Prior knowledge promotes hippocampal separation but cortical assimilation in the left inferior frontal gyrus

Why there are complementary learning systems in the hippocampus and neocortex: insights from the successes and failures of connectionist models of learning and memory

McClelland, J. L., McNaughton, B. L., & O'Reilly, R. C. (1995) · Psychological Review · doi:10.1037/0033-295x.102.3.419 · Cited by 5,256 · see citing works

Depth of Processing and the Retention of Words in Episodic Memory

Craik, F. I. M., & Tulving, E. (1975) · Journal of Experimental Psychology: General · doi:10.1037/0096-3445.104.3.268 · Cited by 4,121 · see citing works

Where is the semantic system? A critical review and meta-analysis of 120 functional neuroimaging studies

Binder, J. R., Desai, R. H., Graves, W. W., & Conant, L. L. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp055 · Cited by 4,060 · see citing works

Representational similarity analysis-connecting the branches of systems neuroscience

Kriegeskorte, N. (2008) · Frontiers in Systems Neuroscience · doi:10.3389/neuro.06.004.2008 · Cited by 3,355 · see citing works

Simple memory: a theory for archicortex

Marr, D. (1971) · Philosophical Transactions of the Royal Society of London. B, Biological Sciences · doi:10.1098/rstb.1971.0078 · Cited by 2,771 · see citing works

Priming and Human Memory Systems

Tulving, E., & Schacter, D. L. (1990) · Science · doi:10.1126/science.2296719 · Cited by 2,595 · 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

Memory systems of the brain: A brief history and current perspective

Squire, L. R. (2004) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2004.06.005 · Cited by 2,269 · see citing works

A spreading activation theory of memory.

Anderson, J. R. (1983) · Journal of Verbal Learning and Verbal Behavior · doi:10.1016/s0022-5371(83)90201-3 · Cited by 2,199 · see citing works

Contextual prerequisites for understanding: Some investigations of comprehension and recall

Bransford, J. D., & Johnson, M. K. (1972) · Journal of Verbal Learning and Verbal Behavior · doi:10.1016/s0022-5371(72)80006-9 · Cited by 2,131 · see citing works

The neurobiology of semantic memory

Binder, J. R., & Desai, R. H. (2011) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2011.10.001 · Cited by 2,114 · see citing works

Information-based functional brain mapping

Kriegeskorte, N., Goebel, R., & Bandettini, P. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0600244103 · Cited by 2,113 · see citing works

Role of left inferior prefrontal cortex in retrieval of semantic knowledge: A reevaluation

Thompson‐Schill, S. L., D’Esposito, M., Aguirre, G. K., & Farah, M. J. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.26.14792 · Cited by 2,111 · see citing works

The hippocampal-VTA loop: controlling the entry of information into long-term memory

Lisman, J. E., & Grace, A. A. (2005) · Neuron · doi:10.1016/j.neuron.2005.05.002 · Cited by 1,983 · see citing works

Building Memories: Remembering and Forgetting of Verbal Experiences as Predicted by Brain Activity

Wagner, A. D., Schacter, D. L., Rotte, M., Koutstaal, W., Maril, A., Dale, A. M., Rosen, B. R., & Buckner, R. L. (1998) · Science · doi:10.1126/science.281.5380.1188 · Cited by 1,620 · see citing works

Pattern Separation in the Dentate Gyrus and CA3 of the Hippocampus

Leutgeb, J. K., Leutgeb, S., Moser, M.-B., & Moser, E. I. (2007) · Science · doi:10.1126/science.1135801 · Cited by 1,601 · 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

Left ventrolateral prefrontal cortex and the cognitive control of memory

Badre, D., & Wagner, A. D. (2007) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2007.06.015 · Cited by 1,471 · see citing works

A generalized form of context-dependent psychophysiological interactions (gPPI): A comparison to standard approaches

McLaren, D. G., Ries, M. L., Xu, G., & Johnson, S. C. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.03.068 · Cited by 1,445 · 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

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

Computational analysis of the role of the hippocampus in memory

Treves, A., & Rolls, E. T. (1994) · Hippocampus · doi:10.1002/hipo.450040319 · Cited by 1,272 · see citing works

Schemas and Memory Consolidation.

Tse, D., Langston, R. F., Kakeyama, M., Bethus, I., Spooner, P. A., Wood, E. R., Witter, M. P., & Morris, R. G. M. (2007) · Science · doi:10.1126/science.1135935 · Cited by 1,244 · see citing works

Is memory schematic

Alba, J. W., & Hasher, L. (1983) · Psychological Bulletin · doi:10.1037/0033-2909.93.2.203 · Cited by 1,169 · 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

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

Perirhinal and parahippocampal cortices of the macaque monkey: Cortical afferents

Suzuki, W., & Amaral, D. G. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903500402 · Cited by 1,134 · see citing works

Ventromedial hypothalamic neurons control a defensive emotion state

Kunwar, P. S., Zelikowsky, M., Remedios, R., Cai, H., Balban, M. Y., Meister, M., & Anderson, D. J. (2015) · eLife · doi:10.7554/elife.06633 · Cited by 1,112 · see citing works

Long-axis specialization of the human hippocampus

Poppenk, J., Evensmoen, H. R., Moscovitch, M., & Nadel, L. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.03.005 · Cited by 1,100 · 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

Pattern Separation in the Human Hippocampal CA3 and Dentate Gyrus

Bakker, A., Kirwan, C. B., Miller, M. I., & Stark, C. E. L. (2008) · Science · doi:10.1126/science.1152882 · Cited by 1,050 · see citing works

The reverse hierarchy theory of visual perceptual learning

Ahissar, M., & Hochstein, S. (2004) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2004.08.011 · Cited by 1,005 · see citing works

Prefrontal and medial temporal lobe interactions in long-term memory

Simons, J. S., & Spiers, H. J. (2003) · Nature Reviews Neuroscience · doi:10.1038/nrn1178 · Cited by 961 · see citing works

Neural systems for recognition of familiar faces

Gobbini, M. I., & Haxby, J. V. (2007) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2006.04.015 · Cited by 958 · see citing works

Hippocampal conjunctive encoding, storage, and recall: Avoiding a trade‐off

O'Reilly, R. C., & McClelland, J. L. (1994) · Hippocampus · doi:10.1002/hipo.450040605 · Cited by 914 · see citing works

Dissociable Controlled Retrieval and Generalized Selection Mechanisms in Ventrolateral Prefrontal Cortex

Badre, D., Poldrack, R. A., Paré-Blagoev, E. J., Insler, R. Z., & Wagner, A. D. (2005) · Neuron · doi:10.1016/j.neuron.2005.07.023 · Cited by 914 · 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

A proposed function for hippocampal theta rhythm: separate phases of encoding and retrieval enhance reversal of prior learning

Hasselmo, M. E., Bodelón, C., & Wyble, B. P. (2002) · Neural Computation · doi:10.1162/089976602317318965 · Cited by 875 · see citing works

Prefrontal–hippocampal interactions in episodic memory

Eichenbaum, H. (2017) · Nature Reviews Neuroscience · doi:10.1038/nrn.2017.74 · Cited by 870 · see citing works

How schema and novelty augment memory formation

van Kesteren, M. T. R., Ruiter, D. J., Fernández, G., & Henson, R. N. (2012) · Trends in Neurosciences · doi:10.1016/j.tins.2012.02.001 · Cited by 860 · see citing works

Tools of the trade: psychophysiological interactions and functional connectivity

O’Reilly, J. X., Woolrich, M. W., Behrens, T. E. J., Smith, S. M., & Johansen-Berg, H. (2012) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nss055 · Cited by 765 · see citing works

Brain networks underlying episodic memory retrieval

Rugg, M. D., & Vilberg, K. L. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2012.11.005 · Cited by 751 · see citing works

Neurobiology of Schemas and Schema-Mediated Memory

Gilboa, A., & Marlatte, H. (2017) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2017.04.013 · Cited by 742 · see citing works

Deconvolving BOLD activation in event-related designs for multivoxel pattern classification analyses

Mumford, J. A., Turner, B. O., Ashby, F. G., & Poldrack, R. A. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.08.076 · Cited by 729 · see citing works

Homo naledi, a new species of the genus Homo from the Dinaledi chamber. South Africa.

Berger, L. R., Hawks, J., de Ruiter, D. J., Churchill, S. E., Schmid, P., Delezene, L. K., Kivell, T. L., Garvin, H. M., Williams, S. A., DeSilva, J. M., et al. (2015) · eLife · doi:10.7554/elife.09560 · Cited by 703 · see citing works

Retrieval of propositional information from long-term memory

Anderson, J. R. (1974) · Cognitive Psychology · doi:10.1016/0010-0285(74)90021-8 · Cited by 674 · see citing works

Distinct prefrontal cortex activity associated with item memory and source memory for visual shapes

Slotnick, S. D., Moo, L. R., Segal, J. B., & Hart, J. (2003) · Cognitive Brain Research · doi:10.1016/s0926-6410(03)00082-x · Cited by 654 · see citing works

Rhythms of the hippocampal network

Colgin, L. L. (2016) · Nature reviews. Neuroscience · doi:10.1038/nrn.2016.21 · Cited by 654 · see citing works

STRUCTURAL ENCODING AND IDENTIFICATION IN FACE PROCESSING: ERP EVIDENCE FOR SEPARATE MECHANISMS

Shlomo Bentin, A., & Deouell, L. Y. (2000) · Cognitive Neuropsychology · doi:10.1080/026432900380472 · Cited by 653 · see citing works

Schema-dependent gene activation and memory encoding in neocortex

Tse, D., Takeuchi, T., Kakeyama, M., Kajii, Y., Okuno, H., Tohyama, C., Bito, H., & Morris, R. G. M. (2011) · Science · doi:10.1126/science.1205274 · Cited by 618 · see citing works

What is a memory schema? A historical perspective on current neuroscience literature

Ghosh, V. E., & Gilboa, A. (2014) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2013.11.010 · Cited by 529 · 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

Projections from neocortex mediate top-down control of memory retrieval

Rajasethupathy, P., Sankaran, S., Marshel, J. H., Kim, C. K., Ferenczi, E., Lee, S. Y., Berndt, A., Ramakrishnan, C., Jaffe, A., Lo, M., et al. (2015) · Nature · doi:10.1038/nature15389 · Cited by 509 · see citing works

Dynamics of learning and recall at excitatory recurrent synapses and cholinergic modulation in rat hippocampal region CA3

Hasselmo, M. E., Schnell, E., & Barkai, E. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-07-05249.1995 · Cited by 463 · see citing works

Persistent schema-dependent hippocampal-neocortical connectivity during memory encoding and postencoding rest in humans

van Kesteren, M. T. R., Fernández, G., Norris, D. G., & Hermans, E. J. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0914892107 · Cited by 444 · see citing works

Correction: Corrigendum: Streptococcus agalactiae clones infecting humans were selected and fixed through the extensive use of tetracycline

Cunha, V. D., Davies, M. R., Douarre, P.-E., Rosinski‐Chupin, I., Margarit, I., Spinali, S., Perkins, T., Lechat, P., Dmytruk, N., Sauvage, E., et al. (2015) · Nature Communications · doi:10.1038/ncomms7108 · Cited by 438 · see citing works

Shaping of Object Representations in the Human Medial Temporal Lobe Based on Temporal Regularities

Schapiro, A. C., Kustner, L. V., & Turk-Browne, N. B. (2012) · Current Biology · doi:10.1016/j.cub.2012.06.056 · Cited by 430 · see citing works

Learning-related representational changes reveal dissociable integration and separation signatures in the hippocampus and prefrontal cortex

Schlichting, M. L., Mumford, J. A., & Preston, A. R. (2015) · Nature Communications · doi:10.1038/ncomms9151 · Cited by 381 · see citing works

Specificity of priming: a cognitive neuroscience perspective

Schacter, D. L., Dobbins, I. G., & Schnyer, D. M. (2004) · Nature reviews. Neuroscience · doi:10.1038/nrn1534 · Cited by 311 · see citing works

The fan effect: New results and new theories.

Anderson, J. R., & Reder, L. M. (1999) · Journal of Experimental Psychology General · doi:10.1037/0096-3445.128.2.186 · Cited by 307 · see citing works

Tracking the flow of hippocampal computation: Pattern separation, pattern completion, and attractor dynamics

Knierim, J. J., & Neunuebel, J. P. (2015) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2015.10.008 · Cited by 305 · see citing works

Neural Similarity Between Encoding and Retrieval is Related to Memory Via Hippocampal Interactions

Ritchey, M., Wing, E. A., LaBar, K. S., & Cabeza, R. E. L. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs258 · Cited by 303 · see citing works

The neural basis of implicit learning and memory: A review of neuropsychological and neuroimaging research

Reber, P. J. (2013) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2013.06.019 · Cited by 296 · see citing works

Incorporating rapid neocortical learning of new schema-consistent information into complementary learning systems theory.

McClelland, J. L. (2013) · Journal of Experimental Psychology General · doi:10.1037/a0033812 · Cited by 273 · see citing works

Multiple Scales of Representation along the Hippocampal Anteroposterior Axis in Humans

Brunec, I. K., Bellana, B., Ozubko, J. D., Man, V. Y., Robin, J., Liu, Z., Grady, C. L., Rosenbaum, R. S., Winocur, G., Barense, M. D., et al. (2018) · Current Biology · doi:10.1016/j.cub.2018.05.016 · Cited by 272 · see citing works

Theta rhythm and the encoding and retrieval of space and time

Hasselmo, M. E., & Stern, C. E. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.06.022 · Cited by 261 · see citing works

Tracking the emergence of conceptual knowledge during human decision making

Kumaran, D., Summerfield, J. J., Hassabis, D., & Maguire, E. A. (2009) · Neuron · doi:10.1016/j.neuron.2009.07.030 · Cited by 260 · see citing works

Memory: organization and control.

Eichenbaum, H. (2017) · Annual Review of Psychology · doi:10.1146/annurev-psych-010416-044131 · Cited by 257 · see citing works

Conceptual Object Representations in Human Anterior Temporal Cortex

Peelen, M. V., & Caramazza, A. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.1953-12.2012 · Cited by 240 · see citing works

Object-Specific Semantic Coding in Human Perirhinal Cortex

Clarke, A., & TYLER, L. K. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.2828-13.2014 · Cited by 238 · see citing works

The impact of study design on pattern estimation for single-trial multivariate pattern analysis

Mumford, J. A., Davis, T., & Poldrack, R. A. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.09.026 · Cited by 237 · see citing works

Controlling for interstimulus perceptual variance abolishes N170 face selectivity

Thierry, G., Martin, C. D., Downing, P. E., & Pegna, A. J. (2007) · Nature Neuroscience · doi:10.1038/nn1864 · Cited by 233 · see citing works

Episodic reinstatement in the medial temporal lobe

Staresina, B. P., Henson, R. N. A., Kriegeskorte, N., & Alink, A. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.4156-12.2012 · Cited by 228 · see citing works

Resistance to forgetting associated with hippocampus-mediated reactivation during new learning

Kuhl, B. A., Shah, A. T., DuBrow, S., & Wagner, A. D. (2010) · Nature Neuroscience · doi:10.1038/nn.2498 · Cited by 225 · see citing works

Retrieval of Associative Information Congruent with Prior Knowledge Is Related to Increased Medial Prefrontal Activity and Connectivity

van Kesteren, M. T. R., Rijpkema, M., Ruiter, D. J., & Fernández, G. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2674-10.2010 · Cited by 224 · see citing works

Fast track to the neocortex: A memory engram in the posterior parietal cortex

Brodt, S., Gais, S., Beck, J., Erb, M., Scheffler, K., & Schönauer, M. (2018) · Science · doi:10.1126/science.aau2528 · Cited by 224 · see citing works

Global Similarity and Pattern Separation in the Human Medial Temporal Lobe Predict Subsequent Memory

LaRocque, K. F., Smith, M. E., Carr, V. A., Witthoft, N., Kalanit Grill-spector, A., & Wagner, A. D. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4293-12.2013 · Cited by 222 · 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

Consolidation Promotes the Emergence of Representational Overlap in the Hippocampus and Medial Prefrontal Cortex

Tompary, A., & Davachi, L. (2017) · Neuron · doi:10.1016/j.neuron.2017.09.005 · Cited by 222 · see citing works

Theory of cortical function

Heeger, D. J. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1619788114 · Cited by 220 · see citing works

Rapid neocortical acquisition of long-term arbitrary associations independent of the hippocampus

Sharon, T., Moscovitch, M., & Gilboa, A. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1005238108 · Cited by 213 · see citing works

Medial Prefrontal Cortex Reduces Memory Interference by Modifying Hippocampal Encoding

Guise, K. G., & Shapiro, M. L. (2017) · Neuron · doi:10.1016/j.neuron.2017.03.011 · Cited by 202 · see citing works

Susceptibility to Memory Interference Effects following Frontal Lobe Damage: Findings from Tests of Paired-Associate Learning

Shimamura, A. P., Jurica, P. J., Mangels, J. A., Gershberg, F. B., & Knight, R. T. (1995) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1995.7.2.144 · Cited by 199 · see citing works

Disambiguating the similar: The dentate gyrus and pattern separation

Schmidt, B., Marrone, D. F., & Markus, E. J. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.08.039 · Cited by 198 · 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

The neural processing of familiar and unfamiliar faces: A review and synopsis

Natu, V. S., & O’Toole, A. J. (2011) · British Journal of Psychology · doi:10.1111/j.2044-8295.2011.02053.x · Cited by 192 · see citing works

How do memory systems detect and respond to novelty?

Kafkas, A., & Montaldi, D. (2018) · Neuroscience Letters · doi:10.1016/j.neulet.2018.01.053 · Cited by 185 · see citing works

Recollection- and familiarity-based decisions reflect memory strength

Wiesmann, M. (2008) · Frontiers in Systems Neuroscience · doi:10.3389/neuro.06.001.2008 · Cited by 177 · see citing works

Rapid and independent memory formation in the parietal cortex

Brodt, S., Pöhlchen, D., Flanagin, V. L., Glasauer, S., Gais, S., & Schönauer, M. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1605719113 · Cited by 168 · see citing works

Overlap among Spatial Memories Triggers Repulsion of Hippocampal Representations

Chanales, A. J. H., Oza, A., Favila, S. E., & Kuhl, B. A. (2017) · Current Biology · doi:10.1016/j.cub.2017.06.057 · Cited by 163 · see citing works

Experience-dependent hippocampal pattern differentiation prevents interference during subsequent learning

Favila, S. E., Chanales, A. J. H., & Kuhl, B. A. (2016) · Nature Communications · doi:10.1038/ncomms11066 · Cited by 162 · see citing works

Neuromodulation by Glutamate and Acetylcholine can Change Circuit Dynamics by Regulating the Relative Influence of Afferent Input and Excitatory Feedback

Giocomo, L. M., & Hasselmo, M. E. (2007) · Molecular Neurobiology · doi:10.1007/s12035-007-0032-z · Cited by 161 · see citing works

Adaptive Top–Down Suppression of Hippocampal Activity and the Purging of Intrusive Memories from Consciousness

Benoit, R. G., Hulbert, J. C., Huddleston, E., & Anderson, M. C. (2014) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00696 · Cited by 158 · see citing works

Reinstatement of associative memories in early visual cortex is signaled by the hippocampus

Bosch, S. E., Jehee, J. F. M., Fernández, G., & Doeller, C. F. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.0805-14.2014 · Cited by 157 · see citing works

Retinotopic activation in response to subjective contours in primary visual cortex

Maertens, M. (2008) · Frontiers in Human Neuroscience · doi:10.3389/neuro.09.002.2008 · Cited by 155 · see citing works

Fast mapping rapidly integrates information into existing memory networks.

Coutanche, M. N., & Thompson‐Schill, S. L. (2014) · Journal of Experimental Psychology General · doi:10.1037/xge0000020 · Cited by 152 · see citing works

The Human Dentate Gyrus Plays a Necessary Role in Discriminating New Memories

Baker, S., Vieweg, P., Gao, F., Gilboa, A., Wolbers, T., Black, S. E., & Rosenbaum, R. S. (2016) · Current Biology · doi:10.1016/j.cub.2016.07.081 · Cited by 148 · see citing works

Memory’s Penumbra: Episodic Memory Decisions Induce Lingering Mnemonic Biases

Duncan, K. D., Sadanand, A., & Davachi, L. (2012) · Science · doi:10.1126/science.1221936 · Cited by 146 · see citing works

Norepinephrine and the dentate gyrus

Harley, C. W. (2007) · Progress in brain research · doi:10.1016/s0079-6123(07)63018-0 · Cited by 143 · see citing works

Intact Memory for Irrelevant Information Impairs Perception in Amnesia

Barense, M. D., Groen, I. I. A., Lee, A. C. H., Yeung, L., Brady, S., Gregori, M., Kapur, N., Bussey, T. J., Saksida, L. M., & Henson, R. N. (2012) · Neuron · doi:10.1016/j.neuron.2012.05.014 · Cited by 142 · see citing works

Mode shifting between storage and recall based on novelty detection in oscillating hippocampal circuits

Meeter, M., Murre, J. M. J., & Talamini, L. M. (2004) · Hippocampus · doi:10.1002/hipo.10214 · Cited by 138 · see citing works

Measuring neural representations with fMRI: practices and pitfalls

Davis, T., & Poldrack, R. A. (2013) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12156 · Cited by 132 · see citing works

Event Congruency Enhances Episodic Memory Encoding through Semantic Elaboration and Relational Binding

Staresina, B. P., Gray, J. C., & Davachi, L. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhn165 · Cited by 125 · see citing works

Revisiting the novelty effect: When familiarity, not novelty, enhances memory.

Poppenk, J., Köhler, S., & Moscovitch, M. (2010) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/a0019900 · Cited by 124 · see citing works

Successful Decoding of Famous Faces in the Fusiform Face Area

Axelrod, V., & Yovel, G. (2015) · PLoS ONE · doi:10.1371/journal.pone.0117126 · Cited by 114 · see citing works

Effects of Prior-Knowledge on Brain Activation and Connectivity During Associative Memory Encoding

Liu, Z., Grady, C. L., & Moscovitch, M. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw047 · Cited by 114 · see citing works

Distinguishing multi-voxel patterns and mean activation: Why, how, and what does it tell us?

Coutanche, M. N. (2013) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/s13415-013-0186-2 · Cited by 111 · see citing works

Rapid Cortical Plasticity Supports Long-Term Memory Formation

Hebscher, M., Wing, E. A., Ryan, J. D., & Gilboa, A. (2019) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2019.09.009 · Cited by 110 · see citing works

Anterior cingulate cortex in schema assimilation and expression

Wang, S.-H., Tse, D., & Morris, R. G. M. (2012) · Learning & Memory · doi:10.1101/lm.026336.112 · Cited by 106 · see citing works

Mnemonic prediction errors bias hippocampal states

Bein, O., Duncan, K. D., & Davachi, L. (2020) · Nature Communications · doi:10.1038/s41467-020-17287-1 · Cited by 103 · see citing works

Overlap between the Neural Correlates of Cued Recall and Source Memory: Evidence for a Generic Recollection Network?

Hayama, H. R., Vilberg, K. L., & Rugg, M. D. (2012) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00202 · Cited by 99 · see citing works

Neural Differentiation of Incorrectly Predicted Memories

Kim, G., Norman, K. A., & Turk‐Browne, N. B. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.3272-16.2017 · Cited by 97 · see citing works

Locus Coeruleus Stimulation Facilitates Long-Term Depression in the Dentate Gyrus That Requires Activation of -Adrenergic Receptors

Hansen, N., & Manahan‐Vaughan, D. (2014) · Cerebral Cortex · doi:10.1093/cercor/bht429 · Cited by 96 · see citing works

Schematic memory components converge within angular gyrus during retrieval

Wagner, I. C., van Buuren, M., Kroes, M. C. W., Gutteling, T. P., van der Linden, M., Morris, R., & Fernández, G. (2015) · eLife · doi:10.7554/elife.09668 · Cited by 92 · see citing works

Initial Investigation of the Effects of an Experimentally Learned Schema on Spatial Associative Memory in Humans

van Buuren, M., Kroes, M. C. W., Wagner, I. C., Genzel, L., Morris, R., & Fernández, G. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.2365-14.2014 · Cited by 91 · see citing works

The Emergence of Knowledge and How it Supports the Memory for Novel Related Information

Sommer, T. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw031 · Cited by 91 · see citing works

How multiple repetitions influence the processing of self-, famous and unknown names and faces: An ERP study

Tacikowski, P., Jednoróg, K., Marchewka, A., & Nowicka, A. (2010) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2010.10.010 · Cited by 89 · see citing works

Delineating the Effect of Semantic Congruency on Episodic Memory: The Role of Integration and Relatedness

Bein, O., Livneh, N., Reggev, N., Gilead, M., Goshen-Gottstein, Y., & Maril, A. (2015) · PLoS ONE · doi:10.1371/journal.pone.0115624 · Cited by 86 · see citing works

N250r and N400 ERP correlates of immediate famous face repetition are independent of perceptual load

Neumann, M. F., & Schweinberger, S. R. (2008) · Brain Research · doi:10.1016/j.brainres.2008.08.039 · Cited by 83 · see citing works

Angular Gyrus Involvement at Encoding and Retrieval Is Associated with Durable But Less Specific Memories

van der Linden, M., Berkers, R. M. W. J., Morris, R., & Fernández, G. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.3603-16.2017 · Cited by 82 · see citing works

Temporal Proximity Promotes Integration of Overlapping Events

Zeithamová, D., & Preston, A. R. (2017) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01116 · Cited by 81 · see citing works

Hippocampal representations as a function of time, subregion, and brain state

Duncan, K. D., & Schlichting, M. L. (2018) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2018.03.006 · Cited by 78 · see citing works

The effects of elaboration on recognition memory

Fisher, R. P., & Craik, F. I. M. (1980) · Memory & Cognition · doi:10.3758/bf03211136 · Cited by 77 · see citing works

Memory for Star Trek : The role of prior knowledge in recognition revisited.

Long, D. L., & Prat, C. S. (2002) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037//0278-7393.28.6.1073 · Cited by 75 · see citing works

Prior knowledge influences on hippocampus and medial prefrontal cortex interactions in subsequent memory

Bein, O., Reggev, N., & Maril, A. (2014) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2014.09.046 · Cited by 73 · see citing works

Computation by oscillations: Implications of experimental data for theoretical models of grid cells

Giocomo, L. M., & Hasselmo, M. E. (2008) · Hippocampus · doi:10.1002/hipo.20501 · Cited by 72 · see citing works

Neural network modeling of the hippocampal formation spatial signals and their possible role in navigation: A modular approach

Sharp, P. E., Blair, H. T., & Brown, M. A., Sr. (1996) · Hippocampus · doi:10.1002/(sici)1098-1063(1996)6:6 · Cited by 64 · see citing works

Decoding the content of recollection within the core recollection network and beyond

Thakral, P. P., Wang, T. H., & Rugg, M. D. (2016) · Cortex · doi:10.1016/j.cortex.2016.12.011 · Cited by 64 · see citing works

Experience is a Double-Edged Sword: A Computational Model of The Encoding/Retrieval Trade-Off With Familiarity

Reder, L. M., Paynter, C. A., Diana, R. A., Ngiam, J., & Dickison, D. (2007) · The Psychology of learning and motivation/The psychology of learning and motivation · doi:10.1016/s0079-7421(07)48007-0 · Cited by 61 · see citing works

Trial-by-Trial Hippocampal Encoding Activation Predicts the Fidelity of Cortical Reinstatement During Subsequent Retrieval

Danker, J. F., Tompary, A., & Davachi, L. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw146 · Cited by 59 · see citing works

Using prior knowledge to minimize interference when learning large amounts of information

Kole, J. A., & Healy, A. F. (2007) · Memory & Cognition · doi:10.3758/bf03195949 · Cited by 56 · see citing works

Why It’s Easier to Remember Seeing a Face We Already Know Than One We Don’t

Reder, L. M., Victoria, L. W., Manelis, A., Oates, J. M., Dutcher, J. M., Bates, J., Cook, S. P., Aizenstein, H. J., Quinlan, J. J., & Gyulai, F. E. (2013) · Psychological Science · doi:10.1177/0956797612457396 · Cited by 56 · see citing works

Semantic Congruence Enhances Memory of Episodic Associations: Role of Theta Oscillations

Atienza, M., Crespo‐García, M., & Cantero, J. L. (2009) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21358 · Cited by 52 · see citing works

The effects of prior knowledge on the encoding of episodic contextual details

Dewitt, M. R., Knight, J. B., Hicks, J. L., & Ball, B. H. (2012) · Psychonomic Bulletin & Review · doi:10.3758/s13423-011-0196-4 · Cited by 51 · see citing works

Event congruency and episodic encoding: A developmental fMRI study

Maril, A., Avital, R., Reggev, N., Barton-Zuckerman, M., Sadeh, T., Ben‐Sira, L., & Livneh, N. (2011) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2011.07.004 · Cited by 50 · see citing works

Neurotransmitters and Novelty: A Systematic Review

Rangel‐Gomez, M., & Meeter, M. (2015) · Journal of Psychopharmacology · doi:10.1177/0269881115612238 · Cited by 48 · see citing works

Memory for Star Trek : The role of prior knowledge in recognition revisited.

Long, D. L., & Prat, C. S. (2002) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/0278-7393.28.6.1073 · Cited by 48 · see citing works

Knowledge Acquisition during Exam Preparation Improves Memory and Modulates Memory Formation

Brod, G., Lindenberger, U., Wagner, A. D., & Shing, Y. L. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0045-16.2016 · Cited by 45 · see citing works

Learning of nondomain facts in high- and low-knowledge domains.

Overschelde, J. P. V., & Healy, A. F. (2001) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037//0278-7393.27.5.1160 · Cited by 42 · see citing works

Representations of individuals in ventral temporal cortex defined by faces and biographies

Verosky, S. C., Todorov, A. T., & Turk‐Browne, N. B. (2013) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2013.07.006 · Cited by 37 · see citing works

Distinct Neural Suppression and Encoding Effects for Conceptual Novelty and Familiarity

Reggev, N., Bein, O., & Maril, A. (2016) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00994 · Cited by 35 · see citing works

Mechanisms supporting superior source memory for familiar items: A multi-voxel pattern analysis study

Poppenk, J., & Norman, K. A. (2012) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2012.07.010 · Cited by 31 · see citing works

Learning of nondomain facts in high- and low-knowledge domains.

Overschelde, J. P. V., & Healy, A. F. (2001) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/0278-7393.27.5.1160 · Cited by 31 · see citing works

The role of prior knowledge in incremental associative learning: An empirical and computational approach

Bein, O., Trzewik, M., & Maril, A. (2019) · Journal of Memory and Language · doi:10.1016/j.jml.2019.03.006 · Cited by 28 · see citing works

Neural Correlates of Enhanced Memory for Meaningful Associations with Age

Amer, T., Giovanello, K. S., Nichol, D. R., Hasher, L., & Grady, C. L. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy334 · Cited by 27 · see citing works

Expert knowledge as mnemonic cues

Bellezza, F. S., & Buck, D. K. (1988) · Applied Cognitive Psychology · doi:10.1002/acp.2350020206 · Cited by 16 · see citing works

Semantic knowledge influences whether novel episodic associations are represented symmetrically or asymmetrically

Popov, V., Zhang, Q., Koch, G. E., Calloway, R. C., & Coutanche, M. N. (2019) · Memory & Cognition · doi:10.3758/s13421-019-00950-4 · Cited by 13 · see citing works

Working with Schemas, Predicting with Schemas

Bein, O., Reggev, N., & Tompary, A. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.3281-17.2018 · Cited by 4 · see citing works

Publisher Correction: Mnemonic prediction errors bias hippocampal states

Bein, O., Duncan, K. D., & Davachi, L. (2020) · Nature Communications · doi:10.1038/s41467-020-19656-2 · Cited by 2 · see citing works

Untitled work

Xiong (1999) · doi:10.1002/(sici)1097-0193(1999)8:2/3

Memory consolidation as an adaptive process

Cowan, E. T., Schapiro, A. C., Dunsmoor, J. E., & Murty, V. P. (2021) · Psychonomic Bulletin & Review · doi:10.3758/s13423-021-01978-x · Cited by 133 · see citing works

From cognitive maps to spatial schemas

Farzanfar, D., Spiers, H. J., Moscovitch, M., & Rosenbaum, R. S. (2023) · Nature Reviews Neuroscience · doi:10.1038/s41583-022-00655-9 · Cited by 115 · see citing works

From remembering to reconstruction: The transformative neural representation of episodic memory.

Xue, G. (2022) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2022.102351 · Cited by 49 · see citing works

Protective effect of naoyikang on D-gal-induced injury in cultured hippocampal neurons

Hu, Y.-E. (2006) · Journal of Nantong University

Effection of polychlorinated biphenyls in cultured hippocampal neuronic cells of rats

Yuhong, W. (2002) · Medical Journal of National Defending Forces in Northwest China

Protective effect of brain-derived neurotrophic factor on Aβ25-35-induced hippocampal neuron injury

Tian, Y. (2011)

Effects of hippocampal PGC-1α on depression-like behaviors and number of astrocytes in hippocampal subregions in mice

Yuhu, D., Yuhu, D., Yanmin, L., et al. (2022) · DOAJ (DOAJ: Directory of Open Access Journals) · doi:10.16016/j.2097-0927.202110068

Morphofunctional Changes in Pyramidal Neurons in Various Hippocampal Fields in Ischemic Postconditioning

Щербак, Н. С., Galagudza, M. M., Yukina, G. Y., et al. (2014) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-014-9957-7