The Medial Temporal Lobe and Recognition Memory

Eichenbaum, H.; Yonelinas, A.P.; Ranganath, C.

doi:10.1146/annurev.neuro.30.051606.094328

Cited by 2,580Memory and Neural MechanismsMemory Processes and InfluencesCognitive Functions and Memory

The Medial Temporal Lobe and Recognition Memory

Open access

Eichenbaum, H., Yonelinas, A.P., Ranganath, C.·2007·Annual Review of Neuroscience

DOI 10.1146/annurev.neuro.30.051606.094328PMC PMC2064941

Open this paper in CoChat — free account

Abstract

The ability to recognize a previously experienced stimulus is supported by two processes: recollection of the stimulus in the context of other information associated with the experience, and a sense of familiarity with the features of the stimulus. Although familiarity and recollection are functionally distinct, there is considerable debate about how these kinds of memory are supported by regions in the medial temporal lobes (MTL). Here, we review evidence for the distinction between recollection and familiarity and then consider the evidence regarding the neural mechanisms of these processes. Evidence from neuropsychological, neuroimaging, and neurophysiological studies of humans, monkeys, and rats indicates that different subregions of the MTL make distinct contributions to recollection and familiarity. The data suggest that the hippocampus is critical for recollection but not familiarity. The parahippocampal cortex also contributes to recollection, possibly via the representation and retrieval of contextual (especially spatial) information, whereas perirhinal cortex contributes to and is necessary for familiarity-based recognition. The findings are consistent with an anatomically guided hypothesis about the functional organization of the MTL and suggest mechanisms by which the anatomical components of the MTL interact to support the phenomenology of recollection and familiarity.

Integrity signals

Registry

Crossref · 10.1146/annurev.neuro.30.051606.094328

Cites

179 of 179 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?

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 [35]
The PHC has been implicated in memory for specific context information.
“the PHC has been implicated in memory for specific context information”
From Delay-dependent contributions of medial temporal lobe regions to episodic memory retrieval (2015) · cites this paper as Eichenbaum et al., 2007

The Cognitive neurosciences
(2005) · Choice Reviews Online · doi:10.5860/choice.43-0626 · Cited by 4,726 · see citing works
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 · see citing works
Self-citation
A process dissociation framework: Separating automatic from intentional uses of memory
Jacoby, L. (1991) · Journal of Memory and Language · doi:10.1016/0749-596x(91)90025-f · Cited by 3,815 · see citing works
Object vision and spatial vision: Two cortical pathways
Mishkin, M., Ungerleider, L. G., & Macko, K. A. (1983) · Trends in Neurosciences · doi:10.1016/0166-2236(83)90190-x · Cited by 2,947 · see citing works
Repetition and the brain: neural models of stimulus-specific effects
Grill-Spector, K., Henson, R., & Martin, A. (2006) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2005.11.006 · Cited by 2,256 · see citing works
Hippocampus, space, and memory
Olton, D. S., Becker, J. T., & Handelmann, G. E. (1979) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00062713 · Cited by 2,018 · see citing works
Human amnesia and the medial temporal region: enduring memory impairment following a bilateral lesion limited to field CA1 of the hippocampus
Zola-Morgan, S., Squire, L., & Amaral, D. (1986) · The Journal of Neuroscience · doi:10.1523/jneurosci.06-10-02950.1986 · Cited by 1,997 · see citing works
How many memory systems are there?
Tulving, E. (1985) · American Psychologist · doi:10.1037/0003-066x.40.4.385 · Cited by 1,909 · 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
Differential Effects of Early Hippocampal Pathology on Episodic and Semantic Memory
Vargha-Khadem, F., Gadian, D. G., Watkins, K. E., Connelly, A., Van Paesschen, W., & Mishkin, M. (1997) · Science · doi:10.1126/science.277.5324.376 · Cited by 1,746 · see citing works
Interpreting the BOLD Signal
Logothetis, N. K., & Wandell, B. A. (2004) · Annual Review of Physiology · doi:10.1146/annurev.physiol.66.082602.092845 · Cited by 1,568 · see citing works
Recognition memory: What are the roles of the perirhinal cortex and hippocampus?
Brown, M. W., & Aggleton, J. P. (2001) · Nature reviews. Neuroscience · doi:10.1038/35049064 · Cited by 1,555 · see citing works
Untitled work
Eichenbaum (2004) · doi:10.1016/j.neuron.2004.08.028 · Cited by 1,464 · see citing works
Self-citation
Cellular networks underlying human spatial navigation
Ekstrom, A. D., Kahana, M. J., Caplan, J. B., Fields, T. A., Isham, E. A., Newman, E. L., & Fried, I. (2003) · Nature · doi:10.1038/nature01964 · Cited by 1,425 · see citing works
Spatial representation in the entorhinal cortex
Fyhn, M., Molden, S., Witter, M. P., Moser, E. I., & Moser, M.-B. (2004) · Science · doi:10.1126/science.1099901 · Cited by 1,339 · see citing works
Declarative and Nondeclarative Memory: Multiple Brain Systems Supporting Learning and Memory
Squire, L. R. (1992) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1992.4.3.232 · Cited by 1,282 · cited 2× · see citing works
“An alternative one-process theory argues that the MTL is equally important for both recollection and familiarity (Squire 1994, Squire & Zola 1998).”
Background
Memory in monkeys severely impaired by combined but not by separate removal of amygdala and hippocampus
Mishkin, M. (1978) · Nature · doi:10.1038/273297a0 · Cited by 1,207 · see citing works
Receiver-operating characteristics in recognition memory: evidence for a dual-process model.
Yonelinas, A. (1994) · Journal of Experimental Psychology. Learning, Memory and Cognition · doi:10.1037/0278-7393.20.6.1341 · Cited by 1,193 · see citing works
Self-citation
Receiver-operating characteristics in recognition memory: Evidence for a dual-process model.
Yonelinas, A. P. (1994) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037//0278-7393.20.6.1341 · Cited by 1,152 · see citing works
Self-citation
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
Two functional components of the hippocampal memory system
Eichenbaum, H., Otto, T., & Cohen, N. J. (1994) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00035391 · Cited by 1,094 · see citing works
Self-citation
Hippocampal Neurons Encode Information about Different Types of Memory Episodes Occurring in the Same Location
Wood, E. R., Dudchenko, P. A., Robitsek, R. J., & Eichenbaum, H. (2000) · Neuron · doi:10.1016/s0896-6273(00)00071-4 · Cited by 992 · see citing works
Self-citation
Spatial memory, recognition memory, and the hippocampus
Broadbent, N. J., Squire, L. R., & Clark, R. E. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0406344101 · Cited by 985 · see citing works
Functional organization of the extrinsic and intrinsic circuitry of the parahippocampal region
Witter, M. P., Groenewegen, H. J., Lopes, F. H. D. S., & Lohman, A. H. M. (1989) · Progress in Neurobiology · doi:10.1016/0301-0082(89)90009-9 · Cited by 918 · 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
Two routes to emotional memory: Distinct neural processes for valence and arousal
Kensinger, E. A., & Corkin, S. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0306408101 · Cited by 848 · cited 3× · see citing works
“…was selectively associated with familiarity and activity in the hippocampus and posterior parahippocampal gyrus was selectively associated with recollection (Daselaar et al. 2006, Davachi et al. 2003, Kensinger & Corkin 2004, Ranganath et al. 2003, Uncapher & Rugg 2005, Weis et al. 2004b).”
BackgroundMethod
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
Three Cases of Enduring Memory Impairment after Bilateral Damage Limited to the Hippocampal Formation
Rempel-Clower, N., Zola, S. M., Squire, L. R., & Amaral, D. G. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-16-05233.1996 · Cited by 815 · see citing works
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 · see citing works
Self-citation
Lesions of perirhinal and parahippocampal cortex that spare the amygdala and hippocampal formation produce severe memory impairment
Zola-Morgan, S. M., Squire, L., Amaral, D., & Suzuki, W. (1989) · Journal of Neuroscience · doi:10.1523/jneurosci.09-12-04355.1989 · Cited by 766 · 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
Hippocampal damage and exploratory preferences in rats: memory for objects, places, and contexts
Mumby, D. G., Gaskin, S., Glenn, M. J., Schramek, T. E., & Lehmann, H. (2002) · Learning & Memory · doi:10.1101/lm.41302 · Cited by 714 · see citing works
The global record of memory in hippocampal neuronal activity
Wood, E. R., Dudchenko, P. A., & Eichenbaum, H. (1999) · Nature · doi:10.1038/17605 · Cited by 707 · see citing works
Self-citation
Dissociable correlates of recollection and familiarity within the medial temporal lobes
Ranganath, C., Yonelinas, A. P., Cohen, M. X., Dy, C. J., Tom, S. M., & D’Esposito, M. (2004) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2003.07.006 · Cited by 689 · see citing works
Self-citation
Major Dissociation Between Medial and Lateral Entorhinal Input to Dorsal Hippocampus
Hargreaves, E. L., Rao, G., Lee, I., & Knierim, J. J. (2005) · Science · doi:10.1126/science.1110449 · Cited by 685 · see citing works
Cortical analysis of visual context.
Bar, M., & Aminoff, E. (2003) · Neuron · doi:10.1016/s0896-6273(03)00167-3 · Cited by 630 · see citing works
Remembering one year later: role of the amygdala and the medial temporal lobe memory system in retrieving emotional memories
Dolcos, F., LaBar, K. S., & Cabeza, R. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0409848102 · Cited by 601 · see citing works
Double Dissociation between the Effects of Peri-Postrhinal Cortex and Hippocampal Lesions on Tests of Object Recognition and Spatial Memory: Heterogeneity of Function within the Temporal Lobe
Winters, B. D., Forwood, S., Cowell, R. A., Saksida, L. M., & Bussey, T. J. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1346-04.2004 · Cited by 588 · see citing works
Components of episodic memory: the contribution of recollection and familiarity
Yonelinas, A. P. (2001) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.2001.0939 · Cited by 547 · see citing works
Self-citation
Category-specific visual responses of single neurons in the human medial temporal lobe
Kreiman, G., Koch, C., & Fried, I. (2000) · Nature Neuroscience · doi:10.1038/78868 · Cited by 541 · see citing works
The Parahippocampal Region: Corticocortical Connectivity
Burwell, R. D. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06717.x · Cited by 513 · see citing works
The Relation between Remembering and Knowing as Bases for Recognition: Effects of Size Congruency
Yonelinas, A., & Jacoby, L. (1995) · Journal of Memory and Language · doi:10.1006/jmla.1995.1028 · Cited by 500 · see citing works
Self-citation
Chunking and consolidation: A theoretical synthesis of semantic networks, configuring in conditioning, S-R versus cognitive learning, normal forgetting, the amnesic syndrome, and the hippocampal arousal system.
Wickelgren, W. A. (1979) · Psychological Review · doi:10.1037/0033-295x.86.1.44 · Cited by 494 · see citing works
The Cognitive Neurosciences
Morris, R. (1996) · Trends in Neurosciences · doi:10.1016/s0166-2236(96)60029-0 · 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
On the delay-dependent involvement of the hippocampus in object recognition memory
HAMMOND, R. (2004) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2004.03.005 · Cited by 476 · see citing works
Hippocampal Contributions to Episodic Encoding: Insights From Relational and Item-Based Learning
Davachi, L., & Wagner, A. D. (2002) · Journal of Neurophysiology · doi:10.1152/jn.2002.88.2.982 · Cited by 475 · see citing works
Recognition memory and the human hippocampus.
Manns, J., Hopkins, R., Reed, J. M., Kitchener, E. G., & Squire, L. (2003) · Neuron · doi:10.1016/s0896-6273(02)01147-9 · Cited by 472 · see citing works
How emotion enhances the feeling of remembering
Sharot, T., Delgado, M., & Phelps, E. (2004) · Nature Neuroscience · doi:10.1038/nn1353 · Cited by 470 · see citing works
Recollection-like memory retrieval in rats is dependent on the hippocampus
Fortin, N. J., Wright, S. P., & Eichenbaum, H. (2004) · Nature · doi:10.1038/nature02853 · Cited by 460 · see citing works
Self-citation
Recollection and familiarity deficits in amnesia: convergence of remember-know, process dissociation, and receiver operating characteristic data.
Yonelinas, A., Kroll, N., Dobbins, I., Lazzara, M. M., & Knight, R. (1998) · Neuropsychology · doi:10.1037/0894-4105.12.3.323 · Cited by 455 · see citing works
Self-citation
Different Contributions of the Hippocampus and Perirhinal Cortex to Recognition Memory
Wan, H., Aggleton, J. P., & Brown, M. W. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-03-01142.1999 · Cited by 449 · see citing works
Event-related brain potential correlates of two states of conscious awareness in memory
Düzel, E., Yonelinas, A. P., Mangun, G. R., Heinze, H., & Tulving, E. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.11.5973 · Cited by 443 · see citing works
Self-citation
Triple Dissociation in the Medial Temporal Lobes: Recollection, Familiarity, and Novelty
Daselaar, S. M., Fleck, M. S., & Cabeza, R. E. L. (2006) · Journal of Neurophysiology · doi:10.1152/jn.01029.2005 · Cited by 438 · see citing works
The neural system that mediates familiarity memory
Montaldi, D., Spencer, T., Roberts, N., & Mayes, A. (2006) · Hippocampus · doi:10.1002/hipo.20178 · Cited by 435 · see citing works
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 · 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
Human recognition memory: a cognitive neuroscience perspective
Rugg, M. D., & Yonelinas, A. P. (2003) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(03)00131-1 · Cited by 417 · see citing works
Self-citation
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
Retrieval Dynamics of Recognition and Frequency Judgments: Evidence for Separate Processes of Familiarity and Recall
Hintzman, D. L., & Curran, T. (1994) · Journal of Memory and Language · doi:10.1006/jmla.1994.1001 · Cited by 388 · see citing works
Neurophysiological Manifestations of Recollective Experience during Recognition Memory Judgments
Smith, M. E. (1993) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1993.5.1.1 · Cited by 383 · see citing works
Recollective qualities modulate hippocampal activation during autobiographical memory retrieval
Addis, D. R., Moscovitch, M., Crawley, A. P., & McAndrews, M. P. (2004) · Hippocampus · doi:10.1002/hipo.10215 · Cited by 383 · see citing works
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 · see citing works
The contribution of recollection and familiarity to recognition and source-memory judgments: A formal dual-process model and an analysis of receiver operating characterstics.
Yonelinas, A. P. (1999) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037//0278-7393.25.6.1415 · Cited by 376 · see citing works
Self-citation
Amygdala Activity Is Associated with the Successful Encoding of Item, But Not Source, Information for Positive and Negative Stimuli
Kensinger, E., & Schacter, D. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.5241-05.2006 · Cited by 371 · see citing works
Single Neurons in the Monkey Hippocampus and Learning of New Associations
Wirth, S., Yanike, M., Frank, L. M., Smith, A. C., Brown, E. N., & SUZUKI, W. A. (2003) · Science · doi:10.1126/science.1084324 · Cited by 356 · see citing works
Perspectives on object-recognition memory following hippocampal damage: lessons from studies in rats
Mumby, D. G. (2001) · Behavioural Brain Research · doi:10.1016/s0166-4328(01)00367-9 · Cited by 356 · see citing works
Developmental amnesia associated with early hypoxic-ischaemic injury
Gadian, D. G. (2000) · Brain · doi:10.1093/brain/123.3.499 · Cited by 355 · 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
Integrated Memory for Object, Place, and Context in Rats: A Possible Model of Episodic-Like Memory?
Eacott, M. J., & Norman, G. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.2975-03.2004 · Cited by 344 · see citing works
Recognition memory: neuronal substrates of the judgement of prior occurrence
Brown, M. W., & Xiang, J. ‐. (1998) · Progress in Neurobiology · doi:10.1016/s0301-0082(98)00002-1 · Cited by 329 · see citing works
Medial temporal lobe activation during encoding and retrieval of novel face‐name pairs
Kirwan, C. B., & Stark, C. E. L. (2004) · Hippocampus · doi:10.1002/hipo.20014 · Cited by 325 · see citing works
Sparing of the familiarity component of recognition memory in a patient with hippocampal pathology.
Aggleton, J., Vann, S., Denby, C., Dix, S., Mayes, A., Roberts, N., & Yonelinas, A. (2005) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2005.01.019 · Cited by 317 · see citing works
Self-citation
A Dissociation of Encoding and Retrieval Processes in the Human Hippocampus
Eldridge, L. L., Engel, S. A., Zeineh, M., Bookheimer, S. Y., & Knowlton, B. J. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.3420-04.2005 · Cited by 315 · see citing works
Recognition memory and the operating characteristic.
Egan, J. P. (1958) · Cited by 315 · see citing works
Neural Correlates of Relational Memory: Successful Encoding and Retrieval of Semantic and Perceptual Associations
Prince, S. E., Daselaar, S. M., & Cabeza, R. E. L. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2540-04.2005 · Cited by 314 · see citing works
Memory in the Cerebral Cortex: An Empirical Approach to Neural Networks in the Human and Nonhuman Primate
Paulsen, J. S. (1996) · American Journal of Psychiatry · doi:10.1176/ajp.153.11.1496 · Cited by 309 · see citing works
Neural substrates of visual stimulus-stimulus association in rhesus monkeys
Murray, E. A., Gaffan, D., & Mishkin, M. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-10-04549.1993 · Cited by 300 · see citing works
Remembering and knowing: two different expressions of declarative memory.
Knowlton, B. J., & Squire, L. R. (1995) · Journal of Experimental Psychology. Learning, Memory and Cognition · doi:10.1037//0278-7393.21.3.699 · Cited by 297 · see citing works
Single-Trial Learning of Novel Stimuli by Individual Neurons of the Human Hippocampus-Amygdala Complex
Rutishauser, U., Mamelak, A. N., & Schuman, E. M. (2006) · Neuron · doi:10.1016/j.neuron.2006.02.015 · Cited by 296 · see citing works
Hippocampal Place Cells Acquire Location-Specific Responses to the Conditioned Stimulus during Auditory Fear Conditioning
Moita, M. A. P., Rosis, S., Zhou, Y., LeDoux, J. E., & Blair, H. T. (2003) · Neuron · doi:10.1016/s0896-6273(03)00033-3 · Cited by 295 · see citing works
Electrophysiological dissociation of the neural correlates of recollection and familiarity
Woodruff, C. C., Hayama, H. R., & Rugg, M. D. (2006) · Brain Research · doi:10.1016/j.brainres.2006.05.019 · Cited by 292 · see citing works
The Neuropsychology of Memory Illusions: False Recall and Recognition in Amnesic Patients
Schacter, D., Verfaellie, M., & Pradere, D. (1996) · Journal of Memory and Language · doi:10.1006/jmla.1996.0018 · Cited by 291 · see citing works
Transient Inactivation of Perirhinal Cortex Disrupts Encoding, Retrieval, and Consolidation of Object Recognition Memory
Winters, B. D., & Bussey, T. J. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.3827-04.2005 · Cited by 283 · 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
Human amnesia and animal models of amnesia: Performance of amnesic patients on tests designed for the monkey.
Squire, L. R., Zola-Morgan, S. M., & Chen, K. S. (1988) · Behavioral Neuroscience · doi:10.1037//0735-7044.102.2.210 · Cited by 276 · see citing works
The hippocampus supports both the recollection and the familiarity components of recognition memory.
Wais, P. E., Wixted, J., Hopkins, R., & Squire, L. (2006) · Neuron · doi:10.1016/j.neuron.2005.12.020 · Cited by 275 · see citing works
Models of recognition: A review of arguments in favor of a dual-process account
Diana, R. A., Reder, L. M., Arndt, J., & Park, H. (2006) · Psychonomic Bulletin & Review · doi:10.3758/bf03193807 · Cited by 271 · see citing works
Backward Spreading of Memory-Retrieval Signal in the Primate Temporal Cortex
Naya, Y., Yoshida, M., & Miyashita, Y. (2001) · Science · doi:10.1126/science.291.5504.661 · Cited by 267 · see citing works
Effects of attention and confidence on the hypothesized ERP correlates of recollection and familiarity
Curran, T. (2004) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2003.12.011 · Cited by 266 · see citing works
A critical role for the anterior hippocampus in relational memory: Evidence from an fMRI study comparing associative and item recognition
Sullivan Giovanello, K., Schnyer, D. M., & Verfaellie, M. (2004) · Hippocampus · doi:10.1002/hipo.10182 · Cited by 265 · see citing works
Memory Strength and Repetition Suppression: Multimodal Imaging of Medial Temporal Cortical Contributions to Recognition
Gonsalves, B. D., Kahn, I., Curran, T., Norman, K. A., & Wagner, A. D. (2005) · Neuron · doi:10.1016/j.neuron.2005.07.013 · Cited by 263 · see citing works
Relative sparing of item recognition memory in a patient with adult‐onset damage limited to the hippocampus
Mayes, A. R., Holdstock, J. S., Isaac, C. L., Hunkin, N. M., & Roberts, N. P. (2002) · Hippocampus · doi:10.1002/hipo.1111 · Cited by 262 · see citing works
Fos Imaging Reveals Differential Patterns of Hippocampal and Parahippocampal Subfield Activation in Rats in Response to Different Spatial Memory Tests
Vann, S. D., Brown, M. W., Erichsen, J. T., & Aggleton, J. P. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-07-02711.2000 · Cited by 260 · see citing works
One-Trial Memory for Object-Place Associations after Separate Lesions of Hippocampus and Posterior Parahippocampal Region in the Monkey
Málková, L., & Mishkin, M. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-05-01956.2003 · Cited by 239 · see citing works
Time course of item and associative information: Implications for global memory models.
Gronlund, S. D., & Ratcliff, R. (1989) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037//0278-7393.15.5.846 · Cited by 233 · see citing works
Neuronal activity in the hippocampus during delayed non‐match to sample performance in rats: Evidence for hippocampal processing in recognition memory
Otto, T., & Eichenbaum, H. (1992) · Hippocampus · doi:10.1002/hipo.450020310 · Cited by 232 · see citing works
Self-citation
The neural basis of the butcher-on-the-bus phenomenon: when a face seems familiar but is not remembered
Yovel, G., & Paller, K. A. (2003) · NeuroImage · doi:10.1016/j.neuroimage.2003.09.034 · Cited by 230 · see citing works
Recall-to-Reject in Recognition: Evidence from ROC Curves
Rotello, C. M., Macmillan, N. A., & Tassel, G. V. (2000) · Journal of Memory and Language · doi:10.1006/jmla.1999.2701 · Cited by 228 · see citing works
Human amnesia and animal models of amnesia: Performance of amnesic patients on tests designed for the monkey.
Squire, L. R., Zola-Morgan, S. M., & Chen, K. S. (1988) · Behavioral Neuroscience · doi:10.1037/0735-7044.102.2.210 · Cited by 227 · see citing works
Making Memories without Trying: Medial Temporal Lobe Activity Associated with Incidental Memory Formation during Recognition
Stark, C. E. L., & Okado, Y. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-17-06748.2003 · Cited by 220 · see citing works
The Hippocampal/Parahippocampal Regions and Recognition Memory: Insights from Visual Paired Comparison versus Object-Delayed Nonmatching in Monkeys
Nemanic, S., Alvarado, M. C., & Bachevalier, J. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3763-03.2004 · Cited by 217 · see citing works
Dissociable Effects of Lesions to the Perirhinal Cortex and the Postrhinal Cortex on Memory for Context and Objects in Rats.
Norman, G., & Eacott, M. J. (2005) · Behavioral Neuroscience · doi:10.1037/0735-7044.119.2.557 · Cited by 217 · see citing works
Encoding activity in anterior medial temporal lobe supports subsequent associative recognition
Jackson, O., & Schacter, D. L. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2003.09.050 · Cited by 211 · see citing works
Signal-Detection, Threshold, and Dual-Process Models of Recognition Memory: ROCs and Conscious Recollection
Yonelinas, A. P., Dobbins, I. G., Szymanski, M. D., Dhaliwal, H. S., & King, L. (1996) · Consciousness and Cognition · doi:10.1006/ccog.1996.0026 · Cited by 211 · see citing works
Self-citation
Luddites must not block progress in genetics
Wood, D. (1999) · Nature · doi:10.1038/16564 · Cited by 208 · see citing works
Episodic Encoding Is More than the Sum of Its Parts: An fMRI Investigation of Multifeatural Contextual Encoding
Uncapher, M. R., Otten, L. J., & Rugg, M. D. (2006) · Neuron · doi:10.1016/j.neuron.2006.08.011 · Cited by 206 · see citing works
Recognition memory for faces: When familiarity supports associative recognition judgments
Yonelinas, A., Kroll, N., Dobbins, I., & Soltani, M. (1999) · Psychonomic Bulletin & Review · doi:10.3758/bf03212975 · Cited by 204 · see citing works
Self-citation
Dissociations of processes in recognition memory: Effects of interference and of response speed.
Yonelinas, A. P., & Jacoby, L. L. (1994) · Canadian Journal of Experimental Psychology/Revue canadienne de psychologie expérimentale · doi:10.1037/1196-1961.48.4.516 · Cited by 201 · see citing works
Self-citation
Entorhinal Cortex Lesions Disrupt the Relational Organization of Memory in Monkeys
Buckmaster, C. A., Eichenbaum, H., Amaral, D. G., SUZUKI, W. A., & Rapp, P. R. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1532-04.2004 · Cited by 198 · see citing works
Self-citation
Neurotoxic Hippocampal Lesions Have No Effect on Odor Span and Little Effect on Odor Recognition Memory But Produce Significant Impairments on Spatial Span, Recognition, and Alternation
Dudchenko, P. A., Wood, E. R., & Eichenbaum, H. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-08-02964.2000 · Cited by 198 · see citing works
Self-citation
Hippocampal cell firing correlates of delayed-match-to-sample performance in the rat.
Hampson, R. E., Heyser, C. J., & Deadwyler, S. A. (1993) · Behavioral Neuroscience · doi:10.1037/0735-7044.107.5.715 · Cited by 194 · see citing works
A Mini-Review of fMRI Studies of Human Medial Temporal Lobe Activity Associated with Recognition Memory
Henson, R. N. (2005) · The Quarterly Journal of Experimental Psychology Section B · doi:10.1080/02724990444000113 · Cited by 184 · see citing works
Slope of the receiver-operating characteristic in recognition memory.
Glanzer, M., Kim, K., Hilford, A., & Adams, J. K. (1999) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/0278-7393.25.2.500 · Cited by 182 · see citing works
The Neurophysiology of Memory
SUZUKI, W. A., & Eichenbaum, H. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06726.x · Cited by 175 · see citing works
Self-citation
Is Organic Amnesia Caused by a Selective Deficit in Remembering Contextual Information?
Mayes, A. R., Meudell, P. R., & Pickering, A. D. (1985) · Cortex · doi:10.1016/s0010-9452(85)80026-5 · Cited by 174 · see citing works
Item recognition is less impaired than recall and associative recognition in a patient with selective hippocampal damage
Holdstock, J., Mayes, A., Gong, Q., Roberts, N., & Kapur, N. (2005) · Hippocampus · doi:10.1002/hipo.20046 · Cited by 174 · see citing works
Critical role of the parahippocampal region for paired-associate learning in rats.
Bunsey, M. D., & Eichenbaum, H. (1993) · Behavioral Neuroscience · doi:10.1037//0735-7044.107.5.740 · Cited by 164 · see citing works
Self-citation
Isolating the contributions of familiarity and source information to item recognition: A time course analysis.
Brian Mcelree, A., Dolan, P. O., & Jacoby, L. L. (1999) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037//0278-7393.25.3.563 · Cited by 161 · see citing works
On the nature of associative information in recognition memory.
Kelley, R., & Wixted, J. T. (2001) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/0278-7393.27.3.701 · Cited by 160 · see citing works
Item memory, source memory, and the medial temporal lobe: concordant findings from fMRI and memory-impaired patients.
Gold, J., Smith, C., Bayley, P., Shrager, Y., Brewer, J., Stark, C. E. L., Hopkins, R., & Squire, L. (2006) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.0602716103 · Cited by 159 · see citing works
Content-specificity of the neural correlates of recollection
Woodruff, C. C., Johnson, J. D., Uncapher, M. R., & Rugg, M. D. (2005) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2004.10.013 · Cited by 158 · see citing works
Visual presentation of novel objects and new spatial arrangements of objects differentially activates the medial temporal lobe subareas in humans
Pihlajamäki, M., Tanila, H., Könönen, M., Hänninen, T., Hämäläinen, A., Soininen, H., & Aronen, H. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03282.x · Cited by 156 · see citing works
Effects of Unilateral Prefrontal Lesions on Familiarity, Recollection, and Source Memory
Duarte, A., Ranganath, C., & Knight, R. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.1392-05.2005 · Cited by 153 · see citing works
Self-citation
The Role of Trace Strength in Recency and Frequency Judgements by Amnesic and Control Subjects
Huppert, F., & Piercy, M. (1978) · Quarterly Journal of Experimental Psychology · doi:10.1080/14640747808400681 · Cited by 152 · see citing works
Empirical generality of data from recognition memory receiver-operating characteristic functions and implications for the global memory models.
Ratcliff, R., McKoon, G., & Tindall, M. L. (1994) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/0278-7393.20.4.763 · Cited by 152 · see citing works
Status of recognition memory in amnesia.
Verfaellie, M., & Treadwell, J. (1993) · Neuropsychology · doi:10.1037/0894-4105.7.1.5 · Cited by 151 · see citing works
Recognition memory for single items and for associations in amnesic patients.
Turriziani, P., Fadda, L., Caltagirone, C., & Carlesimo, G. (2004) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2003.10.003 · Cited by 149 · see citing works
Intact Recollection Memory in High-performing Older Adults: ERP and Behavioral Evidence
Duarte, A., Ranganath, C., Trujillo, C., & Knight, R. T. (2006) · Journal of Cognitive Neuroscience · doi:10.1162/089892906775249988 · Cited by 145 · see citing works
Memory Deficits Characterized by Patterns of Lesions to the Hippocampus and Parahippocampal Cortex
Bohbot, V. D., Allen, J. J. B., & Nadel, L. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06737.x · Cited by 140 · see citing works
Rats with lesions of the hippocampus are impaired on the delayed nonmatching‐to‐sample task†
Clark, R. E., West, A. N., Zola, S. M., & Squire, L. R. (2001) · Hippocampus · doi:10.1002/hipo.1035 · Cited by 135 · see citing works
Discriminating preexperimental (semantic) from learned (episodic) associations: A speed-accuracy study
Dosher, B. (1984) · Cognitive Psychology · doi:10.1016/0010-0285(84)90019-7 · Cited by 135 · see citing works
Disproportionate deficit in associative recognition relative to item recognition in global amnesia
Giovanello, K. S., Verfaellie, M. H., & Keane, M. M. (2003) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/cabn.3.3.186 · Cited by 131 · see citing works
Recollection and familiarity in dense hippocampal amnesia: a case study.
Cipolotti, L., Bird, C., Good, T., MacManus, D., Rudge, P., & Shallice, T. (2006) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2005.05.014 · Cited by 126 · see citing works
Status of recognition memory in amnesia.
Verfaellie, M. H., & Treadwell, J. R. (1993) · Neuropsychology · doi:10.1037//0894-4105.7.1.5 · Cited by 123 · see citing works
Item and Order Recognition Memory in Subjects with Hypoxic Brain Injury
Hopkins, R. O., Kesner, R. P., & Goldstein, M. (1995) · Brain and Cognition · doi:10.1006/brcg.1995.1016 · Cited by 121 · see citing works
Neuropsychology of memory
Matthews, W. A. (1986) · Biological Psychology · doi:10.1016/0301-0511(86)90008-6 · Cited by 120 · see citing works
Hippocampal damage equally impairs memory for single items and memory for conjunctions
Stark, C. E. L., & Squire, L. R. (2003) · Hippocampus · doi:10.1002/hipo.10085 · Cited by 120 · see citing works
Positional firing properties of postrhinal cortex neurons
Burwell, R. D., & Hafeman, D. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00160-x · Cited by 119 · see citing works
Time course of item and associative information: Implications for global memory models.
Gronlund, S. D., & Ratcliff, R. (1989) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/0278-7393.15.5.846 · Cited by 118 · see citing works
Dual-Process Models of Associative Recognition in Young and Older Adults: Evidence From Receiver Operating Characteristics.
Healy, M. R., Light, L. L., & Chung, C. (2005) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/0278-7393.31.4.768 · Cited by 116 · see citing works
Encoding and the Durability of Episodic Memory: A Functional Magnetic Resonance Imaging Study
Uncapher, M. R., & Rugg, M. D. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.1641-05.2005 · Cited by 112 · see citing works
Recapitulating emotional context: activity of amygdala, hippocampus and fusiform cortex during recollection and familiarity
Fenker, D., Schott, B., Richardson-Klavehn, A., Heinze, H., & Düzel, E. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04033.x · Cited by 111 · see citing works
Recognition memory in rats—II. Neuroanatomical substrates
Steckler, T., Drinkenburg, W. H. I. M., Sahgal, A., & Aggleton, J. P. (1998) · Progress in Neurobiology · doi:10.1016/s0301-0082(97)00061-0 · Cited by 108 · see citing works
Modification of the responses of hippocampal neurons in the monkey during the learning of a conditional spatial response task
Cahusac, P., Rolls, E. T., Miyashita, Y., & Niki, H. (1993) · Hippocampus · doi:10.1002/hipo.450030104 · Cited by 108 · see citing works
Visual memory task for rats reveals an essential role for hippocampus and perirhinal cortex
Prusky, G. T., Douglas, R. M., Nelson, L., Shabanpoor, A., & Sutherland, R. J. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0308528101 · Cited by 108 · see citing works
Process dissociation between contextual retrieval and item recognition.
Weis, S., Specht, K., Klaver, P., Tendolkar, I., Willmes, K., Ruhlmann, J., Elger, C. E., & Fernández, G. (2004) · PubMed · Cited by 108 · see citing works
An analysis of signal detection and threshold models of source memory.
Slotnick, S., Klein, S., Dodson, C. S., & Shimamura, A. (2000) · Journal of Experimental Psychology. Learning, Memory and Cognition · doi:10.1037//0278-7393.26.6.1499 · Cited by 107 · see citing works
Material-specific deficits in “remembering” in patients with unilateral temporal lobe epilepsy and excisions
Moscovitch, D. A., & McAndrews, M. P. (2002) · Neuropsychologia · doi:10.1016/s0028-3932(01)00213-5 · Cited by 91 · see citing works
Isolating the contributions of familiarity and source information to item recognition: A time course analysis.
McElree, B., Dolan, P. O., & Jacoby, L. L. (1999) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/0278-7393.25.3.563 · Cited by 91 · see citing works
Multiple memory systems in the visual cortex.
Desimone, R., Miller, E. K., Chelazzi, L., & Lueschow, A. (1995) · Cited by 89 · see citing works
Six Regularities of Source Recognition.
Glanzer, M., Hilford, A., & Kim, K. (2004) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/0278-7393.30.6.1176 · Cited by 89 · see citing works
Recognition Memory and Modality Judgments: A Comparison of Retrieval Dynamics
Hintzman, D. L., & Caulton, D. A. (1997) · Journal of Memory and Language · doi:10.1006/jmla.1997.2511 · Cited by 89 · see citing works
Comparison of the Effects of Damage to the Perirhinal and Parahippocampal Cortex on Transverse Patterning and Location Memory in Rhesus Macaques
Alvarado, M. C., & Bachevalier, J. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.4457-04.2005 · Cited by 87 · see citing works
Long-Term Amnesia: A Review and Detailed Illustrative Case Study
Mayes, A. R., Isaac, C. L., Holdstock, J. S., Cariga, P., Gummer, A., & Roberts, N. P. (2003) · Cortex · doi:10.1016/s0010-9452(08)70855-4 · Cited by 78 · see citing works
Lag-sensitive repetition suppression effects in the anterior parahippocampal gyrus
Brozinsky, C. J., Yonelinas, A. P., Kroll, N. E. A., & Charan Ranganath, A. (2005) · Hippocampus · doi:10.1002/hipo.20087 · Cited by 73 · see citing works
Self-citation
Regularities of source recognition: ROC analysis.
Hilford, A., Glanzer, M., Kim, K., & DeCarlo, L. T. (2002) · Journal of Experimental Psychology General · doi:10.1037//0096-3445.131.4.494 · Cited by 72 · see citing works
Regency and Frequency Judgements in Alcoholic Amnesics and Normal People with Poor Memory
Meudell, P. R., Mayes, A. R., Ostergaard, A. L., & Pickering, A. D. (1985) · Cortex · doi:10.1016/s0010-9452(58)80001-5 · Cited by 69 · see citing works
The role of the temporal lobes in recognizing visuospatial materials: remembering versus knowing.
Blaxton, T., & Theodore, W. (1997) · Brain and Cognition · doi:10.1006/brcg.1997.0902 · Cited by 68 · see citing works
An analysis of signal detection and threshold models of source memory.
Slotnick, S. D., Klein, S. A., Dodson, C. S., et al. (2000) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/0278-7393.26.6.1499 · Cited by 64 · see citing works
Mild hypoxia disrupts recollection, not familiarity
Yonelinas, A., Quamme, J., Widaman, K., Kroll, N., Sauvé, M., & Knight, R. (2004) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/cabn.4.3.393 · Cited by 61 · see citing works
Self-citation
The von Restorff Effect in Amnesia: The Contribution of the Hippocampal System to Novelty-Related Memory Enhancements
Kishiyama, M., Yonelinas, A., & Lazzara, M. M. (2004) · Journal of Cognitive Neuroscience · doi:10.1162/089892904322755511 · Cited by 61 · see citing works
Self-citation
Comparison of the retrieval of item versus spatial position information.
Gronlund, S. D., Edwards, M. B., & Ohrt, D. D. (1997) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037//0278-7393.23.5.1261 · Cited by 55 · see citing works
Fornix-fimbria section and working memory deficits in rats: Stimulus complexity and stimulus size.
Cassaday, H. J., & Rawlins, J. N. P. (1995) · Behavioral Neuroscience · doi:10.1037//0735-7044.109.4.594 · Cited by 49 · see citing works
The contribution of recollection and familiarity to recognition and source-memory judgments: a formal dual-process model and an analysis of receiver operating characteristics.
Yonelinas, A. (1999) · Journal of Experimental Psychology. Learning, Memory and Cognition · doi:10.1037/0278-7393.25.6.1415 · Cited by 47 · see citing works
Self-citation
Objects and Positions in Visual Scenes: Effects of Perirhinal and Postrhinal Cortex Lesions in the Rat.
Gaffan, E. A., Healey, A. N., & Eacott, M. J. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.5.992 · Cited by 45 · see citing works
Regularities of source recognition: ROC analysis.
Hilford, A., Glanzer, M., Kim, K., et al. (2002) · Journal of Experimental Psychology General · doi:10.1037/0096-3445.131.4.494 · Cited by 44 · see citing works
Fornix-fimbria section and working memory deficits in rats: Stimulus complexity and stimulus size.
Cassaday, H. J., & Rawlins, J. N. P. (1995) · Behavioral Neuroscience · doi:10.1037/0735-7044.109.4.594 · Cited by 41 · see citing works
Comparison of the retrieval of item versus spatial position information.
Gronlund, S. D., Edwards, M. B., & Ohrt, D. D. (1997) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/0278-7393.23.5.1261 · Cited by 38 · see citing works
Bilateral Thalamic Lesions Affect Recollection-and Familiarity-Based Recognition Memory Judgments
Kishiyama, M. M., Yonelinas, A. P., Kroll, N. E. A., Lazzara, M. M., Nolan, E. C., Jones, E. G., & Jagust, W. J. (2005) · Cortex · doi:10.1016/s0010-9452(08)70296-x · Cited by 37 · see citing works
Self-citation
The effects of hippocampectomy on performance by rats of a running recognition task using long lists of non-spatial items
Steele, K., & Rawlins, J. N. P. (1993) · Behavioural Brain Research · doi:10.1016/0166-4328(93)90043-p · Cited by 33 · see citing works
Electrophysiological studies of retrieval processing
Rugg, Herron, J., & Morcom, A. (2002) · UCL Discovery (University College London) · Cited by 22 · see citing works
Neural Correlates of Successful Declarative Memory Formation and Retrieval: The Anatomical Overlap
WEIS, S., Klaver, P., REUL, J., Elger, C. E., & Fernández, G. (2004) · Cortex · doi:10.1016/s0010-9452(08)70950-x · Cited by 19 · see citing works
Why are Amnesic Judgements of Recency and Frequency Made in a Qualitatively Different Way from those of Normal People?
Mayes, A. R., Baddeley, A., Cockburn, J., Meudell, P. R., Pickering, A. D., & Wilson, B. M. (1989) · Cortex · doi:10.1016/s0010-9452(89)80061-9 · Cited by 14 · see citing works
Episodic memory, semantic memory, and amnesia
Squire, L. R., & Zola, S. M. (1998) · Hippocampus · doi:10.1002/(sici)1098-1063(1998)8:3
Untitled work
Friedman (2000) · doi:10.1002/1097-0029(20001001)51:1

Flagged first, then by citations

Sorted by citations

Pattern separation in the hippocampus
Yassa, M. A., & Stark, C. E. L. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2011.06.006 · Cited by 1,544 · see citing works
Interplay of Hippocampus and Prefrontal Cortex in Memory
Preston, A. R., & Eichenbaum, H. (2013) · Current Biology · doi:10.1016/j.cub.2013.05.041 · Cited by 1,389 · see citing works
Self-citation
Two cortical systems for memory-guided behaviour
Ranganath, C., & Ritchey, M. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3338 · Cited by 1,377 · see citing works
Self-citation
The hippocampus and memory: insights from spatial processing
Bird, C. M., & Burgess, N. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2335 · Cited by 1,313 · see citing works
The ventral visual pathway: an expanded neural framework for the processing of object quality
Kravitz, D. J., Saleem, K. S., Baker, C. I., Ungerleider, L. G., & Mishkin, M. (2012) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2012.10.011 · Cited by 1,154 · see citing works
Imaging recollection and familiarity in the medial temporal lobe: a three-component model
Diana, R. A., Yonelinas, A. P., & Ranganath, C. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2007.08.001 · Cited by 1,154 · see citing works
Self-citation
The Molecular and Systems Biology of Memory
Kandel, E. R., Dudai, Y., & Mayford, M. R. (2014) · Cell · doi:10.1016/j.cell.2014.03.001 · Cited by 1,134 · 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
The anatomy of memory: an interactive overview of the parahippocampal–hippocampal network
van Strien, N. M., Cappaert, N. L. M., & Witter, M. P. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2614 · Cited by 1,041 · see citing works
Recognition memory and the medial temporal lobe: a new perspective
Squire, L. R., Wixted, J. T., & Clark, R. E. (2007) · Nature reviews. Neuroscience · doi:10.1038/nrn2154 · Cited by 1,013 · see citing works
Theta-gamma coupling increases during the learning of item-context associations
Tort, A. B. L., Komorowski, R. W., Manns, J. R., Kopell, N. J., & Eichenbaum, H. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0911331106 · Cited by 919 · see citing works
Self-citation
Prefrontal–hippocampal interactions in episodic memory
Eichenbaum, H. (2017) · Nature Reviews Neuroscience · doi:10.1038/nrn.2017.74 · Cited by 870 · see citing works
Self-citation
The role of the parahippocampal cortex in cognition
Aminoff, E., Kveraga, K., & Bar, M. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.06.009 · Cited by 855 · see citing works
Evidence for grid cells in a human memory network
Doeller, C. F., Barry, C., & Burgess, N. (2010) · Nature · doi:10.1038/nature08704 · Cited by 828 · 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
Sleep-dependent memory triage: evolving generalization through selective processing
Stickgold, R., & Walker, M. P. (2013) · Nature Neuroscience · doi:10.1038/nn.3303 · Cited by 755 · see citing works
Cognition in schizophrenia: core psychological and neural mechanisms
Barch, D. M., & Ceaser, A. E. (2011) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2011.11.015 · Cited by 752 · see citing works
The Cognitive Neuroscience of Human Memory Since H.M.
Squire, L. R., & Wixted, J. T. (2011) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-061010-113720 · Cited by 749 · 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
A model for memory systems based on processing modes rather than consciousness
Henke, K. (2010) · Nature reviews. Neuroscience · doi:10.1038/nrn2850 · Cited by 666 · 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
Self-citation
Source monitoring 15 years later: What have we learned from fMRI about the neural mechanisms of source memory?
Mitchell, K., & Johnson, M. K. (2009) · Psychological Bulletin · doi:10.1037/a0015849 · Cited by 656 · see citing works
The Restless Engram: Consolidations Never End
Dudai, Y. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062111-150500 · Cited by 644 · see citing works
Targeted enhancement of cortical-hippocampal brain networks and associative memory
Wang, J. X., Rogers, L. M., Gross, E. Z., Ryals, A. J., Dokucu, M. E., Brandstatt, K. L., Hermiller, M. S., & Voss, J. L. (2014) · Science · doi:10.1126/science.1252900 · Cited by 615 · see citing works
Memory retrieval and the parietal cortex: A review of evidence from a dual-process perspective
Vilberg, K. L., & Rugg, M. D. (2008) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2008.01.004 · Cited by 612 · 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
Nasal Respiration Entrains Human Limbic Oscillations and Modulates Cognitive Function
Zelano, C., Jiang, H., Zhou, G., Arora, N., Schuele, S., Rosenow, J., & Gottfried, J. A. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.2586-16.2016 · Cited by 599 · see citing works
Assessing rodent hippocampal involvement in the novel object recognition task. A review
Cohen, S. J., & Stackman, R. W. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.08.002 · Cited by 592 · see citing works
Sex differences in brain activation to emotional stimuli: A meta-analysis of neuroimaging studies
Stevens, J. S., & Hamann, S. (2012) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2012.03.011 · Cited by 588 · see citing works
Automated volumetry and regional thickness analysis of hippocampal subfields and medial temporal cortical structures in mild cognitive impairment
Yushkevich, P. A., Pluta, J. B., Wang, H., Xie, L., Ding, S., Gertje, E. C., Mancuso, L., Kliot, D., Das, S. R., & Wolk, D. A. (2014) · Human Brain Mapping · doi:10.1002/hbm.22627 · Cited by 587 · see citing works
Mapping the human brain's cortical-subcortical functional network organization
Ji, J. L., Spronk, M., Kulkarni, K. R., Repovš, G., Anticevic, A., & Cole, M. W. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.10.006 · Cited by 573 · see citing works
Recollection and familiarity: Examining controversial assumptions and new directions
Yonelinas, A. P., Aly, M., Wang, W., & Koen, J. D. (2010) · Hippocampus · doi:10.1002/hipo.20864 · Cited by 571 · see citing works
“For example, in a review of remember/know, source memory and ROC studies that included recollection and familiarity contrasts, 16 of 19 studies showed that the hippocampus was involved in recollection, whereas only two showed hippocampal involvement in familiarity (Eichenbaum et al., 2007).”
BackgroundMethodResultInfluentialSelf-citation
Object recognition memory: Neurobiological mechanisms of encoding, consolidation and retrieval
Winters, B. D., Saksida, L. M., & Bussey, T. J. (2008) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2008.04.004 · Cited by 568 · see citing works
Memory Transformation and Systems Consolidation
Winocur, G., & Moscovitch, M. (2011) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617711000683 · Cited by 557 · see citing works
Identifying the brain's most globally connected regions
Cole, M. W., Pathak, S., & Schneider, W. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.11.001 · Cited by 557 · see citing works
Hippocampal-Neocortical Interactions in Memory Formation, Consolidation, and Reconsolidation
Wang, S., & Morris, R. (2009) · Annual Review of Psychology · doi:10.1146/annurev.psych.093008.100523 · Cited by 536 · see citing works
Memory enhancement induced by hypothalamic/fornix deep brain stimulation
Hamani, C., McAndrews, M. P., Cohn, M., Oh, M. Y., Zumsteg, D., Shapiro, C. M., Wennberg, R. A., & Lozano, A. M. (2008) · Annals of Neurology · doi:10.1002/ana.21295 · Cited by 530 · see citing works
Frontal midline theta oscillations during working memory maintenance and episodic encoding and retrieval
Hsieh, L.-T., & Ranganath, C. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2013.08.003 · Cited by 525 · see citing works
Self-citation
Episodic memory retrieval, parietal cortex, and the default mode network: functional and topographic analyses
Sestieri, C., Corbetta, M., Romani, G. L., & Shulman, G. L. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.3335-10.2011 · Cited by 523 · see citing works
On the Integration of Space, Time, and Memory
Eichenbaum, H. (2017) · Neuron · doi:10.1016/j.neuron.2017.06.036 · Cited by 512 · see citing works
Self-citation
Distinct Cortical Anatomy Linked to Subregions of the Medial Temporal Lobe Revealed by Intrinsic Functional Connectivity
Kahn, I., Andrews‐Hanna, J. R., Vincent, J. L., Snyder, A. Z., & Buckner, R. L. (2008) · Journal of Neurophysiology · doi:10.1152/jn.00077.2008 · Cited by 490 · 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
Memory formation and long-term retention in humans and animals: Convergence towards a transformation account of hippocampal–neocortical interactions
Winocur, G., Moscovitch, M., & Bontempi, B. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.04.016 · Cited by 486 · 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
Self-citation
A contextual binding theory of episodic memory: systems consolidation reconsidered
Yonelinas, A. P., Ranganath, C., Ekstrom, A. D., & Wiltgen, B. J. (2019) · Nature reviews. Neuroscience · doi:10.1038/s41583-019-0150-4 · Cited by 447 · see citing works
Self-citation
The role of the hippocampus in navigation is memory
Eichenbaum, H. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00005.2017 · Cited by 430 · see citing works
Self-citation
Functional correlates of the lateral and medial entorhinal cortex: objects, path integration and local-global reference frames
Knierim, J. J., Neunuebel, J. P., & Deshmukh, S. S. (2014) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0369 · Cited by 425 · see citing works
What Does the Anatomical Organization of the Entorhinal Cortex Tell Us?
Canto, C. B., Wouterlood, F. G., & Witter, M. P. (2008) · Neural Plasticity · doi:10.1155/2008/381243 · Cited by 418 · 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
Gradual changes in hippocampal activity support remembering the order of events
Manns, J. R., Howard, M. W., & Eichenbaum, H. (2007) · Neuron · doi:10.1016/j.neuron.2007.08.017 · Cited by 397 · see citing works
Self-citation
Vascular hippocampal plasticity after aerobic exercise in older adults.
Maass, A., Düzel, S., Goerke, M., Becke, A., Sobieray, U., Neumann, K., Lövden, M., Lindenberger, U., Bäckman, L., Braun-Dullaeus, R., et al. (2015) · Molecular Psychiatry · doi:10.1038/mp.2014.114 · Cited by 382 · see citing works
Modulation of aesthetic value by semantic context: An fMRI study
Kirk, U., Skov, M., Hulme, O., Christensen, M. S., & Zeki, S. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2008.10.009 · Cited by 381 · see citing works
A unified framework for the functional organization of the medial temporal lobes and the phenomenology of episodic memory
Ranganath, C. (2010) · Hippocampus · doi:10.1002/hipo.20852 · Cited by 375 · see citing works
Self-citation
Going beyond LTM in the MTL: A synthesis of neuropsychological and neuroimaging findings on the role of the medial temporal lobe in memory and perception
Graham, K. S., Barense, M. D., & Lee, A. C. H. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.01.001 · Cited by 374 · see citing works
Hippocampal Representation of Related and Opposing Memories Develop within Distinct, Hierarchically Organized Neural Schemas
McKenzie, S., Frank, A. J., Kinsky, N. R., Porter, B., Rivière, P. D., & Eichenbaum, H. (2014) · Neuron · doi:10.1016/j.neuron.2014.05.019 · Cited by 373 · see citing works
Self-citation
The hippocampal indexing theory and episodic memory: Updating the index
Teyler, T. J., & Rudy, J. W. (2007) · Hippocampus · doi:10.1002/hipo.20350 · Cited by 373 · see citing works
Robust Conjunctive Item–Place Coding by Hippocampal Neurons Parallels Learning What Happens Where
Komorowski, R. W., Manns, J. R., & Eichenbaum, H. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.1378-09.2009 · Cited by 372 · see citing works
Self-citation
Oscillations and Episodic Memory: Addressing the Synchronization/Desynchronization Conundrum
Hanslmayr, S., Staresina, B. P., & Bowman, H. (2016) · Trends in Neurosciences · doi:10.1016/j.tins.2015.11.004 · Cited by 364 · see citing works
Generalization through the recurrent interaction of episodic memories: A model of the hippocampal system.
Kumaran, D., & McClelland, J. L. (2012) · Psychological Review · doi:10.1037/a0028681 · Cited by 358 · see citing works
Towards a functional organization of episodic memory in the medial temporal lobe
Eichenbaum, H., Sauvage, M., Fortin, N., Komorowski, R., & Lipton, P. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2011.07.006 · Cited by 354 · see citing works
Self-citation
The Eyes Have It: Hippocampal Activity Predicts Expression of Memory in Eye Movements
Hannula, D. E., & Ranganath, C. (2009) · Neuron · doi:10.1016/j.neuron.2009.08.025 · Cited by 352 · see citing works
Self-citation
The evolution of episodic memory
Allen, T. A., & Fortin, N. J. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1301199110 · Cited by 350 · see citing works
Hippocampal Activity Patterns Carry Information about Objects in Temporal Context
Hsieh, L., Gruber, M. J., Jenkins, L. J., & Ranganath, C. (2014) · Neuron · doi:10.1016/j.neuron.2014.01.015 · Cited by 347 · see citing works
Self-citation
Opposing Mechanisms Support the Voluntary Forgetting of Unwanted Memories
Benoit, R. G., & Anderson, M. C. (2012) · Neuron · doi:10.1016/j.neuron.2012.07.025 · Cited by 339 · see citing works
Working Memory in the Prefrontal Cortex
Funahashi, S. (2017) · Brain Sciences · doi:10.3390/brainsci7050049 · Cited by 339 · see citing works
CA1 pyramidal cell diversity enabling parallel information processing in the hippocampus
Soltesz, I., & Losonczy, A. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0118-0 · Cited by 333 · see citing works
Can physical exercise in old age improve memory and hippocampal function?
Duzel, E., van Praag, H., & Sendtner, M. (2016) · Brain · doi:10.1093/brain/awv407 · Cited by 329 · see citing works
Relational memory and the hippocampus: Representations and methods
Konkel, A. (2009) · Frontiers in Neuroscience · doi:10.3389/neuro.01.023.2009 · Cited by 329 · see citing works
How the hippocampus preserves order: the role of prediction and context
Davachi, L., & DuBrow, S. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2014.12.004 · Cited by 328 · see citing works
The hippocampus supports high-resolution binding in the service of perception, working memory and long-term memory
Yonelinas, A. P. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.05.030 · Cited by 328 · see citing works
Self-citation
The rodent hippocampus is essential for nonspatial object memory
Cohen, S. J., Munchow, A. H., Rios, L. M., Zhang, G., Ásgeirsdóttir, H. N., & Stackman, R. W. (2013) · Current Biology · doi:10.1016/j.cub.2013.07.002 · Cited by 325 · see citing works
CA1 neurons in the human hippocampus are critical for autobiographical memory, mental time travel, and autonoetic consciousness
Bartsch, T., Döhring, J., Rohr, A., Jansen, O., & Deuschl, G. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1110266108 · Cited by 325 · see citing works
The slow forgetting of emotional episodic memories: an emotional binding account
Yonelinas, A. P., & Ritchey, M. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.02.009 · Cited by 322 · see citing works
Self-citation
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
The Necessity of the Medial Temporal Lobe for Statistical Learning
Schapiro, A. C., Gregory, E., Landau, B., McCloskey, M. E., & Turk‐Browne, N. B. (2014) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00578 · Cited by 315 · see citing works
Memory and Space: Towards an Understanding of the Cognitive Map
Schiller, D., Eichenbaum, H., Buffalo, E. A., Davachi, L., Foster, D. J., Leutgeb, S., & Ranganath, C. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.2618-15.2015 · Cited by 315 · see citing works
Self-citation
Effects of aging on the neural correlates of successful item and source memory encoding.
Dennis, N. A., Hayes, S. M., Prince, S. E., Madden, D. J., Huettel, S. A., & Cabeza, R. E. L. (2008) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/0278-7393.34.4.791 · Cited by 314 · 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
“Within the hippocampal formation (HPC), the perirhinal cortex (PRh) is thought to be crucial in signaling familiarity-based ‘‘what’’ information, whereas the parahippocampal cortex (PH) is involved in processing ‘‘where’’ events occur (Eichenbaum et al., 2007; Ranganath, 2010).”
Background
Contributions of episodic retrieval and mentalizing to autobiographical thought: evidence from functional neuroimaging, resting-state connectivity, and fMRI meta-analyses
Andrews-Hanna, J. R., Saxe, R., & Yarkoni, T. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.01.032 · Cited by 313 · see citing works
Neural changes underlying the development of episodic memory during middle childhood
Ghetti, S., & Bunge, S. A. (2012) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2012.05.002 · Cited by 312 · 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
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
Lateralized human hippocampal activity predicts navigation based on sequence or place memory
Iglói, K., Doeller, C. F., Berthoz, A., Rondi‐Reig, L., & Burgess, N. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1004243107 · Cited by 299 · see citing works
Medial temporal lobe connectivity and its associations with cognition in early Alzheimer’s disease
Berron, D., van Westen, D., Ossenkoppele, R., Strandberg, O. T., & Hansson, O. (2020) · Brain · doi:10.1093/brain/awaa068 · Cited by 298 · see citing works
A disproportionate role for the fornix and mammillary bodies in recall versus recognition memory
Tsivilis, D., Vann, S. D., Denby, C. E., Roberts, N., Mayes, A. R., Montaldi, D., & Aggleton, J. P. (2008) · Nature Neuroscience · doi:10.1038/nn.2149 · Cited by 297 · 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
Differential Connectivity of Perirhinal and Parahippocampal Cortices within Human Hippocampal Subregions Revealed by High-Resolution Functional Imaging
Libby, L. A., Ekstrom, A. D., Ragland, J. D., & Ranganath, C. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.3711-11.2012 · Cited by 296 · see citing works
Self-citation
The contribution of the human posterior parietal cortex to episodic memory
Sestieri, C., Shulman, G. L., & Corbetta, M. (2017) · Nature reviews. Neuroscience · doi:10.1038/nrn.2017.6 · Cited by 294 · see citing works
fMRI studies of successful emotional memory encoding: A quantitative meta-analysis
Murty, V. P., Ritchey, M., Adcock, R. A., & LaBar, K. S. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.07.030 · Cited by 293 · see citing works
Distinct Neural Circuits for the Formation and Retrieval of Episodic Memories
Roy, D. S., 北村, 貴., Okuyama, T., Ogawa, S. K., Sun, C., Obata, Y., Yoshiki, A., & Tonegawa, S. (2017) · Cell · doi:10.1016/j.cell.2017.07.013 · Cited by 293 · see citing works
A Hippocampal Marker of Recollection Memory Ability among Healthy Young Adults: Contributions of Posterior and Anterior Segments
Poppenk, J., & Moscovitch, M. (2011) · Neuron · doi:10.1016/j.neuron.2011.10.014 · Cited by 292 · see citing works
Evidence for holistic episodic recollection via hippocampal pattern completion
Horner, A. J., Bisby, J. A., Bush, D., Lin, W., & Burgess, N. (2015) · Nature Communications · doi:10.1038/ncomms8462 · Cited by 290 · see citing works
The hippocampal-striatal axis in learning, prediction and goal-directed behavior
Pennartz, C. M. A., Ito, R., Verschure, P. F. M. J., Battaglia, F. P., & Robbins, T. W. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2011.08.001 · Cited by 287 · see citing works
The Effects of Healthy Aging, Amnestic Mild Cognitive Impairment, and Alzheimer’s Disease on Recollection and Familiarity: A Meta-Analytic Review
Koen, J. D., & Yonelinas, A. P. (2014) · Neuropsychology Review · doi:10.1007/s11065-014-9266-5 · Cited by 283 · see citing works
Self-citation
Perirhinal Cortex Supports Encoding and Familiarity-Based Recognition of Novel Associations
Haskins, A., Yonelinas, A. P., Quamme, J. R., & Ranganath, C. (2008) · Neuron · doi:10.1016/j.neuron.2008.07.035 · Cited by 281 · see citing works
Self-citation
Medial Temporal Lobe Activity Predicts Successful Relational Memory Binding
Hannula, D. E., & Ranganath, C. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.3086-07.2008 · Cited by 280 · see citing works
Self-citation
Map Making: Constructing, Combining, and Inferring on Abstract Cognitive Maps
Park, S. A., Miller, D. S., Nili, H., Ranganath, C., & Boorman, E. D. (2020) · Neuron · doi:10.1016/j.neuron.2020.06.030 · Cited by 277 · see citing works
Self-citation
Egocentric coding of external items in the lateral entorhinal cortex
Wang, C., Chen, X., Lee, H., Deshmukh, S. S., Yoganarasimha, D., Savelli, F., & Knierim, J. J. (2018) · Science · doi:10.1126/science.aau4940 · Cited by 276 · see citing works
Mind the Gap: Binding Experiences across Space and Time in the Human Hippocampus
Staresina, B. P., & Davachi, L. (2009) · Neuron · doi:10.1016/j.neuron.2009.06.024 · Cited by 273 · see citing works
The parahippocampal gyrus links the default‐mode cortical network with the medial temporal lobe memory system
Ward, A. M., Schultz, A. P., Huijbers, W., Dijk, K. R. A. V., Hedden, T., & Sperling, R. A. (2013) · Human Brain Mapping · doi:10.1002/hbm.22234 · Cited by 271 · see citing works

Dissociable correlates of recollection and familiarity within the medial temporal lobes
Ranganath, C., Yonelinas, A. P., Cohen, M. X., Dy, C. J., Tom, S. M., & D’Esposito, M. (2004) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2003.07.006 · Cited by 689 · see citing works
Self-citation
Imaging recollection and familiarity in the medial temporal lobe: a three-component model
Diana, R. A., Yonelinas, A. P., & Ranganath, C. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2007.08.001 · Cited by 1,154 · see citing works
Self-citation
within the medial temporal lobes
Charan Ranganath, A., A, A. P. Y., Cohen, M. X., B, C. J. D., Tom, S. M., & Mark D’esposito, B. (2003)
Recognition memory and the medial temporal lobe: a new perspective
Squire, L. R., Wixted, J. T., & Clark, R. E. (2007) · Nature reviews. Neuroscience · doi:10.1038/nrn2154 · Cited by 1,013 · see citing works
Tangled Up in Confounds - Unravelling the Controversial Roles of MTL-structures in Familiarity and Recollection
Marzolla, M. C. (2018) · Cited by 1 · see citing works

Authors: Eichenbaum, H., Yonelinas, A. P., & Ranganath, C.
Affiliations: Boston University (US)
University of California, Davis (US)
Department of Psychology, University of California, Davis, California 95616;,
ORCID: Eichenbaum, H.
Yonelinas, A.P.
Venue: Annual Review of Neuroscience
Publisher: Annual Reviews
Published: 2007-07-01
Volume: 30
Issue: 1
Pages: 123-152
ISSN: 0147-006X (ISSN-L)
1545-4126
DOI: 10.1146/annurev.neuro.30.051606.094328
PMC: PMC2064941
OpenAlex: W2170972933
Semantic Scholar: 9d620ada4eec7c2732dc3b390cc95adc3d39387c
Cited by: 2,580
References: 169
Citations by year: 2026: 73 · 2025: 122 · 2024: 108 · 2023: 102 · 2022: 105 · 2021: 123 · 2020: 150 · 2019: 147 · 2018: 148 · 2017: 165 · 2016: 141 · 2015: 136 · 2014: 149 · 2013: 185 · 2012: 173
FWCI: 9.69
Type: journal article
Language: en
Open access: green
www.ncbi.nlm.nih.gov
Locations: Annual Review of Neuroscience (publishedVersion)
PubMed (publishedVersion)
Europe PMC (PubMed Central) (acceptedVersion)
PubMed Central (acceptedVersion)
Funders: National Institute of Mental Health (MH-71702, MH67821, MH059352, MH51570, R01MH051570, MH 52090, R01MH083734, P50MH071702, R01MH059352, R01MH052090)
National Institute of Neurological Disorders and Stroke (NS40813, P01NS040813)
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: medial temporal lobe, recognition memory, recollection, familiarity, hippocampus, parahippocampal cortex, perirhinal cortex, contextual memory, spatial memory, memory retrieval
MeSH terms: Animals, Evoked Potentials, Hippocampus, Humans, Memory, Models, Neurological, Neural Pathways, Temporal Lobe, Parahippocampal Gyrus, Recognition, Psychology, Models, Animal

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

The Medial Temporal Lobe and Recognition Memory

Abstract

Integrity signals

Claims the paper makes

Claims other papers make about this one

Cites

Cited by

Related

Record

About these checks