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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:

Temporal context and latent state inference in the hippocampal splitter signal
Éléonore Duvelle, Roddy M. Grieves, Matthijs A. A. van der Meer
eLife (2023) Vol. 12
Open Access | Times Cited: 32

Showing 1-25 of 32 citing articles:

The homogenous hippocampus: How hippocampal cells process available and potential goals
Neil McNaughton, David M. Bannerman
Progress in Neurobiology (2024) Vol. 240, pp. 102653-102653
Open Access | Times Cited: 25
Single neurons in the human medial temporal lobe flexibly shift representations across spatial and memory tasks
Thomas Donoghue, Runnan Cao, Claire Z. Han, et al.
Hippocampus (2023) Vol. 33, Iss. 5, pp. 600-615
Open Access | Times Cited: 19
Learning produces a hippocampal cognitive map in the form of an orthogonalized state machine
Weinan Sun, Johan Winnubst, Maanasa Natrajan, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 16
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: 5
Perceptual-Cognitive Training Paradigms for Understanding Cognition and Cortical Visual Impairments
Ashim Pandey, Dipesh Shrestha, Sujaya Neupane
IntechOpen eBooks (2025)
Closed Access
Working memory features are embedded in hippocampal place fields
Viktor Varga, Peter Petersen, Ipshita Zutshi, et al.
Cell Reports (2024) Vol. 43, Iss. 3, pp. 113807-113807
Open Access | Times Cited: 4
Hippocampal output suppresses orbitofrontal cortex schema cell formation
Wenhui Zong, Jingfeng Zhou, Matthew P.H. Gardner, et al.
Nature Neuroscience (2025)
Open Access
Expectancy-related changes in firing of dopamine neurons depend on hippocampus
Zhewei Zhang, Yuji K. Takahashi, Marlian Montesinos-Cartegena, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 3
Localized APP expression results in progressive network dysfunction by disorganizing spike timing
Silvia Viana da Silva, Matthias G. Haberl, Kshitij Gaur, et al.
Neuron (2023) Vol. 112, Iss. 1, pp. 124-140.e6
Open Access | Times Cited: 7
Paradoxical replay can protect contextual task representations from destructive interference when experience is unbalanced
H. Isaac Chen, Matthijs A. A. van der Meer
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
Hidden state inference requires abstract contextual representations in ventral hippocampus
Karyna Mishchanchuk, Gabrielle C. Gregoriou, Albert J. Qü, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
Hippocampal and orbitofrontal neurons contribute to complementary aspects of associative structure
Huixin Lin, Jingfeng Zhou
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 2
Parallel maturation of rodent hippocampal memory and CA1 task representations
Juraj Bevandić, Federico Stella, H. Freyja Ólafsdóttir
Current Biology (2024)
Closed Access | Times Cited: 2
Hidden state inference requires abstract contextual representations in the ventral hippocampus
Karyna Mishchanchuk, Gabrielle C. Gregoriou, Albert J. Qü, et al.
Science (2024) Vol. 386, Iss. 6724, pp. 926-932
Open Access | Times Cited: 2
Single neurons in the human medial temporal lobe flexibly shift representations across spatial and memory tasks
Thomas Donoghue, Runnan Cao, Claire Z. Han, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 6
Using multi‐task experiments to test principles of hippocampal function
Claire Z. Han, Thomas Donoghue, Runnan Cao, et al.
Hippocampus (2023) Vol. 33, Iss. 5, pp. 646-657
Open Access | Times Cited: 6
Accounting for multiscale processing in adaptive real-world decision-making via the hippocampus
Dhruv Mehrotra, Laurette Dubé
Frontiers in Neuroscience (2023) Vol. 17
Open Access | Times Cited: 5
Expectancy-related changes in firing of dopamine neurons depend on hippocampus
Yuji K. Takahashi, Zhewei Zhang, Marlian Montesinos-Cartegena, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 4
Linking temporal coordination of hippocampal activity to memory function
Guillaume Etter, James E. Carmichael, Sylvain Williams
Frontiers in Cellular Neuroscience (2023) Vol. 17
Open Access | Times Cited: 4
Distinguishing examples while building concepts in hippocampal and artificial networks
Louis Kang, Taro Toyoizumi
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 1
Theta cycle dynamics of spatial representations in the lateral septum
Katarzyna Bzymek, Fabian Kloosterman
(2024)
Open Access | Times Cited: 1
Integration of rate and phase codes by hippocampal cell-assemblies supports flexible encoding of spatiotemporal context
Eleonora Russo, Nadine Becker, Aleks P. F. Domanski, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 1
Learning Temporal Relationships Between Symbols with Laplace Neural Manifolds
Marc W. Howard, Zahra G. Esfahani, Long Bao Le, et al.
Computational Brain & Behavior (2024)
Closed Access | Times Cited: 1
Latent Representations in Hippocampal Network Model Co-Evolve with Behavioral Exploration of Task Structure
Ian Cone, Claudia Clopath
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 3
Distinguishing examples while building concepts in hippocampal and artificial networks
Louis Kang, Taro Toyoizumi
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 2
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