The DOI matches its Crossref record; 62 of the 62 references it cites were found in a registry or an index.
Persistently active neurons in human medial frontal and medial temporal lobe support working memory
Open accessAbstract
Persistent neural activity is a putative mechanism for the maintenance of working memories. Persistent activity relies on the activity of a distributed network of areas, but the differential contribution of each area remains unclear. We recorded single neurons in the human medial frontal cortex and medial temporal lobe while subjects held up to three items in memory. We found persistently active neurons in both areas. Persistent activity of hippocampal and amygdala neurons was stimulus-specific, formed stable attractors and was predictive of memory content. Medial frontal cortex persistent activity, on the other hand, was modulated by memory load and task set but was not stimulus-specific. Trial-by-trial variability in persistent activity in both areas was related to memory strength, because it predicted the speed and accuracy by which stimuli were remembered. This work reveals, in humans, direct evidence for a distributed network of persistently active neurons supporting working memory maintenance.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source says what the claim attributes to it.
In the citing paper
“A central finding is that concept cells fire when concepts are held in working memory (Kamiński et al., 2017; Kornblith et al., 2017) and become active when these concepts are retrieved from long-term memory (Gelbard-Sagiv et al., 2008).”
From Conscious Processing and the Global Neuronal Workspace Hypothesis (2020) · cites this paper as Kamiński et al., 2017
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Delorme, A., & Makeig, S. (2004) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2003.10.009 · Cited by 24,371
Brainard, D. H. (1997) · Spatial Vision · doi:10.1163/156856897x00357 · Cited by 20,012
Neural networks and physical systems with emergent collective computational abilities.
Hopfield, J. J. (1982) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.79.8.2554 · Cited by 19,270
Nonparametric statistical testing of EEG- and MEG-data
Maris, E., & Oostenveld, R. (2007) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2007.03.024 · Cited by 8,496
Cognitive and emotional influences in anterior cingulate cortex
Bush, G., Luu, P., & Posner, M. I. (2000) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(00)01483-2 · Cited by 6,259
Working Memory: Theories, Models, and Controversies
Baddeley, A. (2012) · Annual Review of Psychology · doi:10.1146/annurev-psych-120710-100422 · Cited by 4,271
Large-scale automated synthesis of human functional neuroimaging data.
Yarkoni, T., Poldrack, R. A., Nichols, T. E., Van Essen, D. C., & Wager, T. D. (2011) · Nature Methods · doi:10.1038/nmeth.1635 · Cited by 3,686 · cited 1×
“In neuroimaging studies MFC activity is consistently related to WM 14 and it has been suggested that the MFC supports executive functions through persistent neuronal activity 15 .”
The amygdala: vigilance and emotion
Davis, M., & Whalen, P. J. (2001) · Molecular Psychiatry · doi:10.1038/sj.mp.4000812 · Cited by 2,882
Mnemonic coding of visual space in the monkey's dorsolateral prefrontal cortex
Funahashi, S., Bruce, C. J., & Goldman-Rakic, P. S. (1989) · Journal of Neurophysiology · doi:10.1152/jn.1989.61.2.331 · Cited by 2,685
Squire, L. R., Stark, C. E. L., & Clark, R. E. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144130 · Cited by 2,680
Flagged first, then by citations
Cited by
Sorted by citations
Conscious Processing and the Global Neuronal Workspace Hypothesis
Mashour, G. A., Roelfsema, P., Changeux, J.-P., & Dehaene, S. (2020) · Neuron · doi:10.1016/j.neuron.2020.01.026 · Cited by 1,164
A high-resolution probabilistic in vivo atlas of human subcortical brain nuclei
Pauli, W. M., Nili, A. N., & Tyszka, J. M. (2018) · Scientific Data · doi:10.1038/sdata.2018.63 · Cited by 515
Persistent Spiking Activity Underlies Working Memory
Constantinidis, C., Funahashi, S., Lee, D., Murray, J. D., Qi, X.-L., Wang, M., & Arnsten, A. F. T. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.2486-17.2018 · Cited by 291
A Closer Look at the Hippocampus and Memory
Voss, J. L., Bridge, D. J., Cohen, N. J., & Walker, J. A. (2017) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2017.05.008 · Cited by 272
Accurate Estimation of Neural Population Dynamics without Spike Sorting
Trautmann, E. M., Stavisky, S. D., Lahiri, S., Ames, K. C., Kaufman, M. T., O’Shea, D. J., Vyas, S., Sun, X., Ryu, S. I., Ganguli, S., et al. (2019) · Neuron · doi:10.1016/j.neuron.2019.05.003 · Cited by 255
Taghia, J., Cai, W., Ryali, S., Kochalka, J., Nicholas, J., Chen, T., & Menon, V. (2018) · Nature Communications · doi:10.1038/s41467-018-04723-6 · Cited by 200
Multidimensional processing in the amygdala
Gothard, K. M. (2020) · Nature reviews. Neuroscience · doi:10.1038/s41583-020-0350-y · Cited by 174
Control of working memory by phase–amplitude coupling of human hippocampal neurons
Daume, J., Kamiński, J., Gómez-Palacio-Schjetnan, A., Salimpour, Y., Khan, U., Kyzar, M., Reed, C. M., Anderson, W. S., Valiante, T. A., Mamelak, A. N., et al. (2024) · Nature · doi:10.1038/s41586-024-07309-z · Cited by 187
Self-citationThe what, where and how of delay activity
Sreenivasan, K. K., & D’Esposito, M. (2019) · Nature reviews. Neuroscience · doi:10.1038/s41583-019-0176-7 · Cited by 165
Neural mechanisms of attending to items in working memory
Manohar, S., Zokaei, N., Fallon, S. J., Vogels, T. P., & Husain, M. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.03.017 · Cited by 153
Flexible recruitment of memory-based choice representations by the human medial frontal cortex
Minxha, J., Adolphs, R., Fusi, S., Mamelak, A. N., & Rutishauser, U. (2020) · Science · doi:10.1126/science.aba3313 · Cited by 141
Self-citationTaxidis, J., Pnevmatikakis, E. A., Dorian, C. C., Mylavarapu, A. L., Arora, J. S., Samadian, K. D., Hoffberg, E. A., & Golshani, P. (2020) · Neuron · doi:10.1016/j.neuron.2020.08.028 · Cited by 139
Attractor dynamics gate cortical information flow during decision-making
Finkelstein, A., Fontolan, L., Economo, M. N., Li, N., Romani, S., & Svoboda, K. (2021) · Nature Neuroscience · doi:10.1038/s41593-021-00840-6 · Cited by 134
Abstract representations emerge in human hippocampal neurons during inference
Courellis, H. S., Minxha, J., Cardenas, A. R., Kimmel, D. L., Reed, C. M., Valiante, T. A., Salzman, C. D., Mamelak, A. N., Fusi, S., & Rutishauser, U. (2024) · Nature · doi:10.1038/s41586-024-07799-x · Cited by 150
Self-citationNeurons detect cognitive boundaries to structure episodic memories in humans
Zheng, J., Schjetnan, A. G. P., Yebra, M., Gomes, B. A., Mosher, C. P., Kalia, S. K., Valiante, T. A., Mamelak, A. N., Kreiman, G., & Rutishauser, U. (2022) · Nature Neuroscience · doi:10.1038/s41593-022-01020-w · Cited by 129
Self-citationNeuronal ensembles: Building blocks of neural circuits
Yuste, R., Cossart, R., & Yaksi, E. (2024) · Neuron · doi:10.1016/j.neuron.2023.12.008 · Cited by 137
Boran, E., Fedele, T., Klaver, P., Hilfiker, P., Stieglitz, L. H., Grünwald, T., & Sarnthein, J. (2019) · Science Advances · doi:10.1126/sciadv.aav3687 · Cited by 105
Dynamic causal brain circuits during working memory and their functional controllability
Cai, W., Ryali, S., Pasumarthy, R., Talasila, V., & Menon, V. (2021) · Nature Communications · doi:10.1038/s41467-021-23509-x · Cited by 105
Debates on the dorsomedial prefrontal/dorsal anterior cingulate cortex: insights for future research
Clairis, N., & Lopez‐Persem, A. (2023) · Brain · doi:10.1093/brain/awad263 · Cited by 109
Yue, Q., Martin, R. C., Hamilton, A. C., & Rose, N. S. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy037 · Cited by 94
Brzezicka, A., Kamiński, J., Reed, C. M., Chung, J. M., Mamelak, A. N., & Rutishauser, U. (2019) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01417 · Cited by 89
Self-citationHippocampal Network Reorganization Underlies the Formation of a Temporal Association Memory
Ahmed, M. S., Priestley, J. B., Castro, A., Stefanini, F., Canales, A. S. S., Balough, E. M., Lavoie, E., Mazzucato, L., Fusi, S., & Losonczy, A. (2020) · Neuron · doi:10.1016/j.neuron.2020.04.013 · Cited by 86
The Architecture of Human Memory: Insights from Human Single-Neuron Recordings
Rutishauser, U., Reddy, L., Mormann, F., & Sarnthein, J. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1648-20.2020 · Cited by 85
Self-citationProbing the limits of activity-silent non-conscious working memory
Trübutschek, D., Marti, S., Ueberschär, H., & Dehaene, S. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1820730116 · Cited by 88
Reevaluating the Role of Persistent Neural Activity in Short-Term Memory
Masse, N. Y., Rosen, M. C., & Freedman, D. J. (2020) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2019.12.014 · Cited by 84
Evidence accumulation relates to perceptual consciousness and monitoring
Pereira, M., Mégevand, P., Tan, M. X., Chang, W., Wang, S., Rezai, A. R., Seeck, M., Corniola, M. V., Momjian, S., Bernasconi, F., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-23540-y · Cited by 109
Billig, A. J., Lad, M., Sedley, W., & Griffiths, T. D. (2022) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2022.102326 · Cited by 90
Persistent Activity During Working Memory From Front to Back
Curtis, C. E., & Sprague, T. C. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.696060 · Cited by 83
Cognitive neuroscience perspective on memory: overview and summary
Sridhar, S., Khamaj, A., & Asthana, M. K. (2023) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2023.1217093 · Cited by 80
Anterior Intraparietal Area: A Hub in the Observed Manipulative Action Network
Lanzilotto, M., Ferroni, C. G., Livi, A., Gerbella, M., Maranesi, M., Borra, E., Passarelli, L., Gamberini, M., Fogassi, L., Bonini, L., et al. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz011 · Cited by 76
Kamiński, J., & Rutishauser, U. (2019) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.14213 · Cited by 84
Self-citationRepresentation and computation in visual working memory
Bays, P. M., Schneegans, S., Ma, W. J., & Brady, T. F. (2024) · Nature Human Behaviour · doi:10.1038/s41562-024-01871-2 · Cited by 116
Resolving the prefrontal mechanisms of adaptive cognitive behaviors: A cross-species perspective
Hanganu‐Opatz, I. L., Klausberger, T., Sigurdsson, T., Nieder, A., Jacob, S. N., Bartos, M., Sauer, J., Durstewitz, D., Leibold, C., & Diester, I. (2023) · Neuron · doi:10.1016/j.neuron.2023.03.017 · Cited by 79
Stable maintenance of multiple representational formats in human visual short-term memory
Liu, J., Zhang, H., Yu, T., Ni, D., Ren, L., Yang, Q., Lu, B., Wang, D., Heinen, R. M., Axmacher, N., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2006752117 · Cited by 75
Theta-phase dependent neuronal coding during sequence learning in human single neurons
Reddy, L., Self, M. W., Zoefel, B., Poncet, M., Possel, J. K., Peters, J. C., Baayen, J. C., Idema, S., VanRullen, R., & Roelfsema, P. R. (2021) · Nature Communications · doi:10.1038/s41467-021-25150-0 · Cited by 76
Wang, L., Wlotko, E. W., Alexander, E., Schoot, L., Kim, M. J., Warnke, L., & Kuperberg, G. R. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1733-19.2020 · Cited by 70
Romo, R., & Rossi-Pool, R. (2020) · Neuron · doi:10.1016/j.neuron.2019.11.033 · Cited by 72
No Pattern Separation in the Human Hippocampus
Quiroga, R. Q. (2020) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2020.09.012 · Cited by 70
Differential Brain Mechanisms of Selection and Maintenance of Information during Working Memory
Quentin, R., King, J.-R., Sallard, E., Fishman, N. S., Thompson, R., Buch, E. R., & Cohen, L. G. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2764-18.2019 · Cited by 66
Kamiński, J., Brzezicka, A., Mamelak, A. N., & Rutishauser, U. (2020) · Neuron · doi:10.1016/j.neuron.2020.01.032 · Cited by 63
Self-citationLançon, K., Qu, C., Navratilova, E., Porreca, F., & Séguéla, P. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109933 · Cited by 60
Information flows from hippocampus to auditory cortex during replay of verbal working memory items
Dimakopoulos, V. S., Mégevand, P., Stieglitz, L. H., Imbach, L., & Sarnthein, J. (2022) · eLife · doi:10.7554/elife.78677 · Cited by 58
Decoding a Decision Process in the Neuronal Population of Dorsal Premotor Cortex
Rossi-Pool, R., Zainos, A., Álvarez, M., Zizumbo, J., Vergara, J. R. A., & Romo, R. (2017) · Neuron · doi:10.1016/j.neuron.2017.11.023 · Cited by 56
Agent-based representations of objects and actions in the monkey pre-supplementary motor area
Livi, A., Lanzilotto, M., Maranesi, M., Fogassi, L., Rizzolatti, G., & Bonini, L. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1810890116 · Cited by 51
The Hippocampal Horizon: Constructing and Segmenting Experience for Episodic Memory
Ross, T. W., & Easton, A. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.11.038 · Cited by 50
Encoding of Target Detection during Visual Search by Single Neurons in the Human Brain
Wang, S., Mamelak, A. N., Adolphs, R., & Rutishauser, U. (2018) · Current Biology · doi:10.1016/j.cub.2018.04.092 · Cited by 48
Self-citationPrefrontal cortex and cognitive aging in macaque monkeys
Upright, N. A., & Baxter, M. G. (2021) · American Journal of Primatology · doi:10.1002/ajp.23250 · Cited by 45
Neural population dynamics of human working memory
Li, H.-H., & Curtis, C. E. (2023) · Current Biology · doi:10.1016/j.cub.2023.07.067 · Cited by 51
Brain-Inspired Learning, Perception, and Cognition: A Comprehensive Review
Jiao, L., Ma, M., He, P., Geng, X., Liu, X., Liu, F., Ma, W., Yang, S., Hou, B., & Tang, X. (2024) · IEEE Transactions on Neural Networks and Learning Systems · doi:10.1109/tnnls.2024.3401711 · Cited by 54
Mosher, C. P., Wei, Y., Kamiński, J., Nandi, A., Mamelak, A. N., Anastassiou, C. A., & Rutishauser, U. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.02.027 · Cited by 46
Self-citationAnterior–Posterior Hippocampal Dynamics Support Working Memory Processing
Li, J., Cao, D., Dimakopoulos, V., Shi, W., Yu, S., Fan, L., Stieglitz, L. H., Imbach, L., Sarnthein, J., & Jiang, T. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1287-21.2021 · Cited by 49
Balancing Flexibility and Interference in Working Memory
Buschman, T. J. (2021) · Annual Review of Vision Science · doi:10.1146/annurev-vision-100419-104831 · Cited by 46
Memory retrieval modulates spatial tuning of single neurons in the human entorhinal cortex
Qasim, S. E., Miller, J. F., Inman, C. S., Gross, R. E., Willie, J. T., Lega, B. C., Lin, J.-J., Sharan, A. D., Wu, C., Sperling, M. R., et al. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0523-z · Cited by 47
Reframing the debate: The distributed systems view of working memory
Lorenc, E. S., & Sreenivasan, K. K. (2021) · Visual Cognition · doi:10.1080/13506285.2021.1899091 · Cited by 44
Multisensory Neurons in the Primate Amygdala
Morrow, J. K., Mosher, C. P., & Gothard, K. M. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2903-18.2019 · Cited by 48
Li, J., Cao, D., Dimakopoulos, V. S., Yu, S., Xiao, X., Imbach, L., Stieglitz, L. H., Sarnthein, J., & Jiang, T. (2023) · Nature Communications · doi:10.1038/s41467-023-38571-w · Cited by 42
Carlson, A. A., Rutishauser, U., & Mamelak, A. N. (2018) · Stereotactic and Functional Neurosurgery · doi:10.1159/000493548 · Cited by 44
Self-citationBausch, M., Niediek, J., Reber, T. P., Mackay, S., Boström, J. P., Elger, C. E., & Mormann, F. (2021) · Nature Communications · doi:10.1038/s41467-021-26327-3 · Cited by 42
Anterior-Posterior Hippocampal Dynamics Support Working Memory Processing
Li, J., Cao, D., Dimakopoulos, V. S., Shi, W., Yu, S. P., Fan, L., Stieglitz, L. H., Imbach, L., Sarnthein, J., & Jiang, T. (2022) · Repository for Publications and Research Data (ETH Zurich) · doi:10.3929/ethz-c-000529862 · Cited by 41
Boran, E., Fedele, T., Steiner, A. C., Hilfiker, P., Stieglitz, L. H., Grünwald, T., & Sarnthein, J. (2020) · Scientific Data · doi:10.1038/s41597-020-0364-3 · Cited by 41
Faraut, M. C. M., Carlson, A. A., Sullivan, S. M., Tudusciuc, O., Ross, I. B., Reed, C. M., Chung, J. M., Mamelak, A. N., & Rutishauser, U. (2018) · Scientific Data · doi:10.1038/sdata.2018.10 · Cited by 41
Self-citationDependence of Working Memory on Coordinated Activity Across Brain Areas
Rezayat, E., Clark, K., Dehaqani, M. A., & Noudoost, B. (2022) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2021.787316 · Cited by 43
Impaired Cognitive Function after Perineuronal Net Degradation in the Medial Prefrontal Cortex
Paylor, J. W., Wendlandt, E., Freeman, T. S., Greba, Q., Marks, W. N., Howland, J. G., & Winship, I. R. (2018) · eNeuro · doi:10.1523/eneuro.0253-18.2018 · Cited by 39
Neuronal spike-rate adaptation supports working memory in language processing
Fitz, H., Uhlmann, M., den Broek, D. V., Duarte, R., Peter Hagoort, A., & Petersson, K. M. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2000222117 · Cited by 35
Quiroga, R. Q. (2023) · Hippocampus · doi:10.1002/hipo.23527 · Cited by 43
Testing Models of Human Declarative Memory at the Single-Neuron Level
Rutishauser, U. (2019) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2019.03.006 · Cited by 36
Self-citationTemporal signals underlying a cognitive process in the dorsal premotor cortex
Rossi-Pool, R., Zizumbo, J., Álvarez, M., Vergara, J., Zainos, A., & Romo, R. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1820474116 · Cited by 33
Nieder, A. (2024) · Physiological Reviews · doi:10.1152/physrev.00014.2024 · Cited by 36
Neuronal codes for arithmetic rule processing in the human brain
Kutter, E. F., Boström, J. P., Elger, C. E., Nieder, A., & Mormann, F. (2022) · Current Biology · doi:10.1016/j.cub.2022.01.054 · Cited by 33
Neurons in human pre-supplementary motor area encode key computations for value-based choice
Aquino, T. G., Cockburn, J., Mamelak, A. N., Rutishauser, U., & O’Doherty, J. P. (2023) · Nature Human Behaviour · doi:10.1038/s41562-023-01548-2 · Cited by 37
Self-citationValue-Related Neuronal Responses in the Human Amygdala during Observational Learning
Aquino, T. G., Minxha, J., Dunne, S., Ross, I. B., Mamelak, A. N., Rutishauser, U., & O’Doherty, J. P. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.2897-19.2020 · Cited by 28
Self-citationThe medial temporal lobe supports the quality of visual short-term memory representation
Xie, W., Chapeton, J. I., Bhasin, S., Zawora, C., Wittig, J. H., Inati, S. K., Zhang, W., & Zaghloul, K. A. (2023) · Nature Human Behaviour · doi:10.1038/s41562-023-01529-5 · Cited by 33
Abstract goal representation in visual search by neurons in the human pre-supplementary motor area
Wang, S., Mamelak, A. N., Adolphs, R., & Rutishauser, U. (2019) · Brain · doi:10.1093/brain/awz279 · Cited by 30
Self-citationRepresentation and computation in working memoryPreprint
Bays, P. M., Schneegans, S., Ma, W. J., & Brady, T. F. (2022) · doi:10.31234/osf.io/kubr9 · Cited by 31
Timescales of learning in prefrontal cortex
Miller, J. A., & Constantinidis, C. (2024) · Nature reviews. Neuroscience · doi:10.1038/s41583-024-00836-8 · Cited by 30
Clairis, N., & Pessiglione, M. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.1795-21.2022 · Cited by 28
Eisenkolb, V. M., Held, L. M., Utzschmid, A., Lin, X., Krieg, S. M., Meyer, B., Gempt, J., & Jacob, S. N. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112467 · Cited by 30
Borderie, A., Caclin, A., Lachaux, J.-P., Perrone‐Bertolotti, M., Hoyer, R. S., Kahane, P., Catenoix, H., Tillmann, B., & Albouy, P. (2024) · PLoS Biology · doi:10.1371/journal.pbio.3002512 · Cited by 29
Neurons as will and representation
Fried, I. (2021) · Nature reviews. Neuroscience · doi:10.1038/s41583-021-00543-8 · Cited by 29
Surgical and Electrophysiological Techniques for Single-Neuron Recordings in Human Epilepsy Patients
Minxha, J., Mamelak, A. N., & Rutishauser, U. (2017) · Neuromethods · doi:10.1007/978-1-4939-7549-5_14 · Cited by 27
Self-citationStaudigl, T., Minxha, J., Mamelak, A. N., Gothard, K. M., & Rutishauser, U. (2022) · Science Advances · doi:10.1126/sciadv.abl6037 · Cited by 27
Self-citationDysregulated neuromodulation in the anterior cingulate cortex in chronic pain
Lançon, K., & Séguéla, P. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1289218 · Cited by 29
Boran, E., Hilfiker, P., Stieglitz, L. H., Grünwald, T., Sarnthein, J., & Klaver, P. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119123 · Cited by 30
Vines, L., Sotelo, D., Johnson, A., Dennis, E., Manza, P., Volkow, N. D., & Wang, G. (2022) · Intelligent Medicine · doi:10.1016/j.imed.2022.03.001 · Cited by 26
Cognitive neurophysiology of the prefrontal cortex
Helfrich, R. F., & Knight, R. T. (2019) · Handbook of clinical neurology · doi:10.1016/b978-0-12-804281-6.00003-3 · Cited by 25
Working Memory: From Neural Activity to the Sentient Mind
Jaffe, R. J., & Constantinidis, C. (2021) · Comprehensive physiology · doi:10.1002/cphy.c210005 · Cited by 32
Theta phase precession supports memory formation and retrieval of naturalistic experience in humans
Zheng, J., Yebra, M., Gómez-Palacio-Schjetnan, A., Patel, K., Katz, C. N., Kyzar, M., Mosher, C. P., Kalia, S. K., Chung, J. M., Reed, C. M., et al. (2024) · Nature Human Behaviour · doi:10.1038/s41562-024-01983-9 · Cited by 28
Self-citationInvolvement of TRPC4 and 5 Channels in Persistent Firing in Hippocampal CA1 Pyramidal Cells
Arboit, A., Reboreda, A., & Yoshida, M. (2020) · Cells · doi:10.3390/cells9020365 · Cited by 25
How TRPC Channels Modulate Hippocampal Function
Gualdani, R., & Gailly, P. L. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21113915 · Cited by 22
Daume, J., Kamiński, J., Salimpour, Y., Gómez-Palacio-Schjetnan, A., Anderson, W. S., Valiante, T. A., Mamelak, A. N., & Rutishauser, U. (2024) · Neuron · doi:10.1016/j.neuron.2024.09.013 · Cited by 27
Self-citationSisterson, N. D., Carlson, A. A., Rutishauser, U., Mamelak, A. N., Flagg, M. E., Pouratian, N., Salimpour, Y., Anderson, W. S., & Richardson, R. M. (2021) · Neurosurgery · doi:10.1093/neuros/nyaa592 · Cited by 23
Self-citationStrategies, debates, and adversarial collaboration in working memory: The 51st Bartlett Lecture
Logie, R. H. (2023) · Quarterly Journal of Experimental Psychology · doi:10.1177/17470218231194037 · Cited by 23
Individual variation in working memory is associated with fear extinction performance
Stout, D. M., Acheson, D. T., Moore, T. M., Gur, R. C., Baker, D. G., Geyer, M. A., & Risbrough, V. B. (2018) · Behaviour Research and Therapy · doi:10.1016/j.brat.2018.01.002 · Cited by 22
Medial prefrontal cortex and the temporal control of action
Zhang, Q., Weber, M. A., & Narayanan, N. (2020) · International review of neurobiology · doi:10.1016/bs.irn.2020.11.004 · Cited by 19
Discrete memories of a continuous world: A working memory perspective on event segmentation
Güler, B., Adıgüzel, Z., Uysal, B., & Günseli, E. (2023) · Current Research in Behavioral Sciences · doi:10.1016/j.crbeha.2023.100145 · Cited by 22
Li, C., Song, J.-R., Zhao, J., Wang, C., Zhang, C., Wang, H.-D., Zhang, Q., Liu, D.-F., Ma, Z., Yuan, J., et al. (2022) · Surgery for Obesity and Related Diseases · doi:10.1016/j.soard.2022.07.007 · Cited by 21
Adaptive Value Normalization in the Prefrontal Cortex Is Reduced by Memory Load
Holper, L., van Brussel, L. D., Schmidt, L., Schulthess, S., Burke, C. J., Louie, K., Seifritz, E., & Tobler, P. N. (2017) · eNeuro · doi:10.1523/eneuro.0365-17.2017 · Cited by 16
Persistent but Labile Synaptic Plasticity at Excitatory Synapses
Pradier, B., Lanning, K. M., Taljan, K. T., Feuille, C. J., Nagy, M. A., & Kauer, J. A. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.2772-17.2018 · Cited by 18
Human hippocampal ripples signal encoding of episodic memories
Sakon, J. J., Halpern, D. J., Schonhaut, D. R., & Kahana, M. J. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.0111-23.2023 · Cited by 16
Working memory and active sampling of the environment: Medial temporal contributions
Pollmann, S., & Schneider, W. X. (2022) · Handbook of clinical neurology · doi:10.1016/b978-0-12-823493-8.00029-8 · Cited by 16
Metadata
- Authors
- Kamiński, J., Sullivan, S., Chung, J. M., Ross, I. B., Mamelak, A. N., & Rutishauser, U.
- Affiliations
- California Institute of Technology (US)
- Cedars-Sinai Medical Center (US)
- Huntington Hospital (US)
- Corresponding author
- Rutishauser, Ueli
- Venue
- Nature Neuroscience
- Published
- 2017-02-20
- Volume
- 20
- Issue
- 4
- Pages
- 590-601
- ISSN
- 1097-6256 (ISSN-L)
- 1546-1726
- PMC
- PMC5374017
- OpenAlex
- W2590265405
- Cited by
- 264
- References
- 62
- Citations by year
- 2026: 25 · 2025: 34 · 2024: 37 · 2023: 34 · 2022: 27 · 2021: 24 · 2020: 34 · 2019: 19 · 2018: 16 · 2017: 13
- FWCI
- 12.88
- Type
- journal article
- Language
- en
- Update notices
- erratum (2017-08-01)
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- CaltechAUTHORS (California Institute of Technology) (submittedVersion)
- Funders
- Cedars-Sinai Medical Center
- National Institute of Mental Health (R01MH110831, P50MH094258)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Keywords
- working memory, persistent activity, medial frontal cortex, medial temporal lobe, hippocampus, amygdala, attractor dynamics, memory maintenance, memory load, memory strength, single-unit recording, distributed neural networks
- MeSH terms
- Amygdala, Frontal Lobe, Gyrus Cinguli, Hippocampus, Humans, Memory, Short-Term, Motor Cortex, Neurons, Photic Stimulation, Temporal Lobe
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review