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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:

Strengthened Temporal Coordination within Pre-existing Sequential Cell Assemblies Supports Trajectory Replay
Usman Farooq, Jérémie Sibille, Kefei Liu, et al.
Neuron (2019) Vol. 103, Iss. 4, pp. 719-733.e7
Open Access | Times Cited: 74

Showing 1-25 of 74 citing articles:

Dynamics of Awake Hippocampal-Prefrontal Replay for Spatial Learning and Memory-Guided Decision Making
Justin D. Shin, Wenbo Tang, Shantanu P. Jadhav
Neuron (2019) Vol. 104, Iss. 6, pp. 1110-1125.e7
Open Access | Times Cited: 163
Preexisting hippocampal network dynamics constrain optogenetically induced place fields
Sam McKenzie, Roman Huszár, Daniel F. English, et al.
Neuron (2021) Vol. 109, Iss. 6, pp. 1040-1054.e7
Open Access | Times Cited: 142
Consolidation of human skill linked to waking hippocampo-neocortical replay
Ethan R. Buch, Leonardo Claudino, Romain Quentin, et al.
Cell Reports (2021) Vol. 35, Iss. 10, pp. 109193-109193
Open Access | Times Cited: 107
Hippocampo-cortical circuits for selective memory encoding, routing, and replay
Ryan E. Harvey, Heath L. Robinson, Can Liu, et al.
Neuron (2023) Vol. 111, Iss. 13, pp. 2076-2090.e9
Open Access | Times Cited: 65
Excitability mediates allocation of pre-configured ensembles to a hippocampal engram supporting contextual conditioned threat in mice
Andrew J. Mocle, Adam I. Ramsaran, Alexander D. Jacob, et al.
Neuron (2024) Vol. 112, Iss. 9, pp. 1487-1497.e6
Closed Access | Times Cited: 35
Sleep loss diminishes hippocampal reactivation and replay
Bapun Giri, Nathaniel R. Kinsky, Utku Kaya, et al.
Nature (2024) Vol. 630, Iss. 8018, pp. 935-942
Open Access | Times Cited: 16
The brain in motion: How ensemble fluidity drives memory-updating and flexibility
William Mau, Michael E. Hasselmo, Denise J. Cai
eLife (2020) Vol. 9
Open Access | Times Cited: 117
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
Retuning of hippocampal representations during sleep
Kourosh Maboudi, Bapun Giri, Hiroyuki Miyawaki, et al.
Nature (2024) Vol. 629, Iss. 8012, pp. 630-638
Open Access | Times Cited: 12
Remapping revisited: how the hippocampus represents different spaces
André A. Fenton
Nature reviews. Neuroscience (2024) Vol. 25, Iss. 6, pp. 428-448
Closed Access | Times Cited: 11
The Ontogeny of Hippocampus-Dependent Memories
Flavio Donato, Cristina M. Alberini, Dima Amso, et al.
Journal of Neuroscience (2020) Vol. 41, Iss. 5, pp. 920-926
Open Access | Times Cited: 54
Backbone spiking sequence as a basis for preplay, replay, and default states in human cortex
Alex Vaz, John H. Wittig, Sara K. Inati, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 22
The generative grammar of the brain: a critique of internally generated representations
George Drăgoi
Nature reviews. Neuroscience (2023) Vol. 25, Iss. 1, pp. 60-75
Closed Access | Times Cited: 18
Dynamic prediction of goal location by coordinated representation of prefrontal-hippocampal theta sequences
Yimeng Wang, Xueling Wang, Ling Wang, et al.
Current Biology (2024) Vol. 34, Iss. 9, pp. 1866-1879.e6
Closed Access | Times Cited: 7
Neuronal sequences in population bursts encode information in human cortex
Weizhen Xie, John H. Wittig, Julio I. Chapeton, et al.
Nature (2024) Vol. 635, Iss. 8040, pp. 935-942
Closed Access | Times Cited: 7
On the methods for reactivation and replay analysis
David Tingley, Adrien Peyrache
Philosophical Transactions of the Royal Society B Biological Sciences (2020) Vol. 375, Iss. 1799, pp. 20190231-20190231
Open Access | Times Cited: 49
Cell assemblies, sequences and temporal coding in the hippocampus
George Drăgoi
Current Opinion in Neurobiology (2020) Vol. 64, pp. 111-118
Open Access | Times Cited: 44
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
De novo inter-regional coactivations of preconfigured local ensembles support memory
Hiroyuki Miyawaki, Kenji Mizuseki
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 26
Effects of theta phase precessing optogenetic intervention on hippocampal neuronal reactivation and spatial maps
Yuki Aoki, Taiki Yokoi, Shota Morikawa, et al.
iScience (2023) Vol. 26, Iss. 7, pp. 107233-107233
Open Access | Times Cited: 13
Beneficial effects of cruceta (Acanthocereus tetragonus) on metabolic syndrome
Karla Lizzeth Morales-Cano, Carolina Peña-Montes, Rosa María Oliart‐Ros, et al.
Elsevier eBooks (2025), pp. 221-249
Closed Access
Spaces and sequences in the hippocampus: a homological perspective
Andrey Babichev, Vladmir Vashin, Yuri Dabaghian
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Sleep stages antagonistically modulate reactivation drift
Lars Bollmann, Péter Baracskay, Federico Stella, et al.
Neuron (2025)
Open Access
Experience reorganizes content-specific memory traces in macaques
Saman Abbaspoor, Ayman Aljishi, Kari L. Hoffman
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Hippocampal reactivation and replay: Findings and insights from rodent studies
Brian Kim, Kamran Diba
Elsevier eBooks (2025)
Closed Access
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