Brain functional connectivity upon awakening from sleep predicts interindividual differences in dream recall frequency
Open accessAbstract
Why do some individuals recall dreams every day while others hardly ever recall one? We hypothesized that sleep inertia—the transient period following awakening associated with brain and cognitive alterations—could be a key mechanism to explain interindividual differences in dream recall at awakening. To test this hypothesis, we measured the brain functional connectivity (combined electroencephalography–functional magnetic resonance imaging) and cognition (memory and mental calculation) of high dream recallers (HR, n = 20) and low dream recallers (LR, n = 18) in the minutes following awakening from an early-afternoon nap. Resting-state scans were acquired just after or before a 2 min mental calculation task, before the nap, 5 min after awakening from the nap, and 25 min after awakening. A comic was presented to the participants before the nap with no explicit instructions to memorize it. Dream(s) and comic recall were collected after the first post-awakening scan. As expected, between-group contrasts of the functional connectivity at 5 min post-awakening revealed a pattern of enhanced connectivity in HR within the default mode network (DMN) and between regions of the DMN and regions involved in memory processes. At the behavioral level, a between-group difference was observed in dream recall, but not comic recall. Our results provide the first evidence that brain functional connectivity right after awakening is associated with interindividual trait differences in dream recall and suggest that the brain connectivity of HR at awakening facilitates the maintenance of the short-term memory of the dream during the sleep–wake transition.
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- Interpretationcitation§ Discussion · p. 7
The cerebral functioning of high dream recallers and low dream recallers is different, as previously demonstrated with EEG and PET.
“our findings confirm that the cerebral functioning of HR and LR is different, as previously demonstrated with EEG and PET [9, 10, 13]”
Quote in the paperNot a substantial claim1 of 3 sources checked- cites [9] Eichenlaub, 2014, Brain reactivity differentiates subjects with high and low dream recall frequencies during both sleep and wakefulness, Cereb Cortex. source
- cites [10] Vallat, 2017, Increased evoked potentials to arousing auditory stimuli during sleep: implication for the understanding of dream recall, Front Hum Neurosci. source
- cites [13] Eichenlaub, 2014, Resting brain activity varies with dream recall frequency between subjects, Neuropsychopharmacology. source
- Findingown data§ Functional connectivity · p. 6
There were no significant group differences in functional connectivity of the three default mode network seeds during the pre-nap resting-state scan.
“First, we did not find any significant group differences in the functional connectivity of any of the three seeds during the pre-nap resting-state scan. In other words, the two groups did not differ in the DMN functional connectivity before the nap.”
Quote in the paperSubstantial claim - Findingown data§ Dream recall · p. 6
When combining both groups, dream recall did not significantly differ after awakening from N2 versus N3 sleep.
“Lastly, when combining participants from both groups, we did not find a significant between-stage difference in dream recall after awakening from the nap. That is, dream recall was not significantly different after awakening from N2 or N3 sleep ( X 2 = 0.08, p = 0.78).”
Quote in the paperNot a substantial claim - Findingown data§ Dream recall · p. 6
After awakening from partial sleep deprivation in the sleep unit, a significantly higher proportion of high dream recallers (65%) than low dream recallers (22%) reported a full or contentless dream.
“After awakening from the partial sleep deprivation in the sleep unit, significantly more HR reported dreams than did LR (65% of HR and 22% of LR reported a full or a white [contentless] dream; X 2 = 7.0, p = 0.008).”
Quote in the paperSubstantial claim - Findingown data§ Functional connectivity · p. 6
Significant group-by-time interaction effects were found for all three default mode network seeds.
“We found significant interaction effects between group and time for all three seeds, which are reported in Supplementary Table S1.”
Quote in the paperSubstantial claim
- Findingown data§ Dream recall · p. 6
After awakening from the 45-minute nap inside the MRI, a significantly higher proportion of high dream recallers (75%) than low dream recallers (33%) reported a dream.
“A similar effect was observed after awakening from the 45 min nap inside the MRI (75% of HR vs. 33% of LR, X 2 = 6.7, p = 0.010; see Table 2).”
Quote in the paperSubstantial claim - Findingown data§ Abstract · p. 2
At 5 minutes after awakening, high dream recallers showed greater functional connectivity than low dream recallers within the default mode network and between default mode network regions and memory-related regions, including MPFC-precuneus, PCC-right PFC, PCC-SFG, LP-SFG, and LP-right AG.
“As expected, between-group contrasts of the functional connectivity at 5 min post-awakening revealed a pattern of enhanced connectivity in HR within the default mode network (DMN) and between regions of the DMN and regions involved in memory processes.”
- Also stated in: § Functional connectivity · p. 6 · plain
“The larger group effect was observed at 5 min post-awakening. The functional connectivity of MPFC, PCC, and LP was increased in HR as compared to LR, specifically between the MPFC and the precuneus, the PCC and the right PFC, the PCC and the superior frontal gyrus (SFG), the LP and the SFG, and the LP and the right angular gyrus (AG).”
Quote in the paperSubstantial claim - Also stated in: § Functional connectivity · p. 6 · plain
- Findingown data§ Discussion · p. 7
There was no significant group difference in behavioral impairment caused by sleep inertia, as measured by a mental calculation task.
“we did not find a significant group difference in the behavioral impairment caused by sleep inertia (as measured by a mental calculation task, Figure 2)”
Quote in the paperNot a substantial claim - Findingown data§ Discussion · p. 7
There was no significant difference between high dream recallers and low dream recallers in dream recall after awakening from N3 sleep.
“but not from N3 sleep”
Quote in the paperSubstantial claim - Findingown data§ Discussion · p. 7
High dream recallers and low dream recallers differed in dream recall after awakening from the nap.
“we have found a group difference in dream recall after awakening from the nap between the two groups”
Quote in the paperSubstantial claim - Findingown data§ Discussion · p. 7
High dream recallers and low dream recallers did not differ significantly in recall of a comic strip presented just before the nap.
“despite no significant difference in the recall of a comic strip that was presented to the participants just before the nap”
Quote in the paperSubstantial claim - Findingown data§ Discussion · p. 7
Compared with low dream recallers, high dream recallers showed increased functional connectivity between default mode network regions and several regions known to be involved in memory processes at 5 min post-awakening.
“Compared to LR, HR showed increased functional connectivity between regions of the DMN and several regions known to be involved in memory processes at 5 min post-awakening”
Quote in the paperSubstantial claim - Findingown data§ Discussion · p. 7
High dream recallers showed increased functional connectivity between the medial prefrontal cortex and the right putamen at 25 min post-awakening compared with low dream recallers.
“and between the MPFC and the right putamen at 25 min post-awakening”
Quote in the paperSubstantial claim - Findingown data§ Discussion · p. 7
Several differences in brain functional connectivity between high dream recallers and low dream recallers were found at 5 min post-awakening.
“we found several differences in brain functional connectivity between the two groups at 5 min post-awakening (Figure 3)”
Quote in the paperSubstantial claim - Findingown data§ Discussion · p. 7
Significantly more high dream recallers than low dream recallers recalled a dream after being awakened from N2 sleep.
“significantly more HR than LR recalled a dream after being awakened from N2 sleep”
Quote in the paperSubstantial claim - Findingown data§ Discussion · p. 7
Between-group contrasts at 5 min post-awakening revealed enhanced connectivity in high dream recallers within the default mode network and between the default mode network and the right prefrontal cortex and angular gyrus.
“Between-group contrasts of the functional connectivity at 5 min post-awakening revealed a pattern of enhanced connectivity in HR within the DMN and between the DMN and the right PFC and AG.”
Quote in the paperSubstantial claim - Findingown data§ Conclusion · p. 9
High dream recallers showed higher functional connectivity upon awakening between regions involved in short-term and episodic memory.
“HR showed a higher functional connectivity upon awakening between regions involved in short term and episodic memory”
Quote in the paperSubstantial claim - Findingown data§ Conclusion · p. 9
The present study showed that interindividual trait differences in dream recall frequency are associated with differences in brain functional connectivity in the first minutes following awakening.
“The present study showed that interindividual trait differences in DRF are associated with differences in brain functional connectivity in the first minutes following awakening.”
Quote in the paperSubstantial claim - Findingown data§ Discussion · p. 7
No group differences in functional connectivity were found during the pre-nap scan.
“no group differences in functional connectivity were found during the pre-nap scan”
Quote in the paperSubstantial claim - Interpretationown data§ Statement of Significance · p. 2
The functional state of the brain immediately upon awakening from sleep partly explains why some individuals recall dreams frequently and others rarely.
“we present evidence that the answer to this question lies in part in the functional state of the brain immediately upon awakening from sleep.”
Quote in the paperSubstantial claim - Premisecitation§ Introduction · p. 3
The MPFC and TPJ are involved in dream production and/or recall.
“The MPFC and TPJ are known to be involved in dream production and/or recall. Indeed, lesions of one or both regions induce cessation of dream reports [21, 22]”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [21] Solms, 1997
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [22] Solms, 2000, Dreaming and REM sleep are controlled by different brain mechanisms, Behav Brain Sci. source
- Study design and conductown data§ Functional connectivity · p. 6
There were no group differences in motion parameters at any of the three resting-state scans.
“Importantly, there was no group difference in motion parameters at any of the three resting-state scans, as indexed by the framewise displacement [45] and the number of scans that were defined as outliers by the Artifact Detection Toolbox (all p 's > 0.4).”
Quote in the paperSubstantial claim - Interpretationown data§ Abstract · p. 2
The brain connectivity of high dream recallers upon awakening facilitates maintaining short-term memory of the dream during the sleep-wake transition.
“and suggest that the brain connectivity of HR at awakening facilitates the maintenance of the short-term memory of the dream during the sleep-wake transition.”
Quote in the paperSubstantial claim - Interpretationown data§ Abstract · p. 2
Brain functional connectivity immediately after awakening is associated with interindividual trait differences in dream recall.
“Our results provide the first evidence that brain functional connectivity right after awakening is associated with interindividual trait differences in dream recall”
- Also stated in: § Statement of Significance · p. 2 · hedged
“Our results show a pattern of enhanced connectivity in HR within the default mode network (DMN) and between the DMN and regions associated with memory processes, therefore suggesting that trait differences in dream recall are associated with a specific brain functioning during the sleep-wake transition.”
Quote in the paperSubstantial claim - Also stated in: § Statement of Significance · p. 2 · hedged
- Interpretationown data§ Discussion · p. 7
Specific group differences in memory-related brain regions are present during the sleep-wake transition.
“show that specific group differences in memory-related brain regions are present during the sleep-wake transition”
Quote in the paperSubstantial claim - Premisecitation§ Discussion · p. 7
Sleep inertia interferes more with memory retrieval on awakening than with memory consolidation.
“It is generally admitted that sleep inertia interferes more with memory retrieval on awakening than with memory consolidation [14, 32, 47, 48].”
Quote in the paperSubstantial claim0 of 4 sources checked- cites [14] Tassi, 2000, Sleep inertia, Sleep Med Rev. source
- cites [32] Conduit, 2004, Poor recall of eye-movement signals from Stage 2 compared to REM sleep: implications for models of dreaming, Conscious Cogn. source
- cites [47] Bonnet, 1983, Memory for events occurring during arousal from sleep, Psychophysiology. source
- cites [48] Dinges, 1990, Are you awake? Cognitive performance and reverie during the hypnopompic state source
- Interpretationreasoning§ High-recallers (HR, n=20) > Low-recallers (LR, n=18) · p. 8
Brain activity at awakening is a critical parameter to explain the difference in dream recall frequency between high dream recallers and low dream recallers.
“we argue that brain activity at awakening is a critical parameter to explain the difference in DRF between HR and LR”
Quote in the paperSubstantial claim- Rests on an assumption: The impact of partial sleep deprivation on functional connectivity, if any, was similar in high dream recallers and low dream recallers.
- Interpretationreasoning§ Conclusion · p. 9
The higher functional connectivity in high dream recallers could facilitate the maintenance in short-term memory of the pre-awakening experience, the dream, and thus promote dream recall.
“which could facilitate the maintenance in short term memory of the pre-awakening experience (i.e. the dream) and thus promote dream recall”
Quote in the paperSubstantial claim - Interpretationown data§ Conclusion · p. 9
These results contribute to the growing body of evidence that trait differences in dream recall are supported by trait neurophysiological differences between high dream recallers and low dream recallers.
“these results contribute to the growing body of evidence that trait differences in dream recall are supported by trait neurophysiological differences between HR and LR”
Quote in the paperSubstantial claim - Interpretationown data§ Discussion · p. 7
The post-awakening functional connectivity changes were specific to the post-awakening period.
“therefore suggesting that these changes were specific to the post-awakening period”
Quote in the paperSubstantial claim - Premisecitation§ Limitations and future directions · p. 9
Naps are usually taken as a strategy to compensate for sleep loss.
“naps are usually taken as a strategy to compensate for sleep loss [58]”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [58] Faraut, 2017, Napping: a public health issue. From epidemiological to laboratory studies, Sleep Med Rev. source
- Interpretationreasoning§ Discussion · p. 7
The regions more functionally connected in high dream recallers than low dream recallers during the first minutes after awakening are almost the same as those associated with retrieval success.
“These are almost the same regions found to be more functionally connected in HR than in LR during the first minutes following awakening.”
Quote in the paperSubstantial claim - Interpretationown data§ Limitations and future directions · p. 9
Our results provide evidence that a specific pattern of functional connectivity upon awakening, involving the default mode network and memory-related brain areas, is related to interindividual differences in dream recall.
“our results provide evidence that a specific pattern of functional connectivity upon awakening, involving the DMN and memory-related brain areas, is related to interindividual differences in dream recall”
Quote in the paperSubstantial claim - Interpretationown data§ Discussion · p. 7
Increased default mode network connectivity upon awakening in high dream recallers facilitates the maintenance of dreams in short-term memory during the sleep-wake transition.
“our findings suggest that an increased DMN connectivity upon awakening in HR facilitates the maintenance of dreams in short-term memory during the sleep-wake transition”
Quote in the paperSubstantial claim - Interpretationreasoning§ Discussion · p. 7
The pattern of enhanced functional connectivity within the default mode network in high dream recallers at awakening facilitates the maintenance of short-term memory content during the sleep-wake transition rather than long-term memory recall.
“These findings suggest that the pattern of enhanced functional connectivity within the DMN in HR at awakening facilitates the maintenance of short term memory content during the transition between sleep and wake rather than long-term memory recall.”
Quote in the paperSubstantial claim - Interpretationreasoning§ High-recallers (HR, n=20) > Low-recallers (LR, n=18) · p. 8
The increased functional connectivity in high dream recallers after awakening would promote successful dream recall at awakening by facilitating the maintenance of short-term memory.
“our results suggest that the increased functional connectivity in HR after awakening would promote successful dream recall at awakening by facilitating the maintenance of short-term memory”
Quote in the paperSubstantial claim- Rests on an assumption: The impact of partial sleep deprivation on functional connectivity, if any, was similar in high dream recallers and low dream recallers.
- Classified as probably not a substantial claim. 18
- May combine two claims. 16
Classified as probably not a substantial claim.
Premisecitation§ Introduction · p. 3The default mode network is a set of functionally coupled brain areas involved in mind-wandering and episodic memory retrieval.
“Indeed, the DMN is a set of functionally coupled brain areas [23, 24] involved in mind-wandering and episodic memory retrieval [25]”
Quote in the paperSubstantial claim1 of 3 sources checked- cites [23] Raichle, 2001, A default mode of brain function, Proc Natl Acad Sci U S A. source
The opening section describes an organized default mode comprising brain areas that consistently decrease their activity across tasks, and the Discussion identifies several of those areas. The passages do not establish that the areas are functionally coupled. The mind-wandering and episodic-memory clause is attached to a different citation [25], so it is not judged here. (LLM, conf=0.82)
Experimental — accuracy not yet measured - cites [24] Sestieri, 2011, Episodic memory retrieval, parietal cortex, and the default mode network: functional and topographic analyses, J Neurosci. source
- cites [25] Legrand, 2009, What is self-specific? Theoretical investigation and critical review of neuroimaging results, Psychol Rev. source
May combine two claims.
Premisecitation§ Introduction · p. 3High dream recallers have increased regional cerebral blood flow in the MPFC and TPJ at rest during wake and sleep, and increased white matter density in the MPFC.
“Noteworthy, we found that HR have an increased regional cerebral blood flow in the medial prefrontal cortex (MPFC) and temporoparietal junction (TPJ) at rest (during wake and sleep), as well as an increased white matter density in the MPFC [20].”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [20] Vallat, 2018, Dream recall frequency is associated with medial prefrontal cortex white-matter density, Front Psychol. source
Classified as probably not a substantial claim. May combine two claims.
Premisecitation§ Introduction · p. 3The default mode network is typically hyperconnected during REM sleep, which has the highest rate of successful dream recall, and hypoconnected during N3 sleep, which has the lowest rate.
“Coherent with this, it is noteworthy that the DMN is typically hyperconnected during rapid eye movement (REM) sleep, the sleep stage associated with the highest rate of successful dream recall, and hypoconnected during N3 sleep, the sleep stage associated with the lowest rate of successful dream recall [28-31].”
Quote in the paperSubstantial claim1 of 4 sources checked- cites [28] Cavallero, 1992, Slow wave sleep dreaming, Sleep. source
- cites [29] Nielsen, 2000, A review of mentation in REM and NREM sleep: “covert” REM sleep as a possible reconciliation of two opposing models, Behav Brain Sci. source
- cites [30] Horovitz, 2009, Decoupling of the brain’s default mode network during deep sleep, Proc Natl Acad Sci U S A. source
The Results and Discussion report reduced frontal–posterior DMN connectivity during deep sleep, supporting the deep-sleep portion of the claim. The paper does not establish REM hyperconnectivity or compare dream-recall rates across sleep stages; it also does not specifically identify its deep-sleep finding as N3. No page numbers are available in our copy. (LLM, conf=0.88)
Experimental — accuracy not yet measured - cites [31] Wu, 2012, Variations in connectivity in the sensorimotor and default-mode networks during the first nocturnal sleep cycle, Brain Connect. source
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductcitation§ Behavioral tests · p. 4Participants trained on the descending subtraction task before the MRI session to avoid a practice effect.
“In the evening at the sleep unit, participants trained on the DST (six blocks of 2 min each), which was used to evaluate cognitive performances during the MRI session on the following day, to avoid a practice effect over the first trials [34].”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [34] Dinges, 1985, Assessing performance upon abrupt awakening from naps during quasi-continuous operations, Behav Res Methods Instrum Comput source
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Premisecitation§ Introduction · p. 3High dream recallers show more intra-sleep wakefulness than low dream recallers, with no differences in other sleep parameters.
“Results showed more intra-sleep wakefulness in HR than in LR (with no differences in other sleep parameters), which is coherent with the idea that periods of wakefulness during sleep are necessary to encode dream content into long-term memory [8].”
Quote in the paperNot a substantial claim1 of 2 sources checked- cites [9] Eichenlaub, 2014, Brain reactivity differentiates subjects with high and low dream recall frequencies during both sleep and wakefulness, Cereb Cortex. source
- cites [10] Vallat, 2017, Increased evoked potentials to arousing auditory stimuli during sleep: implication for the understanding of dream recall, Front Hum Neurosci. source
The Results (Sleep Parameters) show more wakefulness after sleep onset in high dream recallers, and the Discussion identifies awakening duration as the key difference. However, Table 1 also marks total sleep time as significantly different between groups, so the unqualified claim of no differences in other sleep parameters is not supported. (LLM, conf=0.88)
Experimental — accuracy not yet measured
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Premisecitation§ Introduction · p. 3Intra-sleep awakening promotes dream recall, as confirmed by objective sleep measurements.
“Intra-sleep awakening-which is both a state and a trait factor-was also hypothesized to promote dream recall [7, 8], a hypothesis that was recently confirmed using objective sleep measurements.”
Quote in the paperNot a substantial claim1 of 4 sources checked- cites [7] Schredl, 2003, Factors of home dream recall: a structural equation model, J Sleep Res. source
- cites [8] Koulack, 1976, Dream recall and dream recall failure: an arousal-retrieval model, Psychol Bull source
- cites [9] Eichenlaub, 2014, Brain reactivity differentiates subjects with high and low dream recall frequencies during both sleep and wakefulness, Cereb Cortex. source
- cites [10] Vallat, 2017, Increased evoked potentials to arousing auditory stimuli during sleep: implication for the understanding of dream recall, Front Hum Neurosci. source
The Discussion (‘Intra-Sleep Awakenings and Dream Recall’) reports objectively measured awakening durations and identifies duration as the best predictor of dream recall. It says the results support the arousal-retrieval model, but the observational finding does not establish that awakenings cause dream recall or definitively confirm the hypothesis. (LLM, conf=0.82)
Experimental — accuracy not yet measured
Probably not a substantial claim: may not pass S3 (load-bearing).
Premisecitation§ Behavioral tests · p. 4The descending subtraction task has been previously used to demonstrate performance deficits and normalization in the first 30 minutes after awakening.
“The DST has been previously used to evidence performance deficit and normalization in the first 30 min post awakening [34-36].”
Quote in the paperNot a substantial claim1 of 3 sources checked- cites [34] Dinges, 1985, Assessing performance upon abrupt awakening from naps during quasi-continuous operations, Behav Res Methods Instrum Comput source
The Instrumentation section identifies and describes the descending subtraction task, and the Results report DST performance deficits immediately after awakening. The introductory passage says post-awakening impairment generally does not last beyond 15–30 minutes, but the paper does not show DST performance normalizing within that period. (LLM, conf=0.87)
Experimental — accuracy not yet measured - cites [35] Evans, 1975
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [36] Stampi, 1990, Ultrashort sleep schedules: sleep architecture and the recuperative value of multiple 80- 50- and 20-min naps source
Classified as probably not a substantial claim.
Premisecitation§ Discussion · p. 7Short-term memory consistently involves the prefrontal cortex and angular gyrus.
“the known cerebral correlates of short-term memory, which consistently involve the PFC and AG [49, 50]”
Quote in the paperSubstantial claim1 of 2 sources checked- cites [49] Christophel, 2017, The distributed nature of working memory, Trends Cogn Sci. source
The 'Storage of Working Memory Contents' section reports working-memory-related activity in the PFC and parietal cortex. It does not identify the angular gyrus specifically, and its account of distributed activity does not establish that both regions are consistently involved. (LLM, conf=0.86)
Experimental — accuracy not yet measured - cites [50] Caclin, 2018, Musical and verbal short-term memory: insights from neurodevelopmental and neurological disorders, Ann N Y Acad Sci source
Probably not a substantial claim: may not pass S3 (load-bearing).
Premisecitation§ High-recallers (HR, n=20) > Low-recallers (LR, n=18) · p. 8More than 95% of dream reports involve characters.
“more than 95% of dream reports involve characters [55]”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [55] Vallat, 2017, Characteristics of the memory sources of dreams: A new version of the content-matching paradigm to take mundane and remote memories into account, PLoS One. source
May combine two claims.
Findingown data§ Descending subtraction task · p. 6There was no significant main effect of group or group-by-time interaction for descending subtraction task performance.
“Contrary to our hypothesis, there was no significant main effect of group or interaction between group and time for the DST performance.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown data§ Descending subtraction task · p. 6There was no significant effect of time on the percentage of mistakes in the descending subtraction task.
“There was no main effect of time in the percentage of mistakes, a finding in line with the generally held view that speed is more impaired than accuracy during sleep inertia [15].”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown data§ Functional connectivity · p. 6At 25 minutes post-awakening, there were almost no group differences in functional connectivity, except increased MPFC-putamen connectivity in high dream recallers.
“Similarly, there were almost no group differences during the 25-min post-awakening resting-state scan, except increased connectivity between the MPFC and the putamen in HR.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown data§ Abstract · p. 2There was a between-group difference in dream recall but not in comic recall.
“At the behavioral level, a between-group difference was observed in dream recall, but not comic recall.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown data§ Memory recall · p. 6There was no significant group difference in the final memory score for the comic story content questionnaire.
“For the recall of the comic, no significant group difference was found in the final memory score to the questionnaire about the story content (on a scale from 0 to 10: HR = 5.6 ± 2.0; LR = 4.7 ± 2.7; p = 0.26).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Findingown data§ Descending subtraction task · p. 6Descending subtraction task performance (total responses and percentage correct) was significantly reduced at 5 minutes post-awakening compared to pre-nap and 25 minutes post-awakening.
“Specifically, the total number of responses and the percentage of correct responses were reduced at 5 min p-a compared to pre-nap and 25 min p-a (all p 's < 0.05).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown data§ Memory recall · p. 6There was a trend for a higher number of words during free recall of the comic in high dream recallers than low dream recallers.
“However, there was a tendency for a significantly higher number of words during free recall in HR than LR (HR = 223.8 ± 113 words; LR = 156.1 ± 98 words; p = 0.056).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown data§ Dream recall · p. 6The between-group difference in dream recall after the nap was significant for participants awakened in N2 sleep (75% HR vs 17% LR) but not for those awakened in N3 sleep.
“The between-group difference in dream recall after the nap was significant for participants that were awakened in N2 sleep (75% of HR and 17% of LR, X 2 = 4.6, p = 0.03), but not for participants that were awakened in N3 sleep (Table 2).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingreasoning§ Sleep parameters · p. 5Several participants were unable to reach and maintain N2 and N3 sleep during the 45-minute nap due to discomfort of the MRI environment.
“As expected and due to the inherent discomfort of the MRI environment, several participants were not able to reach and maintain N2 and N3 sleep during the 45 min nap slot.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim. May combine two claims.
Premisecitation§ Introduction · p. 3The period immediately after awakening is marked by sleep inertia, a transient state of impaired vigilance and cognition that usually dissipates within 30 minutes.
“The wake period immediately following awakening from sleep is indeed marked by sleep inertia, a transient state of impaired vigilance and cognition that usually dissipates within the first 30 min after awakening [14-16].”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [14] Tassi, 2000, Sleep inertia, Sleep Med Rev. source
- cites [15] Trotti, 2017, Waking up is the hardest thing I do all day: sleep inertia and sleep drunkenness, Sleep Med Rev. source
- cites [16] Vallat, 2019, Hard to wake up? The cerebral correlates of sleep inertia assessed using combined behavioral, EEG and fMRI measures, Neuroimage. source
May combine two claims.
Premisecitation§ Introduction · p. 3Low dream recallers recall fewer dreams than high dream recallers regardless of awakening sleep stage, even when awakenings are experimentally controlled, indicating state factors cannot fully compensate for trait factors.
“Remarkably, LR still recall significantly fewer dreams than HR regardless of the sleep stage in which they are awakened, even when the number of awakenings is increased and experimentally controlled during a night in the lab [9, 11-13], showing that state factors cannot completely compensate for trait factors.”
Quote in the paperSubstantial claim0 of 4 sources checked- cites [9] Eichenlaub, 2014, Brain reactivity differentiates subjects with high and low dream recall frequencies during both sleep and wakefulness, Cereb Cortex. source
- cites [11] Goodenough, 1959, A comparison of “dreamers” and “nondreamers”: eye movements, electroencephalograms, and the recall of dreams, J Abnorm Soc Psychol source
- cites [12] Pagel, 2003, Non-dreamers, Sleep Med. source
- cites [13] Eichenlaub, 2014, Resting brain activity varies with dream recall frequency between subjects, Neuropsychopharmacology. source
May combine two claims.
Study design and conductown data§ Sleep parameters · p. 6In the final sample, high and low dream recallers did not differ in age, BMI, education, habitual sleep duration, or sex ratio, apart from dream recall frequency.
“The two groups differed in DRF (HR = 6.5 ± 0.7 dream reports per week, LR = 0 ± 0 dream report per week, p < 0.001), but did not differ for all the other variables including age (HR = 22.5 ± 2.5 years, LR = 22.7 ± 2.4 years, p = 0.86), BMI (HR = 22.9 ± 2.6 kg/ m 2 , LR = 21.8 ± 2.2 kg/m 2 , p = 0.15), education (HR = 3.8 ± 2.5 years of higher education, LR = 3.6 ± 1.3 years of higher education,”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Premisecitation§ Introduction · p. 3Prior research has identified state and trait factors contributing to intra- and interindividual variability in dream recall.
“Previous research identified several state and trait factors that participate in intra- and interindividual variability in dream recall, respectively [1, 2].”
Quote in the paperNot a substantial claim0 of 2 sources checkedMay combine two claims.
Study design and conductown data§ Sleep parameters · p. 6There were no significant group differences in any sleep parameters during the nap or in the latency between awakening and the two post-awakening resting-state scans.
“Importantly, there was no significant group difference for any of the sleep parameters considered or in the latency between the awakening and the two post-awakening resting-state scans.”
Quote in the paperSubstantial claimMay combine two claims.
Interpretationcitation§ Introduction · p. 3Sleep inertia varies within and between individuals and is a candidate explanation for state and trait variability in dream recall.
“Because sleep inertia can largely vary both within and between individuals, it represents a good candidate to explain both state and trait variability in dream recall [7, 17, 18].”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [7] Schredl, 2003, Factors of home dream recall: a structural equation model, J Sleep Res. source
- cites [17] Koukkou, 1983, Dreaming: the functional state-shift hypothesis. A neuropsychophysiological model, Br J Psychiatry. source
- cites [18] Morel, 1991, The electrophysiological correlates of dream recall and nonrecall from stage 2 sleep, Can J Psychol. source
May combine two claims.
Study design and conductown data§ Participants · p. 4The high and low dream recaller groups did not differ in age, BMI, habitual sleep duration, or education level, apart from dream recall frequency.
“Apart from the DRF ( p < 0.001), the two groups did not differ in other assessed parameters, including age, BMI, habitual sleep duration, or education level (all p 's ≥ 0.25).”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
Premisecitation§ Discussion · p. 7A meta-analysis of episodic encoding and retrieval found that the precuneus, prefrontal cortex, superior frontal gyrus, and angular gyrus were among the largest clusters associated with retrieval success.
“a meta-analysis of the brain areas associated with episodic encoding and retrieval [46] found that the precuneus, PFC, SFG, and AG were among the largest clusters associated with retrieval success”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [46] Spaniol, 2009, Event-related fMRI studies of episodic encoding and retrieval: meta-analyses using activation likelihood estimation, Neuropsychologia. source
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown data§ Sleep parameters · p. 6One participant was excluded due to technical failure, leaving 38 participants (20 high dream recallers and 18 low dream recallers) in the final analysis.
“One subject out of the 39 remaining was discarded because of a technical failure during data acquisition, leading thus to a total of 38 participants included in the final analysis (20 HR and 18 LR).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoning§ EEG and eye movement recordings · p. 5Eye movements were monitored during the experiment to ensure participants did not close their eyes during resting-state scans.
“To ensure that the participants were not closing their eyes during the resting state scans, eye movements were monitored during the experiment using an EyeLink 1000 fMRI eye-tracking system (SR Research Ontario, Canada).”
Quote in the paperNot a substantial claim
The authors state this as an assumption.
Participants already familiar with the MRI environment are less anxious and therefore more likely to fall asleep.
“we assumed that participants who are already familiar to the MR environment might be less anxious and therefore more prone to fall asleep”
The paper relies on this without support.
The impact of partial sleep deprivation on functional connectivity, if any, was similar in high dream recallers and low dream recallers.
“it is likely that the impact of the partial sleep deprivation on the functional connectivity, if any, was similar in HR and LR (though this remains to be tested)”
The paper relies on this without support.
Sleep inertia is higher following sleep deprivation.
“because sleep inertia is known to be higher following sleep deprivation”
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?
Higher spontaneous activity within the DMN and higher functional connectivity at awakening between its core regions in HR compared to LR support the hypothesis of a global differential cognitive and brain functioning between high and low dream recallers.
“The finding of a higher spontaneous activity within the DMN, along with a higher functional connectivity at awakening between its core regions in HR compared to LR7,10 support the hypothesis of a global differential cognitive and brain functioning between high and low dream recallers.”
From High Dream Recall Frequency is Associated with Increased Creativity and Default Mode Network Connectivity (2022) · cites this paper as [10]
HR show increased fMRI functional connectivity between DMN nodes and memory regions 5 minutes post awakening compared to LR.
“In a second study conducted on an independent set of participants, we also observed an increased fMRI functional connectivity between the nodes of the DMN and memory regions 5 minutes post awakening in HR as compared to LR.10”
From High Dream Recall Frequency is Associated with Increased Creativity and Default Mode Network Connectivity (2022) · cites this paper as [10]
Prior works have highlighted several neurophysiological differences between HR and LR during sleep and wakefulness.
“prior works have highlighted several neurophysiological differences between high dream recallers (HR) and low dream recallers (LR), not only during sleep but also during wakefulness.7–10”
From High Dream Recall Frequency is Associated with Increased Creativity and Default Mode Network Connectivity (2022) · cites this paper as [10]
Apart from DRF, HR and LR did not significantly differ in age, sex ratio, BMI, habitual sleep duration and education.
“Apart from the DRF (p < 0.001), the two groups did not significantly differ in age, sex ratio, body mass index (BMI), habitual sleep duration and education.10”
From High Dream Recall Frequency is Associated with Increased Creativity and Default Mode Network Connectivity (2022) · cites this paper as [10]
A previously published analysis of the same dataset showed that HR have increased DMN functional connectivity compared to LR during the second resting-state scan.
“A previously published analysis of the same dataset has shown that HR have increased DMN functional connectivity compared to LR during the second resting-state scan.10”
From High Dream Recall Frequency is Associated with Increased Creativity and Default Mode Network Connectivity (2022) · cites this paper as [10]
Statistics recomputed
Every reported test result, recomputed from its test statistic and degrees of freedom. A result shows as not adding up only once an independent check has confirmed it.
- ConsistentF(2, 72) = 6.04reported p = .004 · recomputed p = .004
“F (2, 72) = 6.04, p = .004”
- ConsistentF(2, 72) = 4.29reported p = .017 · recomputed p = .017
“F (2, 72) = 4.29, p = .017”
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Self-check results appear here once an independent check has confirmed them.
Cites
A default mode of brain function
Raichle, M. E., MacLeod, A. M., Snyder, A. Z., Powers, W. J., Gusnard, D. A., & Shulman, G. L. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.2.676 · Cited by 12,190 · see citing works
Power, J. D., Barnes, K. A., Snyder, A. Z., Schlaggar, B. L., & Petersen, S. E. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.10.018 · Cited by 7,429 · see citing works
(2007) · Cited by 6,530 · see citing works
<i>Conn</i> : A Functional Connectivity Toolbox for Correlated and Anticorrelated Brain Networks
Whitfield-Gabrieli, S., & Nieto-Castanon, A. (2012) · Brain Connectivity · doi:10.1089/brain.2012.0073 · Cited by 4,885 · see citing works
A component based noise correction method (CompCor) for BOLD and perfusion based fMRI
Behzadi, Y., Restom, K., Liau, J., & Liu, T. T. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.04.042 · Cited by 4,502 · see citing works
Buckner, R. L., & Carroll, D. C. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2006.11.004 · Cited by 2,691 · see citing works
Pingouin: statistics in Python
Vallat, R. (2018) · Journal of Open Source Software · doi:10.21105/joss.01026 · Cited by 1,780 · see citing works
Self-citationMind-wandering as spontaneous thought: a dynamic framework
Christoff, K., Irving, Z. C., Fox, K. C. R., Spreng, R. N., & Andrews-Hanna, J. R. (2016) · Nature Reviews Neuroscience · doi:10.1038/nrn.2016.113 · Cited by 1,376 · see citing works
Effect of subjective perspective taking during simulation of action: a PET investigation of agency
Ruby, P., & Decety, J. (2001) · Nature Neuroscience · doi:10.1038/87510 · Cited by 1,182 · see citing works
Self-citationThe visual scoring of sleep in adults
Silber, M. H., Ancoli-Israel, S., Bonnet, M. H., Chokroverty, S., Grigg-Damberger, M. M., Hirshkowitz, M., Kapen, S., Keenan, S. A., Kryger, M. H., Penzel, T., et al. (2007) · Journal of Clinical Sleep Medicine · doi:10.5664/jcsm.26814 · Cited by 1,064 · see citing works
The Distributed Nature of Working Memory
Christophel, T. B., Klink, P. C., Spitzer, B., Roelfsema, P. R., & Haynes, J.-D. (2017) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2016.12.007 · Cited by 882 · see citing works
Vyazovskiy, V. V., Olcese, U., Hanlon, E. C., Nir, Y., Cirelli, C., & Tononi, G. (2011) · Nature · doi:10.1038/nature10009 · Cited by 865 · see citing works
(1968) · Clinical Pharmacology & Therapeutics · doi:10.1002/cpt196896815 · Cited by 828 · see citing works
Spaniol, J., Davidson, P. S. R., Kim, A. S. N., Han, H., Moscovitch, M., & Grady, C. L. (2009) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2009.02.028 · Cited by 791 · see citing works
Weissenbacher, A., Kasess, C., Gerstl, F., Lanzenberger, R., Moser, E., & Windischberger, C. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.05.005 · Cited by 776 · see citing works
The neural correlates of dreaming
Siclari, F., Baird, B., Perogamvros, L., Bernardi, G., LaRocque, J. J., Riedner, B., Boly, M., Postle, B. R., & Tononi, G. (2017) · Nature Neuroscience · doi:10.1038/nn.4545 · Cited by 712 · see citing works
Fox, K. C. R., Spreng, R. N., Ellamil, M., Andrews-Hanna, J. R., & Christoff, K. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.02.039 · Cited by 690 · see citing works
Decoupling of the brain's default mode network during deep sleep
Horovitz, S. G., Braun, A. R., Carr, W. S., Picchioni, D., Balkin, T. J., Fukunaga, M., & Duyn, J. H. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0901435106 · Cited by 685 · see citing works
Promises and limitations of human intracranial electroencephalography
Parvizi, J., & Kastner, S. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0108-2 · Cited by 631 · see citing works
Dreaming and REM sleep are controlled by different brain mechanisms
Solms, M. (2000) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00003988 · Cited by 595 · see citing works
Functional neuroimaging of normal human sleep by positron emission tomography
Maquet (2000) · Journal of Sleep Research · doi:10.1046/j.1365-2869.2000.00214.x · Cited by 581 · see citing works
Sestieri, C., Corbetta, M., Romani, G. L., & Shulman, G. L. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.3335-10.2011 · Cited by 523 · see citing works
Nielsen, T. A. (2000) · Behavioral and Brain Sciences · doi:10.1017/s0140525x0000399x · Cited by 521 · see citing works
Functional neuroimaging of normal human sleep by positron emission tomography
Aquet, P. I. M. (2000) · Cited by 496 · see citing works
What is self-specific? Theoretical investigation and critical review of neuroimaging results
Legrand, D., & Ruby, P. (2009) · Psychological Review · doi:10.1037/a0014172 · Cited by 470 · see citing works
Self-citationTassi, P., & Muzet, A. (2000) · Sleep Medicine Reviews · doi:10.1053/smrv.2000.0098 · Cited by 458 · see citing works
Dreaming and episodic memory: a functional dissociation?
Fosse, M. J., Fosse, R., Hobson, J. A., & Stickgold, R. J. (2003) · Journal of Cognitive Neuroscience · doi:10.1162/089892903321107774 · Cited by 388 · see citing works
Lucid dreaming verified by volitional communication during REM sleep
La Berge, S. P., Nagel, L. E., Dement, W. C., & Zarcone, V. P. (1981) · Perceptual and Motor Skills · doi:10.2466/pms.1981.52.3.727 · Cited by 240 · see citing works
Waking up is the hardest thing I do all day: sleep inertia and sleep drunkenness
Trotti, L. M. (2017) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2016.08.005 · Cited by 227 · see citing works
Napping: a public health issue. From epidemiological to laboratory studies
Faraut, B., Andrillon, T., Vecchierini, M.-F., & Leger, D. (2017) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2016.09.002 · Cited by 217 · see citing works
Assessing performance upon abrupt awakening from naps during quasi-continuous operations
Dinges, D. F., Orne, M. T., & Orne, E. C. (1985) · Behavior Research Methods, Instruments, & Computers · doi:10.3758/bf03200895 · Cited by 185 · see citing works
Reliability and Stability of a Dream Recall Frequency Scale
Schredl, M. (2004) · Perceptual and Motor Skills · doi:10.2466/pms.98.3c.1422-1426 · Cited by 177 · see citing works
Cavallero, C., Cicogna, P., Natale, V., Occhionero, M., & Zito, A. (1992) · Sleep · doi:10.1093/sleep/15.6.562 · Cited by 173 · see citing works
Goodenough, D. R., Shapiro, A., Holden, M., & Steinschriber, L. (1959) · The Journal of Abnormal and Social Psychology · doi:10.1037/h0040532 · Cited by 168 · see citing works
Increased sleep pressure reduces resting state functional connectivity
Sämann, P. G., Tully, C., Spoormaker, V. I., Wetter, T. C., Holsboer, F., Wehrle, R., & Czisch, M. (2010) · Magnetic Resonance Materials in Physics Biology and Medicine · doi:10.1007/s10334-010-0213-z · Cited by 157 · see citing works
Factors of home dream recall: a structural equation model
Schredl, M., Wittmann, L., Ciric, P., & GÖtz, S. (2003) · Journal of Sleep Research · doi:10.1046/j.1365-2869.2003.00344.x · Cited by 145 · see citing works
Dream recall and dream recall failure: an arousal-retrieval model
Koulack, D., & Goodenough, D. R. (1976) · Psychological Bulletin · doi:10.1037/0033-2909.83.5.975 · Cited by 145 · see citing works
Chow, H. M., Horovitz, S. G., Carr, W. S., Picchioni, D., Coddington, N., Fukunaga, M., Xu, Y., Balkin, T. J., Duyn, J. H., & Braun, A. R. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1217691110 · Cited by 139 · see citing works
Marzano, C., Ferrara, M., Mauro, F., Moroni, F., Gorgoni, M., Tempesta, D., Cipolli, C., & De Gennaro, L. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.0412-11.2011 · Cited by 137 · see citing works
Dreaming: The Functional State-Shift Hypothesis
Koukkou, M., & Lehmann, D. (1983) · British Journal of Psychiatry · doi:10.1192/bjp.142.3.221 · Cited by 135 · see citing works
Dream reporting following abrupt and gradual awakenings from different types of sleep
Goodenough, D. R., Lewis, H. B., Shapiro, A., Jaret, L., & Sleser, I. (1965) · Journal of Personality and Social Psychology · doi:10.1037/h0022424 · Cited by 128 · see citing works
Are you awake? Cognitive performance and reverie during the hypnopompic state
Dinges, D. F. (2004) · Sleep and cognition. · doi:10.1037/10499-012 · Cited by 124 · see citing works
The neural substrate for dreaming: is it a subsystem of the default network?
William Domhoff, G. (2011) · Consciousness and Cognition · doi:10.1016/j.concog.2011.03.001 · Cited by 118 · see citing works
Sleep and the functional connectome
Picchioni, D., Duyn, J. H., & Horovitz, S. G. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.067 · Cited by 115 · see citing works
Dreaming and the default network: A review, synthesis, and counterintuitive research proposal
Domhoff, G. W., & Fox, K. C. R. (2015) · Consciousness and Cognition · doi:10.1016/j.concog.2015.01.019 · Cited by 111 · see citing works
Are life episodes replayed during dreaming?
Schwartz, S. (2003) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(03)00162-1 · Cited by 109 · see citing works
Resting brain activity varies with dream recall frequency between subjects
Eichenlaub, J.-B., Nicolas, A., Daltrozzo, J., Redouté, J., Costes, N., & Ruby, P. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2014.6 · Cited by 107 · see citing works
Self-citationBaylor, G. W., & Corrado Cavallero, P. (2001) · SLEEP · doi:10.1093/sleep/24.2.165 · Cited by 105 · see citing works
Eichenlaub, J.-B., Bertrand, O., Morlet, D., & Ruby, P. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhs388 · Cited by 101 · see citing works
Self-citationHeterogeneity of arousals in human sleep: A stereo-electroencephalographic study
Peter‐Derex, L., Magnin, M., & Bastuji, H. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.07.057 · Cited by 90 · see citing works
NREM mentation: relation to personality, orientation time, and time of night
Pivik, T., & Foulkes, D. (1968) · Journal of Consulting and Clinical Psychology · doi:10.1037/h0025489 · Cited by 89 · see citing works
Reduced alpha power associated with the recall of mentation from Stage 2 and Stage REM sleep
Esposito, M. J., Nielsen, T. A., & Paquette, T. (2004) · Psychophysiology · doi:10.1111/j.1469-8986.00143.x · Cited by 86 · see citing works
Vallat, R., Meunier, D., Nicolas, A., & Ruby, P. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2018.09.033 · Cited by 84 · see citing works
Self-citationTribl, G. G., Wetter, T. C., & Schredl, M. (2013) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2012.05.001 · Cited by 76 · see citing works
Cortical activation patterns herald successful dream recall after NREM and REM sleep
Chellappa, S. L., Frey, S., Knoblauch, V., & Cajochen, C. (2011) · Biological Psychology · doi:10.1016/j.biopsycho.2011.03.004 · Cited by 75 · see citing works
Memory sources of dreams: the incorporation of autobiographical rather than episodic experiences
Malinowski, J., & Horton, C. L. (2014) · Journal of Sleep Research · doi:10.1111/jsr.12134 · Cited by 73 · see citing works
Reducing the gradient artefact in simultaneous EEG-fMRI by adjusting the subject's axial position
Mullinger, K. J., Yan, W. X., & Bowtell, R. W. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.09.079 · Cited by 70 · see citing works
Circadian and ultradian influences on dreaming: A dual rhythm model
Wamsley, E. J., Hirota, Y., Tucker, M. A., Smith, M. R., & Antrobus, J. S. (2007) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2006.09.021 · Cited by 69 · see citing works
Experimental research on dreaming: state of the art and neuropsychoanalytic perspectives
Ruby, P. M. (2011) · Frontiers in Psychology · doi:10.3389/fpsyg.2011.00286 · Cited by 63 · see citing works
Self-citationTemporal references in dreams and autobiographical memory.
Grenier, J., Cappeliez, P., St-Onge, M., Vachon, J., Vinette, S., Roussy, F., Mercier, P., Lortie-Lussier, M., & De Koninck, J. (2005) · Memory & Cognition · doi:10.3758/bf03195317 · Cited by 57 · see citing works
Vallat, R., Chatard, B., Blagrove, M., & Ruby, P. (2017) · PLOS ONE · doi:10.1371/journal.pone.0185262 · Cited by 55 · see citing works
Self-citationMemory for events occurring during arousal from sleep
Bonnet, M. H. (1983) · Psychophysiology · doi:10.1111/j.1469-8986.1983.tb00906.x · Cited by 54 · see citing works
EEG-fMRI Methods for the Study of Brain Networks during Sleep
Duyn, J. H. (2012) · Frontiers in Neurology · doi:10.3389/fneur.2012.00100 · Cited by 53 · see citing works
Vallat, R., Lajnef, T., Eichenlaub, J.-B., Berthomier, C., Jerbi, K., Morlet, D., & Ruby, P. M. (2017) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2017.00132 · Cited by 53 · see citing works
Self-citationWu, C. W., Liu, P.-Y., Tsai, P.-J., Wu, Y.-C., Hung, C.-S., Tsai, Y.-C., Cho, K.-H., Biswal, B. B., Chen, C.-J., & Lin, C.-P. (2012) · Brain Connectivity · doi:10.1089/brain.2012.0075 · Cited by 52 · see citing works
Vyazovskiy, V. V., Cui, N., Rodriguez, A. V., Funk, C. M., Cirelli, C., & Tononi, G. (2014) · SLEEP · doi:10.5665/sleep.3926 · Cited by 45 · see citing works
Reliability and stability of a dream recall frequency scale
SCHREDL, M. (2004) · Perceptual and Motor Skills · doi:10.2466/pms.98.3.1422-1426 · Cited by 45 · see citing works
Sleep: An Open-Source Python Software for Visualization, Analysis, and Staging of Sleep Data
Combrisson, E., Vallat, R., Eichenlaub, J., et al. (2017) · Frontiers in Neuroinformatics · doi:10.3389/fninf.2017.00060 · Cited by 44 · see citing works
Self-citationPower, J. D., Barnes, K. A., Snyder, A. Z., Schlaggar, B. L., & Petersen, S. E. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.01.069 · Cited by 42 · see citing works
Plailly, J., Villalba, M., Vallat, R., Nicolas, A., & Ruby, P. (2019) · Scientific Reports · doi:10.1038/s41598-019-51497-y · Cited by 40 · see citing works
Self-citationWong, W., Noreika, V., Móró, L., Revonsuo, A., Windt, J., Valli, K., & Tsuchiya, N. (2020) · Neuroscience of Consciousness · doi:10.1093/nc/niaa006 · Cited by 40 · see citing works
Pagel, J. F. (2003) · Sleep Medicine · doi:10.1016/s1389-9457(02)00255-1 · Cited by 37 · see citing works
Dream recall, dream length, and sleep duration: state or trait factor
Schredl, M., & Reinhard, I. (2008) · Perceptual and Motor Skills · doi:10.2466/pms.106.2.633-636 · Cited by 33 · see citing works
Dream recall frequency is associated with medial prefrontal cortex white-matter density
Vallat, R., Eichenlaub, J.-B., Nicolas, A., & Ruby, P. (2018) · Frontiers in Psychology · doi:10.3389/fpsyg.2018.01856 · Cited by 31 · see citing works
Self-citationIs It a Good Idea to Cultivate Lucid Dreaming?
Vallat, R., & Ruby, P. M. (2019) · Frontiers in Psychology · doi:10.3389/fpsyg.2019.02585 · Cited by 30 · see citing works
Self-citationSleep and dream habits in a sample of French college students who report no sleep disorders
Vallat, R., Eskinazi, M., Nicolas, A., & Ruby, P. M. (2018) · Journal of Sleep Research · doi:10.1111/jsr.12659 · Cited by 26 · see citing works
Self-citationEEG correlates of dream recall in depressed outpatients and healthy controls
Rochlen, A., Hoffmann, R., & Armitage, R. (1998) · Dreaming · doi:10.1023/b:drem.0000005901.68193.1f · Cited by 24 · see citing works
Musical and verbal short-term memory: insights from neurodevelopmental and neurological disorders
Caclin, A., & Tillmann, B. (2018) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13733 · Cited by 20 · see citing works
The electrophysiological correlates of dream recall and nonrecall from stage 2 sleep
Morel, C. R., Hoffmann, R. F., & Moffitt, A. R. (1991) · Canadian Journal of Psychology / Revue canadienne de psychologie · doi:10.1037/h0084276 · Cited by 18 · see citing works
Ultradian and circadian modulation of dream recall: EEG correlates and age effects
Chellappa, S. L., & Cajochen, C. (2013) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2013.03.006 · Cited by 15 · see citing works
Partial memory reinstatement while (lucid) dreaming to change the dream environment
Mallett, R. (2020) · Consciousness and Cognition · doi:10.1016/j.concog.2020.102974 · Cited by 15 · see citing works
Conduit, R., Crewther, S. G., & Coleman, G. (2004) · Consciousness and Cognition · doi:10.1016/j.concog.2004.06.008 · Cited by 14 · see citing works
Intermediate-Term Memory as a Bridge between Working and Long-Term Memory
Kamiński, J. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0604-17.2017 · Cited by 14 · see citing works
Cook, M. R., Cohen, H. D., & Orne, M. T. (1972) · doi:10.21236/ada117379 · Cited by 12 · see citing works
Wong, W., Noreika, V., Móró, L., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/643593 · Cited by 12 · see citing works
Fox, K. C. R., Spreng, R. N., Ellamil, M., Andrews‐Hanna, J. R., & Kalina Christoff, A. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.02.052 · Cited by 7 · see citing works
Vallat, R., Chatard, B., Blagrove, M., & Ruby, P. M. (2018) · PLoS ONE · doi:10.1371/journal.pone.0193440 · Cited by 2 · see citing works
Self-citationErratum to: The visual scoring of sleep in adults
Silber, M. H., Ancoli-Israel, S., Bonnet, M. H., Chokroverty, S., Grigg-Damberger, M. M., Hirshkowitz, M., Kapen, S., Keenan, S. A., Kryger, M. H., Penzel, T., et al. (2007) · Journal of Clinical Sleep Medicine · doi:10.5664/jcsm.26927
Flagged first, then by citations
Research works printed but not linked: 4
- Solms, 1997, Institute for Research in Behavioral Neuroscience.The neuropsychology of dreams: A clinico-anatomical study
- Stampi, 1990, Ultrashort sleep schedules: sleep architecture and the recuperative value of multiple 80- 50- and 20-min naps, 71
- Wittmann, 2004, NREM sleep dream recall, dream report length and cortical activation, 54
- Maquet, 2005, Human cognition during REM sleep and the activity profile within frontal and parietal cortices: a reappraisal of functional neuroimaging data., 219
Cited by
Sorted by citations
What about dreams ? State of the art and open questions
Scarpelli, S., Alfonsi, V., Gorgoni, M., & Gennaro, L. D. (2022) · Journal of Sleep Research · doi:10.1111/jsr.13609 · Cited by 68 · see citing works
“between areas of the DMN and memory-related regions immediately after the awakening (Vallat et al., 2020); and (d) larger event-related”
BackgroundSleep medicine: Practice, challenges and new frontiers
Parrino, L., Halász, P., Szűcs, A., THOMAS, R. J., Azzi, N., Rausa, F., Pizzarotti, S., Zilioli, A., Misirocchi, F., & Mutti, C. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2022.966659 · Cited by 29 · see citing works
Sleep and dreaming in the light of reactive and predictive homeostasis.
Simor, P., Peigneux, P., & Bódizs, R. (2023) · Neuroscience and Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105104 · Cited by 18 · see citing works
Zhuravlev, M. О., Викторович, А. М., Kiselev, A. R., Simonyan, M. A., Novikov, M. Y., Selskii, A. O., Ukolov, R. V., Drapkina, O. M., Orlova, A. A., Penzel, T., et al. (2023) · Scientific Reports · doi:10.1038/s41598-023-35376-1 · Cited by 26 · see citing works
Vallat, R., Türker, B., Nicolas, A., & Ruby, P. (2022) · Nature and Science of Sleep · doi:10.2147/nss.s342137 · Cited by 22 · see citing works
Self-citationSikka, P., Valli, K., Revonsuo, A., & Tuominen, J. (2021) · Consciousness and Cognition · doi:10.1016/j.concog.2021.103189 · Cited by 13 · see citing works
Putois, B., Leslie, W., Asfeld, C., Sierro, C., Higgins, S., & Ruby, P. M. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.00724 · Cited by 15 · see citing works
Self-citationRuby, P., Masson, R., Chatard, B., Hoyer, R., Bottemanne, L., Vallat, R., & Bidet-Caulet, A. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhab445 · Cited by 12 · see citing works
Self-citationNew strategies for the cognitive science of dreaming
Mallett, R., Konkoly, K. R., Nielsen, T., Carr, M., & Paller, K. A. (2024) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2024.10.004 · Cited by 11 · see citing works
Stephan, A., Cataldi, J., Virk, A. S., & Siclari, F. (2025) · Current Biology · doi:10.1016/j.cub.2025.06.064 · Cited by 11 · see citing works
“11 These changes typically revert over several minutes, in parallel to the reestablishment of functional connectivity patterns of wakefulness 11,12 and cognitive performance.”
Dream recall frequency is associated with attention rather than with working memory abilities
Blain, S., de la Chapelle, A., Caclin, A., Bidet‐Caulet, A., & Ruby, P. (2022) · Journal of Sleep Research · doi:10.1111/jsr.13557 · Cited by 9 · see citing works
Self-citationRelationship Between Epilepsy and Dreaming: Current Knowledge, Hypotheses, and Perspectives
de la Chapelle, A., Frauscher, B., Valomon, A., Ruby, P. M., & Peter‐Derex, L. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.717078 · Cited by 7 · see citing works
Self-citationStucky, B. (2025) · Nature and Science of Sleep · doi:10.2147/nss.s506461 · Cited by 7 · see citing works
“139,175,176 177–179 This aligns with the previously discussed functional state–shift hypothesis, particularly since the effect of the awakening is only present in NREM sleep.”
Nightmares, Chronotype, Urbanicity, and Personality: An Online Study
Schredl, M., & Göritz, A. S. (2020) · Clocks & Sleep · doi:10.3390/clockssleep2030029 · Cited by 5 · see citing works
“One might speculate—as dream recall frequency is also associated with conscientiousness in this sample—whether regular sleep patterns, more often found in morning types than in evening types who can show dramatic social jet lags on weekends with very late bedtimes [30], might facilitate dream recall due to less pronou…”
BackgroundThe association of brain injury severity with dream cessation and nightmares
Fisher-Hicks, S., Lovett, V. E., Wood, R. L., & Blagrove, M. (2025) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2025.109209 · Cited by 2 · see citing works
"Pandemic Dreams are Susceptible to Priming and Unrelated to COVID-19 Exposure"
Gallagher, S. P., & Incelli, N. A. (2021) · Journal of Evidence-Based Psychotherapies · doi:10.24193/jebp.2021.2.18 · Cited by 3 · see citing works
de la Chapelle, A., Serres-Blain, S., Elshafei, A., Schwartz, D., Daligault, S., Jung, J., Ruby, P., Caclin, A., & Bidet-Caulet, A. (2025) · Scientific Reports · doi:10.1038/s41598-025-03378-w · Cited by 3 · see citing works
Self-citationMutti, C., Siclari, F., & Rosenzweig, I. (2024) · Journal of Sleep Research · doi:10.1111/jsr.14338 · Cited by 3 · see citing works
“Furthermore, an enhanced functional connectivity within the default mode network and other brain regions involved in the memory processing has also been documented among high dream recallers in the first moments after awakening (Vallat et al., 2020).”
A Prediction Nomogram for Severe Obstructive Sleep Apnea in Snoring Patients: A Retrospective Study
Teng, G., Zhang, R., Zhou, J., Wang, Y., & Zhang, N. (2023) · Nature and Science of Sleep · doi:10.2147/nss.s406384 · Cited by 3 · see citing works
“Among them, dream recall refers to being able to recall dreams at least 5 mornings a week.(16,17) In addition, patients were asked to complete the Epworth Sleepiness Scale, which scores patients on the likelihood of falling asleep in eight different situations.”
BackgroundSikka, P., Valli, K., Revonsuo, A., & Tuominen, J. (2021) · doi:10.31234/osf.io/f9av6 · Cited by 2 · see citing works
Yakovenko, I. A., & Ea, C. (2025) · Journal of Evolutionary Biochemistry and Physiology · doi:10.1134/s0022093025060146 · Cited by 1 · see citing works
“Studies by a group of authors [22] showed that after awakening in the first five minutes, increased functional connectivity between DMN areas and several areas involved in memory processes was observed in a group of subjects who were good at remembering dreams.”
Que nous disent les rêves des enfants ?
Ruby, P. M. (2023) · Enfances & Psy · doi:10.3917/ep.095.0013 · Cited by 1 · see citing works
Self-citationIncrease of both bottom-up and top-down attentional processes in high dream recallersPreprint
Ruby, P. M., Masson, R., Chatard, B., Hoyer, R. S., Bottemanne, L., Vallat, R., & Bidet‐Caulet, A. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.06.16.448743 · Cited by 1 · see citing works
“These new findings confirm that HR and LR exhibit different neurophysiological traits (Eichenlaub et al., 2014a; Eichenlaub et al., 2014b; Ruby et al., 2013; Vallat et al., 2017; Vallat et al., 2018a; Vallat et al., 2020), which nonetheless translate in similar behavioral performance in the CAT task.”
ResultSelf-citationAuditory selective attention during a working memory task with melodies: a MEG studyPreprint
Aurélien, D. L. C., Salomé, S.-B., Alma, E., Denis, S., Sébastien, D., Julien, J., Perrine, R., Anne, C., & Aurélie, B.-C. (2023) · bioRxiv · doi:10.1101/2023.09.19.558422
Poor dream recall associates with Alzheimer’s disease biomarkers and dementia riskPreprint
Lipnicki, D. M., Valentí, M., Valeriano-Lorenzo, E., Vella, A. S., Zea‐Sevilla, M. A., Ricciardi, M., Frades, B., Martinez, M., Wagner, S., Sachdev, P. S., et al. (2025) · medRxiv · doi:10.1101/2025.09.16.25335946 · Cited by 1 · see citing works
Kumar, G., Naaz, S., Jabin, N., Sasidharan, A., Nagendra, R. P., Yadav, R., & Kutty, B. M. (2025) · Consciousness and Cognition · doi:10.1016/j.concog.2025.103869 · Cited by 1 · see citing works
Dream recall during the day triggered by daytime events: frequency and influencing factors
Schredl, M. (2025) · Somnologie - Schlafforschung und Schlafmedizin · doi:10.1007/s11818-025-00535-1
Maffeo, M. L. (2026) · Cambridge University Press eBooks · doi:10.1017/9781009322348.005
Poor dream recall associates with Alzheimer's disease biomarkers and dementia risk
Lipnicki, D. M., Valenti, M., Valeriano-Lorenzo, E., Vella, A. S., Zea‐Sevilla, M. A., Ricciardi, M., Frades, B., Martinez, M., Wagner, S., Sachdev, P. S., et al. (2026) · Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring · doi:10.1002/dad2.70322
Mapping human sleep-state brain function with simultaneous EEG and neuroimaging: A systematic review
Pollatou, A., Tays, G. D., Skeiky, L., Coon, W. G., Scholl, C. A., Abad, N., Metzger, E., Marinelli, L., Ajala, A., Yeh, P., et al. (2026) · NeuroImage · doi:10.1016/j.neuroimage.2026.122122 · Cited by 1 · see citing works
- Authors
- Vallat, R., Nicolas, A., & Ruby, P.
- Affiliations
- Department of Psychology, Center for Human Sleep Science, University of California, Berkeley, CA
- Lyon 1 Université (FR)
- Venue
- Sleep
- Publisher
- Oxford University Press (OUP)
- Published
- 2020-06-28
- Volume
- 43
- Issue
- 12
- ISSN
- 0161-8105 (ISSN-L)
- 1550-9109
- OpenAlex
- W3037540166
- Cited by
- 31
- References
- 86
- Citations by year
- 2026: 3 · 2025: 8 · 2024: 2 · 2023: 5 · 2022: 4 · 2021: 6 · 2020: 3
- FWCI
- 1.81
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model (vor)
- Locations
- SLEEP (publishedVersion)
- PubMed (publishedVersion)
- HAL (Le Centre pour la Communication Scientifique Directe) (submittedVersion)
- Funders
- Université de Lyon (ANR-11-IDEX-0007)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Sleep and related disorders
- Life Sciences › Neuroscience › Cognitive Neuroscience › EEG and Brain-Computer Interfaces
- Keywords
- dream recall, sleep inertia, awakening, brain functional connectivity, default mode network, individual differences, short-term memory, sleep-wake transition
- MeSH terms
- Brain, Dreams, Electroencephalography, Humans, Mental Recall, Sleep
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