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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:

Hippocampal replay of experience at real-world speeds
Eric L. Denovellis, Anna K. Gillespie, Michael E. Coulter, et al.
eLife (2021) Vol. 10
Open Access | Times Cited: 56

Showing 1-25 of 56 citing articles:

Hippocampal replay reflects specific past experiences rather than a plan for subsequent choice
Anna K. Gillespie, Daniela A. Astudillo Maya, Eric L. Denovellis, et al.
Neuron (2021) Vol. 109, Iss. 19, pp. 3149-3163.e6
Open Access | Times Cited: 142
Flexible rerouting of hippocampal replay sequences around changing barriers in the absence of global place field remapping
John Widloski, David J. Foster
Neuron (2022) Vol. 110, Iss. 9, pp. 1547-1558.e8
Open Access | Times Cited: 89
Consciousness and sleep
Giulio Tononi, Mélanie Boly, Chiara Cirelli
Neuron (2024) Vol. 112, Iss. 10, pp. 1568-1594
Closed Access | Times Cited: 19
A systems model of alternating theta sweeps via firing rate adaptation
Zilong Ji, Tianhao Chu, Si Wu, et al.
Current Biology (2025)
Open Access | Times Cited: 3
Imagination as a fundamental function of the hippocampus
Alison E. Comrie, Loren M. Frank, Kenneth Kay
Philosophical Transactions of the Royal Society B Biological Sciences (2022) Vol. 377, Iss. 1866
Open Access | Times Cited: 53
Dynamic synchronization between hippocampal representations and stepping
Abhilasha Joshi, Eric L. Denovellis, Abhijith Mankili, et al.
Nature (2023) Vol. 617, Iss. 7959, pp. 125-131
Open Access | Times Cited: 35
How our understanding of memory replay evolves
Zhe Chen, Matthew A. Wilson
Journal of Neurophysiology (2023) Vol. 129, Iss. 3, pp. 552-580
Open Access | Times Cited: 26
Hippocampal neuronal activity is aligned with action plans
Ipshita Zutshi, Athina Apostolelli, Wannan Yang, et al.
Nature (2025) Vol. 639, Iss. 8053, pp. 153-161
Open Access | Times Cited: 1
Temporally delayed linear modelling (TDLM) measures replay in both animals and humans
Yunzhe Liu, Raymond J. Dolan, Cameron Higgins, et al.
eLife (2021) Vol. 10
Open Access | Times Cited: 46
Replay in minds and machines
Lennart Wittkuhn, Samson Chien, Sam Hall-McMaster, et al.
Neuroscience & Biobehavioral Reviews (2021) Vol. 129, pp. 367-388
Open Access | Times Cited: 34
Spatial Learning Drives Rapid Goal Representation in Hippocampal Ripples without Place Field Accumulation or Goal-Oriented Theta Sequences
Brad E. Pfeiffer
Journal of Neuroscience (2022) Vol. 42, Iss. 19, pp. 3975-3988
Open Access | Times Cited: 27
Bidirectional synaptic changes in deep and superficial hippocampal neurons following in vivo activity
Marcus Berndt, Massimo Trusel, Todd F. Roberts, et al.
Neuron (2023) Vol. 111, Iss. 19, pp. 2984-2994.e4
Open Access | Times Cited: 14
Is episodic-like memory like episodic memory?
James R. Davies, Nicola S. Clayton
Philosophical Transactions of the Royal Society B Biological Sciences (2024) Vol. 379, Iss. 1913
Open Access | Times Cited: 5
The generative neural microdynamics of cognitive processing
Daniel McNamee
Current Opinion in Neurobiology (2024) Vol. 85, pp. 102855-102855
Open Access | Times Cited: 4
Closed-loop modulation of remote hippocampal representations with neurofeedback
Michael E. Coulter, Anna K. Gillespie, Joshua Chu, et al.
Neuron (2025) Vol. 113, Iss. 6, pp. 949-961.e3
Open Access
Neurons in the medial prefrontal cortex that are not modulated by hippocampal sharp-wave ripples are involved in spatial tuning and signaling upcoming choice
Hanna den Bakker, Fabian Kloosterman
(2025)
Open Access
Neurons in the medial prefrontal cortex that are not modulated by hippocampal sharp-wave ripples are involved in spatial tuning and signaling upcoming choice
Hanna den Bakker, Fabian Kloosterman
(2025)
Open Access
Hippocampal reactivation and replay: Findings and insights from rodent studies
Brian Kim, Kamran Diba
Elsevier eBooks (2025)
Closed Access
A large majority of awake hippocampal sharp-wave ripples feature spatial trajectories with momentum
Emma Krause, Jan Drugowitsch
Neuron (2021) Vol. 110, Iss. 4, pp. 722-733.e8
Open Access | Times Cited: 26
Spyglass: a framework for reproducible and shareable neuroscience research
Kyu Hyun Lee, Eric L. Denovellis, Ryan Ly, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 3
Activity Subspaces in Medial Prefrontal Cortex Distinguish States of the World
Silvia Maggi, Mark D. Humphries
Journal of Neuroscience (2022) Vol. 42, Iss. 20, pp. 4131-4146
Open Access | Times Cited: 14
Memory reactivations during sleep: a neural basis of dream experiences?
Claudia Picard‐Deland, Giulio Bernardi, Lisa Genzel, et al.
Trends in Cognitive Sciences (2023) Vol. 27, Iss. 6, pp. 568-582
Open Access | Times Cited: 8
Navigation Through the Complex World: The Neurophysiology of Decision-Making Processes
Ugurcan Mugan, Seiichiro Amemiya, Paul S. Regier, et al.
Springer eBooks (2024), pp. 109-139
Closed Access | Times Cited: 2
Hippocampal representations of alternative possibilities are flexibly generated to meet cognitive demands
Alison E. Comrie, Emily J. Monroe, Ari E. Kahn, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
Neural ensembles in navigation: From single cells to population codes
Emily A Aery Jones, Lisa M. Giocomo
Current Opinion in Neurobiology (2022) Vol. 78, pp. 102665-102665
Open Access | Times Cited: 12
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