Long‐term monitoring of hippocampus‐dependent behavior in naturalistic settings: Mutant mice lacking neurotrophin receptor TrkB in the forebrain show spatial learning but impaired behavioral flexibility

Synaptic Activity and the Construction of Cortical Circuits

Katz, L. C., & Shatz, C. J. (1996) · Science · doi:10.1126/science.274.5290.1133 · Cited by 3,048 · see citing works

NEUROTROPHINS AND SYNAPTIC PLASTICITY

McAllister, A. K., Katz, L. C., & Lo, D. C. (1999) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.22.1.295 · Cited by 1,337 · see citing works

BDNF Regulates the Maturation of Inhibition and the Critical Period of Plasticity in Mouse Visual Cortex

Huang, Z. J., Kirkwood, A., Pizzorusso, T., Porciatti, V., Morales, B., Bear, M. F., Maffei, L., & Tonegawa, S. (1999) · Cell · doi:10.1016/s0092-8674(00)81509-3 · Cited by 1,198 · see citing works

Essential Role for TrkB Receptors in Hippocampus-Mediated Learning

Minichiello, L., Korte, M., Wolfer, D., Kühn, R., Unsicker, K., Cestari, V., Rossi-Arnaud, C., Lipp, H.-P., Bonhoeffer, T., & Klein, R. (1999) · Neuron · doi:10.1016/s0896-6273(00)80853-3 · Cited by 799 · see citing works

Impaired Hippocampal Representation of Space in CA1-Specific NMDAR1 Knockout Mice

McHugh, T. J., Blum, K. I., Tsien, J. Z., Tonegawa, S., & Wilson, M. A. (1996) · Cell · doi:10.1016/s0092-8674(00)81828-0 · Cited by 593 · see citing works

Involvement of Brain-Derived Neurotrophic Factor in Spatial Memory Formation and Maintenance in a Radial Arm Maze Test in Rats

Mizuno, M., Yamada, K., Olariu, A., Nawa, H., & NABESHIMA, T. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-18-07116.2000 · Cited by 549 · see citing works

Learning deficit in BDNF mutant mice.

Linnarsson, S., Björklund, A., & Ernfors, P. (1997) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1997.tb01687.x · Cited by 471 · see citing works

The Role of Brain-Derived Neurotrophic Factor Receptors in the Mature Hippocampus: Modulation of Long-Term Potentiation through a Presynaptic Mechanism involving TrkB

Xu, B., Gottschalk, W., Chow, A., Wilson, R. I., Schnell, E., Zang, K., Wang, D., Nicoll, R. A., Lu, B., & Reichardt, L. F. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-18-06888.2000 · Cited by 401 · see citing works

Hippocampal lesions cause learning deficits in inbred mice in the Morris water maze and conditioned-fear task

Logue, S. F., Paylor, R., & Wehner, J. M. (1997) · Behavioral Neuroscience · doi:10.1037/0735-7044.111.1.104 · Cited by 385 · see citing works

Hippocampal lesions cause learning deficits in inbred mice in the Morris water maze and conditioned-fear task.

Logue, S. F., Paylor, R. E., & Wehner, J. M. (1997) · Behavioral Neuroscience · doi:10.1037//0735-7044.111.1.104 · Cited by 379 · see citing works

Mice lacking the gene encoding tissue-type plasminogen activator show a selective interference with late-phase long-term potentiation in both Schaffer collateral and mossy fiber pathways.

Huang, Y.-Y., Bach, M. E., Lipp, H., Zhuo, M., Wolfer, D. P., Hawkins, R. D., Schoonjans, L., Kandel, E. R., Godfraind, J., Mulligan, R. C., et al. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.16.8699 · Cited by 330 · see citing works

Behavioral and anatomical deficits in mice homozygous for a modified ?-amyloid precursor protein gene

Müller, U. (1994) · Cell · doi:10.1016/0092-8674(94)90066-3 · Cited by 308 · see citing works

Neurotrophins and activity-dependent development of the neocortex

Bonhoeffer, T. (1996) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(96)80017-1 · Cited by 297 · see citing works

Role of neurotrophic factors in neuronal development

Henderson, C. E. (1996) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(96)80010-9 · Cited by 294 · see citing works

Deprivation of endogenous brain-derived neurotrophic factor results in impairment of spatial learning and memory in adult rats

Mu, J.-S., Li, W., Yao, Z., & Zhou, X. (1999) · Brain Research · doi:10.1016/s0006-8993(99)01592-9 · Cited by 282 · see citing works

A role for BDNF in the late-phase of hippocampal long-term potentiation

Körte, M., Kang, H., Bonhoeffer, T., & Schuman, E. M. (1998) · Neuropharmacology · doi:10.1016/s0028-3908(98)00035-5 · Cited by 268 · see citing works

Structural and Functional Properties of the TRK Family of Neurotrophin Receptors

Barbacid, M. (1995) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1995.tb26693.x · Cited by 268 · see citing works

Changes in brain nerve growth factor levels and nerve growth factor receptors in rats exposed to environmental enrichment for one year

Pham, T. M., Ickes, B. R., Albeck, D. S., Söderström, S., Granholm, A.-C., & Mohammed, A. H. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00316-4 · Cited by 262 · see citing works

Neurotrophins and activity-dependent plasticity

Thoenen, H. (2000) · Progress in brain research · doi:10.1016/s0079-6123(00)28016-3 · Cited by 256 · see citing works

Learning upregulates brain-derived neurotrophic factor messenger ribonucleic acid: A mechanism to facilitate encoding and circuit maintenance?

Kesslak, J. P., So, V., Choi, J., Cotman, C. W., & Gómez‐Pinilla, F. (1998) · Behavioral Neuroscience · doi:10.1037//0735-7044.112.4.1012 · Cited by 253 · see citing works

Mice Expressing Activated CaMKII Lack Low Frequency LTP and Do Not Form Stable Place Cells in the CA1 Region of the Hippocampus

Rotenberg, A., Mayford, M. R., Hawkins, R. D., Kandel, E. R., & Muller, R. U. (1996) · Cell · doi:10.1016/s0092-8674(00)81829-2 · Cited by 234 · see citing works

Learning upregulates brain-derived neurotrophic factor messenger ribonucleic acid: A mechanism to facilitate encoding and circuit maintenance?

Kesslak, J. P., So, V., Choi, J. J., et al. (1998) · Behavioral Neuroscience · doi:10.1037/0735-7044.112.4.1012 · Cited by 212 · see citing works

Analysing hippocampal function in transgenic mice: an ethological perspective

Gerlai, R. T., & Clayton, N. S. (1999) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01346-0 · Cited by 211 · see citing works

Deficits in Memory Tasks of Mice with CREB Mutations Depend on Gene DosagePreprint

Gass, P., Wolfer, D. P., Balschun, D., Rudolph, D., Frey, U., Lipp, H.-P., & Schütz, G. (1998) · Learning & Memory · doi:10.1101/lm.5.4.274 · Cited by 210 · see citing works

Genetically modified mice and cognition

Lipp, H., & Wolfer, D. P. (1998) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(98)80151-7 · Cited by 203 · see citing works

Abnormal Hippocampal Spatial Representations in αCaMKII ^T286A and CREB ^αΔ− Mice

Cho, Y. H., Giese, K. P., Tanila, H., Silva, A. J., & Eichenbaum, H. (1998) · Science · doi:10.1126/science.279.5352.867 · Cited by 189 · see citing works

Neurotrophin Regulation of the Developing Nervous System: Analyses of Knockout Mice

Conover, J. C., & Yancopoulos, G. D. (1997) · Reviews in the Neurosciences · doi:10.1515/revneuro.1997.8.1.13 · Cited by 184 · see citing works

Molecular and cellular actions of chronic electroconvulsive seizures.

Duman, R. S., & Vaidya, V. A. (1998) · PubMed · Cited by 176 · see citing works

Dissecting the Behaviour of Transgenic Mice: Is it the Mutation, the Genetic Background, or the Environment?

Wolfer, D. P., & Lipp, H. (2000) · Experimental Physiology · doi:10.1111/j.1469-445x.2000.02095.x · Cited by 165 · see citing works

Modulation of hippocampal synaptic transmission and plasticity by neurotrophins

Lu, B., & Gottschalk, W. (2000) · Progress in brain research · doi:10.1016/s0079-6123(00)28020-5 · Cited by 158 · see citing works

Molecular and Cellular Actions of Chronic Electroconvulsive Seizures

Duman, R. S., & Vaidya, V. A. (1998) · Journal of Ect · doi:10.1097/00124509-199809000-00004 · Cited by 154 · see citing works

Severe learning deficits in apolipoprotein E-knockout mice in a water maze task

Oitzl, M. S., Mulder, M. T., Lucassen, P. J., Havekes, L. M., Grootendorst, J., & de Kloet, E. R. (1997) · Brain Research · doi:10.1016/s0006-8993(96)01448-5 · Cited by 142 · see citing works

Assessing the effects of the 129/Sv genetic background on swimming navigation learning in transgenic mutants: a study using mice with a modified β-amyloid precursor protein gene

Wolfer, D. P., Müller, U., Stagljar, M., & Lipp, H. (1997) · Brain Research · doi:10.1016/s0006-8993(97)00673-2 · Cited by 124 · see citing works

Parallel Instabilities of Long-Term Potentiation, Place Cells, and Learning Caused by Decreased Protein Kinase A Activity

Rotenberg, A., Abel, T. G., Hawkins, R. D., Kandel, E. R., & Muller, R. U. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-21-08096.2000 · Cited by 122 · see citing works

Swimming navigation and structural variations of the infrapyramidal mossy fibers in the hippocampus of the mouse

Schöpke, R., Wolfer, D. P., Lipp, H., & Leisinger-Trigona, M.-C. (1991) · Hippocampus · doi:10.1002/hipo.450010322 · Cited by 121 · see citing works

Neurobiological bases of spatial learning in the natural environment

Lee, D., Miyasato, L. E., & Clayton, N. S. (1998) · Neuroreport · doi:10.1097/00001756-199805110-00076 · Cited by 98 · see citing works

Intact spatial learning and memory in transgenic mice with reduced BDNF

Montkowski, A., & Holsboer, F. (1997) · Neuroreport · doi:10.1097/00001756-199702100-00040 · Cited by 93 · see citing works

Lesions of the limbic system: Their effects upon hypotheses and frustration

Isaacson, R. L., & Kimble, D. P. (1972) · Behavioral Biology · doi:10.1016/s0091-6773(72)80170-6 · Cited by 92 · see citing works

Some effects of hippocampal lesions on the behavior of mongolian gerbils

Glickman, S. E., Higgins, T. J. V., & Isaacson, R. L. (1970) · Physiology & Behavior · doi:10.1016/0031-9384(70)90185-x · Cited by 88 · see citing works

Transgenic Mice Overexpressing Truncated trkB Neurotrophin Receptors in Neurons Show Increased Susceptibility to Cortical Injury after Focal Cerebral Ischemia

Saarelainen, T., Lukkarinen, J. A., Koponen, S., Gröhn, O. H. J., Jolkkonen, J., Koponen, E., Haapasalo, A., Alhonen, L. I., Wong, G., Koıstınaho, J., et al. (2000) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.2000.0863 · Cited by 87 · see citing works

Hippocampal Damage: Effects on Dopaminergic Systems of the Basal Ganglia

Isaacson, R. L. (1984) · International review of neurobiology · doi:10.1016/s0074-7742(08)60683-2 · Cited by 67 · see citing works

Hippocampal mossy fibers and swimming navigation in mice: Correlations with size and left‐right asymmetries

Bernasconi‐Guastalla, S., Wolfer, D. P., & Lipp, H. (1994) · Hippocampus · doi:10.1002/hipo.450040107 · Cited by 65 · see citing works

Bax and Bak proteins require caspase activity to trigger apoptosis in sympathetic neurons

Martinou, I., Missotten, M., Fernandez, P.-A., Sadoul, R., & Martinou, J. (1998) · Neuroreport · doi:10.1097/00001756-199801050-00004 · Cited by 64 · see citing works

Intracerebroventricular administration of brain-derived neurotrophic factor in adult rats affects analgesia and spontaneous behaviour but not memory retention in a Morris Water Maze task

Cirulli, F., Berry, A., & Alleva, E. (2000) · Neuroscience Letters · doi:10.1016/s0304-3940(00)01173-3 · Cited by 57 · see citing works

Regulation of Synaptic Function by Neurotrophic Factors in Vertebrates and Invertebrates: Implications for Development and LearningPreprint

McKay, S. E., Purcell, A. L., & Carew, T. J. (1999) · Learning & Memory · doi:10.1101/lm.6.3.193 · Cited by 43 · see citing works

Unilateral hippocampal lesions in newborn and adult rats: effects on spatial memory and BDNF gene expression

van Praag, H., Qu, P. M., Elliott, R. C., Wu, H., Dreyfus, C. F., & Black, I. B. (1998) · Behavioural Brain Research · doi:10.1016/s0166-4328(97)00117-4 · Cited by 43 · see citing works

Temporal and spatial adaptation to food restriction in mice under naturalistic conditions

Dell’Omo, G., Ricceri, L., Wolfer, D. P., Полетаева, И. И., & Lipp, H. (2000) · Behavioural Brain Research · doi:10.1016/s0166-4328(00)00234-5 · Cited by 43 · see citing works

Hippocampal mossy fiber sprouting is not impaired in brain-derived neurotrophic factor-deficient mice

Bender, R. A., Heimrich, B., Meyer, M., & Frotscher, M. (1998) · Experimental Brain Research · doi:10.1007/s002210050413 · Cited by 42 · see citing works

Shc-binding site in the TrkB receptor is not required for hippocampal long-term potentiation

Körte, M., Minichiello, L., Klein, R., & Bonhoeffer, T. (2000) · Neuropharmacology · doi:10.1016/s0028-3908(99)00273-7 · Cited by 37 · see citing works

The effects of combined prefrontal cortical and hippocampal damage on dopamine-related behaviors in rats

Lipska, B. K., Jaskiw, G. E., & Weinberger, D. R. (1994) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(94)90220-8 · Cited by 27 · see citing works

Neurotrophin-evoked rapid excitation of central neurons

Kafitz, K. W., Rose, C. R., & Konnerth, A. (2000) · Progress in brain research · doi:10.1016/s0079-6123(00)28021-7 · Cited by 13 · see citing works

Hippocampal lesions and temporally chained conditioned stimuli in a conditioned suppression paradigm

Leaton, R. N., & Borszcz, G. S. (1990) · Psychobiology · doi:10.3758/bf03327219 · Cited by 12 · see citing works

The effects of cortical or hippocampal damage on behavioral flexibility in the rat

Terry, P., & Oakley, D. A. (1990) · Psychobiology · doi:10.3758/bf03333087 · Cited by 9 · see citing works

The Psychobiology of Spatial Behavior: The Hippocampal Formation and Spatial Mapping

Nadel, L. (1995) · Springer eBooks · doi:10.1007/978-94-011-0091-5_13 · Cited by 9 · see citing works

The effects of unilateral destruction of fimbria-fornix and supracallosal pathways in the rat

Buzsáki, G., Ryan, J. P., & Isaacson, R. L. (1989) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(89)90932-1 · Cited by 6 · see citing works

Untitled work

(2000) · doi:10.1002/(sici)1098-1063(2000)10:1

Untitled work

Mattson, M. (1999) · doi:10.1002/(sici)1097-4547(19991001)58:1

Variant BDNF (Val66Met) impact on brain structure and function

Bath, K. G., & Lee, F. S. (2006) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/cabn.6.1.79 · Cited by 325 · see citing works

Neurobehavioral assessment in the information age

Tecott, L. H., & Nestler, E. J. (2004) · Nature Neuroscience · doi:10.1038/nn1225 · Cited by 218 · see citing works

Learning deficits in forebrain-restricted brain-derived neurotrophic factor mutant mice

Gorski, J. A., Balogh, S. A., Wehner, J. M., & Jones, K. R. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00426-3 · Cited by 218 · see citing works

M 2 Muscarinic Acetylcholine Receptor Knock-Out Mice Show Deficits in Behavioral Flexibility, Working Memory, and Hippocampal Plasticity

Seeger, T., Fedorova, I. D., Zheng, F., Miyakawa, T., Koustova, E., Gomeza, J., Basile, A. S., Alzheimer, C., & Wess, J. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3581-04.2004 · Cited by 214 · see citing works

Laboratory environments and rodents' behavioural needs: a review

Balcombe, J. P. (2006) · Laboratory Animals · doi:10.1258/002367706777611488 · Cited by 176 · see citing works

A comparison of wild-caught wood mice and bank voles in the Intellicage: assessing exploration, daily activity patterns and place learning paradigms

Galsworthy, M. J., Amrein, I., Kuptsov, P. A., Полетаева, И. И., Zinn, P. O., Rau, A., Vyssotski, A. L., & Lipp, H. (2004) · Behavioural Brain Research · doi:10.1016/j.bbr.2004.06.021 · Cited by 171 · see citing works

Transgenic mice overexpressing the full-length neurotrophin receptor trkB exhibit increased activation of the trkB–PLCγ pathway, reduced anxiety, and facilitated learning

Koponen, E., Võikar, V., Riekki, R., Saarelainen, T., Rauramaa, T., Rauvala, H., Taira, T., & Castrén, E. (2004) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2004.01.006 · Cited by 170 · see citing works

Intrahippocampal administration of BDNF in adult rats affects short‐term behavioral plasticity in the Morris water maze and performance in the elevated plus‐maze

Cirulli, F., Berry, A., Chiarotti, F., & Alleva, E. (2004) · Hippocampus · doi:10.1002/hipo.10220 · Cited by 167 · see citing works

Lab Mice in the Field: Unorthodox Daily Activity and Effects of a Dysfunctional Circadian Clock Allele

Daan, S., Spoelstra, K., Albrecht, U., Schmutz, I., Daan, M., Daan, B., Rienks, F., Poletaeva, I., Dell'Omo, G., Vyssotski, A., et al. (2011) · Journal of Biological Rhythms · doi:10.1177/0748730410397645 · Cited by 149 · see citing works

Increased BDNF levels and NTRK2 gene association suggest a disruption of BDNF/TrkB signaling in autism

Correia, C., Coutinho, A. M., Sequeira, A. F., Sousa, I., Venda, L. L., Almeida, J. P., Abreu, R., Lobo, C., Miguel, T. S., Conroy, J., et al. (2010) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2010.00627.x · Cited by 146 · see citing works

Conditional gene targeting in the mouse nervous system: Insights into brain function and diseases

Gavériaux‐Ruff, C., & Kieffer, B. L. (2007) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2006.12.003 · Cited by 146 · see citing works

Ecological validity of social interaction tests in rats and mice

Kondrakiewicz, K., Kostecki, M., Szadzińska, W., & Knapska, E. (2019) · Genes, Brain and Behavior · doi:10.1111/gbb.12525 · Cited by 136 · see citing works

The individuality of mice

Lathe, R. (2004) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2004.00083.x · Cited by 135 · see citing works

IntelliCage as a tool for measuring mouse behavior – 20 years perspective

Kiryk, A., Janusz, A. K., Zglinicki, B., Turkes, E., Knapska, E., Konopka, W., Lipp, H.-P., & Kaczmarek, L. (2020) · Behavioural Brain Research · doi:10.1016/j.bbr.2020.112620 · Cited by 126 · see citing works

Three Pillars of Automated Home-Cage Phenotyping of Mice: Novel Findings, Refinement, and Reproducibility Based on Literature and Experience

Võikar, V., & Gaburro, S. (2020) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2020.575434 · Cited by 119 · see citing works

Mouse models of genetic effects on cognition: Relevance to schizophrenia

Papaleo, F., Lipska, B. K., & Weinberger, D. R. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.04.025 · Cited by 104 · see citing works

Network Modeling of Adult Neurogenesis: Shifting Rates of Neuronal Turnover Optimally Gears Network Learning according to Novelty Gradient

Chambers, R. A., & Conroy, S. K. (2007) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2007.19.1.1 · Cited by 103 · see citing works

BDNF Locally Potentiates GABAergic Presynaptic Machineries: Target-selective Circuit Inhibition

Ohba, S. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh130 · Cited by 97 · see citing works

Sustained expression of brain-derived neurotrophic factor is required for maintenance of dendritic spines and normal behavior

Vigers, A. J., Amin, D. S., Talley-Farnham, T., Gorski, J. A., Xu, B., & Jones, K. R. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.03.031 · Cited by 95 · see citing works

Neurotrophins Enhance CaMKII Activity and Rescue Amyloid-β-Induced Deficits in Hippocampal Synaptic Plasticity

Zeng, Y., Zhao, D., & Xie, C.-W. (2010) · Journal of Alzheimer s Disease · doi:10.3233/jad-2010-100264 · Cited by 93 · see citing works

Social interactions impact on the dopaminergic system and drive individuality

Torquet, N., Marti, F., Campart, C., Tolu, S., Nguyen, C., Oberto, V. J., Benallaoua, M., Naudé, J., Didienne, S., Debray, N., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-05526-5 · Cited by 88 · see citing works

Brief social isolation in early adolescence affects reversal learning and forebrain BDNF expression in adult rats

Xiao, H., Wang, W., Xue, X., Shao, F., & Li, N. (2011) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2011.07.008 · Cited by 84 · see citing works

Spatial memory deficits in middle‐aged mice correlate with lower exploratory activity and a subordinate status: role of hippocampal neurotrophins

Francia, N., Cirulli, F., Chiarotti, F., Antonelli, A., Aloe, L., & Alleva, E. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04585.x · Cited by 77 · see citing works

Neuroimmunologic and Neurotrophic Interactions in Autism Spectrum Disorders: Relationship to Neuroinflammation

Ohja, K., Gozal, E., Fahnestock, M. L., Cai, L., Cai, J., Freedman, J. H., Switala, A., El-Baz, A. S., & Barnes, G. N. (2018) · NeuroMolecular Medicine · doi:10.1007/s12017-018-8488-8 · Cited by 65 · see citing works

Impaired spatial memory in APP-overexpressing mice on a homocysteinemia-inducing diet

Bernardo, A., McCord, M. C., Troen, A. M., Allison, J. D., & McDonald, M. P. (2006) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2006.05.035 · Cited by 59 · see citing works

The impact of genetic background on neurodegeneration and behavior in seizured mice

Mohajeri, M. H., Madani, R., Saini, K., Lipp, H., Nitsch, R. M., & Wolfer, D. P. (2004) · Genes Brain & Behavior · doi:10.1111/j.1601-1848.2004.00073.x · Cited by 58 · see citing works

Automated dissection of permanent effects of hippocampal or prefrontal lesions on performance at spatial, working memory and circadian timing tasks of C57BL/6 mice in IntelliCage

Võikar, V., Krackow, S., Lipp, H., Rau, A., Colacicco, G., & Wolfer, D. P. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.08.048 · Cited by 57 · see citing works

A comparison of learning and memory characteristics of young and middle-aged wild-type mice in the IntelliCage

Mechan, A. O., Wyss, A., Rieger, H., & Mohajeri, M. H. (2009) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2009.02.018 · Cited by 56 · see citing works

Deficits in LTP and recognition memory in the genetically hypertensive rat are associated with decreased expression of neurotrophic factors and their receptors in the dentate gyrus

Hennigan, A., Callaghan, C. K., Kealy, J., Rouine, J., & Kelly, Á. M. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.09.037 · Cited by 51 · see citing works

Synapse formation in adult barrel cortex following naturalistic environmental enrichment

Landers, M. S., Knott, G. W., Lipp, H., Полетаева, И. И., & Welker, E. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.10.040 · Cited by 48 · see citing works

Neurobehavioral Tests in Rat Models of Degenerative Brain Diseases

Urbach, Y. K., Bode, F. J., Nguyen, H. P., Rieß, O., & von Hörsten, S. (2009) · Methods in molecular biology · doi:10.1007/978-1-60327-389-3_24 · Cited by 46 · see citing works

Impaired behavioural flexibility and memory in mice lacking GDNF family receptor α2

Võikar, V., Rossi, J., Rauvala, H., & Airaksinen, M. S. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03475.x · Cited by 47 · see citing works

A behavioral comparison of the common laboratory rat strains Lister Hooded, Lewis, Fischer 344 and Wistar in an automated homecage system

Clemens, L. E., Jansson, E., Portal, E., Rieß, O., & Nguyen, H. P. (2013) · Genes Brain & Behavior · doi:10.1111/gbb.12093 · Cited by 39 · see citing works

Female behavior drives the formation of distinct social structures in C57BL/6J versus wild-derived outbred mice in field enclosures

Vogt, C. C., Zipple, M. N., Sprockett, D. D., Miller, C. H., Hardy, S. X., Arthur, M. K., Greenstein, A. M., Colvin, M. S., Michel, L. M., Moeller, A. H., et al. (2024) · BMC Biology · doi:10.1186/s12915-024-01809-0 · Cited by 39 · see citing works

Designing animal-friendly behavioral tests for neuroscience research: The importance of an ethological approach

d’Isa, R., & Gerlai, R. T. (2023) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.1090248 · Cited by 41 · see citing works

Captivating Behaviour: Mouse Models, Experimental Genetics and Reductionist Returns in the Neurosciences

Davies, G. F. (2010) · The Sociological Review · doi:10.1111/j.1467-954x.2010.01911.x · Cited by 40 · see citing works

The best-laid plans go oft awry: synaptogenic growth factor signaling in neuropsychiatric disease

Williams, A. J., & Umemori, H. (2014) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2014.00004 · Cited by 37 · see citing works

Adult Hippocampal Neurogenesis in Mammals (and Humans): The Death of a Central Dogma in Neuroscience and its Replacement by a New Dogma

Oppenheim, R. W. (2019) · Developmental Neurobiology · doi:10.1002/dneu.22674 · Cited by 38 · see citing works

TrkB but not trkC receptors are necessary for postnatal maintenance of hippocampal spines

von Bohlen und Halbach, O., Minichiello, L., & Unsicker, K. (2008) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2007.02.028 · Cited by 37 · see citing works

The Relationship Between Dominance Rank and Spatial Ability Among Male Meadow Voles (Microtus pennsylvanicus).

Spritzer, M. D., Meikle, D. B., & Solomon, N. G. (2004) · Journal of comparative psychology · doi:10.1037/0735-7036.118.3.332 · Cited by 37 · see citing works

IntelliCage: the development and perspectives of a mouse- and user-friendly automated behavioral test system

Lipp, H., Krackow, S., Turkes, E., Benner, S., Endo, T., & Russig, H. (2024) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2023.1270538 · Cited by 35 · see citing works

Automated behavioral analysis of mice using INTELLICAGE: inter-laboratory comparisons and validation with exploratory behavior and spatial learning

Litvin, O. I., Galsworthy, M. J., Zinn, P. O., Neuhäusser-Wespy, F., Würbel, H., & Nitsch, R. M. (2005) · Cited by 33 · see citing works

(R)-fluoxetine enhances cognitive flexibility and hippocampal cell proliferation in mice

Marwari, S., & Dawe, G. S. (2018) · Journal of Psychopharmacology · doi:10.1177/0269881118754733 · Cited by 28 · see citing works

Challenges and advanced concepts for the assessment of learning and memory function in mice

Lang, B., Kahnau, P., Hohlbaum, K., Mieske, P., Andresen, N., Boon, M. N., Thöne‐Reineke, C., Lewejohann, L., & Diederich, K. (2023) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2023.1230082 · Cited by 27 · see citing works

Recentering neuroscience on behavior: The interface between brain and environment is a privileged level of control of neural activity

Branchi, I. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104678 · Cited by 26 · see citing works

Association study of neurotrophic tyrosine kinase receptor type 2 (NTRK2) and childhood‐onset mood disorders

Adams, J. H., Wigg, K. G., King, N. A., Burcescu, I., Vetró, Á., Kiss, E., Baji, I., George, C. J., Kennedy, J. L., Kovács, M., et al. (2004) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.30084 · Cited by 25 · see citing works

The effects of living in an outdoor enclosure on hippocampal plasticity and anxiety‐like behavior in response to nematode infection

Cope, E. C., Opendak, M. M., LaMarca, E. A., Murthy, S. S., Park, C. Y., Olson, L. B., Martinez, S., Leung, J. M., Graham, A. L., & Gould, E. (2018) · Hippocampus · doi:10.1002/hipo.23033 · Cited by 24 · see citing works

Blueprints for measuring natural behavior

Puścian, A., & Knapska, E. (2022) · iScience · doi:10.1016/j.isci.2022.104635 · Cited by 21 · see citing works

Activation of TrkB in Parvalbumin interneurons is required for the promotion of reversal learning in spatial and fear memory by antidepressants

Jetsonen, E., Didio, G., Winkel, F., Pou, M. L., Boj, C., Kuczynski-Noyau, L., Võikar, V., Guirado, R., Taira, T., Lauri, S. E., et al. (2023) · Neuropsychopharmacology · doi:10.1038/s41386-023-01562-y · Cited by 22 · see citing works

New candidate proteins for Benzo(a)pyrene-induced spatial learning and memory deficits

Chen, C., Tang, Y. M., Shuqun, C., Jiang, X., Youbin, Q., Yinyin, X., Tang, Q., & Tu, B. (2011) · The Journal of Toxicological Sciences · doi:10.2131/jts.36.163 · Cited by 21 · see citing works

Refining learning and memory assessment in laboratory rodents. An ethological perspective.

Branchi, I., & Ricceri, L. (2004) · PubMed · Cited by 20 · see citing works

Social Determinants of Inter-Individual Variability and Vulnerability: The Role of Dopamine

Fauré, P., Fayad, S. L., Solié, C., & Reynolds, L. M. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.836343 · Cited by 17 · see citing works

A Polymorphism in the BDNF Gene (rs11030101) is Associated With Negative Symptoms in Chinese Han Patients With Schizophrenia

Ping, J., Zhang, J., Wan, J., Huang, C., Luo, J., Du, B., & Jiang, T. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.849227 · Cited by 18 · see citing works

Roaming in a Land of Milk and Honey: Life Trajectories and Metabolic Rate of Female Inbred Mice Living in a Semi Naturalistic Environment

Mieske, P., Diederich, K., & Lewejohann, L. (2021) · Animals · doi:10.3390/ani11103002 · Cited by 16 · see citing works

Bidirectional changes in water-maze learning following recombinant adenovirus-associated viral vector (rAAV)-mediated brain-derived neurotrophic factor expression in the rat hippocampus

Pietropaolo, S., Paterna, J., Büeler, H., Feldon, J., & Yee, B. K. (2007) · Behavioural Pharmacology · doi:10.1097/fbp.0b013e3282da0bf6 · Cited by 15 · see citing works

Natural neurobiology and behavior of the mouse: Relevance for behavioral studies in the laboratory

Lipp, H.-P., & Wolfer, D. P. (2013) · Behavioral Genetics of the Mouse · doi:10.1017/cbo9781139541022.003 · Cited by 13 · see citing works

Uncovering the determinants of brain functioning, behavior and their interplay in the light of context

Branchi, I. (2024) · European Journal of Neuroscience · doi:10.1111/ejn.16331 · Cited by 13 · see citing works

Elemental and Configural Associative Learning in Spatial Tasks: Could Zebrafish be Used to Advance Our Knowledge?

Buatois, A., & Gerlai, R. T. (2020) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2020.570704 · Cited by 13 · see citing works

Behavior is movement only but how to interpret it? Problems and pitfalls in translational neuroscience—a 40-year experience

Lipp, H., & Wolfer, D. P. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.958067 · Cited by 11 · see citing works

How can ethology inform the neuroscience of fear, aggression and dominance?

Battivelli, D., Fan, Z., Hu, H., & Gross, C. T. (2024) · Nature reviews. Neuroscience · doi:10.1038/s41583-024-00858-2 · Cited by 11 · see citing works

Catch me if you can: free-living mice show a highly flexible dodging behaviour suggestive of intentional tactical deception

d’Isa, R., Parsons, M. H., Chrzanowski, M., Bębas, P., & Stryjek, R. (2024) · Royal Society Open Science · doi:10.1098/rsos.231692 · Cited by 9 · see citing works

Robotic animals as new tools in rodent neuroscience research: proposed applications of zooinspired robots for mouse behavioral testing

d’Isa, R. (2025) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2025.1545352 · Cited by 8 · see citing works

A Pluralist Framework for the Philosophy of Social Neuroscience

Barberis, S., Branca, M., & Venturelli, A. (2017) · Springer eBooks · doi:10.1007/978-3-319-68421-5_21 · Cited by 2 · see citing works

Conditional Transgenesis and Recombination to Study the Molecular Mechanisms of Brain Plasticity and Memory

Baumgärtel, K., Fernández, C., Johansson, T., & Mansuy, I. M. (2007) · Springer eBooks · doi:10.1007/978-3-540-35109-2_13 · Cited by 5 · see citing works

Evaluation of methods and applications for behavioural profiling of transgenic mice

Võikar, V. (2006) · Työväentutkimus Vuosikirja · Cited by 2 · see citing works

Cell proliferation and cell survival in the dentate gyrus of adult mice under naturalistic conditions

Santoso, A. (2009) · Elektronische Hochschulschriften der LMU München (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.10676 · Cited by 2 · see citing works

Mutants at large: ethology meets transgenic technology!

Gerlai, R. T. (2002) · Trends in Neurosciences · doi:10.1016/s0166-2236(02)02205-1 · Cited by 1 · see citing works

General

Crusio, W. E., Sluyter, F., Gerlai, R. T., & Pietropaolo, S. (2013) · Cambridge University Press eBooks · doi:10.1017/cbo9781139541022.002 · Cited by 1 · see citing works

The role of bHLH transcription factor NEX in neuronal differentiation and experience-dependent plasticity

Mikhailova, O. (2008) · doi:10.53846/goediss-3382 · Cited by 1 · see citing works

Rodent Behavior: Approaches

Tecott, L. H., & Nestler, E. J. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.00887-1

Diversité des effets de la nicotine sur les neurones dopaminergiques de l’aire tegmentale ventrale

Nguyen, C. (2020) · theses.fr (ABES) · doi:10.70675/57dc4740z36f1z4ee7z87e7z960af8c4a43e

Home-cage monitoring methods reveal age- and strain-related differences in motor, thermal, and cognitive functions in male mice of two inbred strains

Faisal, M., Radyushkin, K., & Baumgart, J. (2026) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2026.110773

Essential Role for TrkB Receptors in Hippocampus-Mediated Learning

Minichiello, L., Korte, M., Wolfer, D., Kühn, R., Unsicker, K., Cestari, V., Rossi-Arnaud, C., Lipp, H.-P., Bonhoeffer, T., & Klein, R. (1999) · Neuron · doi:10.1016/s0896-6273(00)80853-3 · Cited by 799 · see citing works

Learning through Trk-ing

Wiedemann, C. G. (2007) · Nature reviews. Neuroscience · doi:10.1038/nrn2077

Reviewed by:

Kleinknecht, K. R., Bedenk, B. T., Kaltwasser, S. F., Grünecker, B., Yen, Y.-C., Czisch, M., Wotjak, C. T., Oitzl, M. S., Eichenbaum, H., Wotjak, C. T., et al. (2012)

Nicotinic receptor-mediated regulation of dopamine transporter activity in rat prefrontal cortex

Drew, A. E., Derbez, A. E., & Werling, L. L. (2000) · Synapse · doi:10.1002/1098-2396(200010)38:1 · Cited by 89 · see citing works

Regional- and Age-Dependent Reduction in trkB Receptor Expression in the Hippocampus Is Associated with Altered Spine Morphologies

Halbach, O. V. B. U., Krause, S., Medina, D. L., Sciarretta, C., Minichiello, L., & Unsicker, K. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.08.025 · Cited by 64 · see citing works