Medial temporal lobe activity during source retrieval reflects information type, not memory strength

Diana, Rachel A.; Yonelinas, Andrew P.; Ranganath, Charan

doi:10.1162/jocn.2009.21335

Cited by 191Memory Processes and InfluencesMemory and Neural MechanismsCognitive Functions and Memory

Medial temporal lobe activity during source retrieval reflects information type, not memory strength

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Diana, Rachel A., Yonelinas, Andrew P., Ranganath, Charan·2010·Journal of Cognitive Neuroscience

DOI 10.1162/jocn.2009.21335PMC PMC2862119

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Abstract

The medial temporal lobes (MTLs) are critical for episodic memory but the functions of MTL subregions are controversial. According to memory strength theory, MTL subregions collectively support declarative memory in a graded manner. In contrast, other theories assert that MTL subregions support functionally distinct processes. For instance, one view is that perirhinal cortex (PRc) processes item information, parahippocampal cortex (PHc) processes context information, and the hippocampus binds item and context. Here, we report two experiments that tested competing predictions from these models. In these studies, subjects encoded color-word associations by imagining color either as a contextual association (context detail condition) or as a feature of the item to be encoded (item detail condition). Results showed that encoding color information as an item detail improved source recognition in amnesic patients with recollection deficits. Furthermore, event-related fMRI data from healthy subjects revealed PRc activation associated with successful retrieval of item details, whereas activation in the hippocampus and PHc was associated with recollection-based source retrieval. The qualitatively different patterns of results observed in PRc and hippocampus/PHc are inconsistent with a memory strength account and are consistent with the idea that different MTL regions process different types of episodic information.

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The prior literature is most consistent with a role for the PRC in item processing.
“the prior literature is most consistent with a role for the PRC in item processing”
From Delay-dependent contributions of medial temporal lobe regions to episodic memory retrieval (2015) · cites this paper as Diana et al., 2010

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Detection Theory: A User's Guide
Macmillan, N. A., & Creelman, C. D. (1991) · Cited by 5,415 · 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
Detection theory: A user's guide
Lories, G. (1993) · Behavioural Processes · doi:10.1016/0376-6357(93)90083-4 · Cited by 2,927 · see citing works
The Medial Temporal Lobe and Recognition Memory
Eichenbaum, H., Yonelinas, A. P., & Ranganath, C. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.30.051606.094328 · Cited by 2,580 · see citing works
Self-citation
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
Memory, amnesia, and the hippocampal system
(1994) · Choice Reviews Online · doi:10.5860/choice.31-5148 · Cited by 1,533 · see citing works
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 Variability of Human, BOLD Hemodynamic Responses
Aguirre, G. K., Zarahn, E., & D’Esposito, M. (1998) · NeuroImage · doi:10.1006/nimg.1998.0369 · Cited by 1,224 · 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
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
Item, context and relational episodic encoding in humans
Davachi, L. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2006.10.012 · Cited by 1,138 · 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
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
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
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
Associative memory and the medial temporal lobes
Mayes, A. R., Montaldi, D., & Migo, E. M. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2006.12.003 · Cited by 681 · 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
Self-citation
Effects of extensive temporal lobe damage or mild hypoxia on recollection and familiarity
Yonelinas, A., Kroll, N., Quamme, J., Lazzara, M. M., Sauvé, M., Widaman, K., & Knight, R. (2002) · Nature Neuroscience · doi:10.1038/nn961 · Cited by 554 · see citing works
Memory, amnesia, and the hippocampal system
Holmes, G. L. (1994) · Journal of Epilepsy · doi:10.1016/0896-6974(94)90099-x · Cited by 422 · see citing works
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
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
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
Differential Encoding Mechanisms for Subsequent Associative Recognition and Free Recall
Staresina, B. P., & Davachi, L. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.2877-06.2006 · Cited by 306 · see citing works
Effect of unitization on associative recognition in amnesia
Quamme, J., Yonelinas, A., & Norman, K. A. (2007) · Hippocampus · doi:10.1002/hipo.20257 · Cited by 297 · see citing works
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
The human medial temporal lobe processes online representations of complex objects
Barense, M. D., Gaffan, D., & Graham, K. S. (2007) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2007.05.023 · Cited by 279 · see citing works
Hippocampal, parahippocampal and occipital-temporal contributions to associative and item recognition memory: an fMRI study
Yonelinas, A. P., Hopfinger, J. B., Buonocore, M. H., Kroll, N. E. A., & Baynes, K. (2001) · Neuroreport · doi:10.1097/00001756-200102120-00035 · Cited by 243 · see citing works
Selective and Shared Contributions of the Hippocampus and Perirhinal Cortex to Episodic Item and Associative Encoding
Staresina, B. P., & Davachi, L. (2008) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2008.20104 · Cited by 222 · see citing works
The effects of unitization on familiarity-based source memory: Testing a behavioral prediction derived from neuroimaging data.
Diana, R. A., Yonelinas, A. P., & Ranganath, C. (2008) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/0278-7393.34.4.730 · Cited by 216 · see citing works
Dissociation of the neural correlates of recognition memory according to familiarity, recollection, and amount of recollected information
Vilberg, K. L., & Rugg, M. D. (2007) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2007.02.027 · Cited by 213 · 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
Removal of Confounding Effects of Global Signal in Functional MRI Analyses
Desjardins, A. E., Kiehl, K. A., & Liddle, P. F. (2001) · NeuroImage · doi:10.1006/nimg.2000.0719 · Cited by 185 · see citing works
Using event-related fMRI to assess delay-period activity during performance of spatial and nonspatial working memory tasks
Postle, B. R., Zarahn, E., & D’Esposito, M. (2000) · Brain Research Protocols · doi:10.1016/s1385-299x(99)00053-7 · Cited by 164 · see citing works
The contribution of familiarity to associative memory in amnesia.
Giovanello, K., Keane, M., & Verfaellie, M. (2006) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2006.03.004 · Cited by 143 · see citing works
Activity in the Medial Temporal Lobe Predicts Memory Strength, Whereas Activity in the Prefrontal Cortex Predicts Recollection
Kirwan, C. B., Wixted, J. T., & Squire, L. R. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.3456-08.2008 · Cited by 141 · see citing works
ERP correlates of source memory: Unitized source information increases familiarity-based retrieval
Diana, R. A., van den Boom, W., Yonelinas, A. P., & Charan Ranganath, A. (2010) · Brain Research · doi:10.1016/j.brainres.2010.10.030 · 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
In Search of Recollection and Familiarity Signals in the Hippocampus
Wais, P. E., Squire, L. R., & Wixted, J. T. (2009) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21190 · Cited by 103 · see citing works
Recognition memory for faces and scenes in amnesia: Dissociable roles of medial temporal lobe structures
Taylor, K. J., Henson, R. N., & Graham, K. S. (2007) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2007.04.004 · Cited by 100 · see citing works
Hippocampal atrophy is the critical brain change in patients with hypoxic amnesia
Paola, M. D., Caltagirone, C., Fadda, L., Sabatini, U., Serra, L., & Carlesimo, G. A. (2008) · Hippocampus · doi:10.1002/hipo.20432 · Cited by 93 · see citing works
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 47 · see citing works
Decrements in Hippocampal Activity with Item Repetition during Continuous Recognition: An fMRI Study
Suzuki, M., Johnson, J. D., & Rugg, M. D. (2010) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2010.21535 · Cited by 39 · see citing works
Electrical impedance and volume changes in brain during preparation for electron microscopy
Nevis, A. H., & Collins, G. H. (1967) · Brain Research · doi:10.1016/0006-8993(67)90219-3 · Cited by 38 · see citing works
Contributions of the medial temporal lobe to declarative memory retrieval: Manipulating the amount of contextual retrievalPreprint
Tendolkar, I., Arnold, J., Petersson, K. M., Weis, S., Brockhaus‐Dumke, A., van Eijndhoven, P., Buitelaar, J. K., & Fernández, G. (2008) · Learning & Memory · doi:10.1101/lm.916708 · Cited by 30 · see citing works
Recollection, familiarity and memory strength: confusion about confounds
Diana, R. A., & Charan Ranganath, A. (2011) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2011.06.001 · Cited by 26 · see citing works
Memory Strength Effects in fMRI Studies: A Matter of Confidence
de Zubicaray, G. I., McMahon, K. L., Dennis, S. J., & Dunn, J. C. (2010) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2010.21601 · Cited by 13 · see citing works
Pre-experimental Familiarization Increases Hippocampal Activity for Both Targets and Lures in Recognition Memory: An fMRI Study
de Zubicaray, G. I., McMahon, K. L., Hayward, L. E., & Dunn, J. C. (2011) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00092 · Cited by 9 · see citing works
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Xiong (1999) · doi:10.1002/(sici)1097-0193(1999)8:2/3

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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
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
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
“, 2007), and it can play a role in associative and source memory under conditions that promote unitization of item–item or item–source information (Staresina and Davachi, 2006; Haskins et al., 2008; Diana et al., 2010).”
BackgroundResultInfluentialSelf-citation
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
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
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 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
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
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
“…in both humans and animals have revealed that two brain areas, the hippocampus (HPC) and medial prefrontal cortex (mPFC), are essential for the encoding and retrieval of episodic memories (Kennedy and Shapiro, 2004; Hasselmo and Eichenbaum, 2005; Diana et al., 2010; Preston and Eichenbaum, 2013).”
Background
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
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
Cortico-hippocampal systems involved in memory and cognition
Ritchey, M., Libby, L. A., & Ranganath, C. (2015) · Progress in brain research · doi:10.1016/bs.pbr.2015.04.001 · Cited by 268 · see citing works
The role of recollection and familiarity in the functional differentiation of the medial temporal lobes
Montaldi, D., & Mayes, A. R. (2010) · Hippocampus · doi:10.1002/hipo.20853 · Cited by 259 · see citing works
Prefrontal and medial temporal lobe activity at encoding predicts temporal context memory
Jenkins, L. J., & Ranganath, C. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.1337-10.2010 · Cited by 213 · see citing works
Object and spatial mnemonic interference differentially engage lateral and medial entorhinal cortex in humans
Reagh, Z. M., & Yassa, M. A. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1411250111 · Cited by 225 · see citing works
Binding Items and Contexts
Ranganath, C. (2010) · Current Directions in Psychological Science · doi:10.1177/0963721410368805 · Cited by 214 · see citing works
Perirhinal and Parahippocampal Cortices Differentially Contribute to Later Recollection of Object- and Scene-Related Event Details
Staresina, B. P., Duncan, K. D., & Davachi, L. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4978-10.2011 · Cited by 192 · see citing works
Cortico-hippocampal network connections support the multidimensional quality of episodic memory
Cooper, R. A., & Ritchey, M. (2019) · eLife · doi:10.7554/elife.45591 · Cited by 156 · see citing works
Item memory, context memory and the hippocampus: fMRI evidence
Rugg, M. D., Vilberg, K. L., Mattson, J. T., Yu, S. S., Johnson, J. D., & Suzuki, M. (2012) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2012.06.004 · Cited by 153 · see citing works
Examining ERP correlates of recognition memory: Evidence of accurate source recognition without recollection
Addante, R. J., Ranganath, C., & Yonelinas, A. P. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.04.031 · Cited by 148 · see citing works
Delay-dependent contributions of medial temporal lobe regions to episodic memory retrieval
Ritchey, M., Montchal, M. E., Yonelinas, A. P., & Ranganath, C. (2015) · eLife · doi:10.7554/elife.05025 · Cited by 148 · see citing works
Self-citation
Memory for the Order of Events in Specific Sequences: Contributions of the Hippocampus and Medial Prefrontal Cortex
DeVito, L. M., & Eichenbaum, H. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4202-10.2011 · Cited by 144 · see citing works
Memory signals are temporally dissociated in and across human hippocampus and perirhinal cortex
Staresina, B. P., Fell, J., Lam, A. T. A. D., Axmacher, N., & Henson, R. N. (2012) · Nature Neuroscience · doi:10.1038/nn.3154 · Cited by 130 · see citing works
Associative memory in aging: The effect of unitization on source memory.
Bastin, C., Diana, R. A., Simon, J., Collette, F., Yonelinas, A. P., & Salmon, É. (2013) · Psychology and Aging · doi:10.1037/a0031566 · Cited by 125 · see citing works
Content Representation in the Human Medial Temporal Lobe
Liang, J. C., Wagner, A. D., & Preston, A. R. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr379 · Cited by 123 · see citing works
Dynamic Theta Networks in the Human Medial Temporal Lobe Support Episodic Memory
Solomon, E. A., Stein, J. M., Das, S. R., Gorniak, R., Sperling, M. R., Worrell, G. A., Inman, C. S., Tan, R. J., Jobst, B. C., Rizzuto, D. S., et al. (2018) · Current Biology · doi:10.1016/j.cub.2019.02.020 · Cited by 116 · see citing works
An integrative memory model of recollection and familiarity to understand memory deficits
Bastin, C., Besson, G., Simon, J., Delhaye, E., Geurten, M., Willems, S. J., & Salmon, É. (2019) · Behavioral and Brain Sciences · doi:10.1017/s0140525x19000621 · Cited by 121 · see citing works
Multiple interacting brain areas underlie successful spatiotemporal memory retrieval in humans
Schedlbauer, A. M., Copara, M. S., Watrous, A. J., & Ekstrom, A. D. (2014) · Scientific Reports · doi:10.1038/srep06431 · Cited by 119 · see citing works
Familiarity and recollection produce distinct eye movement, pupil and medial temporal lobe responses when memory strength is matched
Kafkas, A., & Montaldi, D. (2012) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2012.08.001 · Cited by 117 · see citing works
The importance of unitization for familiarity-based learning.
Parks, C. M., & Yonelinas, A. P. (2014) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/xlm0000068 · Cited by 114 · see citing works
ERP correlates of source memory: Unitized source information increases familiarity-based retrieval
Diana, R. A., van den Boom, W., Yonelinas, A. P., & Charan Ranganath, A. (2010) · Brain Research · doi:10.1016/j.brainres.2010.10.030 · Cited by 108 · see citing works
Double Dissociation between Hippocampal and Parahippocampal Responses to Object–Background Context and Scene Novelty
Howard, L. R., Kumaran, D., Ólafsdóttir, H. F., & Spiers, H. J. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.6055-10.2011 · Cited by 99 · see citing works
Distinct hippocampal functional networks revealed by tractography-based parcellation
Adnan, A., Barnett, A. J., Moayedi, M., McCormick, C., Cohn, M., & McAndrews, M. P. (2015) · Brain Structure and Function · doi:10.1007/s00429-015-1084-x · Cited by 94 · see citing works
Human neural systems underlying rigid and flexible forms of allocentric spatial representation
Zhang, H., & Ekstrom, A. D. (2012) · Human Brain Mapping · doi:10.1002/hbm.21494 · Cited by 81 · see citing works
Recollection, familiarity, and content-sensitivity in lateral parietal cortex: a high-resolution fMRI study
Johnson, J. D., Suzuki, M., & Rugg, M. D. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00219 · Cited by 74 · see citing works
Developmental Differences in Relations Between Episodic Memory and Hippocampal Subregion Volume During Early Childhood
Riggins, T., Blankenship, S. L., Mulligan, E. M., Warnell, K. R., & Redcay, E. (2015) · Child Development · doi:10.1111/cdev.12445 · Cited by 78 · see citing works
Cortical reinstatement and the confidence and accuracy of source memory
Thakral, P. P., Wang, T. H., & Rugg, M. D. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.01.003 · Cited by 75 · see citing works
Familiarity in source memory
Mollison, M. V., & Curran, T. (2012) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2012.06.027 · Cited by 73 · see citing works
Stimulus content and the neural correlates of source memory
Duarte, A., Henson, R. N., & Graham, K. S. (2010) · Brain Research · doi:10.1016/j.brainres.2010.11.086 · Cited by 73 · see citing works
Binding neutral information to emotional contexts: Brain dynamics of long-term recognition memory
Ventura‐Bort, C., Löw, A., Wendt, J., Moltó, J., Poy, R., Dolcos, F., Hamm, A. O., & Weymar, M. (2015) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-015-0385-0 · Cited by 74 · see citing works
The human hippocampus contributes to both the recollection and familiarity components of recognition memory
Merkow, M. B., Burke, J. F., & Kahana, M. J. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1513145112 · Cited by 72 · see citing works
A Critical Role for the Hippocampus and Perirhinal Cortex in Perceptual Learning of Scenes and Faces: Complementary Findings from Amnesia and fMRI
Mundy, M. E., Downing, P. E., Dwyer, D. M., Honey, R. C., & Graham, K. S. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2958-12.2013 · Cited by 69 · see citing works
Activity reductions in perirhinal cortex predict conceptual priming and familiarity-based recognition
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Kragel, J. E., Morton, N. W., & Polyn, S. M. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3378-14.2015 · Cited by 64 · see citing works
Aging Affects the Interaction between Attentional Control and Source Memory: An fMRI Study
Dulas, M. R., & Duarte, A. (2014) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00663 · Cited by 60 · see citing works
A Review of the Neural and Behavioral Consequences for Unitizing Emotional and Neutral Information
Murray, B. D., & Kensinger, E. A. (2013) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2013.00042 · Cited by 61 · see citing works
Medial temporal lobe contributions to cued retrieval of items and contexts
Hannula, D. E., Libby, L. A., Yonelinas, A. P., & Ranganath, C. (2013) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2013.02.011 · Cited by 61 · see citing works
Neuroanatomical correlates of genetic risk for bipolar disorder: A voxel-based morphometry study in bipolar type I patients and healthy first degree relatives
Sarıçiçek, A., Yalın, N., Hıdıroğlu, C., Çavuşoğlu, B., Taş, C., Ceylan, D., Zorlu, N., Ada, E., Tunca, Z., & Özerdem, A. (2015) · Journal of Affective Disorders · doi:10.1016/j.jad.2015.06.055 · Cited by 57 · see citing works
Episodic memory and event construction in aging and amnesia
Romero, K., & Moscovitch, M. (2012) · Journal of Memory and Language · doi:10.1016/j.jml.2012.05.002 · Cited by 58 · see citing works
Development of memory for spatial context: Hippocampal and cortical contributions
DeMaster, D., Pathman, T., & Ghetti, S. (2013) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2013.05.026 · Cited by 58 · see citing works
Electrophysiological evidence for the effects of unitization on associative recognition memory in older adults
Zheng, Z., Li, J., Xiao, F., Broster, L. S., & Jiang, Y. (2015) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2015.03.006 · Cited by 57 · see citing works
Differential contributions of subregions of medial temporal lobe to memory system in amnestic mild cognitive impairment: insights from fMRI study
Chen, J., Duan, X., Shu, H., Wang, Z., Long, Z., Liu, D., Liao, W., Shi, Y., Chen, H., & Zhang, Z. (2016) · Scientific Reports · doi:10.1038/srep26148 · Cited by 55 · see citing works
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 50 · see citing works
Could masked conceptual primes increase recollection? The subtleties of measuring recollection and familiarity in recognition memory
Taylor, J. R., & Henson, R. N. (2012) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2012.07.029 · Cited by 53 · see citing works
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 52 · see citing works
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 50 · see citing works
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 · see citing works
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 47 · see citing works
The effects of unitization on the contribution of familiarity and recollection processes to associative recognition memory: Evidence from event-related potentials
Zheng, Z., Li, J., Xiao, F., Broster, L. S., Jiang, Y., & Ming-jing, X. (2015) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2015.01.003 · Cited by 46 · see citing works
Hippocampal metabolites and memory performances in patients with amnestic mild cognitive impairment and Alzheimer’s disease
Watanabe, T., Shiino, A., & Akiguchi, I. (2012) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2012.01.006 · Cited by 45 · see citing works
Medial temporal lobe reinstatement of content-specific details predicts source memory
Liang, J. C., & Preston, A. R. (2016) · Cortex · doi:10.1016/j.cortex.2016.09.011 · Cited by 45 · see citing works
A Role for Perirhinal Cortex in Memory for Novel Object–Context Associations
Watson, H. C., Wilding, E. L., & Graham, K. S. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.5751-11.2012 · Cited by 44 · see citing works
Age-related changes in overcoming proactive interference in associative memory: The role of PFC-mediated executive control processes at retrieval
Dulas, M. R., & Duarte, A. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.02.017 · Cited by 40 · see citing works
Connectivity Profiles Reveal a Transition Subarea in the Parahippocampal Region That Integrates the Anterior Temporal–Posterior Medial Systems
Zhuo, J., Fan, L., Liu, Y., Zhang, Y., Yu, C., & Jiang, T. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1975-15.2016 · Cited by 41 · see citing works
Disentangling Spatial Perception and Spatial Memory in the Hippocampus: A Univariate and Multivariate Pattern Analysis fMRI Study
Lee, A. C. H., Brodersen, K. H., & Rudebeck, S. R. (2012) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00301 · Cited by 41 · see citing works
Decrements in Hippocampal Activity with Item Repetition during Continuous Recognition: An fMRI Study
Suzuki, M., Johnson, J. D., & Rugg, M. D. (2010) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2010.21535 · Cited by 39 · see citing works
Associative memory and its cerebral correlates in Alzheimer׳s disease: Evidence for distinct deficits of relational and conjunctive memory
Bastin, C., Bahri, M. A., Miévis, F., Lemaire, C. F., Collette, F., Genon, S., Simon, J., Guillaume, B., Diana, R. A., Yonelinas, A. P., et al. (2014) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2014.08.023 · Cited by 36 · see citing works
Cerebellar degeneration affects cortico-cortical connectivity in motor learning networks
Tzvi, E., Zimmermann, C., Bey, R., Münte, T. F., Nitschke, M. F., & Krämer, U. M. (2017) · NeuroImage Clinical · doi:10.1016/j.nicl.2017.07.012 · Cited by 39 · see citing works
Variations in recollection: The effects of complexity on source recognition
Parks, C., Murray, L. J., Elfman, K. W., & Yonelinas, A. (2011) · Journal of Experimental Psychology. Learning, Memory and Cognition · doi:10.1037/a0022798 · Cited by 41 · see citing works
What’s in a context? Cautions, limitations, and potential paths forward
Stark, S. M., Reagh, Z. M., Yassa, M. A., & Stark, C. E. L. (2017) · Neuroscience Letters · doi:10.1016/j.neulet.2017.05.022 · Cited by 37 · see citing works
Neurocomputational account of memory and perception: Thresholded and graded signals in the hippocampus
Elfman, K. W., Aly, M., & Yonelinas, A. P. (2014) · Hippocampus · doi:10.1002/hipo.22345 · Cited by 35 · see citing works
Item and source memory for emotional associates is mediated by different retrieval processes
Ventura‐Bort, C., Dolcos, F., Wendt, J., Wirkner, J., Hamm, A. O., & Weymar, M. (2017) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2017.12.015 · Cited by 34 · see citing works
Unitization mitigates interference by intrinsic negative emotion in familiarity and recollection of associative memory: Electrophysiological evidence
Han, M., Mao, X., Kartvelishvili, N., Li, W., & Guo, C. (2018) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-018-0636-y · Cited by 32 · see citing works
Item familiarity and controlled associative retrieval in Alzheimer's disease: an fMRI study.
Genon, S., Collette, F., Feyers, D., Phillips, C., Salmon, E., & Bastin, C. (2013) · Cortex; a journal devoted to the study of the nervous system and behavior · doi:10.1016/j.cortex.2012.11.017 · Cited by 30 · see citing works
Examining the causes of memory strength variability: Recollection, attention failure, or encoding variability?
Koen, J., Aly, M., Wang, W.-C., & Yonelinas, A. (2013) · Journal of Experimental Psychology. Learning, Memory and Cognition · doi:10.1037/a0033671 · Cited by 21 · see citing works
Novelty preference in patients with developmental amnesia
Muñoz, M., Chadwick, M. J., Pérez-Hernández, E., Vargha‐Khadem, F., & Mishkin, M. (2010) · Hippocampus · doi:10.1002/hipo.20836 · Cited by 31 · see citing works
Extrastriate cortex and medial temporal lobe regions respond differentially to visual feature overlap within preferred stimulus category
Mundy, M. E., Downing, P. E., & Graham, K. S. (2012) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2012.07.006 · Cited by 31 · see citing works
Unitization improves source memory in older adults: An event-related potential study.
Zheng, Z., Li, J., Xiao, F., Ren, W., & He, R.-Q. (2016) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2016.06.025 · Cited by 26 · see citing works
Misrecollection prevents older adults from benefitting from semantic relatedness of the memoranda in associative memory
Delhaye, E., Tibon, R., Gronau, N., Levy, D. A., & Bastin, C. (2017) · Neuropsychology, development, and cognition. Section B, Aging, neuropsychology and cognition · doi:10.1080/13825585.2017.1358351 · Cited by 24 · see citing works
Dissociable neural correlates of item and context retrieval in the medial temporal lobes
Wang, W., Yonelinas, A. P., & Charan Ranganath, A. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.05.029 · Cited by 29 · see citing works
False memory for context activates the parahippocampal cortex
Karanian, J. M., & Slotnick, S. D. (2014) · Cognitive Neuroscience · doi:10.1080/17588928.2014.938035 · Cited by 28 · see citing works
Neural synchronization as a function of engagement with the narrative
Ohad, T., & Yeshurun, Y. (2023) · NeuroImage · doi:10.1016/j.neuroimage.2023.120215 · Cited by 32 · see citing works
A meta-analysis of event-related potential correlates of recognition memory
Morcom, A., Kwon, S., Rugg, M. D., Curran, T., & Wiegand, R. (2023) · Psychonomic Bulletin & Review · doi:10.3758/s13423-023-02309-y · Cited by 35 · see citing works
Contributions of Feature Binding During Encoding and Functional Connectivity of the Medial Temporal Lobe Structures to Episodic Memory Deficits Across the Prodromal and First-Episode Phases of Schizophrenia
Haut, K. M., van Erp, T. G. M., Knowlton, B. J., Bearden, C. E., Subotnik, K. L., Ventura, J., Nuechterlein, K. H., & Cannon, T. D. (2014) · Clinical Psychological Science · doi:10.1177/2167702614533949 · Cited by 28 · see citing works
Preserved hippocampal novelty responses following anterior temporal‐lobe resection that impairs familiarity but spares recollection
Bowles, B., O’Neil, E. B., Mirsattari, S. M., Poppenk, J., & Köhler, S. (2010) · Hippocampus · doi:10.1002/hipo.20800 · Cited by 28 · see citing works
Recollection-dependent memory for event duration in large-scale spatial navigationPreprint
Brunec, I. K., Ozubko, J. D., Barense, M. D., & Moscovitch, M. (2017) · Learning & Memory · doi:10.1101/lm.044032.116 · Cited by 27 · see citing works
Abnormal semantic knowledge in a case of developmental amnesia
Blumenthal, A., Duke, D., Bowles, B., Gilboa, A., Rosenbaum, R. S., Köhler, S., & McRae, K. (2017) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2017.06.018 · Cited by 26 · see citing works
Names and their meanings: A dual-process account of proper-name encoding and retrieval.
O’Rourke, T., & Balaguer, R. D. D. (2019) · Neuroscience and Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.11.005 · Cited by 20 · see citing works
Recollection, familiarity and memory strength: confusion about confounds
Diana, R. A., & Charan Ranganath, A. (2011) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2011.06.001 · Cited by 26 · see citing works
Short-Term Memory Depends on Dissociable Medial Temporal Lobe Regions in Amnestic Mild Cognitive Impairment
Das, S. R., Mancuso, L., Olson, I. R., Arnold, S. E., & Wolk, D. A. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv022 · Cited by 22 · see citing works
Brain–behavior relationships in source memory: Effects of age and memory ability
Meusel, L.-A., Grady, C. L., Ebert, P. E., & Anderson, N. D. (2017) · Cortex · doi:10.1016/j.cortex.2016.12.023 · Cited by 24 · see citing works
Reconciling the object and spatial processing views of the perirhinal cortex through task‐relevant unitization
Fiorilli, J., Bos, J. J., Grande, X., Lim, J., Düzel, E., & Pennartz, C. M. A. (2021) · Hippocampus · doi:10.1002/hipo.23304 · Cited by 23 · see citing works
Prediction of cognitive performance differences in older age from multimodal neuroimaging data
Krämer, C., Stumme, J., Campos, L. D. C., Dellani, P. R., Rubbert, C., Caspers, J., Caspers, S., & Jockwitz, C. (2023) · GeroScience · doi:10.1007/s11357-023-00831-4 · Cited by 22 · see citing works
Repetition suppression in the medial temporal lobe and midbrain is altered by event overlap
Zeithamová, D., Manthuruthil, C., & Preston, A. R. (2016) · Hippocampus · doi:10.1002/hipo.22622 · Cited by 22 · see citing works
Functional connectivity in category‐selective brain networks after encoding predicts subsequent memory
Collins, J. A., & Dickerson, B. C. (2018) · Hippocampus · doi:10.1002/hipo.23003 · Cited by 23 · see citing works
Recollection‐related hippocampal activity during continuous recognition: A high‐resolution fMRI study
Suzuki, M., Johnson, J. D., & Rugg, M. D. (2010) · Hippocampus · doi:10.1002/hipo.20781 · Cited by 22 · see citing works
Categorical Versus Dimensional Approaches to Autism-Associated Intermediate Phenotypes in 22q11.2 Microdeletion Syndrome
Jalbrzikowski, M., Ahmed, K. H., Patel, A. B., Jonas, R. K., Kushan, L., Chow, C. C., & Bearden, C. E. (2016) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2016.06.007 · Cited by 22 · see citing works
Role of cholinergic receptors in memory retrieval depends on gender and age of memory
Rashid, H., Mahboob, A., & Ahmed, T. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.05.017 · Cited by 22 · see citing works
Impaired perceptual integration and memory for unitized representations are associated with perirhinal cortex atrophy in Alzheimer's disease.
Delhaye, E., Bahri, M., Salmon, E., & Bastin, C. (2019) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2018.09.021 · Cited by 19 · see citing works
Associative memory for conceptually unitized word pairs in mild cognitive impairment is related to the volume of the perirhinal cortex
Delhaye, E., Mechanic-Hamilton, D., Saad, L., Das, S. R., Wisse, L., Yushkevich, P., Wolk, D., & Bastin, C. (2018) · Hippocampus · doi:10.1002/hipo.23063 · Cited by 20 · see citing works

Content-specific source encoding in the human medial temporal lobe.
Awipi, T., & Davachi, L. (2008) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/0278-7393.34.4.769 · Cited by 83 · see citing works
Dissociable neural correlates of item and context retrieval in the medial temporal lobes
Wang, W., Yonelinas, A. P., & Charan Ranganath, A. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.05.029 · Cited by 29 · see citing works
Multiple routes to memory: distinct medial temporal lobe processes build item and source memories
Davachi, L., Mitchell, J. P., & Wagner, A. D. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0337195100 · Cited by 899 · see citing works
Dissociable 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
Domain‐specific retrieval of source information in the medial temporal lobe
Peters, J., Boris Suchan, A., Köster, O., & Daum, I. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05752.x · Cited by 38 · see citing works

Authors: Diana, R. A., Yonelinas, A. P., & Ranganath, C.
Affiliations: University of California, Davis (US)
ORCID: Diana, Rachel A.
Yonelinas, Andrew P.
Venue: Journal of Cognitive Neuroscience
Publisher: MIT Press
Published: 2010-08-01
Volume: 22
Issue: 8
Pages: 1808-1818
ISSN: 0898-929X (ISSN-L)
1530-8898
DOI: 10.1162/jocn.2009.21335
PMC: PMC2862119
OpenAlex: W2099171807
Cited by: 191
References: 47
Citations by year: 2026: 3 · 2025: 3 · 2024: 8 · 2023: 8 · 2022: 4 · 2021: 7 · 2020: 10 · 2019: 16 · 2018: 14 · 2017: 13 · 2016: 8 · 2015: 18 · 2014: 14 · 2013: 13 · 2012: 22
FWCI: 8.39
Type: journal article
Language: en
Open access: green
www.ncbi.nlm.nih.gov
Locations: Journal of Cognitive Neuroscience (publishedVersion)
PubMed (publishedVersion)
PubMed Central (acceptedVersion)
Funders: National Institutes of Health
University of California, Davis
National Institute of Mental Health (MH079621, K99MH083945, MH059352, MH 068721, R01MH083734, R01MH068721, R01MH059352, F32MH079621)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Social Sciences › Psychology › Experimental and Cognitive Psychology › Cognitive Functions and Memory
Keywords: medial temporal lobe, episodic memory, source memory, recollection, perirhinal cortex, parahippocampal cortex, hippocampus, amnesia, event-related fMRI
MeSH terms: Adult, Amnesia, Brain Mapping, Female, Humans, Image Processing, Computer-Assisted, Magnetic Resonance Imaging, Male, Middle Aged, Neuropsychological Tests, Oxygen, Mental Recall, ROC Curve, Temporal Lobe, Recognition, Psychology

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Medial temporal lobe activity during source retrieval reflects information type, not memory strength

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