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:

Signatures of rapid plasticity in hippocampal CA1 representations during novel experiences
James B. Priestley, John C. Bowler, Sebi V. Rolotti, et al.
Neuron (2022) Vol. 110, Iss. 12, pp. 1978-1992.e6
Open Access | Times Cited: 84

Showing 1-25 of 84 citing articles:

Entorhinal cortex directs learning-related changes in CA1 representations
Christine Grienberger, Jeffrey C. Magee
Nature (2022) Vol. 611, Iss. 7936, pp. 554-562
Open Access | Times Cited: 85

Synaptic memory and CaMKII
Roger A. Nicoll, Howard Schulman
Physiological Reviews (2023) Vol. 103, Iss. 4, pp. 2897-2945
Open Access | Times Cited: 37

A thalamic-hippocampal CA1 signal for contextual fear memory suppression, extinction, and discrimination
Heather Ratigan, Seetha Krishnan, Shai Smith, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 25

Direct cortical inputs to hippocampal area CA1 transmit complementary signals for goal-directed navigation
John C. Bowler, Attila Losonczy
Neuron (2023) Vol. 111, Iss. 24, pp. 4071-4085.e6
Open Access | Times Cited: 24

Awake ripples enhance emotional memory encoding in the human brain
Haoxin Zhang, Ivan Skelin, Shiting Ma, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 9

Subfield-specific interneuron circuits govern the hippocampal response to novelty in male mice
Thomas Hainmueller, Aurore Cazala, Li-Wen Huang, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 9

Mouse hippocampal CA1 VIP interneurons detect novelty in the environment and support recognition memory
Suhel Tamboli, Sanjay Singh, Dimitry Topolnik, et al.
Cell Reports (2024) Vol. 43, Iss. 4, pp. 114115-114115
Open Access | Times Cited: 7

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: 7

A consistent map in the medial entorhinal cortex supports spatial memory
Taylor J. Malone, Nai-Wen Tien, Yan Ma, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 6

Coordinated representations for naturalistic memory encoding and retrieval in hippocampal neural subspaces
Dasom Kwon, Jungwoo Kim, Seng Bum Michael Yoo, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access

Mental navigation and the neural mechanisms of insight
Jaan Aru, Moritz Drüke, Juhan Pikamäe, et al.
Trends in Neurosciences (2022) Vol. 46, Iss. 2, pp. 100-109
Open Access | Times Cited: 26

The formation of an expanding memory representation in the hippocampus
Sachin P. Vaidya, Guanchun Li, Raymond A. Chitwood, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 18

A local circuit-basis for spatial navigation and memory processes in hippocampal area CA1
Tristan Geiller, James B. Priestley, Attila Losonczy
Current Opinion in Neurobiology (2023) Vol. 79, pp. 102701-102701
Open Access | Times Cited: 15

A critical role for CaMKII in behavioral timescale synaptic plasticity in hippocampal CA1 pyramidal neurons
Kuo Xiao, Yiding Li, Raymond A. Chitwood, et al.
Science Advances (2023) Vol. 9, Iss. 36
Open Access | Times Cited: 15

Synaptic Basis of Behavioral Timescale Plasticity
Kevin C. Gonzalez, Adrian Negrean, Zhenrui Liao, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 14

Neurosustainability
M. Khalil
Frontiers in Human Neuroscience (2024) Vol. 18
Open Access | Times Cited: 5

Latent representations in hippocampal network model co-evolve with behavioral exploration of task structure
Ian Cone, Claudia Clopath
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 4

Predictive sequence learning in the hippocampal formation
Yusi Chen, Huanqiu Zhang, Mia Cameron, et al.
Neuron (2024) Vol. 112, Iss. 15, pp. 2645-2658.e4
Closed Access | Times Cited: 4

Perpetual step-like restructuring of hippocampal circuit dynamics
Zheyang Zheng, Roman Huszár, Thomas Hainmueller, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 3

Learning, Fast and Slow: Single- and Many-Shot Learning in the Hippocampus
Zhenrui Liao, Attila Losonczy
Annual Review of Neuroscience (2024) Vol. 47, Iss. 1, pp. 187-209
Closed Access | Times Cited: 3

Representational drift as the consequence of ongoing memory storage
Federico Devalle, Licheng Zou, Gloria Cecchini, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Closed Access | Times Cited: 3

Mechanisms of memory-supporting neuronal dynamics in hippocampal area CA3
Yiding Li, John J. Briguglio, Sandro Romani, et al.
Cell (2024)
Open Access | Times Cited: 3

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