Mechanisms underlying working memory for novel information

The episodic buffer: a new component of working memory?

Baddeley, A. (2000) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(00)01538-2 · Cited by 7,359 · see citing works

The medial temporal lobe

Squire, L. R., Stark, C. E. L., & Clark, R. E. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144130 · Cited by 2,680 · see citing works

A Parametric Study of Prefrontal Cortex Involvement in Human Working Memory

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Storage of 7 +/- 2 short-term memories in oscillatory subcycles

Lisman, J. E., & Idiart, M. A. P. (1995) · Science · doi:10.1126/science.7878473 · Cited by 1,471 · see citing works

A Distributed Representation of Temporal Context

Howard, M. W., & Kahana, M. J. (2002) · Journal of Mathematical Psychology · doi:10.1006/jmps.2001.1388 · Cited by 1,174 · see citing works

From Conditioning to Conscious Recollection

Eichenbaum, H., & Cohen, N. J. (2004) · doi:10.1093/acprof:oso/9780195178043.001.0001 · Cited by 1,026 · see citing works

Neural mechanisms for detecting and remembering novel events

Ranganath, C., & Rainer, G. (2003) · Nature Reviews Neuroscience · doi:10.1038/nrn1052 · Cited by 779 · see citing works

Graded persistent activity in entorhinal cortex neurons

Egorov, A. V., Hamam, B. N., Fransén, E., Hasselmo, M. E., & Alonso, A. A. (2002) · Nature · doi:10.1038/nature01171 · Cited by 769 · see citing works

Activity of neurons in anterior inferior temporal cortex during a short- term memory task

Miller, E. K., Li, L., & Desimone, R. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-04-01460.1993 · Cited by 732 · see citing works

Neurocomputational models of working memory

Durstewitz, D., Seamans, J. K., & B, T. J. S. A. (2000) · Nature Neuroscience · doi:10.1038/81460 · Cited by 710 · see citing works

Neural Activity in the Primate Prefrontal Cortex during Associative Learning

Asaad, W. F., Rainer, G., & Miller, E. K. (1998) · Neuron · doi:10.1016/s0896-6273(00)80658-3 · Cited by 593 · see citing works

Lasting Consequences of Bilateral Medial Temporal Lobectomy: Clinical Course and Experimental Findings in H.M.

Corkin, S. (1984) · Seminars in Neurology · doi:10.1055/s-2008-1041556 · Cited by 582 · see citing works

Heightened synaptic plasticity of hippocampal CA1 neurons during a Cholinergically induced rhythmic state

Huerta, P. T., & Lisman, J. E. (1993) · Nature · doi:10.1038/364723a0 · Cited by 564 · see citing works

Selective cognitive dysfunction in acetylcholine M1 muscarinic receptor mutant mice

Anagnostaras, S., Murphy, G. G., Hamilton, S. E., Mitchell, S. L., Rahnama, N. P., Nathanson, N. M., & Silva, A. J. (2002) · Nature Neuroscience · doi:10.1038/nn992 · Cited by 543 · see citing works

Hippocampal sequence-encoding driven by a cortical multi-item working memory buffer

Jensen, O. B., & Lisman, J. E. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.12.001 · Cited by 467 · see citing works

Working Memory for Conjunctions Relies on the Medial Temporal Lobe

Olson, I. R., Page, K., Moore, K., Chatterjee, A., & Verfaellie, M. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1923-05.2006 · Cited by 426 · see citing works

Medial Temporal Lobe Activity Associated with Active Maintenance of Novel Information

Charan Ranganath, A., & D’Esposito, M. (2001) · Neuron · doi:10.1016/s0896-6273(01)00411-1 · Cited by 391 · see citing works

Phase Locking of Single Neuron Activity to Theta Oscillations during Working Memory in Monkey Extrastriate Visual Cortex

Lee, H. B., Simpson, G. V., Logothetis, N. K., & Rainer, G. (2005) · Neuron · doi:10.1016/j.neuron.2004.12.025 · Cited by 388 · see citing works

Object and Place Memory in the Macaque Entorhinal Cortex

SUZUKI, W. A., Miller, E. K., & Desimone, R. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.78.2.1062 · Cited by 383 · see citing works

Doubts about double dissociations between short- and long-term memory

Charan Ranganath, A., & Blumenfeld, R. S. (2005) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2005.06.009 · Cited by 376 · see citing works

Memory Representation within the Parahippocampal Region

Young, B. J., Otto, T., Fox, G. D., & Eichenbaum, H. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-13-05183.1997 · Cited by 363 · see citing works

Neuronal activity related to visual recognition memory: long-term memory and the encoding of recency and familiarity information in the primate anterior and medial inferior temporal and rhinal cortex

Fahy, F. L., Riches, I. P., & Brown, M. W. (1993) · Experimental Brain Research · doi:10.1007/bf00234113 · Cited by 359 · see citing works

Complementary roles of the orbital prefrontal cortex and the perirhinal-entorhinal cortices in an odor-guided delayed-nonmatching-to-sample task.

Otto, T., & Eichenbaum, H. (1992) · Behavioral Neuroscience · doi:10.1037/0735-7044.106.5.762 · Cited by 343 · see citing works

The effects of visual stimulation and memory on neurons of the hippocampal formation and the neighboring parahippocampal gyrus and inferior temporal cortex of the primate

Riches, I. P., Wilson, F., & Mw, B. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-06-01763.1991 · Cited by 336 · see citing works

Complementary roles of the orbital prefrontal cortex and the perirhinal-entorhinal cortices in an odor-guided delayed-nonmatching-to-sample task.

Otto, T., & Eichenbaum, H. (1992) · Behavioral Neuroscience · doi:10.1037//0735-7044.106.5.762 · Cited by 317 · see citing works

Preserved Recognition Memory for Small Sets, and Impaired Stimulus Identification for Large Sets, Following Rhinal Cortex Ablations in Monkeys

Eacott, M. J., Gaffan, D., & Murray, E. A. (1994) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1994.tb01008.x · Cited by 293 · see citing works

Mechanism of Graded Persistent Cellular Activity of Entorhinal Cortex Layer V Neurons

Fransén, E., Tahvildari, B., Egorov, A. V., Hasselmo, M. E., & Alonso, A. A. (2006) · Neuron · doi:10.1016/j.neuron.2006.01.036 · Cited by 279 · see citing works

Monkeys (Macaca fascicularis) with rhinal cortex ablations succeed in object discrimination learning despite 24-hr intertrial intervals and fail at matching to sample despite double sample presentations.

Gaffan, D., & Murray, E. A. (1992) · Behavioral Neuroscience · doi:10.1037//0735-7044.106.1.30 · Cited by 265 · see citing works

Patterns of memory failure after scopolamine treatment: Implications for cholinergic hypotheses of dementia

Beatty, W. W., Butters, N., & Janowsky, D. S. (1986) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(86)90772-7 · Cited by 249 · see citing works

Medial temporal and prefrontal contributions to working memory tasks with novel and familiar stimuli

Stern, C. E., Sherman, S. J., Kirchhoff, B. A., & Hasselmo, M. E. (2001) · Hippocampus · doi:10.1002/hipo.1048 · Cited by 244 · see citing works

Directing the mind's eye: prefrontal, inferior and medial temporal mechanisms for visual working memory

Charan Ranganath, A., & D’Esposito, M. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.03.017 · Cited by 235 · see citing works

Muscarinic Modulation of the Oscillatory and Repetitive Firing Properties of Entorhinal Cortex Layer II Neurons

Klink, R., & Alonso, A. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.77.4.1813 · Cited by 228 · see citing works

Cholinergic Neurotransmission Is Essential for Perirhinal Cortical Plasticity and Recognition Memory

Warburton, E. C., Koder, T., Cho, K., Massey, P. V., Duguid, G., Barker, G. R. I., Aggleton, J. P., Bashir, Z. I., & Brown, M. W. (2003) · Neuron · doi:10.1016/s0896-6273(03)00358-1 · Cited by 226 · see citing works

Visual Working Memory Is Impaired when the Medial Temporal Lobe Is Damaged

Olson, I. R., Moore, K. S., Stark, M., & Chatterjee, A. K. (2006) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2006.18.7.1087 · Cited by 221 · see citing works

Modelling dementia: Effects of scopolamine on memory and attention

Broks, P., Preston, G. C., Traub, M., Poppleton, P., Ward, C., & Stahl, S. M. (1988) · Neuropsychologia · doi:10.1016/0028-3932(88)90004-8 · Cited by 220 · see citing works

Monkeys (Macaca fascicularis) with rhinal cortex ablations succeed in object discrimination learning despite 24-hr intertrial intervals and fail at matching to sample despite double sample presentations.

Gaffan, D., & Murray, E. A. (1992) · Behavioral Neuroscience · doi:10.1037/0735-7044.106.1.30 · Cited by 217 · see citing works

Persistence of Parahippocampal Representation in the Absence of Stimulus Input Enhances Long-Term Encoding: A Functional Magnetic Resonance Imaging Study of Subsequent Memory after a Delayed Match-to-Sample Task

Schon, K., Hasselmo, M. E., LoPresti, M. L., Tricarico, M. D., & Stern, C. E. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.3807-04.2004 · Cited by 191 · see citing works

Novel lists of 7 +/- 2 known items can be reliably stored in an oscillatory short-term memory network: interaction with long-term memory.Preprint

Jensen, O. B., & Lisman, J. E. (1996) · Learning & Memory · doi:10.1101/lm.3.2-3.257 · Cited by 183 · see citing works

Blockade of Central Cholinergic Receptors Impairs New Learning and Increases Proactive Interference in a Word Paired-Associate Memory Task.

Atri, A., Sherman, S. J., Norman, K. A., Kirchhoff, B. A., Nicolas, M. M., Greicius, M. D., Cramer, S. C., Breiter, H. C., Hasselmo, M. E., & Stern, C. E. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.1.223 · Cited by 162 · see citing works

Theta/gamma networks with slow NMDA channels learn sequences and encode episodic memory: role of NMDA channels in recall.Preprint

Jensen, O. B., & Lisman, J. E. (1996) · Learning & Memory · doi:10.1101/lm.3.2-3.264 · Cited by 152 · see citing works

An analysis of the learning deficit following hyoscine administration to man

Crow, T. J., & GROVE-WHITE, I. G. (1973) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.1973.tb08379.x · Cited by 140 · see citing works

Effects of scopolamine on delayed-matching-to-sample and paired associates tests of visual memory and learning in human subjects: comparison with diazepam and implications for dementia

Robbins, T. W., Semple, J., Kumar, R., Truman, M. I., Shorter, J., Ferraro, A., Fox, B., McKay, G., & Matthews, K. (1997) · Psychopharmacology · doi:10.1007/s002130050430 · Cited by 138 · see citing works

Simulations of the Role of the Muscarinic-Activated Calcium-Sensitive Nonspecific Cation Current<i>I_NCM</i>in Entorhinal Neuronal Activity during Delayed Matching Tasks

Fransén, E., Alonso, A. A., & Hasselmo, M. E. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-03-01081.2002 · Cited by 137 · see citing works

Comparison of computational models of familiarity discrimination in the perirhinal cortex

Bogacz, R., & Brown, M. W. (2003) · Hippocampus · doi:10.1002/hipo.10093 · Cited by 134 · see citing works

The animal model of human amnesia: long-term memory impaired and short-term memory intact.

Alvarez, P., Zola-Morgan, S. M., & Squire, L. R. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.12.5637 · Cited by 134 · see citing works

Scopolamine Reduces Persistent Activity Related to Long-Term Encoding in the Parahippocampal Gyrus during Delayed Matching in Humans

Schon, K., Atri, A., Hasselmo, M. E., Tricarico, M. D., LoPresti, M. L., & Stern, C. E. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.1982-05.2005 · Cited by 132 · see citing works

Muscarinic and nicotinic receptor modulation of object and spatial -back working memory in humans

GREEN, A., Ellis, K. A., Ellis, J. R., Bartholomeusz, C., ILIC, S., Croft, R. J., LUANPHAN, K., & NATHAN, P. (2005) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2005.04.010 · Cited by 127 · see citing works

Ionic Mechanism of the Slow Afterdepolarization Induced by Muscarinic Receptor Activation in Rat Prefrontal Cortex

Haj-Dahmane, S., & Andrade, R. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.3.1197 · Cited by 126 · see citing works

Effects of muscarinic blockade in perirhinal cortex during visual recognition

Tang, Y., Mishkin, M., & Aigner, T. G. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.23.12667 · Cited by 125 · see citing works

Comparison of the effects of scopolamine administered before and after acquisition in a test of visual recognition memory in monkeys

Aigner, T. G., Walker, D. L., & Mishkin, M. (1991) · Behavioral and Neural Biology · doi:10.1016/0163-1047(91)80127-z · Cited by 117 · see citing works

Cholinergic Deafferentation of the Entorhinal Cortex in Rats Impairs Encoding of Novel But Not Familiar Stimuli in a Delayed Nonmatch-to-Sample Task

McGaughy, J. A., Koene, R. A., Eichenbaum, H., & Hasselmo, M. E. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2386-05.2005 · Cited by 103 · see citing works

Effects of cholinergic drugs on delayed match-to-sample performance of rhesus monkeys

Penetar, D. M., & McDonough, J. H. (1983) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(83)90399-4 · Cited by 96 · see citing works

Modeling goal-directed spatial navigation in the rat based on physiological data from the hippocampal formation

Koene, R. A., Anatoli Gorchetchnikov, A., Cannon, R. C., & Hasselmo, M. E. (2003) · Neural Networks · doi:10.1016/s0893-6080(03)00106-0 · Cited by 87 · see citing works

Neuronal Responses Related to Long-Term Recognition Memory Processes in Prefrontal Cortex

Xiang, J.-Z., & Brown, M. W. (2004) · Neuron · doi:10.1016/j.neuron.2004.05.013 · Cited by 86 · see citing works

Modelling Hebbian cell assemblies comprised of cortical neurons

Lansner, A., & Fransen, E. J. (1992) · Network Computation in Neural Systems · doi:10.1088/0954-898x_3_2_002 · Cited by 83 · see citing works

Effects of cholinergic deafferentation of the rhinal cortex on visual recognition memory in monkeys

Turchi, J. N., Saunders, R. C., & Mishkin, M. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0409708102 · Cited by 70 · see citing works

Scopolamine affects short-term memory but not inferior temporal neurons

Miller, E. K., & Desimone, R. (1993) · NeuroReport · doi:10.1097/00001756-199301000-00021 · Cited by 66 · see citing works

Muscarinic Activation of a Cation Current and Associated Current Noise in Entorhinal-Cortex Layer-II Neurons

Shalinsky, M. H., Magistretti, J., Ma, L., & Alonso, A. A. (2002) · Journal of Neurophysiology · doi:10.1152/jn.2002.88.3.1197 · Cited by 65 · see citing works

Unilateral Lesions of the Cholinergic Basal Forebrain and Fornix in One Hemisphere and Inferior Temporal Cortex in the Opposite Hemisphere Produce Severe Learning Impairments in Rhesus Monkeys

Easton, A. (2002) · Cerebral Cortex · doi:10.1093/cercor/12.7.729 · Cited by 63 · see citing works

Memory networks in the prefrontal cortex

Fuster, J. M. (2000) · Progress in Brain Research · doi:10.1016/s0079-6123(08)62147-0 · Cited by 51 · see citing works

Effects of Scopolamine on Matching to Sample Paradigm and Related Tests in Human Subjects

Koller, G., Satzger, W., Adam, M., Wagner, M., Kathmann, N., Soyka, M., & Engel, R. R. (2003) · Neuropsychobiology · doi:10.1159/000072883 · Cited by 40 · see citing works

Effects of scopolamine on performance of rats in a delayed-response radial maze task

Bolhuis, J. J., Strijkstra, A. M., & Kramers, R. J. K. (1988) · Physiology & Behavior · doi:10.1016/0031-9384(88)90111-4 · Cited by 31 · see citing works

An opportunity cost model of subjective effort and task performance

Kurzban, R., Duckworth, A., Kable, J. W., & Myers, J. (2013) · Behavioral and Brain Sciences · doi:10.1017/s0140525x12003196 · Cited by 1,381 · see citing works

Consciousness, accessibility, and the mesh between psychology and neuroscience

Block, N. (2007) · Behavioral and Brain Sciences · doi:10.1017/s0140525x07002786 · Cited by 1,146 · see citing works

Modes and models of forebrain cholinergic neuromodulation of cognition

Hasselmo, M. E., & Sarter, M. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2010.104 · Cited by 733 · see citing works

Incorporating Learnable Membrane Time Constant to Enhance Learning of Spiking Neural Networks

Fang, W., Yu, Z., Chen, Y., Masquelier, T., Huang, T., & Tian, Y. (2021) · IEEE/CVF International Conference on Computer Vision (ICCV) · doi:10.1109/iccv48922.2021.00266 · Cited by 673 · 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

Entorhinal Cortex Layer III Input to the Hippocampus Is Crucial for Temporal Association Memory

Suh, J., Rivest, A. J., Nakashiba, T., Tominaga, T., & Tonegawa, S. (2011) · Science · doi:10.1126/science.1210125 · Cited by 352 · see citing works

Neurotrophic factors in Alzheimer’s disease: role of axonal transport

Schindowski, K., Bélarbi, K., & Buée, L. (2008) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2007.00378.x · Cited by 335 · see citing works

Mapping aesthetic musical emotions in the brain

Trost, W., Ethofer, T., Zentner, M., & Vuilleumier, P. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr353 · Cited by 326 · see citing works

Working models of working memory

Barak, O., & Tsodyks, M. V. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.10.008 · Cited by 281 · see citing works

The attentional blink provides episodic distinctiveness: Sparing at a cost.

Wyble, B., Bowman, H., & Nieuwenstein, M. R. (2009) · Journal of Experimental Psychology Human Perception & Performance · doi:10.1037/a0013902 · Cited by 271 · see citing works

Complementary learning systems

O’Reilly, R. C., Bhattacharyya, R., Howard, M. D., & Ketz, N. (2014) · Cognitive Science · doi:10.1111/j.1551-6709.2011.01214.x · Cited by 259 · see citing works

Grid cell firing may arise from interference of theta frequency membrane potential oscillations in single neurons

Hasselmo, M. E., Giocomo, L. M., & Zilli, E. A. (2007) · Hippocampus · doi:10.1002/hipo.20374 · Cited by 246 · see citing works

Neuromodulatory Systems and Their Interactions: A Review of Models, Theories, and Experiments

Avery, M. C., & Krichmar, J. L. (2017) · Frontiers in Neural Circuits · doi:10.3389/fncir.2017.00108 · Cited by 231 · see citing works

Slow and Fast Gamma Rhythms Coordinate Different Spatial Coding Modes in Hippocampal Place Cells

Bieri, K. W., Bobbitt, K. N., & Colgin, L. L. (2014) · Neuron · doi:10.1016/j.neuron.2014.03.013 · Cited by 221 · see citing works

Visual Working Memory Is Impaired when the Medial Temporal Lobe Is Damaged

Olson, I. R., Moore, K. S., Stark, M., & Chatterjee, A. K. (2006) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2006.18.7.1087 · Cited by 221 · see citing works

Grid cell mechanisms and function: Contributions of entorhinal persistent spiking and phase resetting

Hasselmo, M. E. (2008) · Hippocampus · doi:10.1002/hipo.20512 · Cited by 209 · see citing works

Interactions between medial temporal lobe, prefrontal cortex, and inferior temporal regions during visual working memory: a combined intracranial EEG and functional magnetic resonance imaging study

Axmacher, N., Schmitz, D. P., Wagner, T., Elger, C. E., & Fell, J. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.1778-08.2008 · Cited by 204 · see citing works

A Flexible Model of Working Memory

Bouchacourt, F., & Buschman, T. J. (2019) · Neuron · doi:10.1016/j.neuron.2019.04.020 · Cited by 196 · see citing works

Mechanisms of Persistent Activity in Cortical Circuits: Possible Neural Substrates for Working Memory

Zylberberg, J., & Strowbridge, B. W. (2017) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-070815-014006 · Cited by 192 · see citing works

Which computational mechanisms operate in the hippocampus during novelty detection?

Kumaran, D., & Maguire, E. A. (2007) · Hippocampus · doi:10.1002/hipo.20326 · Cited by 197 · see citing works

Rapid instructed task learning: A new window into the human brain’s unique capacity for flexible cognitive control

Cole, M. W., Laurent, P. A., & Stocco, A. (2012) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-012-0125-7 · Cited by 195 · see citing works

Cholinergic modulation of cognitive processing: insights drawn from computational models

Newman, E. L., Gupta, K., Climer, J. R., Monaghan, C. K., & Hasselmo, M. E. (2012) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2012.00024 · Cited by 185 · see citing works

Emotional valence and arousal affect reading in an interactive way: Neuroimaging evidence for an approach-withdrawal framework

CITRON, F. M. M., Gray, M. A., Critchley, H., Weekes, B., & Ferstl, E. C. (2014) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2014.01.002 · Cited by 190 · see citing works

A sense of direction in human entorhinal cortex

Jacobs, J., Kahana, M. J., Ekstrom, A. D., Mollison, M. V., & Fried, I. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0911213107 · Cited by 178 · see citing works

Cholinergic modulation of cognition: Insights from human pharmacological functional neuroimaging

Bentley, P., Driver, J., & Dolan, R. J. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.06.002 · Cited by 173 · see citing works

Acetylcholine and memory: A long, complex and chaotic but still living relationship

Micheau, J., & Marighetto, A. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.11.052 · Cited by 164 · see citing works

The what, where and how of delay activity

Sreenivasan, K. K., & D’Esposito, M. (2019) · Nature reviews. Neuroscience · doi:10.1038/s41583-019-0176-7 · Cited by 156 · see citing works

A model of episodic memory: Mental time travel along encoded trajectories using grid cells

Hasselmo, M. E. (2009) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2009.07.005 · Cited by 157 · see citing works

Recognition memory: Material, processes, and substrates

Brown, M. W., Warburton, E. C., & Aggleton, J. P. (2010) · Hippocampus · doi:10.1002/hipo.20858 · Cited by 138 · see citing works

Activating the medial temporal lobe during oddity judgment for faces and scenes.

Lee, A. C. H., Scahill, V., & Graham, K. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm104 · Cited by 154 · see citing works

Interactions between prefrontal cortex and cerebellum revealed by trace eyelid conditioningPreprint

Kalmbach, B. E., Ohyama, T., Kreider, J. C., Riusech, F., & Mauk, M. D. (2009) · Learning & Memory · doi:10.1101/lm.1178309 · Cited by 136 · see citing works

Regulation of cholinergic activity by the vesicular acetylcholine transporter

Prado, V. F., Roy, A., Kolisnyk, B., Gros, R., & Prado, M. A. M. (2013) · Biochemical Journal · doi:10.1042/bj20121662 · Cited by 133 · see citing works

Assessing behavioural and cognitive domains of autism spectrum disorders in rodents: current status and future perspectives

Kas, M. J., Glennon, J. C., Buitelaar, J., Ey, E., Biemans, B., Crawley, J., Ring, R. H., Lajonchere, C., Esclassan, F., Talpos, J., et al. (2014) · Psychopharmacology · doi:10.1007/s00213-013-3268-5 · Cited by 132 · see citing works

Medial Temporal Lobe Coding of Item and Spatial Information during Relational Binding in Working Memory

Libby, L. A., Hannula, D. E., & Charan Ranganath, A. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0655-14.2014 · Cited by 130 · see citing works

ChAT-ChR2-EYFP Mice Have Enhanced Motor Endurance But Show Deficits in Attention and Several Additional Cognitive Domains

Kolisnyk, B., Guzmán-Lenis, M.-S., Raulic, S., Fan, J., Magalhães, A. C., Feng, G., Gros, R., Prado, V. F., & Prado, M. A. M. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0395-13.2013 · Cited by 125 · see citing works

Astrocyte‐derived kynurenic acid modulates basal and evoked cortical acetylcholine release

Zmarowski, A., Wu, H., Brooks, J. M., Potter, M. C., Pellicciari, R., Schwarcz, R. M., & Bruno, J. P. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06594.x · Cited by 121 · see citing works

Switching between “On” and “Off” states of persistent activity in lateral entorhinal layer III neurons

Tahvildari, B., Fransén, E. A., Alonso, A. A., & Hasselmo, M. E. (2007) · Hippocampus · doi:10.1002/hipo.20270 · Cited by 113 · see citing works

Computational models of cognitive control

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A biologically inspired hierarchical goal directed navigation model

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Replay of Very Early Encoding Representations during Recollection

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Novel scenes improve recollection and recall of words

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mGluR‐dependent persistent firing in entorhinal cortex layer III neurons

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Perirhinal Cortex Contributes to Accuracy in Recognition Memory and Perceptual Discriminations

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Impaired Medial Temporal Repetition Suppression is Related to Failure of Parietal Deactivation in Alzheimer Disease

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Possible role of acetylcholine in regulating spatial novelty effects on theta rhythm and grid cells

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Age-dependent regulation of synaptic connections by dopamine D2 receptors

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Metabotropic Induction of Persistent Activity in Layers II/III of Anterior Cingulate Cortex

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Auditory trace fear conditioning requires perirhinal cortex

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Greater Working Memory Load Results in Greater Medial Temporal Activity at Retrieval

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Differing time dependencies of object recognition memory impairments produced by nicotinic and muscarinic cholinergic antagonism in perirhinal cortexPreprint

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Functional Dissociation within the Entorhinal Cortex for Memory Retrieval of an Association between Temporally Discontiguous Stimuli

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Bridging Integrator 1 (BIN1) Genotype Effects on Working Memory, Hippocampal Volume, and Functional Connectivity in Young Healthy Individuals

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Comparison of Associative Learning-Related Signals in the Macaque Perirhinal Cortex and Hippocampus

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The entorhinal cortex and neurotrophin signaling in Alzheimer’s disease and other disorders

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Activating Developmental Reserve Capacity Via Cognitive Training or Non-invasive Brain Stimulation: Potentials for Promoting Fronto-Parietal and Hippocampal-Striatal Network Functions in Old Age

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Dendritic Generation of mGluR-Mediated Slow Afterdepolarization in Layer 5 Neurons of Prefrontal Cortex

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Bridging Scales in Alzheimer's Disease: Biological Framework for Brain Simulation With The Virtual Brain

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Cellular dynamical mechanisms for encoding the time and place of events along spatiotemporal trajectories in episodic memory

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Hippocampal networks habituate as novelty accumulatesPreprint

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Neurophysiological coding of space and time in the hippocampus, entorhinal cortex, and retrosplenial cortex

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Balancing Flexibility and Interference in Working Memory

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Ligand-Dependent TrkA Activity in Brain Differentially Affects Spatial Learning and Long-Term Memory

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Muscarinic acetylcholine neurotransmission enhances the late-phase of long-term potentiation in the hippocampal–prefrontal cortex pathway of rats in vivo: A possible involvement of monoaminergic systems

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Remembering forward: Neural correlates of memory and prediction in human motor adaptation

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The neural correlates of reward-related trial-and-error learning: An fMRI study with a probabilistic learning taskPreprint

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Cell-Specific Cholinergic Modulation of Excitability of Layer 5B Principal Neurons in Mouse Auditory Cortex

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Forgetting Unwanted Memories: Active Forgetting and Implications for the Development of Psychological Disorders

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Decoding oscillatory representations and mechanisms in memory

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Pharmacological Interventions for the MATRICS Cognitive Domains in Schizophrenia: What’s the Evidence?

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A Working Memory Buffer in Parahippocampal Regions: Evidence from a Load Effect during the Delay Period

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The right parahippocampal gyrus contributes to the formation and maintenance of bound information in working memory

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