Are the Dorsal and Ventral Hippocampus Functionally Distinct Structures?
Open accessAbstract
One literature treats the hippocampus as a purely cognitive structure involved in memory; another treats it as a regulator of emotion whose dysfunction leads to psychopathology. We review behavioral, anatomical, and gene expression studies that together support a functional segmentation into three hippocampal compartments: dorsal, intermediate, and ventral. The dorsal hippocampus, which corresponds to the posterior hippocampus in primates, performs primarily cognitive functions. The ventral (anterior in primates) relates to stress, emotion, and affect. Strikingly, gene expression in the dorsal hippocampus correlates with cortical regions involved in information processing, while genes expressed in the ventral hippocampus correlate with regions involved in emotion and stress (amygdala and hypothalamus).
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
The hippocampus is an important brain region involved in consolidation and storage of long-term memories, cognition and emotional processing.
“The hippocampus is an important brain region involved in the consolidation and storage of long-term memories, cognition and emotional processing [54, 55].”
From Sex chromosomes and sex hormones differently shape microglial properties during normal physiological conditions in the adult mouse hippocampus (2025) · cites this paper as [54]
The Memory & Cognition and Emotion sections link the hippocampus to memory, cognition, and emotional function. The Anatomic Connectivity section suggests a role in memory consolidation, but attributes long-term retention of contextual fear memories to the perirhinal and postrhinal cortices; our copy does not establish that the hippocampus stores long-term memories. (LLM, conf=0.84)
Experimental — accuracy not yet measuredProcessing of sensory signals into memories in rodents involves dorsal hippocampus networks.
“processing of sensory signals into memories in rodents involves dorsal hippocampus networks.9,10”
From Preferential loss of dorsal-hippocampus synapses underlies memory impairments provoked by short, multimodal stress (2014) · cites this paper as [9]
Ventral hippocampus has distinct afferent/efferent connections including robust pathways to amygdala, which may enhance the emotional salience of memories.
“In contrast, ventral hippocampus is endowed with distinct afferent/efferent connections9,11 including robust pathways to amygdala,12,13 which may enhance the emotional salience of memories.9,14”
From Preferential loss of dorsal-hippocampus synapses underlies memory impairments provoked by short, multimodal stress (2014) · cites this paper as [9]
Dorsal hippocampus primarily projects to cortical structures, whereas ventral hippocampus outflow targets subcortical regions including amygdala and hypothalamus.
“dorsal hippocampus primarily projects to cortical structures, whereas outflow from ventral hippocampus targets subcortical regions including amygdala and hypothalamus.9,11,13”
From Preferential loss of dorsal-hippocampus synapses underlies memory impairments provoked by short, multimodal stress (2014) · cites this paper as [9]
Dorsal hippocampus in the rodent, primarily CA1, is the principal location of memory encoding and processing.
“Dorsal hippocampus in the rodent, and primarily CA1, has emerged as the principal location of memory encoding and processing”
From Preferential loss of dorsal-hippocampus synapses underlies memory impairments provoked by short, multimodal stress (2014) · cites this paper as [9]
Ventral hippocampus contributes to a network involved in salience and emotionality.
“ventral hippocampus contributes to a network involved in salience and emotionality.9,10,25,117”
From Preferential loss of dorsal-hippocampus synapses underlies memory impairments provoked by short, multimodal stress (2014) · cites this paper as [9]
The dorsal hippocampus supports spatial navigation learning and memory, and the ventral hippocampus is important for anxiety and stress regulation.
“Studies have shown that different parts of the hippocampus serve these different functions, with the dorsal hippocampus supporting spatial navigation learning and memory, and the ventral hippocampus as important for anxiety and stress regulation (Fanselow and Dong, 2010; Kheirbek et al., 2013).”
From Adult neurogenesis, glia, and the extracellular matrix (2019) · cites this paper as Fanselow and Dong, 2010
The anterior hippocampus in humans is considered analogous to the vHIP in rodents.
“a region that is considered analogous to the vHIP in rodents (22).”
From Perineuronal nets, inhibitory interneurons and anxiety-related ventral hippocampal neuronal oscillations are altered by early life adversity (2019) · cites this paper as [22]
The vHIP is functionally distinct from the dHIP and has been implicated in anxiety regulation.
“The vHIP was analyzed separately as it is functionally distinct from the dHIP and has been implicated in anxiety regulation (22).”
From Perineuronal nets, inhibitory interneurons and anxiety-related ventral hippocampal neuronal oscillations are altered by early life adversity (2019) · cites this paper as [22]
YFP expression in the Amigo2-Cre line was selective and robust in CA2 pyramidal neurons throughout dorsal hippocampus.
“We observed selective and robust YFP expression in CA2 PNs throughout dorsal hippocampus9-11”
From The hippocampal CA2 region is essential for social memory (2014) · cites this paper as [11]
Ventral/temporal hippocampus is more involved in anxiety and emotional processing, while dorsal/septal portions are more involved in learning and memory.
“with ventral/temporal portions more involved in anxiety and emotional processing, and dorsal/septal portions more involved in learning and memory [41].”
From An emerging circuit pharmacology of GABAA receptors (2018) · cites this paper as [41]
The dorsal and ventral hippocampus exhibit functional heterogeneity.
“The dorsal and ventral hippocampus exhibit functional heterogeneity”
From The medial prefrontal cortex - hippocampus circuit that integrates information of object, place and time to construct episodic memory in rodents: Behavioral, anatomical and neurochemical properties (2020) · cites this paper as Fanselow and Dong, 2010
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
LOSS 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 · see citing works
Developments of a water-maze procedure for studying spatial learning in the rat
Morris, R. (1984) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(84)90007-4 · Cited by 7,180 · see citing works
The hippocampus as a spatial map. Preliminary evidence from unit activity in the freely-moving rat
O'Keefe, J., & Dostrovsky, J. (1971) · Brain Research · doi:10.1016/0006-8993(71)90358-1 · Cited by 6,151 · see citing works
Memory and the hippocampus: A synthesis from findings with rats, monkeys, and humans.
Squire, L. R. (1992) · Psychological Review · doi:10.1037/0033-295x.99.2.195 · Cited by 5,376 · see citing works
Gray, J. A. (1982) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00013066 · Cited by 4,477 · see citing works
Paxinos, G. (1985) · Cited by 3,715 · see citing works
The psychology of fear and stress
(1988) · Choice Reviews Online · doi:10.5860/choice.26-2399 · Cited by 3,134 · see citing works
Hypothalamic regulation of sleep and circadian rhythms
Saper, C. B., Scammell, T. E., & Lu, J. (2005) · Nature · doi:10.1038/nature04284 · Cited by 2,804 · see citing works
Spatial localization does not require the presence of local cues
Morris, R. G. M. (1981) · Learning and Motivation · doi:10.1016/0023-9690(81)90020-5 · Cited by 2,699 · see citing works
Modality-Specific Retrograde Amnesia of Fear
Kim, J. J., & Fanselow, M. S. (1992) · Science · doi:10.1126/science.1585183 · Cited by 2,483 · see citing works
Self-citationde Nó, R. L. (1934) · Cited by 1,974 · see citing works
Remembrance of places passed: Spatial memory in rats.
Olton, D. S., & Samuelson, R. J. (1976) · Journal of Experimental Psychology Animal Behavior Processes · doi:10.1037/0097-7403.2.2.97 · Cited by 1,934 · see citing works
Taube, J., Muller, R., & Ranck, J. (1990) · The Journal of Neuroscience · doi:10.1523/jneurosci.10-02-00420.1990 · Cited by 1,809 · see citing works
JACOBSON, L., & SAPOLSKY, R. (1991) · Endocrine Reviews · doi:10.1210/edrv-12-2-118 · Cited by 1,739 · see citing works
Swanson, L. W., & Cowan, W. M. (1977) · The Journal of Comparative Neurology · doi:10.1002/cne.901720104 · Cited by 1,571 · see citing works
Anatomical analysis of afferent projections to the medial prefrontal cortex in the rat
Hoover, W. B., & Vertes, R. P. (2007) · Brain Structure and Function · doi:10.1007/s00429-007-0150-4 · Cited by 1,365 · see citing works
Limbic system mechanisms of stress regulation: Hypothalamo-pituitary-adrenocortical axis
Herman, J. P., Ostrander, M. M., Mueller, N. K., & Figueiredo, H. (2005) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2005.08.006 · Cited by 1,322 · see citing works
Knowing Where and Getting There: A Human Navigation Network
Maguire, E. A., Burgess, N., Donnett, J. G., Frackowiak, R. S. J., Frith, C. D., & O'Keefe, J. (1998) · Science · doi:10.1126/science.280.5365.921 · Cited by 1,303 · see citing works
Theta rhythms coordinate hippocampal-prefrontal interactions in a spatial memory task
Jones, M. W., & Wilson, M. A. (2005) · PLoS Biology · doi:10.1371/journal.pbio.0030402 · Cited by 1,036 · see citing works
Pitkänen, A., Pikkarainen, M., Nurminen, N., & Ylinen, A. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06738.x · Cited by 962 · see citing works
The Involvement of the Anterior Cingulate Cortex in Remote Contextual Fear Memory
Frankland, P., Bontempi, B., Talton, L., Kaczmarek, L., & Silva, A. J. (2004) · Science · doi:10.1126/science.1094804 · Cited by 952 · see citing works
The Head Direction Signal: Origins and Sensory-Motor Integration
Taube, J. S. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.29.051605.112854 · Cited by 916 · see citing works
Reduced fear expression after lesions of the ventral hippocampus
Kjelstrup, K. G., Tuvnes, F. A., Steffenach, H.-A., Murison, R., Moser, E. I., & Moser, M.-B. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.152112399 · Cited by 912 · see citing works
Spatial learning with a minislab in the dorsal hippocampus.
Moser, M., Moser, E. I., Forrest, E., Andersen, P. N., & Morris, R. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.21.9697 · Cited by 902 · see citing works
Organization of intrahippocampal projections originating from CA3 pyramidal cells in the rat
Ishizuka, N., Weber, J., & Amaral, D. G. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902950407 · Cited by 899 · see citing works
Cerebral hemisphere regulation of motivated behavior
Swanson, L. W. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02905-x · Cited by 846 · see citing works
Comparison of spatial firing characteristics of units in dorsal and ventral hippocampus of the rat
Jung, M. W., Wiener, S. I., & McNaughton, B. L. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-12-07347.1994 · Cited by 818 · see citing works
Hikosaka, O., & Wurtz, R. H. (1983) · Journal of Neurophysiology · doi:10.1152/jn.1983.49.5.1285 · Cited by 811 · see citing works
Finite scale of spatial representation in the hippocampus
Kjelstrup, K. B., Solstad, T., Brun, V. H., Hafting, T., Leutgeb, S., Witter, M. P., Moser, E. I., & Moser, M.-B. (2008) · Science · doi:10.1126/science.1157086 · Cited by 760 · see citing works
Corticostriatal-hypothalamic circuitry and food motivation: Integration of energy, action and reward
Kelley, A. E., Baldo, B. A., Pratt, W. E., & Will, M. J. (2005) · Physiology & Behavior · doi:10.1016/j.physbeh.2005.08.066 · Cited by 752 · see citing works
Contextual fear, gestalt memories, and the hippocampus
Fanselow, M. S. (2000) · Behavioural Brain Research · doi:10.1016/s0166-4328(99)00186-2 · Cited by 728 · see citing works
Self-citationTopography of projections from amygdala to bed nuclei of the stria terminalis
Dong, H.-W., Petrovich, G. D., & Swanson, L. W. (2001) · Brain Research Reviews · doi:10.1016/s0165-0173(01)00079-0 · Cited by 714 · see citing works
Self-citation(1997) · Neuroscience · doi:10.1016/s0306-4522(97)00239-x · Cited by 707 · see citing works
An autoradiographic study of the organization of intrahippocampal association pathways in the rat
Swanson, L. W., Wyss, J. M., & Cowan, W. M. (1978) · The Journal of Comparative Neurology · doi:10.1002/cne.901810402 · Cited by 704 · see citing works
The olfactory bulbectomised rat as a model of depression
Song, C., & Leonard, B. E. (2005) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2005.03.010 · Cited by 700 · see citing works
The brain and the stress axis: the neural correlates of cortisol regulation in response to stress
Dedovic, K., Duchesne, A., Andrews, J., Engert, V., & Pruessner, J. C. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.05.074 · Cited by 699 · see citing works
The Neuroscience of Mammalian Associative Learning
Fanselow, M. S., & Poulos, A. M. (2005) · Annual Review of Psychology · doi:10.1146/annurev.psych.56.091103.070213 · Cited by 683 · see citing works
Self-citationWatts, A. G., Swanson, L. W., & Sanchez‐Watts, G. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902580204 · Cited by 678 · see citing works
Recalling Routes around London: Activation of the Right Hippocampus in Taxi Drivers
Maguire, E. A., Frackowiak, R. S. J., & Frith, C. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-18-07103.1997 · Cited by 655 · see citing works
Cenquizca, L. A., & Swanson, L. W. (2007) · Brain Research Reviews · doi:10.1016/j.brainresrev.2007.05.002 · Cited by 640 · see citing works
Combinatorial amygdalar inputs to hippocampal domains and hypothalamic behavior systems.
Petrovich, G., Canteras, N., & Swanson, L. (2001) · Brain research. Brain research reviews · doi:10.1016/s0165-0173(01)00080-7 · Cited by 628 · see citing works
Factors governing one-trial contextual conditioning
Fanselow, M. S. (1990) · Animal Learning & Behavior · doi:10.3758/bf03205285 · Cited by 564 · see citing works
Self-citationDo septal neurons pace the hippocampal theta rhythm?
Stewart, M., & Fox, S. E. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90040-h · Cited by 559 · see citing works
The Influence of Stress Hormones on Fear Circuitry
Rodrigues, S. M., LeDoux, J. E., & Sapolsky, R. M. (2009) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.051508.135620 · Cited by 556 · see citing works
"Psychic blindness" and other symptoms following bilateral temporal lobectomy in Rhesus monkeys.
Klüver, H., & Bucy, P. C. (1937) · American Journal of Physiology-Legacy Content · Cited by 549 · see citing works
Cullinan, W. E., Herman, J. P., & Watson, S. J. (1993) · Journal of Comparative Neurology · doi:10.1002/cne.903320102 · Cited by 541 · see citing works
Cortical connections between rat cingulate cortex and visual, motor, and postsubicular cortices
Vogt, B. A., & Miller, M. W. (1983) · The Journal of Comparative Neurology · doi:10.1002/cne.902160207 · Cited by 528 · see citing works
Dong, H., Petrovich, G. D., Watts, A. G., & Swanson, L. W. (2001) · Journal of Comparative Neurology · doi:10.1002/cne.1079 · Cited by 521 · see citing works
Self-citationThe 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
Synaptic plasticity in the basolateral amygdala induced by hippocampal formation stimulation in vivo
Maren, S., & Fanselow (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-11-07548.1995 · Cited by 499 · see citing works
Macaque monkey retrosplenial cortex: III. Cortical efferents
Kobayashi, Y., & Amaral, D. G. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21346 · Cited by 487 · see citing works
Witter, M. P., & Amaral, D. G. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903070308 · Cited by 480 · see citing works
Structural Evidence for Functional Domains in the Rat Hippocampus
Risold, P., & Swanson, L. W. (1996) · Science · doi:10.1126/science.272.5267.1484 · Cited by 451 · see citing works
Groenewegen, H. J., & Russchen, F. T. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902230303 · Cited by 447 · see citing works
Connections of the retrosplenial granular a cortex in the rat
van Groen, T., & Wyss, J. M. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.903000412 · Cited by 419 · see citing works
Bernard, J. F., Alden, M., & Besson, J. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903290205 · Cited by 411 · see citing works
Mogenson, G. J., Swanson, L. W., & Wu, M. (1983) · Journal of Neuroscience · doi:10.1523/jneurosci.03-01-00189.1983 · Cited by 410 · see citing works
Genomic anatomy of the hippocampus
Thompson, C. L., Pathak, S. D., Jeromin, A., Ng, L. L., MacPherson, C. R., Mortrud, M. T., Cusick, A., Riley, Z. L., Sunkin, S. M., Bernard, A., et al. (2008) · Neuron · doi:10.1016/j.neuron.2008.12.008 · Cited by 403 · see citing works
Bannerman, D. M., Yee, B. K., Good, M. A., Heupel, M. J., Iversen, S. D., & Rawlins, J. N. P. (1999) · Behavioral Neuroscience · doi:10.1037/0735-7044.113.6.1170 · Cited by 397 · see citing works
Choi, D. C., Furay, A. R., Evanson, N. K., Ostrander, M. M., Ulrich-Lai, Y. M., & Herman, J. P. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.4301-06.2007 · Cited by 392 · see citing works
The hippocampus as a cognitive graph.
Muller, R. U., Stead, M., & Pach, J. (1996) · The Journal of general physiology · doi:10.1085/jgp.107.6.663 · Cited by 391 · see citing works
Topographical organization of the entorhinal projection to the dentate gyrus of the monkey
Witter, M., Hoesen, G. W. V., & Amaral, D. (1989) · Journal of Neuroscience · doi:10.1523/jneurosci.09-01-00216.1989 · Cited by 380 · see citing works
Connections between the retrosplenial cortex and the hippocampal formation in the rat: A review
Wyss, J. M., & van Groen, T. (1992) · Hippocampus · doi:10.1002/hipo.450020102 · Cited by 379 · see citing works
The Temporal Lobe and Limbic System
GLOOR, P. (1997) · Medical Entomology and Zoology · Cited by 372 · see citing works
Thoughts, behaviour, and brain dynamics during navigation in the real world
Spiers, H. J., & Maguire, E. A. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.01.037 · Cited by 371 · see citing works
Genomic–anatomic evidence for distinct functional domains in hippocampal field CA1
Dong, H., Swanson, L. W., Chen, L., Fanselow, M. S., & Toga, A. W. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0812608106 · Cited by 361 · see citing works
Self-citationKelley, A. E., Baldo, B. A., & Pratt, W. E. (2005) · Journal of Comparative Neurology · doi:10.1002/cne.20769 · Cited by 352 · see citing works
Risold, P., Thompson, R. H., & Swanson, L. W. (1997) · Brain Research Reviews · doi:10.1016/s0165-0173(97)00007-6 · Cited by 347 · see citing works
Vertes, R. P., Hoover, W. B., Szigeti‐Buck, K., & Léránth, C. (2007) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2006.12.002 · Cited by 345 · see citing works
Chapter 29 The nucleus accumbens: gateway for limbic structures to reach the motor system?
Groenewegen, H. J., Wright, C. I., & Beijer, A. V. J. (1996) · Progress in brain research · doi:10.1016/s0079-6123(08)61883-x · Cited by 344 · see citing works
Witter, M. P., & Amaral, D. G. (2004) · Elsevier eBooks · doi:10.1016/b978-012547638-6/50022-5 · Cited by 344 · see citing works
Swanson, L. W., & Köhler, C. (1986) · Journal of Neuroscience · doi:10.1523/jneurosci.06-10-03010.1986 · Cited by 340 · see citing works
Navigation around London by a taxi driver with bilateral hippocampal lesions
Maguire, E. A., Nannery, R., & Spiers, H. J. (2006) · Brain · doi:10.1093/brain/awl286 · Cited by 335 · see citing works
Walker, D. L., Miles, L. A., & Davis, M. (2009) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2009.06.022 · Cited by 331 · see citing works
Fanselow, M. S. (1986) · Learning and Motivation · doi:10.1016/0023-9690(86)90018-4 · Cited by 326 · see citing works
Self-citationSpatial Memory in the Rat Requires the Dorsolateral Band of the Entorhinal Cortex
Steffenach, H.-A., Witter, M. P., Moser, M., & Moser, E. I. (2005) · Neuron · doi:10.1016/j.neuron.2004.12.044 · Cited by 321 · see citing works
Neural connections of the posteromedial cortex in the macaque
Parvizi, J., Hoesen, G. W. V., Buckwalter, J. A., V, & Damásio, A. R. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0507729103 · Cited by 313 · see citing works
Neuronal Mechanisms of the Orienting Reflex
Stern, J. A. (1976) · The Journal of Nervous and Mental Disease · doi:10.1097/00005053-197611000-00016 · Cited by 307 · see citing works
Hippocampo-Hypothalamic Connections: Origin in Subicular Cortex, Not Ammon's Horn
Swanson, L. W., & Cowan, W. M. (1975) · Science · doi:10.1126/science.49928 · Cited by 305 · see citing works
Trace but not delay fear conditioning requires attention and the anterior cingulate cortex
Han, C. J., O'Tuathaigh, C. M., van Trigt, L., Quinn, J. J., Fanselow, M. S., Mongeau, R., Koch, C., & Anderson, D. J. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2132313100 · Cited by 302 · see citing works
Self-citationConnections of the retrosplenial granular b cortex in the rat
van Groen, T., & Wyss, J. M. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10757 · Cited by 302 · see citing works
Dong, H.-W., & Swanson, L. W. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.20788 · Cited by 290 · see citing works
Self-citationPothuizen, H. H. J., Zhang, W., Jongen‐Rêlo, A. L., Feldon, J., & Yee, B. K. (2004) · European Journal of Neuroscience · doi:10.1111/j.0953-816x.2004.03170.x · Cited by 274 · see citing works
Connections of the posterior nucleus of the amygdala
Canteras, N. S., Simerly, R. B., & Swanson, L. W. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903240203 · Cited by 273 · see citing works
Organization of CA1 projections to the subiculum: A PHA‐L analysis in the rat
Amaral, D. G., Dolorfo, C. L., & Alvarez‐Royo, P. (1991) · Hippocampus · doi:10.1002/hipo.450010410 · Cited by 272 · see citing works
Maren, S., & Holt, W. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.1.97 · Cited by 272 · see citing works
The connections of presubiculum and parasubiculum in the rat
van Groen, T., & Wyss, J. M. (1990) · Brain Research · doi:10.1016/0006-8993(90)90976-i · Cited by 269 · see citing works
Entorhinal cortex of the rat: Organization of intrinsic connections
Dolorfo, C. L., & Amaral, D. G. (1998) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19980817)398:1 · Cited by 268 · see citing works
Haglund, L., Swanson, L. W., & Köhler, C. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902290204 · Cited by 264 · 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
Naber, P. A., da Silva, F. H. L., & Witter, M. P. (2001) · Hippocampus · doi:10.1002/hipo.1028 · Cited by 258 · see citing works
(1975) · Medical Entomology and Zoology · Cited by 252 · see citing works
Regional analysis of hippocampal activation during memory encoding and retrieval: fMRI study
Greicius, M. D., Krasnow, B., Anderson, J. M. B., D, S. E. M., Schatzberg, A. F., Reiss, A. L., & Menon, V. (2002) · Hippocampus · doi:10.1002/hipo.10064 · Cited by 229 · see citing works
Allen reference atlas : a digital color brain atlas of the C57Black/6J male mouse
Dong, H. (2008) · Wiley eBooks · Cited by 228 · see citing works
Self-citationTamamaki, N., & Nojyo, Y. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903530306 · Cited by 225 · see citing works
Naber, P. A., & Witter, M. P. (1998) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19980413)393:3 · Cited by 219 · see citing works
Saunders, R. C., Rosene, D. L., & Hoesen, G. W. V. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902710203 · Cited by 206 · see citing works
Dorsal/ventral hippocampus, fornix, and conditioned place preference
Ferbinteanu, J., & McDonald, R. J. (2001) · Hippocampus · doi:10.1002/hipo.1036 · Cited by 198 · see citing works
From Rapid Place Learning to Behavioral Performance: A Key Role for the Intermediate Hippocampus
Bast, T., Wilson, I. A., Witter, M. P., & Morris, R. (2009) · PLoS Biology · doi:10.1371/journal.pbio.1000089 · Cited by 189 · see citing works
Baxter, M. G., & Murray, E. A. (2001) · Hippocampus · doi:10.1002/1098-1063(2001)11:1 · Cited by 186 · see citing works
Roberts, A., Tomic, D. L., Parkinson, C. H., Roeling, T. A. P., Cutter, D. J., Robbins, T. W., & Everitt, B. J. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21300 · Cited by 184 · see citing works
Distinct opioid circuits determine the palatability and the desirability of rewarding events
Wassum, K. M., Ostlund, S. B., Maidment, N. T., & Balleine, B. W. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0905874106 · Cited by 182 · see citing works
Witter, M. P., & Groenewegen, H. J. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902240305 · Cited by 178 · see citing works
Dorsal hippocampus NMDA receptors differentially mediate trace and contextual fear conditioning
Quinn, J. J., Loya, F., Ma, Q. D., & Fanselow, M. S. (2005) · Hippocampus · doi:10.1002/hipo.20088 · Cited by 166 · see citing works
Self-citationThe role of hippocampus in the pathophysiology of bipolar disorder
Frey, B. N., Andreazza, A. C., Nery, F. G., Martins, M. R., Quevedo, J., Soares, J. C., & Kapczinski, F. (2007) · Behavioural Pharmacology · doi:10.1097/fbp.0b013e3282df3cde · Cited by 162 · see citing works
Analysis of direct hippocampal cortical field CA1 axonal projections to diencephalon in the rat
Cenquizca, L. A., & Swanson, L. W. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.20985 · Cited by 157 · see citing works
Reduced posterior hippocampal volume in posttraumatic stress disorder
Bonne, O., Vythilingam, M., Inagaki, M., Wood, S., Neumeister, A., Nugent, A. C., Snow, J., Luckenbaugh, D. A., Bain, E. E., Drevets, W. C., et al. (2008) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.v69n0707 · Cited by 156 · see citing works
Hunsaker, M. R., & Kesner, R. P. (2007) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2007.08.016 · Cited by 156 · see citing works
Contributions of postrhinal and perirhinal cortex to contextual information processing.
Bucci, D. J., Phillips, R. G., & Burwell, R. D. (2021) · Behavioral Neuroscience · doi:10.1037/bne0000436 · Cited by 154 · see citing works
Hippocampal pathway to the amygdala and stress ulcer development.
Henke, P. G. (1990) · Brain Research Bulletin · doi:10.1016/0361-9230(90)90044-z · Cited by 153 · see citing works
Kishi, T., Tsumori, T., Yokota, S., & Yasui, Y. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.20919 · Cited by 150 · see citing works
Bast, T. (2007) · Reviews in the Neurosciences · doi:10.1515/revneuro.2007.18.3-4.253 · Cited by 149 · see citing works
Rudy, J. W., & Matus-Amat, P. (2005) · Behavioral Neuroscience · doi:10.1037/0735-7044.119.1.154 · Cited by 147 · see citing works
Malin, E. L., & McGaugh, J. L. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0510890103 · Cited by 147 · see citing works
Contributions of postrhinal and perirhinal cortex to contextual information processing.
Bucci, D. J., Phillips, R. G., & Burwell, R. D. (2000) · Behavioral Neuroscience · doi:10.1037//0735-7044.114.5.882 · Cited by 147 · see citing works
Chapter 4 The subiculum: cytoarchitectonically a simple structure, but hodologically complex
Witter, M. P., & Groenewegen, H. J. (1990) · Progress in brain research · doi:10.1016/s0079-6123(08)61240-6 · Cited by 145 · see citing works
Hippocampal Lesion Prevents Spatial Relational Learning in Adult Macaque Monkeys
Lavenex, P. B., Amaral, D. G., & Lavenex, P. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.5412-05.2006 · Cited by 145 · see citing works
Laminar organization of the pyramidal cell layer of the subiculum in the rat
Ishizuka, N. (2001) · The Journal of Comparative Neurology · doi:10.1002/cne.1195 · Cited by 144 · see citing works
Barrientos, R. M., O’Reilly, R. C., & Rudy, J. W. (2002) · Behavioural Brain Research · doi:10.1016/s0166-4328(02)00045-1 · Cited by 143 · see citing works
Zhang, W. (2001) · Behavioural Brain Research · doi:10.1016/s0166-4328(01)00256-x · Cited by 138 · see citing works
Prevention of stress-induced morphological and cognitive consequences
McEwen, B. S., Conrad, C. D., Kuroda, Y., Frankfurt, M., Magariños, A. M., & McKittrick, C. R. (1997) · European Neuropsychopharmacology · doi:10.1016/s0924-977x(97)00064-3 · Cited by 137 · see citing works
Contributions of postrhinal and perirhinal cortex to contextual information processing.
Bucci, D. J., Phillips, R. G., & Burwell, R. D. (2000) · Behavioral Neuroscience · doi:10.1037/0735-7044.114.5.882 · Cited by 136 · see citing works
Gaykema, R. P. A., van der Kuil, J., Hersh, L. B., & Luiten, P. G. M. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90299-4 · Cited by 131 · see citing works
Pandi-Perumal, S. R., Moscovitch, A., Srinivasan, V., Spence, D. W., Cardinali, D. P., & Brown, G. M. (2009) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2009.04.007 · Cited by 128 · see citing works
SUZUKI, W. A., & Amaral, D. G. (1990) · Neuroscience Letters · doi:10.1016/0304-3940(90)90515-b · Cited by 127 · see citing works
Hunsaker, M. R., Fieldsted, P. M., Rosenberg, J. S., & Kesner, R. P. (2008) · Behavioral Neuroscience · doi:10.1037/0735-7044.122.3.643 · Cited by 127 · see citing works
Klur, S., Muller, C., de Vasconcelos, A. P., Ballard, T. M., Lopez, J., Galani, R., Certa, U., & Cassel, J. (2009) · Hippocampus · doi:10.1002/hipo.20562 · Cited by 126 · see citing works
Perirhinal and Postrhinal Contributions to Remote Memory for Context
Burwell, R. D., Bucci, D. J., Sanborn, M. R., & Jutras, M. J. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3781-04.2004 · Cited by 124 · see citing works
Both dorsal and ventral hippocampus contribute to spatial learning in Long–Evans rats
Ferbinteanu, J., Ray, C. A., & McDonald, R. J. (2003) · Neuroscience Letters · doi:10.1016/s0304-3940(03)00473-7 · Cited by 124 · see citing works
Selective immunolesions of hippocampal cholinergic input fail to impair spatial working memory
McMahan, R. W., Sobel, T. J., & Baxter, M. G. (1997) · Hippocampus · doi:10.1002/(sici)1098-1063(1997)7:2 · Cited by 109 · see citing works
Groen, T. V., van Haren, F. J., Witter, M. P., & Groenewegen, H. J. (1986) · The Journal of Comparative Neurology · doi:10.1002/cne.902500407 · Cited by 109 · see citing works
The Temporal Lobe and Limbic System.
MacLean, P. D. (1998) · The Journal of Nervous and Mental Disease · doi:10.1097/00005053-199811000-00015 · Cited by 108 · see citing works
Swanson, C. J., & Kalivas, P. W. (2000) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(24)35306-6 · Cited by 108 · see citing works
Choi, D. C., Evanson, N. K., Furay, A. R., Ulrich‐Lai, Y. M., Ostrander, M. M., & Herman, J. P. (2007) · Endocrinology · doi:10.1210/en.2007-0883 · Cited by 106 · see citing works
Kloosterman, F., van Haeften, T., Witter, M. P., & Lopes, F. H. D. S. (2003) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2003.03046.x · Cited by 105 · see citing works
Exploration and visualization of gene expression with neuroanatomy in the adult mouse brain
Lau, C. C., Ng, L., Thompson, C. L., Pathak, D. S., Kuan, L., Jones, A., & Hawrylycz, M. (2008) · BMC Bioinformatics · doi:10.1186/1471-2105-9-153 · Cited by 102 · see citing works
Integration of the sensory inputs to place cells: What, where, why, and how?
Jeffery, K. J. (2007) · Hippocampus · doi:10.1002/hipo.20322 · Cited by 97 · see citing works
Werner, W., Hoffmann, K.-P., & Dannenberg, S. (1997) · Experimental Brain Research · doi:10.1007/pl00005691 · Cited by 94 · see citing works
Wang, D., Noda, Y., Tsunekawa, H., Zhou, Y., Miyazaki, M., Senzaki, K., & Nabeshima, T. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2007.01.003 · Cited by 89 · see citing works
Rogers, J. L., & Kesner, R. P. (2006) · Behavioral Neuroscience · doi:10.1037/0735-7044.120.4.852 · Cited by 65 · see citing works
Entorhinal cortex of the monkey: VII. Intrinsic connections
Chrobak, J. J., & Amaral, D. G. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.21200 · Cited by 64 · see citing works
NMDA Receptor Modulation of Incidental Learning in Pavlovian Context Conditioning.
Stote, D. L., & Fanselow, M. S. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.1.253 · Cited by 55 · see citing works
Self-citationHarker, K. T., & Whishaw, I. Q. (2004) · Hippocampus · doi:10.1002/hipo.10159 · Cited by 51 · see citing works
Antidepressants and Sleep: A Review
Holshoe, J. M. (2009) · Perspectives In Psychiatric Care · doi:10.1111/j.1744-6163.2009.00221.x · Cited by 51 · see citing works
Spatial relational learning persists following neonatal hippocampal lesions in macaque monkeys
Lavenex, P., Lavenex, P. B., & Amaral, D. G. (2006) · Nature Neuroscience · doi:10.1038/nn1820 · Cited by 51 · see citing works
Hippocampal lesions interfere with long-trace taste aversion conditioning
Koh, M. T., Wheeler, D. S., & Gallagher, M. (2009) · Physiology & Behavior · doi:10.1016/j.physbeh.2009.04.017 · Cited by 46 · see citing works
The hippocampus and Pavlovian fear conditioning: Reply to Bast et al.
Anagnostaras, S., Gale, G. D., & Fanselow, M. (2002) · Hippocampus · doi:10.1002/hipo.10071 · Cited by 44 · see citing works
Self-citationMcGaugh, J. L. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.5.1140 · Cited by 42 · see citing works
Chiba, T. (2000) · Neuroscience Research · doi:10.1016/s0168-0102(00)00183-8 · Cited by 37 · see citing works
Tokita, K., Shimura, T., Nakamura, S., Inoue, T., & Yamamoto, T. (2007) · Brain Research · doi:10.1016/j.brainres.2007.01.023 · Cited by 29 · see citing works
Clark, E. W., & Bernstein, I. L. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.09.030 · Cited by 13 · see citing works
Hoshino, K., Hicks, T. P., Hirano, S., & Norita, M. (2000) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(20000403)419:2 · Cited by 8 · see citing works
Cortico-hippocampal communication by way of parallel parahippocampal-subicular pathways.
Lavenex (2000) · Pure Amsterdam UMC · doi:10.1002/1098-1063(2000)10:4 · Cited by 1 · see citing works
Fashena, D. (1999) · doi:10.1002/(sici)1096-9861(19990412)406:3
Flagged first, then by citations
Research works printed but not linked: 4
- Kocsis B Vertes RP Phase relations of rhythmic neuronal firing in the supramammillary nucleus and mammillary body to the hippocampal theta activity in urethane anesthetized rats Hippocampus 1997 7 204 214 9136050
- Swanson LW Brain Maps III: Structure of the Rat Brain 2004 Third ed Amsterdam Elsevier
- Swanson LW Kohler C Bjorklund A The limbic region. I: The septohippocampal system 1987 Vol. 5 Elsevier
- Swanson LW Wyss JM Cowan WM An autoradiographic study of the organization of intrahippocampal association pathways in the rat J Comp Neurol 1978 181 681 715 690280
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 · see citing works
Regulation of the Hypothalamic‐Pituitary‐Adrenocortical Stress Response
Herman, J. P., McKlveen, J. M., Ghosal, S., Kopp, B., Wulsin, A., Makinson, R., Scheimann, J., & Myers, B. (2016) · Comprehensive Physiology · doi:10.1002/cphy.c150015 · Cited by 1,819 · see citing works
Neuronal circuits for fear and anxiety
Tovote, P., Fadok, J. P., & Lüthi, A. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn3945 · Cited by 1,786 · see citing works
The contextual brain: implications for fear conditioning, extinction and psychopathology
Maren, S., Phan, K. L., & Liberzon, I. (2013) · Nature Reviews Neuroscience · doi:10.1038/nrn3492 · Cited by 1,547 · 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
Adult hippocampal neurogenesis and cognitive flexibility — linking memory and mood
Anacker, C., & Hen, R. (2017) · Nature Reviews Neuroscience · doi:10.1038/nrn.2017.45 · Cited by 1,014 · see citing works
The hippocampal CA2 region is essential for social memory
Hitti, F. L., & Siegelbaum, S. A. (2014) · Nature · doi:10.1038/nature13028 · Cited by 976 · see citing works
A pathophysiological framework of hippocampal dysfunction in ageing and disease
Small, S. A., Schobel, S., Buxton, R. B., Witter, M. P., & Barnes, C. A. (2011) · Nature reviews. Neuroscience · doi:10.1038/nrn3085 · Cited by 920 · see citing works
Neural Networks of the Mouse Neocortex
Zingg, B., Hintiryan, H., Gou, L., Song, M. Y., Bay, M., Bienkowski, M. S., Foster, N. N., Yamashita, S., Bowman, I., Toga, A. W., et al. (2014) · Cell · doi:10.1016/j.cell.2014.02.023 · Cited by 797 · see citing works
Self-citationDifferential Control of Learning and Anxiety along the Dorsoventral Axis of the Dentate Gyrus
Kheirbek, M. A., Drew, L. J., Burghardt, N. S., Costantini, D. O., Tannenholz, L., Ahmari, S. E., Zeng, H., Fenton, A. A., & Hen, R. (2013) · Neuron · doi:10.1016/j.neuron.2012.12.038 · Cited by 713 · see citing works
Shah, S., Lubeck, E., Zhou, W., & Cai, L. (2016) · Neuron · doi:10.1016/j.neuron.2016.10.001 · Cited by 671 · see citing works
Stress, serotonin, and hippocampal neurogenesis in relation to depression and antidepressant effects
Mahar, I., Bambico, F. R., Mechawar, N., & Nobrega, J. N. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.11.009 · Cited by 694 · see citing works
Hippocampal–prefrontal input supports spatial encoding in working memory
Spellman, T., Rigotti, M., Ahmari, S. E., Fusi, S., Gogos, J. A., & Gordon, J. A. (2015) · Nature · doi:10.1038/nature14445 · Cited by 693 · see citing works
Hippocampal synaptic plasticity, spatial memory and anxiety
Bannerman, D. M., Sprengel, R., Sanderson, D. J., McHugh, S. B., Rawlins, J. N. P., Monyer, H., & Seeburg, P. H. (2014) · Nature Reviews Neuroscience · doi:10.1038/nrn3677 · Cited by 688 · see citing works
Diet and depression: Exploring the biological mechanisms of action
Marx, W., Lane, M., Hockey, M., Aslam, H., Berk, M., Walder, K., Borsini, A., Firth, J., Pariante, C. M., Berding, K., et al. (2021) · Molecular Psychiatry · doi:10.1038/s41380-020-00925-x · Cited by 685 · see citing works
Western diet consumption and cognitive impairment: Links to hippocampal dysfunction and obesity
Kanoski, S. E., & Davidson, T. L. (2010) · Physiology & Behavior · doi:10.1016/j.physbeh.2010.12.003 · Cited by 674 · see citing works
Ventral CA1 neurons store social memory
Okuyama, T., Kitamura, T., Roy, D. S., Itohara, S., & Tonegawa, S. (2016) · Science · doi:10.1126/science.aaf7003 · Cited by 657 · see citing works
Regulation and function of adult neurogenesis: from genes to cognition.
Aimone, J. B., Li, Y., Lee, S. W., Clemenson, G. D., Deng, W., & Gage, F. H. (2014) · Physiological Reviews · doi:10.1152/physrev.00004.2014 · Cited by 635 · see citing works
Anxiety Cells in a Hippocampal-Hypothalamic Circuit
Jimenez, J., Su, K., Goldberg, A., Luna, V. M., Biane, J. S., Ordek, G., Zhou, P., Ong, S. K., Wright, M. A., Zweifel, L. S., et al. (2018) · Neuron · doi:10.1016/j.neuron.2018.01.016 · Cited by 606 · see citing works
Bang-Andersen, B., Ruhland, T., Jørgensen, M., Smith, G., Frederiksen, K., Jensen, K. G., Zhong, H., Nielsen, S. M., Hogg, S., Mørk, A., et al. (2011) · Journal of Medicinal Chemistry · doi:10.1021/jm101459g · Cited by 606 · see citing works
Human Hippocampal Neurogenesis Persists in Aged Adults and Alzheimer’s Disease Patients
Tobin, M. K., Musaraca, K., Disouky, A., Shetti, A., Bheri, A., Honer, W. G., Kim, N., Dawe, R. J., Bennett, D. A., Arfanakis, K., et al. (2019) · Cell Stem Cell · doi:10.1016/j.stem.2019.05.003 · Cited by 603 · see citing works
Parallel, Redundant Circuit Organization for Homeostatic Control of Feeding Behavior
Betley, J. N., Cao, Z. F. H., Ritola, K., & Sternson, S. M. (2013) · Cell · doi:10.1016/j.cell.2013.11.002 · Cited by 591 · see citing works
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 · see citing works
Hill, A. S., Sahay, A., & Hen, R. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.85 · Cited by 557 · see citing works
Modulation of the Hypothalamic-Pituitary-Adrenal Axis by Early Life Stress Exposure
van Bodegom, M., Homberg, J. R., & Henckens, M. J. A. G. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00087 · Cited by 562 · see citing works
Regulation of the Hypothalamic‐Pituitary‐Adrenocortical Stress Response
Herman, J. P., McKlveen, J. M., Ghosal, S., Kopp, B., Wulsin, A. C., Makinson, R. A., Scheimann, J. R., & Myers, B. (2016) · Comprehensive physiology · doi:10.1002/j.2040-4603.2016.tb00694.x · Cited by 541 · see citing works
Neuromodulation by Oxytocin and Vasopressin
Stoop, R. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.025 · Cited by 506 · see citing works
Acquiring “the Knowledge” of London's Layout Drives Structural Brain Changes
Woollett, K., & Maguire, E. A. (2011) · Current Biology · doi:10.1016/j.cub.2011.11.018 · Cited by 509 · see citing works
Neurogenesis and generalization: a new approach to stratify and treat anxiety disorders
Kheirbek, M., Klemenhagen, K. C., Sahay, A., & Hen, R. (2012) · Nature Neuroscience · doi:10.1038/nn.3262 · Cited by 543 · see citing works
The role of 5-HT receptors in depression
Yohn, C. N., Gergues, M. M., & Samuels, B. A. (2017) · Molecular Brain · doi:10.1186/s13041-017-0306-y · Cited by 485 · see citing works
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 466 · see citing works
A neoHebbian framework for episodic memory; role of dopamine-dependent late LTP
Lisman, J., Grace, A. A., & Duzel, E. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2011.07.006 · Cited by 465 · see citing works
A quantitative meta-analysis of fMRI studies in bipolar disorder
Chen, C., John Suckling, A., Lennox, B., Ooi, C., & Bullmore, E. T. (2011) · Bipolar Disorders · doi:10.1111/j.1399-5618.2011.00893.x · Cited by 457 · see citing works
Hipposeq: a comprehensive RNA-seq database of gene expression in hippocampal principal neurons
Cembrowski, M. S., Wang, L., Sugino, K., Shields, B. C., & Spruston, N. (2016) · eLife · doi:10.7554/elife.14997 · Cited by 422 · see citing works
Lucassen, P. J., Pruessner, J. C., Sousa, N., Almeida, O. F. X., Dam, A. M. V., Rajkowska, G., Swaab, D. F., & Czéh, B. (2013) · Acta Neuropathologica · doi:10.1007/s00401-013-1223-5 · Cited by 449 · see citing works
Coordination of entorhinal–hippocampal ensemble activity during associative learning
Igarashi, K. M., Lu, L., Colgin, L. L., Moser, M., & Moser, E. I. (2014) · Nature · doi:10.1038/nature13162 · Cited by 435 · see citing works
Treatment resistant depression: A multi-scale, systems biology approach
Akil, H., Gordon, J. A., Hen, R., Javitch, J. A., Mayberg, H. S., McEwen, B. S., Meaney, M. J., & Nestler, E. J. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.08.019 · Cited by 443 · see citing works
The hippocampal–prefrontal pathway: The weak link in psychiatric disorders?
Godsil, B. P., Kiss, J., Spedding, M., & Jay, T. M. (2013) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2012.10.018 · Cited by 434 · see citing works
Neural and cellular mechanisms of fear and extinction memory formation
Orsini, C. A., & Maren, S. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2011.12.014 · Cited by 429 · see citing works
Functions and Dysfunctions of Adult Hippocampal Neurogenesis
Christian, K. M., Song, H., & Ming, G. (2014) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071013-014134 · Cited by 395 · see citing works
Neurobiology of BDNF in fear memory, sensitivity to stress, and stress-related disorders
Notaras, M. J., & van den Buuse, M. (2020) · Molecular Psychiatry · doi:10.1038/s41380-019-0639-2 · Cited by 395 · see citing works
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 · see citing works
Sex differences in anxiety and emotional behavior
Donner, N. C., & Lowry, C. A. (2013) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-013-1271-7 · Cited by 379 · see citing works
Spatial Gene-Expression Gradients Underlie Prominent Heterogeneity of CA1 Pyramidal Neurons
Cembrowski, M. S., Bachman, J. L., Wang, L., Sugino, K., Shields, B. C., & Spruston, N. (2016) · Neuron · doi:10.1016/j.neuron.2015.12.013 · Cited by 328 · see citing works
Morris water maze: a versatile and pertinent tool for assessing spatial learning and memory
Othman, M. Z., Hassan, Z., & Has, A. T. C. (2022) · EXPERIMENTAL ANIMALS · doi:10.1538/expanim.21-0120 · Cited by 375 · see citing works
Fractionation of social brain circuits in autism spectrum disorders
Gotts, S. J., Simmons, W. K., Milbury, L. A., Wallace, G. L., Cox, R. W., & Martin, A. (2012) · Brain · doi:10.1093/brain/aws160 · Cited by 369 · see citing works
Over the river, through the woods: cognitive maps in the hippocampus and orbitofrontal cortex
Wikenheiser, A. M., & Schoenbaum, G. M. (2016) · Nature reviews. Neuroscience · doi:10.1038/nrn.2016.56 · Cited by 353 · see citing works
Placing the paraventricular nucleus of the thalamus within the brain circuits that control behavior
Kirouac, G. J. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.08.005 · Cited by 357 · see citing works
Reduced grid-cell–like representations in adults at genetic risk for Alzheimer’s disease
Kunz, L., Schröder, T. N., Lee, H. L., Montag, C., Lachmann, B., Sariyska, R., Reuter, M., Stirnberg, R., Stöcker, T., Messing-Floeter, P. C., et al. (2015) · Science · doi:10.1126/science.aac8128 · Cited by 345 · see citing works
Hippocampal Activity Patterns Carry Information about Objects in Temporal Context
Hsieh, L., Gruber, M. J., Jenkins, L. J., & Charan Ranganath, A. (2014) · Neuron · doi:10.1016/j.neuron.2014.01.015 · Cited by 347 · see citing works
Selective information routing by ventral hippocampal CA1 projection neurons
Ciocchi, S., Passecker, J., Malagon‐Vina, H., Mikuš, N., & Klausberger, T. (2015) · Science · doi:10.1126/science.aaa3245 · Cited by 344 · see citing works
CA1 pyramidal cell diversity enabling parallel information processing in the hippocampus
Soltesz, I., & Losonczy, A. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0118-0 · Cited by 333 · see citing works
Lambert, C., Zrinzo, L. U., Nagy, Z., Lutti, A., Hariz, M. I., Foltynie, T., Draganski, B., Ashburner, J., & Frackowiak, R. S. J. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.11.082 · Cited by 338 · see citing works
Li, X., Yu, B., Sun, Q., Zhang, Y., Ren, M., Zhang, X., Li, A., Yuan, J., Madisen, L., Luo, Q., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1703601115 · Cited by 329 · see citing works
Joshi, S. H., Espinoza, R. T., Pirnia, T., Shi, J., Wang, Y., Ayers, B., Leaver, A., Woods, R. P., & Narr, K. L. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.02.029 · Cited by 320 · see citing works
Roth, T. L., Zoladz, P. R., Sweatt, J. D., & Diamond, D. M. (2011) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2011.01.013 · Cited by 321 · see citing works
Aggleton, J. P. (2011) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2011.09.005 · Cited by 319 · see citing works
Kundaković, M., & Rocks, D. (2022) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2022.101010 · Cited by 333 · see citing works
Memory and Space: Towards an Understanding of the Cognitive Map
Schiller, D., Eichenbaum, H., Buffalo, E. A., Davachi, L., Foster, D. J., Leutgeb, S., & Charan Ranganath, A. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.2618-15.2015 · Cited by 315 · see citing works
Hippocampal-Prefrontal Interactions in Cognition, Behavior and Psychiatric Disease
Sigurdsson, T., & Duvarci, S. (2016) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00190 · Cited by 309 · see citing works
Libby, L. A., Ekstrom, A. D., Ragland, J. D., & Charan Ranganath, A. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.3711-11.2012 · Cited by 303 · see citing works
Adult Neurogenesis: Beyond Learning and Memory
Cameron, H. A., & Glover, L. R. (2014) · Annual Review of Psychology · doi:10.1146/annurev-psych-010814-015006 · Cited by 302 · see citing works
Npas4 Regulates a Transcriptional Program in CA3 Required for Contextual Memory Formation
Ramamoorthi, K., Fropf, R., Belfort, G. M., Fitzmaurice, H. L., McKinney, R. M., Neve, R. L., Otto, T., & Lin, Y. (2011) · Science · doi:10.1126/science.1208049 · Cited by 295 · see citing works
Poppenk, J., & Moscovitch, M. (2011) · Neuron · doi:10.1016/j.neuron.2011.10.014 · Cited by 302 · see citing works
Hippocampal oxytocin receptors are necessary for discrimination of social stimuli
Raam, T., McAvoy, K. M., Besnard, A., Veenema, A. H., & Sahay, A. (2017) · Nature Communications · doi:10.1038/s41467-017-02173-0 · Cited by 292 · see citing works
O’Neill, P.-K., Gordon, J. A., & Sigurdsson, T. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2378-13.2013 · Cited by 294 · see citing works
Loss of Dickkopf-1 Restores Neurogenesis in Old Age and Counteracts Cognitive Decline
Seib, D. R., Corsini, N. S., Ellwanger, K., Plaas, C., Mateos, Á., Pitzer, C., Niehrs, C., Celikel, T., & Martín-Villalba, A. (2013) · Cell stem cell · doi:10.1016/j.stem.2012.11.010 · Cited by 294 · see citing works
Sublayer-Specific Coding Dynamics during Spatial Navigation and Learning in Hippocampal Area CA1
Danielson, N. B., Zaremba, J. D., Kaifosh, P., Bowler, J., Ladow, M., & Losonczy, A. (2016) · Neuron · doi:10.1016/j.neuron.2016.06.020 · Cited by 288 · see citing works
Neurogenesis and affective disorders
Samuels, B. A., & Hen, R. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07614.x · Cited by 286 · see citing works
DNA methylation atlas of the mouse brain at single-cell resolution
Liu, H., Zhou, J., Tian, W., Luo, C., Bartlett, A., Aldridge, A., Lucero, J., Osteen, J. K., Nery, J. R., Chen, H., et al. (2021) · Nature · doi:10.1038/s41586-020-03182-8 · Cited by 289 · see citing works
Murakami, T. C., Mano, T., Saikawa, S., Horiguchi, S. A., Shigeta, D., Baba, K., Sekiya, H., Shimizu, Y., Tanaka, K. F., Kiyonari, H., et al. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0109-1 · Cited by 290 · see citing works
Stress, anxiety, and dendritic spines: What are the connections?
Leuner, B., & Shors, T. J. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2012.04.021 · Cited by 284 · see citing works
Hippocampal neurogenesis: Learning to remember
Lazarov, O., & Hollands, C. (2016) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2015.12.006 · Cited by 281 · see citing works
Vachon-Presseau, É., Roy, M., Martel, M., Caron, E., Marin, M.-F., Chen, J., Albouy, G., Plante, I., Sullivan, M., Lupien, S., et al. (2013) · Brain : a journal of neurology · doi:10.1093/brain/aws371 · Cited by 285 · see citing works
Ortega-Martinez, S. (2015) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2015.00046 · Cited by 263 · see citing works
Varela, C., Kumar, S., Yang, J. Y., & Wilson, M. A. (2014) · Brain Structure and Function · doi:10.1007/s00429-013-0543-5 · Cited by 277 · see citing works
Kanoski, S. E., & Grill, H. J. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.09.011 · Cited by 278 · see citing works
Cortico-hippocampal systems involved in memory and cognition
Ritchey, M., Libby, L. A., & Ranganath, C. (2015) · Progress in brain research · doi:10.1016/bs.pbr.2015.04.001 · Cited by 268 · see citing works
Novel Object Recognition and Object Location Behavioral Testing in Mice on a Budget
Denninger, J. K., Smith, B. M., & Kirby, E. D. (2018) · Journal of Visualized Experiments · doi:10.3791/58593 · Cited by 273 · see citing works
Kraus, K. S., & Canlon, B. (2012) · Hearing Research · doi:10.1016/j.heares.2012.02.009 · Cited by 263 · see citing works
Osimo, E. F., Beck, K., Marques, T. R., & Howes, O. D. (2018) · Molecular Psychiatry · doi:10.1038/s41380-018-0041-5 · Cited by 264 · see citing works
Duncan, K. D., Ketz, N., Inati, S., & Davachi, L. (2011) · Hippocampus · doi:10.1002/hipo.20933 · Cited by 263 · see citing works
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 · see citing works
Gray Matter Correlates of Posttraumatic Stress Disorder: A Quantitative Meta-Analysis
Kühn, S., & Gallinat, J. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.06.029 · Cited by 259 · see citing works
Memory and cognition in schizophrenia
Guo, J. Y., Ragland, J. D., & Carter, C. S. (2018) · Molecular Psychiatry · doi:10.1038/s41380-018-0231-1 · Cited by 258 · see citing works
Heterogeneity within classical cell types is the rule: lessons from hippocampal pyramidal neurons
Cembrowski, M. S., & Spruston, N. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0125-5 · Cited by 258 · see citing works
A common substrate for prefrontal and hippocampal inhibition of the neuroendocrine stress response
Radley, J. J., & Sawchenko, P. E. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.6040-10.2011 · Cited by 251 · see citing works
The Corticohippocampal Circuit, Synaptic Plasticity, and MemoryPreprint
Basu, J., & Siegelbaum, S. A. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a021733 · Cited by 244 · see citing works
Hippocampal Sirtuin 1 signaling mediates depression-like behavior
Abe-Higuchi, N., Uchida, S., Yamagata, H., Higuchi, F., Hobara, T., Hara, K., Kobayashi, A., & Watanabe, Y. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.01.009 · Cited by 247 · see citing works
Takeuchi, H., Iba, M., Inoue, H., Higuchi, M., Takao, K., Tsukita, K., Karatsu, Y., Iwamoto, Y., Miyakawa, T., Suhara, T., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0021050 · Cited by 247 · see citing works
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 242 · see citing works
Neuronal plasticity and antidepressant actions
Castrén, E., & Hen, R. (2013) · Trends in Neurosciences · doi:10.1016/j.tins.2012.12.010 · Cited by 243 · see citing works
Detecting Representations of Recent and Remote Autobiographical Memories in vmPFC and Hippocampus
Bonnici, H. M., Chadwick, M. J., Lutti, A., Hassabis, D., Weiskopf, N., & Maguire, E. A. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.2475-12.2012 · Cited by 245 · see citing works
Schizophrenia as a disorder of disconnectivity
Schmitt, A., Hasan, A., Gruber, O., & Falkai, P. (2011) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-011-0242-2 · Cited by 244 · see citing works
Galea, L. A. M., Wainwright, S. R., Roes, M., Duarte‐Guterman, P., Chow, C., & Hamson, D. K. (2013) · Journal of Neuroendocrinology · doi:10.1111/jne.12070 · Cited by 238 · see citing works
Kirby, E. D., Muroy, S. E., Sun, W. G., Covarrubias, D., Leong, M. J., Barchas, L. A., & Kaufer, D. (2013) · eLife · doi:10.7554/elife.00362 · Cited by 238 · see citing works
Albert‐Gascó, H., Ros‐Bernal, F., Castillo-Gómez, E., & Olucha-Bordonau, F. E. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21124471 · Cited by 240 · see citing works
Oxytocin stimulates adult neurogenesis even under conditions of stress and elevated glucocorticoids
Leuner, B., Caponiti, J., & Gould, E. (2011) · Hippocampus · doi:10.1002/hipo.20947 · Cited by 237 · see citing works
Adult neurogenesis, glia, and the extracellular matrix
Cope, E. C., & Gould, E. (2019) · Cell Stem Cell · doi:10.1016/j.stem.2019.03.023 · Cited by 236 · see citing works
Annese, J., Schenker-Ahmed, N. M., Bartsch, H., Maechler, P., Sheh, C., Thomas, N., Kayano, J., Ghatan, A., Bresler, N., Frosch, M. P., et al. (2014) · Nature Communications · doi:10.1038/ncomms4122 · Cited by 234 · see citing works
- Authors
- Fanselow, M. S., & Dong, H.-W.
- Affiliations
- University of California, Los Angeles (US)
- Corresponding author
- Fanselow, Michael S.
- Dong, Hong-Wei
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2010-01
- Volume
- 65
- Issue
- 1
- Pages
- 7-19
- ISSN
- 0896-6273 (ISSN-L)
- PMC
- PMC2822727
- OpenAlex
- W2051005796
- Cited by
- 3,358
- References
- 148
- Citations by year
- 2026: 187 · 2025: 215 · 2024: 220 · 2023: 242 · 2022: 246 · 2021: 286 · 2020: 248 · 2019: 235 · 2018: 234 · 2017: 202 · 2016: 193 · 2015: 196 · 2014: 210 · 2013: 165 · 2012: 141
- FWCI
- 10.23
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 1293 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Mental Health (MH083180, MH62122)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- hippocampus, dorsal hippocampus, ventral hippocampus, cognitive function, emotion regulation, stress, gene expression, amygdala, hypothalamus, memory, psychopathology
- MeSH terms
- Animals, Behavior, Animal, Cognition, Emotions, Gene Expression Regulation, Hippocampus, Humans, Memory, Nerve Net, Neural Pathways, Primates
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