Citation Impact
Citing Papers
Potent CRISPR-Cas9 inhibitors from Staphylococcus genomes
2020 StandoutNobel
CRISPR/Cas9 in Genome Editing and Beyond
2016
A noninflammatory mRNA vaccine for treatment of experimental autoimmune encephalomyelitis
2021 StandoutScienceNobel
High-throughput biochemical profiling reveals sequence determinants of dCas9 off-target binding and unbinding
2017 StandoutNobel
Crippling life support for SARS-CoV-2 and other viruses through synthetic lethality
2020 StandoutNobel
Machine learning predicts new anti-CRISPR proteins
2020 StandoutNobel
Ligand-tethered lipid nanoparticles for targeted RNA delivery to treat liver fibrosis
2023 StandoutNobel
Extension of the crRNA enhances Cpf1 gene editing in vitro and in vivo
2018
Improved gRNA secondary structures allow editing of target sites resistant to CRISPR-Cas9 cleavage
2022 StandoutNobel
Engineered receptors for soluble cellular communication and disease sensing
2024 StandoutNatureNobel
The promise and challenge of therapeutic genome editing
2020 StandoutNatureNobel
Controlling CRISPR-Cas9 with ligand-activated and ligand-deactivated sgRNAs
2019 StandoutNobel
Enhancing extracellular vesicle cargo loading and functional delivery by engineering protein-lipid interactions
2024 StandoutNobel
Cell Hashing with barcoded antibodies enables multiplexing and doublet detection for single cell genomics
2018
Is autoimmunity the Achilles' heel of cancer immunotherapy?
2017
CRISPR/Cas9 genome editing in human hematopoietic stem cells
2018
Scrublet: Computational Identification of Cell Doublets in Single-Cell Transcriptomic Data
2019
Genetically encoding multiple functionalities into extracellular vesicles for the targeted delivery of biologics to T cells
2023
Modular and tunable biological feedback control using a de novo protein switch
2019 StandoutNatureNobel
Genome-Editing Technologies: Principles and Applications
2016
A genome-wide CRISPR screen identifies a restricted set of HIV host dependency factors
2016
New CRISPR–Cas systems from uncultivated microbes
2016 StandoutNatureNobel
Genome surgery using Cas9 ribonucleoproteins for the treatment of age-related macular degeneration
2017
The Principles of Engineering Immune Cells to Treat Cancer
2017
CRISPR–Cas9 genome engineering of primary CD4+ T cells for the interrogation of HIV–host factor interactions
2018 StandoutNobel
CRISPR-Cas9 Circular Permutants as Programmable Scaffolds for Genome Modification
2019 StandoutNobel
In vitro and ex vivo strategies for intracellular delivery
2016 Nature
Efficient integration of heterogeneous single-cell transcriptomes using Scanorama
2019
The changing landscape of atherosclerosis
2021 StandoutNature
A high-fidelity Cas9 mutant delivered as a ribonucleoprotein complex enables efficient gene editing in human hematopoietic stem and progenitor cells
2018
Highly efficient homology-driven genome editing in human T cells by combining zinc-finger nuclease mRNA and AAV6 donor delivery
2015
Integrating single-cell transcriptomic data across different conditions, technologies, and species
2018 Standout
A Cas9 Ribonucleoprotein Platform for Functional Genetic Studies of HIV-Host Interactions in Primary Human T Cells
2016 StandoutNobel
The single-cell transcriptional landscape of mammalian organogenesis
2019 StandoutNature
Engineered T cells: the promise and challenges of cancer immunotherapy
2016
Chimeric antigen receptors: driving immunology towards synthetic biology
2016
Next-generation regulatory T cell therapy
2019
Reference-based analysis of lung single-cell sequencing reveals a transitional profibrotic macrophage
2019 Standout
Primary, Adaptive, and Acquired Resistance to Cancer Immunotherapy
2017 Standout
Targeting Treg signaling for the treatment of autoimmune diseases
2015
Pooled Knockin Targeting for Genome Engineering of Cellular Immunotherapies
2020
Nanoparticles for nucleic acid delivery: Applications in cancer immunotherapy
2019
Applications of CRISPR technologies in research and beyond
2016 StandoutNobel
A thermostable Cas9 with increased lifetime in human plasma
2017 StandoutNobel
Chemistry of Class 1 CRISPR-Cas effectors: Binding, editing, and regulation
2020 StandoutNobel
Engineering of monosized lipid-coated mesoporous silica nanoparticles for CRISPR delivery
2020 StandoutNobel
The Biology of CRISPR-Cas: Backward and Forward
2018 StandoutNobel
CRISPR-Based Technologies for the Manipulation of Eukaryotic Genomes
2016 Standout
Cornerstones of CRISPR–Cas in drug discovery and therapy
2016 StandoutNobel
CasX enzymes comprise a distinct family of RNA-guided genome editors
2019 StandoutNatureNobel
Integrative single-cell analysis
2019
Comprehensive Integration of Single-Cell Data
2019 Standout
Organoid single-cell genomic atlas uncovers human-specific features of brain development
2019 StandoutNatureNobel
Human FOXP3+ Regulatory T Cell Heterogeneity and Function in Autoimmunity and Cancer
2019 StandoutNobel
Genome-editing Technologies for Gene and Cell Therapy
2016
The Unexpected Importance of the Primary Structure of the Hydrophobic Part of One-Component Ionizable Amphiphilic Janus Dendrimers in Targeted mRNA Delivery Activity
2022 StandoutNobel
Ionizable Lipid Nanoparticles for In Vivo mRNA Delivery to the Placenta during Pregnancy
2023 StandoutNobel
Single Cell RNA Sequencing in Atherosclerosis Research
2020
Taking regulatory T cells into medicine
2021 StandoutNobel
Targeted and Equally Distributed Delivery of mRNA to Organs with Pentaerythritol-Based One-Component Ionizable Amphiphilic Janus Dendrimers
2023 StandoutNobel
One-Component Multifunctional Sequence-Defined Ionizable Amphiphilic Janus Dendrimer Delivery Systems for mRNA
2021 StandoutNobel
Systematic discovery of natural CRISPR-Cas12a inhibitors
2018 StandoutScienceNobel
CRISPR-CasΦ from huge phages is a hypercompact genome editor
2020 StandoutScienceNobel
SAXSMoW 2.0: Online calculator of the molecular weight of proteins in dilute solution from experimental SAXS data measured on a relative scale
2018
The epigenetic landscape of T cell exhaustion
2016 Science
Tools for translation: non-viral materials for therapeutic mRNA delivery
2017
Chimeric Antigen Receptor Therapy
2018 Standout
Delivery technologies for genome editing
2017
Computational design of mechanically coupled axle-rotor protein assemblies
2022 StandoutScienceNobel
Multiplexed genetic engineering of human hematopoietic stem and progenitor cells using CRISPR/Cas9 and AAV6
2017
Proenkephalin+regulatory T cells expanded by ultraviolet B exposure maintain skin homeostasis with a healing function
2020 StandoutNobel
Targeted Delivery of mRNA with One-Component Ionizable Amphiphilic Janus Dendrimers
2021 StandoutNobel
Cas9 interrogates DNA in discrete steps modulated by mismatches and supercoiling
2020 StandoutNobel
Targeted gene knock-in by homology-directed genome editing using Cas9 ribonucleoprotein and AAV donor delivery
2017 StandoutNobel
CRISPR-Cas guides the future of genetic engineering
2018 StandoutScienceNobel
CAR T cell immunotherapy for human cancer
2018 StandoutScience
Cancer immunotherapy using checkpoint blockade
2018 StandoutScience
Nontoxic nanopore electroporation for effective intracellular delivery of biological macromolecules
2019 StandoutNobel
Works of Rachel E. Gate being referenced
Generation of knock-in primary human T cells using Cas9 ribonucleoproteins
2015 StandoutNobel
CRISPR/Cas9-mediated PD-1 disruption enhances anti-tumor efficacy of human chimeric antigen receptor T cells
2017
A Calmodulin C-Lobe Ca2+-Dependent Switch Governs Kv7 Channel Function
2018
Multiplexed droplet single-cell RNA-sequencing using natural genetic variation
2017