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:

Resolving Heart Regeneration by Replacement Histone Profiling
Joseph Goldman, Guray Kuzu, Nutishia Lee, et al.
Developmental Cell (2017) Vol. 40, Iss. 4, pp. 392-404.e5
Open Access | Times Cited: 105

Showing 1-25 of 105 citing articles:

Cardiac regeneration strategies: Staying young at heart
Eldad Tzahor, Kenneth D. Poss
Science (2017) Vol. 356, Iss. 6342, pp. 1035-1039
Open Access | Times Cited: 327

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

Acoel genome reveals the regulatory landscape of whole-body regeneration
Andrew R. Gehrke, Emily R Neverett, Yi‐Jyun Luo, et al.
Science (2019) Vol. 363, Iss. 6432
Open Access | Times Cited: 153

Kupffer-cell-derived IL-6 is repurposed for hepatocyte dedifferentiation via activating progenitor genes from injury-specific enhancers
Lu Li, Lei Cui, Ping Lin, et al.
Cell stem cell (2023) Vol. 30, Iss. 3, pp. 283-299.e9
Open Access | Times Cited: 58

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

Cardiac ageing: extrinsic and intrinsic factors in cellular renewal and senescence
Natalie Gude, Kathleen M. Broughton, Fareheh Firouzi, et al.
Nature Reviews Cardiology (2018) Vol. 15, Iss. 9, pp. 523-542
Closed Access | Times Cited: 141

Gene regulatory programmes of tissue regeneration
Joseph Goldman, Kenneth D. Poss
Nature Reviews Genetics (2020) Vol. 21, Iss. 9, pp. 511-525
Open Access | Times Cited: 135

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

A map of cis-regulatory elements and 3D genome structures in zebrafish
Hongbo Yang, Yu Luan, Tingting Liu, et al.
Nature (2020) Vol. 588, Iss. 7837, pp. 337-343
Open Access | Times Cited: 121

Structure and function of the Nppa–Nppb cluster locus during heart development and disease
Joyce C.K. Man, Phil Barnett, Vincent M. Christoffels
Cellular and Molecular Life Sciences (2018) Vol. 75, Iss. 8, pp. 1435-1444
Open Access | Times Cited: 103

Zebrafish Models of Cardiac Disease: From Fortuitous Mutants to Precision Medicine
Juan Manuel González‐Rosa
Circulation Research (2022) Vol. 130, Iss. 12, pp. 1803-1826
Open Access | Times Cited: 58

Distinct epicardial gene regulatory programs drive development and regeneration of the zebrafish heart
Michael Weinberger, Filipa C. Simões, Trishalee Gungoosingh, et al.
Developmental Cell (2024) Vol. 59, Iss. 3, pp. 351-367.e6
Open Access | Times Cited: 14

Hallmarks of regeneration
Kenneth D. Poss, Elly M. Tanaka
Cell stem cell (2024) Vol. 31, Iss. 9, pp. 1244-1261
Closed Access | Times Cited: 10

Tbx5a lineage tracing shows cardiomyocyte plasticity during zebrafish heart regeneration
Héctor Sánchez-Iranzo, María Galardi‐Castilla, Carolina Minguillón, et al.
Nature Communications (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 75

Damage-responsive elements in Drosophila regeneration
Elena Vizcaya-Molina, Cecília C. Klein, Florenci Serras, et al.
Genome Research (2018) Vol. 28, Iss. 12, pp. 1852-1866
Open Access | Times Cited: 65

Runx1 promotes scar deposition and inhibits myocardial proliferation and survival during zebrafish heart regeneration
Jana Koth, Xiaonan Wang, Abigail C. Killen, et al.
Development (2020) Vol. 147, Iss. 8
Open Access | Times Cited: 64

Regenerating zebrafish fin epigenome is characterized by stable lineage-specific DNA methylation and dynamic chromatin accessibility
Hyung Joo Lee, Yiran Hou, Yujie Chen, et al.
Genome biology (2020) Vol. 21, Iss. 1
Open Access | Times Cited: 59

Enhancer selection dictates gene expression responses in remote organs during tissue regeneration
Fei Sun, Jianhong Ou, Adam R. Shoffner, et al.
Nature Cell Biology (2022) Vol. 24, Iss. 5, pp. 685-696
Open Access | Times Cited: 34

An enhancer-based gene-therapy strategy for spatiotemporal control of cargoes during tissue repair
Ruorong Yan, Valentina Cigliola, Kelsey A. Oonk, et al.
Cell stem cell (2022) Vol. 30, Iss. 1, pp. 96-111.e6
Open Access | Times Cited: 34

Animal models to study cardiac regeneration
Michael Weinberger, Paul R. Riley
Nature Reviews Cardiology (2023) Vol. 21, Iss. 2, pp. 89-105
Closed Access | Times Cited: 20

Identification and requirements of enhancers that direct gene expression during zebrafish fin regeneration
John Thompson, Jianhong Ou, Nutishia Lee, et al.
Development (2020) Vol. 147, Iss. 14
Open Access | Times Cited: 49

Building bridges, not walls: spinal cord regeneration in zebrafish
Valentina Cigliola, Clayton J. Becker, Kenneth D. Poss
Disease Models & Mechanisms (2020) Vol. 13, Iss. 5
Open Access | Times Cited: 47

Hippo-Yap/Taz signalling in zebrafish regeneration
Susanna E. Riley, Yi Feng, Carsten Gram Hansen
npj Regenerative Medicine (2022) Vol. 7, Iss. 1
Open Access | Times Cited: 27

Page 1 - Next Page

Scroll to top