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Ventral hippocampus-lateral septum circuitry promotes foraging-related memory

Décarie-Spain, L., Liu, C. M., Lauer, L. T., Subramanian, K. S., Bashaw, A. G., Klug, M. E., Gianatiempo, I. H., Suarez, A. N., Noble, E. E., Donohue, K. N., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111402 · Cited by 45 · see citing works

Anterograde transneuronal tracing and genetic control with engineered yellow fever vaccine YFV-17D

Li, E., Guo, J. Q., Oh, S. J., Luo, Y., Lyons, H., Du, W., Arano, R., Kim, Y., Chen, Y.-T., Eitson, J. L., et al. (2021) · Nature Methods · doi:10.1038/s41592-021-01319-9 · Cited by 39 · see citing works

Noncanonical projections to the hippocampal CA3 regulate spatial learning and memory by modulating the feedforward hippocampal trisynaptic pathway

Lin, X., Amalraj, M., Blanton, C., Avila, B., Holmes, T. C., Nitz, D. A., & Xu, X. (2021) · PLoS Biology · doi:10.1371/journal.pbio.3001127 · Cited by 48 · see citing works

Complex roles for reactive astrocytes in the triple transgenic mouse model of Alzheimer disease

Guillemaud, O., Ceyzériat, K., Saint-Georges, T., Cambon, K., Petit, F., Haim, L. B., Sauvage, M.-A. C.-D., Guillermier, M., Bernier, S., Hérard, A., et al. (2019) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2020.02.010 · Cited by 40 · see citing works

Parallel ventral hippocampus-lateral septum pathways differentially regulate approach-avoidance conflict

Yeates, D. C. M., Leavitt, D., Sujanthan, S., Khan, N., Alushaj, D., Lee, A. C. H., & Ito, R. (2022) · Nature Communications · doi:10.1038/s41467-022-31082-0 · Cited by 39 · see citing works

In Situ Ligand-Directed Growth of Gold Nanoparticles in Biological Tissues

Peng, C., Yu, M., & Zheng, J. (2019) · Nano Letters · doi:10.1021/acs.nanolett.9b04911 · Cited by 39 · see citing works

A neural circuit for excessive feeding driven by environmental context in mice

Mohammad, H., Senol, E., Graf, M. R., Lee, C.-Y., Li, Q., Liu, Q., Yeo, X. Y., Wang, M., Laskaratos, A., Xu, F., et al. (2021) · Nature Neuroscience · doi:10.1038/s41593-021-00875-9 · Cited by 37 · see citing works

Contextual Processing elicits Sex Differences in Dorsal Hippocampus Activation following Footshock and Context Fear Retrieval

Colón, L. M., & Poulos, A. M. (2020) · Behavioural Brain Research · doi:10.1016/j.bbr.2020.112771 · Cited by 31 · see citing works

Ventral hippocampal CA1 modulates pain behaviors in mice with peripheral inflammation

Shao, S., Zheng, Y., Fu, Z., Wang, J., Zhang, Y., Wang, C., Qi, X., Gong, T., Ma, L., Lin, X., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112017 · Cited by 34 · see citing works

Fear extinction relies on ventral hippocampal safety codes shaped by the amygdala

Nguyen, R., Koukoutselos, K., Forro, T., & Ciocchi, S. (2023) · Science Advances · doi:10.1126/sciadv.adg4881 · Cited by 35 · see citing works

Hippocampal-medial entorhinal circuit is differently organized along the dorsoventral axis in rodents

Ohara, S., Rannap, M., Tsutsui, K., Draguhn, A., Egorov, A. V., & Witter, M. P. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112001 · Cited by 33 · see citing works

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 32 · see citing works

Adult-born neurons from the dorsal, intermediate, and ventral regions of the longitudinal axis of the hippocampus exhibit differential sensitivity to glucocorticoids

Levone, B. R., Codagnone, M. G., Moloney, G. M., Nolan, Y. M., Cryan, J. F., & O’Leary, O. F. (2020) · Molecular Psychiatry · doi:10.1038/s41380-020-0848-8 · Cited by 32 · see citing works

Activation of ventral CA1 hippocampal neurons projecting to the lateral septum during feeding

Kosugi, K., Yoshida, K., Suzuki, T., Kobayashi, K., Yoshida, K., Mimura, M., & Tanaka, K. F. (2020) · Hippocampus · doi:10.1002/hipo.23289 · Cited by 32 · see citing works

Emotion in action: When emotions meet motor circuits

Braine, A., & Georges, F. E. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105475 · Cited by 32 · see citing works

An open access mouse brain flatmap and upgraded rat and human brain flatmaps based on current reference atlases

Hahn, J. D., Swanson, L. W., Bowman, I., Foster, N. N., Zingg, B., Bienkowski, M. S., Hintiryan, H., & Dong, H. (2020) · The Journal of Comparative Neurology · doi:10.1002/cne.24966 · Cited by 31 · see citing works

Cerebral Microbleeds Are Associated With Increased Brain Iron and Cognitive Impairment in Patients With Cerebral Small Vessel Disease: A Quantitative Susceptibility Mapping Study

Li, J., Nguyen, T. D., Zhang, Q., Guo, L., & Wang, Y. (2022) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.28092 · Cited by 30 · see citing works

The Hippocampus and Social Impairment in Psychiatric DisordersPreprint

Schafer, M., & Schiller, D. (2018) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2018.83.037614 · Cited by 30 · see citing works

Mapping brain-wide excitatory projectome of primate prefrontal cortex at submicron resolution and comparison with diffusion tractography

Yan, M., Yu, W., Lv, Q., Lv, Q., Bo, T., Chen, X., Liu, Y., Zhan, Y., Yan, S., Shen, X., et al. (2022) · eLife · doi:10.7554/elife.72534 · Cited by 28 · see citing works

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 28 · see citing works

Small lesions of the dorsal or ventral hippocampus subregions are associated with distinct impairments in working memory and reference memory retrieval, and combining them attenuates the acquisition rate of spatial reference memory

Hauser, J., López, L. H. L., Feldon, J., Gargiulo, P. Á., & Yee, B. K. (2020) · Hippocampus · doi:10.1002/hipo.23207 · Cited by 27 · see citing works

Dissecting the role of subiculum in epilepsy: Research update and translational potential

Fei, F., Wang, X., Wang, Y., & Chen, Z. (2021) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2021.102029 · Cited by 28 · see citing works

A near‐infrared probe for detecting and interposing amyloid beta oligomerization in early Alzheimer's disease

Li, Q., Moreno‐González, I., Xie, Z., Gamez, N., Vegas‐Gomez, L., Song, Q., Gu, J., Lin, W., Gomez‐Gutierrez, R., & Wu, T. (2022) · Alzheimer s & Dementia · doi:10.1002/alz.12673 · Cited by 28 · see citing works

Iterative Design of Near-Infrared Fluorescent Probes for Early Diagnosis of Alzheimer’s Disease by Targeting Aβ Oligomers

Liu, B., Li, X., Liu, Z., He, B., Xu, H., Cao, J., Zeng, F., Feng, H., Ren, Y., Li, H., et al. (2024) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.4c00252 · Cited by 27 · see citing works

Hippocampal Proteomics Reveals the Role of Glutamatergic Synapse Activation in the Depression Induced by Perfluorooctane Sulfonate

An, Z., Yang, J., Xiao, F., Lv, J., Xing, X., Liu, H., Wang, L., Liu, Y., Zhang, Z., & Guo, H. (2023) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.3c01344 · Cited by 28 · see citing works

Anorexia increases microglial density and cytokine expression in the hippocampus of young female rats

Varman, D. R., Macedo-Mendoza, M., Labrada-Moncada, F. E., Reyes-Ortega, P., Morales, T., Martínez‐Torres, A., & Reyes‐Haro, D. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.01.042 · Cited by 26 · see citing works

Double dissociation of learned approach–avoidance conflict processing and spatial pattern separation along the dorsoventral axis of the dentate gyrus

Yeates, D. C. M., Ussling, A., Lee, A. C. H., & Ito, R. (2019) · Hippocampus · doi:10.1002/hipo.23182 · Cited by 25 · see citing works

Dorsal hippocampus‐ and ACC‐projecting medial septum neurons differentially contribute to the recollection of episodic‐like memory

Jin, T., Chen, R., Shao, M., Yang, X., Ma, L., & Wang, F. (2020) · The FASEB Journal · doi:10.1096/fj.202000398r · Cited by 24 · see citing works

Spatially resolved cell atlas of the teleost telencephalon and deep homology of the vertebrate forebrain

Hegarty, B. E., Gruenhagen, G. W., Johnson, Z. V., Baker, C. M., & Streelman, J. T. (2024) · Communications Biology · doi:10.1038/s42003-024-06315-1 · Cited by 25 · see citing works

A circuit of COCH neurons encodes social-stress-induced anxiety via MTF1 activation of Cacna1h

Jing, W., Zhang, T., Liu, J., Huang, X., Yu, Q., Yu, H., Zhang, Q., Li, H., Deng, M., Zhu, L., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.110177 · Cited by 25 · see citing works

Heritability of hippocampal functional and microstructural organisation

Bayrak, Ş., de Wael, R. V., Schaare, H. L., Hettwer, M. D., Caldairou, B., Bernasconi, A., Bernasconi, N., Bernhardt, B. C., & Valk, S. L. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119656 · Cited by 23 · see citing works

Regional Analysis of the Brain Transcriptome in Mice Bred for High and Low Methamphetamine Consumption

HITZEMANN, R. J., Iancu, O. D., Reed, C. L., Baba, H., Lockwood, D. R., & Phillips, T. J. (2019) · Brain Sciences · doi:10.3390/brainsci9070155 · Cited by 24 · see citing works

Seeing the Forest and Its Trees Together: Implementing 3D Light Microscopy Pipelines for Cell Type Mapping in the Mouse Brain

Newmaster, K. T., Kronman, F. N., Wu, Y.-T., & Kim, Y. (2022) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2021.787601 · Cited by 20 · see citing works

Intersectional, anterograde transsynaptic targeting of neurons receiving monosynaptic inputs from two upstream regions

Kitanishi, T., Tashiro, M., Kitanishi, N., & Mizuseki, K. (2022) · Communications Biology · doi:10.1038/s42003-022-03096-3 · Cited by 22 · see citing works

Distinct contributions of GluA1-containing AMPA receptors of different hippocampal subfields to salience processing, memory and impulse control

Kilonzo, K., Strahnen, D., Prex, V., Gems, J., van der Veen, B., Kapanaiah, S. K. T., Murthy, B. K. B., Schulz, S., Sprengel, R., Bannerman, D. M., et al. (2022) · Translational Psychiatry · doi:10.1038/s41398-022-01863-8 · Cited by 22 · see citing works

Phospholipase D1 Ablation Disrupts Mouse Longitudinal Hippocampal Axis Organization and Functioning

Marinha, L. S., Castanho, I., Silva, R. R., Bravo, F. V., Miranda, A. M., Meira, T., Morais‐Ribeiro, R., Marques, F., Xu, Y., du Jour, K. P., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2020.02.102 · Cited by 23 · see citing works

Immunohistochemical field parcellation of the human hippocampus along its antero-posterior axis

González‐Arnay, E., Pérez-Santos, I., Sánchez, L. J., Cid, E., Gal, B., de la Prida, L. M., & Cavada, C. (2024) · Brain Structure and Function · doi:10.1007/s00429-023-02725-9 · Cited by 25 · see citing works

The interoceptive hippocampus: Mouse brain endocrine receptor expression highlights a dentate gyrus (DG)–cornu ammonis (CA) challenge–sufficiency axis

Lathe, R., Singadia, S., Jordan, C. Y., & Riedel, G. (2020) · PLoS ONE · doi:10.1371/journal.pone.0227575 · Cited by 21 · see citing works

Morphological Development Trajectory and Structural Covariance Network of the Human Fetal Cortical Plate during the Early Second Trimester

Xu, F., Liu, M., Kim, S. Y., Ge, X., Zhang, Z., Tang, Y., Lin, X., Toga, A. W., Liu, S., & Kim, H. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab123 · Cited by 19 · see citing works

Monosynaptic connection from the subiculum to medial mammillary nucleus neurons projecting to the anterior thalamus and Gudden’s ventral tegmental nucleus

Umaba, R., Kitanishi, T., & Mizuseki, K. (2021) · Neuroscience Research · doi:10.1016/j.neures.2021.01.006 · Cited by 19 · see citing works

Homologous laminar organization of the mouse and human subiculum

Bienkowski, M. S., Sepehrband, F., Kurniawan, N. D., Stanis, J., Korobkova, L., Khanjani, N., Clark, K. A., Hintiryan, H., Miller, C. A., & Dong, H. (2021) · Scientific Reports · doi:10.1038/s41598-021-81362-w · Cited by 21 · see citing works

Optogenetic inhibition of the dorsal hippocampus CA3 region during early-stage cocaine-memory reconsolidation disrupts subsequent context-induced cocaine seeking in rats

Qi, S., Tan, S. M., Wang, R., Higginbotham, J. A., Ritchie, J. L., Ibarra, C. K., Arguello, A. A., Christian, R. J., & Fuchs, R. A. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-022-01342-0 · Cited by 19 · see citing works

Neural circuits expressing the serotonin 2C receptor regulate memory in mice and humans

Liu, H., He, Y., Liu, H., Brouwers, B., Yin, N., Lawler, K., Keogh, J. M., Henning, E., Lee, D.-K., Yu, M., et al. (2024) · Science Advances · doi:10.1126/sciadv.adl2675 · Cited by 20 · see citing works

Hippocampal Neuroanatomy

Amaral, D. G., Lavenex, P., & Insausti, R. (2025) · Oxford University Press eBooks · doi:10.1093/med/9780190065324.003.0003 · Cited by 19 · see citing works

Projections of hippocampal CA2 pyramidal neurons: Distinct innervation patterns of CA2 compared to CA3 in rodents

Shinohara, Y., & Kohara, K. (2023) · Hippocampus · doi:10.1002/hipo.23519 · Cited by 18 · see citing works

Chrna2‐OLM interneurons display different membrane properties and h‐current magnitude depending on dorsoventral location

Hilscher, M. M., Nogueira, I., Mikulovic, S., Kullander, K., Leão, R. N., & Leão, K. E. (2019) · Hippocampus · doi:10.1002/hipo.23134 · Cited by 16 · see citing works

Integrating Data Directly into Publications with Augmented Reality and Web-Based Technologies – Schol-AR

Ard, T. D., Bienkowski, M. S., Liew, S., Sepehrband, F., Yan, L., & Toga, A. W. (2022) · Scientific Data · doi:10.1038/s41597-022-01426-y · Cited by 17 · see citing works

Constructing the rodent stereotaxic brain atlas: a survey

Feng, Z., Li, A., Gong, H., & Luo, Q. (2021) · Science China Life Sciences · doi:10.1007/s11427-020-1911-9 · Cited by 16 · see citing works

Parallel Pathways Provide Hippocampal Spatial Information to Prefrontal Cortex

Messanvi, F., Berkun, K., Perkins, A., & Chudasama, Y. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.0846-22.2022 · Cited by 15 · see citing works

Activity‐regulated gene expression across cell types of the mouse hippocampus

Nelson, E. D., Maynard, K. R., Nicholas, K. R., Tran, M. N., Divecha, H. R., Collado‐Torres, L., Hicks, S. C., & Martinowich, K. (2023) · Hippocampus · doi:10.1002/hipo.23548 · Cited by 15 · see citing works

A mouse brain stereotaxic topographic atlas with isotropic 1-μm resolution

Feng, Z., Li, X., Luo, Y., Liu, X., Long, B., Jiang, T., Jia, X., Chen, X., Luo, J., Chai, X., et al. (2025) · Nature · doi:10.1038/s41586-025-09211-8 · Cited by 15 · see citing works

Macroscale connections of the mouse lateral preoptic area and anterior lateral hypothalamic area

Hahn, J. D., Gao, L., Boesen, T., Gou, L., Hintiryan, H., & Dong, H. (2022) · The Journal of Comparative Neurology · doi:10.1002/cne.25331 · Cited by 15 · see citing works

Further refining the boundaries of the hippocampus CA2 with gene expression and connectivity: Potential subregions and heterogeneous cell types

Bienkowski, M. S. (2023) · Hippocampus · doi:10.1002/hipo.23508 · Cited by 16 · see citing works

Hippocampal area CA2 activity supports social investigation following an acute social stress

Radzicki, D., McCann, K. E., Alexander, G. M., & Dudek, S. M. (2024) · Molecular Psychiatry · doi:10.1038/s41380-024-02834-9 · Cited by 15 · see citing works

Lack of redundancy between electrophysiological measures of long-range neuronal communication

Strahnen, D., Kapanaiah, S. K. T., Bygrave, A. M., & Kätzel, D. (2021) · BMC Biology · doi:10.1186/s12915-021-00950-4 · Cited by 15 · see citing works

Hippocampal contextualization of social rewards in mice

Duarte, J. M., Nguyen, R., Kyprou, M., Li, K., Milentijevic, A., Cerquetella, C., Forro, T., & Ciocchi, S. (2024) · Nature Communications · doi:10.1038/s41467-024-53866-2 · Cited by 13 · see citing works

Specific AAV2/PHP.eB-mediated gene transduction of CA2 pyramidal cells via injection into the lateral ventricle

Okamoto, K., Kamikubo, Y., Yamauchi, K., Okamoto, S., Takahashi, M., Ishida, Y., Koike, M., Ikegaya, Y., Sakurai, T., & Hioki, H. (2023) · Scientific Reports · doi:10.1038/s41598-022-27372-8 · Cited by 14 · see citing works

Heterogeneous expression patterns of fibronectin in the mouse subiculum

Kashima, T., Noguchi, A., Ikegaya, Y., & Matsumoto, N. (2019) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2019.04.010 · Cited by 13 · see citing works

Heart failure impairs mood and memory in male rats and down-regulates the expression of numerous genes important for synaptic plasticity in related brain regions

Parent, M. B., Ferreira‐Neto, H. C., Kruemmel, A. R., Althammer, F., Patel, A. A., Keo, S., Whitley, K. E., Cox, D. N., & Stern, J. E. (2021) · Behavioural Brain Research · doi:10.1016/j.bbr.2021.113452 · Cited by 11 · see citing works

Elucidating memory in the brain via single‐cell transcriptomics

Sullivan, K. E., Kendrick, R. M., & Cembrowski, M. S. (2020) · Journal of Neurochemistry · doi:10.1111/jnc.15250 · Cited by 11 · see citing works

Enhanced and Unified Anatomical Labeling for a Common Mouse Brain AtlasPreprint

Chon, U., Vanselow, D. J., Cheng, K. C., & Kim, Y. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/636175 · Cited by 12 · see citing works

Ventral hippocampal cholecystokinin interneurons gate contextual reward memory

Nguyen, R., Sivakumaran, S., Lambe, E. K., & Kim, J. C. (2024) · iScience · doi:10.1016/j.isci.2024.108824 · Cited by 12 · see citing works

HippoGenes: A robust workflow for subregional transcriptomic profiling of the human hippocampusPreprint

Ngo, A., Larivière, S., Royer, J., Smith, M., Rodríguez‐Cruces, R., Hwang, Y., Liu, L., Gan‐Or, Z., Evans, A. C., Bernasconi, A., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.08.04.742581

Homologous laminar organization of the mouse and human subiculum

Bienkowski, M. S., Sepehrband, F., Kurniawan, N. D., Stanis, J., Korobkova, L., Khanjani, N., Clark, K. A., Hintiryan, H., Miller, C. A., & Dong, H. (2021) · Scientific Reports · doi:10.1038/s41598-021-81362-w · Cited by 21 · see citing works

“Genomic neuroanatomy”: novel principles of hippocampal organization gained from analysis of genome-scale in situ hybridization data

Ed, L. (2008) · Frontiers in Neuroinformatics · doi:10.3389/conf.neuro.11.2008.01.153

Mapping Projectome Heterogeneity of Subiculum Neuron Cell Types

Saustad, A. W., & Bienkowski, M. S. (2026) · Hippocampus · doi:10.1002/hipo.70138

Multimodal gradient mapping of rodent hippocampus

Gunnarsdóttir, B., Zerbi, V., & Kelly, C. A. M. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119082 · Cited by 9 · see citing works