Limbic systems for emotion and for memory, but no single limbic system

Spatial view cells and the representation of place in the primate hippocampus

Rolls, E. T. (1999) · Hippocampus · doi:10.1002/(sici)1098-1063(1999)9:4<467::aid-hipo13>3.0.co;2-f · Cited by 299

Projections of thalamic gustatory and lingual areas in the monkey, Macaca fascicularis

Pritchard, T. C., Hamilton, R. B., Morse, J. R., & Norgren, R. (1986) · Journal of Comparative Neurology · doi:10.1002/cne.902440208 · Cited by 294

The amygdala, social behavior, and danger detection

AMARAL, D. G. (2003) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1280.015 · Cited by 293

Hypothalamic neuronal responses associated with the sight of food

Rolls, E. T., Burton, M. J., & Mora, F. (1976) · Brain Research · doi:10.1016/0006-8993(76)91048-9 · Cited by 291

Olfactory Sensory-Specific Satiety in Humans

ROLLS, E., & ROLLS, J. (1997) · Physiology & Behavior · doi:10.1016/s0031-9384(96)00464-7 · Cited by 288

Functions of Neuronal Networks in the Hippocampus and Neocortex in Memory

Rolls, E. T. (1989) · Neural Models of Plasticity · doi:10.1016/b978-0-12-148955-7.50017-5 · Cited by 286

The Noisy BrainStochastic Dynamics as a Principle of Brain Function

Rolls, E. T., & Deco, G. (2010) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780199587865.001.0001 · Cited by 285

The neuronal encoding of information in the brain

Rolls, E. T., & Treves, A. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.08.002 · Cited by 284

Persistence of feelings and sentience after bilateral damage of the insula

Damasio, A., Damasio, H., & Tranel, D. (2013) · Cerebral Cortex · doi:10.1093/cercor/bhs077 · Cited by 282

Gustatory responses of single neurons in the caudolateral orbitofrontal cortex of the macaque monkey

Rolls, E. T., Yaxley, S., & Sienkiewicz, Z. J. (1990) · Journal of Neurophysiology · doi:10.1152/jn.1990.64.4.1055 · Cited by 282

Visual responses of neurons in the dorsolateral amygdala of the alert monkey

Sanghera, M. K., Rolls, E. T., & Roper-Hall, A. (1979) · Experimental Neurology · doi:10.1016/0014-4886(79)90175-4 · Cited by 280

Comparison of prefrontal architecture and connections

Pandya, D. N., & Yeterian, E. H. (1996) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.1996.0127 · Cited by 279

Responses to the Sensory Properties of Fat of Neurons in the Primate Orbitofrontal Cortex

Rolls, E. T., Critchley, H. D., Browning, A. S., Hernadi, I., & Lenard, L. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-04-01532.1999 · Cited by 278

Range-adapting representation of economic value in the orbitofrontal cortex

Padoa-Schioppa, C. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.3751-09.2009 · Cited by 276

A computational theory of episodic memory formation in the hippocampus

Rolls, E. T. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.03.027 · Cited by 276

Gustatory responses of single neurons in the insula of the macaque monkey

Yaxley, S., Rolls, E. T., & Sienkiewicz, Z. J. (1990) · Journal of Neurophysiology · doi:10.1152/jn.1990.63.4.689 · Cited by 262

Cognitive influences on the affective representation of touch and the sight of touch in the human brain

McCabe, C., Rolls, E. T., Bilderbeck, A., & McGlone, F. (2008) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsn005 · Cited by 262

Glutamate-receptor-mediated encoding and retrieval of paired-associate learning

Day, M., Langston, R., & Morris, R. G. M. (2003) · Nature · doi:10.1038/nature01769 · Cited by 261

XI. An investigation into the functions of the occipital and temporal lobes of the monkey's brain

Brown, S., & Sharpey-Schafer, E. A. (1888) · Philosophical Transactions of the Royal Society of London. (B.) · doi:10.1098/rstb.1888.0011 · Cited by 260

Memory: Anatomical Organization of Candidate Brain Regions

Amaral, D. G. (1987) · Comprehensive Physiology · doi:10.1002/cphy.cp010507 · Cited by 259

Hippocampal neurons in the monkey with activity related to the place in which a stimulus is shown

Rolls, E., Miyashita, Y., Cahusac, P., Kesner, R., Niki, H., Feigenbaum, J., & Bach, L. (1989) · The Journal of Neuroscience · doi:10.1523/jneurosci.09-06-01835.1989 · Cited by 256

Organization of cortical afferent input to orbitofrontal areas in the rhesus monkey

Barbas, H. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90132-y · Cited by 256

Entorhinal cortex grid cells can map to hippocampal place cells by competitive learning

Rolls, E. T., Stringer, S. M., & Elliot, T. (2006) · Network: Computation in Neural Systems · doi:10.1080/09548980601064846 · Cited by 254

Representation of Umami Taste in the Human Brain

de Araujo, I. E. T., Kringelbach, M. L., Rolls, E. T., & Hobden, P. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00669.2002 · Cited by 254

Task and Content Modulate Amygdala-Hippocampal Connectivity in Emotional Retrieval

Smith, A. P. R., Stephan, K. E., Rugg, M. D., & Dolan, R. J. (2006) · Neuron · doi:10.1016/j.neuron.2005.12.025 · Cited by 252

Anatomie comparée des circonvolutions cérébrales : le grand lobe limbique et la scissure limbique dans la série des mammifères

Broca, P. (1878) · Medical Entomology and Zoology · Cited by 251

Effects of hunger on the responses of neurons in the lateral hypothalamus to the sight and taste of food

Burton, M. J., Rolls, E. T., & Mora, F. (1976) · Experimental Neurology · doi:10.1016/0014-4886(76)90189-8 · Cited by 251

An attention modulated response to disgust in human ventral anterior insula

Krolak‐Salmon, P., Hénaff, M., Isnard, J., Tallon‐Baudry, C., Guénot, M., Vighetto, A., Bertrand, O., & Mauguière, F. (2003) · Annals of Neurology · doi:10.1002/ana.10502 · Cited by 251

The emergence of grid cells: Intelligent design or just adaptation?

Kropff, E., & Treves, A. (2008) · Hippocampus · doi:10.1002/hipo.20520 · Cited by 250

Projections from behaviorally-defined sectors of the prefrontal cortex to the basal ganglia, septum, and diencephalon of the monkey

Johnson, T. N., Rosvold, H. E., & Mishkin, M. (1968) · Experimental Neurology · doi:10.1016/0014-4886(68)90030-7 · Cited by 248

Principles of behavioral and cognitive neurology, 2nd ed.

Mesulam, M. M. (2000) · Cited by 248

The behavioural final common path

McFarland, D. J., & Sibly, R. M. (1975) · Philosophical Transactions of the Royal Society of London. B, Biological Sciences · doi:10.1098/rstb.1975.0009 · Cited by 245

Involvement of Human Amygdala and Orbitofrontal Cortex in Hunger-Enhanced Memory for Food Stimuli

Morris, J. S., & Dolan, R. J. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-14-05304.2001 · Cited by 240

Borderline Personality Disorder, Impulsivity, and the Orbitofrontal Cortex

Berlin, H. A., Rolls, E. T., & Iversen, S. D. (2005) · American Journal of Psychiatry · doi:10.1176/appi.ajp.162.12.2360 · Cited by 240

One-Trial Memory for Object-Place Associations after Separate Lesions of Hippocampus and Posterior Parahippocampal Region in the Monkey

Malkova, L., & Mishkin, M. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-05-01956.2003 · Cited by 239

An attractor network in the hippocampus: Theory and neurophysiology

Rolls, E. T. (2007) · Learning & Memory · doi:10.1101/lm.631207 · Cited by 238

Neurodynamics of Biased Competition and Cooperation for Attention: A Model With Spiking Neurons

Deco, G., & Rolls, E. T. (2005) · Journal of Neurophysiology · doi:10.1152/jn.01095.2004 · Cited by 238

Spatial View Cells in the Primate Hippocampus

Rolls, E. T., Robertson, R. G., & Georges‐François, P. (1997) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1997.tb01538.x · Cited by 238

Expected Value, Reward Outcome, and Temporal Difference Error Representations in a Probabilistic Decision Task

Rolls, E. T., McCabe, C., & Redoute, J. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm097 · Cited by 236

MOTILITY, BEHAVIOR AND THE BRAIN*: STEREODYNAMIC ORGANIZATION AND NEURAL CO-ORDINATES OF BEHAVIOR

Yakovlev, P. I. (1948) · The Journal of Nervous and Mental Disease · doi:10.1097/00005053-194810740-00001 · Cited by 234

Place memory and scene memory: effects of fornix transection in the monkey

Gaffan, D., & Harrison, S. (1989) · Experimental Brain Research · doi:10.1007/bf00248293 · Cited by 234

Decoding Neuronal Ensembles in the Human Hippocampus

Hassabis, D., Chu, C., Rees, G., Weiskopf, N., Molyneux, P. D., & Maguire, E. A. (2009) · Current Biology · doi:10.1016/j.cub.2009.02.033 · Cited by 231

The Oxford Handbook of Comparative Cognition

(2012) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780195392661.001.0001 · Cited by 231

Gustatory responses in the frontal opercular cortex of the alert cynomolgus monkey

Scott, T. R., Yaxley, S., Sienkiewicz, Z. J., & Rolls, E. T. (1986) · Journal of Neurophysiology · doi:10.1152/jn.1986.56.3.876 · Cited by 228

Warm pleasant feelings in the brain

Rolls, E. T., Grabenhorst, F., & Parris, B. A. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.03.005 · Cited by 227

Spatial View Cells in the Primate Hippocampus: Allocentric View not Head Direction or Eye Position or Place

Georges-Francois, P. (1999) · Cerebral Cortex · doi:10.1093/cercor/9.3.197 · Cited by 223

Umami: a delicious flavor formed by convergence of taste and olfactory pathways in the human brain

McCabe, C., & Rolls, E. T. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05445.x · Cited by 221

Decoding Individual Episodic Memory Traces in the Human Hippocampus

Chadwick, M. J., Hassabis, D., Weiskopf, N., & Maguire, E. A. (2010) · Current Biology · doi:10.1016/j.cub.2010.01.053 · Cited by 219

Afferent connections of the caudolateral orbitofrontal cortex taste area of the primate

Baylis, L. L., Rolls, E. T., & Baylis, G. C. (1995) · Neuroscience · doi:10.1016/0306-4522(94)00449-f · Cited by 217

Functions of the orbitofrontal and pregenual cingulate cortex in taste, olfaction, appetite and emotion

Rolls, E. (2008) · Acta Physiologica Hungarica · doi:10.1556/aphysiol.95.2008.2.1 · Cited by 214

Amygdala damage impairs eye contact during conversations with real people

Spezio, M. L., Huang, P.-Y. S., Castelli, F., & Adolphs, R. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.3789-06.2007 · Cited by 213

How Pleasant and Unpleasant Stimuli Combine in Different Brain Regions: Odor Mixtures

Grabenhorst, F., Rolls, E. T., Margot, C., da Silva, M. A. A. P., & Velazco, M. I. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.3337-07.2007 · Cited by 213

A comparison of the effects of fornix transection and sulcus principalis ablation upon spatial learning by monkeys

Gaffan, D., & Harrison, S. (1989) · Behavioural Brain Research · doi:10.1016/0166-4328(89)90003-x · Cited by 213

Luddites must not block progress in genetics

Wood, D. (1999) · Nature · doi:10.1038/16564 · Cited by 209

How the Brain Represents the Reward Value of Fat in the Mouth

Grabenhorst, F., Rolls, E. T., Parris, B. A., & d'Souza, A. A. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhp169 · Cited by 209

Sensory processing in the brain related to the control of food intake

Rolls, E. T. (2007) · Proceedings of the Nutrition Society · doi:10.1017/s0029665107005332 · Cited by 209

The responsiveness of neurons in the insular gustatory cortex of the macaque monkey is independent of hunger

Yaxley, S., Rolls, E. T., & Sienkiewicz, Z. J. (1988) · Physiology & Behavior · doi:10.1016/0031-9384(88)90074-1 · Cited by 206

Adaptation of Reward Sensitivity in Orbitofrontal Neurons

Kobayashi, S., Pinto de Carvalho, O., & Schultz, W. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4009-09.2010 · Cited by 206

Selective attention to affective value alters how the brain processes taste stimuli

Grabenhorst, F., & Rolls, E. T. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06033.x · Cited by 206

Memory, Attention, and Decision-Making: A unifying computational neuroscience approach

Rolls, E. T. (2007) · Cited by 205

Activity of neurones in the inferotemporal cortex of the alert monkey

Rolls, E. T., Judge, S. J., & Sanghera, M. K. (1977) · Brain Research · doi:10.1016/0006-8993(77)90272-4 · Cited by 198

Brain mechanisms for perceptual and reward-related decision-making

Deco, G., Rolls, E. T., Albantakis, L., & Romo, R. (2013) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2012.01.010 · Cited by 196

Monkeys with rhinal cortex damage or neurotoxic hippocampal lesions are impaired on spatial scene learning and object reversals.

Murray, E. A., Baxter, M. G., & Gaffan, D. (1998) · Behavioral Neuroscience · doi:10.1037//0735-7044.112.6.1291 · Cited by 194

Neurophysiological analysis of brain-stimulation reward in the monkey

Rolls, E. T., Burton, M. J., & Mora, F. (1980) · Brain Research · doi:10.1016/0006-8993(80)91216-0 · Cited by 193

Organization of connections between the amygdaloid complex and the perirhinal and parahippocampal cortices in macaque monkeys

Stefanacci, L., SUZUKI, W. A., & Amaral, D. G. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19961125)375:4<552::aid-cne2>3.0.co;2-0 · Cited by 193

Allocentric and egocentric spatial information processing in the hippocampal formation of the behaving primate

Feigenbaum, J. D., & Rolls, E. T. (1991) · Psychobiology · doi:10.1007/bf03337953 · Cited by 193

Role of the amygdala in decisions under ambiguity and decisions under risk: Evidence from patients with Urbach-Wiethe disease

Brand, M., Grabenhorst, F., Starcke, K., Vandekerckhove, M. M. P., & Markowitsch, H. J. (2007) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2006.09.021 · Cited by 191

Olfactory neuronal responses in the primate orbitofrontal cortex: analysis in an olfactory discrimination task

Critchley, H. D., & Rolls, E. T. (1996) · Journal of Neurophysiology · doi:10.1152/jn.1996.75.4.1659 · Cited by 190

The Role of the Amygdala in Emotional Learning

(1994) · International Review of Neurobiology · doi:10.1016/s0074-7742(08)60305-0 · Cited by 190

Primate Insular/Opercular Taste Cortex: Neuronal Representations of the Viscosity, Fat Texture, Grittiness, Temperature, and Taste of Foods

Verhagen, J. V., Kadohisa, M., & Rolls, E. T. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00321.2004 · Cited by 189

Enhanced affective brain representations of chocolate in cravers vs. non‐cravers

Rolls, E. T., & McCabe, C. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05724.x · Cited by 188

Taste, olfactory and food texture reward processing in the brain and obesity

Rolls, E. T. (2011) · International Journal of Obesity · doi:10.1038/ijo.2010.155 · Cited by 185

AMNESIA IN MAN FOLLOWING TRANSECTION OF THE FORNIX: A REVIEW

GAFFAN, D., & GAFFAN, E. A. (1991) · Brain · doi:10.1093/brain/114.6.2611 · Cited by 182

Neural and Metabolic Control of Macronutrient Intake

(1999) · CRC Press eBooks · doi:10.1201/9780367802059 · Cited by 180

Information About Spatial View in an Ensemble of Primate Hippocampal Cells

Rolls, E. T., Treves, A., Robertson, R. G., Georges-François, P., & Panzeri, S. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.79.4.1797 · Cited by 179

Dissociable Effects of Subtotal Lesions within the Macaque Orbital Prefrontal Cortex on Reward-Guided Behavior

Rudebeck, P. H., & Murray, E. A. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.0091-11.2011 · Cited by 179

Decision‐making and Weber's law: a neurophysiological model

Deco, G., & Rolls, E. T. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04940.x · Cited by 179

Intrinsic connections and architectonics of the superior temporal sulcus in the rhesus monkey

Seltzer, B., & Pandya, D. N. (1989) · Journal of Comparative Neurology · doi:10.1002/cne.902900402 · Cited by 177

Neuronal Representations of Stimuli in the Mouth: The Primate Insular Taste Cortex, Orbitofrontal Cortex and Amygdala

Kadohisa, M., Rolls, E. T., & Verhagen, J. V. (2005) · Chemical Senses · doi:10.1093/chemse/bji036 · Cited by 173

Taste and Olfactory Processing in the Brain and Its Relation to the Control of Eating

Rolls, E. T. (1997) · Critical Reviews™ in Neurobiology · doi:10.1615/critrevneurobiol.v11.i4.20 · Cited by 172

Invariant Visual Object and Face Recognition: Neural and Computational Bases, and a Model, VisNet

Rolls, E. T. (2012) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2012.00035 · Cited by 172

The Functions of the Orbitofrontal Cortex

Rolls, E. T. (1999) · Neurocase · doi:10.1080/13554799908411984 · Cited by 172

Spatial firing correlates of neurons in the hippocampal formation of freely moving rats

Muller, R. U., Kubie, J. L., Bostock, E. M., Taube, J. S., & Quirk, G. J. (1991) · Brain And Space · doi:10.1093/oso/9780198542841.003.0017 · Cited by 170

Orbitofrontal contributions to value-based decision making: evidence from humans with frontal lobe damage

Fellows, L. K. (2011) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2011.06229.x · Cited by 169

Neurophysiology and functions of the primate amygdala.

Rolls, E. T. (1992) · Cited by 167

Combined Unilateral Lesions of the Amygdala and Orbital Prefrontal Cortex Impair Affective Processing in Rhesus Monkeys

Izquierdo, A., & Murray, E. A. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00968.2003 · Cited by 167

The responsiveness of neurones in the frontal opercular gustatory cortex of the macaque monkey is independent of hunger.

Rolls, E. T., Scott, T. R., Sienkiewicz, Z. J., & Yaxley, S. (1988) · The Journal of Physiology · doi:10.1113/jphysiol.1988.sp016984 · Cited by 166

Neurons in the Primate Orbitofrontal Cortex Respond to Fat Texture Independently of Viscosity

Verhagen, J. V., Rolls, E. T., & Kadohisa, M. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00320.2003 · Cited by 163

Central Neural Mechanisms of Taste

Norgren, R. (1984) · Comprehensive physiology · doi:10.1002/cphy.cp010324 · Cited by 163

Representations of the Texture of Food in the Primate Orbitofrontal Cortex: Neurons Responding to Viscosity, Grittiness, and Capsaicin

Rolls, E. T., Verhagen, J. V., & Kadohisa, M. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00515.2003 · Cited by 161

The affective and cognitive processing of touch, oral texture, and temperature in the brain

Rolls, E. T. (2010) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2008.03.010 · Cited by 160

Neuromodulation by Glutamate and Acetylcholine can Change Circuit Dynamics by Regulating the Relative Influence of Afferent Input and Excitatory Feedback

Giocomo, L. M., & Hasselmo, M. E. (2007) · Molecular Neurobiology · doi:10.1007/s12035-007-0032-z · Cited by 160

Orbitofrontal Cortex and Amygdala Contributions to Affect and Action in Primates

MURRAY, E. A., & IZQUIERDO, A. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1401.021 · Cited by 159

Spatial View Cells in the Primate Hippocampus: Effects of Removal of View Details

Robertson, R. G., Rolls, E. T., & Georges‐François, P. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.79.3.1145 · Cited by 157

Taste, olfactory and food texture reward processing in the brain and the control of appetite

Rolls, E. T. (2012) · Proceedings of The Nutrition Society · doi:10.1017/s0029665112000821 · Cited by 156

Olfaction: A Model System for Computational Neuroscience

Davis, J. L., & Eichenbaum, H. (1991) · Cited by 155

Understanding the mechanisms of food intake and obesity

Rolls, E. T. (2007) · Obesity Reviews · doi:10.1111/j.1467-789x.2007.00321.x · Cited by 152

Face-selective and auditory neurons in the primate orbitofrontal cortex

Rolls, E. T., Critchley, H. D., Browning, A. S., & Inoue, K. (2006) · Experimental Brain Research · doi:10.1007/s00221-005-0191-y · Cited by 151

The representation of information about faces in the temporal and frontal lobes

Rolls, E. T. (2006) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2006.04.019 · Cited by 150

Neuroanatomy of the primate amygdala.

Freese, J. L., & Amaral, D. G. (2009) · Cited by 149

Choice, difficulty, and confidence in the brain

Rolls, E. T., Grabenhorst, F., & Deco, G. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.06.073 · Cited by 148

Object, Space, and Object-Space Representations in the Primate Hippocampus

Rolls, E. T., Xiang, J.-Z., & Franco, L. (2005) · Journal of Neurophysiology · doi:10.1152/jn.01063.2004 · Cited by 146

Umami Responses in Mouse Taste Cells Indicate More than One Receptor

Maruyama, Y., Pereira, E., Margolskee, R. F., Chaudhari, N., & Roper, S. D. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.4329-05.2006 · Cited by 145

Taste and Olfactory Processing in the Brain, and Its Relation to the Control of Eating

Rolls, E. T. (1998) · KARGER eBooks · doi:10.1159/000061107 · Cited by 145

The amygdala: is it an essential component of the neural network for social cognition?

Amaral, D. G., Capitanio, J. P., Jourdain, M., Mason, W. A., Mendoza, S. P., & Prather, M. (2003) · Neuropsychologia · doi:10.1016/s0028-3932(02)00154-9 · Cited by 143

Neurophysiology and functions of the primate amygdala, and the neural basis of emotion

Rolls, E. T. (2000) · The Amygdala · doi:10.1093/oso/9780198505013.003.0013 · Cited by 142

Responses of neurons in the primate taste cortex to glutamate

Baylis, L. L., & Rolls, E. T. (1991) · Physiology & Behavior · doi:10.1016/0031-9384(91)90210-f · Cited by 141

Neural models of plasticity: experimental and theoretical approaches

Byrne, J. H., & Berry, W. O. (1990) · Comparative Biochemistry and Physiology Part A Physiology · doi:10.1016/0300-9629(90)90284-y · Cited by 140

The Role of Orbitofrontal Cortex in Decision Making: A Component Process Account

Fellows, L. K. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1401.023 · Cited by 140

Morphological and numerical analysis of synaptic interactions between neurons in deep and superficial layers of the entorhinal cortex of the rat

van Haeften, T., Baks‐te‐Bulte, L., Goede, P. H., Wouterlood, F. G., & Witter, M. P. (2003) · Hippocampus · doi:10.1002/hipo.10144 · Cited by 135

The Role of the Perirhinal Cortex and Hippocampus in Learning, Memory, and Perception

Buckley, M. J. (2005) · The Quarterly Journal of Experimental Psychology Section B · doi:10.1080/02724990444000186 · Cited by 134

Reward-Spatial View Representations and Learning in the Primate Hippocampus

Rolls, E. T., & Xiang, J.-Z. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.1481-05.2005 · Cited by 133

The representation and storage of information in neural networks in the primate cerebral cortex and hippocampus

Rolls, E. T. (1989) · Addison-Wesley Longman Publishing Co., Inc. eBooks · Cited by 131

Specialized Elements of Orbitofrontal Cortex in Primates

Barbas, H. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1401.015 · Cited by 131

From affective value to decision‐making in the prefrontal cortex

Fabian Grabenhorst, B., Rolls, E. T., & Parris, B. A. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06489.x · Cited by 130

Human cortical representation of oral temperature

Guest, S., Grabenhorst, F., Essick, G., Chen, Y., Young, M., McGlone, F., de Araujo, I., & Rolls, E. T. (2007) · Physiology & Behavior · doi:10.1016/j.physbeh.2007.07.004 · Cited by 129

Perirhinal and parahippocampal cortices of the macaque monkey: Intrinsic projections and interconnections

Lavenex, P., SUZUKI, W. A., & Amaral, D. G. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20079 · Cited by 126

A quantitative theory of the functions of the hippocampal CA3 network in memory

Rolls, E. T. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00098 · Cited by 126

The neural and molecular bases of learning

Bruyn, G. W. (1987) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(87)90195-x · Cited by 123

Decision-Making, Errors, and Confidence in the Brain

Rolls, E. T., Fabian Grabenhorst, B., & Deco, G. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00571.2010 · Cited by 123

Projections from the parahippocampal region to the prefrontal cortex in the rat: evidence of multiple pathways

Delatour, B., & Witter, M. P. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2002.01973.x · Cited by 123

Connections of orbital cortex

Price, J. L. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780198565741.003.0003 · Cited by 122

Central Taste Anatomy and Neurophysiology

Scott, T., & Rolls, E. (2003) · CRC Press eBooks · doi:10.1201/9780203911457-38 · Cited by 119

The Noisy Brain: Stochastic Dynamics as a Principle of Brain Function

Dawkins, M. S. (2010) · Animal Behaviour · doi:10.1016/j.anbehav.2010.04.019 · Cited by 118

Selective Attention to Affective Value Alters How the Brain Processes Olfactory Stimuli

Rolls, E. T., Fabian Grabenhorst, B., Margot, C., da Silva, M. A. A. P., & Velazco, M. I. (2008) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2008.20128 · Cited by 116

Responses of Primate Taste Cortex Neurons to the Astringent Tastant Tannic Acid

Critchley, H., & Rolls, E. T. (1996) · Chemical Senses · doi:10.1093/chemse/21.2.135 · Cited by 115

Analysis of behavioural change

Piercy, M. (1970) · Neuropsychologia · doi:10.1016/0028-3932(70)90015-1 · Cited by 114

Monkey hippocampus and learning about spatially directed movements.

Rupniak, N. M. J., & Gaffan, D. (1987) · Europe PMC (PubMed Central) · Cited by 112

Contribution of Genoarchitecture to Understanding Forebrain Evolution and Development, with Particular Emphasis on the Amygdala

Medina, L. M., Bupesh, M., & Abellán, A. (2011) · Brain Behavior and Evolution · doi:10.1159/000330056 · Cited by 112

Synaptic and Spiking Dynamics underlying Reward Reversal in the Orbitofrontal Cortex

Deco, G., & Rolls, E. T. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh103 · Cited by 112

Projections from the lateral, basal, and accessory basal nuclei of the amygdala to the entorhinal cortex in the macaque monkey

Pitkänen, A., Kelly, J. L., & Amaral, D. G. (2002) · Hippocampus · doi:10.1002/hipo.1099 · Cited by 110

Responses of neurons in the primate taste cortex to the glutamate ion and to inosine 5′-monophosphate

Rolls, E. T. (1996) · Physiology & Behavior · doi:10.1016/0031-9384(95)02178-7 · Cited by 109

Orbitofrontal Cortex and Memory Formation

Frey, S., & Petrides, M. (2002) · Neuron · doi:10.1016/s0896-6273(02)00901-7 · Cited by 109

Orbitofrontal cortex: neuronal representation of oral temperature and capsaicin in addition to taste and texture

Kadohisa, M., Rolls, E. T., & Verhagen, J. V. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.04.037 · Cited by 109

Spatial View Cells in the Primate Hippocampus and Memory Recall

Rolls, E. T., & Xiang, J.-Z. (2006) · Reviews in the Neurosciences · doi:10.1515/revneuro.2006.17.1-2.175 · Cited by 108

The Orbitofrontal Cortex: Novelty, Deviation from Expectation, and Memory

Petrides, M. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1401.035 · Cited by 106

What went where? Impaired object‐location learning in patients with right hippocampal lesions

Crane, J., & Milner, B. A. (2004) · Hippocampus · doi:10.1002/hipo.20043 · Cited by 106

The primate amygdala: Neuronal representations of the viscosity, fat texture, temperature, grittiness and taste of foods

Kadohisa, M., Verhagen, J. V., & Rolls, E. T. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2004.12.005 · Cited by 106

A proposed architecture for the neural representation of spatial context

Jeffery, K. J., Anderson, M. I., Hayman, R. M. A., & Chakraborty, S. (2004) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2003.12.002 · Cited by 105

Neural Systems Underlying Decisions about Affective Odors

Rolls, E. T., Fabian Grabenhorst, B., & Parris, B. A. (2009) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21231 · Cited by 101

Functional neuroimaging of umami taste: what makes umami pleasant?

Rolls, E. T. (2009) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.2009.27462r · Cited by 99

Assessing the mechanism of response in the retrosplenial cortex of good and poor navigators

Auger, S. D., & Maguire, E. A. (2013) · Cortex · doi:10.1016/j.cortex.2013.08.002 · Cited by 98

Role of long‐term synaptic modification in short‐term memory

Kesner, R. P., & Rolls, E. T. (2001) · Hippocampus · doi:10.1002/hipo.1040 · Cited by 95

The amygdala: is it an essential component of the neural network for social cognition?

Amaral, D. G., Bauman, M. D., Capitanio, J. P., Lavenex, P., Mason, W. A., Mauldin-Jourdain, M. L., & Mendoza, S. P. (2003) · Neuropsychologia · doi:10.1016/s0028-3932(02)00310-x · Cited by 95

Motility, behavior, and the brain.

YAKOVLEV, P. I. (1946) · PubMed · Cited by 93

Simulation studies of the CA3 hippocampal subfield modelled as an attractor neural network

Rolls, E. T., Treves, A., Foster, D. J., & Pérez-Vicente, C. (1997) · Neural Networks · doi:10.1016/s0893-6080(97)00092-0 · Cited by 92

The Representation of Information About Taste and Odor in the Orbitofrontal Cortex

Rolls, E. T., Critchley, H., Verhagen, J. V., & Kadohisa, M. (2009) · Chemosensory Perception · doi:10.1007/s12078-009-9054-4 · Cited by 91

Reward modulates neuronal activity in the hippocampus of the rat

Hölscher, C., Jacob, W., & Mallot, H. A. (2003) · Behavioural Brain Research · doi:10.1016/s0166-4328(02)00422-9 · Cited by 90

Handbook of Reward and Decision Making

Dreher, J., & Tremblay, L. (2009) · Elsevier eBooks · doi:10.1016/b978-0-12-374620-7.x0001-5 · Cited by 88

The Representation of Umami Taste in the Taste Cortex

Rolls, E. T. (2000) · Journal of Nutrition · doi:10.1093/jn/130.4.960s · Cited by 88

Different representations of relative and absolute subjective value in the human brain

Fabian Grabenhorst, B., & Rolls, E. T. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.06.045 · Cited by 86

Spatial memory and the monkey hippocampus: Not all space is created equal

Lavenex, P. B., & Lavenex, P. (2008) · Hippocampus · doi:10.1002/hipo.20485 · Cited by 85

Open Peer Review by a Selected-Papers Network

Lee, C. J. (2012) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2012.00001 · Cited by 85

Handbook of Olfaction and Gustation

Hirsch, A. R. (1995) · JAMA · doi:10.1001/jama.1995.03530180073039 · Cited by 82

The hippocampus, objects, and their contexts.

Cassaday, H. J., & Rawlins, J. N. P. (1997) · Behavioral Neuroscience · doi:10.1037/0735-7044.111.6.1228 · Cited by 82

Hippocampal Representation of Touch-Guided Behavior in Rats: Persistent and Independent Traces of Stimulus and Reward Location

Itskov, P. M., Vinnik, E., & Diamond, M. E. (2011) · PLoS ONE · doi:10.1371/journal.pone.0016462 · Cited by 81

The Neurophysiology of Taste and Olfaction in Primates, and Umami Flavora

ROLLS, E. T., CRITCHLEY, H. D., BROWNING, A., & HERNADI, I. (1998) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1998.tb10602.x · Cited by 80

The hippocampus, perirhinal cortex and memory in the monkey

Buckley, M. J., & Gaffan, D. (2000) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780198524823.003.0019 · Cited by 80

Neurobiology of the Hippocampus

Gray, J. A. (1985) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.48.1.94-a · Cited by 78

A biased activation theory of the cognitive and attentional modulation of emotion

Rolls, E. T. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00074 · Cited by 76

Perirhinal cortex neuronal activity related to long‐term familiarity memory in the macaque

Hölscher, C., Rolls, E. T., & Xiang, J.-Z. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02903.x · Cited by 75

Gustatory Neural Responses in the Medial Orbitofrontal Cortex of the Old World Monkey

Pritchard, T. C., Edwards, E. M., Smith, C. A., Hilgert, K. G., Gavlick, A. M., Maryniak, T. D., Schwartz, G. J., & Scott, T. R. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0430-05.2005 · Cited by 74

A common neural scale for the subjective pleasantness of different primary rewards

Fabian Grabenhorst, B., D’Souza, A., Parris, B. A., Rolls, E. T., & Passingham, R. E. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.03.043 · Cited by 72

Functions of the primate hippocampus in spatial and nonspatial memory

Rolls, E. T. (1991) · Hippocampus · doi:10.1002/hipo.450010310 · Cited by 67

The effect of satiety on responses of gustatory neurons in the amygdala of alert cynomolgus macaques

Yan, J., & Scott, T. R. (1996) · Brain Research · doi:10.1016/s0006-8993(96)00864-5 · Cited by 67

The Nonhuman Primate Amygdala Is Necessary for the Acquisition but not the Retention of Fear-Potentiated Startle

Antoniadis, E. A., Winslow, J., Davis, M., & Amaral, D. G. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.07.007 · Cited by 66

Reward value invariant place responses and reward site associated activity in hippocampal neurons of behaving rats

Tabuchi, E., Mulder, A. B., & Wiener, S. I. (2002) · Hippocampus · doi:10.1002/hipo.10056 · Cited by 65

Running Recognition of Configural Stimuli by Fornix-Transected Monkeys

Gaffan, D., & Saunders, R. C. (1985) · The Quarterly Journal of Experimental Psychology Section B · doi:10.1080/14640748508402087 · Cited by 63

Neural mediation of memory for time: Role of the hippocampus and medial prefrontal cortex

Kesner, R. P. (1998) · Psychonomic Bulletin & Review · doi:10.3758/bf03208836 · Cited by 62

Attentional Modulation of Affective Versus Sensory Processing: Functional Connectivity and a Top-Down Biased Activation Theory of Selective Attention

Fabian Grabenhorst, B., & Rolls, E. T. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00352.2010 · Cited by 62

The chemical senses

Gottfried, J. A., Small, D. M., & Zald, D. H. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780198565741.003.0006 · Cited by 62

Effects of satiety on self-stimulation of the orbitofrontal cortex in the rhesus monkey

Mora, F., AVRITH, D. B., Phillips, A. G., & Rolls, E. T. (1979) · Neuroscience Letters · doi:10.1016/0304-3940(79)90031-4 · Cited by 61

Attention-Dependent Modulation of Cortical Taste Circuits Revealed by Granger Causality with Signal-Dependent Noise

Luo, Q., Ge, T., Fabian Grabenhorst, B., Feng, J., & Rolls, E. T. (2013) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003265 · Cited by 61

Novel visual stimuli activate a population of neurons in the primate orbitofrontal cortex

Rolls, E. T., Browning, A. S., Inoue, K., & Hernádi, I. (2005) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2005.05.003 · Cited by 60

Componential Granger causality, and its application to identifying the source and mechanisms of the top–down biased activation that controls attention to affective vs sensory processing

Ge, T., Feng, J., Fabian Grabenhorst, B., & Rolls, E. T. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.08.047 · Cited by 60

Theoretical and Neurophysiological Analysis of the Functions of the Primate Hippocampus in MemoryPreprint

Rolls, E. T. (1990) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.1990.055.01.095 · Cited by 57

A hedonically complex odor mixture produces an attentional capture effect in the brain

Fabian Grabenhorst, B., Rolls, E. T., & Margot, C. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.12.023 · Cited by 55

Book Review: Object Categorization, Computer and Human Vision Perspectives

Yu, J., & Joshi, D. (2007) · Journal of Electronic Imaging · doi:10.1117/1.3487487 · Cited by 55

Foundations of neuroeconomic analysis

Levallois, C. (2012) · Journal of Economic Methodology · doi:10.1080/1350178x.2012.662334 · Cited by 52

An electrophysiological and behavioural study of self-stimulation in the orbitofrontal cortex of the rhesus monkey

Mora, F., AVRITH, D. B., & Rolls, E. T. (1980) · Brain Research Bulletin · doi:10.1016/0361-9230(80)90181-1 · Cited by 52

THE NEURAL REPRESENTATION OF ORAL TEXTURE INCLUDING FAT TEXTURE

Rolls, E. T. (2011) · Journal of Texture Studies · doi:10.1111/j.1745-4603.2011.00296.x · Cited by 50

Plasticity of the Hippocampal Place Cell Representation

Jeffery, K. J., & Hayman, R. M. A. (2004) · Reviews in the Neurosciences · doi:10.1515/revneuro.2004.15.5.309 · Cited by 42

The primate amygdala and reinforcement: A dissociation between rule-based and associatively-mediated memory revealed in neuronal activity

Wilson, F. A. W., & Rolls, E. T. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.03.022 · Cited by 39

Top — Down Control of Visual Perception: Attention in Natural Vision

Rolls, E. T. (2008) · Perception · doi:10.1068/p5877 · Cited by 38

Symposium Overview: What Happens to the Pontine Processing? Repercussions of Interspecies Differences in Pontine Taste Representation for Tasting and Feeding

Small, D. M., & Scott, T. R. (2009) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2009.03918.x · Cited by 37

Spatial scene representations formed by self‐organizing learning in a hippocampal extension of the ventral visual system

Rolls, E. T., Tromans, J. M., & Stringer, S. M. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06486.x · Cited by 36

Greater orbitofrontal activity predicts better memory for faces

Frey, S., & Petrides, M. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02714.x · Cited by 34

Taste, Olfactory, Visual, and Somatosensory Representations of the Sensory Properties of Foods in the Brain, and Their Relation to the Control of Food Intake

Rolls, E. T. (1999) · CRC Press eBooks · doi:10.1201/9781420048933.sec3 · Cited by 32

Selective Ablations Reveal That Orbital and Lateral Prefrontal Cortex Play Different Roles in Estimating Predicted Reward Value

Simmons, J. M., Minamimoto, T., Murray, E. A., & Richmond, B. J. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.1802-10.2010 · Cited by 30

Face processing in different brain areas, and critical band masking

Rolls, E. T. (2008) · Journal of Neuropsychology · doi:10.1348/174866407x258903 · Cited by 28

The Perirhinal Cortex and Long-Term Familiarity Memory

Rolls, E. T., Franco, L., & Stringer, S. M. (2005) · The Quarterly Journal of Experimental Psychology Section B · doi:10.1080/02724990444000122 · Cited by 26

Different representations of relative and absolute value in the human brain

Rolls, E. T. (2008) · Frontiers in Human Neuroscience · doi:10.3389/conf.neuro.09.2009.01.201 · Cited by 20

Central Taste Anatomy and Neurophysiology

Scott, T. R., & Rolls, E. T. (2003) · CRC Press eBooks · doi:10.1201/9780203911457.ch33 · Cited by 17

Spatial, Temporal, and Associative Behavioral Functions Associated with Different Subregions of the Hippocampus

Kesner, R. P., Morris, A. M., & Weeden, C. S. S. (2012) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780195392661.013.0018 · Cited by 15

The Neurophysiology and Computational Mechanisms of Object Representation

Rolls, E. T. (2009) · Cambridge University Press eBooks · doi:10.1017/cbo9780511635465.015 · Cited by 12

From reward value to decision-making

Rolls, E. T. (2009) · Elsevier eBooks · doi:10.1016/b978-0-12-374620-7.00005-4 · Cited by 12

Prefrontal cortical projections to the striatum in macaque monkeys: Evidence for an organization related to prefrontal networks

(2000) · doi:10.1002/1096-9861(20000925)425:3

Connectional networks within the orbital and medial prefrontal cortex of macaque monkeys

Carmichael, S. T., & Price, J. L. (1996) · Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19960722)371:2<179::aid-cne1>3.0.co;2-#

The cingulate cortex and limbic systems for emotion, action, and memory

Rolls, E. T. (2019) · Brain Structure and Function · doi:10.1007/s00429-019-01945-2 · Cited by 859

The cingulum bundle: Anatomy, function, and dysfunction

Bubb, E. J., Metzler-Baddeley, C., & Aggleton, J. P. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.05.008 · Cited by 740

The mechanisms for pattern completion and pattern separation in the hippocampus

Rolls, E. T. (2013) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2013.00074 · Cited by 545

A computational theory of hippocampal function, and tests of the theory: New developments

Kesner, R. P., & Rolls, E. T. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.11.009 · Cited by 347

State-dependent architecture of thalamic reticular subnetworks

Halassa, M. M., Chen, Z., Wimmer, R. D., Brunetti, P. M., Zhao, S., Zikopoulos, B., Wang, F., Brown, E. N., & Wilson, M. A. (2014) · Cell · doi:10.1016/j.cell.2014.06.025 · Cited by 309