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Hippocampal sharp-wave ripples linked to visual episodic recollection in humans

Norman, Yitzhak, Yeagle, Erin M., Khuvis, Simon, Harel, Michal, Mehta, Ashesh D., Malach, Rafael·2019·Science

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Abstract

Sharp-wave ripples in the hippocampus: What are the brain mechanisms responsible for episodic memory retrieval? Norman et al. investigated epilepsy patients who had electrodes implanted in the hippocampus and a variety of cortical areas. Using a visual learning paradigm, they examined the temporal relationship between the incidence of hippocampal sharp-wave ripples and recall. Effective encoding of visual information was associated with higher incidence of ripples. Successful recall was preceded by an increased probability of ripples, which were also associated with transient reemergence of activation patterns in higher visual cortical areas. Hippocampal ripples may thus boost recollections during episodic memory retrieval. Science , this issue p. eaax1030

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Delorme, A., & Makeig, S. (2004) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2003.10.009 · Cited by 24,371
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Desikan, R. S., Ségonne, F., Fischl, B., Quinn, B. T., Dickerson, B. C., Blacker, D., Buckner, R. L., Dale, A. M., Maguire, R. P., Hyman, B. T., et al. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.01.021 · Cited by 13,324
Improved Optimization for the Robust and Accurate Linear Registration and Motion Correction of Brain Images
Jenkinson, M., Bannister, P., Brady, M., & Smith, S. (2002) · NeuroImage · doi:10.1006/nimg.2002.1132 · Cited by 11,888
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Smith, S. M. (2002) · Human Brain Mapping · doi:10.1002/hbm.10062 · Cited by 10,496
The control of the false discovery rate in multiple testing under dependency
Benjamini, Y., & Yekutieli, D. (2001) · The Annals of Statistics · doi:10.1214/aos/1013699998 · Cited by 10,490
FieldTrip: open source software for advanced analysis of MEG, EEG, and invasive electrophysiological data
Oostenveld, R., Fries, P., Maris, E., & Schoffelen, J.-M. (2011) · Computational Intelligence and Neuroscience · doi:10.1155/2011/156869 · Cited by 10,323
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Fischl, B. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.01.021 · Cited by 9,526
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Maris, E., & Oostenveld, R. (2007) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2007.03.024 · Cited by 8,496
A global optimisation method for robust affine registration of brain images
Jenkinson, M., & Smith, S. M. (2001) · Medical Image Analysis · doi:10.1016/s1361-8415(01)00036-6 · Cited by 7,018
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Swanson, R. A., Levenstein, D., McClain, K., Tingley, D., & Buzsáki, G. (2020) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2020.02.008 · Cited by 32
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Self-citation
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Self-citation
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Zhang, H., Skelin, I., Ma, S., Paff, M. R., Mnatsakanyan, L., Yassa, M. A., Knight, R. T., & Lin, J. J. (2024) · Nature Communications · doi:10.1038/s41467-023-44295-8 · Cited by 31
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Hagen, E., Chambers, A. R., Einevoll, G. T., Pettersen, K. H., Enger, R., & Stasik, A. J. (2021) · Neuroinformatics · doi:10.1007/s12021-020-09496-2 · Cited by 24
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Lin, R., Meng, X., Chen, F., Li, X., Jensen, O. B., Theeuwes, J., & Wang, B. (2024) · Nature Human Behaviour · doi:10.1038/s41562-024-01852-5 · Cited by 28
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Coelho, C. A. O., Mocle, A. J., Jacob, A. D., Ramsaran, A. I., Rashid, A. J., Köhler, S., Josselyn, S. A., & Frankland, P. W. (2024) · Science Advances · doi:10.1126/sciadv.adn9815 · Cited by 23
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Authors: Norman, Y., Yeagle, E. M., Khuvis, S., Harel, M., Mehta, A. D., & Malach, R.
Affiliations: Weizmann Institute of Science (IL)
Feinstein Institute for Medical Research (US)
Corresponding author: Malach, Rafael
ORCID: Norman, Yitzhak
Yeagle, Erin M.
Khuvis, Simon
Harel, Michal
Mehta, Ashesh D.
Malach, Rafael
Venue: Science
Publisher: American Association for the Advancement of Science (AAAS)
Published: 2019-08-16
Volume: 365
Issue: 6454
ISSN: 0036-8075 (ISSN-L)
1095-9203
DOI: 10.1126/science.aax1030
OpenAlex: W2969121629
Cited by: 270
References: 91
Citations by year: 2026: 32 · 2025: 59 · 2024: 53 · 2023: 33 · 2022: 30 · 2021: 32 · 2020: 27 · 2019: 4
FWCI: 13.54
Type: journal article
Language: en
Open access: closed
Locations: Science (publishedVersion)
PubMed (publishedVersion)
Funders: United States - Israel Binational Science Foundation (2017015)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
Keywords: hippocampal ripples, episodic memory, memory retrieval, memory consolidation, memory encoding, intracranial recordings
MeSH terms: Adult, Female, Hippocampus, Humans, Male, Middle Aged, Mental Recall, Visual Perception, Wakefulness, Young Adult, Brain Waves, Memory, Episodic

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Hippocampal sharp-wave ripples linked to visual episodic recollection in humans

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