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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

The Chromatin Structure of CRISPR-Cas9 Target DNA Controls the Balance between Mutagenic and Homology-Directed Gene-Editing Events
Josephine M. Janssen, Xiaoyu Chen, Jin Liu, et al.
Molecular Therapy — Nucleic Acids (2019) Vol. 16, pp. 141-154
Open Access | Times Cited: 51

Showing 1-25 of 51 citing articles:

Inhibition of histone deacetylase 1 (HDAC1) and HDAC2 enhances CRISPR/Cas9 genome editing
Bin Liu, Siwei Chen, Anouk La Rose, et al.
Nucleic Acids Research (2019) Vol. 48, Iss. 2, pp. 517-532
Open Access | Times Cited: 293
Chromatin context-dependent regulation and epigenetic manipulation of prime editing
Xiaoyi Li, Wei Chen, Beth Martin, et al.
Cell (2024) Vol. 187, Iss. 10, pp. 2411-2427.e25
Open Access | Times Cited: 29
Combinatorial Polycation Synthesis and Causal Machine Learning Reveal Divergent Polymer Design Rules for Effective pDNA and Ribonucleoprotein Delivery
Ramya Kumar, Ngoc Le, Felipe Oviedo, et al.
JACS Au (2022) Vol. 2, Iss. 2, pp. 428-442
Open Access | Times Cited: 42
A multiplex guide RNA expression system and its efficacy for plant genome engineering
Youngbin Oh, Bora Lee, Hyeonjin Kim, et al.
Plant Methods (2020) Vol. 16, Iss. 1
Open Access | Times Cited: 60
Integrating gene delivery and gene-editing technologies by adenoviral vector transfer of optimized CRISPR-Cas9 components
Ignazio Maggio, Hidde A. Zittersteijn, Qian Wang, et al.
Gene Therapy (2020) Vol. 27, Iss. 5, pp. 209-225
Open Access | Times Cited: 56
Advances in Genome Editing and Application to the Generation of Genetically Modified Rat Models
Vanessa Chenouard, Séverine Rémy, Laurent Tesson, et al.
Frontiers in Genetics (2021) Vol. 12
Open Access | Times Cited: 42
Decorating chromatin for enhanced genome editing using CRISPR-Cas9
Evelyn Chen, Enrique Lin-Shiao, Marena Trinidad, et al.
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 49
Open Access | Times Cited: 33
New advances in CRISPR/Cas-mediated precise gene-editing techniques
Chris Richardson, Robert N. Kelsh, Rebecca J. Richardson
Disease Models & Mechanisms (2023) Vol. 16, Iss. 2
Open Access | Times Cited: 21
Chromatin context-dependent regulation and epigenetic manipulation of prime editing
Xiaoyi Li, Wei Chen, Beth Martin, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 21
Improving Precise CRISPR Genome Editing by Small Molecules: Is there a Magic Potion?
Nadja Bischoff, Sandra Wimberger, Marcello Maresca, et al.
Cells (2020) Vol. 9, Iss. 5, pp. 1318-1318
Open Access | Times Cited: 49
Moving Mountains—The BRCA1 Promotion of DNA Resection
Ruth M. Densham, Joanna R. Morris
Frontiers in Molecular Biosciences (2019) Vol. 6
Open Access | Times Cited: 45
mRNA, a Revolution in Biomedicine
Bruno Baptista, Rita Carapito, Nabila Laroui, et al.
Pharmaceutics (2021) Vol. 13, Iss. 12, pp. 2090-2090
Open Access | Times Cited: 38
Meiotic Cas9 expression mediates gene conversion in the male and female mouse germline
Alexander J. Weitzel, Hannah A. Grunwald, Ceri Weber, et al.
PLoS Biology (2021) Vol. 19, Iss. 12, pp. e3001478-e3001478
Open Access | Times Cited: 37
Strategies for Enhancing the Homology-Directed Repair Efficiency of CRISPR-Cas Systems
Wenli Sun, Hui Liu, Wenhao Yin, et al.
The CRISPR Journal (2022) Vol. 5, Iss. 1, pp. 7-18
Closed Access | Times Cited: 25
Improving Homology-Directed Repair in Genome Editing Experiments by Influencing the Cell Cycle
Svetlana Smirnikhina, Milyausha I. Zaynitdinova, Vasilina A. Sergeeva, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 11, pp. 5992-5992
Open Access | Times Cited: 23
A scalable CRISPR/Cas9-based fluorescent reporter assay to study DNA double-strand break repair choice
Paris Roidos, Stéphanie Sungalee, Salvatore Benfatto, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 37
A repackaged CRISPR platform increases homology-directed repair for yeast engineering
Deon Ploessl, Yuxin Zhao, Mingfeng Cao, et al.
Nature Chemical Biology (2021) Vol. 18, Iss. 1, pp. 38-46
Closed Access | Times Cited: 31
Small Molecule MIF Modulation Enhances Ferroptosis by Impairing DNA Repair Mechanisms
Deng Chen, Chunlong Zhao, Jianqiu Zhang, et al.
Advanced Science (2024) Vol. 11, Iss. 32
Open Access | Times Cited: 4
Double-strand break toxicity is chromatin context independent
Anoek Friskes, Lisa Koob, Lenno Krenning, et al.
Nucleic Acids Research (2022) Vol. 50, Iss. 17, pp. 9930-9947
Open Access | Times Cited: 19
Precise homology-directed installation of large genomic edits in human cells with cleaving and nicking high-specificity Cas9 variants
Qian Wang, Jin Liu, Josephine M. Janssen, et al.
Nucleic Acids Research (2023) Vol. 51, Iss. 7, pp. 3465-3484
Open Access | Times Cited: 10
Comparative Analysis of Methods for Assessing On-Target Gene Editing Efficiencies
Bing Yao, Qiangbing Yang, Manuel A. F. V. Gonçalves, et al.
Methods and Protocols (2025) Vol. 8, Iss. 2, pp. 23-23
Open Access
Beyond a few bases: methods for large DNA insertion and gene targeting in plants
Katie Vollen, José M. Alonso, Anna N. Stepanova
The Plant Journal (2025) Vol. 121, Iss. 6
Open Access
An Overview and Comparative Analysis of CRISPR-SpCas9 gRNA Activity Prediction Tools
Hao Yuan, Chunping Song, Huixin Xu, et al.
The CRISPR Journal (2025)
Closed Access
The Off-Targets of Clustered Regularly Interspaced Short Palindromic Repeats Gene Editing
Manuel M. Vicente, Miguel Chaves‐Ferreira, João M. P. Jorge, et al.
Frontiers in Cell and Developmental Biology (2021) Vol. 9
Open Access | Times Cited: 18
Non-immunogenic Induced Pluripotent Stem Cells, a Promising Way Forward for Allogenic Transplantations for Neurological Disorders
Henriette R. Frederiksen, Ulrik Doehn, Pernille Tveden‐Nyborg, et al.
Frontiers in Genome Editing (2021) Vol. 2
Open Access | Times Cited: 17
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