Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Reciprocal analyses in zebrafish and medaka reveal that harnessing the immune response promotes cardiac regeneration
Shih-Lei Lai, Rubén Marín‐Juez, Pedro Luís Moura, et al.
eLife (2017) Vol. 6
Open Access | Times Cited: 258

Showing 1-25 of 258 citing articles:

Single-cell expression profiling reveals dynamic flux of cardiac stromal, vascular and immune cells in health and injury
Nona Farbehi, Ralph Patrick, Aude Dorison, et al.
eLife (2019) Vol. 8
Open Access | Times Cited: 477
Macrophages directly contribute collagen to scar formation during zebrafish heart regeneration and mouse heart repair
Filipa C. Simões, Thomas J. Cahill, Amy Kenyon, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 314
Role of Cardiac Macrophages on Cardiac Inflammation, Fibrosis and Tissue Repair
William P. Lafuse, Daniel J. Wozniak, Murugesan V. S. Rajaram
Cells (2020) Vol. 10, Iss. 1, pp. 51-51
Open Access | Times Cited: 258
Myocardial Polyploidization Creates a Barrier to Heart Regeneration in Zebrafish
Juan Manuel González‐Rosa, Michka Sharpe, Dorothy Field, et al.
Developmental Cell (2018) Vol. 44, Iss. 4, pp. 433-446.e7
Open Access | Times Cited: 236
Zebrafish Regulatory T Cells Mediate Organ-Specific Regenerative Programs
Subhra Prakash Hui, Delicia Z Sheng, Kotaro Sugimoto, et al.
Developmental Cell (2017) Vol. 43, Iss. 6, pp. 659-672.e5
Open Access | Times Cited: 231
Single-cell analysis uncovers that metabolic reprogramming by ErbB2 signaling is essential for cardiomyocyte proliferation in the regenerating heart
Hessel Honkoop, Dennis E. M. de Bakker, Alla Aharonov, et al.
eLife (2019) Vol. 8
Open Access | Times Cited: 221
The epicardium as a hub for heart regeneration
Jingli Cao, Kenneth D. Poss
Nature Reviews Cardiology (2018) Vol. 15, Iss. 10, pp. 631-647
Open Access | Times Cited: 202
Model systems for regeneration: zebrafish
Inês J. Marques, Eleonora Lupi, Nadia Mercader
Development (2019) Vol. 146, Iss. 18
Open Access | Times Cited: 191
The Macrophage in Cardiac Homeostasis and Disease
Kory J. Lavine, Alexander R. Pinto, Slava Epelman, et al.
Journal of the American College of Cardiology (2018) Vol. 72, Iss. 18, pp. 2213-2230
Open Access | Times Cited: 184
A double-edged sword of immuno-microenvironment in cardiac homeostasis and injury repair
Kang Sun, Yi‐yuan Li, Jin Jin
Signal Transduction and Targeted Therapy (2021) Vol. 6, Iss. 1
Open Access | Times Cited: 184
Polyploidy in Cardiomyocytes
Wouter Derks, Olaf Bergmann
Circulation Research (2020) Vol. 126, Iss. 4, pp. 552-565
Open Access | Times Cited: 158
Origin and function of activated fibroblast states during zebrafish heart regeneration
Bo Hu, Sara Lelek, Bastiaan Spanjaard, et al.
Nature Genetics (2022) Vol. 54, Iss. 8, pp. 1227-1237
Open Access | Times Cited: 85
Macrophage-based therapeutic approaches for cardiovascular diseases
Marida Sansonetti, Bashar Al Soodi, Thomas Thum, et al.
Basic Research in Cardiology (2024) Vol. 119, Iss. 1, pp. 1-33
Open Access | Times Cited: 24
Cross-species comparison reveals that Hmga1 reduces H3K27me3 levels to promote cardiomyocyte proliferation and cardiac regeneration
Mara Bouwman, Dennis E. M. de Bakker, Hessel Honkoop, et al.
Nature Cardiovascular Research (2025)
Open Access | Times Cited: 2
Revitalizing the heart: strategies and tools for cardiomyocyte regeneration post-myocardial infarction
Axelle Bois, Catarina Grandela, James Gallant, et al.
npj Regenerative Medicine (2025) Vol. 10, Iss. 1
Open Access | Times Cited: 2
AP-1 Contributes to Chromatin Accessibility to Promote Sarcomere Disassembly and Cardiomyocyte Protrusion During Zebrafish Heart Regeneration
Arica Beisaw, Carsten Kuenne, Stefan Guenther, et al.
Circulation Research (2020) Vol. 126, Iss. 12, pp. 1760-1778
Open Access | Times Cited: 123
The blastema and epimorphic regeneration in mammals
Ashley W. Seifert, Ken Muneoka
Developmental Biology (2017) Vol. 433, Iss. 2, pp. 190-199
Open Access | Times Cited: 121
Specific macrophage populations promote both cardiac scar deposition and subsequent resolution in adult zebrafish
Laura Bevan, Zhi Wei Lim, Byrappa Venkatesh, et al.
Cardiovascular Research (2019) Vol. 116, Iss. 7, pp. 1357-1371
Open Access | Times Cited: 121
The interstitium in cardiac repair: role of the immune–stromal cell interplay
Elvira Forte, Milena B. Furtado, Nadia Rosenthal
Nature Reviews Cardiology (2018) Vol. 15, Iss. 10, pp. 601-616
Open Access | Times Cited: 118
Coronary Revascularization During Heart Regeneration Is Regulated by Epicardial and Endocardial Cues and Forms a Scaffold for Cardiomyocyte Repopulation
Rubén Marín‐Juez, Hadil El‐Sammak, Christian SM Helker, et al.
Developmental Cell (2019) Vol. 51, Iss. 4, pp. 503-515.e4
Open Access | Times Cited: 118
Endocardial Notch Signaling Promotes Cardiomyocyte Proliferation in the Regenerating Zebrafish Heart through Wnt Pathway Antagonism
Long Zhao, Raz Ben-Yair, Caroline E. Burns, et al.
Cell Reports (2019) Vol. 26, Iss. 3, pp. 546-554.e5
Open Access | Times Cited: 99
Immune responses in cardiac repair and regeneration: a comparative point of view
Shih-Lei Lai, Rubén Marín‐Juez, Didier Y. R. Stainier
Cellular and Molecular Life Sciences (2018) Vol. 76, Iss. 7, pp. 1365-1380
Open Access | Times Cited: 92
Peripheral Macrophages Promote Tissue Regeneration in Zebrafish by Fine-Tuning the Inflammatory Response
Rodrigo A. Morales, Miguel L. Allende
Frontiers in Immunology (2019) Vol. 10
Open Access | Times Cited: 90
ZNF281 enhances cardiac reprogramming by modulating cardiac and inflammatory gene expression
Huanyu Zhou, María Gabriela Morales, Hisayuki Hashimoto, et al.
Genes & Development (2017) Vol. 31, Iss. 17, pp. 1770-1783
Open Access | Times Cited: 88
TLR3 Mediates Repair and Regeneration of Damaged Neonatal Heart through Glycolysis Dependent YAP1 Regulated miR-152 Expression
Xiaohui Wang, Tuanzhu Ha, Li Liu, et al.
Cell Death and Differentiation (2018) Vol. 25, Iss. 5, pp. 966-982
Open Access | Times Cited: 87
Page 1 - Next Page

Scroll to top