CRISPR Journal

Papers
(The TQCC of CRISPR Journal is 7. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-09-01 to 2025-09-01.)
ArticleCitations
CRISPR-Cas Gene Perturbation and Editing in Human Induced Pluripotent Stem Cells481
Exploring the Cytoplasmic Retention of CRISPR-Cas9 in Eukaryotic Cells: The Role of Nuclear Localization Signals and Ribosomal Interactions50
Hairpin Internal Nuclear Localization Signals in CRISPR-Cas9 Enhance Editing in Primary Human Lymphocytes48
Adaptation by Type V-A and V-B CRISPR-Cas Systems Demonstrates Conserved Protospacer Selection Mechanisms Between Diverse CRISPR-Cas Types44
Gene Editing Corrects In Vitro a G > A GLB1 Transition from a GM1 Gangliosidosis Patient40
Increasing Genome Editing Efficiency of Cas9 Nucleases by the Simultaneous Use of Transcriptional Activators and Histone Acetyltransferase Activator40
CRISPR Comparison Toolkit: Rapid Identification, Visualization, and Analysis of CRISPR Array Diversity37
Will Advances in Genetic Medicine Lessen the Need for Germline Modifications?36
Inference of CRISPR Edits from Sanger Trace Data33
Editing Properties of Base Editors with SpCas9-NG in Discarded Human Tripronuclear Zygotes31
A Taxonomic and Phylogenetic Classification of Diverse Base Editors30
Acknowledgment of Reviewers 202230
Curing “GFP-itis” in Bacteria with Base Editors: Development of a Genome Editing Science Program Implemented with High School Biology Students28
Novel CRISPR-Associated Gene-Editing Systems Discovered in Metagenomic Samples Enable Efficient and Specific Genome Engineering27
Advances in Cas12a-Based Amplification-Free Nucleic Acid Detection27
Opposing Human Genetic Engineering26
Gene Editing and Rett Syndrome: Does It Make the Cut?24
Generation of a Commercial-Scale Founder Population of Porcine Reproductive and Respiratory Syndrome Virus Resistant Pigs Using CRISPR-Cas22
Early Detection of Wildlife Disease Pathogens Using CRISPR-Cas System Methods21
Generation of Human Isogenic Induced Pluripotent Stem Cell Lines with CRISPR Prime Editing20
Implementing CRISPR-Cas9 Yeast Practicals into Biology Curricula20
Increasing the Targeting Scope of CRISPR Base Editing System Beyond NGG20
Efficient Homology-Directed Repair with Circular Single-Stranded DNA Donors17
CRISPR Crops and Sustainable Agriculture17
Comprehensive Analysis of CRISPR-Cas9 Editing Outcomes in Yeast Xanthophyllomyces dendrorhous17
The Roles and Responsibilities of Scientific Journals in Research Governance: Editorial Policymaking at Nature and Springer Nature (1995–2023)16
CRISPR Rewrites the Future of Medicine15
CRISPR à la carte15
A Story of Perseverance: An Interview with Matthew Porteus15
Evolutionary Biology and Gene Editing of Cat Allergen, Fel d 114
Widespread Impact of Natural Genetic Variations in CRISPR-Cas9 Outcomes14
Gene Editing in the Chagas Disease Vector Rhodnius prolixus by Cas9-Mediated ReMOT Control13
Engineered Antiviral Sensor Targets Infected Mosquitoes13
Evolution of Type IV CRISPR-Cas Systems: Insights from CRISPR Loci in Integrative Conjugative Elements of Acidithiobacillia12
Combined Theoretical, Bioinformatic, and Biochemical Analyses of RNA Editing by Adenine Base Editors12
dCas9 Tells Tales: Probing Gene Function and Transcription Regulation in Cancer12
Institutional Bioethics: From Critical Interdisciplinarity to Cosmopolitanism12
Automated Good Manufacturing Practice-Compatible CRISPR-Cas9 Editing of Hematopoietic Stem and Progenitor Cells for Clinical Treatment of β-Hemoglobinopathies12
Engineering CjCas9 for Efficient Base Editing and Prime Editing11
CRISPR Momentum in the Clinic and the Field11
Specific High-Sensitivity Enzymatic Reporter UnLOCKing-Mediated Detection of Oncogenic BCR::ABL1 and EGFR Rearrangements11
Fanzors: Mysterious TnpB-Like Bacterial Transposon-Related RNA-Guided DNA Nucleases of Eukaryotes11
Rational Engineering of CRISPR-Cas9 Nuclease to Attenuate Position-Dependent Off-Target Effects11
A PCR-Induced Mutagenesis-Restriction Fragment Length Polymorphism Method for the Detection of CRISPR-Induced Indels10
A Fluorescent Reporter Mouse for In Vivo Assessment of Genome Editing with Diverse Cas Nucleases and Prime Editors10
Enhancements of the CRISPR-Cas System in the Silkworm Bombyx mori10
Affordable Pricing of CRISPR Treatments is a Pressing Ethical Imperative10
A Protein-Cutting CRISPR Complex Caught in Action9
A Multiplexed Cas13-Based Assay with Point-of-Care Attributes for Simultaneous COVID-19 Diagnosis and Variant Surveillance9
The CRISPR Revolution in the Drug Discovery Workflow: An Industry Perspective9
Bacterial Retrons Enable Precise Gene Editing in Human Cells9
Rapid and Technically Simple Detection of SARS-CoV-2 Variants Using CRISPR Cas12 and Cas139
It's a Knockout for Cat Allergies?9
Warrior Spirit: An Interview with Victoria Gray, Sickle Cell Pioneer9
Introducing Faith-Based Claims to Ethical Discourse on Scientific Matters8
Acknowledgment of Reviewers 20238
Cas12a-Capture: A Novel, Low-Cost, and Scalable Method for Targeted Sequencing8
Spotlight on Genetic Design in a Spotted Wing Crop Killer8
CRISPR-Cas9-Mediated Correction of TSC2 Pathogenic Variants in iPSCs from Patients with Tuberous Sclerosis Complex Type 28
Navigating Viral Space with CRISPR Technologies7
Five Years of Progress in CRISPR Clinical Trials (2019–2024)7
Reduction of Pre-Existing Adaptive Immune Responses Against SaCas9 in Humans Using Epitope Mapping and Identification7
Base Editing of Somatic Cells Using CRISPR–Cas9 in Drosophila7
Rapid Variant Pathogenicity Analysis by CRISPR Activation of CRB1 Gene Expression in Patient-Derived Fibroblasts7
Genome Editing Headwinds: Can CRISPR Stay on Target?7
The New Old Colonialism7
CRISPR-Cas9 Gene Editing Protects from the A53T-SNCA Overexpression-Induced Pathology of Parkinson's Disease In Vivo7
Genome Editing Therapy for the Blood: Ex Vivo Success and In Vivo Prospects7
Trichostatin A for Efficient CRISPR-Cas9 Gene Editing of Human Pluripotent Stem Cells7
Moving Therapeutic Genome Editing into Global Clinical Trials and Medicine7
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