Evidence map›Paper›PMID 35867767›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

Widespread ripples synchronize human cortical activity during sleep, waking, and memory recall.

Charles W Dickey, Ilya A Verzhbinsky, Xi Jiang, Burke Q Rosen, Sophie Kajfez, Brittany Stedelin, Jerry J Shih, Sharona Ben-Haim, Ahmed M Raslan, Emad N Eskandar and 3 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

56 citing papers in PubMed.

  1. Trial
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  6. Epileptogenicity alters intrahippocampal ripple propagation.medRxiv : the preprint server for health sciences · 2026
    Article
  7. Are physiological oscillations physiological?The Journal of physiology · 2026
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
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  16. Precise temporal dynamics of ripple events support order memory in human hippocampal-cortical circuits.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  17. Review
  18. Article
  19. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Charles W DickeyNeurosciences Graduate Program, University of California San Diego, La Jolla, CA 92093.ORCID 0000-0002-9118-8605
Ilya A VerzhbinskyNeurosciences Graduate Program, University of California San Diego, La Jolla, CA 92093.ORCID 0000-0002-7890-8559
Xi JiangNeurosciences Graduate Program, University of California San Diego, La Jolla, CA 92093.
Burke Q RosenNeurosciences Graduate Program, University of California San Diego, La Jolla, CA 92093.ORCID 0000-0002-5049-8316
Sophie KajfezDepartment of Radiology, University of California San Diego, La Jolla, CA 92093.
Brittany StedelinDepartment of Neurological Surgery, Oregon Health & Science University, Portland, OR 97239.ORCID 0000-0001-5368-4299
Jerry J ShihDepartment of Neurosciences, University of California San Diego, La Jolla, CA 92093.
Sharona Ben-HaimDepartment of Neurological Surgery, University of California San Diego, La Jolla, CA 92093.ORCID 0000-0002-3864-6443
Ahmed M RaslanDepartment of Neurological Surgery, Oregon Health & Science University, Portland, OR 97239.
Emad N EskandarDepartment of Neurological Surgery, Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, NY 10461.
Jorge Gonzalez-MartinezDepartment of Neurological Surgery, University of Pittsburgh, Pittsburgh, PA 15260.
Sydney S CashDepartment of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114.ORCID 0000-0002-4557-6391
Eric HalgrenDepartment of Radiology, University of California San Diego, La Jolla, CA 92093.

Funding

Neurosciences Graduate Training ProgramT32NS061847 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Brenda L Bloodgood · 2008 to 2026
$7.7M
TRAINING PROGRAM IN COGNITIVE NEUROSCIENCET32MH020002 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SEJNOWSKI, TERRENCE J · 1999 to 2020
$6.1M
From ion channel dynamics to human EEG and MEG: multiscale neuronal models validated by human dataRF1MH117155 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BAZHENOV, MAKSIM V, CASH, SYDNEY S · 2018 to 2018
$3.7M
NIMH NIH HHS RF1 MH117155NIMH NIH HHS T32 MH020002NINDS NIH HHS T32 NS061847
6 · The paper itself

Abstract

Declarative memory encoding, consolidation, and retrieval require the integration of elements encoded in widespread cortical locations. The mechanism whereby such "binding" of different components of mental events into unified representations occurs is unknown. The "binding-by-synchrony" theory proposes that distributed encoding areas are bound by synchronous oscillations enabling enhanced communication. However, evidence for such oscillations is sparse. Brief high-frequency oscillations ("ripples") occur in the hippocampus and cortex and help organize memory recall and consolidation. Here, using intracranial recordings in humans, we report that these ∼70-ms-duration, 90-Hz ripples often couple (within ±500 ms), co-occur (≥ 25-ms overlap), and, crucially, phase-lock (have consistent phase lags) between widely distributed focal cortical locations during both sleep and waking, even between hemispheres. Cortical ripple co-occurrence is facilitated through activation across multiple sites, and phase locking increases with more cortical sites corippling. Ripples in all cortical areas co-occur with hippocampal ripples but do not phase-lock with them, further suggesting that cortico-cortical synchrony is mediated by cortico-cortical connections. Ripple phase lags vary across sleep nights, consistent with participation in different networks. During waking, we show that hippocampo-cortical and cortico-cortical coripples increase preceding successful delayed memory recall, when binding between the cue and response is essential. Ripples increase and phase-modulate unit firing, and coripples increase high-frequency correlations between areas, suggesting synchronized unit spiking facilitating information exchange. co-occurrence, phase synchrony, and high-frequency correlation are maintained with little decrement over very long distances (25 cm). Hippocampo-cortico-cortical coripples appear to possess the essential properties necessary to support binding by synchrony during memory retrieval and perhaps generally in cognition.

Indexed as

Cerebral CortexHippocampusMemory ConsolidationMental RecallSleepWakefulnessElectrocorticographyHumanscortexhippocampusnon-rapid eye movement sleeprippleswaking

Identifiers

PMID35867767
PMCPMC9282280

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.