationic lipid-mediated delivery of proteins enables efficient protein-based genome editing in vitro and in vivo (2014)
- High-throughput profiling of off-target DNA cleavage reveals RNA-programmed Cas9 nuclease specificity (2013)
- Evolved Cas9 variants with broad PAM compatibility and high DNA specificity (2018)
- Sequence-Controlled Polymers (2013)
- Base editing: precision chemistry on the genome and transcriptome of living cells (2018)
- CRISPR-Based Technologies for the Manipulation of Eukaryotic Genomes (2016)
- Methods for the directed evolution of proteins (2015)
- Improving cytidine and adenine base editors by expression optimization and ancestral reconstruction (2018)
- Fusion of catalytically inactive Cas9 to FokI nuclease improves the specificity of genome modification (2014)
- A Small-Molecule Inhibitor of Tgf-β Signaling Replaces Sox2 in Reprogramming by Inducing Nanog (2009)
- Phage-assisted evolution of an adenine base editor with improved Cas domain compatibility and activity (2020)
- Increasing the genome-targeting scope and precision of base editing with engineered Cas9-cytidine deaminase fusions (2017)
- Sequence Determinants of Intracellular Phase Separation by Complex Coacervation of a Disordered Protein (2016)
- The Behaviour of 5-Hydroxymethylcytosine in Bisulfite Sequencing (2010)
- Improved base excision repair inhibition and bacteriophage Mu Gam protein yields C:G-to-T:A base editors with higher efficiency and product purity (2017)
- Prime genome editing in rice and wheat (2020)
- Efficient delivery of genome-editing proteins using bioreducible lipid nanoparticles (2016)
- A system for the continuous directed evolution of biomolecules (2011)
- A bacterial cytidine deaminase toxin enables CRISPR-free mitochondrial base editing (2020)
- DNA‐Templated Organic Synthesis: Nature's Strategy for Controlling Chemical Reactivity Applied to Synthetic Molecules (2004)
- Enhanced prime editing systems by manipulating cellular determinants of editing outcomes (2021)
- Treatment of autosomal dominant hearing loss by in vivo delivery of genome editing agents (2017)
- Predictable and precise template-free CRISPR editing of pathogenic variants (2018)
- Engineered virus-like particles for efficient in vivo delivery of therapeutic proteins (2022)
- Cytosine and adenine base editing of the brain, liver, retina, heart and skeletal muscle of mice via adeno-associated viruses (2020)
- Improving the DNA specificity and applicability of base editing through protein engineering and protein delivery (2017)
- Evaluation and minimization of Cas9-independent off-target DNA editing by cytosine base editors (2020)
- Prime editing for precise and highly versatile genome manipulation (2022)
- Therapeutic in vivo delivery of gene editing agents (2022)
- Programmable m6A modification of cellular RNAs with a Cas13-directed methyltransferase (2020)
- Massively parallel assessment of human variants with base editor screens (2021)
- Evolution of an adenine base editor into a small, efficient cytosine base editor with low off-target activity (2022)
- Phage-assisted evolution and protein engineering yield compact, efficient prime editors (2023)
- CRISPR-free base editors with enhanced activity and expanded targeting scope in mitochondrial and nuclear DNA (2022)
- DNA capture by a CRISPR-Cas9–guided adenine base editor (2020)
- Efficient in vivo base editing via single adeno-associated viruses with size-optimized genomes encoding compact adenine base editors (2022)
- Engineered virus-like particles for transient delivery of prime editor ribonucleoprotein complexes in vivo (2024)
- Efficient prime editing in mouse brain, liver and heart with dual AAVs (2023)
- Efficient in vivo genome editing prevents hypertrophic cardiomyopathy in mice (2023)
- Small-molecule discovery through DNA-encoded libraries (2023)
- Ex vivo prime editing of patient haematopoietic stem cells rescues sickle-cell disease phenotypes after engraftment in mice (2023)
- Efficient site-specific integration of large genes in mammalian cells via continuously evolved recombinases and prime editing (2024)
- Branched chemically modified poly(A) tails enhance the translation capacity of mRNA (2024)
Immediate Impact
42 by Nobel laureates 98 from Science/Nature 205 standout
Citing Papers
The road to fully programmable protein catalysis
2022 StandoutNatureNobel
The promise and challenge of therapeutic genome editing
2020 StandoutNatureNobel
Works of David R. Liu being referenced
Treatment of autosomal dominant hearing loss by in vivo delivery of genome editing agents
2017 StandoutNature
Efficient delivery of genome-editing proteins using bioreducible lipid nanoparticles
2016 Standout
Author Peers
| Author | Last Decade | Papers | Cites | ||||
|---|---|---|---|---|---|---|---|
| David R. Liu | 45346 | 10095 | 3506 | 4101 | 274 | 50.4k | |
| Jonathan S. Weissman | 66333 | 8084 | 521 | 3979 | 289 | 76.8k | |
| Jennifer A. Doudna | 69285 | 12026 | 323 | 7603 | 355 | 75.9k | |
| Wendell A. Lim | 23512 | 3965 | 480 | 2207 | 158 | 30.0k | |
| Phillip A. Sharp | 75784 | 17227 | 494 | 5702 | 428 | 91.6k | |
| Osamu Nureki | 19105 | 2923 | 444 | 1905 | 362 | 23.3k | |
| Feng Zhang | 74434 | 14566 | 216 | 7552 | 177 | 82.9k | |
| Dinshaw J. Patel | 44668 | 3411 | 2134 | 5481 | 555 | 50.8k | |
| Robert Tjian | 55642 | 13805 | 621 | 5474 | 336 | 69.0k | |
| Yi Zhang | 52178 | 9200 | 414 | 3526 | 413 | 59.2k | |
| Hidde L. Ploegh | 29898 | 4445 | 2561 | 1120 | 604 | 61.2k |
All Works
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