New behavioral protocols to extend our knowledge of rodent object recognition memory

The Rat Brain in Stereotaxic Coordinates

Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585 · see citing works

Statistical principles in experimental design.

Winer, B. J. (1962) · McGraw-Hill Book Company · doi:10.1037/11774-000 · Cited by 27,137 · see citing works

Statistical Methods for Psychology.

Gudgeon, A. C., & Howell, D. C. (1994) · Journal of the Royal Statistical Society Series D (The Statistician) · doi:10.2307/2348956 · Cited by 8,277 · see citing works

A new one-trial test for neurobiological studies of memory in rats. 1: behavioral data

Ennaceur, A., & Delacour, J. (1988) · Behavioural Brain Research · doi:10.1016/0166-4328(88)90157-x · Cited by 3,223 · see citing works

The Medial Temporal Lobe and Recognition Memory

Eichenbaum, H., Yonelinas, A. P., & Ranganath, C. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.30.051606.094328 · Cited by 2,580 · see citing works

Episodic memory, amnesia, and the hippocampal–anterior thalamic axis

Aggleton, J. P., & Brown, M. W. (1999) · Behavioral and Brain Sciences · doi:10.1017/s0140525x99002034 · Cited by 1,879 · see citing works

Recognition memory: What are the roles of the perirhinal cortex and hippocampus?

Brown, M. W., & Aggleton, J. P. (2001) · Nature reviews. Neuroscience · doi:10.1038/35049064 · Cited by 1,555 · see citing works

Medial Frontal Cortex Mediates Perceptual Attentional Set Shifting in the Rat

Birrell, J. M., & Brown, V. J. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-11-04320.2000 · Cited by 1,421 · see citing works

Recognition memory and the medial temporal lobe: a new perspective

Squire, L. R., Wixted, J. T., & Clark, R. E. (2007) · Nature reviews. Neuroscience · doi:10.1038/nrn2154 · Cited by 1,013 · see citing works

Effects on visual recognition of combined and separate ablations of the entorhinal and perirhinal cortex in rhesus monkeys

Meunier, M., Bachevalier, J., Mishkin, M., & Murray, E. A. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-12-05418.1993 · Cited by 900 · see citing works

Lesions of perirhinal and parahippocampal cortex that spare the amygdala and hippocampal formation produce severe memory impairment

Zola-Morgan, S. M., Squire, L., Amaral, D., & Suzuki, W. (1989) · Journal of Neuroscience · doi:10.1523/jneurosci.09-12-04355.1989 · Cited by 766 · see citing works

Impaired Recognition Memory in Rats after Damage to the Hippocampus

Clark, R. E., Zola, S. M., & Squire, L. R. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-23-08853.2000 · Cited by 740 · see citing works

Spontaneous object recognition and object location memory in rats: the effects of lesions in the cingulate cortices, the medial prefrontal cortex, the cingulum bundle and the fornix

Ennaceur, A., Neave, N., & Aggleton, J. P. (1997) · Experimental Brain Research · doi:10.1007/pl00005603 · Cited by 670 · see citing works

Extending the spontaneous preference test of recognition: evidence of object-location and object-context recognition

Dix, S. L., & Aggleton, J. P. (1999) · Behavioural Brain Research · doi:10.1016/s0166-4328(98)00079-5 · Cited by 598 · see citing works

Double Dissociation between the Effects of Peri-Postrhinal Cortex and Hippocampal Lesions on Tests of Object Recognition and Spatial Memory: Heterogeneity of Function within the Temporal Lobe

Winters, B. D., Forwood, S., Cowell, R. A., Saksida, L. M., & Bussey, T. J. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1346-04.2004 · Cited by 588 · see citing works

Object recognition memory and the rodent hippocampus

Broadbent, N. J., Gaskin, S., Squire, L. R., & Clark, R. E. (2010) · Learning & Memory · doi:10.1101/lm.1650110 · Cited by 568 · see citing works

Object recognition memory: Neurobiological mechanisms of encoding, consolidation and retrieval

Winters, B. D., Saksida, L. M., & Bussey, T. J. (2008) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2008.04.004 · Cited by 568 · see citing works

An analysis of short-term visual memory in the monkey.

Mishkin, M. M., & Delacour, J. (1975) · Journal of Experimental Psychology Animal Behavior Processes · doi:10.1037/0097-7403.1.4.326 · Cited by 470 · see citing works

Interleaving brain systems for episodic and recognition memory.

Aggleton, J., & Brown, M. W. (2006) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2006.08.003 · Cited by 465 · see citing works

Recollection-like memory retrieval in rats is dependent on the hippocampus

Fortin, N. J., Wright, S. P., & Eichenbaum, H. (2004) · Nature · doi:10.1038/nature02853 · Cited by 460 · see citing works

Rhinal cortex lesions and object recognition in rats.

Mumby, D. G., & Pinel, J. P. J. (1994) · Behavioral Neuroscience · doi:10.1037//0735-7044.108.1.11 · Cited by 412 · see citing works

Perspectives on object-recognition memory following hippocampal damage: lessons from studies in rats

Mumby, D. G. (2001) · Behavioural Brain Research · doi:10.1016/s0166-4328(01)00367-9 · Cited by 356 · see citing works

Neurotoxic lesions of the perirhinal cortex do not mimic the behavioural effects of fornix transection in the rat

Ennaceur, A., Neave, N., & Aggleton, J. P. (1996) · Behavioural Brain Research · doi:10.1016/0166-4328(96)00006-x · Cited by 351 · see citing works

Rhinal cortex lesions and object recognition in rats.

Mumby, D. G., & Pinel, J. P. J. (1994) · Behavioral Neuroscience · doi:10.1037/0735-7044.108.1.11 · Cited by 348 · see citing works

Complementary roles of the orbital prefrontal cortex and the perirhinal-entorhinal cortices in an odor-guided delayed-nonmatching-to-sample task.

Otto, T., & Eichenbaum, H. (1992) · Behavioral Neuroscience · doi:10.1037/0735-7044.106.5.762 · Cited by 343 · see citing works

Complementary roles of the orbital prefrontal cortex and the perirhinal-entorhinal cortices in an odor-guided delayed-nonmatching-to-sample task.

Otto, T., & Eichenbaum, H. (1992) · Behavioral Neuroscience · doi:10.1037//0735-7044.106.5.762 · Cited by 317 · see citing works

Variation in visual acuity within pigmented, and between pigmented and albino rat strains

Prusky, G. T., Harker, K. T., Douglas, R. M., & Whishaw, I. Q. (2002) · Behavioural Brain Research · doi:10.1016/s0166-4328(02)00126-2 · Cited by 310 · see citing works

The role of the hippocampus in memory for the temporal order of a sequence of odors.

Kesner, R. P., Gilbert, P. E., & Barua, L. A. (2002) · Behavioral Neuroscience · doi:10.1037//0735-7044.116.2.286 · Cited by 309 · see citing works

The role of the hippocampus in memory for the temporal order of a sequence of odors.

Kesner, R. P., Gilbert, P. E., & Barua, L. A. (2002) · Behavioral Neuroscience · doi:10.1037/0735-7044.116.2.286 · Cited by 261 · see citing works

Hippocampal lesions that abolish spatial maze performance spare object recognition memory at delays of up to 48 hours

Forwood, S., Winters, B. D., & Bussey, T. J. (2004) · Hippocampus · doi:10.1002/hipo.20059 · Cited by 259 · see citing works

Distinct patterns of behavioural impairments resulting from fornix transection or neurotoxic lesions of the perirhinal and postrhinal cortices in the rat

Bussey, T. J., Duck, J., Muir, J. L., & Aggleton, J. P. (2000) · Behavioural Brain Research · doi:10.1016/s0166-4328(00)00155-8 · Cited by 252 · see citing works

Episodic-like memory in mice: Simultaneous assessment of object, place and temporal order memory

Dere, E., Huston, J. P., & Silva, M. A. D. S. (2005) · Brain Research Protocols · doi:10.1016/j.brainresprot.2005.08.001 · Cited by 242 · see citing works

The effects of fornix and medial prefrontal lesions on delayed non-matching-to-sample by rats

Shaw, C., & Aggleton, J. P. (1993) · Behavioural Brain Research · doi:10.1016/0166-4328(93)90051-q · Cited by 181 · see citing works

Impaired object recognition with increasing levels of feature ambiguity in rats with perirhinal cortex lesions

Norman, G., & Eacott, M. J. (2003) · Behavioural Brain Research · doi:10.1016/s0166-4328(03)00176-1 · Cited by 175 · see citing works

Perirhinal cortex resolves feature ambiguity in configural object recognition and perceptual oddity tasksPreprint

Bartko, S. J., Winters, B. D., Cowell, R. A., Saksida, L. M., & Bussey, T. J. (2007) · Learning & Memory · doi:10.1101/lm.749207 · Cited by 172 · see citing works

One-Trial Object Recognition by Rats

Aggleton, J. P. (1985) · The Quarterly Journal of Experimental Psychology Section B · doi:10.1080/14640748508401171 · Cited by 166 · see citing works

Lesions of the rat perirhinal cortex spare the acquisition of a complex configural visual discrimination yet impair object recognition.

Aggleton, J. P., Albasser, M. M., Aggleton, D. J., Poirier, G. L., & Pearce, J. M. (2010) · Behavioral Neuroscience · doi:10.1037/a0018320 · Cited by 166 · see citing works

Retrograde and anterograde object recognition in rats with hippocampal lesions

Gaskin, S., Tremblay, A., & Mumby, D. G. (2003) · Hippocampus · doi:10.1002/hipo.10154 · Cited by 160 · see citing works

Nonrecurring-items delayed nonmatching-to-sample in rats: A new paradigm for testing nonspatial working memory

Mumby, D. G., Pinel, J. P. J., & Wood, E. R. (1990) · Psychobiology · doi:10.3758/bf03327250 · Cited by 145 · see citing works

What is it like to be a rat? Rat sensory perception and its implications for experimental design and rat welfare

Burn, C. C. (2008) · Applied Animal Behaviour Science · doi:10.1016/j.applanim.2008.02.007 · Cited by 133 · see citing works

Qualitatively different modes of perirhinal–hippocampal engagement when rats explore novel vs. familiar objects as revealed by c‐Fos imaging

Albasser, M. M., Poirier, G. L., & Aggleton, J. P. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.07042.x · Cited by 131 · see citing works

RECOGNITION MEMORY IN RATS—I.CONCEPTS AND CLASSIFICATION

Steckler, T., Drinkenburg, W. H. I. M., Sahgal, A., & Aggleton, J. P. (1998) · Progress in Neurobiology · doi:10.1016/s0301-0082(97)00060-9 · Cited by 126 · see citing works

A Distributed Cortical Representation Underlies Crossmodal Object Recognition in Rats

Winters, B. D., & Reid, J. M. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.6073-09.2010 · Cited by 119 · see citing works

Visual memory task for rats reveals an essential role for hippocampus and perirhinal cortex

Prusky, G. T., Douglas, R. M., Nelson, L., Shabanpoor, A., & Sutherland, R. J. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0308528101 · Cited by 108 · see citing works

A comparison between Dark Agouti and Sprague-Dawley rats in their behaviour on the elevated plus-maze, open-field apparatus and activity meters, and their response to diazepam

Mechan, A. O., Moran, P. M., Elliott, M. J., Young, A. M., Joseph, M. H., & Green, R. A. (2001) · Psychopharmacology · doi:10.1007/s002130100902 · Cited by 96 · see citing works

Beyond Spatial Memory: The Anterior Thalamus and Memory for the Temporal Order of a Sequence of Odor Cues

Wolff, M., Gibb, S., & Dalrymple‐Alford, J. C. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.5481-05.2006 · Cited by 91 · see citing works

Perirhinal cortex damage and anterograde object-recognition in rats after long retention intervals

Mumby, D. G., Piterkin, P., Lecluse, V., & LEHMANN, H. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2007.07.026 · Cited by 78 · see citing works

The role of the hippocampus in mnemonic integration and retrieval: complementary evidence from lesion and inactivation studies

Iordanova, M., Burnett, D. J., Aggleton, J., Good, M., & Honey, R. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.07010.x · Cited by 69 · see citing works

An animal model of recognition memory and medial temporal lobe amnesia: History and current issues

Clark, R. E., & Squire, L. R. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.02.004 · Cited by 68 · see citing works

A limited role for the hippocampus in the modulation of novel-object preference by contextual cues

Piterkin, P., Cole, E., Cossette, M.-P., Gaskin, S., & Mumby, D. G. (2008) · Learning & Memory · doi:10.1101/lm.1035508 · Cited by 65 · see citing works

A reaffirmation of the retrosplenial contribution to rodent navigation: reviewing the influences of lesion, strain, and task

Harker, K. T., & Whishaw, I. Q. (2004) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.06.005 · Cited by 57 · see citing works

Selective disconnection of the hippocampal formation projections to the mammillary bodies produces only mild deficits on spatial memory tasks: Implications for fornix function

Vann, S. D., Erichsen, J. T., O’Mara, S. M., & Aggleton, J. P. (2010) · Hippocampus · doi:10.1002/hipo.20796 · Cited by 57 · see citing works

3 – Concepts and Classification1

Zimmerman, B. J. (1979) · Academic Press eBooks · Cited by 49 · see citing works

Testing the importance of the retrosplenial navigation system: lesion size but not strain matters: a reply to Harker and Whishaw

Aggleton, J. P., & Vann, S. D. (2004) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.08.003 · Cited by 42 · see citing works

Impaired "episodic-like" object memory in adult APPswe transgenic mice.

Good, M. A., Hale, G., & Staal, V. (2007) · Behavioral Neuroscience · doi:10.1037/0735-7044.121.2.443 · Cited by 40 · see citing works

The ability of different strains of rats to acquire a visual nonmatching-to-sample task

Aggleton, J. P. (1996) · Psychobiology · doi:10.3758/bf03331952 · Cited by 18 · see citing works

Lesions of the perirhinal cortex do not impair integration of visual and geometric information in rats.

Horne, M. R., Iordanova, M. D., Albasser, M. M., Aggleton, J. P., Honey, R. C., & Pearce, J. M. (2010) · Behavioral Neuroscience · doi:10.1037/a0019287 · Cited by 18 · see citing works

Distinct roles of medial and lateral entorhinal cortex in spatial cognition

Van Cauter, T., Camon, J., Alvernhe, A., Elduayen, C., Sargolini, F., & Save, E. (2013) · Cerebral Cortex · doi:10.1093/cercor/bhs033 · Cited by 196 · see citing works

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

Chao, O. Y., de Souza Silva, M. A., Yang, Y.-M., & Huston, J. P. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.04.007 · Cited by 158 · see citing works

Neuronal circuitry for recognition memory of object and place in rodent models

Chao, O. Y.-H., Nikolaus, S., Yang, Y., & Huston, J. P. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104855 · Cited by 157 · see citing works

A review of behavioral methods for the evaluation of cognitive performance in animal models: Current techniques and links to human cognition

Ghafarimoghadam, M., Mashayekh, R., Gholami, M., Fereydani, P., Shelley-Tremblay, J. F., Kandezi, N., Sabouri, E., & Motaghinejad, M. (2021) · Physiology & Behavior · doi:10.1016/j.physbeh.2021.113652 · Cited by 133 · see citing works

Rigor and reproducibility in rodent behavioral research

Gulinello, M. E., Mitchell, H. A., Chang, Q., O’Brien, W. T., Zhou, Z., Abel, T. G., Wang, L., Corbin, J. G., Veeraragavan, S., Samaco, R. C., et al. (2018) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2018.01.001 · Cited by 116 · see citing works

Medial prefrontal cortex role in recognition memory in rodents

Morici, J. F., Bekinschtein, P., & Weisstaub, N. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.06.030 · Cited by 119 · see citing works

Aerobic exercise upregulates the BDNF-Serotonin systems and improves the cognitive function in rats

Pietrelli, A., Matković, L., Vacotto, M., López‐Costa, J. J., Basso, N., & Brusco, A. (2018) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2018.05.007 · Cited by 102 · see citing works

Hippocampus and neocortex: recognition and spatial memory

Vann, S. D., & Albasser, M. M. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.02.002 · Cited by 86 · see citing works

What pharmacological interventions indicate concerning the role of the perirhinal cortex in recognition memory

Brown, M. W., Barker, G. R. I., Aggleton, J. P., & Warburton, E. C. (2012) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2012.07.034 · Cited by 84 · see citing works

Contrasting brain activity patterns for item recognition memory and associative recognition memory: insights from immediate-early gene functional imaging

Aggleton, J. P., Brown, M. W., & Albasser, M. M. (2012) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2012.05.018 · Cited by 79 · see citing works

A high-fat high-sugar diet in adolescent rats impairs social memory and alters chemical markers characteristic of atypical neuroplasticity and parvalbumin interneuron depletion in the medial prefrontal cortex

Reichelt, A. C., Gibson, G. D., Abbott, K. N., & Hare, D. J. (2019) · Food & Function · doi:10.1039/c8fo02118j · Cited by 65 · see citing works

Erythropoietin improves motor and cognitive deficit, axonal pathology, and neuroinflammation in a combined model of diffuse traumatic brain injury and hypoxia, in association with upregulation of the erythropoietin receptor

Hellewell, S. C., Yan, E. B., Alwis, D. S., Bye, N., & Morganti-Kossmann, M. C. (2013) · Journal of Neuroinflammation · doi:10.1186/1742-2094-10-156 · Cited by 63 · see citing works

Moving beyond standard procedures to assess spontaneous recognition memory

Ameen‐Ali, K. E., Easton, A., & Eacott, M. J. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.03.013 · Cited by 59 · see citing works

Advances in the behavioural testing and network imaging of rodent recognition memory

Kinnavane, L., Albasser, M. M., & Aggleton, J. P. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.07.049 · Cited by 59 · see citing works

Selective increases in inter-individual variability in response to environmental enrichment in female mice

Körholz, J., Zocher, S., Grzyb, A. N., Morisse, B., Poetzsch, A., Ehret, F., Schmied, C., & Kempermann, G. (2018) · eLife · doi:10.7554/elife.35690 · Cited by 58 · see citing works

Evidence that the rat hippocampus has contrasting roles in object recognition memory and object recency memory

Albasser, M. M., Amin, E., Lin, T.-C. E., Iordanova, M. D., & Aggleton, J. P. (2012) · Behavioral Neuroscience · doi:10.1037/a0029754 · Cited by 58 · see citing works

Anterior Thalamic Inputs Are Required for Subiculum Spatial Coding, with Associated Consequences for Hippocampal Spatial Memory

Frost, B. E., Martin, S. K., Cafalchio, M., Islam, M. N., Aggleton, J. P., & O’Mara, S. M. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.2868-20.2021 · Cited by 59 · see citing works

Long-lasting memory deficits in mice withdrawn from cocaine are concomitant to neuroadaptations in hippocampal basal activity, GABAergic interneurons and adult neurogenesis

de Guevara‐Miranda, D. L., Millón, C., Rosell‐Valle, C., Pérez-Fernández, M., Missiroli, M., Serrano, A., Pavón, F. J., de Fonseca, F. R., Martínez‐Losa, M., Álvarez‐Dolado, M., et al. (2017) · Disease Models & Mechanisms · doi:10.1242/dmm.026682 · Cited by 52 · see citing works

Dimebon enhances hippocampus-dependent learning in both appetitive and inhibitory memory tasks in mice

Vignisse, J., Steinbusch, H. W. M., Bolkunov, A., Costa-Nunes, J. P., Santos, A. I., Grandfils, C., Бачурин, С. О., & Strekalova, T. V. (2010) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2010.12.007 · Cited by 51 · see citing works

Conversion of short-term to long-term memory in the novel object recognition paradigm

Moore, S. J., Deshpande, K. S., Stinnett, G. S., Seasholtz, A. F., & Murphy, G. G. (2013) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.06.014 · Cited by 49 · see citing works

The retrosplenial cortex and object recency memory in the rat

Powell, A. L., Vann, S. D., Olarte‐Sánchez, C. M., Kinnavane, L., Davies, M., Amin, E., Aggleton, J. P., & Nelson, A. J. D. (2017) · European Journal of Neuroscience · doi:10.1111/ejn.13577 · Cited by 49 · see citing works

Distributed interactive brain circuits for object-in-place memory: A place for time?

Aggleton, J. P., & Nelson, A. J. D. (2020) · Brain and Neuroscience Advances · doi:10.1177/2398212820933471 · Cited by 50 · see citing works

Dysgranular retrosplenial cortex lesions in rats disrupt cross-modal object recognitionPreprint

Hindley, E. L., Nelson, A. J. D., Aggleton, J. P., & Vann, S. D. (2014) · Learning & Memory · doi:10.1101/lm.032516.113 · Cited by 47 · see citing works

Perirhinal cortex lesions uncover subsidiary systems in the rat for the detection of novel and familiar objects

Albasser, M. M., Amin, E., Iordanova, M. D., Brown, M. W., Pearce, J. M. S., & Aggleton, J. P. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07755.x · Cited by 43 · see citing works

Perirhinal cortex lesions impair tests of object recognition memory but spare novelty detection

Olarte‐Sánchez, C. M., Amin, E., Warburton, E. C., & Aggleton, J. P. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.13106 · Cited by 42 · see citing works

The melatonin metabolite N1‐acetyl‐5‐methoxykynuramine facilitates long‐term object memory in young and aging mice

Iwashita, H., Matsumoto, Y., Maruyama, Y., Watanabe, K., Chiba, A., & Hattori, A. (2020) · Journal of Pineal Research · doi:10.1111/jpi.12703 · Cited by 41 · see citing works

Dissociation of recognition and recency memory judgments after anterior thalamic nuclei lesions in rats.

Dumont, J. R., & Aggleton, J. P. (2013) · Behavioral Neuroscience · doi:10.1037/a0032750 · Cited by 40 · see citing works

Anterior thalamic nuclei lesions in rats disrupt markers of neural plasticity in distal limbic brain regions

Dumont, J. R., Amin, E., Poirier, G. L., Albasser, M. M., & Aggleton, J. P. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.08.027 · Cited by 40 · see citing works

Assessing spatial pattern separation in rodents using the object pattern separation task

van Goethem, N. P., van Hagen, B. T. J., & Prickaerts, J. (2018) · Nature Protocols · doi:10.1038/s41596-018-0013-x · Cited by 40 · see citing works

Separate but interacting recognition memory systems for different senses: The role of the rat perirhinal cortexPreprint

Albasser, M. M., Amin, E., Iordanova, M. D., Brown, M. W., Pearce, J. M., & Aggleton, J. P. (2011) · Learning & Memory · doi:10.1101/lm.2132911 · Cited by 39 · see citing works

A new behavioural apparatus to reduce animal numbers in multiple types of spontaneous object recognition paradigms in rats

Ameen‐Ali, K. E., Eacott, M. J., & Easton, A. (2012) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2012.08.006 · Cited by 37 · see citing works

Memory impairment due to fipronil pesticide exposure occurs at the GABAA receptor level, in rats

Godinho, A. F., Souza, A. C. D. O., Carvalho, C. C., Horta, D. F., Fraia, D. D., Anselmo, F., Chaguri, J. L., & Faria, C. A. (2016) · Physiology & Behavior · doi:10.1016/j.physbeh.2016.06.035 · Cited by 37 · see citing works

Mammilliothalamic tract lesions disrupt tests of visuo-spatial memory.

Nelson, A. J. D., & Vann, S. D. (2014) · Behavioral Neuroscience · doi:10.1037/bne0000001 · Cited by 34 · see citing works

The influence of context on recognition memory in monkeys: Effects of hippocampal, parahippocampal and perirhinal lesions

Bachevalier, J., Nemanic, S., & Alvarado, M. C. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.07.010 · Cited by 33 · see citing works

Strain-Dependent Variations in Spatial Learning and in Hippocampal Synaptic Plasticity in the Dentate Gyrus Of Freely Behaving Rats

Manahan‐Vaughan, D., & Schwegler, H. (2011) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2011.00007 · Cited by 31 · see citing works

Perirhinal cortex lesions in rats: Novelty detection and sensitivity to interference.

Albasser, M. M., Olarte‐Sánchez, C. M., Amin, E., Brown, M. W., Kinnavane, L., & Aggleton, J. P. (2015) · Behavioral Neuroscience · doi:10.1037/bne0000049 · Cited by 29 · see citing works

Linagliptin treatment improves cerebrovascular function and remodeling and restores reduced cerebral perfusion in Type 2 diabetes

Hardigan, T., Abdul, Y., Abdelsaid, M. A., Coucha, M. M., Elshafey, S., Li, W., Johnson, M. H., & Ergul, A. (2016) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00057.2016 · Cited by 28 · see citing works

5-HT2a receptor in mPFC influences context-guided reconsolidation of object memory in perirhinal cortex

Morici, J. F., Miranda, M., Gallo, F. T., Zanoni, M. B., Bekinschtein, P., & Weisstaub, N. (2018) · eLife · doi:10.7554/elife.33746 · Cited by 28 · see citing works

Chemogenetics Reveal an Anterior Cingulate–Thalamic Pathway for Attending to Task-Relevant Information

Bubb, E. J., Aggleton, J. P., O’Mara, S. M., & Nelson, A. J. D. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa353 · Cited by 27 · see citing works

The neural basis of nonvisual object recognition memory in the rat.

Albasser, M. M., Olarte‐Sánchez, C. M., Amin, E., Horne, M. R., Newton, M. J., Warburton, E. C., & Aggleton, J. P. (2012) · Behavioral Neuroscience · doi:10.1037/a0031216 · Cited by 25 · see citing works

Reconciling the object and spatial processing views of the perirhinal cortex through task‐relevant unitization

Fiorilli, J., Bos, J. J., Grande, X., Lim, J., Düzel, E., & Pennartz, C. M. A. (2021) · Hippocampus · doi:10.1002/hipo.23304 · Cited by 23 · see citing works

Mapping parahippocampal systems for recognition and recency memory in the absence of the rat hippocampus

Kinnavane, L., Amin, E., Horne, M., & Aggleton, J. P. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12740 · Cited by 21 · see citing works

The importance of mammillary body efferents for recency memory: towards a better understanding of diencephalic amnesia

Nelson, A. J. D., & Vann, S. D. (2016) · Brain Structure and Function · doi:10.1007/s00429-016-1330-x · Cited by 22 · see citing works

Early-Delayed, Radiation-Induced Cognitive Deficits in Adult Rats are Heterogeneous and Age-Dependent

Forbes, M. E., Paitsel, M., Bourland, J. D., & Riddle, D. R. (2014) · Radiation Research · doi:10.1667/rr13662.1 · Cited by 21 · see citing works

Development of the hippocampal CA2 region and the emergence of social recognition

Diethorn, E. J., & Gould, E. (2023) · Developmental Neurobiology · doi:10.1002/dneu.22919 · Cited by 20 · see citing works

Contrasting networks for recognition memory and recency memory revealed by immediate-early gene imaging in the rat

Olarte-Sánchez, C. M., Kinnavane, L., Amin, E., & Aggleton, J. P. (2014) · Behavioral Neuroscience · doi:10.1037/a0037055 · Cited by 18 · see citing works

One-trial object recognition memory in the domestic rabbit (Oryctolagus cuniculus) is disrupted by NMDA receptor antagonists

Hoffman, K. L., & Basurto, E. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.04.049 · Cited by 18 · see citing works

Putting memory in context: Dissociating memories by distinguishing the nature of context

Robertson, B.-A., Eacott, M. J., & Easton, A. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.10.045 · Cited by 17 · see citing works

Continual Trials Spontaneous Recognition Tasks in Mice: Reducing Animal Numbers and Improving Our Understanding of the Mechanisms Underlying Memory

Chan, M., Eacott, M. J., Sanderson, D. J., Wang, J., Sun, M., & Easton, A. (2018) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2018.00214 · Cited by 15 · see citing works

Early memory consolidation window enables drug induced state-dependent memory

Osorio‐Gómez, D., Saldivar-Mares, K. S., Perera-López, A., McGaugh, J. L., & Bermúdez‐Rattoni, F. (2018) · Neuropharmacology · doi:10.1016/j.neuropharm.2018.11.033 · Cited by 16 · see citing works

Automated Visual Cognitive Tasks for Recording Neural Activity Using a Floor Projection Maze

Jacobson, T. K., Ho, J. W., Kent, B. W., Yang, F., & Burwell, R. D. (2014) · Journal of Visualized Experiments · doi:10.3791/51316 · Cited by 15 · see citing works

The Effects of Galactic Cosmic Rays on the Central Nervous System: From Negative to Unexpectedly Positive Effects That Astronauts May Encounter

Kokhan, V. S., & Dobynde, M. I. (2023) · Biology · doi:10.3390/biology12030400 · Cited by 13 · see citing works

Object Novelty Recognition Memory

Ennaceur, A. (2018) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-812012-5.00001-x · Cited by 11 · see citing works

Stimulus-seeking in rats is accompanied by increased c-Fos expression in hippocampal CA1 as well as short 22 kHz and flat 50 kHz calls

Robakiewicz, I., Polak, M., Rawska, M., Alberski, D., Polowy, R., Wytrychiewicz‐Pankowska, K., Syperek, M., Matysiak, J., & Filipkowski, R. K. (2019) · Acta Neurobiologiae Experimentalis · doi:10.21307/ane-2019-029 · Cited by 11 · see citing works

Immediate-Early Gene Expression in Neural Circuits Related to Object Recognition Memory

Barbosa, F. F., & Silva, R. H. (2018) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-812012-5.00018-5 · Cited by 11 · see citing works

The remarkable hypoxia tolerance in Brandt's voles ( Lasiopodomys brandtii )

Li, W., Dong, Y., Dong, Q., Sun, H. Q., Zhang, Y., & Wang, Z. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.15012 · Cited by 10 · see citing works

Cholinergic input to the hippocampus is not required for a model of episodic memory in the rat, even with multiple consecutive events

Seel, S. V., Eacott, M. J., Langston, R. F., & Easton, A. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.06.001 · Cited by 9 · see citing works

Perirhinal cortex and the recognition of relative familiarity

Ameen‐Ali, K. E., Sivakumaran, M. H., Eacott, M. J., O’Connor, A. R., Ainge, J. A., & Easton, A. (2021) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2021.107439 · Cited by 8 · see citing works

Methodological Approaches to the Behavioural Investigation of Visual Perception in Rodents

Zoccolan, D., & Filippo, A. D. (2018) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-812012-5.00005-7 · Cited by 8 · see citing works

Lactational Exposure to Fipronil Pesticide in Low Dose Impairs Memory in Rat Offspring

Montanha, F. P., & Machado, F. D. (2016) · Journal of Neurological Disorders · doi:10.4172/2329-6895.1000279 · Cited by 7 · see citing works

AnMei decoction ameliorates cognitive impairment in rats with chronic sleep deprivation by mitigating hippocampal neuroinflammation and restoring synaptic architecture

Xu, Z., Zhang, J.-L., Li, F., Xu, B., Xia, J., Wang, P., & Xie, G. (2024) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2024.119101 · Cited by 6 · see citing works

Effects of Endogenous and Exogenous N-Acety-5-Methoxy Kynuramine on Object Recognition Memory in Male C3H Mice

Iwashita, H., Sano, M., & Chiba, A. (2022) · Hormones and Behavior · doi:10.1016/j.yhbeh.2023.105329 · Cited by 6 · see citing works

Rats recognize spatial and temporal attributes in a new object recognition memory task with multiple trials

Araujo, A. P. D. C., de Lucena, J. D., Drieskens, D. C., Neves, L. R., Pugliane, K. C., Belchior, H., Castelo‐Branco, R., & Barbosa, F. F. (2020) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2020.108936 · Cited by 6 · see citing works

Dissociating the effects of distraction and proactive interference on object memory through tests of novelty preference

Landreth, K., Simanaviciute, U., Fletcher, J., Grayson, B., Grant, R. A., Harte, M., & Gigg, J. (2021) · Brain and Neuroscience Advances · doi:10.1177/23982128211003199 · Cited by 5 · see citing works

Post-learning caffeine administration improves ‘what-when’ and ‘what-where’ components of episodic-like memory in rats

Dias, A. L. A., Golzio, A. M. F. D. O., Santos, B. H. D. L., Salvadori, M. G. D. S. S., dos Santos, S. G., da Silva, M. S., de Almeida, R. N., & Barbosa, F. F. (2022) · Behavioural Brain Research · doi:10.1016/j.bbr.2022.113982 · Cited by 5 · see citing works

Anterior thalamic function is required for spatial coding in the subiculum and is necessary for spatial memoryPreprint

Frost, B. E., Martin, S. K., Cafalchio, M., Islam, M. N., Aggleton, J. P., & O’Mara, S. M. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.01.31.928762 · Cited by 5 · see citing works

Assessing episodic memory in rodents using spontaneous object recognition tasks

Barbosa, F. F., & Castelo‐Branco, R. (2022) · Emerging Topics in Life Sciences · doi:10.1042/etls20220010 · Cited by 4 · see citing works

Using the Spontaneous Object Recognition Memory Tasks to Uncover the Neural Circuitry of Recognition Memory

Warburton, E. C. (2018) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-812012-5.00013-6 · Cited by 3 · see citing works

Between similarity and difference: network dynamics of the hippocampal- parahippocampal circuitry in pattern separation of male Wistar rats

Araujo, A. P. D. C., Parente, J. S., Coutinho, S. L. D. O., Castelo‐Branco, R., Meurer, Y. D. S. R., & Barbosa, F. F. (2025) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2025.1648536 · Cited by 2 · see citing works

Working and Reference Memory Impairments Induced by Passive Chronic Cocaine Administration in Mice

Mañas‐Padilla, M. C., Ávila‐Gámiz, F., Gil‐Rodríguez, S., Salido, L. S., Santín, L. J., & Castilla‐Ortega, E. (2021) · Neuromethods · doi:10.1007/978-1-0716-1748-9_11 · Cited by 2 · see citing works

Perirhinal Cortex Lesions and Spontaneous Object Recognition Memory in Rats

Aggleton, J. P. (2018) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-812012-5.00012-4 · Cited by 1 · see citing works

Dissociating the effects of distraction and proactive interference on object memory through tests of novelty preferencePreprint

Landreth, K., Simanaviciute, U., Fletcher, J., Grayson, B., Grant, R. A., Harte, M., & Gigg, J. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.08.16.253179 · Cited by 1 · see citing works

The effects of dietary probiotic administration on anxiety and cognition

O’Hagan, C. (2015) · ORCA Online Research @Cardiff (Cardiff University)

The role of the anterior thalamic nuclei for properties of episodic memory: what, when, where

Dumont, J. R. (2012) · UPT. Syiah Kuala University Library (Syiah Kuala University)

INFLUÊNCIA DO TAMANHO DA NINHADA SOBRE O DECLÍNIO COGNITIVO E A MORFOLOGIA MICROGLIAL DA CAMADA MOLECULAR DO GIRO DENTEADO EM Rattus novergicus

Augusto‐Oliveira, M. (2012)

Demarcating the anatomical structure of the claustrum: piecing together a new functional puddlePreprint

Dillingham, C. M., Frost, B. E., Jankowski, M. M., Lambert, M. A., & O’Mara, S. M. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/179879

Cognitive Correlates of Anterolateral Entorhinal Cortex Volume Differences in Older Adults

Yeung, L. (2017) · TSpace (University of Toronto)

Novel tests of complex recognition memory in animals and humans

Ameen‐Ali, K. E. (2015) · Durham e-Theses (Durham University)

Bases neuronales de l’apprentissage associatif multisensoriel : implication différentielle du cortex entorhinal et de l’hippocampe chez le rat

Boisselier, L. (2016) · theses.fr (ABES) · doi:10.70675/ca67629fz2635z4501z95e1z49cf0b9b0be1

The bow-tie maze: A new one-session test for object recognition in rats

John, A. (2009) · Frontiers in Behavioral Neuroscience · doi:10.3389/conf.neuro.08.2009.09.073

Perirhinal Cortex Lesions and Spontaneous Object Recognition Memory in Rats

Aggleton, J. P. (2018) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-812012-5.00012-4 · Cited by 1 · see citing works

Advances in the behavioural testing and network imaging of rodent recognition memory

Kinnavane, L., Albasser, M. M., & Aggleton, J. P. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.07.049 · Cited by 59 · see citing works

Object recognition in rats and mice: a one-trial non-matching-to-sample learning task to study 'recognition memory'

Bevins, R. A., & Besheer, J. (2006) · Nature Protocols · doi:10.1038/nprot.2006.205 · Cited by 1,278 · see citing works

An associative analysis of object memory

Ward-Robinson, J., & Bonardi, C. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.10.046 · Cited by 16 · see citing works