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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:

Amputation‐induced reactive oxygen species signaling is required for axolotl tail regeneration
Nour W. Al Haj Baddar, Adarsh Chithrala, S. Randal Voss
Developmental Dynamics (2018) Vol. 248, Iss. 2, pp. 189-196
Open Access | Times Cited: 45

Showing 1-25 of 45 citing articles:

Mitochondrial function in spinal cord injury and regeneration
Paula G. Slater, Miguel E. Domínguez-Romero, Maximiliano Villarreal, et al.
Cellular and Molecular Life Sciences (2022) Vol. 79, Iss. 5
Closed Access | Times Cited: 57
Evolutionarily divergent mTOR remodels translatome for tissue regeneration
Olena Zhulyn, Hannah D. Rosenblatt, Leila Shokat, et al.
Nature (2023) Vol. 620, Iss. 7972, pp. 163-171
Closed Access | Times Cited: 34
Cellular and molecular roles of reactive oxygen species in wound healing
Matthew Hunt, Mónica S. Torres, Etty Bachar‐Wikstrom, et al.
Communications Biology (2024) Vol. 7, Iss. 1
Open Access | Times Cited: 12
Deep evolutionary origin of limb and fin regeneration
Sylvain Darnet, Aline Cutrim Dragalzew, Danielson B. Amaral, et al.
Proceedings of the National Academy of Sciences (2019) Vol. 116, Iss. 30, pp. 15106-15115
Open Access | Times Cited: 64
Synergistic ferroptosis-gemcitabine chemotherapy of the gemcitabine loaded carbonaceous nanozymes to enhance the treatment and magnetic resonance imaging monitoring of pancreatic cancer
Gaorui Zhang, Nianlu Li, Yafei Qi, et al.
Acta Biomaterialia (2022) Vol. 142, pp. 284-297
Closed Access | Times Cited: 27
Weak magnetic fields modulate superoxide to control planarian regeneration
Luke J. Kinsey, Alanna V. Van Huizen, Wendy S. Beane
Frontiers in Physics (2023) Vol. 10
Open Access | Times Cited: 15
Eya2 promotes cell cycle progression by regulating DNA damage response during vertebrate limb regeneration
Konstantinos Sousounis, Donald M. Bryant, Jose Martinez Fernandez, et al.
eLife (2020) Vol. 9
Open Access | Times Cited: 36
Appendage regeneration is context dependent at the cellular level
Can Aztekin
Open Biology (2021) Vol. 11, Iss. 7
Open Access | Times Cited: 28
Regeneration of Lumbriculus variegatus requires post‐amputation production of reactive oxygen species
Freya R. Beinart, Kathy M. Gillen
Development Growth & Differentiation (2025)
Open Access
Death fuels growth: Emerging players bridging apoptosis and cell proliferation in Drosophila and beyond
Caitlin Hounsell, Yun Fan
Seminars in Cell and Developmental Biology (2025) Vol. 169, pp. 103602-103602
Open Access
The quest for the perfect healing of human skin wounds: promising models
PraIlaria Dal Prà, Anna Chiarini, Daniele De Santis, et al.
Regenesis repair rehabilitation. (2025)
Open Access
Towards comparative analyses of salamander limb regeneration
Varun B. Dwaraka, S. Randal Voss
Journal of Experimental Zoology Part B Molecular and Developmental Evolution (2019) Vol. 336, Iss. 2, pp. 129-144
Open Access | Times Cited: 28
Cellular response to spinal cord injury in regenerative and non-regenerative stages in Xenopus laevis
Gabriela Edwards‐Faret, Karina González‐Pinto, Arantxa Cebrián‐Silla, et al.
Neural Development (2021) Vol. 16, Iss. 1
Open Access | Times Cited: 21
Hydrogen peroxide is necessary during tail regeneration in juvenile axolotl
Belfran Alcides Carbonell Medina, Juliana Zapata Cardona, Jean Paul Delgado
Developmental Dynamics (2021) Vol. 251, Iss. 6, pp. 1054-1076
Closed Access | Times Cited: 21
An early Shh–H2O2 reciprocal regulatory interaction controls the regenerative program during zebrafish fin regeneration
Marion Thauvin, Rodolphe Matias de Sousa, Marine Alves, et al.
Journal of Cell Science (2022) Vol. 135, Iss. 6
Open Access | Times Cited: 15
Duox is the primary NADPH oxidase responsible for ROS production during adult caudal fin regeneration in zebrafish
Kunal Chopra, Milda Folkmanaitė, Liam Stockdale, et al.
iScience (2023) Vol. 26, Iss. 3, pp. 106147-106147
Open Access | Times Cited: 7
HDAC Regulates Transcription at the Outset of Axolotl Tail Regeneration
S. Randal Voss, Larissa V. Ponomareva, Varun B. Dwaraka, et al.
Scientific Reports (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 20
The engine initiating tissue regeneration: does a common mechanism exist during evolution?
Yanmei Liu, Wilson Pak-Kin Lou, Ji‐Feng Fei
Cell Regeneration (2021) Vol. 10, Iss. 1
Open Access | Times Cited: 16
The rich evolutionary history of the Reactive Oxygen Species metabolic arsenal shapes its mechanistic plasticity at the onset of metazoan regeneration
Aurore Vullien, Aldine Amiel, Loeiza Baduel, et al.
Molecular Biology and Evolution (2024) Vol. 42, Iss. 1
Open Access | Times Cited: 2
Post-amputation reactive oxygen species production is necessary for axolotls limb regeneration
Belfran Carbonell-M, Juliana Zapata Cardona, Jean Paul Delgado
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 11
The sooner, the better: ROS, kinases and nutrients at the onset of the damage response in Drosophila
Florenci Serras
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 10
Total synthesis of griseusins and elucidation of the griseusin mechanism of action
Yinan Zhang, Qing Ye, Larissa V. Ponomareva, et al.
Chemical Science (2019) Vol. 10, Iss. 32, pp. 7641-7648
Open Access | Times Cited: 16
The amazing and anomalous axolotls as scientific models
Carly J. Adamson, Nikolas Morrison‐Welch, Crystal D. Rogers
Developmental Dynamics (2022) Vol. 251, Iss. 6, pp. 922-933
Open Access | Times Cited: 9
Reactive Oxygen Species Signaling Differentially Controls Wound Healing and Regeneration
Alanna V. Van Huizen, Samantha J. Hack, Jacqueline M. Greene, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 9
Key Proteins for Regeneration in A. mexicanum
Aylin Del Moral‐Morales, Cynthia Sámano, José Antonio Ocampo-Cervantes, et al.
Scientifica (2024) Vol. 2024, Iss. 1
Open Access | Times Cited: 1
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