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:

Induction of resistance to chimeric antigen receptor T cell therapy by transduction of a single leukemic B cell
Marco Ruella, Jun Xu, David M. Barrett, et al.
Nature Medicine (2018) Vol. 24, Iss. 10, pp. 1499-1503
Open Access | Times Cited: 534

Showing 1-25 of 534 citing articles:

Engineering strategies to overcome the current roadblocks in CAR T cell therapy
Sarwish Rafiq, Christopher S. Hackett, Renier J. Brentjens
Nature Reviews Clinical Oncology (2019) Vol. 17, Iss. 3, pp. 147-167
Open Access | Times Cited: 1123

Mechanisms of resistance to CAR T cell therapy
Nirali N. Shah, Terry J. Fry
Nature Reviews Clinical Oncology (2019)
Open Access | Times Cited: 836

Recent advances and discoveries in the mechanisms and functions of CAR T cells
Rebecca C. Larson, Marcela V. Maus
Nature reviews. Cancer (2021) Vol. 21, Iss. 3, pp. 145-161
Open Access | Times Cited: 634

An introduction to chimeric antigen receptor (CAR) T‐cell immunotherapy for human cancer
Steven Feins, Weimin Kong, Erik F. Williams, et al.
American Journal of Hematology (2019) Vol. 94, Iss. S1
Open Access | Times Cited: 485

Tumor Immunology and Tumor Evolution: Intertwined Histories
Jérôme Galon, Daniela Bruni
Immunity (2020) Vol. 52, Iss. 1, pp. 55-81
Open Access | Times Cited: 457

Ionizable Lipid Nanoparticle-Mediated mRNA Delivery for Human CAR T Cell Engineering
Margaret M. Billingsley, Nathan Singh, Pranali Ravikumar, et al.
Nano Letters (2020) Vol. 20, Iss. 3, pp. 1578-1589
Open Access | Times Cited: 444

CAR exosomes derived from effector CAR-T cells have potent antitumour effects and low toxicity
Wenyan Fu, Changhai Lei, Shuowu Liu, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 374

Side-effect management of chimeric antigen receptor (CAR) T-cell therapy
Maria‐Luisa Schubert, Michael Schmitt, L. Wang, et al.
Annals of Oncology (2020) Vol. 32, Iss. 1, pp. 34-48
Open Access | Times Cited: 360

Engineering and Design of Chimeric Antigen Receptors
Sònia Guedan, Hugo Calderón, Avery D. Posey, et al.
Molecular Therapy — Methods & Clinical Development (2018) Vol. 12, pp. 145-156
Open Access | Times Cited: 348

γδ T cells: pleiotropic immune effectors with therapeutic potential in cancer
Bruno Silva‐Santos, Sofia Mensurado, Seth B. Coffelt
Nature reviews. Cancer (2019) Vol. 19, Iss. 7, pp. 392-404
Open Access | Times Cited: 327

Emerging Cellular Therapies for Cancer
Sònia Guedan, Marco Ruella, Carl H. June
Annual Review of Immunology (2018) Vol. 37, Iss. 1, pp. 145-171
Open Access | Times Cited: 324

Recent advances in CAR-T cell engineering
Ruihao Huang, Xiaoping Li, Yundi He, et al.
Journal of Hematology & Oncology (2020) Vol. 13, Iss. 1
Open Access | Times Cited: 297

Late Events after Treatment with CD19-Targeted Chimeric Antigen Receptor Modified T Cells
Ana Cordeiro, Evandro D. Bezerra, Alexandre V. Hirayama, et al.
Biology of Blood and Marrow Transplantation (2019) Vol. 26, Iss. 1, pp. 26-33
Open Access | Times Cited: 295

Universal CARs, universal T cells, and universal CAR T cells
Juanjuan Zhao, Quande Lin, Yongping Song, et al.
Journal of Hematology & Oncology (2018) Vol. 11, Iss. 1
Open Access | Times Cited: 257

Chimeric antigen receptor natural killer (CAR-NK) cell design and engineering for cancer therapy
Ying Gong, Roel G. J. Klein Wolterink, Jianxiang Wang, et al.
Journal of Hematology & Oncology (2021) Vol. 14, Iss. 1
Open Access | Times Cited: 248

Impaired Death Receptor Signaling in Leukemia Causes Antigen-Independent Resistance by Inducing CAR T-cell Dysfunction
Nathan Singh, Yong Gu Lee, Olga Shestova, et al.
Cancer Discovery (2020) Vol. 10, Iss. 4, pp. 552-567
Open Access | Times Cited: 241

Engineering the next-generation of CAR T-cells with CRISPR-Cas9 gene editing
Alexander Dimitri, Friederike Herbst, Joseph A. Fraietta
Molecular Cancer (2022) Vol. 21, Iss. 1
Open Access | Times Cited: 215

CAR-T Cell Therapy in Hematological Malignancies: Current Opportunities and Challenges
Xiaomin Zhang, Lingling Zhu, Hui Zhang, et al.
Frontiers in Immunology (2022) Vol. 13
Open Access | Times Cited: 209

Genetically engineered T cells for cancer immunotherapy
Dan Li, Xue Li, Weilin Zhou, et al.
Signal Transduction and Targeted Therapy (2019) Vol. 4, Iss. 1
Open Access | Times Cited: 205

Gut microbiome correlates of response and toxicity following anti-CD19 CAR T cell therapy
Melody Smith, Anqi Dai, Guido Ghilardi, et al.
Nature Medicine (2022) Vol. 28, Iss. 4, pp. 713-723
Open Access | Times Cited: 192

Applications of Surface Modification Technologies in Nanomedicine for Deep Tumor Penetration
Zimu Li, Xiaoting Shan, Zhidong Chen, et al.
Advanced Science (2020) Vol. 8, Iss. 1
Open Access | Times Cited: 180

CAR T-cell therapy is effective for CD19-dim B-lymphoblastic leukemia but is impacted by prior blinatumomab therapy
Vinodh Pillai, Kavitha Muralidharan, Wenzhao Meng, et al.
Blood Advances (2019) Vol. 3, Iss. 22, pp. 3539-3549
Open Access | Times Cited: 173

Hypoxia as a driver of resistance to immunotherapy
Joanna Kopecka, Iris C. Salaroglio, Elisabeth Pérez-Ruíz, et al.
Drug Resistance Updates (2021) Vol. 59, pp. 100787-100787
Open Access | Times Cited: 173

Scalable Manufacturing of CAR T Cells for Cancer Immunotherapy
Mohamed Abou‐El‐Enein, Magdi Elsallab, Steven A. Feldman, et al.
Blood Cancer Discovery (2021) Vol. 2, Iss. 5, pp. 408-422
Open Access | Times Cited: 170

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