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Times Cited: 579
Times Cited: 579
Times Cited
Times Co-cited
Similarity
Multiplex genome engineering using CRISPR/Cas systems.
Le Cong, F Ann Ran, David Cox, Shuailiang Lin, Robert Barretto, Naomi Habib, Patrick D Hsu, Xuebing Wu, Wenyan Jiang, Luciano A Marraffini,[...]. Science 2013
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Search-and-replace genome editing without double-strand breaks or donor DNA.
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A programmable dual-RNA-guided DNA endonuclease in adaptive bacterial immunity.
Martin Jinek, Krzysztof Chylinski, Ines Fonfara, Michael Hauer, Jennifer A Doudna, Emmanuelle Charpentier. Science 2012
Martin Jinek, Krzysztof Chylinski, Ines Fonfara, Michael Hauer, Jennifer A Doudna, Emmanuelle Charpentier. Science 2012
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Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage.
Alexis C Komor, Yongjoo B Kim, Michael S Packer, John A Zuris, David R Liu. Nature 2016
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Programmable base editing of A•T to G•C in genomic DNA without DNA cleavage.
Nicole M Gaudelli, Alexis C Komor, Holly A Rees, Michael S Packer, Ahmed H Badran, David I Bryson, David R Liu. Nature 2017
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RNA-guided human genome engineering via Cas9.
Prashant Mali, Luhan Yang, Kevin M Esvelt, John Aach, Marc Guell, James E DiCarlo, Julie E Norville, George M Church. Science 2013
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Advances in genome editing through control of DNA repair pathways.
Charles D Yeh, Christopher D Richardson, Jacob E Corn. Nat Cell Biol 2019
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Homology-mediated end joining-based targeted integration using CRISPR/Cas9.
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In vivo genome editing using Staphylococcus aureus Cas9.
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Microhomology-mediated end-joining-dependent integration of donor DNA in cells and animals using TALENs and CRISPR/Cas9.
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Genome editing with CRISPR-Cas nucleases, base editors, transposases and prime editors.
Andrew V Anzalone, Luke W Koblan, David R Liu. Nat Biotechnol 2020
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One-step generation of mice carrying mutations in multiple genes by CRISPR/Cas-mediated genome engineering.
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Rationally engineered Cas9 nucleases with improved specificity.
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Enhanced homology-directed human genome engineering by controlled timing of CRISPR/Cas9 delivery.
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Development of a gene-editing approach to restore vision loss in Leber congenital amaurosis type 10.
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Cpf1 is a single RNA-guided endonuclease of a class 2 CRISPR-Cas system.
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Knock-in of large reporter genes in human cells via CRISPR/Cas9-induced homology-dependent and independent DNA repair.
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In vivo genome editing via the HITI method as a tool for gene therapy.
Keiichiro Suzuki, Juan Carlos Izpisua Belmonte. J Hum Genet 2018
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Double nicking by RNA-guided CRISPR Cas9 for enhanced genome editing specificity.
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Development and applications of CRISPR-Cas9 for genome engineering.
Patrick D Hsu, Eric S Lander, Feng Zhang. Cell 2014
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One-step generation of mice carrying reporter and conditional alleles by CRISPR/Cas-mediated genome engineering.
Hui Yang, Haoyi Wang, Chikdu S Shivalila, Albert W Cheng, Linyu Shi, Rudolf Jaenisch. Cell 2013
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High-fidelity CRISPR-Cas9 nucleases with no detectable genome-wide off-target effects.
Benjamin P Kleinstiver, Vikram Pattanayak, Michelle S Prew, Shengdar Q Tsai, Nhu T Nguyen, Zongli Zheng, J Keith Joung. Nature 2016
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High levels of AAV vector integration into CRISPR-induced DNA breaks.
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A high-fidelity Cas9 mutant delivered as a ribonucleoprotein complex enables efficient gene editing in human hematopoietic stem and progenitor cells.
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Highly efficient CRISPR/Cas9-mediated knock-in in zebrafish by homology-independent DNA repair.
Thomas O Auer, Karine Duroure, Anne De Cian, Jean-Paul Concordet, Filippo Del Bene. Genome Res 2014
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Enhanced proofreading governs CRISPR-Cas9 targeting accuracy.
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Genome engineering using the CRISPR-Cas9 system.
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Chemically modified guide RNAs enhance CRISPR-Cas genome editing in human primary cells.
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Increasing the efficiency of homology-directed repair for CRISPR-Cas9-induced precise gene editing in mammalian cells.
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Predictable and precise template-free CRISPR editing of pathogenic variants.
Max W Shen, Mandana Arbab, Jonathan Y Hsu, Daniel Worstell, Sannie J Culbertson, Olga Krabbe, Christopher A Cassa, David R Liu, David K Gifford, Richard I Sherwood. Nature 2018
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Virus-Mediated Genome Editing via Homology-Directed Repair in Mitotic and Postmitotic Cells in Mammalian Brain.
Jun Nishiyama, Takayasu Mikuni, Ryohei Yasuda. Neuron 2017
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Cas9-crRNA ribonucleoprotein complex mediates specific DNA cleavage for adaptive immunity in bacteria.
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Evolved Cas9 variants with broad PAM compatibility and high DNA specificity.
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Base editing: precision chemistry on the genome and transcriptome of living cells.
Holly A Rees, David R Liu. Nat Rev Genet 2018
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Long-term evaluation of AAV-CRISPR genome editing for Duchenne muscular dystrophy.
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In vivo genome editing with a small Cas9 orthologue derived from Campylobacter jejuni.
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Identification of preexisting adaptive immunity to Cas9 proteins in humans.
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Highly efficient therapeutic gene editing of human hematopoietic stem cells.
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Therapeutic genome editing: prospects and challenges.
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Genome editing. The new frontier of genome engineering with CRISPR-Cas9.
Jennifer A Doudna, Emmanuelle Charpentier. Science 2014
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Targeted nucleotide editing using hybrid prokaryotic and vertebrate adaptive immune systems.
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ZFN, TALEN, and CRISPR/Cas-based methods for genome engineering.
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Nanoparticle delivery of Cas9 ribonucleoprotein and donor DNA in vivo induces homology-directed DNA repair.
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Repair of double-strand breaks induced by CRISPR-Cas9 leads to large deletions and complex rearrangements.
Michael Kosicki, Kärt Tomberg, Allan Bradley. Nat Biotechnol 2018
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CRISPR-Cas9 genome editing induces a p53-mediated DNA damage response.
Emma Haapaniemi, Sandeep Botla, Jenna Persson, Bernhard Schmierer, Jussi Taipale. Nat Med 2018
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Enrichment of G2/M cell cycle phase in human pluripotent stem cells enhances HDR-mediated gene repair with customizable endonucleases.
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A mechanism for the suppression of homologous recombination in G1 cells.
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10
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.