Cited by 959Memory Processes and InfluencesMemory and Neural MechanismsFunctional Brain Connectivity Studies

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Coherent Spontaneous Activity Identifies a Hippocampal-Parietal Memory Network

Vincent, Justin L., Snyder, Abraham Z., Fox, Michael D., Shannon, Benjamin J., Andrews, Jessica R., Raichle, Marcus E., Buckner, Randy L.·2006·Journal of Neurophysiology

DOI 10.1152/jn.00048.2006

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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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Control of goal-directed and stimulus-driven attention in the brain
Corbetta, M., & Shulman, G. L. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn755 · Cited by 12,881
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
Self-citation
Co-Planar Stereotaxic Atlas of the Human Brain
Talairach, J., & Tournoux, P. (1988) · Medical Entomology and Zoology · Cited by 11,798
Functional connectivity in the motor cortex of resting human brain using echo‐planar mri
Biswal, B., Zerrin Yetkin, F., Haughton, V. M., & Hyde, J. S. (1995) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910340409 · Cited by 9,812
The human brain is intrinsically organized into dynamic, anticorrelated functional networks
Fox, M. D., Snyder, A. Z., Vincent, J. L., Corbetta, M., Van Essen, D. C., & Raichle, M. E. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504136102 · Cited by 8,553
Self-citation
The fusiform face area: a module in human extrastriate cortex specialized for face perception
Kanwisher, N., McDermott, J., & Chun, M. M. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-11-04302.1997 · Cited by 7,738
Neuronal Oscillations in Cortical Networks
Buzsáki, G., & Draguhn, A. (2004) · Science · doi:10.1126/science.1099745 · Cited by 6,576
Functional connectivity in the resting brain: a network analysis of the default mode hypothesis
Greicius, M. D., Krasnow, B., Reiss, A. L., & Menon, V. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0135058100 · Cited by 6,358
Untitled work
(1983) · Medical Entomology and Zoology · Cited by 6,051
Memory and the hippocampus: A synthesis from findings with rats, monkeys, and humans.
Squire, L. R. (1992) · Psychological Review · doi:10.1037/0033-295x.99.2.195 · Cited by 5,376
Memory and consciousness.
Tulving, E. (1985) · Canadian Psychology / Psychologie canadienne · doi:10.1037/h0080017 · Cited by 4,638
The principles of psychology, Vol I.
James, W. (1890) · doi:10.1037/10538-000 · Cited by 4,514
Dynamic magnetic resonance imaging of human brain activity during primary sensory stimulation.
Kwong, K. K., Belliveau, J. W., Chesler, D. A., Goldberg, I. E., Weisskoff, R. M., Poncelet, B. P., Kennedy, D. N., Hoppel, B. E., Cohen, M. S., & Turner, R. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.12.5675 · Cited by 4,212
The Nature of Recollection and Familiarity: A Review of 30 Years of Research
Yonelinas, A. P. (2002) · Journal of Memory and Language · doi:10.1006/jmla.2002.2864 · Cited by 3,840
Default-mode network activity distinguishes Alzheimer’s disease from healthy aging: evidence from functional MRI
Greicius, M. D., Srivastava, G., Reiss, A. L., & Menon, V. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0308627101 · Cited by 3,684
Intrinsic signal changes accompanying sensory stimulation: functional brain mapping with magnetic resonance imaging.
Ogawa, S., Tank, D. W., Menon, R., Ellermann, J. M., Kim, S. G., Merkle, H., & Ugurbil, K. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.13.5951 · Cited by 3,681
Searching for a baseline: Functional imaging and the resting human brain
Gusnard, D. A., & Raichle, M. E. (2001) · Nature Reviews Neuroscience · doi:10.1038/35094500 · Cited by 3,371
Self-citation
Medial prefrontal cortex and self-referential mental activity: Relation to a default mode of brain function
Gusnard, D. A., Akbudak, E., Shulman, G. L., & Raichle, M. E. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.071043098 · Cited by 2,997
Self-citation
PsyScope: An interactive graphic system for designing and controlling experiments in the psychology laboratory using Macintosh computers
Cohen, J., MacWhinney, B., Flatt, M., & Provost, J. (1993) · Behavior Research Methods, Instruments, & Computers · doi:10.3758/bf03204507 · Cited by 2,802
Development and neurophysiology of mentalizing
Frith, U., & Frith, C. D. (2003) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.2002.1218 · Cited by 2,306
Molecular, structural, and functional characterization of Alzheimer's disease: evidence for a relationship between default activity, amyloid, and memory
Buckner, R. L., Snyder, A. Z., Shannon, B. J., LaRossa, G., Sachs, R., Fotenos, A. F., Sheline, Y. I., Klunk, W. E., Mathis, C. A., Morris, J. C., et al. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.2177-05.2005 · Cited by 2,140
Self-citation
Characterization of the decision-making deficit of patients with ventromedial prefrontal cortex lesions
Bechara, A., Tranel, D., & Damásio, H. (2000) · Brain · doi:10.1093/brain/123.11.2189 · Cited by 1,903
Common blood flow changes across visual tasks: II. Decreases in cerebral cortex
Shulman, G. L., Fiez, J. A., Corbetta, M., Buckner, R. L., Miezin, F. M., Raichle, M. E., & Petersen, S. E. (1997) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1997.9.5.648 · Cited by 1,890
Self-citation
Episodic memory, amnesia, and the hippocampal–anterior thalamic axis
Aggleton, J. P., & Brown, M. W. (1999) · Behavioral and Brain Sciences · doi:10.1017/s0140525x99002034 · Cited by 1,879
Reverse replay of behavioural sequences in hippocampal place cells during the awake state
Foster, D. J., & Wilson, M. A. (2006) · Nature · doi:10.1038/nature04587 · Cited by 1,727
Interacting Minds--A Biological Basis
Frith, C. D., & Frith, U. (1999) · Science · doi:10.1126/science.286.5445.1692 · Cited by 1,714
SPACE AND ATTENTION IN PARIETAL CORTEX
Colby, C. L., & Goldberg, M. E. (1999) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.22.1.319 · Cited by 1,710
Dynamics of ongoing activity: explanation of the large variability in evoked cortical responses
Arieli, A., Sterkin, A., Grinvald, A., & Aertsen, A. (1996) · Science · doi:10.1126/science.273.5283.1868 · Cited by 1,660
BRAIN WORK AND BRAIN IMAGING
Raichle, M. E., & Mintun, M. A. (2006) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.29.051605.112819 · Cited by 1,630
Self-citation
The connections of the middle temporal visual area (MT) and their relationship to a cortical hierarchy in the macaque monkey
Maunsell, J., & van Essen, D. (1983) · The Journal of Neuroscience · doi:10.1523/jneurosci.03-12-02563.1983 · Cited by 1,602
Parietal lobe contributions to episodic memory retrieval
Wagner, A. D., Shannon, B. J., Kahn, I., & Buckner, R. L. (2005) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2005.07.001 · Cited by 1,571
Self-citation
Memory, amnesia, and the hippocampal system
(1994) · Choice Reviews Online · doi:10.5860/choice.31-5148 · Cited by 1,533
The Return of Phineas Gage: Clues About the Brain from the Skull of a Famous Patient
Damásio, H., Grabowski, T. J., Frank, R. J., Galaburda, A. M., & Damásio, A. R. (1994) · Science · doi:10.1126/science.8178168 · Cited by 1,520
Functional analysis of human MT and related visual cortical areas using magnetic resonance imaging
Tootell, R. B. H., Reppas, J. B., Kwong, K. K., Malach, R., Born, R. T., Brady, T., Rosen, B. R., & Belliveau, J. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-04-03215.1995 · Cited by 1,434
Frequencies contributing to functional connectivity in the cerebral cortex in "resting-state" data.
Cordes, D., Haughton, V. M., Arfanakis, K., Carew, J. D., Turski, P. A., Moritz, C. H., Quigley, M., & Meyerand, M. E. (2001) · PubMed Central · Cited by 1,402
Spontaneous low‐frequency BOLD signal fluctuations: An fMRI investigation of the resting‐state default mode of brain function hypothesis
Fransson, P. (2005) · Human Brain Mapping · doi:10.1002/hbm.20113 · Cited by 1,388
Separating respiratory-variation-related fluctuations from neuronal-activity-related fluctuations in fMRI
Birn, R. M., Diamond, J. B., Smith, M. A., & Bandettini, P. A. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.02.048 · Cited by 1,381
Preclinical Evidence of Alzheimer's Disease in Persons Homozygous for the ε4 Allele for Apolipoprotein E
Reiman, E. M., Caselli, R. J., Yun, L. S., Chen, K., Bandy, D., Minoshima, S., Thibodeau, S. N., & Osborne, D. (1996) · New England Journal of Medicine · doi:10.1056/nejm199603213341202 · Cited by 1,366
Correlated neuronal activity and the flow of neural information
Salinas, E., & Sejnowski, T. J. (2001) · Nature Reviews Neuroscience · doi:10.1038/35086012 · Cited by 1,333
Functional Heterogeneity in Cingulate Cortex: The Anterior Executive and Posterior Evaluative Regions
Vogt, B. A., Finch, D. M., & Olson, C. R. (1992) · Cerebral Cortex · doi:10.1093/cercor/2.6.435-a · Cited by 1,315
Buchbesprechungen / Book Reviews
Förstl, H. (2006) · Zeitschrift für Psychiatrie Psychologie und Psychotherapie · doi:10.1024/1661-4747.54.1.68a · Cited by 1,308
Intentional Maps in Posterior Parietal Cortex
Andersen, R. A., & Buneo, C. A. (2002) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.25.112701.142922 · Cited by 1,294 · cited 2×
“…memory may seem surprising because traditional views suggest that parietal cortex subserves processes associated with sensory-motor integration and visual-spatial attention (Andersen and Buneo 2002; Colby and Goldberg 1999; Corbetta and Shulman 2002; Heilman and Gonzalez Rothi 1993; Mesulam 1999).”
Background
Neural mechanisms of autonomic, affective, and cognitive integration
Critchley, H. D. (2005) · Journal of Comparative Neurology · doi:10.1002/cne.20749 · Cited by 1,214
A Population-Average, Landmark- and Surface-based (PALS) atlas of human cerebral cortex
Van Essen, D. C. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.06.058 · Cited by 1,151
Perirhinal and parahippocampal cortices of the macaque monkey: Cortical afferents
Suzuki, W., & Amaral, D. G. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903500402 · Cited by 1,149
Spatial attention and neglect: parietal, frontal and cingulate contributions to the mental representation and attentional targeting of salient extrapersonal events
Mesulam, M.-M. (1999) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.1999.0482 · Cited by 1,096
A Parametric Manipulation of Factors Affecting Task-induced Deactivation in Functional Neuroimaging
McKiernan, K. A., Kaufman, J. N., Kucera-Thompson, J., & Binder, J. R. (2003) · Journal of Cognitive Neuroscience · doi:10.1162/089892903321593117 · Cited by 1,080
Conceptual Processing during the Conscious Resting State: A Functional MRI Study
Binder, J. R., Frost, J. A., Hammeke, T. A., Bellgowan, P. S. F., Rao, S. M., & Cox, R. W. (1999) · Journal of Cognitive Neuroscience · doi:10.1162/089892999563265 · Cited by 1,066
Turning on and off recurrent balanced cortical activity
Shu, Y., Hasenstaub, A., & McCormick, D. A. (2003) · Nature · doi:10.1038/nature01616 · Cited by 1,054
Selective averaging of rapidly presented individual trials using fMRI
Dale, A. M., & Buckner, R. L. (1997) · Human Brain Mapping · doi:10.1002/(sici)1097-0193(1997)5:5 · Cited by 1,034
Self-citation
Neocortical Network Activity In Vivo Is Generated through a Dynamic Balance of Excitation and Inhibition
Haider, B., Duque, A., Hasenstaub, A. R., & McCormick, D. A. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.5297-05.2006 · Cited by 962
Cortical connections of visual area MT in the macaque
Ungerleider, L. G., & Desimone, R. (1986) · The Journal of Comparative Neurology · doi:10.1002/cne.902480204 · Cited by 954
Reward processing in primate orbitofrontal cortex and basal ganglia
Schultz, W. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.272 · Cited by 942
Spontaneously emerging cortical representations of visual attributes
Kenet, T., Bibitchkov, D., Tsodyks, M., Grinvald, A., & Arieli, A. (2003) · Nature · doi:10.1038/nature02078 · Cited by 924
Cortical networks for working memory and executive functions sustain the conscious resting state in man
Mazoyer, B., Zago, L., Mellet, E., Bricogne, S., Etard, O., Houdé, O., Crivello, F., Joliot, M., Petit, L., & Tzourio-Mazoyer, N. (2001) · Brain Research Bulletin · doi:10.1016/s0361-9230(00)00437-8 · Cited by 906
Remembering episodes: a selective role for the hippocampus during retrieval
Eldridge, L. L., Knowlton, B. J., Furmanski, C. S., Bookheimer, S. Y., & Engel, S. A. (2000) · Nature Neuroscience · doi:10.1038/80671 · Cited by 906
Corticocortical connections of anatomically and physiologically defined subdivisions within the inferior parietal lobule
Andersen, R., Asanuma, C., Essick, G., & Siegel, R. M. (1990) · The Journal of comparative neurology · doi:10.1002/cne.902960106 · Cited by 853
The entorhinal cortex of the monkey: II. Cortical afferents
Insausti, R., Amaral, D. G., & Cowan, W. M. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902640306 · Cited by 835
Recollection and Familiarity in Recognition Memory: An Event-Related Functional Magnetic Resonance Imaging Study
Henson, R. N. A., Rugg, M. D., Shallice, T., Josephs, O., & Dolan, R. J. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-10-03962.1999 · Cited by 835
Separating the brain regions involved in recollection and familiarity in recognition memory
Yonelinas, A. P., Otten, L. J., Shaw, K. N., & Rugg, M. D. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.5295-04.2005 · Cited by 813
Posterior parietal cortex in rhesus monkey: I. Parcellation of areas based on distinctive limbic and sensory corticocortical connections
Cavada, C., & Goldman-Rakic, P. (1989) · The Journal of comparative neurology · doi:10.1002/cne.902870402 · Cited by 812
When zero is not zero: the problem of ambiguous baseline conditions in fMRI
Stark, C. E. L., & Squire, L. R. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.221462998 · Cited by 724
Dissociation of the neural correlates of implicit and explicit memory
Rugg, M. D., Mark, R. E., Walla, P., Schloerscheidt, A. M., Birch, C. S., & Allan, K. (1998) · Nature · doi:10.1038/33396 · Cited by 723
Anatomic Localization and Quantitative Analysis of Gradient Refocused Echo-Planar fMRI Susceptibility Artifacts
Ojemann, J. G., Akbudak, E., Snyder, A. Z., McKinstry, R. C., Raichle, M. E., & Conturo, T. E. (1997) · NeuroImage · doi:10.1006/nimg.1997.0289 · Cited by 699
Self-citation
Neural Systems for Visual Orienting and Their Relationships to Spatial Working Memory
Corbetta, M., Kincade, J. M., & Shulman, G. L. (2002) · Journal of Cognitive Neuroscience · doi:10.1162/089892902317362029 · Cited by 698
Category-Specific Cortical Activity Precedes Retrieval During Memory Search
Polyn, S. M., Natu, V. S., Cohen, J. D., & Norman, K. A. (2005) · Science · doi:10.1126/science.1117645 · Cited by 690
Mapping of Contralateral Space in Retinotopic Coordinates by a Parietal Cortical Area in Humans
Sereno, M. I., Pitzalis, S., & Martinez, A. (2001) · Science · doi:10.1126/science.1063695 · Cited by 682
Functional anatomical studies of explicit and implicit memory retrieval tasks
Buckner, R. L., Petersen, S., Ojemann, J. G., Miezin, F. M., Squire, L., & Raichle, M. E. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-01-00012.1995 · Cited by 678
Self-citation
Very Slow Activity Fluctuations in Monkey Visual Cortex: Implications for Functional Brain Imaging
Leopold, D. A. (2003) · Cerebral Cortex · doi:10.1093/cercor/13.4.422 · Cited by 675
Coherent spontaneous activity accounts for trial-to-trial variability in human evoked brain responses
Fox, M. D., Snyder, A. Z., Zacks, J. M., & Raichle, M. E. (2006) · Nature Neuroscience · doi:10.1038/nn1616 · Cited by 660
Self-citation
Episodic memory and common sense: how far apart?
Tulving, E. (2001) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2001.0937 · Cited by 607
Remembering the past: two facets of episodic memory explored with positron emission tomography
(1995) · American Journal of Psychiatry · doi:10.1176/ajp.152.11.1576 · Cited by 593
The Inferior Parietal Lobule Is the Target of Output from the Superior Colliculus, Hippocampus, and Cerebellum
Clower, D. M., West, R. A., Lynch, J. C., & Strick, P. L. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-16-06283.2001 · Cited by 563
"Memory of the future": an essay on the temporal organization of conscious awareness.
Ingvar, D. H. (1985) · PubMed · Cited by 519
Retrieval processing and episodic memory
Rugg, M. D., & Wilding, E. L. (2000) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(00)01445-5 · Cited by 518
Neuroimaging studies of autobiographical event memory
Maguire, E. A. (2001) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.2001.0944 · Cited by 513
Emotion-induced changes in human medial prefrontal cortex: II. During anticipatory anxiety.
Simpson, J., Drevets, W., Snyder, A., Gusnard, D., & Raichle, M. (2001) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.98.2.688 · Cited by 491
Self-citation
Macaque monkey retrosplenial cortex: III. Cortical efferents
Kobayashi, Y., & Amaral, D. G. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21346 · Cited by 487
Retrosplenial amnesia
VALENSTEIN, E., BOWERS, D., VERFAELLIE, M., HEILMAN, K. M., DAY, A., & WATSON, R. T. (1987) · Brain · doi:10.1093/brain/110.6.1631 · Cited by 487
Regional Cerebral Metabolic Alterations in Dementia of the Alzheimer Type
Friedland, R. P., Budinger, T. F., Ganz, E., Yano, Y., Mathis, C. A., Koss, B., Ober, B. A., Huesman, R. H., & Derenzo, S. (1983) · Journal of Computer Assisted Tomography · doi:10.1097/00004728-198308000-00003 · Cited by 468
Functional-anatomic correlates of remembering and knowing
Wheeler, M. E., & Buckner, R. L. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2003.11.001 · Cited by 434
Self-citation
Cellular Mechanisms Contributing to Response Variability of Cortical NeuronsIn Vivo
Azouz, R., & Gray, C. M. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-06-02209.1999 · Cited by 404
Reflective self-awareness and conscious states: PET evidence for a common midline parietofrontal core
Kjaer, T. W., Nowak, M., & Lou, H. C. (2002) · NeuroImage · doi:10.1006/nimg.2002.1230 · Cited by 395
Brain Activity during Episodic Retrieval of Autobiographical and Laboratory Events: An fMRI Study using a Novel Photo Paradigm
Cabeza, R. E. L., Prince, S. E., Daselaar, S. M., Greenberg, D. L., Budde, M. D., Dolcos, F., LaBar, K. S., & Rubin, D. C. (2004) · Journal of Cognitive Neuroscience · doi:10.1162/0898929042568578 · Cited by 395
Macaque monkey retrosplenial cortex: II. Cortical afferents
Kobayashi, Y., & Amaral, D. G. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10883 · Cited by 387
Functional-Neuroanatomic Correlates of Recollection: Implications for Models of Recognition Memory
Kahn, I., Davachi, L., & Wagner, A. D. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.0624-04.2004 · Cited by 380
Behavioral Neurology and Neuropsychology
Farah, M. J., & Feinberg, T. E. (1996) · Medical Entomology and Zoology · Cited by 377
Remembering and Knowing
Gardiner, J. M. (2008) · Elsevier eBooks · doi:10.1016/b978-012370509-9.00167-4 · Cited by 375
Internal Dynamics Determine the Cortical Response to Thalamic Stimulation
MacLean, J. N., Watson, B. O., Aaron, G. B., & Yuste, R. (2005) · Neuron · doi:10.1016/j.neuron.2005.09.035 · Cited by 373
Differential modulation of a common memory retrieval network revealed by positron emission tomography
Maguire, E. A., & Mummery, C. J. (1999) · Hippocampus · doi:10.1002/(sici)1098-1063(1999)9:1 · Cited by 365
New insights into the functions of the superior temporal cortex
Karnath, H. (2001) · Nature reviews. Neuroscience · doi:10.1038/35086057 · Cited by 357
In defense of the signal detection interpretation of remember/know judgments
Wixted, J. T., & Stretch, V. (2004) · Psychonomic Bulletin & Review · doi:10.3758/bf03196616 · Cited by 353
Functional Dissociation among Components of Remembering: Control, Perceived Oldness, and Content
Wheeler, M. E., & Buckner, R. L. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-09-03869.2003 · Cited by 327
Self-citation
Memory orientation and success: separable neurocognitive components underlying episodic recognition
Dobbins, I. G., Rice, H. J., Wagner, A. D., & Schacter, D. L. (2002) · Neuropsychologia · doi:10.1016/s0028-3932(02)00164-1 · Cited by 318
Perirhinal and parahippocampal cortices of the macaque monkey: Projections to the neocortex
Lavenex, P., SUZUKI, W. A., & Amaral, D. G. (2002) · The Journal of Comparative Neurology · doi:10.1002/cne.10243 · Cited by 317
Neural connections of the posteromedial cortex in the macaque
Parvizi, J., Hoesen, G. W. V., Buckwalter, J. A., V, & Damásio, A. R. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0507729103 · Cited by 312
Correlations in Low-Frequency BOLD Fluctuations Reflect Cortico-Cortical Connections
Lowe, M. J., Džemidžić, M., Lurito, J. T., Mathews, V. P., & Phillips, M. D. (2000) · NeuroImage · doi:10.1006/nimg.2000.0654 · Cited by 305
Barrages of Synaptic Activity Control the Gain and Sensitivity of Cortical Neurons
Shu, Y., Hasenstaub, A., Badoual, M., Bal, T., & McCormick, D. A. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-32-10388.2003 · Cited by 298
Neural Correlates of Episodic Retrieval Success
Konishi, S., Wheeler, M. E., Donaldson, D. I., & Buckner, R. L. (2000) · NeuroImage · doi:10.1006/nimg.2000.0614 · Cited by 288
Self-citation
Emotion-induced changes in human medial prefrontal cortex: I. During cognitive task performance
Simpson, J. R., Snyder, A. Z., Gusnard, D. A., & Raichle, M. E. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.2.683 · Cited by 278
Self-citation
Functional-Anatomic Correlates of Memory Retrieval That Suggest Nontraditional Processing Roles for Multiple Distinct Regions within Posterior Parietal Cortex
Shannon, B. J., & Buckner, R. L. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.2625-04.2004 · Cited by 263
Self-citation
A modality‐independent approach to spatial normalization of tomographic images of the human brain
Lancaster, J. L., Glass, T. G., Lankipalli, B. R., Downs, H., Mayberg, H. S., & Fox, P. T. (1995) · Human Brain Mapping · doi:10.1002/hbm.460030305 · Cited by 256
Differential connections of the perirhinal and parahippocampal cortex with the orbital and medial prefrontal networks in macaque monkeys
Kondo, H., Saleem, K. S., & Price, J. L. (2005) · Journal of Comparative Neurology · doi:10.1002/cne.20796 · Cited by 236
Architecture and connections of retrosplenial area 30 in the rhesus monkey (macaca mulatta).
Morris, R., Petrides, M., & Pandya, D. Ν. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00672.x · Cited by 226
Preserved Neural Correlates of Priming in Old Age and Dementia
Lustig, C., & Buckner, R. L. (2004) · Neuron · doi:10.1016/j.neuron.2004.04.002 · Cited by 212
Self-citation
FDG PET and Differential Diagnosis of Dementia
Herholz, K. (1995) · Alzheimer Disease & Associated Disorders · doi:10.1097/00002093-199505000-00004 · Cited by 201
Widespread functional connectivity and fMRI fluctuations in human visual cortex in the absence of visual stimulation
Nir, Y., Hasson, U., Levy, I., Yeshurun, Y., & Malach, R. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2005.11.018 · Cited by 199
Recognition memory for new associations: electrophysiological evidence for the role of recollection
Donaldson, D. I., & Rugg, M. D. (1998) · Neuropsychologia · doi:10.1016/s0028-3932(97)00143-7 · Cited by 192
Combining independent component analysis and correlation analysis to probe interregional connectivity in fMRI task activation datasets
Arfanakis, K., Cordes, D., Haughton, V. M., Moritz, C. H., Quigley, M. A., & Meyerand, M. E. (2000) · Magnetic Resonance Imaging · doi:10.1016/s0730-725x(00)00190-9 · Cited by 191
Persistence and brain circuitry
Gusnard, D. A., Ollinger, J. M., Shulman, G. L., Cloninger, C. R., Price, J. L., Essen, D. C. V., & Raichle, M. E. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0538050100 · Cited by 177
Self-citation
Retrieval Success is Accompanied by Enhanced Activation in Anterior Prefrontal Cortex During Recognition Memory: An Event-Related fMRI Study
McDermott, K. B., Jones, T. C., Petersen, S. E., Lageman, S. K., & Roediger, H. L., III (2000) · Journal of Cognitive Neuroscience · doi:10.1162/08989290051137503 · Cited by 156
Free will versus survival: Brain systems that underlie intrinsic constraints on behavior
Price, J. (2005) · The Journal of comparative neurology · doi:10.1002/cne.20750 · Cited by 141
Some Temporal and Parietal Cortical Connections Converge in CA1 of the Primate Hippocampus
Rockland, K. S. (1999) · Cerebral Cortex · doi:10.1093/cercor/9.3.232 · Cited by 125
The chronoarchitecture of the cerebral cortex
Bartels, A., & Zeki, S. (2005) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2005.1627 · Cited by 107
The ageing brain: normal and abnormal memory
The American Association for Research into Nervous and Mental Diseases, & Albert, M. (1997) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.1997.0152 · Cited by 84
Successful episodic memory retrieval of newly learned faces activates a left fronto-parietal network
Leube, D., Erb, M., Grodd, W., Bartels, M., & Kircher, T. T. J. (2003) · Cognitive Brain Research · doi:10.1016/j.cogbrainres.2003.09.008 · Cited by 68
The growth of human brain mapping
Fox, P. T. (1997) · Human Brain Mapping · doi:10.1002/(sici)1097-0193(1997)5:1 · Cited by 66
Rapid Self-Paced Event-Related Functional MRI: Feasibility and Implications of Stimulus- versus Response-Locked Timing
Maccotta, L., Zacks, J. M., & Buckner, R. L. (2001) · NeuroImage · doi:10.1006/nimg.2001.0912 · Cited by 59
Self-citation
Neuronal Networks: Flip-Flops in theBrain
McCormick, D. A. (2005) · Current Biology · doi:10.1016/j.cub.2005.04.009 · Cited by 38
Slow vasomotor fluctuation in fMRI of anesthetized child brain
Kiviniemi, V., Jauhiainen, J., Tervonen, O., P��kk�, E., Oikarinen, J., Vainionp��, V., Rantala, H., & Biswal, B. (2000) · Magnetic Resonance in Medicine · doi:10.1002/1522-2594(200009)44:3

Research works printed but not linked: 2

Heilman KM and Gonzalez Rothi LJ. Apraxia. In: Clinical Neuropsychology , edited by Heilman KM, and Valenstein E. Oxford, UK: Oxford Univ. Press, 1993, p. 141–163.
10.1002/(SICI)1098-1063(1999)9:1<62::AID-HIPO7>3.0.CO;2-K · DOI

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Self-citation
The Brain's Default Network: Anatomy, Function, and Relevance to Disease
Buckner, R. L., Andrews‐Hanna, J. R., & Schacter, D. L. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1440.011 · Cited by 9,761
“In fact, many of the major neocortical regions constituting the default network can be revealed by placing a seed region in the hippocampal formation and mapping those cortical regions that show spontaneous correlation (Vincent et al. 2006).”
BackgroundMethodInfluentialSelf-citation
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Buckner, R. L., Krienen, F. M., Castellanos, A., Diaz, J. C., & Yeo, B. T. T. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00339.2011 · Cited by 7,304
Self-citation
Dissociable intrinsic connectivity networks for salience processing and executive control
Seeley, W. W., Menon, V., Schatzberg, A. F., Keller, J., Glover, G. H., Kenna, H., Reiss, A. L., & Greicius, M. D. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5587-06.2007 · Cited by 7,426
“Previous work using both ROI analyses (Greicius et al., 2003; Fox et al., 2005; Fransson, 2005; Vincent et al., 2006) and ICA (Greicius and Menon, 2004; Beckmann et al.”
Method
Spontaneous fluctuations in brain activity observed with functional magnetic resonance imaging
Fox, M. D., & Raichle, M. E. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2201 · Cited by 6,700
Self-citation

See all 959

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)
ORCID: Snyder, Abraham Z.
Fox, Michael D.
Raichle, Marcus E.
Buckner, Randy L.
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
DOI: 10.1152/jn.00048.2006
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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Coherent Spontaneous Activity Identifies a Hippocampal-Parietal Memory Network

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