Prefrontal and medial temporal lobe interactions in long-term memory

Simons, Jon S.; Spiers, Hugo J.

doi:10.1038/nrn1178

Cited by 962Memory and Neural MechanismsMemory Processes and InfluencesCognitive Functions and Memory

Prefrontal and medial temporal lobe interactions in long-term memory

Simons, Jon S., Spiers, Hugo J.·2003·Nature Reviews Neuroscience

DOI 10.1038/nrn1178

Open this paper in CoChat — free account

Integrity signals

Registry

Crossref · 10.1038/nrn1178

Cites

142 of 142 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

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?

These regions have been correlated with top-down control operations often employed during retrieval and may be related to item-specific search operations.
“These regions have been correlated with top-down control operations often employed during retrieval (Simons and Spiers, 2003; Badre and Wagner, 2007) and may be related to item-specific search operations (Makino et al., 2004; Long et al., 2010).”
From Neural Correlates of Long-Term Memory Enhancement Following Retrieval Practice (2021) · cites this paper as Simons and Spiers, 2003
The amount of information generated and potentially encoded during a task can modulate BOLD activity in the hippocampus and lateral prefrontal cortex.
“Because the strength of BOLD activity during fMRI, particularly in the hippocampus and lateral prefrontal cortex (for review, see Simons and Spiers 2003; e.g., see Martin et al. 2011), can be modulated by the amount of information that is generated and potentially encoded during a task”
From Neural Mechanisms of Episodic Retrieval Support Divergent Creative Thinking (2019) · cites this paper as Simons and Spiers 2003
The medial temporal, medial prefrontal, midline and parietal brain regions make up a core network engaged during episodic recall and imagining the future.
“For instance, the medial temporal, medial prefrontal, midline and parietal brain regions make up a ‘core network’ that is engaged during episodic recall and imagining the future [25–27,33–36]”
From Is episodic-like memory <i>like</i> episodic memory? (2024) · cites this paper as [33]
The connectivity between the hippocampus and the neocortex in mammalian brains allows for close interactions and information pathways between these structures.
“Research on humans, non-human primates and rodents suggests that the connectivity between the hippocampus and the neocortex in mammalian brains allows for close interactions and information pathways between these structures [33,129].”
From Is episodic-like memory <i>like</i> episodic memory? (2024) · cites this paper as [33]

Untitled work
(1978) · UA Campus Repository (The University of Arizona) · Cited by 8,010 · see citing works
LOSS OF RECENT MEMORY AFTER BILATERAL HIPPOCAMPAL LESIONS
Scoville, W. B., & Milner, B. (1957) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp.20.1.11 · Cited by 7,322 · see citing works
Place navigation impaired in rats with hippocampal lesions
Morris, R. G. M., Garrud, P., Rawlins, J. N. P., & O'Keefe, J. (1982) · Nature · doi:10.1038/297681a0 · Cited by 6,340 · see citing works
The hippocampus as a spatial map. Preliminary evidence from unit activity in the freely-moving rat
O'Keefe, J., & Dostrovsky, J. (1971) · Brain Research · doi:10.1016/0006-8993(71)90358-1 · Cited by 6,151 · see citing works
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 · see citing works
Why there are complementary learning systems in the hippocampus and neocortex: insights from the successes and failures of connectionist models of learning and memory
McClelland, J. L., McNaughton, B. L., & O'Reilly, R. C. (1995) · Psychological Review · doi:10.1037/0033-295x.102.3.419 · Cited by 5,256 · see citing works
The hippocampus as a cognitive map
Passingham, R. E. (1979) · Neuroscience · doi:10.1016/0306-4522(79)90015-0 · Cited by 5,128 · see citing works
The Cognitive neurosciences
(2005) · Choice Reviews Online · doi:10.5860/choice.43-0626 · Cited by 4,726 · see citing works
Attention to Action: Willed and Automatic Control of Behavior
Norman, D. A., & Shallice, T. (1986) · Consciousness and Self-Regulation · doi:10.1007/978-1-4757-0629-1_1 · Cited by 4,455 · see citing works
Simple memory: a theory for archicortex
Marr, D. (1971) · Philosophical Transactions of the Royal Society of London. B, Biological Sciences · doi:10.1098/rstb.1971.0078 · Cited by 2,771 · see citing works
Common regions of the human frontal lobe recruited by diverse cognitive demands
Duncan, J., & Owen, A. M. (2000) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01633-7 · Cited by 2,498 · see citing works
Memory consolidation, retrograde amnesia and the hippocampal complex
Nadel, L., & Moscovitch, M. (1997) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(97)80010-4 · Cited by 1,924 · see citing works
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 · see citing works
Human Brain Function
Frackowiak, R. S. J. (1997) · Cited by 1,713 · see citing works
Varieties of Memory and Consciousness: Essays in Honour of Endel Tulving
Roediger, H. L., III, & Craik, F. I. M. (2014) · Medical Entomology and Zoology · Cited by 1,654 · see citing works
Building Memories: Remembering and Forgetting of Verbal Experiences as Predicted by Brain Activity
Wagner, A. D., Schacter, D. L., Rotte, M., Koutstaal, W., Maril, A., Dale, A. M., Rosen, B. R., & Buckner, R. L. (1998) · Science · doi:10.1126/science.281.5380.1188 · Cited by 1,620 · see citing works
Hemispheric encoding/retrieval asymmetry in episodic memory: positron emission tomography findings.
Tulving, E., Kapur, S., Craik, F. I. M., Moscovitch, M., & Houle, S. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.6.2016 · Cited by 1,597 · see citing works
Memory, amnesia, and the hippocampal system
(1994) · Choice Reviews Online · doi:10.5860/choice.31-5148 · Cited by 1,533 · see citing works
Functional specialization for semantic and phonological processing in the left inferior prefrontal cortex
Poldrack, R. A., Wagner, A. D., Prull, M. W., Desmond, J. E., Glover, G. H., & Gabrieli, J. D. E. (1999) · NeuroImage · doi:10.1006/nimg.1999.0441 · Cited by 1,448 · see citing works
Neural Mechanisms of Visual Working Memory in Prefrontal Cortex of the Macaque
Miller, E. K., Erickson, C. A., & Desimone, R. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-16-05154.1996 · Cited by 1,441 · see citing works
Dissociation of object and spatial processing domains in primate prefrontal cortex.
Wilson, F. A., Scalaidhe, S. P. Ó., & Goldman-Rakic, P. (1993) · Science · doi:10.1126/science.8316836 · Cited by 1,374 · see citing works
Consciousness and Self-Regulation
SCHWARTZ, G. E. R., & Shapiro, D. L. (1978) · Springer eBooks · doi:10.1007/978-1-4684-2571-0 · Cited by 1,370 · see citing works
Frontal lobes and human memory: Insights from functional neuroimaging
Fletcher, P. C. (2001) · Brain · doi:10.1093/brain/124.5.849 · Cited by 1,348 · see citing works
Knowing Where and Getting There: A Human Navigation Network
Maguire, E. A., Burgess, N., Donnett, J. G., Frackowiak, R. S. J., Frith, C. D., & O'Keefe, J. (1998) · Science · doi:10.1126/science.280.5365.921 · Cited by 1,303 · see citing works
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 1,134 · see citing works
Categorical Representation of Visual Stimuli in the Primate Prefrontal Cortex
Freedman, D. J., Riesenhuber, M., Poggio, T., & Miller, E. K. (2001) · Science · doi:10.1126/science.291.5502.312 · Cited by 1,123 · see citing works
Making Memories: Brain Activity that Predicts How Well Visual Experience Will Be Remembered
Brewer, J. B., Zhao, Z., Desmond, J. E., Glover, G. H., & Gabrieli, J. D. E. (1998) · Science · doi:10.1126/science.281.5380.1185 · Cited by 1,108 · see citing works
Memory consolidation and the medial temporal lobe: a simple network model.
Alvarez, P., & Squire, L. R. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.15.7041 · Cited by 1,054 · see citing works
The role of the anterior prefrontal cortex in human cognition
Koechlin, É., Basso, G., Pietrini, P., Panzer, S., & Grafman, J. H. (1999) · Nature · doi:10.1038/20178 · Cited by 1,046 · see citing works
Emotion-related learning in patients with social and emotional changes associated with frontal lobe damage.
Rolls, E. T., Hornak, J., Wade, D., & McGrath, J. (1994) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp.57.12.1518 · Cited by 1,005 · see citing works
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 · see citing works
Effects on visual recognition of combined and separate ablations of the entorhinal and perirhinal cortex in rhesus monkeys
Meunier, M., Bachevalier, J., Mishkin, M., & Murray, E. A. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-12-05418.1993 · Cited by 900 · see citing works
Multiple routes to memory: distinct medial temporal lobe processes build item and source memories
Davachi, L., Mitchell, J. P., & Wagner, A. D. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0337195100 · Cited by 899 · see citing works
Dissociable functions in the medial and lateral orbitofrontal cortex: Evidence from human neuroimaging studies
Elliott, R. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.308 · Cited by 887 · see citing works
An adaptive coding model of neural function in prefrontal cortex
Duncan, J. (2001) · Nature Reviews Neuroscience · doi:10.1038/35097575 · Cited by 874 · see citing works
Conjunctive representations in learning and memory: Principles of cortical and hippocampal function.
O'Reilly, R. C., & Rudy, J. W. (2001) · Psychological Review · doi:10.1037//0033-295x.108.2.311 · Cited by 865 · see citing works
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 · see citing works
Hemispheric Specialization in Human Dorsal Frontal Cortex and Medial Temporal Lobe for Verbal and Nonverbal Memory Encoding
Kelley, W. M., Miezin, F. M., McDermott, K. B., Buckner, R. L., Raichle, M. E., Cohen, N. J., Ollinger, J. M., Akbudak, E., Conturo, T. E., Snyder, A. Z., et al. (1998) · Neuron · doi:10.1016/s0896-6273(00)80474-2 · Cited by 823 · see citing works
The Well-Worn Route and the Path Less Traveled
Hartley, T., Maguire, E. A., Spiers, H. J., & Burgess, N. (2003) · Neuron · doi:10.1016/s0896-6273(03)00095-3 · Cited by 817 · see citing works
Self-citation
Dual pathways connecting the dorsolateral prefrontal cortex with the hippocampal formation and parahippocampal cortex in the rhesus monkey
Goldman‐Rakic, P. S., Selemon, L. D., & Schwartz, M. L. (1984) · Neuroscience · doi:10.1016/0306-4522(84)90166-0 · Cited by 782 · see citing works
Maintenance versus Manipulation of Information Held in Working Memory: An Event-Related fMRI Study
D’Esposito, M., Postle, B. R., Ballard, D., & Lease, J. (1999) · Brain and Cognition · doi:10.1006/brcg.1999.1096 · Cited by 779 · see citing works
Fast Backprojections from the Motion to the Primary Visual Area Necessary for Visual Awareness
Pascual-Leone, A., & Walsh, V. (2001) · Science · doi:10.1126/science.1057099 · Cited by 761 · see citing works
Memory in the Cerebral Cortex
FOSTER, J. M. (1996) · The Journal of Nervous and Mental Disease · doi:10.1097/00005053-199606000-00014 · Cited by 755 · see citing works
Impaired Recognition Memory in Rats after Damage to the Hippocampus
Clark, R. E., Zola, S. M., & Squire, L. R. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-23-08853.2000 · Cited by 740 · see citing works
What's new with the amnesic patient H.M.?
Corkin, S. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn726 · Cited by 726 · see citing works
A Neural Mechanism for Working and Recognition Memory in Inferior Temporal Cortex
Miller, E. K., Li, L., & Desimone, R. (1991) · Science · doi:10.1126/science.1962197 · Cited by 706 · see citing works
The frontopolar cortex and human cognition: Evidence for a rostrocaudal hierarchical organization within the human prefrontal cortex
Kalina Christoff, A., & Gabrieli, J. D. E. (2000) · Psychobiology · doi:10.3758/bf03331976 · Cited by 684 · see citing works
Hippocampal Efferents Reach Widespread Areas of Cerebral Cortex and Amygdala in the Rhesus Monkey
Rosene, D. L., & Hoesen, G. W. V. (1977) · Science · doi:10.1126/science.410102 · Cited by 678 · see citing works
Do Rats Have Prefrontal Cortex? The Rose-Woolsey-Akert Program Reconsidered
Preuss, T. M. (1995) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1995.7.1.1 · Cited by 666 · see citing works
Dissociation of human mid-dorsolateral from posterior dorsolateral frontal cortex in memory processing.
Petrides, M., Alivisatos, B., Evans, A. C., & Meyer, E. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.3.873 · Cited by 660 · see citing works
Top-down signal from prefrontal cortex in executive control of memory retrieval
Tomita, H., Ohbayashi, M., Nakahara, K., Hasegawa, I., & Miyashita, Y. (1999) · Nature · doi:10.1038/44372 · Cited by 615 · see citing works
Control of Response Selection by Reinforcer Value Requires Interaction of Amygdala and Orbital Prefrontal Cortex
Baxter, M. G., Parker, A., Lindner, C. C. C., Izquierdo, A. D., & Murray, E. A. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-11-04311.2000 · Cited by 582 · see citing works
Effects of extensive temporal lobe damage or mild hypoxia on recollection and familiarity
Yonelinas, A., Kroll, N., Quamme, J., Lazzara, M. M., Sauvé, M., Widaman, K., & Knight, R. (2002) · Nature Neuroscience · doi:10.1038/nn961 · Cited by 554 · see citing works
Conscious recollection and the human hippocampal formation: evidence from positron emission tomography.
Schacter, D. L., Alpert, N. M., Savage, C. R., Rauch, S. L., & Albert, M. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.1.321 · Cited by 552 · see citing works
PET studies of encoding and retrieval: The HERA model
Nyberg, L. H., Cabeza, R. E. L., & Tulving, E. (1996) · Psychonomic Bulletin & Review · doi:10.3758/bf03212412 · Cited by 544 · see citing works
Lesions of the perirhinal and parahippocampal cortices in the monkey produce long-lasting memory impairment in the visual and tactual modalities
Suzuki, W., Zola-Morgan, S. M., Squire, L., & Amaral, D. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-06-02430.1993 · Cited by 543 · see citing works
Humans and great apes share a large frontal cortex
Semendeferi, K., Lu, A., Schenker-Ahmed, N. M., & Damasio, H. (2002) · Nature Neuroscience · doi:10.1038/nn814 · Cited by 540 · see citing works
Prefrontal–Temporal Circuitry for Episodic Encoding and Subsequent Memory
Kirchhoff, B. A., Wagner, A. D., Maril, A., & Stern, C. E. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-16-06173.2000 · Cited by 536 · see citing works
Cross-modal and cross-temporal association in neurons of frontal cortex
Fuster, J. M., Bodner, M., & Kroger, J. K. (2000) · Nature · doi:10.1038/35012613 · Cited by 528 · see citing works
Retrieval without recollection: An experimental analysis of source amnesia
Schacter, D. L., Harbluk, J. L., & McLachlan, D. R. C. (1984) · Journal of Verbal Learning and Verbal Behavior · doi:10.1016/s0022-5371(84)90373-6 · Cited by 528 · see citing works
Memory for the temporal order of events in patients with frontal lobe lesions and amnesic patients.
Shimamura, A., Janowsky, J., & Squire, L. (1990) · Neuropsychologia · doi:10.1016/0028-3932(90)90004-8 · Cited by 524 · see citing works
Confabulation and the control of recollection
Burgess, P. W. (1996) · Memory · doi:10.1080/096582196388906 · Cited by 509 · see citing works
A temporoparietal and prefrontal network for retrieving the spatial context of lifelike events
Burgess, N., Maguire, E. A., Spiers, H. J., & O'Keefe, J. (2001) · NeuroImage · doi:10.1006/nimg.2001.0806 · Cited by 502 · see citing works
Self-citation
Executive Control during Episodic Retrieval
Dobbins, I. G., Foley, H. A., Schacter, D. L., & Wagner, A. D. (2002) · Neuron · doi:10.1016/s0896-6273(02)00858-9 · Cited by 501 · see citing works
The effects of hippocampal lesions upon spatial and non-spatial tests of working memory
Aggleton, J. P., Hunt, P. R., & Rawlins, J. N. P. (1986) · Behavioural Brain Research · doi:10.1016/0166-4328(86)90011-2 · Cited by 496 · see citing works
Right prefrontal cortex and episodic memory retrieval: a functional MRI test of the monitoring hypothesis
Henson, R. N., Shallice, T., & Dolan, R. J. (1999) · Brain · doi:10.1093/brain/122.7.1367 · Cited by 479 · see citing works
Impaired Recognition Memory in Monkeys after Damage Limited to the Hippocampal Region
Zola, S. M., Squire, L. R., Teng, E., Stefanacci, L., Buffalo, E. A., & Clark, R. E. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-01-00451.2000 · Cited by 477 · see citing works
The Prefrontal CortexExecutive and Cognitive Functions
Roberts, A., Robbins, T. W., & Weiskrantz, L. (1998) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780198524410.001.0001 · Cited by 468 · see citing works
Long-term plasticity in hippocampal place-cell representation of environmental geometry
Lever, C., Wills, T., Cacucci, F., Burgess, N., & O'Keefe, J. (2002) · Nature · doi:10.1038/416090a · Cited by 465 · see citing works
Episodic memory and the self in a case of isolated retrograde amnesia
Levine, B. (1998) · Brain · doi:10.1093/brain/121.10.1951 · Cited by 462 · see citing works
Memory in the cerebral cortex
Fuster, J. M. (1999) · Cited by 456 · see citing works
Topographically specific hippocampal projections target functionally distinct prefrontal areas in the rhesus monkey
Barbas, H., & Blatt, G. J. (1995) · Hippocampus · doi:10.1002/hipo.450050604 · Cited by 453 · see citing works
The Predictive Value of Changes in Effective Connectivity for Human Learning
Büchel, C., Coull, J. T., & Friston, K. J. (1999) · Science · doi:10.1126/science.283.5407.1538 · Cited by 447 · see citing works
Perceptual–mnemonic functions of the perirhinal cortex
Murray, E. A. (1999) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(99)01303-0 · Cited by 441 · see citing works
Object Recognition and Location Memory in Monkeys with Excitotoxic Lesions of the Amygdala and Hippocampus
Murray, E. A., & Mishkin, M. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-16-06568.1998 · Cited by 434 · see citing works
Prospective coding for objects in primate prefrontal cortex
Rainer, G., Rao, S. C., & Miller, E. K. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-13-05493.1999 · Cited by 432 · cited 1× · see citing works
“This prefrontal neuronal signal acts in a prospective manner in associative learning, initially reflecting the sample cue and then, before presentation of a test cue, reflecting the expected target stimulus that was previously associated with the sampl”
Background
Neuroanatomy (Text and Atlas)
Hlavin, L. (1990) · Neurology · doi:10.1212/wnl.40.2.388-c · Cited by 426 · see citing works
Memory, amnesia, and the hippocampal system
Holmes, G. L. (1994) · Journal of Epilepsy · doi:10.1016/0896-6974(94)90099-x · Cited by 422 · see citing works
Differentiating the roles of the hippocampus complex and the neocortex in long-term memory storage: Evidence from the study of semantic dementia and Alzheimer's disease.
Graham, K. S., & Hodges, J. R. (1997) · Neuropsychology · doi:10.1037/0894-4105.11.1.77 · Cited by 421 · see citing works
Prefrontal Contributions to Executive Control: fMRI Evidence for Functional Distinctions within Lateral Prefrontal Cortex
Wagner, A. D., Maril, A., Bjork, R. A., & Schacter, D. L. (2001) · NeuroImage · doi:10.1006/nimg.2001.0936 · Cited by 421 · see citing works
Amnesia: A disconnection syndrome?
Warrington, E. K., & Weiskrantz, L. (1982) · Neuropsychologia · doi:10.1016/0028-3932(82)90099-9 · Cited by 416 · see citing works
The role of the rostral frontal cortex (area 10) in prospective memory: a lateral versus medial dissociation
Burgess, P. W., Scott, S. K., & Frith, C. D. (2003) · Neuropsychologia · doi:10.1016/s0028-3932(02)00327-5 · Cited by 415 · see citing works
Brain Activity Underlying Encoding and Retrieval of Source Memory
Cansino, S. (2002) · Cerebral Cortex · doi:10.1093/cercor/12.10.1048 · Cited by 413 · see citing works
The functional roles of prefrontal cortex in episodic memory
Fletcher, P. C., Shallice, T., & Dolan, R. J. (1998) · Cited by 389 · see citing works
Memory for events and their spatial context: models and experiments
Burgess, N., Becker, S., King, J. A., & O'Keefe, J. (2001) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.2001.0948 · Cited by 377 · see citing works
Late Onset of Anterior Prefrontal Activity during True and False Recognition: An Event-Related fMRI Study
Schacter, D. L., Buckner, R. L., Koutstaal, W., Dale, A. M., & Rosen, B. R. (1997) · NeuroImage · doi:10.1006/nimg.1997.0305 · Cited by 373 · see citing works
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 362 · see citing works
Neuronal activity related to visual recognition memory: long-term memory and the encoding of recency and familiarity information in the primate anterior and medial inferior temporal and rhinal cortex
Fahy, F. L., Riches, I. P., & Brown, M. W. (1993) · Experimental Brain Research · doi:10.1007/bf00234113 · Cited by 359 · see citing works
Neurotoxic lesions of the perirhinal cortex do not mimic the behavioural effects of fornix transection in the rat
Ennaceur, A., Neave, N., & Aggleton, J. P. (1996) · Behavioural Brain Research · doi:10.1016/0166-4328(96)00006-x · Cited by 351 · see citing works
Free recall and recognition in a network model of the hippocampus: simulating effects of scopolamine on human memory function
Hasselmo, M. E., & Wyble, B. (1997) · Behavioural Brain Research · doi:10.1016/s0166-4328(97)00048-x · Cited by 337 · see citing works
The effects of visual stimulation and memory on neurons of the hippocampal formation and the neighboring parahippocampal gyrus and inferior temporal cortex of the primate
Riches, I. P., Wilson, F., & Mw, B. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-06-01763.1991 · Cited by 336 · see citing works
Amnesia and recognition memory: A re-analysis of psychometric data
Aggleton, J. P., & Shaw, C. (1996) · Neuropsychologia · doi:10.1016/0028-3932(95)00150-6 · Cited by 323 · see citing works
Material-specific lateralization of prefrontal activation during episodic encoding and retrieval
Wagner, A. D., Poldrack, R. A., Eldridge, L. L., Desmond, J. E., Glover, G. H., & Gabrieli, J. D. E. (1998) · Neuroreport · doi:10.1097/00001756-199811160-00026 · Cited by 321 · see citing works
The functional roles of prefrontal cortex in episodic memory. I. Encoding
Fletcher, P. C. (1998) · Brain · doi:10.1093/brain/121.7.1239 · Cited by 318 · see citing works
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 · see citing works
Neuroanatomy: Text and Atlas
Martin, J. H. (1989) · Cited by 295 · see citing works
Functional brain maps of retrieval mode and recovery of episodic information
Nyberg, L. H., Tulving, E., Habib, R., Nilsson, L., Kapur, S., Houle, S., Cabeza, R. E. L., & McIntosh, A. R. (1995) · Neuroreport · doi:10.1097/00001756-199512000-00060 · Cited by 292 · see citing works
Time-Dependent Relationship between the Dorsal Hippocampus and the Prefrontal Cortex in Spatial Memory
Lee, I., & Kesner, R. P. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-04-01517.2003 · Cited by 287 · see citing works
A familiarity signal in human anterior medial temporal cortex?
Henson, R. N., Cansino, S., Herron, J. E., Robb, W. G. K., & Rugg, M. D. (2003) · Hippocampus · doi:10.1002/hipo.10117 · Cited by 277 · see citing works
The Role of the Prefrontal Cortex in Recognition Memory and Memory for Source: An fMRI Study
Rugg, M. D., Fletcher, P. C., Chua, P. M.-L., & Dolan, R. J. (1999) · NeuroImage · doi:10.1006/nimg.1999.0488 · Cited by 275 · see citing works
The effects of bilateral hippocampal damage on fMRI regional activations and interactions during memory retrieval
Maguire, E. A. (2001) · Brain · doi:10.1093/brain/124.6.1156 · Cited by 266 · see citing works
Strategic search and retrieval inhibition: The role of the frontal lobes
della Rocchetta, A. I., & Milner, B. A. (1993) · Neuropsychologia · doi:10.1016/0028-3932(93)90049-6 · Cited by 260 · see citing works
Preserved Recognition in a Case of Developmental Amnesia: Implications for the Acaquisition of Semantic Memory?
Baddeley, A., Vargha-Khadem, F., & Mishkin, M. (2001) · Journal of Cognitive Neuroscience · doi:10.1162/08989290151137403 · Cited by 257 · see citing works
A comparison of egocentric and allocentric spatial memory in a patient with selective hippocampal damage.
Holdstock, J., Mayes, A., Cezayirli, E., Isaac, C., Aggleton, J., & Roberts, N. (2000) · Neuropsychologia · doi:10.1016/s0028-3932(99)00099-8 · Cited by 252 · see citing works
Selective Perceptual Impairments After Perirhinal Cortex Ablation
Buckley, M. J., Booth, M. C. A., Rolls, E. T., & Gaffan, D. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-24-09824.2001 · Cited by 249 · see citing works
Hippocampal amnesia
Spiers, H. J., Maguire, E. A., & Burgess, N. (2001) · Neurocase · doi:10.1076/neur.7.5.357.16245 · Cited by 249 · see citing works
Self-citation
Neuronal computations underlying the firing of place cells and their role in navigation
Burgess, N., & O'Keefe, J. M. (1996) · Hippocampus · doi:10.1002/(sici)1098-1063(1996)6:6 · Cited by 240 · see citing works
The Cognitive Neurosciences
Poeppel, D. 1., Mangun, G. R. 1., & Gazzaniga, M. S. 1. (1995) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1995.7.4.514 · Cited by 222 · see citing works
Task-dependency of the Neural Correlates of Episodic Encoding as Measured by fMRI
Otten, L. J. (2001) · Cerebral Cortex · doi:10.1093/cercor/11.12.1150 · Cited by 216 · see citing works
Long-term retrograde amnesia...the crucial role of the hippocampus.
Cipolotti, L., Shallice, T., Chan, D., Fox, N., Scahill, R., Harrison, G., Stevens, J., & Rudge, P. (2001) · Neuropsychologia · doi:10.1016/s0028-3932(00)00103-2 · Cited by 212 · see citing works
The Laminar Pattern of Connections between Prefrontal and Anterior Temporal Cortices in the Rhesus Monkey is Related to Cortical Structure and Function
Rempel-Clower, N. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.9.851 · Cited by 203 · see citing works
Retinotopic organization of early visual spatial attention effects as revealed by PET and ERPs
Woldorff, M. G., Fox, P. T., Matzke, M., Lancaster, J. L., Veeraswamy, S., Zamarripa, F., Seabolt, M., Glass, T. G., Gao, J., Martin, C. C., et al. (1997) · Human Brain Mapping · doi:10.1002/(sici)1097-0193(1997)5:4 · Cited by 195 · see citing works
Set-and Code-Specific Activation in the Frontal Cortex: An fMRI Study of Encoding and Retrieval of Faces and Words
McDermott, K., Buckner, R., Petersen, S., Kelley, W. M., & Sanders, A. (1999) · Journal of Cognitive Neuroscience · doi:10.1162/089892999563698 · Cited by 193 · see citing works
A hierarchical neuronal network for planning behavior
Dehaene, S., & Changeux, J. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.24.13293 · Cited by 187 · see citing works
Inferotemporal‐frontal Disconnection: The Uncinate Fascicle and Visual Associative Learning in Monkeys
Eacott, M. J., & Gaffan, D. (1992) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1992.tb00157.x · Cited by 152 · see citing works
Responses of single neurons in the hippocampus of the macaque related to recognition memory
Rolls, E. T., Cahusac, P., Feigenbaum, J. D., & Miyashita, Y. (1993) · Experimental Brain Research · doi:10.1007/bf00228398 · Cited by 142 · see citing works
Robotic and neuronal simulation of the hippocampus and rat navigation
Burgess, N., Donnett, J. G., Jeffery, K. J., & O'Keefe, J. M. (1997) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.1997.0140 · Cited by 142 · see citing works
Callosal Window Between Prefrontal Cortices: Cognitive Interaction to Retrieve Long-Term Memory
Hasegawa, I., Fukushima, T., Ihara, T., & Miyashita, Y. (1998) · Science · doi:10.1126/science.281.5378.814 · Cited by 136 · see citing works
Feeling-of-knowing in episodic memory: an event-related fMRI study
Maril, A., Simons, J., Mitchell, J. P., Schwartz, B. L., & Schacter, D. L. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00014-4 · Cited by 120 · see citing works
Self-citation
Interaction of ventral and orbital prefrontal cortex with inferotemporal cortex in conditional visuomotor learning.
Bussey, T. J., Wise, S. P., & Murray, E. A. (2002) · Behavioral Neuroscience · doi:10.1037/0735-7044.116.4.703 · Cited by 110 · see citing works
Simulation of spatial learning in the Morris water maze by a neural network model of the hippocampal formation and nucleus accumbens
Brown, M. A., Sr., & Sharp, P. E. (1995) · Hippocampus · doi:10.1002/hipo.450050304 · Cited by 103 · see citing works
Semantic knowledge and episodic memory for faces in semantic dementia.
Simons, J. S., Graham, K. S., Galton, C. J., Patterson, K. E., & Hodges, J. R. (2001) · Neuropsychology · doi:10.1037/0894-4105.15.1.101 · Cited by 102 · see citing works
Self-citation
Interaction of Inferior Temporal Cortex with Frontal Cortex and Basal Forebrain: Double Dissociation in Strategy Implementation and Associative Learning
Gaffan, D., Easton, A., & Parker, A. J. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-16-07288.2002 · Cited by 99 · see citing works
Recollection-based memory in frontotemporal dementia: implications for theories of long-term memory
Simons, J. S. (2002) · Brain · doi:10.1093/brain/awf247 · Cited by 98 · see citing works
Self-citation
Perceptual and Mnemonic Matching-To-Sample in Humans: Contributions of The Hippocampus, Perirhinal and Other Medial Temporal Lobe Cortices
Holdstock, J. S., Gutnikov, S. A., Gaffan, D., & Mayes, A. R. (2000) · Cortex · doi:10.1016/s0010-9452(08)70843-8 · Cited by 93 · see citing works
Effects of aging and axotomy on the expression of neurotrophin receptors in primary sensory neurons
Bergman, E., Fundín, B. T., & Ulfhake, B. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19990802)410:3 · Cited by 90 · see citing works
The effects of mammillary body and combined amygdalar-fornix lesions on tests of delayed non-matching-to-sample in the rat
Aggleton, J. P., Hunt, P. R., & Shaw, C. (1990) · Behavioural Brain Research · doi:10.1016/0166-4328(90)90006-z · Cited by 90 · see citing works
A Computational Model of Prefrontal Control in Free Recall: Strategic Memory Use in the California Verbal Learning Task
Becker, S., & Lim, J. C. (2003) · Journal of Cognitive Neuroscience · doi:10.1162/089892903322370744 · Cited by 88 · see citing works
Neuroanatomy
Wolf, M. K. (1997) · Neurology · doi:10.1212/wnl.48.1.300-a · Cited by 86 · see citing works
Medial dorsal thalamic lesions and working memory in the rat
Hunt, P. R., & Aggleton, J. P. (1991) · Behavioral and Neural Biology · doi:10.1016/0163-1047(91)80141-z · Cited by 82 · see citing works
Inferotemporal-frontal disconnection and fornix transection in visuomotor conditional learning by monkeys
Gaffan, D., & HARRISON, S. (1988) · Behavioural Brain Research · doi:10.1016/0166-4328(88)90018-6 · Cited by 81 · see citing works
Functional interactions between the medial temporal lobes and posterior neocortex related to episodic memory retrieval
Köhler, S., McIntosh, A. R., Moscovitch, M., & Winocur, G. (1998) · Cerebral Cortex · doi:10.1093/cercor/8.5.451 · Cited by 76 · see citing works
Specialized systems for the processing of mnemonic information within the primate frontal cortex
Petrides, M. (1998) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780198524410.003.0008 · Cited by 76 · see citing works
The Recognition Memory Deficit Caused by Mediodorsal Thalamic Lesion in Non‐human Primates: A Comparison with Rhinal Cortex Lesion
Parker, A. J., Eacott, M. J., & Gaffan, D. (1997) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1997.tb01659.x · Cited by 74 · see citing works
Delayed Matching by Fornix-Transected Monkeys: The Sample, the Push and the Bait
Gaffan, D., Shields, C., & Harrison, S. (1984) · The Quarterly Journal of Experimental Psychology Section B · doi:10.1080/14640748408402210 · Cited by 46 · see citing works
Perceptual and Semantic Components of Memory for Objects and Faces: A PET Study
Simons, J. S., Graham, K. S., Owen, A. M., Patterson, K. E., & Hodges, J. R. (2001) · Journal of Cognitive Neuroscience · doi:10.1162/08989290152001862 · Cited by 44 · see citing works
Self-citation
Perceptual and semantic contributions to episodic memory: evidence from semantic dementia and Alzheimer's disease
Simons, J. S., Graham, K. S., & Hodges, J. R. (2002) · Journal of Memory and Language · doi:10.1016/s0749-596x(02)00003-7 · Cited by 37 · see citing works
Self-citation
Ventromedial Temporal Lobe Pathology in Dementia, Brain Trauma, and Schizophrenia
Hoesen, G. W. V., Augustinack, J. C., & REDMAN, S. J. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb09290.x · Cited by 24 · see citing works
Models and experiments
Miller, J. S., & Drillon, M. (2001) · Wiley-VCH eBooks · Cited by 11 · see citing works
Cortico-hippocampal communication by way of parallel parahippocampal-subicular pathways.
Lavenex (2000) · Pure Amsterdam UMC · doi:10.1002/1098-1063(2000)10:4 · Cited by 1 · see citing works
Untitled work
Lepage (1998) · doi:10.1002/(sici)1098-1063(1998)8:4
Untitled work
(1999) · doi:10.1002/(sici)1098-1063(1999)9:5

Flagged first, then by citations

2 of the 144 references couldn’t be matched to a known paper.

Sorted by citations

Updating P300: An integrative theory of P3a and P3b
Polich, J. (2007) · Clinical Neurophysiology · doi:10.1016/j.clinph.2007.04.019 · Cited by 7,919 · see citing works
Visual objects in context
Bar, M. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1476 · Cited by 1,613 · see citing works
The Influences of Emotion on Learning and Memory
Chai, M. T., Amin, H. U., Saad, M. N. M., & Malik, A. S. (2017) · Frontiers in Psychology · doi:10.3389/fpsyg.2017.01454 · Cited by 1,652 · see citing works
The nature of individual differences in working memory capacity: Active maintenance in primary memory and controlled search from secondary memory.
Unsworth, N., & Engle, R. W. (2007) · Psychological Review · doi:10.1037/0033-295x.114.1.104 · Cited by 1,307 · see citing works
Deconstructing episodic memory with construction
Hassabis, D., & Maguire, E. A. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2007.05.001 · Cited by 1,229 · see citing works
Intermediate phenotypes and genetic mechanisms of psychiatric disorders
Meyer-Lindenberg, A., & Weinberger, D. R. (2006) · Nature reviews. Neuroscience · doi:10.1038/nrn1993 · Cited by 1,216 · see citing works
Episodic memory and beyond: the hippocampus and neocortex in transformation
Moscovitch, M., Cabeza, R., Winocur, G., & Nadel, L. (2016) · Annual Review of Psychology · doi:10.1146/annurev-psych-113011-143733 · Cited by 1,062 · see citing works
Event-related fMRI studies of episodic encoding and retrieval: meta-analyses using activation likelihood estimation
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
The gateway hypothesis of rostral prefrontal cortex (area 10) function
Burgess, P. W., Dumontheil, I., & Gilbert, S. J. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2007.05.004 · Cited by 753 · see citing works
Functional neuroimaging of autobiographical memory
Cabeza, R., & St Jacques, P. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2007.02.005 · Cited by 736 · see citing works
The Episodic Memory System: Neurocircuitry and Disorders
Dickerson, B. C., & Eichenbaum, H. (2009) · Neuropsychopharmacology · doi:10.1038/npp.2009.126 · Cited by 658 · see citing works
Neural activity that predicts subsequent memory and forgetting: A meta-analysis of 74 fMRI studies
Kim, H. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.09.045 · Cited by 605 · see citing works
Top-down and bottom-up attention to memory: a hypothesis (AtoM) on the role of the posterior parietal cortex in memory retrieval
Ciaramelli, E., Grady, C. L., & Moscovitch, M. (2008) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2008.03.022 · Cited by 534 · see citing works
The role of the hippocampus in flexible cognition and social behavior
Rubin, R. D., Watson, P. D., Duff, M. C., & Cohen, N. J. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00742 · Cited by 489 · see citing works
Autobiographical memory and sense of self.
Prebble, S. C., Addis, D. R., & Tippett, L. J. (2013) · Psychological Bulletin · doi:10.1037/a0030146 · Cited by 466 · see citing works
Executive function
Gilbert, S. J., & Burgess, P. W. (2008) · Current Biology · doi:10.1016/j.cub.2007.12.014 · Cited by 455 · see citing works
The effects of acute stress on episodic memory: A meta-analysis and integrative review.
Shields, G. S., Sazma, M. A., McCullough, A. M., & Yonelinas, A. P. (2017) · Psychological Bulletin · doi:10.1037/bul0000100 · Cited by 450 · see citing works
Interleaving brain systems for episodic and recognition memory.
Aggleton, J., & Brown, M. W. (2006) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2006.08.003 · Cited by 465 · see citing works
Dissociable effects of arousal and valence on prefrontal activity indexing emotional evaluation and subsequent memory: an event-related fMRI study
Dolcos, F., LaBar, K. S., & Cabeza, R. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2004.05.015 · Cited by 439 · see citing works
The touchscreen operant platform for testing learning and memory in rats and mice
Horner, A. E., Heath, C. J., Hvoslef‐Eide, M., Kent, B. A., Kim, C. H., Nilsson, S. R. O., Alsiö, J., Oomen, C. A., Holmes, A., Saksida, L. M., et al. (2013) · Nature Protocols · doi:10.1038/nprot.2013.122 · Cited by 412 · see citing works
Sleep transforms the cerebral trace of declarative memories
Gais, S., Albouy, G., Boly, M., Dang-Vu, T. T., Darsaud, A., Desseilles, M., Rauchs, G., Schabus, M., Sterpenich, V., Vandewalle, G., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0705454104 · Cited by 412 · see citing works
Effects of Healthy Aging on Hippocampal and Rhinal Memory Functions: An Event-Related fMRI Study
Daselaar, S. M., Fleck, M. S., Dobbins, I. G., Madden, D. J., & Cabeza, R. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhj112 · Cited by 392 · see citing works
Episodic memory in normal aging and Alzheimer disease: Insights from imaging and behavioral studies
Tromp, D., Dufour, A., Lithfous, S., Pebayle, T., & Després, O. (2015) · Ageing Research Reviews · doi:10.1016/j.arr.2015.08.006 · Cited by 390 · see citing works
When less means more: deactivations during encoding that predict subsequent memory
Daselaar, S. M., Prince, S. E., & Cabeza, R. E. L. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2004.07.031 · Cited by 389 · see citing works
The Basic-Systems Model of Episodic Memory
Rubin, D. C. (2006) · Perspectives on Psychological Science · doi:10.1111/j.1745-6916.2006.00017.x · Cited by 374 · see citing works
Psychosocial stress impairs working memory at high loads: an association with cortisol levels and memory retrieval
Oei, N. Y. L., Everaerd, W. T. A. M., Elzinga, B. M., van Well, S., & Bermond, B. (2006) · Stress · doi:10.1080/10253890600965773 · Cited by 373 · see citing works
Effects of memory training on cortical thickness in the elderly
Engvig, A., Fjell, A., Westlye, L., Moberget, T., Sundseth, Ø., Larsen, V. A., & Walhovd, K. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.05.041 · Cited by 383 · see citing works
Working, declarative and procedural memory in specific language impairment
Lum, J. A. G., Conti‐Ramsden, G., Page, D., & Ullman, M. T. (2011) · Cortex · doi:10.1016/j.cortex.2011.06.001 · Cited by 364 · see citing works
Neural correlates of emotion–cognition interactions: A review of evidence from brain imaging investigations
Dolcos, F., Iordan, A. D., & Dolcos, S. (2011) · Journal of Cognitive Psychology · doi:10.1080/20445911.2011.594433 · Cited by 355 · see citing works
Episodic memory across the lifespan: The contributions of associative and strategic components
Shing, Y. L., Werkle‐Bergner, M., Brehmer, Y., Müller, V., Li, S., & Lindenberger, U. (2009) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2009.11.002 · Cited by 348 · see citing works
Labile or stable: opposing consequences for memory when reactivated during waking and sleep
Diekelmann, S., Büchel, C., Born, J., & Rasch, B. (2011) · Nature Neuroscience · doi:10.1038/nn.2744 · Cited by 344 · see citing works
Optically Stimulated Artificial Synapse Based on Layered Black Phosphorus
Ahmed, T., Kuriakose, S., Mayes, E. L. H., Ramanathan, R., Bansal, V., Bhaskaran, M. C., Sriram, S., & Walia, S. (2019) · Small · doi:10.1002/smll.201900966 · Cited by 333 · see citing works
The Formation of Recent and Remote Memory Is Associated with Time-Dependent Formation of Dendritic Spines in the Hippocampus and Anterior Cingulate Cortex
Restivo, L., Vetere, G., Bontempi, B., & Ammassari‐Teule, M. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.0966-09.2009 · Cited by 322 · see citing works
Multiple anatomical systems embedded within the primate medial temporal lobe: Implications for hippocampal function
Aggleton, J. P. (2011) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2011.09.005 · Cited by 319 · see citing works
Recent advances in the neuropsychopharmacology of serotonergic hallucinogens
Halberstadt, A. L. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.07.016 · Cited by 312 · see citing works
“The PFC exerts top-down executive control over processing in temporal and parietal cortices (Tomita et al., 1999; Simons and Spiers, 2003; Merchant et al., 2011; Crowe et al., 2013).”
Background
A systematic review and meta-analysis of rTMS effects on cognitive enhancement in mild cognitive impairment and Alzheimer's disease
Chou, Y.-H., Ton That, V., & Sundman, M. (2020) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2019.08.020 · Cited by 319 · see citing works
Prefrontal-Hippocampal Interactions in Memory and Emotion
Jin, J., & Maren, S. (2015) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00170 · Cited by 313 · see citing works
“Indeed, considerable data suggests that communication between these brain areas is essential for episodic memory processes (Simons and Spiers, 2003; Preston and Eichenbaum, 2013).”
Background
Hippocampal-Prefrontal Interactions in Cognition, Behavior and Psychiatric Disease
Sigurdsson, T., & Duvarci, S. (2016) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00190 · Cited by 309 · see citing works
New Circuits for Old Memories
Wiltgen, B. J., Brown, R. A. M., Talton, L. E., & Silva, A. J. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.015 · Cited by 309 · see citing works
The temporal context model in spatial navigation and relational learning: toward a common explanation of medial temporal lobe function across domains
Howard, M. W., Fotedar, M. S., Datey, A. V., & Hasselmo, M. E. (2005) · Psychological Review · doi:10.1037/0033-295x.112.1.75 · Cited by 283 · see citing works
Distributed Representations in Memory: Insights from Functional Brain Imaging
Rissman, J., & Wagner, A. D. (2012) · Annual Review of Psychology · doi:10.1146/annurev-psych-120710-100344 · Cited by 299 · see citing works
New translational assays for preclinical modelling of cognition in schizophrenia: The touchscreen testing method for mice and rats
Bussey, T. J., Holmes, A., Lyon, L., Mar, A. C., McAllister, K. A. L., Nithianantharajah, J., Oomen, C. A., & Saksida, L. M. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.04.011 · Cited by 299 · see citing works
Using the MATRICS to guide development of a preclinical cognitive test battery for research in schizophrenia
Young, J. W., Powell, S. B., Risbrough, V. B., Marston, H. M., & Geyer, M. A. (2009) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2009.02.004 · Cited by 299 · see citing works
Revisiting the Functional Anatomy of the Human Brain: Toward a Meta-Networking Theory of Cerebral Functions
Herbet, G., & Duffau, H. (2020) · Physiological Reviews · doi:10.1152/physrev.00033.2019 · Cited by 299 · see citing works
Frequency-specific network connectivity increases underlie accurate spatiotemporal memory retrieval
Watrous, A. J., Tandon, N., Conner, C. R., Pieters, T., & Ekstrom, A. D. (2013) · Nature Neuroscience · doi:10.1038/nn.3315 · Cited by 296 · see citing works
The neural basis of implicit learning and memory: A review of neuropsychological and neuroimaging research
Reber, P. J. (2013) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2013.06.019 · Cited by 296 · see citing works
Development of abstract thinking during childhood and adolescence: the role of rostrolateral prefrontal cortex
Dumontheil, I. (2014) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2014.07.009 · Cited by 293 · see citing works
Multiple cognitive deficits during the transition to Alzheimer's disease
Bäckman, L., Jones, S., Berger, A., Laukka, E. J., & Small, B. J. (2004) · Journal of Internal Medicine · doi:10.1111/j.1365-2796.2004.01386.x · Cited by 293 · see citing works
Hippocampal-prefrontal theta oscillations support memory integration
Backus, A. R., Schoffelen, J.-M., Szebényi, S., Hanslmayr, S., & Doeller, C. F. (2016) · Current Biology · doi:10.1016/j.cub.2015.12.048 · Cited by 288 · see citing works
The Influence of Prior Knowledge on Memory: A Developmental Cognitive Neuroscience Perspective
Brod, G., Werkle‐Bergner, M., & Shing, Y. L. (2013) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2013.00139 · Cited by 287 · see citing works
Prefrontal cortex and neural mechanisms of executive function
Funahashi, S., & Andreau, J. M. (2013) · Journal of Physiology-Paris · doi:10.1016/j.jphysparis.2013.05.001 · Cited by 285 · see citing works
Active Forgetting: Adaptation of Memory by Prefrontal Control
Anderson, M. C., & Hulbert, J. C. (2021) · Annual Review of Psychology · doi:10.1146/annurev-psych-072720-094140 · Cited by 279 · see citing works
Neural predictors of individual differences in response to math tutoring in primary-grade school children
Supekar, K., Swigart, A. G., Tenison, C., Jolles, D., Rosenberg‐Lee, M., Fuchs, L. S., & Menon, V. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1222154110 · Cited by 270 · see citing works
Memory Dysfunction
Budson, A. E., & Price, B. H. (2005) · New England Journal of Medicine · doi:10.1056/nejmra041071 · Cited by 262 · see citing works
Baseline and longitudinal grey matter changes in newly diagnosed Parkinson’s disease: ICICLE-PD study
Mak, E., Su, L., Williams, G. B., Firbank, M., Lawson, R. A., Yarnall, A. J., Duncan, G. W., Owen, A. M., Khoo, T. K., Brooks, D. J., et al. (2015) · Brain · doi:10.1093/brain/awv211 · Cited by 261 · see citing works
Memory: organization and control.
Eichenbaum, H. (2017) · Annual Review of Psychology · doi:10.1146/annurev-psych-010416-044131 · Cited by 257 · see citing works
Temporal clustering and sequencing in short-term memory and episodic memory.
Farrell, S. (2012) · Psychological Review · doi:10.1037/a0027371 · Cited by 240 · see citing works
Frontotemporal connections in episodic memory and aging: a diffusion MRI tractography study
Metzler-Baddeley, C., Jones, D. K., Belaroussi, B., Aggleton, J. P., & O'Sullivan, M. J. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.2317-11.2011 · Cited by 247 · see citing works
Episodic memory-related activation in schizophrenia: meta-analysis
Achim, A. M., & Lepage, M. (2005) · The British Journal of Psychiatry · doi:10.1192/bjp.187.6.500 · Cited by 244 · see citing works
Associative and strategic components of episodic memory: A life-span dissociation.
Shing, Y. L., Werkle‐Bergner, M., Li, S., & Lindenberger, U. (2008) · Journal of Experimental Psychology General · doi:10.1037/0096-3445.137.3.495 · Cited by 233 · see citing works
Contralateral cortico-ponto-cerebellar pathways reconstruction in humans in vivo: implications for reciprocal cerebro-cerebellar structural connectivity in motor and non-motor areas
Palesi, F., Rinaldis, A. D., Castellazzi, G., Calamante, F., Muhlert, N., Chard, D., Tournier, J., Magenes, G., D'Angelo, E. U., & Wheeler‐Kingshott, C. A. M. G. (2017) · Scientific Reports · doi:10.1038/s41598-017-13079-8 · Cited by 234 · see citing works
Precise Slow Oscillation–Spindle Coupling Promotes Memory Consolidation in Younger and Older Adults
Muehlroth, B. E., Sander, M. C., Fandakova, Y., Grandy, T. H., Rasch, B., Shing, Y. L., & Werkle‐Bergner, M. (2019) · Scientific Reports · doi:10.1038/s41598-018-36557-z · Cited by 227 · see citing works
Functional connectivity with the hippocampus during successful memory formation
Charan Ranganath, A., Heller, A. S., Cohen, M. X., Brozinsky, C. J., & Rissman, J. (2005) · Hippocampus · doi:10.1002/hipo.20141 · Cited by 224 · see citing works
A unifying account of angular gyrus contributions to episodic and semantic cognition
Humphreys, G. F., Lambon Ralph, M. A., & Simons, J. S. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2021.01.006 · Cited by 220 · see citing works
Self-citation
The right hippocampus participates in short-term memory maintenance of object–location associations
Piekema, C., Kessels, R. P. C., Mars, R. B., Petersson, K. M., & Fernández, G. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.06.035 · Cited by 208 · see citing works
Brain mechanisms of reality monitoring
Simons, J. S., Garrison, J. R., & Johnson, M. K. (2017) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2017.03.012 · Cited by 202 · see citing works
Self-citation
Diversity and plasticity of microglial cells in psychiatric and neurological disorders
Nakagawa, Y., & Chiba, K. (2015) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2015.06.010 · Cited by 208 · see citing works
Memory Function and the Hippocampus
Opitz, B. (2014) · Monographs in clinical neuroscience/Frontiers of neurology and neuroscience/Monographs in neural sciences · doi:10.1159/000356422 · Cited by 209 · see citing works
Dopamine-Dependent Interactions between Limbic and Prefrontal Cortical Plasticity in the Nucleus Accumbens: Disruption by Cocaine Sensitization
Goto, Y., & Grace, A. A. (2005) · Neuron · doi:10.1016/j.neuron.2005.06.017 · Cited by 204 · see citing works
Episodic retrieval and the cortical binding of relational activity
Shimamura, A. P. (2011) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/s13415-011-0031-4 · Cited by 205 · see citing works
Hippocampal brain-network coordination during volitional exploratory behavior enhances learning
Voss, J. L., Gonsalves, B. D., Federmeier, K. D., Tranel, D., & Cohen, N. J. (2010) · Nature Neuroscience · doi:10.1038/nn.2693 · Cited by 203 · see citing works
Cingulate cortex projections to the parahippocampal region and hippocampal formation in the rat
Jones, B. F., & Witter, M. P. (2007) · Hippocampus · doi:10.1002/hipo.20330 · Cited by 201 · see citing works
Visual and spatial working memory: From boxes to networks
Zimmer, H. D. (2008) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2008.05.016 · Cited by 200 · see citing works
Involvement of rostral prefrontal cortex in selection between stimulus‐oriented and stimulus‐independent thought
Gilbert, S. J., Frith, C. D., & Burgess, P. W. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.03981.x · Cited by 193 · see citing works
Youthful brains in older adults: Preserved neuroanatomy in the default mode and salience networks contributes to youthful memory in superaging
Sun, F. W., Stepanovic, M. R., Andreano, J., Barrett, L. F., Touroutoglou, A., & Dickerson, B. C. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.1492-16.2016 · Cited by 191 · see citing works
Abnormal Functional Connectivity of Hippocampus During Episodic Memory Retrieval Processing Network in Amnestic Mild Cognitive Impairment
Bai, F., Zhang, Z., Watson, D. R., Yu, H., Shi, Y., Yuan, Y., Zang, Y., Zhu, C., & Qian, Y. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.10.017 · Cited by 183 · see citing works
Generators of the intracranial P50 response in auditory sensory gating
Korzyukov, O., Pflieger, M. E., Wagner, M., Bowyer, S. M., Rosburg, T., Sundaresan, K., Elger, C. E., & Boutros, N. N. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2006.12.011 · Cited by 183 · see citing works
Age-Related Functional Changes of Prefrontal Cortex in Long-Term Memory: A Repetitive Transcranial Magnetic Stimulation Study
Rossi, S., Miniussi, C., Pasqualetti, P., Babiloni, C., Rossini, P. M., & Cappa, S. F. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.0703-04.2004 · Cited by 184 · see citing works
Long-lasting, dissociable improvements in working memory and long-term memory in older adults with repetitive neuromodulation
Grover, S., Wen, W., Viswanathan, V., Gill, C. T., & Reinhart, R. M. G. (2022) · Nature Neuroscience · doi:10.1038/s41593-022-01132-3 · Cited by 187 · see citing works
What did you do yesterday? A meta-analysis of sex differences in episodic memory.
Asperholm, M., Högman, N., Rafi, J., & Herlitz, A. (2019) · Psychological Bulletin · doi:10.1037/bul0000197 · Cited by 182 · see citing works
Enhancing cognitive control through neurofeedback: A role of gamma-band activity in managing episodic retrieval
Keizer, A. W., Verment, R. S., & Hommel, B. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.11.023 · Cited by 180 · see citing works
Common and unique gray matter correlates of episodic memory dysfunction in frontotemporal dementia and alzheimer's disease
Irish, M., Piguet, O., Hodges, J. R., & Hornberger, M. (2013) · Human Brain Mapping · doi:10.1002/hbm.22263 · Cited by 171 · see citing works
Age-related deficits in associative memory: The influence of impaired strategic retrieval.
Cohn, M., Emrich, S. M., & Moscovitch, M. (2008) · Psychology and Aging · doi:10.1037/0882-7974.23.1.93 · Cited by 172 · see citing works
False memories with age: neural and cognitive underpinnings
Devitt, A. L., & Schacter, D. L. (2016) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2016.08.030 · Cited by 171 · see citing works
Cerebral blood flow associated with creative performance: A comparative study
Chávez-Eakle, R. A., Graff‐Guerrero, A., Garcı́a-Reyna, J. C., Vaugier, V., & Cruz-Fuentes, C. S. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.07.059 · Cited by 169 · see citing works
Memory Systems, Processing Modes, and Components: Functional Neuroimaging Evidence
Cabeza, R., & Moscovitch, M. (2013) · Perspectives on Psychological Science · doi:10.1177/1745691612469033 · Cited by 163 · see citing works
Distinct contributions of the hippocampus and medial prefrontal cortex to the “what–where–when” components of episodic-like memory in mice
DeVito, L. M., & Eichenbaum, H. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2009.09.014 · Cited by 164 · see citing works
Transcranial Magnetic Stimulation to Address Mild Cognitive Impairment in the Elderly: A Randomized Controlled Study
Marra, H., Myczkowski, M. L., Memória, C. M., Arnaut, D., Ribeiro, P. L., Mansur, C. G., Alberto, R. L., Bellini, B. B., da Silva, A. A. F., Tortella, G., et al. (2015) · Behavioural Neurology · doi:10.1155/2015/287843 · Cited by 161 · see citing works
Neuromodulation and aging: implications of aging neuronal gain control on cognition
Li, S., & Rieckmann, A. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.07.009 · Cited by 164 · see citing works
A functional magnetic resonance imaging study mapping the episodic memory encoding network in temporal lobe epilepsy
Sidhu, M. K., Stretton, J., Winston, G. P., Bonelli, S. B., Centeno, M., Vollmar, C., Symms, M. R., Thompson, P. J., Koepp, M. J., & Duncan, J. S. (2013) · Brain · doi:10.1093/brain/awt099 · Cited by 154 · see citing works
Differential contributions of hippocampus and medial prefrontal cortex to self-projection and self-referential processing
Kurczek, J., Wechsler, E., Ahuja, S., Jensen, U., Cohen, N. J., Tranel, D., & Duff, M. (2015) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2015.05.002 · Cited by 157 · see citing works
Sequence of information processing for emotions through pathways linking temporal and insular cortices with the amygdala
Höistad, M., & Barbas, H. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2007.12.043 · Cited by 157 · see citing works
The brain angiotensin system and extracellular matrix molecules in neural plasticity, learning, and memory
Wright, J. W., & Harding, J. W. (2004) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2004.03.003 · Cited by 156 · see citing works
Progression from selective to general involvement of hippocampal subfields in schizophrenia
Ho, N. F., Iglesias, J. E., Sum, M. Y., Kuswanto, C. N., Sitoh, Y. Y., de Souza, J., Hong, Z., Fischl, B. R., Roffman, J. L., Zhou, J. H., et al. (2016) · Molecular Psychiatry · doi:10.1038/mp.2016.4 · Cited by 151 · see citing works
The role of experience in adolescent cognitive development: Integration of executive, memory, and mesolimbic systems
Murty, V. P., Calabro, F. J., & Luna, B. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.07.034 · Cited by 152 · see citing works
Association between prefrontal activity and volume change in prefrontal and medial temporal lobes in aging and dementia: A review
Maillet, D., & Rajah, M. N. (2012) · Ageing Research Reviews · doi:10.1016/j.arr.2012.11.001 · Cited by 145 · see citing works
Dual Neural Network Model for the Evolution of Speech and Language
Hage, S. R., & Nieder, A. (2016) · Trends in Neurosciences · doi:10.1016/j.tins.2016.10.006 · Cited by 148 · see citing works
Evidence of Neuronal Compensation During Episodic Memory in Subjective Memory Impairment
Erk, S. (2011) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2011.80 · Cited by 147 · see citing works
Age-related white matter microstructural differences partly mediate age-related decline in processing speed but not cognition
Salami, A., Eriksson, J., Nilsson, L., & Nyberg, L. H. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2011.09.001 · Cited by 147 · see citing works
Glucocorticoids Decrease Hippocampal and Prefrontal Activation during Declarative Memory Retrieval in Young Men
Oei, N. Y. L., Elzinga, B. M., Wolf, O. T., de Ruiter, M. B., Damoiseaux, J. S., Kuijer, J. P. A., Veltman, D. J., Scheltens, P., & Rombouts, S. A. R. B. (2007) · Brain Imaging and Behavior · doi:10.1007/s11682-007-9003-2 · Cited by 146 · see citing works

Authors: Simons, J. S., & Spiers, H. J.
Affiliations: University College London (GB)
MRC Cognition and Brain Sciences Unit (GB)
ORCID: Simons, Jon S.
Spiers, Hugo J.
Venue: Nature Reviews Neuroscience
Publisher: Springer Science and Business Media LLC
Published: 2003-08
Volume: 4
Issue: 8
Pages: 637-648
ISSN: 1471-003X (ISSN-L)
1471-0048
DOI: 10.1038/nrn1178
OpenAlex: W2168918294
Cited by: 961
References: 144
Citations by year: 2026: 21 · 2025: 39 · 2024: 39 · 2023: 27 · 2022: 30 · 2021: 51 · 2020: 44 · 2019: 49 · 2018: 55 · 2017: 67 · 2016: 54 · 2015: 60 · 2014: 47 · 2013: 49 · 2012: 38
FWCI: 3.13
Type: journal article
Language: en
Open access: closed
Licence: www.springer.com/tdm (tdm)
Locations: Nature reviews. Neuroscience (publishedVersion)
PubMed (publishedVersion)
UCL Discovery (University College London) (submittedVersion)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
Social Sciences › Psychology › Experimental and Cognitive Psychology › Cognitive Functions and Memory
Keywords: prefrontal cortex, medial temporal lobe, long-term memory, memory encoding, memory retrieval, cognitive control, structural connectivity, computational modelling
MeSH terms: Animals, Humans, Memory, Neural Pathways, Temporal Lobe, Prefrontal Cortex

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Prefrontal and medial temporal lobe interactions in long-term memory

Integrity signals

Claims the paper makes

Claims other papers make about this one

Cites

Cited by

Related

Record

About these checks