The DOI matches its Crossref record; 110 of the 110 references it cites were found in a registry or an index.
Long-axis specialization of the human hippocampus
Abstract
Investigation of the hippocampus has historically focused on computations within the trisynaptic circuit. However, discovery of important anatomical and functional variability along its long axis has inspired recent proposals of long-axis functional specialization in both the animal and human literatures. Here, we review and evaluate these proposals. We suggest that various long-axis specializations arise out of differences between the anterior (aHPC) and posterior hippocampus (pHPC) in large-scale network connectivity, the organization of entorhinal grid cells, and subfield compositions that bias the aHPC and pHPC towards pattern completion and separation, respectively. The latter two differences give rise to a property, reflected in the expression of multiple other functional specializations, of coarse, global representations in anterior hippocampus and fine-grained, local representations in posterior hippocampus.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“One possible explanation for the different engagement of the posterior and anterior HPC in generalization relates to spatial scale, with the posterior HPC encoding room or junction spaces, and the anterior HPC encoding large-scale (outdoor) spaces 76 .”
From From cognitive maps to spatial schemas (2023) · cites this paper as [76]
In the citing paper
“with MTT/TTT predicting that the hippocampus, and in particular the posterior hippocampus, would play a more important role if detailed processing is required (Poppenk et al. 2013).”
From Hippocampal and Retrosplenial Goal Distance Coding After Long-term Consolidation of a Real-World Environment (2019) · cites this paper as Poppenk et al. 2013
In the citing paper
“and the posterior locus agrees with the view that posterior hippocampus processes fine detail, such as spatial metric information (Poppenk et al. 2013).”
From Hippocampal and Retrosplenial Goal Distance Coding After Long-term Consolidation of a Real-World Environment (2019) · cites this paper as Poppenk et al. 2013
In the citing paper
“In contrast, posterior hippocampus contributed equally to subsequent hits and false alarms, consistent with its role in representing detailed contextual information that more generally supports recollection (59).”
From Neural mechanisms of reactivation-induced updating that enhance and distort memory (2013) · cites this paper as [59]
In the citing paper
“A related line of research suggests that the hippocampus and ventromedial prefrontal cortex (vmPFC) support flexible memory processes that allow memories to be combined and used in novel ways, and that contribute to memory updating.”
From Neural mechanisms of reactivation-induced updating that enhance and distort memory (2013) · cites this paper as [59]
In the citing paper
“Additionally, the anterior hippocampus represents global context through its connections with vmPFC and related schematic processes that could support the incorporation of novel information (59).”
From Neural mechanisms of reactivation-induced updating that enhance and distort memory (2013) · cites this paper as [59]
In the citing paper
“Besides, the connectivity of the hippocampus varies along its anterior–posterior axis, with the posterior part being more strongly connected to the PCC (Poppenk et al., 2013).”
From Hippocampal subfield volumetry in mild cognitive impairment, Alzheimer's disease and semantic dementia (2013) · cites this paper as Poppenk et al., 2013
Citations
Cites
(1978) · UA Campus Repository (The University of Arizona) · Cited by 8,010
Self-citationLOSS OF RECENT MEMORY AFTER BILATERAL HIPPOCAMPAL LESIONS
Scoville, W. B., & Milner, B. (1957) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp.20.1.11 · Cited by 7,322
The hippocampus as a cognitive map
Passingham, R. E. (1979) · Neuroscience · doi:10.1016/0306-4522(79)90015-0 · Cited by 5,128
Microstructure of a spatial map in the entorhinal cortex
Hafting, T., Fyhn, M., Molden, S., Moser, M.-B., & Moser, E. I. (2005) · Nature · doi:10.1038/nature03721 · Cited by 4,068
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
The reward circuit: linking primate anatomy and human imaging
Haber, S. N., & Knutson, B. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2009.129 · Cited by 3,718
Are the Dorsal and Ventral Hippocampus Functionally Distinct Structures?
Fanselow, M. S., & Dong, H.-W. (2010) · Neuron · doi:10.1016/j.neuron.2009.11.031 · Cited by 3,358
Where do you know what you know? The representation of semantic knowledge in the human brain
Patterson, K., Nestor, P. J., & Rogers, T. T. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2277 · Cited by 2,706
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
Place Cells, Grid Cells, and the Brain's Spatial Representation System
Moser, E. I., Kropff, E., & Moser, M.-B. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.31.061307.090723 · Cited by 1,934
Flagged first, then by citations
Cited by
Sorted by citations
Functional organization of the hippocampal longitudinal axis
Strange, B. A., Witter, M. P., Lein, E. S., & Moser, E. I. (2014) · Nature reviews. Neuroscience · doi:10.1038/nrn3785 · Cited by 1,738
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
The Molecular and Systems Biology of Memory
Kandel, E. R., Dudai, Y., & Mayford, M. R. (2014) · Cell · doi:10.1016/j.cell.2014.03.001 · Cited by 1,134
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
Self-citationPrefrontal–hippocampal interactions in episodic memory
Eichenbaum, H. (2017) · Nature Reviews Neuroscience · doi:10.1038/nrn.2017.74 · Cited by 870
Topographic organization of the human subcortex unveiled with functional connectivity gradients
Tian, Y., Margulies, D. S., Breakspear, M. J., & Zalesky, A. (2020) · Nature Neuroscience · doi:10.1038/s41593-020-00711-6 · Cited by 808
What Learning Systems do Intelligent Agents Need? Complementary Learning Systems Theory Updated
Kumaran, D., Hassabis, D., & McClelland, J. L. (2016) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2016.05.004 · Cited by 759
Domain generality versus modality specificity: the paradox of statistical learning
Frost, R., Armstrong, B. C., Siegelman, N., & Christiansen, M. H. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2014.12.010 · Cited by 601
Anterior hippocampus: the anatomy of perception, imagination and episodic memory
Zeidman, P., & Maguire, E. A. (2016) · Nature Reviews Neuroscience · doi:10.1038/nrn.2015.24 · Cited by 542
Schapiro, A. C., Turk‐Browne, N. B., Botvinick, M., & Norman, K. A. (2016) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2016.0049 · Cited by 530
The hippocampus in aging and disease: From plasticity to vulnerability
Bartsch, T., & Wulff, P. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.07.084 · Cited by 499
Schlichting, M. L., Mumford, J. A., & Preston, A. R. (2015) · Nature Communications · doi:10.1038/ncomms9151 · Cited by 381
The hippocampus and related neocortical structures in memory transformation
Sekeres, M. J., Winocur, G., & Moscovitch, M. (2018) · Neuroscience Letters · doi:10.1016/j.neulet.2018.05.006 · Cited by 370
Self-citationStructural imaging of hippocampal subfields in healthy aging and Alzheimer’s disease
de Florès, R., Joie, R. L., & Chételat, G. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.08.033 · Cited by 387
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 363
The slow forgetting of emotional episodic memories: an emotional binding account
Yonelinas, A. P., & Ritchey, M. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.02.009 · Cited by 341
Memory and Space: Towards an Understanding of the Cognitive Map
Schiller, D., Eichenbaum, H., Buffalo, E. A., Davachi, L., Foster, D. J., Leutgeb, S., & Ranganath, C. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.2618-15.2015 · Cited by 340
Howard, L. R., Javadi, A. H., Yu, Y., Mill, R. D., Morrison, L. C., Knight, R., Loftus, M. M., Staskute, L., & Spiers, H. J. (2014) · Current Biology · doi:10.1016/j.cub.2014.05.001 · Cited by 298
Medial temporal lobe connectivity and its associations with cognition in early Alzheimer’s disease
Berron, D., van Westen, D., Ossenkoppele, R., Strandberg, O. T., & Hansson, O. (2020) · Brain · doi:10.1093/brain/awaa068 · Cited by 310
Hierarchical dynamics as a macroscopic organizing principle of the human brain
Raut, R. V., Snyder, A. Z., & Raichle, M. E. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2003383117 · Cited by 307
La Joie, R., Perrotin, A., de La Sayette, V., Egret, S., Doeuvre, L., Belliard, S., Eustache, F., Desgranges, B., & Chételat, G. (2013) · NeuroImage: Clinical · doi:10.1016/j.nicl.2013.08.007 · Cited by 290
Bakker, A., Albert, M., Krauss, G. L., Speck, C. L., & Gallagher, M. (2015) · NeuroImage Clinical · doi:10.1016/j.nicl.2015.02.009 · Cited by 295
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 305
Self-citationCortico-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 293
Robin, J., & Moscovitch, M. (2017) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2017.07.016 · Cited by 266
Self-citationMemory: organization and control.
Eichenbaum, H. (2017) · Annual Review of Psychology · doi:10.1146/annurev-psych-010416-044131 · Cited by 257
Memory hierarchies map onto the hippocampal long axis in humans
Collin, S. H. P., Milivojevic, B., & Doeller, C. F. (2015) · Nature Neuroscience · doi:10.1038/nn.4138 · Cited by 256
Anatomical and microstructural determinants of hippocampal subfield functional connectome embedding
de Wael, R. V., Larivière, S., Caldairou, B., Hong, S., Margulies, D. S., Jefferies, E., Bernasconi, A., Smallwood, J., Bernasconi, N., & Bernhardt, B. C. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1803667115 · Cited by 248
Prefrontal–hippocampal pathways underlying inhibitory control over memory
Anderson, M. C., Bunce, J. G., & Barbas, H. (2015) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2015.11.008 · Cited by 269
Hippocampal—diencephalic—cingulate networks for memory and emotion: an anatomical guide
Bubb, E. J., Kinnavane, L., & Aggleton, J. P. (2017) · Brain and Neuroscience Advances · doi:10.1177/2398212817723443 · Cited by 234
Persistence of hippocampal multivoxel patterns into postencoding rest is related to memory
Tambini, A., & Davachi, L. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1308499110 · Cited by 230
A Brain System for Auditory Working Memory
Kumar, S., Joseph, S., Gander, P. E., Barascud, N., Halpern, A. R., & Griffiths, T. D. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.4341-14.2016 · Cited by 242
Temporal binding within and across events
DuBrow, S., & Davachi, L. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.07.011 · Cited by 226
Human hippocampus represents space and time during retrieval of real-world memories
Nielson, D. M., Smith, T. A., Sreekumar, V., Dennis, S. J., & Sederberg, P. B. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1507104112 · Cited by 245
Deconstructing the Posterior Medial Episodic Network
Ritchey, M., & Cooper, R. A. (2020) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2020.03.006 · Cited by 236
Reagh, Z. M., & Yassa, M. A. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1411250111 · Cited by 239
Bienkowski, M. S., Bowman, I., Song, M. Y., Gou, L., Ard, T., Cotter, K., Zhu, M., Benavidez, N. L., Yamashita, S., Abu-Jaber, J., et al. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0241-y · Cited by 224
Tompary, A., & Davachi, L. (2017) · Neuron · doi:10.1016/j.neuron.2017.09.005 · Cited by 235
Tanti, A., & Belzung, C. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.08.017 · Cited by 226
Interactions between human orbitofrontal cortex and hippocampus support model-based inference
Wang, F., Schoenbaum, G. M., & Kahnt, T. (2020) · PLoS Biology · doi:10.1371/journal.pbio.3000578 · Cited by 229
Functionally distinct high and low theta oscillations in the human hippocampus
Goyal, A., Miller, J. F., Qasim, S. E., Watrous, A. J., Zhang, H., Stein, J. M., Inman, C. S., Gross, R. E., Willie, J. T., Lega, B. C., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-15670-6 · Cited by 215
O’Leary, O. F., & Cryan, J. F. (2014) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2014.09.011 · Cited by 221
Hippocampal and prefrontal processing of network topology to simulate the future
Javadi, A.-H., Emo, B., Howard, L. R., Zisch, F. E., Yu, Y., Knight, R., Pinelo Silva, J., & Spiers, H. J. (2017) · Nature Communications · doi:10.1038/ncomms14652 · Cited by 207
Neurocognitive Aging and the Hippocampus across Species
Leal, S. L., & Yassa, M. A. (2015) · Trends in Neurosciences · doi:10.1016/j.tins.2015.10.003 · Cited by 221
The quartet theory of human emotions: An integrative and neurofunctional model
Koelsch, S., Jacobs, A. M., Menninghaus, W., Liebal, K., Klann-Delius, G., von Scheve, C., & Gebauer, G. (2015) · Physics of Life Reviews · doi:10.1016/j.plrev.2015.03.001 · Cited by 216
Sex Hormones and Cognition: Neuroendocrine Influences on Memory and Learning
Hamson, D. K., Roes, M., & Galea, L. A. M. (2016) · Comprehensive physiology · doi:10.1002/cphy.c150031 · Cited by 216
Parallel Regulation of Memory and Emotion Supports the Suppression of Intrusive Memories
Gagnepain, P., Hulbert, J. C., & Anderson, M. C. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.2732-16.2017 · Cited by 221
Episodic memory: Neuronal codes for what, where, and when
Sugar, J., & Moser, M. (2019) · Hippocampus · doi:10.1002/hipo.23132 · Cited by 216
Bowman, C. R., & Zeithamová, D. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.2811-17.2018 · Cited by 215
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 207
Gilboa, A., & Moscovitch, M. (2021) · Neuron · doi:10.1016/j.neuron.2021.04.025 · Cited by 174
Self-citationMcCormick, C., St‐Laurent, M., Ty, A., Valiante, T. A., & McAndrews, M. P. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht324 · Cited by 192
Ito, R., & Lee, A. C. H. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.07.039 · Cited by 188
Building concepts one episode at a time: The hippocampus and concept formation
Mack, M. L., Love, B. C., & Preston, A. R. (2017) · Neuroscience Letters · doi:10.1016/j.neulet.2017.07.061 · Cited by 183
False memories with age: neural and cognitive underpinnings
Devitt, A. L., & Schacter, D. L. (2016) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2016.08.030 · Cited by 171
Constructing, Perceiving, and Maintaining Scenes: Hippocampal Activity and Connectivity
Zeidman, P., Mullally, S. L., & Maguire, E. A. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu266 · Cited by 187
Vogel, J. W., Joie, R. L., Grothe, M. J., Diaz-Papkovich, A., Doyle, A., Vachon‐Presseau, É., Lepage, C., de Wael, R. V., Thomas, R. A., Iturria‐Medina, Y., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-14518-3 · Cited by 168
A human memory circuit derived from brain lesions causing amnesia
Ferguson, M. A., Lim, C. S., Cooke, D. L., Darby, R. R., Wu, O., Rost, N. S., Corbetta, M., Grafman, J. H., & Fox, M. (2019) · Nature Communications · doi:10.1038/s41467-019-11353-z · Cited by 168
Intrinsic connectivity reveals functionally distinct cortico-hippocampal networks in the human brain
Barnett, A. J., Reilly, W., Dimsdale-Zucker, H. R., Mızrak, E., Reagh, Z. M., & Ranganath, C. (2021) · PLoS Biology · doi:10.1371/journal.pbio.3001275 · Cited by 172
Boecker, R., Holz, N. E., Buchmann, A. F., Blomeyer, D., Plichta, M. M., Wolf, I., Baumeister, S., Meyer-Lindenberg, A., Banaschewski, T., Brandeis, D., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0104185 · Cited by 157
Joie, R. L., Landeau, B., Perrotin, A., Bejanin, A., Egret, S., Pèlerin, A., Mézenge, F., Belliard, S., Sayette, V. D. L., Eustache, F., et al. (2014) · Neuron · doi:10.1016/j.neuron.2014.01.026 · Cited by 165
Gulyaeva, N. V. (2018) · Neurochemical Research · doi:10.1007/s11064-018-2662-0 · Cited by 156
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
The role of the hippocampus in memory and mental construction
Sheldon, S., & Levine, B. (2016) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13006 · Cited by 155
Khan, S. A., Keaser, M. L., Meiller, T. F., & Seminowicz, D. A. (2014) · Pain · doi:10.1016/j.pain.2014.04.022 · Cited by 157
Ding, S., & Hoesen, G. W. V. (2015) · The Journal of Comparative Neurology · doi:10.1002/cne.23786 · Cited by 158
Dale, E., Pehrson, A. L., Jeyarajah, T., Li, Y., Leiser, S. C., Smagin, G. N., Olsen, C. K., & Sánchez, C. (2015) · CNS Spectrums · doi:10.1017/s1092852915000425 · Cited by 156
Murty, V. P., Calabro, F. J., & Luna, B. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.07.034 · Cited by 167
Wolosin, S. M., Zeithamová, D., & Preston, A. R. (2012) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00237 · Cited by 162
Age differences in hippocampal subfield volumes from childhood to late adulthood
Daugherty, A. M., Bender, A. R., Raz, N., & Ofen, N. (2015) · Hippocampus · doi:10.1002/hipo.22517 · Cited by 149
Schlichting, M. L., & Preston, A. R. (2015) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2015.11.005 · Cited by 164
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
A protocol for manual segmentation of medial temporal lobe subregions in 7 Tesla MRI
Berron, D., Vieweg, P., Hochkeppler, A., Pluta, J. B., Ding, S., Maass, A., Luther, A., Xie, L., Das, S. R., Wolk, D. A., et al. (2017) · NeuroImage Clinical · doi:10.1016/j.nicl.2017.05.022 · Cited by 148
Two distinct scene processing networks connecting vision and memory
Baldassano, C., Esteva, A., Fei-Fei, L., & Beck, D. M. (2016) · eneuro · doi:10.1523/eneuro.0178-16.2016 · Cited by 144
Murty, V. P., Tompary, A., Adcock, R. A., & Davachi, L. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.4032-15.2016 · Cited by 141
Boundaries Shape Cognitive Representations of Spaces and Events
Brunec, I. K., Moscovitch, M., & Barense, M. D. (2018) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2018.03.013 · Cited by 149
Self-citationMaruszak, A., & Thuret, S. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00095 · Cited by 147
Stimulation of the Posterior Cortical-Hippocampal Network Enhances Precision of Memory Recollection
Nilakantan, A. S., Bridge, D. J., Gagnon, E. P., VanHaerents, S. A., & Voss, J. L. (2017) · Current Biology · doi:10.1016/j.cub.2016.12.042 · Cited by 136
Functional connectivity and network analysis of midbrain and brainstem nuclei
Bär, K.-J., de la Cruz, F., Schumann, A., Koehler, S., Sauer, H., Critchley, H., & Wagner, G. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.03.071 · Cited by 134
The hippocampus in multiple sclerosis
Rocca, M. A., Barkhof, F., Luca, J. D., Frisén, J., Geurts, J. J. G., Hulst, H. E., Sastre‐Garriga, J., Filippi, M., Barkhof, F., Ciccarelli, O., et al. (2018) · The Lancet Neurology · doi:10.1016/s1474-4422(18)30309-0 · Cited by 134
Insight Reconfigures Hippocampal-Prefrontal Memories
Milivojevic, B., Vicente-Grabovetsky, A., & Doeller, C. F. (2015) · Current Biology · doi:10.1016/j.cub.2015.01.033 · Cited by 137
Aggleton, J. P., & Christiansen, K. (2015) · Progress in brain research · doi:10.1016/bs.pbr.2015.03.003 · Cited by 135
Aggleton, J. P., Wright, N. F., Rosene, D. L., & Saunders, R. C. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv019 · Cited by 133
Development of Hippocampal–Prefrontal Cortex Interactions through Adolescence
Calabro, F. J., Murty, V. P., Jalbrzikowski, M., Tervo‐Clemmens, B., & Luna, B. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz186 · Cited by 139
Separate elements of episodic memory subserved by distinct hippocampal-prefrontal connections
Barker, G. R. I., Banks, P. J., Scott, H., Ralph, G. S., Mitrophanous, K. A., Wong, L.-F., Bashir, Z. I., Uney, J. B., & Warburton, E. C. (2017) · Nature Neuroscience · doi:10.1038/nn.4472 · Cited by 124
Kraguljac, N. V., White, D. M., Hadley, N. T., Hadley, J. A., Hoef, L. V., Davis, E., & Lahti, A. C. (2016) · Schizophrenia Bulletin · doi:10.1093/schbul/sbv228 · Cited by 129
Kim, H. (2014) · Hippocampus · doi:10.1002/hipo.22387 · Cited by 133
Staresina, B. P., Michelmann, S., Bonnefond, M., Jensen, O. B., Axmacher, N., & Fell, J. (2016) · eLife · doi:10.7554/elife.17397 · Cited by 130
Neurofunctional topography of the human hippocampus
Robinson, J. L., Barron, D. S., Kirby, L. A. J., Bottenhorn, K. L., Hill, A. C., Murphy, J. E., Katz, J. S., Salibi, N., Eickhoff, S. B., & Fox, P. T. (2015) · Human Brain Mapping · doi:10.1002/hbm.22987 · Cited by 125
The many dimensions of human hippocampal organization and (dys)function
Genon, S., Bernhardt, B. C., Joie, R. L., Amunts, K., & Eickhoff, S. B. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2021.10.003 · Cited by 119
Grady, C. L. (2019) · Hippocampus · doi:10.1002/hipo.23164 · Cited by 127
Kaboodvand, N., Bäckman, L., Nyberg, L. H., & Salami, A. (2018) · Human Brain Mapping · doi:10.1002/hbm.23983 · Cited by 124
Xie, L., Wisse, L. E. M., Pluta, J. B., de Florès, R., Piskin, V., Manjón, J. V., Wang, H., Das, S. R., Ding, S., Wolk, D. A., et al. (2019) · Human Brain Mapping · doi:10.1002/hbm.24607 · Cited by 120
Predictive Representations in Hippocampal and Prefrontal Hierarchies
Brunec, I. K., & Momennejad, I. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1327-21.2021 · Cited by 123
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
Self-citationA neurobiological enquiry into the origins of our experience of the sublime and beautiful
Ishizu, T. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00891 · Cited by 115
Effects of Maternal Hypothyroidism on Offspring Hippocampus and Memory
Willoughby, K. A., McAndrews, M. P., & ROVET, J. F. (2013) · Thyroid · doi:10.1089/thy.2013.0215 · Cited by 121
The Cognitive Control of Eating and Body Weight: It’s More Than What You “Think”
Davidson, T. L., Jones, S., Roy, M., & Stevenson, R. J. (2019) · Frontiers in Psychology · doi:10.3389/fpsyg.2019.00062 · Cited by 125
Generalization and the hippocampus: More than one story?
Zeithamová, D., & Bowman, C. R. (2020) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2020.107317 · Cited by 123
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 125
Self-citation
Metadata
- Authors
- Poppenk, J., Evensmoen, H. R., Moscovitch, M., & Nadel, L.
- Affiliations
- Princeton University (US)
- Norwegian University of Science and Technology (NO)
- University of Toronto (CA)
- University of Arizona (US)
- Corresponding author
- Poppenk, Jordan
- Moscovitch, Morris
- Nadel, Lynn
- Venue
- Trends in Cognitive Sciences
- Publisher
- Elsevier BV
- Published
- 2013-05
- Volume
- 17
- Issue
- 5
- Pages
- 230-240
- ISSN
- 1364-6613 (ISSN-L)
- OpenAlex
- W2072427931
- Cited by
- 1,100
- References
- 110
- Citations by year
- 2026: 93 · 2025: 88 · 2024: 96 · 2023: 87 · 2022: 68 · 2021: 110 · 2020: 110 · 2019: 88 · 2018: 78 · 2017: 76 · 2016: 71 · 2015: 67 · 2014: 46 · 2013: 20
- FWCI
- 5.78
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Trends in Cognitive Sciences (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- hippocampus, anterior hippocampus, posterior hippocampus, trisynaptic circuit, pattern completion, pattern separation, hippocampal subfields, spatial representation, functional specialization
- MeSH terms
- Animals, Brain Mapping, Hippocampus, Humans, Functional Laterality, Models, Neurological, Nerve Net, Mental Recall
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review