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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 Remapping after Partial Inactivation of the Medial Entorhinal Cortex
Chenglin Miao, Qichen Cao, Hiroshi Ito, et al.
Neuron (2015) Vol. 88, Iss. 3, pp. 590-603
Open Access | Times Cited: 126

Showing 1-25 of 126 citing articles:

DREADDs for Neuroscientists
Bryan L. Roth
Neuron (2016) Vol. 89, Iss. 4, pp. 683-694
Open Access | Times Cited: 1540
What Is a Cognitive Map? Organizing Knowledge for Flexible Behavior
Timothy E.J. Behrens, Timothy Müller, James C. R. Whittington, et al.
Neuron (2018) Vol. 100, Iss. 2, pp. 490-509
Open Access | Times Cited: 872
Spatial representation in the hippocampal formation: a history
Edvard I Moser, May‐Britt Moser, Bruce L. McNaughton
Nature Neuroscience (2017) Vol. 20, Iss. 11, pp. 1448-1464
Closed Access | Times Cited: 490
Dentate gyrus circuits for encoding, retrieval and discrimination of episodic memories
Thomas Hainmueller, Marlene Bartos
Nature reviews. Neuroscience (2020) Vol. 21, Iss. 3, pp. 153-168
Open Access | Times Cited: 374
Silencing Neurons: Tools, Applications, and Experimental Constraints
J. Simon Wiegert, Mathias Mahn, Matthias Prigge, et al.
Neuron (2017) Vol. 95, Iss. 3, pp. 504-529
Open Access | Times Cited: 297
Sublayer-Specific Coding Dynamics during Spatial Navigation and Learning in Hippocampal Area CA1
Nathan Danielson, Jeffrey D. Zaremba, Patrick Kaifosh, et al.
Neuron (2016) Vol. 91, Iss. 3, pp. 652-665
Open Access | Times Cited: 269
Functionally Distinct Neuronal Ensembles within the Memory Engram
Xiaochen Sun, Max J. Bernstein, Meizhen Meng, et al.
Cell (2020) Vol. 181, Iss. 2, pp. 410-423.e17
Open Access | Times Cited: 212
Ten Years of Grid Cells
David C Rowland, Yasser Roudi, May‐Britt Moser, et al.
Annual Review of Neuroscience (2016) Vol. 39, Iss. 1, pp. 19-40
Open Access | Times Cited: 208
Hippocampal awake replay in fear memory retrieval
Chun-Ting Wu, Daniel Christopher Haggerty, Caleb Kemere, et al.
Nature Neuroscience (2017) Vol. 20, Iss. 4, pp. 571-580
Open Access | Times Cited: 201
Gamma rhythm communication between entorhinal cortex and dentate gyrus neuronal assemblies
Antonio Fernández‐Ruiz, Azahara Oliva, Marisol Soula, et al.
Science (2021) Vol. 372, Iss. 6537
Open Access | Times Cited: 181
Disrupted Place Cell Remapping and Impaired Grid Cells in a Knockin Model of Alzheimer's Disease
Heechul Jun, Allen Bramian, Shogo Soma, et al.
Neuron (2020) Vol. 107, Iss. 6, pp. 1095-1112.e6
Open Access | Times Cited: 139
Entorhinal cortex dysfunction in Alzheimer's disease
Kei M. Igarashi
Trends in Neurosciences (2022) Vol. 46, Iss. 2, pp. 124-136
Open Access | Times Cited: 122
Impaired path integration in mice with disrupted grid cell firing
Mariana Gil, Mihai Ancău, Magdalene I. Schlesiger, et al.
Nature Neuroscience (2017) Vol. 21, Iss. 1, pp. 81-91
Open Access | Times Cited: 158
Stellate cells drive maturation of the entorhinal-hippocampal circuit
Flavio Donato, R. Irene Jacobsen, May‐Britt Moser, et al.
Science (2017) Vol. 355, Iss. 6330
Open Access | Times Cited: 141
Parvalbumin and Somatostatin Interneurons Control Different Space-Coding Networks in the Medial Entorhinal Cortex
Chenglin Miao, Qichen Cao, May‐Britt Moser, et al.
Cell (2017) Vol. 171, Iss. 3, pp. 507-521.e17
Open Access | Times Cited: 128
Evidence for a subcircuit in medial entorhinal cortex representing elapsed time during immobility
James G. Heys, Daniel A. Dombeck
Nature Neuroscience (2018) Vol. 21, Iss. 11, pp. 1574-1582
Open Access | Times Cited: 128
Medial Entorhinal Cortex Selectively Supports Temporal Coding by Hippocampal Neurons
Nick T.M. Robinson, James B. Priestley, Jon W. Rueckemann, et al.
Neuron (2017) Vol. 94, Iss. 3, pp. 677-688.e6
Open Access | Times Cited: 123
Hippocampal neurons represent events as transferable units of experience
Chen Sun, Wannan Yang, Jared Martin, et al.
Nature Neuroscience (2020) Vol. 23, Iss. 5, pp. 651-663
Closed Access | Times Cited: 117
Chronic Loss of CA2 Transmission Leads to Hippocampal Hyperexcitability
Roman Boehringer, Denis Polygalov, Arthur Huang, et al.
Neuron (2017) Vol. 94, Iss. 3, pp. 642-655.e9
Open Access | Times Cited: 104
A Novel Mechanism for the Grid-to-Place Cell Transformation Revealed by Transgenic Depolarization of Medial Entorhinal Cortex Layer II
Benjamin R. Kanter, Christine Lykken, Daniel Avesar, et al.
Neuron (2017) Vol. 93, Iss. 6, pp. 1480-1492.e6
Open Access | Times Cited: 102
Origin and role of path integration in the cognitive representations of the hippocampus: computational insights into open questions
Francesco Savelli, James Knierim
Journal of Experimental Biology (2019) Vol. 222, Iss. Suppl_1
Open Access | Times Cited: 90
Hippocampal Remapping and Its Entorhinal Origin
Patrick Latuske, Olga Kornienko, Laura Kohler, et al.
Frontiers in Behavioral Neuroscience (2018) Vol. 11
Open Access | Times Cited: 89
CA1-projecting subiculum neurons facilitate object–place learning
Yanjun Sun, Suoqin Jin, Xiaoxiao Lin, et al.
Nature Neuroscience (2019) Vol. 22, Iss. 11, pp. 1857-1870
Open Access | Times Cited: 87
Manipulating Hippocampal Place Cell Activity by Single-Cell Stimulation in Freely Moving Mice
Maria Diamantaki, Stefano Coletta, Khaled Nasr, et al.
Cell Reports (2018) Vol. 23, Iss. 1, pp. 32-38
Open Access | Times Cited: 84
Multiple Maps of the Same Spatial Context Can Stably Coexist in the Mouse Hippocampus
Liron Sheintuch, Nitzan Geva, Hadas Baumer, et al.
Current Biology (2020) Vol. 30, Iss. 8, pp. 1467-1476.e6
Open Access | Times Cited: 79
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