Cited by 1,186Memory and Neural MechanismsNeuroscience and Neuropharmacology ResearchNeurogenesis and neuroplasticity mechanisms

The DOI matches its Crossref record.

The Hippocampus Book

·2006·Oxford University Press eBooks

DOI 10.1093/acprof:oso/9780195100273.001.0001

Open this paper in CoChat — free account

Abstract

Abstract The hippocampus is one of a group of remarkable structures embedded within the brain's medial temporal lobe. Long known to be important for memory, it has been a prime focus of neuroscience research for many years. This book aims to facilitate developments in the field in a major way by bringing together contributions by leading international scientists knowledgeable about hippocampal anatomy, physiology, and function. This book offers an up-to-date account of what the hippocampus does, how it does it, and what happens when things go wrong. At the same time, it illustrates how research focusing on this single brain structure has revealed principles of wider generality for the whole brain in relation to anatomical connectivity, synaptic plasticity, cognition and behavior, and computational algorithms. Well-organized in its presentation of both theory and experimental data, this book illustrates the astonishing progress that has been made in unraveling the workings of the brain.

Integrity signals

Registry

Crossref · 10.1093/acprof:oso/9780195100273.001.0001

Cites

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Sorted by citations

Items 401–500 of 999

Short-term high-fat diet consumption impairs synaptic plasticity in the aged hippocampus via IL-1 signaling
Olmo, B. M. G., Bettes, M. N., DeMarsh, J. W., Zhao, F., Askwith, C. C., & Barrientos, R. M. (2023) · npj Science of Food · doi:10.1038/s41538-023-00211-4 · Cited by 33
A theory of the neural mechanisms underlying negative cognitive bias in major depression
Jiang, Y. (2024) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2024.1348474 · Cited by 43
Structural hippocampal alterations, perceived stress, and coping deficiencies in patients with anorexia nervosa
Burkert, N. T., Koschutnig, K., Ebner, F., & Freidl, W. (2015) · International Journal of Eating Disorders · doi:10.1002/eat.22397 · Cited by 33
Non-homogeneous stereological properties of the rat hippocampus from high-resolution 3D serial reconstruction of thin histological sections
Ropireddy, D., Bachus, S. E., & Ascoli, G. A. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2011.12.055 · Cited by 35
Effect of VGLUT inhibitors on glutamatergic synaptic transmission in the rodent hippocampus and prefrontal cortex
Neale, S. A., Copeland, C. S., & Salt, T. E. (2013) · Neurochemistry International · doi:10.1016/j.neuint.2013.10.001 · Cited by 35
The effects of black garlic ethanol extract on the spatial memory and estimated total number of pyramidal cells of the hippocampus of monosodium glutamate-exposed adolescent male Wistar rats
Hermawati, E., Sari, D. C. R., & Partadiredja, G. (2014) · Anatomical Science International · doi:10.1007/s12565-014-0262-x · Cited by 35
Mammillothalamic and Mammillotegmental Tracts as New Targets for Dementia and Epilepsy Treatment
Balak, N., Balkuv, E., Karadağ, A., Başaran, R., Biçeroğlu, H., Erkan, B., & Tanrıöver, N. (2017) · World Neurosurgery · doi:10.1016/j.wneu.2017.10.168 · Cited by 34
The brain's best kept secret is its degenerate structure
Albantakis, L., Bernard, C., Brenner, N., Marder, E., & Narayanan, R. (2024) · The Journal of Neuroscience · doi:10.1523/jneurosci.1339-24.2024 · Cited by 34
Mean-field models for heterogeneous networks of two-dimensional integrate and fire neurons
Nicola, W., & Campbell, S. A. (2013) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2013.00184 · Cited by 34
“This is contradictory to the observation that burst firing is ubiquitous in this region (Andersen et al., 2006, section 5.3.5).”
BackgroundResultInfluential
Novel long-range inhibitory nNOS-expressing hippocampal cells
Wick, Z. C., Tetzlaff, M. R., & Krook-Magnuson, E. I. (2019) · eLife · doi:10.7554/elife.46816 · Cited by 37
New boundaries and dissociation of the mouse hippocampus along the dorsal‐ventral axis based on glutamatergic, GABAergic and catecholaminergic receptor densities
Lothmann, K., Deitersen, J., Zilles, K., Amunts, K., & Herold, C. (2020) · Hippocampus · doi:10.1002/hipo.23262 · Cited by 34
Developmental regulation of gene expression and astrocytic processes may explain selective hippocampal vulnerability
Lavenex, P., Sugden, S. G., Davis, R. R., Gregg, J. P., & Lavenex, P. B. (2009) · Hippocampus · doi:10.1002/hipo.20730 · Cited by 33
Network bursting using experimentally constrained single compartment CA3 hippocampal neuron models with adaptation
Dur-e-Ahmad, M., Nicola, W., Campbell, S. A., & Skinner, F. K. (2011) · Journal of Computational Neuroscience · doi:10.1007/s10827-011-0372-6 · Cited by 33
Influence of slow oscillation on hippocampal activity and ripples through cortico-hippocampal synaptic interactions, analyzed by a cortical-CA3-CA1 network model
Taxidis, J., Mizuseki, K., Mason, R., & Owen, M. R. (2013) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2013.00003 · Cited by 35
Intrinsic mechanisms stabilize encoding and retrieval circuits differentially in a hippocampal network model
Hummos, A., Franklin, C. C., & Nair, S. S. (2014) · Hippocampus · doi:10.1002/hipo.22324 · Cited by 33
Constitutive activation of CREB in mice enhances temporal association learning and increases hippocampal CA1 neuronal spine density and complexity
Serita, T., Fukushima, H., & Kida, S. (2017) · Scientific Reports · doi:10.1038/srep42528 · Cited by 37
Molecular fingerprinting of principal neurons in the rodent hippocampus: A neuroinformatics approach
Hamilton, D. J., White, C. M., Rees, C. L., Wheeler, D. W., & Ascoli, G. A. (2017) · Journal of Pharmaceutical and Biomedical Analysis · doi:10.1016/j.jpba.2017.03.062 · Cited by 30
Unpredictable Chronic Mild Stress Suppresses the Incorporation of New Neurons at the Caudal Pole of the Chicken Hippocampal Formation
Gualtieri, F., Armstrong, E. A., Longmoor, G., D’Eath, R. B., Sandilands, V., Boswell, T., & Smulders, T. V. (2019) · Scientific Reports · doi:10.1038/s41598-019-43584-x · Cited by 31
“Blood samples were collected at three time points during the experiment: (1) before the stress manipulation, (2) two weeks into the stress manipulation and (3) during the penultimate week of stress treatment, for quantification of H/L ratios and baseline CORT.”
Whole-brain hippocampal sparing radiation therapy: Volume-modulated arc therapy vs intensity-modulated radiation therapy case study
Lee, K., Lenards, N., & Holson, J. (2015) · Medical dosimetry · doi:10.1016/j.meddos.2015.06.003 · Cited by 32
Simultaneous measurement of cholinergic tone and neuronal network dynamics in vivo in the rat brain using a novel choline oxidase based electrochemical biosensor
Santos, R. M., Laranjinha, J. A. N., Barbosa, R. M., & Sirota, A. (2015) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2015.02.003 · Cited by 33
A computational study on how theta modulated inhibition can account for the long temporal windows in the entorhinal–hippocampal loop
Cutsuridis, V., & Poirazi, P. (2015) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2015.02.002 · Cited by 30
A hippocampus-accumbens code guides goal-directed appetitive behavior
Barnstedt, O., Mocellin, P., & Remy, S. (2024) · Nature Communications · doi:10.1038/s41467-024-47361-x · Cited by 31
A simple model for Behavioral Time Scale Synaptic Plasticity (BTSP) provides content addressable memory with binary synapses and one-shot learning
Wu, Y., & Maass, W. (2025) · Nature Communications · doi:10.1038/s41467-024-55563-6 · Cited by 36
Quantitative T1 and T2 MRI signal characteristics in the human brain: different patterns of MR contrasts in normal ageing
Knight, M. J., McCann, B., Tsivos, D., Coulthard, E. J., & Kauppinen, R. A. (2016) · Magnetic Resonance Materials in Physics Biology and Medicine · doi:10.1007/s10334-016-0573-0 · Cited by 33
Theta-frequency selectivity in the somatic spike-triggered average of rat hippocampal pyramidal neurons is dependent on HCN channels
Das, A., & Narayanan, R. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00356.2017 · Cited by 33
Pattern separation and completion of distinct axonal inputs transmitted via micro-tunnels between co-cultured hippocampal dentate, CA3, CA1 and entorhinal cortex networks
Poli, D., Wheeler, B. C., DeMarse, T. B., & Brewer, G. J. (2018) · Journal of Neural Engineering · doi:10.1088/1741-2552/aabc20 · Cited by 31
“Anatomically, the larger number of DG neurons than the primary inputs from layer II of the entorhinal cortex (EC) suggests a fanout of information needed for pattern separation (Andersen et al 2006).”
Background
Memory impairments and increased GFAP expression in hippocampal astrocytes following hypercaloric diet in rats
Bondan, E. F., Cardoso, C. V., Martins, M. D. F. M., & Otton, R. (2019) · Arquivos de Neuro-Psiquiatria · doi:10.1590/0004-282x20190091 · Cited by 33
Synaptic Development and Neuronal Myelination Are Altered with Growth Restriction in Fetal Guinea Pigs
Piorkowska, K., Thompson, J. A., Nygard, K. L., Matushewski, B. J., Hammond, R. R., & Richardson, B. S. (2014) · Developmental Neuroscience · doi:10.1159/000363696 · Cited by 30
Endogenous serotonin facilitates hippocampal long-term potentiation at CA3/CA1 synapses
Mlinar, B., Stocca, G., & Corradetti, R. (2014) · Journal of Neural Transmission · doi:10.1007/s00702-014-1246-7 · Cited by 34
Crosstalk and transitions between multiple spatial maps in an attractor neural network model of the hippocampus: Collective motion of the activity
Monasson, R., & Rosay, S. (2014) · Physical Review E · doi:10.1103/physreve.89.032803 · Cited by 31
Crosstalk and transitions between multiple spatial maps in an attractor neural network model of the hippocampus: Phase diagram
Monasson, R., & Rosay, S. (2013) · Physical Review E · doi:10.1103/physreve.87.062813 · Cited by 31
Acute Stress, But not Corticosterone, Disrupts Short- and Long-Term Synaptic Plasticity in Rat Dorsal Subiculum Via Glucocorticoid Receptor Activation
MacDougall, M. J., & Howland, J. G. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs247 · Cited by 31
Feline Temporal Lobe Epilepsy: Review of the Experimental Literature
Kitz, S., Thalhammer, J. G., Glantschnigg, U., et al. (2017) · Journal of Veterinary Internal Medicine · doi:10.1111/jvim.14699 · Cited by 31
Delineation of hippocampal subregions using T1-weighted magnetic resonance images at 3 Tesla
Rhindress, K., Ikuta, T., Wellington, R. L., Malhotra, A. K., & Szeszko, P. R. (2014) · Brain Structure and Function · doi:10.1007/s00429-014-0854-1 · Cited by 30
A comprehensive protocol for manual segmentation of the medial temporal lobe structures.
Moore, M., Hu, Y., Woo, S., O'Hearn, D., Iordan, A., Dolcos, S., & Dolcos, F. (2014) · Journal of Visualized Experiments · doi:10.3791/50991 · Cited by 43
Effects of Voluntary Exercise on Cell Proliferation and Neurogenesis in the Dentate Gyrus of Adult FMR1 Knockout Mice
Pinar, C., Yau, S., Sharp, Z., Shamei, A., Fontaine, C. J., Meconi, A., Lottenberg, C. P., & Christie, B. R. (2018) · Brain Plasticity · doi:10.3233/bpl-170052 · Cited by 28
A Role for the Longitudinal Axis of the Hippocampus in Multiscale Representations of Large and Complex Spatial Environments and Mnemonic Hierarchies
Harland, B. C., Contreras, M., & Fellous, J. (2018) · InTech eBooks · doi:10.5772/intechopen.71165 · Cited by 29
Entorhinal cortex stimulation induces dentate gyrus neurogenesis through insulin receptor signaling
Ronaghi, A., Zibaii, M. I., Pandamooz, S., Nourzei, N., Motamedi, F., Ahmadiani, A., & Dargahi, L. (2018) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2018.11.011 · Cited by 30
Consequences of space radiation on the brain and cardiovascular system
Davis, C. M., Allen, A. R., & Bowles, D. E. (2021) · Journal of Environmental Science and Health Part C · doi:10.1080/26896583.2021.1891825 · Cited by 30
Magnetoencephalography can reveal deep brain network activities linked to memory processes
López‐Madrona, V. J., Villalon, S. M., Badier, J., Trébuchon, A., Velmurugan, J., Bartoloméi, F., Carron, R., Barborică, A., Vulliémoz, S., Alario, F. ‐., et al. (2022) · Human Brain Mapping · doi:10.1002/hbm.25987 · Cited by 26
Graph Theoretic and Motif Analyses of the Hippocampal Neuron Type Potential Connectome
Rees, C. L., Wheeler, D. W., Hamilton, D. J., White, C. M., Komendantov, A. O., & Ascoli, G. A. (2016) · eNeuro · doi:10.1523/eneuro.0205-16.2016 · Cited by 30
Driving and regulating temporal association learning coordinated by entorhinal-hippocampal network
北村, 貴. (2017) · Neuroscience Research · doi:10.1016/j.neures.2017.04.005 · Cited by 33
Deciphering the Contribution of Oriens-Lacunosum/Moleculare (OLM) Cells to Intrinsic θ Rhythms Using Biophysical Local Field Potential (LFP) Models
Chatzikalymniou, A. P., & Skinner, F. K. (2018) · eNeuro · doi:10.1523/eneuro.0146-18.2018 · Cited by 32
Spatial tuning and brain state account for dorsal hippocampal CA1 activity in a non-spatial learning task
Shan, K. Q., Lubenov, E. V., Papadopoulou, M., & Siapas, A. G. (2016) · eLife · doi:10.7554/elife.14321 · Cited by 27
Repeated exposures to diisopropylfluorophosphate result in structural disruptions of myelinated axons and persistent impairments of axonal transport in the brains of rats
Naughton, S. X., Hernandez, C. M., Beck, W. D., Poddar, I., Yanasak, N. E., Lin, P., & Terry, A. V. (2018) · Toxicology · doi:10.1016/j.tox.2018.06.004 · Cited by 29
Evolutionary shifts dramatically reorganized the human hippocampal complex
Schilder, B. M., Petry, H. M., & Hof, P. R. (2019) · The Journal of Comparative Neurology · doi:10.1002/cne.24822 · Cited by 31
Stress, memory, and implications for major depression
de Sousa, G. M., Vargas, H. D. Q., Barbosa, F. F., & Coelho, N. L. G. (2021) · Behavioural Brain Research · doi:10.1016/j.bbr.2021.113410 · Cited by 32
Memory in ASD: have we been barking up the wrong tree?
Boucher, J., & Mayes, A. R. (2012) · Autism · doi:10.1177/1362361311417738 · Cited by 32
Hippocampal subregion volume changes associated with antipsychotic treatment in first-episode psychosis
Rhindress, K., Robinson, D. G., Gallego, J. A., Wellington, R. L., Malhotra, A. K., & Szeszko, P. R. (2017) · Psychological Medicine · doi:10.1017/s0033291717000137 · Cited by 29
Dentate granule and mossy cells exhibit distinct spatiotemporal responses to local change in a one-dimensional landscape of visual-tactile cues
Jung, D., Kim, S., Sariev, A., Sharif, F., Kim, D., & Royer, S. (2019) · Scientific Reports · doi:10.1038/s41598-019-45983-6 · Cited by 27
Aging, neurogenesis, and caloric restriction in different model organisms.
Arslan-Ergül, A., Ozdemir, A. T., & Adams, M. M. (2013) · Europe PMC (PubMed Central) · Cited by 32
Hippocampal mitochondrial dysfunction and psychiatric-relevant behavioral deficits in spinocerebellar ataxia 1 mouse model
Tichánek, F., Šalomová, M., Jedlička, J., Kuncová, J., Pitule, P., Macanova, T., Petránková, Z., Tůma, Z., & Cendelín, J. (2020) · Scientific Reports · doi:10.1038/s41598-020-62308-0 · Cited by 28
A neurohybrid memristive system for adaptive stimulation of hippocampus
Gerasimova, S. A., Lebedeva, A., Fedulina, A., Koryazhkina, M. N., Belov, A. I., Mishchenko, M. A., Matveeva, M., Guseinov, D. V., Mikhaylov, A. N., Kazantsev, V., et al. (2021) · Chaos Solitons & Fractals · doi:10.1016/j.chaos.2021.110804 · Cited by 29
RGS14 Regulation of Post-Synaptic Signaling and Spine Plasticity in Brain
Harbin, N. H., Bramlett, S. N., Montañez‐Miranda, C., Terzioğlu, G., & Hepler, J. R. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22136823 · Cited by 24
Degree and pattern of calbindin immunoreactivity in granule cells of the dentate gyrus differ in mesial temporal sclerosis, cortical malformation- and tumor-related epilepsies
Ábrahám, H., Richter, Z., Gyimesi, C., Horváth, Z., Janszky, J., Doczi, T. P., & Seress, L. (2011) · Brain Research · doi:10.1016/j.brainres.2011.05.010 · Cited by 28
Decoding illusory self-location from activity in the human hippocampus
Guterstam, A., Björnsdotter, M., Bergouignan, L., Gentile, G., Li, T., & Ehrsson, H. H. (2015) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2015.00412 · Cited by 31
“ORIGINAL RESEARCH published: 15 July 2015 doi: 10.3389/fnhum.2015.00412 Edited by: Klaus Gramann, Berlin Institute of Technology, Germany Reviewed by: Soyun Kim, University of California, Irvine, USA Amir-Homayoun Javadi, University College London, UK *Correspondence: Arvid Guterstam, Department of Neuroscience, Karol…”
Influential
Rearing‐environment‐dependent hippocampal local field potential differences in wild‐type and inositol trisphosphate receptor type 2 knockout mice
Tanaka, M., Wang, X., Mikoshiba, K., Hirase, H., & Shinohara, Y. (2017) · The Journal of Physiology · doi:10.1113/jp274573 · Cited by 26
Effective Connectivity of Hippocampal Neural Network and Its Alteration in Mg2+-Free Epilepsy Model
Gong, X., Li, J.-B., Lu, Q.-C., Liang, P.-J., & Zhang, P.-M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0092961 · Cited by 28
Manganese‐enhanced magnetic resonance imaging detects mossy fiber sprouting in the pilocarpine model of epilepsy
Malheiros, J. M., Polli, R. S., Paiva, F. F., et al. (2012) · Epilepsia · doi:10.1111/j.1528-1167.2012.03521.x · Cited by 27
A detailed anatomical and mathematical model of the hippocampal formation for the generation of sharp-wave ripples and theta-nested gamma oscillations
Aussel, A., Buhry, L., Tyvaert, L., & Ranta, R. (2018) · Journal of Computational Neuroscience · doi:10.1007/s10827-018-0704-x · Cited by 30
“As it is commonly accepted that the hippocampal formation receives most of its external inputs through the entorhinal cortex, only these neurons receive external stimulation in our model (Andersen et al. 2007).”
Background
Modelling unitary fields and the single‐neuron contribution to local field potentials in the hippocampus
Teleńczuk, M. T., Teleńczuk, B., & Alain Destexhe, A. (2020) · The Journal of Physiology · doi:10.1113/jp279452 · Cited by 27
Memory and dendritic spines loss, and dynamic dendritic spines changes are age-dependent in the rat
Aguilar‐Hernández, L., Vázquez-Hernández, A. J., de-Lima-Mar, D. F., Vázquez‐Roque, R. A., Tendilla‐Beltrán, H., & Flores, G. (2020) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2020.101858 · Cited by 29
Microglia Loss and Astrocyte Activation Cause Dynamic Changes in Hippocampal [18F]DPA-714 Uptake in Mouse Models of Depression
Guo, J., Qiu, T., Wang, L., Shi, L., Ai, M., Xia, Z., Peng, Z., Zheng, A., Li, X., & Kuang, L. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.802192 · Cited by 26
Recognition Memory Induces Natural LTP-like Hippocampal Synaptic Excitation and Inhibition
Sánchez‐Rodríguez, I., Temprano‐Carazo, S., Jeremic, D., Delgado-Garcia, J. M., Gruart, A., Navarro‐López, J. D., & Jiménez‐Díaz, L. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231810806 · Cited by 27
Modulation of local field potentials by high-frequency stimulation of afferent axons in the hippocampal CA1 region
Yu, Y., Feng, Z., Cao, J., Guo, Z., Wang, Z., Hu, N., & Wei, X. F. (2015) · Journal of Integrative Neuroscience · doi:10.1142/s0219635216500011 · Cited by 27
Cilostazol improves hippocampus-dependent long-term memory in mice
Yanai, S., Semba, Y., Ito, H., & Endo, S. (2014) · Psychopharmacology · doi:10.1007/s00213-014-3442-4 · Cited by 28
Flexible theta sequence compression mediated via phase precessing interneurons
Chadwick, A., van Rossum, M. C. W., & Nolan, M. F. (2016) · eLife · doi:10.7554/elife.20349 · Cited by 26
Combinatorial brain decoding of people's whereabouts during visuospatial navigation
de Beeck, H. O. (2013) · Frontiers in Neuroscience · doi:10.3389/fnins.2013.00078 · Cited by 27
Oscillation-Induced Signal Transmission and Gating in Neural Circuits
Jahnke, S., Memmesheimer, R.-M., & Timme, M. (2014) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003940 · Cited by 26
A Role for Matrix Metalloproteases in Antidepressant Efficacy
Alaiyed, S., & Conant, K. E. (2019) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2019.00117 · Cited by 26
“Since each PV interneuron can contact hundreds of pyramidal cells (Andersen et al., 2006), PNN disruption may influence pyramidal cell activity at the population level.”
Background
The Presence of the Temporal Horn Exacerbates the Vulnerability of Hippocampus During Head Impacts
Zhou, Z., Li, X., Domel, A. G., Dennis, E. L., Georgiadis, M., Liu, Y., Raymond, S., Grant, G. A., Kleiven, S., Camarillo, D. B., et al. (2022) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2022.754344 · Cited by 25
Integration of exteroceptive and interoceptive information within the hippocampus: a computational study
Kassab, R., & Alexandre, F. (2015) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00087 · Cited by 25
Proteogenomics of the human hippocampus: The road ahead
Kang, M., Byun, K., Kim, J. H., Park, N. H., Heinsen, H., Ravid, R., Steinbusch, H. W. M., Lee, B., & Park, Y. M. (2015) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2015.02.010 · Cited by 27
Encoding Binary Neural Codes in Networks of Threshold-Linear Neurons
Curto, C., Degeratu, A., & Itskov, V. (2013) · Neural Computation · doi:10.1162/neco_a_00504 · Cited by 24
Impacts of Spike Shape Variations on Synaptic Communication
Ramezani, H., & Akan, Ö. B. (2018) · IEEE Transactions on NanoBioscience · doi:10.1109/tnb.2018.2838056 · Cited by 25
Optimizing brain performance: Identifying mechanisms of adaptive neurobiological plasticity
Lambert, K. G., Eisch, A. J., Galea, L. A. M., Kempermann, G., & Merzenich, M. M. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.06.033 · Cited by 26
“However, this statement overlooks the fact that the hippocampus subserves a range of brain functions (Andersen et al., 2007; Scharfman, 2011), which includes memory but also mood regulation.”
Background
Hippocampal Neurophysiology Across Species
Las, L., & Ulanovsky, N. (2014) · Springer eBooks · doi:10.1007/978-3-7091-1292-2_16 · Cited by 24
Non‐spatial expertise and hippocampal gray matter volume in humans
Woollett, K., Glensman, J., & Maguire, E. A. (2008) · Hippocampus · doi:10.1002/hipo.20465 · Cited by 26
Electrophysiological insights into the enduring effects of early life stress on the brain
Ali, I. Y., Salzberg, M. R., French, C. R., & Jones, N. C. (2010) · Psychopharmacology · doi:10.1007/s00213-010-2125-z · Cited by 27
Hippocampal-Dependent Inhibitory Learning and Memory Processes in the Control of Eating and Drug Taking
Clasen, M. M., Riley, A. L., & Davidson, T. L. (2020) · Current Pharmaceutical Design · doi:10.2174/1381612826666200206091447 · Cited by 23
Comparison and Reliability of Hippocampal Subfield Segmentations Within FreeSurfer Utilizing T1- and T2-Weighted Multispectral MRI Data
Seiger, R., Hammerle, F. P., Godbersen, G. M., Reed, M. B., Spurny‐Dworak, B., Handschuh, P. A., Klöbl, M., Unterholzner, J., Gryglewski, G., Vanicek, T., et al. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.666000 · Cited by 25
Reversible Behavioral Deficits in Rats during a Cycle of Demyelination-Remyelination of the Fimbria
Grinkina, N., Abdel-Baki, S. G., & Bergold, P. J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0053775 · Cited by 25
An in vitro seizure model from human hippocampal slices using multi-electrode arrays
Hsiao, M.-C., Yu, P.-N., Song, D. B., Liu, C. Y., Heck, C. N., Millett, D., & Berger, T. W. (2014) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2014.09.010 · Cited by 27
The Wobbler Mouse Model of Amyotrophic Lateral Sclerosis (ALS) Displays Hippocampal Hyperexcitability, and Reduced Number of Interneurons, but No Presynaptic Vesicle Release Impairments
Thielsen, K. D., Moser, J., Schmitt‐John, T., Jensen, M. S., Jensen, K., & Holm, M. M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0082767 · Cited by 25
Variant BDNF-Val66Met Polymorphism is Associated with Layer-Specific Alterations in GABAergic Innervation of Pyramidal Neurons, Elevated Anxiety and Reduced Vulnerability of Adolescent Male Mice to Activity-Based Anorexia
Chen, Y.-W., Surgent, O. J., Rana, B. S., Lee, F., & Aoki, C. J. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw210 · Cited by 25
Triclosan Impairs Hippocampal Synaptic Plasticity and Spatial Memory in Male Rats
Arias‐Cavieres, A., More, J., Vicente, J. M., Adasme, T., Hidalgo, J., Valdés, J. L., Humeres, A., Valdés-Undurraga, I., Sánchez, G., Hidalgo, C., et al. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00429 · Cited by 27
“The hippocampus, which mediates the formation of long-term memories and is critical for memory consolidation, is a well-established model to study neuronal function (Andersen et al., 2006).”
Background
The race to learn: Spike timing and STDP can coordinate learning and recall in CA3
Nolan, C. R., Wyeth, G. F., Milford, M. J., & Wiles, J. (2010) · Hippocampus · doi:10.1002/hipo.20777 · Cited by 25
Sertraline effects on cerebrospinal fluid monoamines and species-typical socioemotional behavior of female cynomolgus monkeys
Shively, C. A., Register, T. C., Higley, J. D., & Willard, S. L. (2013) · Psychopharmacology · doi:10.1007/s00213-013-3329-9 · Cited by 25
Prospective Optimization
B, T. J. S. A., Howard Poizner, A., LYNCH, G. S., Gepshtein, S., & Greenspan, R. J. (2014) · Proceedings of the IEEE · doi:10.1109/jproc.2014.2314297 · Cited by 25
“Classical conditioning, which might seem like a weak way to learn about the world, could thus lead to near-optimal strategies for finding food, shelter, and mates over many trials [6].”
Background
Neonatal Ethanol and Choline Treatments Alter the Morphology of Developing Rat Hippocampal Pyramidal Neurons in Opposite Directions
Goeke, C. M., Roberts, M. L., Hashimoto, J. G., Finn, D. A., & Guizzetti, M. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.01.031 · Cited by 26
Vascular mapping of the human hippocampus using Ferumoxytol-enhanced MRI
Buch, S., Chen, Y., Jella, P. K., Ge, Y., & Haacke, E. M. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.118957 · Cited by 27
Memory-inspired spiking hyperdimensional network for robust online learning
Zou, Z., Alimohamadi, H., Zakeri, A., Imani, F., Kim, Y., Najafi, M. H., & Imani, M. (2022) · Scientific Reports · doi:10.1038/s41598-022-11073-3 · Cited by 47
Hippocampal theta-dependent eyeblink classical conditioning: Coordination of a distributed learning system
Berry, S. D., & Hoffmann, L. C. (2010) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2010.11.014 · Cited by 24
High dose of 8-OH-DPAT decreases maximal dentate gyrus activation and facilitates granular cell plasticity in vivo
Orbán, G., Pierucci, M., Benigno, A., et al. (2013) · Experimental Brain Research · doi:10.1007/s00221-013-3594-1 · Cited by 24
Localization and Intrinsic Function
Rathkopf, C. A. (2013) · Philosophy of Science · doi:10.1086/668878 · Cited by 26
Behavioral alterations are associated with vitamin B12 deficiency in the transcobalamin receptor/CD320 KO mouse
Arora, K., Sequeira, J. M., Hernandez, A. I., Alarcón, J. M., & Quadros, E. V. (2017) · PLoS ONE · doi:10.1371/journal.pone.0177156 · Cited by 26
A memristive plasticity model of voltage-based STDP suitable for recurrent bidirectional neural networks in the hippocampus
Diederich, N., Bartsch, T., Kohlstedt, H., & Ziegler, M. (2018) · Scientific Reports · doi:10.1038/s41598-018-27616-6 · Cited by 25
Stores, Channels, Glue, and Trees: Active Glial and Active Dendritic Physiology
Ashhad, S., & Narayanan, R. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-1223-5 · Cited by 25
Impairments of Synaptic Plasticity Induction Threshold and Network Oscillatory Activity in the Hippocampus Underlie Memory Deficits in a Non-Transgenic Mouse Model of Amyloidosis
Mayordomo‐Cava, J., Iborra‐Lázaro, G., Djebari, S., Temprano‐Carazo, S., Sánchez‐Rodríguez, I., Jeremic, D., Gruart, A., Delgado-Garcia, J. M., Jiménez‐Díaz, L., & Navarro‐López, J. D. (2020) · Biology · doi:10.3390/biology9070175 · Cited by 21
Calretinin expression in hilar mossy cells of the hippocampal dentate gyrus of nonhuman primates and humans
Seress, L., Ábrahám, H., Czéh, B., Fuchs, E., & Léránth, C. (2008) · Hippocampus · doi:10.1002/hipo.20403 · Cited by 24

Venue: Oxford University Press eBooks
Publisher: Oxford University Press
Published: 2006-12-14
DOI: 10.1093/acprof:oso/9780195100273.001.0001
OpenAlex: W644076287
Cited by: 1,186
References: 0
Citations by year: 2026: 15 · 2025: 33 · 2024: 37 · 2023: 32 · 2022: 44 · 2021: 68 · 2020: 71 · 2019: 67 · 2018: 79 · 2017: 66 · 2016: 60 · 2015: 78 · 2014: 91 · 2013: 108 · 2012: 68
FWCI: 12.76
Type: book
Language: en
Open access: closed
Locations: Oxford University Press eBooks (publishedVersion)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Keywords: hippocampus, medial temporal lobe, memory, hippocampal anatomy, hippocampal dysfunction, synaptic plasticity, structural connectivity, cognition and behavior, computational neuroscience, brain function

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

The Hippocampus Book

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cited by

Related

Metadata

Record

About these checks