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

The DOI matches its Crossref record; 179 of the 179 references it cites were found in a registry or an index.

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 Cognitive neurosciences
(2005) · Choice Reviews Online · doi:10.5860/choice.43-0626 · Cited by 4,726
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
Self-citation
A process dissociation framework: Separating automatic from intentional uses of memory
Jacoby, L. L. (1991) · Journal of Memory and Language · doi:10.1016/0749-596x(91)90025-f · Cited by 3,817
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
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
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
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
How many memory systems are there?
Tulving, E. (1985) · American Psychologist · doi:10.1037/0003-066x.40.4.385 · Cited by 1,909
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
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

Show all 169 references

Research works printed but not linked: 5

10.1037//0735-7044.107.5.715 · DOI
Squire LR, 1994, Memory Systems, 203
10.1037//0003-066X.40.4.385 · DOI · Paper page
Weis S, 2004, Neuroreport, 15, 2729
10.1037//0894-4105.12.3.323 · DOI

Sorted by citations

Items 701–800 of 1,017

Early Exposure to Volatile Anesthetics Impairs Long-Term Associative Learning and Recognition Memory
Lee, B. H., Chan, J. T., Hazarika, O. D., Vutskits, L., & Sall, J. W. (2014) · PLoS ONE · doi:10.1371/journal.pone.0105340 · Cited by 53
Preserved and Impaired Emotional Memory in Alzheimer’s Disease
Klein-Koerkamp, Y., Baciu, M., & Hot, P. (2012) · Frontiers in Psychology · doi:10.3389/fpsyg.2012.00331 · Cited by 55
Aberrant resting-state connectivity in non-psychotic individuals with auditory hallucinations
Diederen, K. M. J., Neggers, S. F. W., de Weijer, A. D., van Lutterveld, R., Daalman, K., Eickhoff, S. B., Clos, M., Kahn, R. S., & Sommer, I. E. (2012) · Psychological Medicine · doi:10.1017/s0033291712002541 · Cited by 53
Representation of memories in the cortical–hippocampal system: Results from the application of population similarity analyses
McKenzie, S., Keene, C. S., Farovik, A., Bladon, J. H., Place, R., Komorowski, R. W., & Eichenbaum, H. (2015) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2015.12.008 · Cited by 57
Self-citation
Distinguishing the precision of spatial recollection from its success: Evidence from healthy aging and unilateral mesial temporal lobe resection
Nilakantan, A. S., Bridge, D. J., VanHaerents, S. A., & Voss, J. L. (2018) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2018.07.035 · Cited by 53
Neural correlates of the Dunning–Kruger effect
Muller, A., Sirianni, L. A., & Addante, R. J. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14935 · Cited by 60
Prior knowledge promotes hippocampal separation but cortical assimilation in the left inferior frontal gyrus
Bein, O., Reggev, N., & Maril, A. (2020) · Nature Communications · doi:10.1038/s41467-020-18364-1 · Cited by 52
Cued memory decline in biomarker-defined preclinical Alzheimer disease
Papp, K. V., Rentz, D. M., Mormino, E. C., Schultz, A. P., Amariglio, R. E., Quiroz, Y., Johnson, K. A., & Sperling, R. A. (2017) · Neurology · doi:10.1212/wnl.0000000000003812 · Cited by 52
Dissociating distinct cortical networks associated with subregions of the human medial temporal lobe using precision neuroimaging
Reznik, D., Trampel, R., Weiskopf, N., Witter, M. P., & Doeller, C. F. (2023) · Neuron · doi:10.1016/j.neuron.2023.05.029 · Cited by 52
Local Functional Connectivity as a Pre-Surgical Tool for Seizure Focus Identification in Non-Lesion, Focal Epilepsy
Weaver, K. E., Chaovalitwongse, W. A., Novotny, E. J., Poliakov, A. V., Grabowski, T. J., & Ojemann, J. G. (2013) · Frontiers in Neurology · doi:10.3389/fneur.2013.00043 · Cited by 52
Selective familiarity deficits after left anterior temporal-lobe removal with hippocampal sparing are material specific
Martin, C. B., Bowles, B., Mirsattari, S. M., & Köhler, S. (2011) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2011.03.012 · Cited by 55
Differential effects of normal aging on recollection of concrete and abstract words.
Peters, J., & Daum, I. (2008) · Neuropsychology · doi:10.1037/0894-4105.22.2.255 · Cited by 52
Task-Selective Memory Effects for Successfully Implemented Encoding Strategies
Leshikar, E. D., Duarte, A., & Hertzog, C. K. (2012) · PLoS ONE · doi:10.1371/journal.pone.0038160 · Cited by 52
COMT Val108/158 Met Genotype Affects Neural but not Cognitive Processing in Healthy Individuals
Dennis, N. A., Need, A. C., LaBar, K. S., Waters, S., Cirulli, E. T., Kragel, J. E., Goldstein, D. B., & Cabeza, R. E. L. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp132 · Cited by 53
Spatial learning‐induced increase in agmatine levels at hippocampal CA1 synapses
Leitch, B., Shevtsova, O., Reusch, K., Bergin, D. H., & Liu, P. (2010) · Synapse · doi:10.1002/syn.20828 · Cited by 52
Age- and performance-related differences in hippocampal contributions to episodic retrieval
Sastre, M., Wendelken, C., Lee, J. K., Bunge, S. A., & Ghetti, S. (2016) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2016.01.003 · Cited by 52
Cognitive control and episodic memory in adolescents with autism spectrum disorders
Solomon, M., McCauley, J. B., Iosif, A., Carter, C. S., & Ragland, J. D. (2016) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2016.05.013 · Cited by 56
Pre-stimulus thalamic theta power predicts human memory formation
Sweeney‐Reed, C. M., Zaehle, T., Voges, J., Schmitt, F. C., Buentjen, L., Kopitzki, K., Richardson‐Klavehn, A., Hinrichs, H., Heinze, H., Knight, R. T., et al. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.05.042 · Cited by 57
Coding of Object Size and Object Category in Human Visual Cortex
Julian, J. B., Ryan, J., & Epstein, R. A. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw150 · Cited by 54
Scene-selective coding by single neurons in the human parahippocampal cortex
Mormann, F., Kornblith, S., Cerf, M., Ison, M. J., Kraskov, A., Tran, M., Knieling, S., Quiroga, R. Q., Koch, C., & Fried, I. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1608159113 · Cited by 54
From the Cover: 2.45-GHz Microwave Radiation Impairs Hippocampal Learning and Spatial Memory: Involvement of Local Stress Mechanism-Induced Suppression of iGluR/ERK/CREB Signaling
Shahin, S., Banerjee, S., Swarup, V., Singh, S. P., & Chaturvedi, C. M. (2017) · Toxicological Sciences · doi:10.1093/toxsci/kfx221 · Cited by 52
Large-scale network integration in the human brain tracks temporal fluctuations in memory encoding performance
Keerativittayayut, R., Aoki, R., Sarabi, M. T., Jimura, K., & Nakahara, K. (2018) · eLife · doi:10.7554/elife.32696 · Cited by 54
United we fall: All-or-none forgetting of complex episodic events.
Joensen, B. H., Gaskell, M. G., & Horner, A. J. (2019) · Journal of Experimental Psychology General · doi:10.1037/xge0000648 · Cited by 55
The effects of aging on material-independent and material-dependent neural correlates of contextual binding
Dulas, M. R., & Duarte, A. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.05.036 · Cited by 52
Visual perception and memory systems: from cortex to medial temporal lobe
Khan, Z. U., Martín‐Montañez, E., & Baxter, M. G. (2011) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-011-0641-6 · Cited by 53
Reduced prefrontal activation during working and long‐term memory tasks and impaired patient‐reported cognition among cancer survivors postchemotherapy compared with healthy controls
Wang, L., Apple, A. C., Schroeder, M. P., Ryals, A. J., Voss, J. L., Gitelman, D. R., Sweet, J. J., Butt, Z. A., Cella, D. F., & Wagner, L. I. (2015) · Cancer · doi:10.1002/cncr.29737 · Cited by 53
Hippocampus at 25
Eichenbaum, H., Amaral, D. G., Buffalo, E. A., Buzsáki, G., Cohen, N. J., Davachi, L., Frank, L. M., Heckers, S., Morris, R., Moser, E. I., et al. (2016) · Hippocampus · doi:10.1002/hipo.22616 · Cited by 55
Self-citation
From learning to forgetting: Behavioral, circuitry, and molecular properties define the different functional states of the recognition memory trace
Romero‐Granados, R., Fontán‐Lozano, Á., Delgado-Garcia, J. M., & Carrión, Á. M. (2009) · Hippocampus · doi:10.1002/hipo.20669 · Cited by 54
Roles of human hippocampal subfields in retrieval of spatial and temporal context
Kyle, C. T., Smuda, D. N., Hassan, A. S., & Ekstrom, A. D. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.10.034 · Cited by 54
Sexually dimorphic alterations in locomotion and reversal learning after adolescent tetrahydrocannabinol exposure in the rat
Harte, L. C., & Dow-Edwards, D. (2010) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2010.05.001 · Cited by 51
Functional independence within the self-memory system: New insights from two cases of developmental amnesia
Picard, L., Mayor-Dubois, C., Maeder, P. P., Kalenzaga, S., Abram, M., Duval, C., Eustache, F., Roulet‐Perez, E., & Piolino, P. (2012) · Cortex · doi:10.1016/j.cortex.2012.10.003 · Cited by 54
A demonstration that the hippocampus supports both recollection and familiarity
Kirwan, C. B., Wixted, J. T., & Squire, L. R. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0912543107 · Cited by 54
Double dissociation between familiarity and recollection in Parkinson's disease as a function of encoding tasks
Cohn, M., Moscovitch, M., & Davidson, P. S. R. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.10.013 · Cited by 51
Monkeys Recall and Reproduce Simple Shapes from Memory
Basile, B. M., & Hampton, R. R. (2011) · Current Biology · doi:10.1016/j.cub.2011.03.044 · Cited by 52
The Role of Relational Binding in Item Memory: Evidence from Face Recognition in a Case of Developmental Amnesia
Olsen, R. K., Lee, Y., Kube, J., Rosenbaum, R. S., Grady, C. L., Moscovitch, M., & Ryan, J. D. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3987-14.2015 · Cited by 57
Hippocampal activity during recognition memory co‐varies with the accuracy and confidence of source memory judgments
Yu, S. S., Johnson, J. D., & Rugg, M. D. (2011) · Hippocampus · doi:10.1002/hipo.20982 · Cited by 51
Differential effects of white noise in cognitive and perceptual tasks
Herweg, N. A., & Bunzeck, N. (2015) · Frontiers in Psychology · doi:10.3389/fpsyg.2015.01639 · Cited by 51
Distinct Medial Temporal Lobe Network States as Neural Contexts for Motivated Memory Formation
Murty, V. P., & Adcock, R. A. (2017) · Springer eBooks · doi:10.1007/978-3-319-50406-3_15 · Cited by 55
Acute stress throughout the memory cycle: Diverging effects on associative and item memory.
Goldfarb, E. V., Tompary, A., Davachi, L., & Phelps, E. A. (2018) · Journal of Experimental Psychology General · doi:10.1037/xge0000472 · Cited by 54
Progression from Feature-Specific Brain Activity to Hippocampal Binding during Episodic Encoding
Cooper, R. A., & Ritchey, M. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.1971-19.2019 · Cited by 56
Alpha Rhythms Reveal When and Where Item and Associative Memories Are Retrieved
Martín-Buro, M. C., Wimber, M., Henson, R. N., & Staresina, B. P. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1982-19.2020 · Cited by 53
Neural Development of Memory and Metamemory in Childhood and Adolescence: Toward an Integrative Model of the Development of Episodic Recollection
Ghetti, S., & Fandakova, Y. (2020) · Annual Review of Developmental Psychology · doi:10.1146/annurev-devpsych-060320-085634 · Cited by 51
Declarative Memory
Davachi, L., & Dobbins, I. G. (2008) · Current Directions in Psychological Science · doi:10.1111/j.1467-8721.2008.00559.x · Cited by 55
Superadditive memory strength for item and source recognition: The role of hierarchical relational binding in the medial temporal lobe.
Shimamura, A. P., & Wickens, T. D. (2009) · Psychological Review · doi:10.1037/a0014500 · Cited by 55
Mnemonic prediction errors promote detailed memoriesPreprint
Bein, O., Plotkin, N. A., & Davachi, L. (2021) · Learning & Memory · doi:10.1101/lm.053410.121 · Cited by 54
The nature of recollection in behavior and the brain
Slotnick, S. D. (2013) · Neuroreport · doi:10.1097/wnr.0b013e328362e47e · Cited by 50
Establishment of Emotional Memories Is Mediated by Vagal Nerve Activation: Evidence from Noninvasive taVNS
Ventura‐Bort, C., Wirkner, J., Wendt, J., Hamm, A. O., & Weymar, M. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.2329-20.2021 · Cited by 54
Episodic Recollection Difficulties in ASD Result from Atypical Relational Encoding: Behavioral and Neural Evidence
Gaigg, S., Bowler, D., Ecker, C., Calvo‐Merino, B., & Murphy, D. (2015) · Autism Research · doi:10.1002/aur.1448 · Cited by 62
ERPs and Neural Oscillations during Volitional Suppression of Memory Retrieval
Depue, B. E., Ketz, N., Mollison, M. V., Nyhus, E., Banich, M. T., & Curran, T. (2013) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00418 · Cited by 50
Differential Contributions of Executive and Episodic Memory Functions to Problem Solving in Younger and Older Adults
Vandermorris, S., Sheldon, S., Winocur, G., & Moscovitch, M. (2013) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617713000982 · Cited by 57
Comparison of Associative Learning-Related Signals in the Macaque Perirhinal Cortex and Hippocampus
Yanike, M., Wirth, S., Smith, A. C., Brown, E. N., & SUZUKI, W. A. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhn156 · Cited by 51
Memory Retrieval in Mice and MenPreprint
Ben-Yakov, A., Dudai, Y., & Mayford, M. R. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a021790 · Cited by 54
Spatial and stimulus-type tuning in the LEC, MEC, POR, PrC, CA1, and CA3 during spontaneous item recognition memory: Spatial and Stimulus-Type Tunings in Recognition Memory
Beer, Z., Chwiesko, C., Kitsukawa, T., & Sauvage, M. M. (2013) · Hippocampus · doi:10.1002/hipo.22195 · Cited by 49
Neural stem cell apoptosis after low‐methylmercury exposures in postnatal hippocampus produce persistent cell loss and adolescent memory deficits
Sokolowski, K., Obiorah, M., Robinson, K. R., McCandlish, E. F., Buckley, B., & DiCicco-Bloom, E. M. (2013) · Developmental Neurobiology · doi:10.1002/dneu.22119 · Cited by 50
Imaging genetics of cognitive functions: Focus on episodic memory
Rasch, B., Papassotiropoulos, A., & de Quervain, D. J. ‐. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.01.001 · Cited by 51
Differential age effects for implicit and explicit conceptual associative memory.
Dew, I. T. Z., & Giovanello, K. S. (2010) · Psychology and Aging · doi:10.1037/a0019940 · Cited by 49
Recollective performance advantages for implicit memory tasks
Sheldon, S., & Moscovitch, M. (2010) · Memory · doi:10.1080/09658211.2010.499876 · Cited by 49
Neural evidence for a 3-state model of visual short-term memory
Nee, D. E., & Jonides, J. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.02.019 · Cited by 52
The entorhinal cortex and neurotrophin signaling in Alzheimer’s disease and other disorders
Scharfman, H. E., & Chao, M. V. (2013) · Cognitive Neuroscience · doi:10.1080/17588928.2013.826184 · Cited by 52
Damage to the lateral prefrontal cortex impairs familiarity but not recollection
Aly, M., Yonelinas, A. P., Kishiyama, M. M., & Knight, R. T. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.07.043 · Cited by 49
Self-citation
Adaptation to cognitive context and item information in the medial temporal lobes
Diana, R. A., Yonelinas, A. P., & Ranganath, C. (2012) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2012.07.035 · Cited by 49
Self-citation
Neurobiological Aspects of Face Recognition: The Role of Oxytocin
Lopatina, O. L., Komleva, Y. K., Gorina, Y. V., Higashida, H., & Salmina, A. B. (2018) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2018.00195 · Cited by 53
Recognition memory: Adding a response deadline eliminates recollection but spares familiarityPreprint
Sauvage, M. M., Beer, Z., & Eichenbaum, H. (2010) · Learning & Memory · doi:10.1101/lm.1647710 · Cited by 50
Self-citation
A High‐resolution study of hippocampal and medial temporal lobe correlates of spatial context and prospective overlapping route memory
Brown, T. I., Hasselmo, M. E., & Stern, C. E. (2014) · Hippocampus · doi:10.1002/hipo.22273 · Cited by 51
The object pattern separation (OPS) task: A behavioral paradigm derived from the object recognition task
van Hagen, B. T. J., van Goethem, N. P., Lagatta, D. C., & Prickaerts, J. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.10.041 · Cited by 48
Effects of cannabinoid CB1 receptor antagonist rimonabant in consolidation and reconsolidation of methamphetamine reward memory in mice
Yu, L., Wang, X., Zhao, M., Liu, Y., Li, Y., Li, F.-Q., Wang, X., Xue, Y.-X., & Lü, L. (2009) · Psychopharmacology · doi:10.1007/s00213-008-1450-y · Cited by 48
Cognitive Neuroscience of Memory
Slotnick, S. D. (2017) · Cambridge University Press eBooks · doi:10.1017/9781316026687 · Cited by 49
Dissociable medial temporal pathways for encoding emotional item and context information
Ritchey, M., Wang, S.-F., Yonelinas, A. P., & Ranganath, C. (2018) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2018.12.015 · Cited by 49
Self-citation
Working Memory in Alzheimer’s Disease and Parkinson’s Disease
Zokaei, N., & Husain, M. (2019) · Current topics in behavioral neurosciences · doi:10.1007/7854_2019_103 · Cited by 52
Anatomy and White Matter Connections of the Parahippocampal Gyrus
Lin, Y., Dhanaraj, V., Mackenzie, A., Young, I. M., Tanglay, O., Briggs, R. G., Chakraborty, A. R., Hormovas, J., Fonseka, R. D., Kim, S. J., et al. (2021) · World Neurosurgery · doi:10.1016/j.wneu.2020.12.136 · Cited by 50
Brain‐derived neurotrophic factor val66met polymorphism and hippocampal activation during episodic encoding and retrieval tasks
Dennis, N. A., Cabeza, R. E. L., Need, A. C., Waters, S., Goldstein, D. B., & LaBar, K. S. (2010) · Hippocampus · doi:10.1002/hipo.20809 · Cited by 48
Cognitive Neuroscience Perspectives on Motivation and Learning: Revisiting Self‐Determination Theory
Luria, E., Shalom, M., & Levy, D. A. (2020) · Mind Brain and Education · doi:10.1111/mbe.12275 · Cited by 62
Intrinsic brain indices of verbal working memory capacity in children and adolescents
Yang, Z., Jutagir, D. R., Koyama, M. S., Craddock, R. C., Yan, C., Shehzad, Z. E., Castellanos, F. X., Martino, A. D., & Milham, M. P. (2015) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2015.07.007 · Cited by 47
Modulation of encoding and retrieval by recollection and familiarity: Mapping the medial temporal lobe networks
de Vanssay-Maigne, A., Noulhiane, M., Devauchelle, A.-D., Rodrigo, S., Baudoin‐Chial, S., Meder, J. F., Oppenheim, C., Chiron, C., & Chassoux, F. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.06.086 · Cited by 57
Cholinergic modulation of hippocampal CA1 basal-dendritic long-term potentiation
Doralp, S., & Leung, L.-W. S. (2008) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2008.05.013 · Cited by 47
Dissecting medial temporal lobe contributions to item and associative memory formation
Qin, S., Rijpkema, M., Tendolkar, I., Piekema, C., Hermans, E. J., Binder, M., Petersson, K. M., Luo, J., & Fernández, G. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.02.039 · Cited by 49
Multivariate pattern analysis of the human medial temporal lobe revealed representationally categorical cortex and representationally agnostic hippocampus
Huffman, D. J., & Stark, C. E. L. (2014) · Hippocampus · doi:10.1002/hipo.22321 · Cited by 51
Parahippocampal cortex activation during context reinstatement predicts item recollection.
Diana, R. A., Yonelinas, A. P., & Ranganath, C. (2013) · Journal of Experimental Psychology General · doi:10.1037/a0034029 · Cited by 47
Self-citation
Familiarity, but not recollection, supports the between-subject production effect in recognition memory.
Fawcett, J. M., & Ozubko, J. D. (2016) · Canadian Journal of Experimental Psychology/Revue canadienne de psychologie expérimentale · doi:10.1037/cep0000089 · Cited by 47
Developmental changes in plasticity, synaptic, glia and connectivity protein levels in rat dorsal hippocampus
Travaglia, A., Bisaz, R., Cruz, E., & Alberini, C. M. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.08.005 · Cited by 50
Perirhinal firing patterns are sustained across large spatial segments of the task environment
Bos, J. J., Vinck, M. A., Mourik-Donga, L. A. V., Jackson, J. C., Witter, M. P., & Pennartz, C. M. A. (2017) · Nature Communications · doi:10.1038/ncomms15602 · Cited by 47
Abnormal functional connectivity density in patients with major depressive disorder with comorbid insomnia
Gong, L., Xu, R., Liu, D., Zhang, C., Huang, Q., Zhang, B., & Xi, C. (2020) · Journal of Affective Disorders · doi:10.1016/j.jad.2020.01.088 · Cited by 48
Transcranial Electric Current Stimulation During Associative Memory Encoding: Comparing tACS and tDCS Effects in Healthy Aging
Klink, K., Peter, J., Wyss, P., & Klöppel, S. (2020) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2020.00066 · Cited by 49
Attentional Selection
Theeuwes, J., & Failing, M. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108891288 · Cited by 50
The hippocampus supports encoding of between-domain associations within working memoryPreprint
Piekema, C., Kessels, R. P. C., Rijpkema, M., & Fernández, G. (2009) · Learning & Memory · doi:10.1101/lm.1283109 · Cited by 47
Effects of learning experience on forgetting rates of item and associative memoriesPreprint
Yang, J., Zhan, L., Wang, Y., Du, X., Zhou, W., Ning, X., Sun, Q. Y., & Moscovitch, M. (2016) · Learning & Memory · doi:10.1101/lm.041210.115 · Cited by 51
Default Network Connectivity in Medial Temporal Lobe Amnesia
Hayes, S. M., Salat, D. H., & Verfaellie, M. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.0700-12.2012 · Cited by 46
NMDA signaling in CA1 mediates selectively the spatial component of episodic memory
Place, R., Lykken, C., Beer, Z., Suh, J., McHugh, T. J., Tonegawa, S., Eichenbaum, H., & Sauvage, M. M. (2012) · Learning & Memory · doi:10.1101/lm.025254.111 · Cited by 46
Self-citation
Dopamine D1 receptor activity modulates object recognition memory consolidation in the perirhinal cortex but not in the hippocampus
Balderas, I., Moreno‐Castilla, P., & Bermudez‐Rattoni, F. (2013) · Hippocampus · doi:10.1002/hipo.22143 · Cited by 46
Perception and Memory in the Ventral Visual Stream and Medial Temporal Lobe
Martin, C. B., & Barense, M. D. (2023) · Annual Review of Vision Science · doi:10.1146/annurev-vision-120222-014200 · Cited by 54
Long-Term Functional Outcomes and Correlation with Regional Brain Connectivity by MRI Diffusion Tractography Metrics in a Near-Term Rabbit Model of Intrauterine Growth Restriction
Illa, M., Eixarch, E., Batallé, D., Arbat‐Plana, A., Muñoz‐Moreno, E., Figueras, F., & Gratacós, E. (2013) · PLoS ONE · doi:10.1371/journal.pone.0076453 · Cited by 46
A Broader View of Perirhinal Function: From Recognition Memory to Fluency-Based Decisions
Dew, I. T. Z., & Cabeza, R. E. L. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1413-13.2013 · Cited by 46
Scene construction in schizophrenia.
Raffard, S., D’Argembeau, A., Bayard, S., Boulenger, J., & der Linden, M. V. (2010) · Neuropsychology · doi:10.1037/a0019113 · Cited by 53
Amygdala lesions selectively impair familiarity in recognition memory
Farovik, A., Place, R., Miller, D. R., & Eichenbaum, H. (2011) · Nature Neuroscience · doi:10.1038/nn.2919 · Cited by 48
Self-citation
A critical role of the human hippocampus in an electrophysiological measure of implicit memory
Addante, R. J. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2014.12.069 · Cited by 51
A single trial analysis of EEG in recognition memory: Tracking the neural correlates of memory strength
Ratcliff, R., Sederberg, P. B., Smith, T. A., & Childers, R. (2016) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2016.09.026 · Cited by 47
Estimation of effective connectivity using multi-layer perceptron artificial neural network
Talebi, N., Nasrabadi, A. M., & Mohammad-Rezazadeh, I. (2017) · Cognitive Neurodynamics · doi:10.1007/s11571-017-9453-1 · Cited by 46
The effect of prior knowledge on post-encoding brain connectivity and its relation to subsequent memory
Liu, Z., Grady, C. L., & Moscovitch, M. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.11.032 · Cited by 52
Effect of Volatile Organic Chemicals in Chrysanthemum indicum Linné on Blood Pressure and Electroencephalogram
Kim, D., Goo, Y., Cho, J., Lee, J.-K., Lee, D. Y., Sin, S. M., Kil, Y. S., Jeong, W. M., Ko, K. H., Yang, K. J., et al. (2018) · Molecules · doi:10.3390/molecules23082063 · Cited by 46
Encoding of long-term associations through neural unitization in the human medial temporal lobe
Rey, H. G., Falco, E. D., Ison, M. J., Valentı́n, A., Alarcón, G., Selway, R., Richardson, M. P., & Quiroga, R. Q. (2018) · Nature Communications · doi:10.1038/s41467-018-06870-2 · Cited by 48

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

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks