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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:

Causes and consequences of representational drift
Michael E. Rule, Timothy O’Leary, Christopher D. Harvey
Current Opinion in Neurobiology (2019) Vol. 58, pp. 141-147
Open Access | Times Cited: 203

Showing 1-25 of 203 citing articles:

If deep learning is the answer, what is the question?
Andrew Saxe, Stephanie Nelli, Christopher Summerfield
Nature reviews. Neuroscience (2020) Vol. 22, Iss. 1, pp. 55-67
Open Access | Times Cited: 339
Representational drift in primary olfactory cortex
Carl E. Schoonover, Sarah Ohashi, Richard Axel, et al.
Nature (2021) Vol. 594, Iss. 7864, pp. 541-546
Open Access | Times Cited: 248
Representational drift in the mouse visual cortex
Daniel Deitch, Alon Rubin, Yaniv Ziv
Current Biology (2021) Vol. 31, Iss. 19, pp. 4327-4339.e6
Open Access | Times Cited: 163
Ion Channel Degeneracy, Variability, and Covariation in Neuron and Circuit Resilience
Jean‐Marc Goaillard, Eve Marder
Annual Review of Neuroscience (2021) Vol. 44, Iss. 1, pp. 335-357
Open Access | Times Cited: 157
Hippocampal remapping as hidden state inference
Honi Sanders, Matthew A. Wilson, Samuel J. Gershman
eLife (2020) Vol. 9
Open Access | Times Cited: 148
How to build a cognitive map
James C. R. Whittington, David McCaffary, Jacob J. W. Bakermans, et al.
Nature Neuroscience (2022) Vol. 25, Iss. 10, pp. 1257-1272
Closed Access | Times Cited: 135
Representational drift: Emerging theories for continual learning and experimental future directions
Laura N. Driscoll, Lea Duncker, Christopher D. Harvey
Current Opinion in Neurobiology (2022) Vol. 76, pp. 102609-102609
Closed Access | Times Cited: 94
Time and experience differentially affect distinct aspects of hippocampal representational drift
Nitzan Geva, Daniel Deitch, Alon Rubin, et al.
Neuron (2023) Vol. 111, Iss. 15, pp. 2357-2366.e5
Open Access | Times Cited: 67
Active experience, not time, determines within-day representational drift in dorsal CA1
Dorgham Khatib, Aviv Ratzon, Mariell Sellevoll, et al.
Neuron (2023) Vol. 111, Iss. 15, pp. 2348-2356.e4
Open Access | Times Cited: 51
Neuronal ensembles: Building blocks of neural circuits
Rafael Yuste, Rosa Cossart, Emre Yaksi
Neuron (2024) Vol. 112, Iss. 6, pp. 875-892
Open Access | Times Cited: 33
Dynamic representation of appetitive and aversive stimuli in nucleus accumbens shell D1- and D2-medium spiny neurons
Ana Verónica Domingues, Tawan T. A. Carvalho, Gabriela J. Martins, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access | Times Cited: 2
Slow Drift of Neural Activity as a Signature of Impulsivity in Macaque Visual and Prefrontal Cortex
Benjamin R. Cowley, A. C. Snyder, Katerina Acar, et al.
Neuron (2020) Vol. 108, Iss. 3, pp. 551-567.e8
Open Access | Times Cited: 119
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: 113
Stable task information from an unstable neural population
Michael E. Rule, Adrianna Loback, Dhruva V. Raman, et al.
eLife (2020) Vol. 9
Open Access | Times Cited: 85
Long-term stability of cortical ensembles
Jesús Pérez-Ortega, Tzitzitlini Alejandre-García, Rafael Yuste
eLife (2021) Vol. 10
Open Access | Times Cited: 66
The neural bases for timing of durations
Albert Tsao, S. Aryana Yousefzadeh, Warren H. Meck, et al.
Nature reviews. Neuroscience (2022) Vol. 23, Iss. 11, pp. 646-665
Closed Access | Times Cited: 59
The representation of context in mouse hippocampus is preserved despite neural drift
Alexandra T. Keinath, Coralie‐Anne Mosser, Mark P. Brandon
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 55
Contribution of behavioural variability to representational drift
Sadra Sadeh, Claudia Clopath
eLife (2022) Vol. 11
Open Access | Times Cited: 52
Self-healing codes: How stable neural populations can track continually reconfiguring neural representations
Michael E. Rule, Timothy O’Leary
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 7
Open Access | Times Cited: 41
In vivo ephaptic coupling allows memory network formation
Dimitris A. Pinotsis, Earl K. Miller
Cerebral Cortex (2023) Vol. 33, Iss. 17, pp. 9877-9895
Open Access | Times Cited: 37
Quasiuniversal scaling in mouse-brain neuronal activity stems from edge-of-instability critical dynamics
Guillermo B. Morales, Serena Di Santo, Miguel A. Muñoz
Proceedings of the National Academy of Sciences (2023) Vol. 120, Iss. 9
Open Access | Times Cited: 33
Holographic stimulation of opposing amygdala ensembles bidirectionally modulates valence-specific behavior via mutual inhibition
Sean C. Piantadosi, Zhe Zhou, Carina Pizzano, et al.
Neuron (2023) Vol. 112, Iss. 4, pp. 593-610.e5
Closed Access | Times Cited: 33
Coordinated drift of receptive fields in Hebbian/anti-Hebbian network models during noisy representation learning
Shanshan Qin, Shiva Farashahi, David Lipshutz, et al.
Nature Neuroscience (2023) Vol. 26, Iss. 2, pp. 339-349
Closed Access | Times Cited: 30
Stimulus novelty uncovers coding diversity in visual cortical circuits
Marina Garrett, Peter A. Groblewski, Alex T. Piet, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 24
A manifold neural population code for space in hippocampal coactivity dynamics independent of place fields
Eliott R. J. Levy, Simón Carrillo Segura, Eunhye Park, et al.
Cell Reports (2023) Vol. 42, Iss. 10, pp. 113142-113142
Open Access | Times Cited: 22
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