Rhinal cortex ablations fail to disrupt reinforcer devaluation effects in rhesus monkeys (Macaca mulatta).

Handbook of Sensory Physiology

Sanders, M. D. (1975) · British Journal of Ophthalmology · doi:10.1136/bjo.59.2.111-c · Cited by 7,166 · see citing works

The Neuropsychology of Memory

Squire, L. R. (1984) · Springer eBooks · doi:10.1007/978-3-642-70094-1_32 · Cited by 2,126 · see citing works

Contemporary Animal Learning Theory

LoLordo, V. M., & Dickinson, A. (1982) · The American Journal of Psychology · doi:10.2307/1422669 · Cited by 891 · see citing works

The Amygdaloid Complex

Marburg, O. (2007) · Stereotactic and Functional Neurosurgery · doi:10.1159/000105833 · Cited by 387 · see citing works

The amygdala and reward

Baxter, M. G., & Murray, E. A. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn875 · Cited by 1,200 · see citing works

Control of Response Selection by Reinforcer Value Requires Interaction of Amygdala and Orbital Prefrontal Cortex

Baxter, M. G., Parker, A., Lindner, C. C. C., Izquierdo, A. D., & Murray, E. A. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-11-04311.2000 · Cited by 582 · see citing works

Neural systems and cue-induced cocaine craving

Bonson, K. (2002) · Neuropsychopharmacology · doi:10.1016/s0893-133x(01)00371-2 · Cited by 507 · see citing works

Role of perirhinal cortex in object perception, memory, and associations

Murray, E. A., & Richmond, B. J. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00195-1 · Cited by 319 · see citing works

Localization of Dysfunction in Major Depressive Disorder: Prefrontal Cortex and Amygdala

Murray, E. A., Wise, S. P., & Drevets, W. C. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.09.041 · Cited by 208 · see citing works

Transient Inactivation of Orbitofrontal Cortex Blocks Reinforcer Devaluation in Macaques

West, E. A., DesJardin, J. T., Gale, K., & Málková, L. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.3295-11.2011 · Cited by 137 · see citing works

Response Differences in Monkey TE and Perirhinal Cortex: Stimulus Association Related to Reward Schedules

Liu, Z., & Richmond, B. J. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.83.3.1677 · Cited by 134 · see citing works

GABA_A-Mediated Inhibition of Basolateral Amygdala Blocks Reward Devaluation in Macaques

Wellman, L. L., Gale, K., & Malkova, L. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.2257-04.2005 · Cited by 126 · see citing works

The effects of selective amygdala, orbital frontal cortex or hippocampal formation lesions on reward assessment in nonhuman primates

Machado, C. J., & Bachevalier, J. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05525.x · Cited by 120 · see citing works

The neurocognitive bases of human multimodal food perception: Consciousness

Verhagen, J. V. (2006) · Brain Research Reviews · doi:10.1016/j.brainresrev.2006.09.002 · Cited by 109 · see citing works

Neurotoxic Lesions of the Medial Mediodorsal Nucleus of the Thalamus Disrupt Reinforcer Devaluation Effects in Rhesus Monkeys

Mitchell, A. S., Browning, P. G. F., & Baxter, M. G. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1914-07.2007 · Cited by 100 · see citing works

Learning motivational significance of visual cues for reward schedules requires rhinal cortex

Liu, Z., Murray, E. A., & Richmond, B. J. (2000) · Nature Neuroscience · doi:10.1038/81841 · Cited by 95 · see citing works

Neural Estimates of Imagined Outcomes in the Orbitofrontal Cortex Drive Behavior and Learning

Takahashi, Y. K., Chang, C. Y., Lucantonio, F., Haney, R. Z., Berg, B. A., Yau, H., Bonci, A., & Schoenbaum, G. M. (2013) · Neuron · doi:10.1016/j.neuron.2013.08.008 · Cited by 81 · see citing works

Amount of training affects associatively-activated event representation

Holland, P. C. (1998) · Neuropharmacology · doi:10.1016/s0028-3908(98)00038-0 · Cited by 75 · see citing works

Impairments in visual discrimination learning and recognition memory produced by neurotoxic lesions of rhinal cortex in rhesus monkeys

Baxter, M. G., & Murray, E. A. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01491.x · Cited by 69 · see citing works

What, if anything, is the medial temporal lobe, and how can the amygdala be part of it if there is no such thing?

Murray, E. A., & Wise, S. P. (2004) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2004.05.005 · Cited by 45 · see citing works

Behavioral outcomes of late‐onset or early‐onset orbital frontal cortex (areas 11/13) lesions in rhesus monkeys

Bachevalier, J., Machado, C. J., & Kazama, A. M. (2011) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2011.06211.x · Cited by 39 · see citing works

Measuring reward assessment in a semi-naturalistic context: The effects of selective amygdala, orbital frontal or hippocampal lesions

Machado, C. J., & Bachevalier, J. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.06.035 · Cited by 35 · see citing works

Interaction Between Orbital Prefrontal and Rhinal Cortex Is Required for Normal Estimates of Expected Value

Clark, A. M., Bouret, S., Young, A. M., Murray, E. A., & Richmond, B. J. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3605-12.2013 · Cited by 31 · see citing works

Cognitive Aging in Nonhuman Primates

Baxter, M. G. (2001) · Elsevier eBooks · doi:10.1016/b978-012351830-9/50028-7 · Cited by 24 · see citing works

The visual prefrontal cortex of anthropoids: interaction with temporal cortex in decision making and its role in the making of ‘visual animals’

Eldridge, M. A. G., Hines, B. E., & Murray, E. A. (2021) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2021.02.012 · Cited by 21 · see citing works

Cognitive functions of the temporal lobe in the dog: A review

Kowalska, D. M. (2000) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/s0278-5846(00)00110-x · Cited by 20 · see citing works

Visual agnosia and Klüver-Bucy syndrome in marmosets (Callithrix jacchus) following ablation of inferotemporal cortex, with additional mnemonic effects of immunotoxic lesions of cholinergic projections to medial temporal areas.

Ridley, R., Warner, K. A., Maclean, C. J., Gaffan, D., & Baker, H. (2001) · Brain Research · doi:10.1016/s0006-8993(01)02187-4 · Cited by 20 · see citing works

Rhinal cortex lesions produce mild deficits in visual discrimination learning for an auditory secondary reinforcer in rhesus monkeys.

Baxter, M. G., Hadfield, W. S., & Murray, E. A. (1999) · Behavioral Neuroscience · doi:10.1037//0735-7044.113.2.243 · Cited by 19 · see citing works

A visual, position-independent instrumental reinforcer devaluation task for rats

West, E. A., Forcelli, P. A., Murnen, A. T., Gale, K., & Málková, L. (2010) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2010.11.004 · Cited by 15 · see citing works

Macaques fail to develop habit responses during extended training on a reinforcer devaluation task.

LaFlamme, E. M., Ahmed, F., Forcelli, P. A., & Málková, L. (2022) · Behavioral Neuroscience · doi:10.1037/bne0000503 · Cited by 9 · see citing works

Functional neuroanatomy of human emotion

Morris, J. C., & Dolan, R. (2003) · Elsevier eBooks · doi:10.1016/b978-012264841-0/50020-2 · Cited by 11 · see citing works

The Role of Perirhinal Cortex in Visual Discrimination Learning for Visual Secondary Reinforcement in Rats.

Eacott, M. J., Norman, G., & Gaffan, E. A. (2003) · Behavioral Neuroscience · doi:10.1037/0735-7044.117.6.1318 · Cited by 8 · see citing works

Effects of systemic cholinergic antagonism on reinforcer devaluation in macaques

Waguespack, H. F., Málková, L., Forcelli, P. A., & Turchi, J. N. (2018) · Neuroscience Letters · doi:10.1016/j.neulet.2018.05.003 · Cited by 7 · see citing works

Effects of the anterior temporal lobe lesions, separate or combined with hippocampal damage, on spatial delayed responses guided by auditory stimulus

Kowalska, D. M. (1999) · Acta Neurobiologiae Experimentalis · doi:10.55782/ane-1999-1315 · Cited by 7 · see citing works

Temporal-orbitofrontal pathway regulates choices across physical reward and visual novelty

Ogasawara, T., Xu, K., Snyder, A. Z., Perlmutter, J. S., Tu, Z., Minamimoto, T., Inoue, K., Takada, M., & Monosov, I. E. (2026) · Neuron · doi:10.1016/j.neuron.2025.12.011 · Cited by 2 · see citing works

Chemogenetic Disruption of Monkey Perirhinal Neurons Projecting to the Rostromedial Caudate Impairs Associative Learning

Wang, W., Eldridge, M. A. G., Setogawa, T., Webster-Bass, S., Miyazaki, N. L., Pearl, J. E., Liow, J., Lerchner, W., Li, B., Turchi, J. N., et al. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.0491-25.2025

Rhinal cortex lesions produce mild deficits in visual discrimination learning for an auditory secondary reinforcer in rhesus monkeys.

Baxter, M. G., Hadfield, W. S., & Murray, E. A. (1999) · Behavioral Neuroscience · doi:10.1037//0735-7044.113.2.243 · Cited by 19 · see citing works

Anterior rhinal cortex and amygdala: dissociation of their contributions to memory and food preference in rhesus monkeys.

Murray, E. A., Gaffan, E. A., & Flint, R. W. (1996) · PubMed · Cited by 74 · see citing works

Comparison of emotional responses in monkeys with rhinal cortex or amygdala lesions.

Meunier, M., & Bachevalier, J. (2002) · Emotion · doi:10.1037/1528-3542.2.2.147 · Cited by 32 · see citing works

Access of object representations to reinforcer value

(2005) · Psychology Press eBooks · doi:10.4324/9780203989388-19

Rhinal Cortex Removal Produces Amnesia for Preoperatively Learned Discrimination Problems But Fails to Disrupt Postoperative Acquisition and Retention in Rhesus Monkeys

Thornton, J. A., Rothblat, L. A., & Murray, E. A. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-21-08536.1997 · Cited by 85 · see citing works