The DOI matches its Crossref record; 44 of the 44 references it cites were found in a registry or an index.
Medial Temporal Theta/Alpha Power Enhancement Precedes Successful Memory Encoding: Evidence Based on Intracranial EEG
Open accessAbstract
Not only poststimulus, but also prestimulus neural activity has been shown to be predictive for later successful memory encoding. However, it is still not clear which medial temporal lobe processes precede effective memory formation. Here, our aim was to investigate whether such prestimulus markers for successful memory encoding can be specified based on intracranial recordings directly from the hippocampus and rhinal cortex. For this purpose, we analyzed subsequent memory effects during a continuous word recognition paradigm in 31 presurgical epilepsy patients. We found that rhinal and hippocampal theta and successive alpha power enhancement before word presentation predicted successful memory encoding. Previous studies suggest that stimulus-triggered hippocampal theta activity is particularly related to memory retrieval and activation of a mnemonic context, whereas the alpha rhythm reflects inhibitory top-down control of task processing and executive functioning. In line with these suggestions, we propose that the observed medial temporal theta and alpha power increases before stimulus presentation reflect activation of contextual information and inhibitory top-down control processes preparing for stimulus-triggered memory processing.
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 source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Theta activity in waking is considered a condition favoring the encoding of new information and associated synaptic plastic processes in hippocampal networks (64,371,612,1251).”
From About Sleep's Role in Memory (2013) · cites this paper as [371]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“(1) the amount of theta power present at the time individuals are asked to recall a stimulus is associated with the recall of that stimulus (Fell et al., 2011; Guderian, Schott, Richardson-Klavehn, & Duzel, 2009; Lega, Jacobs, & Kahana, 2012; Watrous et al., 2013)”
From Brain oscillations, hypnosis, and hypnotizability (2015) · cites this paper as Fell et al., 2011
Experimental — accuracy not yet measured
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
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
EEG alpha oscillations: The inhibition–timing hypothesis
Klimesch, W., Sauseng, P., & Hanslmayr, S. (2006) · Brain Research Reviews · doi:10.1016/j.brainresrev.2006.06.003 · Cited by 3,890
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
Driving fast-spiking cells induces gamma rhythm and controls sensory responses
Cardin, J. A., Carlén, M., Meletis, K., Knoblich, U., Zhang, F., Deisseroth, K., Tsai, L.-H., & Moore, C. I. (2009) · Nature · doi:10.1038/nature08002 · Cited by 2,603
The Medial Temporal Lobe and Recognition Memory
Eichenbaum, H., Yonelinas, A. P., & Ranganath, C. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.30.051606.094328 · Cited by 2,580
A cortical–hippocampal system for declarative memory
Eichenbaum, H. (2000) · Nature reviews. Neuroscience · doi:10.1038/35036213 · Cited by 1,817
Ray, W. J., & Cole, H. W. (1985) · Science · doi:10.1126/science.3992243 · Cited by 1,146
Reward-motivated learning: mesolimbic activation precedes memory formation
Adcock, R. A., Thangavel, A., Whitfield-Gabrieli, S., Knutson, B., & Gabrieli, J. D. E. (2006) · Neuron · doi:10.1016/j.neuron.2006.03.036 · Cited by 977
Buzsáki, G. (2005) · Hippocampus · doi:10.1002/hipo.20113 · Cited by 872
Theta and gamma oscillations predict encoding and retrieval of declarative memory
Osipova, D., Takashima, A., Oostenveld, R., Fernández, G., Maris, E., & Jensen, O. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.1948-06.2006 · Cited by 671
Cited by
Sorted by citations
Rasch, B., & Born, J. (2013) · Physiological Reviews · doi:10.1152/physrev.00032.2012 · Cited by 2,783
“Theta activity in waking is considered a condition favoring the encoding of new information and associated synaptic plastic processes in hippocampal networks (64, 371, 612, 1251).”
BackgroundLisman, J. E., & Jensen, O. (2013) · Neuron · doi:10.1016/j.neuron.2013.03.007 · Cited by 1,609
Carhart-Harris, R. L., Leech, R., Hellyer, P. J., Shanahan, M., Feilding, A., Tagliazucchi, E., Chialvo, D. R., & Nutt, D. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00020 · Cited by 1,252
Theta Oscillations in Human Memory
Herweg, N. A., Solomon, E. A., & Kahana, M. J. (2020) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2019.12.006 · Cited by 620
Hsieh, L.-T., & Ranganath, C. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2013.08.003 · Cited by 525
Oscillatory power decreases and long-term memory: the information via desynchronization hypothesis
Hanslmayr, S., Staudigl, T., & Fellner, M.-C. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2012.00074 · Cited by 543
Beyond the FRN: Broadening the time-course of EEG and ERP components implicated in reward processing
Glazer, J. E., Kelley, N. J., Pornpattananangkul, N., Mittal, V. A., & Nusslock, R. (2018) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2018.02.002 · Cited by 381
Communication between Brain Areas Based on Nested Oscillations
Bonnefond, M., Kästner, S., & Jensen, O. B. (2017) · eNeuro · doi:10.1523/eneuro.0153-16.2017 · Cited by 302
Oscillatory activity in the monkey hippocampus during visual exploration and memory formation
Jutras, M. J., Fries, P., & Buffalo, E. A. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1302351110 · Cited by 291
Jacobs, J. (2013) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0304 · Cited by 279
Direct Brain Stimulation Modulates Encoding States and Memory Performance in Humans
Ezzyat, Y., Kragel, J. E., Burke, J. F., Levy, D. F., Lyalenko, A., Wanda, P. A., O’Sullivan, L., Hurley, K. B., Busygin, S., Pedisich, I., et al. (2017) · Current Biology · doi:10.1016/j.cub.2017.03.028 · Cited by 242
Theta Oscillations at Encoding Mediate the Context-Dependent Nature of Human Episodic Memory
Staudigl, T., & Hanslmayr, S. (2013) · Current Biology · doi:10.1016/j.cub.2013.04.074 · Cited by 246
Lega, B. C., Burke, J., Jacobs, J., & Kahana, M. J. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu232 · Cited by 230
High vs Low Frequency Neural Oscillations in Schizophrenia
Moran, L. V., & Hong, L. E. (2011) · Schizophrenia Bulletin · doi:10.1093/schbul/sbr056 · Cited by 219
Infants’ preferences for native speakers are associated with an expectation of information
Begus, K., Gliga, T., & Southgate, V. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1603261113 · Cited by 186
Cicchese, J. J., & Berry, S. D. (2016) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2016.00001 · Cited by 173
Acetylcholine bidirectionally regulates learning and memory
Huang, Q., Liao, C., Ge, F., Ao, J., & Liu, T. (2022) · Journal of Neurorestoratology · doi:10.1016/j.jnrt.2022.100002 · Cited by 181
Tan, E., Troller‐Renfree, S. V., Morales, S., Buzzell, G. A., McSweeney, M., Antúnez, M., & Fox, N. A. (2024) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2024.101404 · Cited by 193
Human intracranial high-frequency activity maps episodic memory formation in space and time
Burke, J. F., Long, N. M., Zaghloul, K. A., Sharan, A. D., Sperling, M. R., & Kahana, M. J. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.06.067 · Cited by 149
Grounding language processing on basic neurophysiological principles
Friederici, A. D., & Singer, W. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.03.012 · Cited by 154
Frequency-specific electrophysiologic correlates of resting state fMRI networks
Hacker, C. D., Snyder, A. Z., Pahwa, M., Corbetta, M., & Leuthardt, E. C. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.01.054 · Cited by 146
The rhythm of learning: Theta oscillations as an index of active learning in infancy
Begus, K., & Bonawitz, E. B. (2020) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2020.100810 · Cited by 163
Movement-Related Theta Rhythm in Humans: Coordinating Self-Directed Hippocampal Learning
Kaplan, R., Doeller, C. F., Barnes, G. R., Vladimir Litvak, A., Düzel, E., Bandettini, P. A., & Burgess, N. (2012) · PLoS Biology · doi:10.1371/journal.pbio.1001267 · Cited by 151
Neuronal oscillations: unavoidable and useful?
Singer, W. (2017) · European Journal of Neuroscience · doi:10.1111/ejn.13796 · Cited by 153
Stiso, J., Khambhati, A. N., Menara, T., Kahn, A. E., Stein, J. M., Das, S. R., Gorniak, R., Tracy, J. I., Litt, B., Davis, K. A., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2019.08.008 · Cited by 136
Medial prefrontal theta phase coupling during spatial memory retrieval
Kaplan, R., Bush, D., Bonnefond, M., Bandettini, P. A., Barnes, G. R., Doeller, C. F., & Burgess, N. (2014) · Hippocampus · doi:10.1002/hipo.22255 · Cited by 146
Nir, R., Sinai, A., Moont, R., Harari, E., & Yarnitsky, D. (2011) · Clinical Neurophysiology · doi:10.1016/j.clinph.2011.08.006 · Cited by 139
Decreases in theta and increases in high frequency activity underlie associative memory encoding
Greenberg, J. A., Burke, J. F., Haque, R. U., Kahana, M. J., & Zaghloul, K. A. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.03.077 · Cited by 127
Duncan, K. D., Tompary, A., & Davachi, L. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0521-14.2014 · Cited by 126
Staresina, B. P., Michelmann, S., Bonnefond, M., Jensen, O. B., Axmacher, N., & Fell, J. (2016) · eLife · doi:10.7554/elife.17397 · Cited by 130
Self-citationHuman hippocampal theta power indicates movement onset and distance travelled
Bush, D., Bisby, J. A., Bird, C. M., Gollwitzer, S., Rodionov, R., Diehl, B., McEvoy, A. W., Walker, M. C., & Burgess, N. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1708716114 · Cited by 112
Avraham, G., Morehead, J. R., Kim, H. E., & Ivry, R. B. (2021) · PLoS Biology · doi:10.1371/journal.pbio.3001147 · Cited by 102
Expected reward modulates encoding-related theta activity before an event
Gruber, M. J., Watrous, A. J., Ekstrom, A. D., Ranganath, C., & Otten, L. J. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2012.07.064 · Cited by 108
Hermiller, M. S., Chen, Y. F., Parrish, T. B., & Voss, J. L. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0486-20.2020 · Cited by 109
Brain oscillations, hypnosis, and hypnotizability
Jensen, M. P., Adachi, T., & Hakimian, S. (2015) · American Journal of Clinical Hypnosis · doi:10.1080/00029157.2014.976786 · Cited by 98
Functional networks of the brain: from connectivity restoration to dynamic integration
Hramov, A. E., Frolov, N. S., Maksimenko, V. A., Kurkin, S., Kazantsev, V., & Pisarchik, A. N. (2020) · Physics-Uspekhi · doi:10.3367/ufne.2020.06.038807 · Cited by 100
Rhythmic Working Memory Activation in the Human Hippocampus
Leszczyński, M., Fell, J., & Axmacher, N. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.09.081 · Cited by 95
Self-citationPeri-encoding predictors of memory encoding and consolidation
Cohen, N., Pell, L., Edelson, M. G., Ben-Yakov, A., Pine, A., & Dudai, Y. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.11.002 · Cited by 98
Intracranial recordings and human memory
Johnson, E. L., & Knight, R. T. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.07.021 · Cited by 88
Fellner, M.-C., Bäuml, K. T., & Hanslmayr, S. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.04.121 · Cited by 89
Neural Oscillations: Understanding a Neural Code of Pain
Kim, J. A., & Davis, K. D. (2020) · The Neuroscientist · doi:10.1177/1073858420958629 · Cited by 92
Using single-trial EEG to predict and analyze subsequent memory
Noh, E., Herzmann, G., Curran, T., & de Sa, V. R. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.09.028 · Cited by 81
Ryan, J. D., Shen, K., & Liu, Z. (2019) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.14256 · Cited by 86
Johnson, E. L., Kam, J. W. Y., Tzovara, A., & Knight, R. T. (2020) · Journal of Neural Engineering · doi:10.1088/1741-2552/abb7a5 · Cited by 80
Differential effects of ongoing EEG beta and theta power on memory formation
Scholz, S., Schneider, S. L., & Rose, M. (2017) · PLoS ONE · doi:10.1371/journal.pone.0171913 · Cited by 78
Septohippocampal Neuromodulation Improves Cognition after Traumatic Brain Injury
Lee, D. J., Gurkoff, G. G., Izadi, A., Seidl, S. E., Echeverri, A., Melnik, M., Berman, R. F., Ekstrom, A. D., Muizelaar, J. P., Lyeth, B. G., et al. (2015) · Journal of Neurotrauma · doi:10.1089/neu.2014.3744 · Cited by 82
The role of cortical beta oscillations in time estimation
Kulashekhar, S., Pekkola, J., Palva, J. M., & Palva, S. (2016) · Human Brain Mapping · doi:10.1002/hbm.23239 · Cited by 77
The Sync/deSync Model: How a Synchronized Hippocampus and a Desynchronized Neocortex Code Memories
Parish, G., Hanslmayr, S., & Bowman, H. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.2561-17.2018 · Cited by 69
Rapid Improvement in Visual Selective Attention Related to Action Video Gaming Experience
Qiu, N., Ma, W., Fan, X., Zhang, Y., Li, Y., Yan, Y., Zhou, Z., Li, F., Gong, D., & Yao, D. (2018) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2018.00047 · Cited by 76
Oscillatory EEG dynamics underlying automatic chunking during sentence processing
Bonhage, C., Meyer, L., Gruber, T., Friederici, A. D., & Mueller, J. L. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.03.018 · Cited by 72
Infant EEG theta modulation predicts childhood intelligence
Jones, E. J. H., Goodwin, A., Orekhova, E. V., Charman, T., Dawson, G., Webb, S. J., & Johnson, M. H. (2020) · Scientific Reports · doi:10.1038/s41598-020-67687-y · Cited by 73
Begus, K., & Southgate, V. (2018) · Springer eBooks · doi:10.1007/978-3-319-77182-3_2 · Cited by 75
Brain oscillations track the formation of episodic memories in the real world
Griffiths, B., Mazaheri, A., Debener, S., & Hanslmayr, S. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.09.021 · Cited by 67
Sheehan, T. C., Sreekumar, V., Inati, S. K., & Zaghloul, K. A. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.2389-17.2017 · Cited by 67
Gorgoni, M., D’Atri, A., Scarpelli, S., Reda, F., & Gennaro, L. D. (2019) · Sleep Medicine · doi:10.1016/j.sleep.2019.06.025 · Cited by 73
The role of the anterior nuclei of the thalamus in human memory processing
Sweeney‐Reed, C. M., Buentjen, L., Voges, J., Schmitt, F. C., Zaehle, T., Kam, J. W. Y., Kaufmann, J., Heinze, H., Hinrichs, H., Knight, R. T., et al. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.02.046 · Cited by 66
Developmental change in EEG theta activity in the medial prefrontal cortex during response control
Liu, Z., Woltering, S., & Lewis, M. D. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.08.054 · Cited by 74
Functional connectivity and oscillatory neuronal activity in the resting human brain
Ganzetti, M., & Mantini, D. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.02.032 · Cited by 61
Theta rhythmicity governs human behavior and hippocampal signals during memory-dependent tasks
Wal, M. T., Domingo, J. L., Lifanov, J., Roux, F., Kolibius, L. D., Gollwitzer, S., Lang, J., Hamer, H. M., Rollings, D. T., Sawlani, V., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-27323-3 · Cited by 62
Self-citationPre-stimulus thalamic theta power predicts human memory formation
Sweeney‐Reed, C. M., Zaehle, T., Voges, J., Schmitt, F. C., Buentjen, L., Kopitzki, K., Richardson‐Klavehn, A., Hinrichs, H., Heinze, H., Knight, R. T., et al. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.05.042 · Cited by 57
Canolty, R. T., Ganguly, K., & Carmena, J. M. (2012) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002809 · Cited by 52
Aktürk, T., de Graaf, T. A., Güntekin, B., Hanoğlu, L., & Sack, A. T. (2022) · Scientific Reports · doi:10.1038/s41598-022-18665-z · Cited by 55
Blocking of irrelevant memories by posterior alpha activity boosts memory encoding
Park, H., Lee, D. S., Kang, E., Kang, H., Hahm, J., Kim, J. S., Chung, C. K., & Jensen, O. B. (2014) · Human Brain Mapping · doi:10.1002/hbm.22452 · Cited by 64
Fornical Closed-Loop Stimulation for Alzheimer’s Disease
Senova, S., Chaillet, A., & Lozano, A. M. (2018) · Trends in Neurosciences · doi:10.1016/j.tins.2018.03.015 · Cited by 53
Cortical theta wanes for language
Hermes, D., Miller, K. J., Vansteensel, M. J., Edwards, E., Ferrier, C. H., Bleichner, M. G., van Rijen, P. C., Aarnoutse, E. J., & Ramsey, N. F. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.07.029 · Cited by 51
Brain computer interface to enhance episodic memory in human participants
Burke, J. F., Merkow, M. B., Jacobs, J., Kahana, M. J., & Zaghloul, K. A. (2015) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.01055 · Cited by 54
Prestimulus theta in the human hippocampus predicts subsequent recognition but not recall
Merkow, M. B., Burke, J. F., Stein, J. M., & Kahana, M. J. (2014) · Hippocampus · doi:10.1002/hipo.22335 · Cited by 54
Nokia, M. S., Sisti, H. M., Choksi, M. R., & Shors, T. J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0031375 · Cited by 51
Crespo‐García, M., Zeiller, M., Leupold, C., Kreiselmeyer, G., Rampp, S., Hamer, H. M., & Dalal, S. S. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.08.021 · Cited by 49
Zhang, H., Morrone, M. C., & Alais, D. (2019) · Scientific Reports · doi:10.1038/s41598-018-37918-4 · Cited by 45
Ripples reflect a spectrum of synchronous spiking activity in human anterior temporal lobe
Tong, A. P. S., Vaz, A. P., Wittig, J. H., Inati, S. K., & Zaghloul, K. A. (2021) · eLife · doi:10.7554/elife.68401 · Cited by 42
The predictive role of pre-cue EEG rhythms on MI-based BCI classification performance
Bamdadian, A., Guan, C., Ang, K. K., & Xu, J. (2014) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2014.06.011 · Cited by 48
Bunce, J. G., Zikopoulos, B., Feinberg, M. D., & Barbas, H. (2013) · The Journal of Comparative Neurology · doi:10.1002/cne.23413 · Cited by 46
Sweeney‐Reed, C. M., Zaehle, T., Voges, J., Schmitt, F. C., Buentjen, L., Kopitzki, K., Hinrichs, H., Heinze, H., Rugg, M. D., Knight, R. T., et al. (2015) · eLife · doi:10.7554/elife.07578 · Cited by 48
What Turns Assistive into Restorative Brain-Machine Interfaces?
Gharabaghi, A. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00456 · Cited by 51
The anterior and centromedian thalamus: Anatomy, function, and dysfunction in epilepsy
Warsi, N. M., Yan, H., Suresh, H., Wong, S. M., Arski, O. N., Gorodetsky, C., Zhang, K., Gouveia, F. V., & Ibrahim, G. M. (2022) · Epilepsy Research · doi:10.1016/j.eplepsyres.2022.106913 · Cited by 45
Hippocampal Theta and Episodic Memory
Rudoler, J. H., Herweg, N. A., & Kahana, M. J. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.1045-22.2022 · Cited by 45
Hippocampal theta activity during encoding promotes subsequent associative memory in humans
Joensen, B. H., Bush, D., Vivekananda, U., Horner, A. J., Bisby, J. A., Diehl, B., Miserocchi, A., McEvoy, A. W., Walker, M. C., & Burgess, N. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad162 · Cited by 45
The EEG as an index of neuromodulator balance in memory and mental illness
Vakalopoulos, C. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00063 · Cited by 45
Remembered or Forgotten?—An EEG-Based Computational Prediction Approach
Sun, X., Qian, C., Chen, Z., Wu, Z., Luo, B., & Pan, G. (2016) · PLoS ONE · doi:10.1371/journal.pone.0167497 · Cited by 45
Phase separation of competing memories along the human hippocampal theta rhythm
Kerrén, C., van Bree, S., Griffiths, B., & Wimber, M. (2022) · eLife · doi:10.7554/elife.80633 · Cited by 37
Fleischmann, R., Tränkner, S., Kraft, A., Schmidt, S. H., Schreiber, S. J., & Brandt, S. A. (2019) · Pilot and Feasibility Studies · doi:10.1186/s40814-018-0388-z · Cited by 42
Bidirectional propagation of low frequency oscillations over the human hippocampal surface
Kleen, J. K., Chung, J. E., Sellers, K. K., Zhou, J. J., Triplett, M., Lee, K., Tooker, A., Haque, R., & Chang, E. F. (2021) · Nature Communications · doi:10.1038/s41467-021-22850-5 · Cited by 38
Changing temporal context in human temporal lobe promotes memory of distinct episodes
El-Kalliny, M. M., Wittig, J. H., Sheehan, T. C., Sreekumar, V., Inati, S. K., & Zaghloul, K. A. (2019) · Nature Communications · doi:10.1038/s41467-018-08189-4 · Cited by 41
Elfman, K. W., Aly, M., & Yonelinas, A. P. (2014) · Hippocampus · doi:10.1002/hipo.22345 · Cited by 35
Bauer, R. H., Fels, M., Royter, V., Raco, V., & Gharabaghi, A. (2016) · Clinical Neurophysiology · doi:10.1016/j.clinph.2016.06.020 · Cited by 37
Does the Cerebral Cortex Exploit High-Dimensional, Non-linear Dynamics for Information Processing?
Singer, W., & Lazăr, A. (2016) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2016.00099 · Cited by 36
Bagnato, S., Boccagni, C., Prestandrea, C., Fingelkurts, A. A., Fingelkurts, A. A., & Galardi, G. (2016) · Archives of Physical Medicine and Rehabilitation · doi:10.1016/j.apmr.2016.09.132 · Cited by 36
Hawco, C. S., Armony, J. L., Daskalakis, Z. J., Berlim, M. T., Chakravarty, M. M., Pike, G. B., & Lepage, M. (2017) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2017.00404 · Cited by 33
Salari, N., & Rose, M. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.10.037 · Cited by 41
Cross‐regional phase amplitude coupling supports the encoding of episodic memories
Wang, D. X., Schmitt, K., Seger, S. E., Davila, C. E., & Lega, B. C. (2021) · Hippocampus · doi:10.1002/hipo.23309 · Cited by 33
Driving working memory with frequency‐tuned noninvasive brain stimulation
Albouy, P., Baillet, S., & Zatorre, R. J. (2018) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13664 · Cited by 34
Labruna, L., Stark‐Inbar, A., Breska, A., Dabit, M., Vanderschelden, B., Nitsche, M. A., & Ivry, R. B. (2019) · Brain stimulation · doi:10.1016/j.brs.2019.03.008 · Cited by 32
Intention to encode boosts memory-related pre-stimulus EEG beta power
Schneider, S. L., & Rose, M. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.11.024 · Cited by 32
Cortical Low-Frequency Power and Progressive Phase Synchrony Precede Successful Memory Encoding
Haque, R. U., Wittig, J. H., Damera, S. R., Inati, S. K., & Zaghloul, K. A. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0687-15.2015 · Cited by 29
Targeted memory reactivation in human REM sleep elicits detectable reactivation
Abdellahi, M. E. A., Koopman, A. C. M., Treder, M. S., & Lewis, P. A. (2023) · eLife · doi:10.7554/elife.84324 · Cited by 31
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
Strunk, J., & Duarte, A. (2018) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2019.01.005 · Cited by 25
Direct electrical brain stimulation of human memory: lessons learnt and future perspectives
Kucewicz, M. T., Worrell, G. A., & Axmacher, N. (2022) · Brain · doi:10.1093/brain/awac435 · Cited by 27
Self-citationHypothesis-driven methods to augment human cognition by optimizing cortical oscillations
Horschig, J. M., Zumer, J. M., & Bahramisharif, A. (2014) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2014.00119 · Cited by 26
Metadata
- Authors
- Fell, J., Ludowig, E., Staresina, B. P., Wagner, T., Kranz, T., Elger, C. E., & Axmacher, N.
- Affiliations
- University of Bonn (DE)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2011-04-06
- Volume
- 31
- Issue
- 14
- Pages
- 5392-5397
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6622710
- OpenAlex
- W2025180344
- Cited by
- 203
- References
- 44
- Citations by year
- 2026: 5 · 2025: 11 · 2024: 9 · 2023: 13 · 2022: 18 · 2021: 19 · 2020: 16 · 2019: 9 · 2018: 17 · 2017: 13 · 2016: 14 · 2015: 11 · 2014: 17 · 2013: 18 · 2012: 9
- FWCI
- 7.64
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Deutsche Forschungsgemeinschaft
- Volkswagen Foundation (I/79878)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- memory encoding, medial temporal lobe, hippocampus, rhinal cortex, theta power, alpha power, subsequent memory effect, word recognition, top-down control, contextual information, epilepsy patients, intracranial EEG
- MeSH terms
- Adolescent, Adult, Alpha Rhythm, Brain Mapping, Child, Child, Preschool, Electroencephalography, Epilepsy, Temporal Lobe, Female, Hippocampus, Humans, Male, Middle Aged, Neuropsychological Tests, Photic Stimulation, Reaction Time, Temporal Lobe, Theta Rhythm, Vocabulary, Statistics, Nonparametric, Recognition, Psychology, Young Adult
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