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Coherent Spontaneous Activity Identifies a Hippocampal-Parietal Memory Network
Abstract
Despite traditional theories emphasizing parietal contributions to spatial attention and sensory-motor integration, functional MRI (fMRI) experiments in normal subjects suggest that specific regions within parietal cortex may also participate in episodic memory. Here we examined correlations in spontaneous blood-oxygenation-level-dependent (BOLD) signal fluctuations in a resting state to identify the network associated with the hippocampal formation (HF) and determine whether parietal regions were elements of that network. In the absence of task, stimuli, or explicit mnemonic demands, robust correlations were observed between activity in the HF and several parietal regions (including precuneus, posterior cingulate, retrosplenial cortex, and bilateral inferior parietal lobule). These HF-correlated regions in parietal cortex were spatially distinct from those correlated with the motion-sensitive MT+ complex. Reanalysis of event-related fMRI studies of recognition memory showed that the regions spontaneously correlated with the HF (but not MT+) were also modulated during directed recollection. These regions showed greater activity to successfully recollected items as compared with other trial types. Together, these results associate specific regions of parietal cortex that are sensitive to successful recollection with the HF.
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“This set of brain regions has also been called the “episodic memory network” (e.g., Vincent et al. 2006) or the “default network” (e.g., Raichle et al. 2001) and is active when people recall the past (e.g., Buckner & Carroll 2007; Schacter et al. 2007; see McDermott et al. 2009 for a meta-analysis), imagine the future (e.g., Addis et al. 2007; see Hassabis & Maguire 2009; Moulton & Kosslyn 2009;”
From The brain basis of emotion: a meta-analytic review (2012) · cites this paper as Vincent et al. 2006
In the citing paper
“Activity in the different resting state networks has been linked to different functions (Laird et al., 2011) and the degree of correlation has been shown to be related to behavioral outcomes (Vincent et al., 2006) and clinical conditions (Greichius, 2008).”
From Oxytocin effects on complex brain networks are moderated by experiences of maternal love withdrawal (2013) · cites this paper as Vincent et al., 2006
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“The FC maps of the mPFC seeds for each participant were identified on the basis of the correlations of low-frequency fMRI fluctuations, and Fisher’s r-to-z transformation was used to convert the correlation maps into z maps (Vincent et al., 2006).”
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“Other networks were also studied using the seed-region functional connectivity approach, such as the default-mode network [83–86], the attentional networks [42, 83, 87], and memory networks [46, 88].”
MethodFamiliarity and Conceptual Priming Engage Distinct Cortical Networks
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“One popular hypothesis is that parietal cortex interacts with medial temporal structures to coordinate retrieval (Vincent et al. 2006).”
BackgroundAge-related effects in working memory recognition modulated by retroactive interference.
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The embodied transcendental: a Kantian perspective on neurophenomenology
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“…functions—e.g., the medial temporal lobe subsystem, together with PCC/Rsp, is implicated in successful retrieval of detailed information from memory (Vincent et al., 2006); the MPFC subsystem is typically engaged by self-referential judgment tasks (Gusnard et al., 2001; Qin and Northoff, 2011)—the…”
BackgroundIndividual susceptibility to TMS affirms the precuneal role in meta-memory upon recollection
Ye, Q., Zou, F., Dayan, M., Lau, H. C., Hu, Y., & Kwok, S. C. (2019) · Brain Structure and Function · doi:10.1007/s00429-019-01909-6 · Cited by 36
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“A topographically similar connection between the hippocampus and retrosplenial cortex has also been seen in the correlation structure of functional neuroimaging signals in humans (Vincent et al., 2006).”
BackgroundSelf-citationSpontaneous future cognition: the past, present and future of an emerging topic
Cole, S. N., & Kvavilashvili, L. (2019) · Psychological Research · doi:10.1007/s00426-019-01193-3 · Cited by 49
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Hippocampal and neocortical oscillatory contributions to visuospatial binding and comparison.
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Low-dose Propofol–induced Amnesia Is Not due to a Failure of Encoding
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Dissociable components of the reward circuit are involved in appraisal versus choice
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“The same sets of regions have been dissociated using resting-state functional connectivity, between sub-networks of the Default Mode Network (Vincent et al., 2006; Andrews-Hanna et al., 2010; Shenhav and Buckner, 2014; Christoff et al., 2016).”
MethodAltered functional connectivity between hypothalamus and limbic system in fibromyalgia
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Hippocampal signals for strong memory when associative memory is available and when it is not
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“Specially, by placing seed regions in brain areas, many functional networks have been shown to be coherent in their spontaneous activity, including the somatomotor [13, 14], visual [15, 16], default mode [17, 18], language [15, 19], memory [20, 21] and dorsal and ventral attention networks [22].”
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“…between the hippocampus–right dlPFC. Theta phase synchronization has been considered an important indicator of top–down control and communication between the lateral PFC and medial temporal lobe, including the hippocampus (Vincent et al., 2006; Depue et al., 2013; Daume et al., 2017a,b).”
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“, sets of interconnected regions defined based on studies in which task-induced activation would typically either increase or decrease compared to an ‘at rest’ baseline (Fox et al., 2005; Fransson, 2005; Kim et al., 2010; Vincent et al., 2006).”
BackgroundOpposing amygdala and ventral striatum connectivity during emotion identification
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Priming Picture Naming with a Semantic Task: An fMRI Investigation
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“Episodic memory retrieval and recollection is one of the mechanisms put forward to account for the repetition priming effect [74,75].”
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Seibert, T. M., & Brewer, J. B. (2011) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2011.04.010 · Cited by 30
Butt, O. H., Benson, N. C., Datta, R., & Aguirre, G. K. (2015) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2015.00025 · Cited by 33
“Modest spatial smoothing increases the sensitivity and specificity of the final correlation structure (Vincent et al., 2006), while decreasing spatial noise (Greicius et al., 2003).”
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“Because the precuneus is functionally connected to these regions during the resting state (Libby et al., 2012; Margulies et al., 2009; Vincent et al., 2006), this region might constitute a hub of the brain network underlying the visuotactile texture matching, by functionally connecting with the medial temporal lobe an…”
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“(2008), activation from the “remember–know” contrast and hippocampal-correlated DN activation overlapped in the hippocampus and posterior DN regions (Cavanna, 2007; Vincent et al., 2006; Wagner et al., 2005).”
BackgroundJoint Sparse Representation of Brain Activity Patterns in Multi-Task fMRI Data
Ramezani, M., Marble, K., Trang, H. P., Johnsrude, I. S., & Abolmaesumi, P. (2014) · IEEE Transactions on Medical Imaging · doi:10.1109/tmi.2014.2340816 · Cited by 31
“The PBC functional maps are cortical areas that are associated with cognitive control networks [40], language function (Wernicke’s and Broca’s area [41]), motor function (hand, foot, and tongue [42]), retinal field maps [43], and auditory responsive cortex [44].”
BackgroundDefault Network and Intelligence Difference
Song, M., Liu, Y., Zhou, Y., Wang, K., Yu, C., & Jiang, T. (2009) · IEEE Transactions on Autonomous Mental Development · doi:10.1109/tamd.2009.2029312 · Cited by 35
“Additionally, the functional connectivity of HF showed imperfect overlap with the default network [47].”
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Jiang, H., He, N., Sun, Y., Jian, F., Bian, L., Shen, J.-K., Yan, F., Pan, S., & Sun, Q. (2016) · Clinical Endocrinology · doi:10.1111/cen.13277 · Cited by 31
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“Secondly, it has been shown to be activated during successful retrieval (Vincent et al., 2006), and BOLD activity in the inferior parietal cortex and angular gyrus during encoding was reported to be associated with primacy recall (Sommer et al., 2006).”
BackgroundWahlheim, C. N., Christensen, A. P., Reagh, Z. M., & Cassidy, B. S. (2021) · Hippocampus · doi:10.1002/hipo.23393 · Cited by 31
“Indeed, the prominent structural and functional connectivity between the hippocampus and parietal regions has led some to suggest that there is a ’parietal memory network’ within the DMN that supports episodic memory (75, 76).”
BackgroundPorto, F. H. D. G., Coutinho, A. M., Pinto, A. L. D. S., Gualano, B., Duran, F., Prando, S., Ono, C. R., Spíndola, L., de Oliveira, M. O., do Vale, P. H. F., et al. (2015) · Journal of Alzheimer s Disease · doi:10.3233/jad-150033 · Cited by 34
““task-negative” brain networks [66, 68, 69].”
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Structural correlates of subjective and objective memory performance in multiple sclerosis
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“The posterior medial system, on the other hand, seems to play a key role in the encoding and retrieval of the contextual features of a stimulus such as the temporal, spatial, or social milieux (Aggleton et al., 1995; Vann et al., 2009; Vincent et al., 2006).”
BackgroundFunctional brain networks involved in reality monitoring
Metzak, P. D., Lavigne, K. M., & Woodward, T. S. (2015) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2015.05.014 · Cited by 30
“Similar patterns of deactivity are essentially ubiquitous when performing effortful cognitive tasks, and has been termed the DMN (or task negative network) (Greicius et al., 2003; Raichle et al., 2001; Vincent et al., 2006).”
InfluentialMendelsohn, A. (2010) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2010.00018 · Cited by 30
Seidman, L. J., Rosso, I. M., Thermenos, H. W., Makris, N., Juelich, R. J., Gabrieli, J. D. E., Faraone, S. V., Tsuang, M. T., & Whitfield, S. (2014) · Schizophrenia Research · doi:10.1016/j.schres.2014.09.011 · Cited by 30
“Interestingly, this region also is one of the core regions of the default mode network (DMN) in healthy subjects (Vincent et al., 2006; Buckner et al., 2008; Kahn et al., 2008; Greicius et al., 2009) and patients with schizophrenia (Kumari et al.”
Encoding Social Interactions: The Neural Correlates of True and False Memories
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“In addition, parietal regions appeared to interact with the hippocampal formation during successful recognition (Vincent et al., 2006).”
BackgroundA Differentiation Account of Recognition Memory: Evidence from fMRI
Criss, A. H., Wheeler, M. E., & McClelland, J. L. (2012) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00292 · Cited by 29
“Vincent and colleagues used hippocampal ROIs as seed points and found correlated voxels in bilateral AG (Kahn, Andrews-Hanna, Vincent, Snyder, & Buckner, 2008; Vincent et al., 2006).”
BackgroundAnterior Thalamic High Frequency Band Activity Is Coupled with Theta Oscillations at Rest
Sweeney‐Reed, C. M., Zaehle, T., Voges, J., Schmitt, F. C., Buentjen, L., Borchardt, V., Walter, M., Hinrichs, H., Heinze, H., Rugg, M. D., et al. (2017) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2017.00358 · Cited by 29
“Indeed, although specific brain regions have been consistently identified as being active during the resting state (Fox et al., 2006; Vincent et al., 2006), the processes that are engaged would be expected to differ between participants when not performing a specified cognitive task, since the…”
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Reduced functional connectivity supports statistical learning of temporally distributed regularities
Park, J., Janacsek, K., Németh, D., & Jeon, H. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119459 · Cited by 29
Salimpoor, V. N., Chang, C., & Menon, V. (2009) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21234 · Cited by 30
“(BA 30), is tightly coupled to the hippocampal formation (Parvizi, Van hoesen, Buckwalter, & Damasio, 2006) and is also thought to be involved in directed recollection of previously seen items (Cavanna & Trimble, 2006; Vincent et al., 2006).”
BackgroundPCC characteristics at rest in 10-year memory decliners
Bernard, C., Dilharreguy, B., Helmer, C., Chanraud, S., Amieva, H., Dartigues, J., Michèle Allard, A., & Catheline, G. (2015) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2015.07.002 · Cited by 31
MODELING FLUCTUATIONS IN DEFAULT-MODE BRAIN NETWORK USING A SPIKING NEURAL NETWORK
Yamanishi, T., Liu, J., & Nishimura, H. (2012) · International Journal of Neural Systems · doi:10.1142/s0129065712500165 · Cited by 28
Schoo, L. A., van Zandvoort, M. J. E., Biessels, G. J., Kappelle, L. J., Postma, A., & de Haan, E. H. F. (2010) · Journal of Neuropsychology · doi:10.1348/174866410x504059 · Cited by 28
“The hippocampus and the surrounding medial temporal lobe (MTL) have long been acknowledged as important structures for episodic memory (Squire, Stark, & Clark, 2004).”
BackgroundInfluentialBehrendt, R. (2013) · Reviews in the Neurosciences · doi:10.1515/revneuro-2012-0088 · Cited by 28
“The default-mode network of regions commonly coactivated during the resting state (including also the ventral anterior cingulate and rostral medial prefrontal cortex) is functionally connected with the hippocampus, consistent with the notion that the default-mode network is closely involved in episodic memory processi…”
BackgroundResultBiskup, C. S., Helmbold, K., Baurmann, D., Klasen, M., Gaber, T. J., Bubenzer‐Busch, S., Königschulte, W., Fink, G. R., & Zepf, F. D. (2016) · Acta Psychiatrica Scandinavica · doi:10.1111/acps.12573 · Cited by 30
Process-Specific Alliances (PSAs) in Cognitive Neuroscience
Cabeza, R. E. L., Stanley, M. L., & Moscovitch, M. (2018) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2018.08.005 · Cited by 28
“Finally, meeting Requirement 3, AG and HC are not only structurally connected [29,30] and coactive during rest [31], but, critically, they show task-related fCon during recollection [32–34].”
BackgroundFfytche, D. H., & Wible, C. G. (2014) · Schizophrenia Bulletin · doi:10.1093/schbul/sbu041 · Cited by 27
Construction and use of mental models: Organizing principles for the science of brain and mind
Duncan, J. (2024) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2024.109062 · Cited by 35
Bhushan, C., Chong, M., Choi, S., Joshi, A. A., Haldar, J. P., Damásio, H., & Leahy, R. M. (2016) · PLoS ONE · doi:10.1371/journal.pone.0158504 · Cited by 27
“An early example from Vincent et al. shows real-time brain dynamics from data used to explore resting networks (https://youtu.be/VaQ66lDZ-08 and https://youtu.be/3nCBLw9Z-xU) [36, 39] but the dynamics do not clearly show coherent activity in regions forming the default mode and other networks.”
Lee, T., & Xue, S. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.13828 · Cited by 25
“This study extended previous understanding of the DMN by statistically and systematically examining the roles of the subcortical structures that has been sporadically addressed in previous research (Greicius et al., 2004; Vincent et al., 2006; Buckner et al., 2008).”
BackgroundMethodInfluentialHelmchen, C., Machner, B., Rother, M., Spliethoff, P., Göttlich, M., & Sprenger, A. (2020) · Human Brain Mapping · doi:10.1002/hbm.24963 · Cited by 27
“Seed-based connectivity (FC) analysis was performed to investigate the functional connectivity of a brain region of interest (ROI) to all the other voxel in the brain (Biswal, Yetkin, Haughton, & Hyde, 1995; Vincent et al., 2006).”
MethodKim, K., Sherwood, M. S., McIntire, L. K., McKinley, R. A., & Charan Ranganath, A. (2021) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01725 · Cited by 28
DiNicola, L. M., Sun, W., & Buckner, R. L. (2023) · Journal of Neurophysiology · doi:10.1152/jn.00277.2023 · Cited by 28
“This possibility is raised by the small DLPFC region consistently observed in analyses of networks coupled to posterior para-hippocampal cortex (39), distinct from regions associated with cognitive control (40).”
BackgroundSelf-citationAltered Functional Connectivity of the Default Mode Network in Low-Empathy Subjects
Kim, S. J., Kim, S. E., Kim, H.-E., Han, K., Jeong, B., Kim, J., Namkoong, K., & Kim, J.-W. (2017) · Yonsei Medical Journal · doi:10.3349/ymj.2017.58.5.1061 · Cited by 29
The developmental trajectory of 1H-MRS brain metabolites from childhood to adulthood
Thomson, A. R., Hwa, H., Pasanta, D., Hopwood, B., Powell, H., Lawrence, R., Gracia-Tabuenca, Z., Arichi, T., Edden, R. A. E., Chai, X. J., et al. (2024) · Cerebral Cortex · doi:10.1093/cercor/bhae046 · Cited by 31
Kronman, C. A., Kern, K. L., Nauer, R. K., Dunne, M. F., Storer, T. W., & Schön, K. (2019) · Hippocampus · doi:10.1002/hipo.23169 · Cited by 26
“An early resting-state fMRI study by Vincent et al. (2006) demonstrated that BOLD signal fluctuations in the rHC and lHC correlate with fluctuations in the PCC, mPFC, and LTC in young adults.”
BackgroundWu, J., He, Y., Liang, S., Liu, Z., Huang, J., Tao, J., Chen, L., Chan, C. C. H., & Lee, T. M. C. (2023) · American Journal of Geriatric Psychiatry · doi:10.1016/j.jagp.2023.04.008 · Cited by 27
Stufflebeam, S. M., & Rosen, B. R. (2007) · Neuroimaging Clinics of North America · doi:10.1016/j.nic.2007.07.005 · Cited by 32
“Although speculative, it may be that the memory system, especially the declarative memory system, might be activated in the so-called resting state [69].”
BackgroundYamada, T., Ohta, H., Watanabe, H., Kanai, C., Tani, M., Ohno, T., Takayama, Y., Iwanami, A., Kato, N., & Hashimoto, R. (2012) · PLoS ONE · doi:10.1371/journal.pone.0043220 · Cited by 29
“First, time-series data of each voxel in the individual brain were regressed out for the six parameters of head movement, mean signal intensity in the whole scanning range, and mean intensity in the white matter and cerebrospinal fluid (CSF) regions as previously described [30].”
MethodWolf, T., Doherty, M., Kallogjeri, D., Coalson, R. S., Nicklaus, J. E., Ma, C. X., Schlaggar, B. L., & Piccirillo, J. F. (2016) · Oncology · doi:10.1159/000447744 · Cited by 27
Default mode network deactivation during odor–visual association
Karunanayaka, P., Wilson, D. A., Tobia, M. J., Martinez, B., Meadowcroft, M. D., Eslinger, P. J., & Yang, Q. X. (2016) · Human Brain Mapping · doi:10.1002/hbm.23440 · Cited by 27
“…connected to the DMN through posteromedial regions (extending from the posterior cingulate to precuneus and lateral parietal regions), is deactivated and considered essential for successful memory formation [Greicius et al., 2004; Kahn et al., 2008; Sperling et al., 2003; Vincent et al., 2006].”
BackgroundLeft posterior parietal cortex participates in both task preparation and episodic retrieval
Phillips, J. S., Velanova, K., Wolk, D. A., & Wheeler, M. E. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.02.044 · Cited by 26
“Connectivity ana lyses suggest the e xistence of s uch a channel b etween the parietal lobes and medial temporal lobe memory areas (Vincent et al., 2006).”
Biological markers of aging and mental health: A seed and soil model of neurocognitive disorders
McDonough, I. M., & Allen, R. S. (2018) · Aging & Mental Health · doi:10.1080/13607863.2018.1531383 · Cited by 23
“…is notable because it is closely tied to the default mode network (DMN)—sometimes being characterized within the DMN (Greicius, Srivastava, Reiss, & Menon, 2004; Vincent et al., 2006) and other times being separate from, but closely interacting with regions within the DMN (Westlye et al., 2011).”
BackgroundKumar, V. A., Lee, J., Liu, H., Allen, J. W., Filippi, C. G., Holodny, A. I., Hsu, K. A., Jain, R., McAndrews, M. P., Peck, K. K., et al. (2023) · American Journal of Neuroradiology · doi:10.3174/ajnr.a8067 · Cited by 29
Castro, P., Luppi, A. I., Tagliazucchi, E., Perl, Y. S., Naçi, L., Owen, A. M., Sitt, J. D., Alain Destexhe, A., & Cofré, R. (2024) · Communications Biology · doi:10.1038/s42003-024-06858-3 · Cited by 34
The Role of Prospection in Steep Temporal Reward Discounting in Gambling Addiction
Wiehler, A., Bromberg, U., & Peters, J. (2015) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2015.00112 · Cited by 24
Primary Cognitive Factors Impaired after Glioma Surgery and Associated Brain Regions
Niki, C., Kumada, T., Maruyama, T., Tamura, M., Kawamata, T., & Muragaki, Y. (2020) · Behavioural Neurology · doi:10.1155/2020/7941689 · Cited by 24
“Concerning the parietal lobe, robust correlations have been found between the activities of the hippocampal regions during successful memory retrieval, suggesting a hippocampal-parietal memory network [50, 51].”
BackgroundPatil, A. U., Madathil, D., & Huang, C. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.607988 · Cited by 26
“, 2015) related to episodic and semantic memory, language, and visual, attention, and social cognition (Vincent et al., 2006; Seghier et al., 2010; Price et al., 2015).”
BackgroundHigher-dimensional neural representations predict better episodic memory
Sheng, J., Zhang, L., Liu, C., Liu, J., Feng, J., Zhou, Y., Hu, H., & Xue, G. (2022) · Science Advances · doi:10.1126/sciadv.abm3829 · Cited by 24
“As a result, PMR has been considered an extension of the hippocampal memory system (73, 74).”
BackgroundCombining task-evoked and spontaneous activity to improve pre-operative brain mapping with fMRI
Fox, M., Qian, T., Madsen, J. R., Wang, D., Li, M., Ge, M., Zuo, H., Groppe, D. M., Mehta, A. D., Hong, B., et al. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.09.030 · Cited by 25
“Similar to the somatomotor system, language and memory systems have been mapped using spontaneous activity recorded with fMRI (McCormick et al., 2013; Tie et al., 2014; Vincent et al., 2006).”
Self-citationRamanan, S., Marstaller, L., Hodges, J. R., Piguet, O., & Irish, M. (2020) · Cortex · doi:10.1016/j.cortex.2019.12.026 · Cited by 24
Sharma, N., Murari, G., Vandermorris, S., Verhoeff, N. P. L. G., Herrmann, N., Chen, J. J., & Mah, L. (2021) · Journal of Alzheimer s Disease · doi:10.3233/jad-201579 · Cited by 24
Das, A., & Menon, V. (2021) · Cortex · doi:10.1016/j.cortex.2021.11.012 · Cited by 24
McHugo, M., Rogers, B. P., Talati, P., Woodward, N. D., & Heckers, S. (2015) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2015.00092 · Cited by 25
“org ventromedial prefrontal, parahippocampal, and posterior inferior parietal cortices rather than the core midline areas (18, 56, 57).”
BackgroundNiedźwieńska, A., Kvavilashvili, L., Ashaye, K., & Neckar, J. (2017) · Neuropsychology · doi:10.1037/neu0000378 · Cited by 24
“The involvement of these posterior brain areas in focal PM tasks is important because they constitute key parts of the brain’s default network, especially the posterior cingulate cortex and the inferior parietal lobe, which not only have anatomical connections with the medial temporal lobe structures, but also functio…”
BackgroundDunn, J., Choudhary, P., Teh, M. M., Macdonald, I. A., Hunt, K. F., Marsden, P. K., & Amiel, S. A. (2018) · Diabetologia · doi:10.1007/s00125-018-4622-2 · Cited by 26
“The lateral parietal cortex shows functional connectivity with the hippocampal formation and is associated with recollection of experiences [41, 45].”
BackgroundFunctional network interactions at rest underlie individual differences in memory abilityPreprint
van Buuren, M., Wagner, I. C., & Fernández, G. (2018) · Learning & Memory · doi:10.1101/lm.048199.118 · Cited by 24
“While the DMN is assumed to be related to memory reconstruction and retrieval (Vincent et al. 2006; Kim 2015), the FPN is thought to underlie attention and cognitive control processes contributing to memory retrieval (Vincent et al. 2008).”
MethodMaoz, U., Rutishauser, U., Kim, S., Cai, X., Lee, D., & Koch, C. (2013) · Frontiers in Neuroscience · doi:10.3389/fnins.2013.00225 · Cited by 22
“…November 2013 | Volume 7 | Article 225 | 13 brain activity (Fox et al., 2007) thought to be involved in responding to stimuli in conjunction with stimulus-evoked activity (Arieli et al., 1996; Wang, 2002; Leopold et al., 2003; Ress and Heeger, 2003; Fox et al., 2006; Vincent et al., 2006).”
BackgroundLocal Signal Time-Series during Rest Used for Areal Boundary Mapping in Individual Human Brains
Hirose, S., Watanabe, T., Jimura, K., Katsura, M., Kunimatsu, A., Abe, O., Ohtomo, K., Miyashita, Y., & Konishi, S. (2012) · PLoS ONE · doi:10.1371/journal.pone.0036496 · Cited by 23
“Resting state functional connectivity, measures of correlation of low-frequency BOLD signal between brain regions during resting [1–4], has revealed strong functional correlation between distant brain regions [5–13].”
Background
Metadata
- Authors
- Vincent, J. L., Snyder, A. Z., Fox, M. D., Shannon, B. J., Andrews, J. R., Raichle, M. E., & Buckner, R. L.
- Affiliations
- Washington University in St. Louis (US)
- Venue
- Journal of Neurophysiology
- Publisher
- American Physiological Society
- Published
- 2006-12
- Volume
- 96
- Issue
- 6
- Pages
- 3517-3531
- ISSN
- 0022-3077 (ISSN-L)
- 1522-1598
- OpenAlex
- W2066667961
- Cited by
- 959
- References
- 122
- Citations by year
- 2026: 15 · 2025: 22 · 2024: 34 · 2023: 28 · 2022: 29 · 2021: 46 · 2020: 29 · 2019: 48 · 2018: 55 · 2017: 43 · 2016: 39 · 2015: 57 · 2014: 53 · 2013: 71 · 2012: 69
- FWCI
- 27.18
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Neurophysiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute on Aging (P 50 AG05681, P50AG005681, P01 AG0 3991, P01AG003991)
- National Institute of Neurological Disorders and Stroke (NS 06833)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Keywords
- hippocampal formation, parietal cortex, episodic memory, spontaneous neuronal activity, memory networks, precuneus, posterior cingulate cortex, retrosplenial cortex, inferior parietal lobule, recollection, recognition memory, spatial attention
- MeSH terms
- Adolescent, Adult, Algorithms, Brain Mapping, Cognition, Data Interpretation, Statistical, Electrophysiology, Female, Hippocampus, Humans, Functional Laterality, Magnetic Resonance Imaging, Male, Memory, Nerve Net, Oxygen, Parietal Lobe, Mental Recall
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