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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:

The firing rate speed code of entorhinal speed cells differs across behaviorally relevant time scales and does not depend on medial septum inputs
Holger Dannenberg, Craig Kelley, Alec Hoyland, et al.
Journal of Neuroscience (2019), pp. 1450-18
Open Access | Times Cited: 48

Showing 1-25 of 48 citing articles:

A temporal record of the past with a spectrum of time constants in the monkey entorhinal cortex
Ian M. Bright, Miriam L. R. Meister, Nathanael A. Cruzado, et al.
Proceedings of the National Academy of Sciences (2020) Vol. 117, Iss. 33, pp. 20274-20283
Open Access | Times Cited: 89
Cooling of Medial Septum Reveals Theta Phase Lag Coordination of Hippocampal Cell Assemblies
Peter Petersen, György Buzsáki
Neuron (2020) Vol. 107, Iss. 4, pp. 731-744.e3
Open Access | Times Cited: 79
Microcircuits for spatial coding in the medial entorhinal cortex
John J. Tukker, Prateep Beed, Michael Brecht, et al.
Physiological Reviews (2021) Vol. 102, Iss. 2, pp. 653-688
Open Access | Times Cited: 61
Functional network topography of the medial entorhinal cortex
Horst A. Obenhaus, Weijian Zong, R. Irene Jacobsen, et al.
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 7
Open Access | Times Cited: 51
Gated transformations from egocentric to allocentric reference frames involving retrosplenial cortex, entorhinal cortex, and hippocampus
Andrew S. Alexander, Jennifer C. Robinson, Chantal E. Stern, et al.
Hippocampus (2023) Vol. 33, Iss. 5, pp. 465-487
Open Access | Times Cited: 35
A Brainstem Locomotor Circuit Drives the Activity of Speed Cells in the Medial Entorhinal Cortex
Miguel M. Carvalho, Nouk Tanke, Emilio Kropff, et al.
Cell Reports (2020) Vol. 32, Iss. 10, pp. 108123-108123
Open Access | Times Cited: 51
Adaptive integration of self-motion and goals in posterior parietal cortex
Andrew S. Alexander, Janet C. Tung, G. William Chapman, et al.
Cell Reports (2022) Vol. 38, Iss. 10, pp. 110504-110504
Open Access | Times Cited: 28
Optogenetic silencing of medial septal GABAergic neurons disrupts grid cell spatial and temporal coding in the medial entorhinal cortex
Jennifer C. Robinson, Johnson Ying, Michael E. Hasselmo, et al.
Cell Reports (2024) Vol. 43, Iss. 8, pp. 114590-114590
Open Access | Times Cited: 6
Neurophysiological coding of space and time in the hippocampus, entorhinal cortex, and retrosplenial cortex
Andrew S. Alexander, Jennifer C. Robinson, Holger Dannenberg, et al.
Brain and Neuroscience Advances (2020) Vol. 4, pp. 239821282097287-239821282097287
Open Access | Times Cited: 39
Optogenetic suppression of the medial septum impairs working memory maintenance
Zachary M. Gemzik, Margaret M. Donahue, Amy L. Griffin
Learning & Memory (2021) Vol. 28, Iss. 10, pp. 361-370
Open Access | Times Cited: 36
Cell type, sub-region, and layer-specific speed representation in the hippocampal–entorhinal circuit
Motosada Iwase, Takuma Kitanishi, Kenji Mizuseki
Scientific Reports (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 37
Effects of visual inputs on neural dynamics for coding of location and running speed in medial entorhinal cortex
Holger Dannenberg, Hallie Lazaro, Pranav Nambiar, et al.
eLife (2020) Vol. 9
Open Access | Times Cited: 36
Cortical Integration of Vestibular and Visual Cues for Navigation, Visual Processing, and Perception
Sepiedeh Keshavarzi, Mateo Vélez‐Fort, Troy W. Margrie
Annual Review of Neuroscience (2023) Vol. 46, Iss. 1, pp. 301-320
Open Access | Times Cited: 11
Septo-hippocampal dynamics and the encoding of space and time
Jennifer C. Robinson, Jacob H. Wilmot, Michael E. Hasselmo
Trends in Neurosciences (2023) Vol. 46, Iss. 9, pp. 712-725
Open Access | Times Cited: 11
Cholinergic dynamics in the septo-hippocampal system provide phasic multiplexed signals for spatial novelty and correlate with behavioral states
Fatemeh Farokhi Moghadam, Blanca Erika Gutiérrez-Guzmán, Xihui Zheng, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Tiling of large-scaled environments by grid cells requires experience
Blanca Erika Gutiérrez-Guzmán, J. Jesús Hernández-Pérez, Holger Dannenberg
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Impairment of theta oscillations in the hippocampal CA1 region may mediate age-dependent movement alternations in the 5xFAD mouse model of Alzheimer’s disease
Hong Ni, Zhongzhao Guo, Jie Wang, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access
Medial septal theta stimulation enhances spatial working memory performance in rats
Zachary M. Gemzik, Amy L. Griffin
Learning & Memory (2025) Vol. 32, Iss. 4, pp. a054075-a054075
Open Access
Spatial periodicity in grid cell firing is explained by a neural sequence code of 2-D trajectories
Rebecca RG, Giorgio A. Ascoli, Nate M Sutton, et al.
(2025)
Open Access
Time to put the mammillothalamic pathway into context
Christopher M. Dillingham, Michal M. Milczarek, James C. Perry, et al.
Neuroscience & Biobehavioral Reviews (2020) Vol. 121, pp. 60-74
Open Access | Times Cited: 28
Internally generated time in the rodent hippocampus is logarithmically compressed
Rui Cao, John Bladon, Stephen J. Charczynski, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 18
Two septal-entorhinal GABAergic projections differentially control coding properties of spatially tuned neurons in the medial entorhinal cortex
Magdalene I. Schlesiger, Tobias Ruff, Duncan A. A. MacLaren, et al.
Cell Reports (2021) Vol. 34, Iss. 9, pp. 108801-108801
Open Access | Times Cited: 20
Optogenetic pacing of medial septum parvalbumin-positive cells disrupts temporal but not spatial firing in grid cells
Mikkel Elle Lepperød, Ane Charlotte Christensen, Kristian Kinden Lensjø, et al.
Science Advances (2021) Vol. 7, Iss. 19
Open Access | Times Cited: 19
The influence of emotion on temporal context models
Lynn J. Lohnas, Marc W. Howard
Cognition & Emotion (2024), pp. 1-29
Open Access | Times Cited: 2
A temporal record of the past with a spectrum of time constants in the monkey entorhinal cortex
Ian M. Bright, Miriam L. R. Meister, Nathanael A. Cruzado, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2019)
Open Access | Times Cited: 18
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