Cortical remodelling induced by activity of ventral tegmental dopamine neurons

Neuronal Synchrony: A Versatile Code for the Definition of Relations?

Singer, W. (1999) · Neuron · doi:10.1016/s0896-6273(00)80821-1 · Cited by 2,581 · see citing works

CORTICAL PLASTICITY: From Synapses to Maps

Buonomano, D. V., & Merzenich, M. M. (1998) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.21.1.149 · Cited by 2,083 · see citing works

A framework for mesencephalic dopamine systems based on predictive Hebbian learning

Montague, P., Dayan, P., & Sejnowski, T. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-05-01936.1996 · Cited by 2,066 · see citing works

Neural substrates for the effects of rehabilitative training on motor recovery after ischemic infarct

Nudo, R. J., Wise, B. M., SiFuentes, F., & Milliken, G. W. (1996) · Science · doi:10.1126/science.272.5269.1791 · Cited by 1,911 · see citing works

Neuronal Coding of Prediction Errors

Schultz, W., & Dickinson, A. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.473 · Cited by 1,427 · see citing works

Information processing in the primate visual system: an integrated systems perspective

Van Essen, D. C., Anderson, C. H., & Felleman, D. J. (1992) · Science · doi:10.1126/science.1734518 · Cited by 1,266 · see citing works

Plasticity in the frequency representation of primary auditory cortex following discrimination training in adult owl monkeys

Recanzone, G., Schreiner, C., & Merzenich, M. (1993) · The Journal of Neuroscience · doi:10.1523/jneurosci.13-01-00087.1993 · Cited by 1,266 · see citing works

Plasticity and Primary Motor Cortex

Sanes, J. N., & Donoghue, J. P. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.393 · Cited by 1,202 · see citing works

Cortical Map Reorganization Enabled by Nucleus Basalis Activity

Kilgard, M. P., & Merzenich, M. M. (1998) · Science · doi:10.1126/science.279.5357.1714 · Cited by 1,197 · see citing works

Dopamine neurons report an error in the temporal prediction of reward during learning

Hollerman, J. R., & Schultz, W. (1998) · Nature Neuroscience · doi:10.1038/1124 · Cited by 1,103 · see citing works

Learning-Induced LTP in Neocortex

Rioult-Pedotti, M.-S., Friedman, D. J., & Donoghue, J. P. (2000) · Science · doi:10.1126/science.290.5491.533 · Cited by 1,014 · see citing works

Ventral tegmental (A10) system: neurobiology. 1. Anatomy and connectivity

Oades, R. D., & Halliday, G. M. (1987) · Brain Research Reviews · doi:10.1016/0165-0173(87)90011-7 · Cited by 1,008 · see citing works

Functional reorganization of primary somatosensory cortex in adult owl monkeys after behaviorally controlled tactile stimulation

Jenkins, W. M., Merzenich, M. M., Ochs, M. T., Allard, T., & Guic-Robles, E. (1990) · Journal of Neurophysiology · doi:10.1152/jn.1990.63.1.82 · Cited by 937 · see citing works

Interhemispheric Synchronization of Oscillatory Neuronal Responses in Cat Visual Cortex

Engel, A. K., Peter König, B., Kreiter, A. K., & Singer, W. (1991) · Science · doi:10.1126/science.252.5009.1177 · Cited by 914 · see citing works

A mechanism for generation of long-range synchronous fast oscillations in the cortex

Traub, R. D., Whittington, M. A., Stanford, I. M., & Jefferys, J. G. R. (1996) · Nature · doi:10.1038/383621a0 · Cited by 701 · see citing works

Extrathalamic Modulation of Cortical Function

Foote, S. L., & Morrison, J. (1987) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.10.030187.000435 · Cited by 480 · see citing works

Induction of a physiological memory in the cerebral cortex by stimulation of the nucleus basalis.

Bakin, J. S., & Weinberger, N. M. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.20.11219 · Cited by 478 · see citing works

The cerebral cortex of the rat

(1991) · Comparative Biochemistry and Physiology Part A Physiology · doi:10.1016/0300-9629(91)90172-9 · Cited by 416 · see citing works

Distribution of dopaminergic receptors in the primate cerebral cortex: Quantitative autoradiographic analysis using [3H]raclopride, [3H]spiperone and [3H]SCH23390

Lidow, M. S., Goldman-Rakic, P. S., Gallager, D. W., & Rakic, P. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90003-7 · Cited by 394 · see citing works

Essential Role of D1 But Not D2 Receptors in the NMDA Receptor-Dependent Long-Term Potentiation at Hippocampal-Prefrontal Cortex SynapsesIn Vivo

Gurden, H., Takita, M., & Jay, T. M. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-22-j0003.2000 · Cited by 366 · see citing works

Plasticity of temporal information processing in the primary auditory cortex

Kilgard, M. P., & Merzenich, M. M. (1998) · Nature Neuroscience · doi:10.1038/3729 · Cited by 298 · see citing works

Electrophysiological studies of acetylcholine and the role of the basal forebrain in the somatosensory cortex of the cat. II. Cortical neurons excited by somatic stimuli

Tremblay, N. A., Warren, R. A., & Dykes, R. W. (1990) · Journal of Neurophysiology · doi:10.1152/jn.1990.64.4.1212 · Cited by 221 · see citing works

Association areas of the cerebral cortex

Pandya, D. Ν., & Seltzer, B. (1982) · Trends in Neurosciences · doi:10.1016/0166-2236(82)90219-3 · Cited by 218 · see citing works

Classical conditioning rapidly induces specific changes in frequency receptive fields of single neurons in secondary and ventral ectosylvian auditory cortical fields

Diamond, D. M., & Weinberger, N. M. (1986) · Brain Research · doi:10.1016/0006-8993(86)91144-3 · Cited by 185 · see citing works

D1/D5 Dopamine Receptors Inhibit Depotentiation at CA1 Synapses via cAMP-Dependent Mechanism

Otmakhova, N. A., & Lisman, J. E. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-04-01270.1998 · Cited by 176 · see citing works

Role of the Basal Forebrain Cholinergic Projection in Somatosensory Cortical Plasticity

Sachdev, R. N. S., Lu, S., Wiley, R. G., & Ebner, F. F. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.79.6.3216 · Cited by 116 · see citing works

Induction of receptive field plasticity in the auditory cortex of the guinea pig during instrumental avoidance conditioning.

Bakin, J. S., South, D. A., & Weinberger, N. M. (1996) · Behavioral Neuroscience · doi:10.1037//0735-7044.110.5.905 · Cited by 90 · see citing works

Dopaminergic and Serotonergic Neurotransmission Systems Are Differentially Involved in Auditory Cortex Learning: A Long‐Term Microdialysis Study of Metabolites

Stark, H., & Scheich, H. (1997) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1997.68020691.x · Cited by 86 · see citing works

Induction of receptive field plasticity in the auditory cortex of the guinea pig during instrumental avoidance conditioning.

Bakin, J. S., South, D. A., & Weinberger, N. M. (1996) · Behavioral Neuroscience · doi:10.1037/0735-7044.110.5.905 · Cited by 77 · see citing works

The identification of some sources of afferent input to the rat nucleus basalis magnocellularis by retrograde transport of horseradish peroxidase

Haring, J. H., & Wang, R. Y. (1986) · Brain Research · doi:10.1016/0006-8993(86)91290-4 · Cited by 64 · see citing works

Dopamine D2 receptors are organized in bands in normal human temporal cortex

Goldsmith, S. K., & Joyce, J. N. (1996) · Neuroscience · doi:10.1016/0306-4522(96)00132-7 · Cited by 50 · see citing works

Model of autism: increased ratio of excitation/inhibition in key neural systems

Rubenstein, J. L. R., & Merzenich, M. M. (2003) · Genes, Brain and Behavior · doi:10.1034/j.1601-183x.2003.00037.x · Cited by 2,768 · see citing works

Getting formal with dopamine and reward

Schultz, W. (2002) · Neuron · doi:10.1016/s0896-6273(02)00967-4 · Cited by 2,574 · see citing works

Long-term dendritic spine stability in the adult cortex

Grutzendler, J., Kasthuri, N., & Gan, W.-B. (2002) · Nature · doi:10.1038/nature01276 · Cited by 1,198 · see citing works

Neuronal Reward and Decision Signals: From Theories to Data

Schultz, W. (2015) · Physiological Reviews · doi:10.1152/physrev.00023.2014 · Cited by 1,126 · see citing works

Behavioral dopamine signals.

Schultz, W. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.03.007 · Cited by 1,028 · see citing works

Learned predictions of error likelihood in the anterior cingulate cortex

Brown, J. W., & Braver, T. S. (2005) · Science · doi:10.1126/science.1105783 · Cited by 928 · see citing works

Exercising your brain: A review of human brain plasticity and training-induced learning.

Green, C. S., & Bavelier, D. (2008) · Psychology and Aging · doi:10.1037/a0014345 · Cited by 660 · see citing works

Removing brakes on adult brain plasticity: From molecular to behavioral interventions

Bavelier, D., Levi, D. M., Li, R. W., Dan, Y., & Hensch, T. K. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4812-10.2010 · Cited by 589 · see citing works

The origin of mind: Evolution of brain, cognition, and general intelligence.

Geary, D. C. (2005) · doi:10.1037/10871-000 · Cited by 551 · see citing works

Brain plasticity through the life span: Learning to learn and action video games

Bavelier, D., Green, C. S., Pouget, A., & Schrater, P. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-060909-152832 · Cited by 541 · see citing works

Environmental influences on the pace of brain development

Tooley, U. A., Bassett, D. S., & Mackey, A. P. (2021) · Nature reviews. Neuroscience · doi:10.1038/s41583-021-00457-5 · Cited by 488 · see citing works

Plasticity of Cortical Excitatory-Inhibitory Balance

Froemke, R. C. (2015) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071714-034002 · Cited by 458 · see citing works

Toward a neurobiology of delusions

Corlett, P. R., Taylor, J. R., Wang, X.-J., Fletcher, P. C., & Krystal, J. H. (2010) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2010.06.007 · Cited by 394 · see citing works

From drugs to deprivation: A Bayesian framework for understanding models of psychosis

Corlett, P. R., Frith, C. D., & Fletcher, P. C. (2009) · Psychopharmacology · doi:10.1007/s00213-009-1561-0 · Cited by 367 · see citing works

Reconciling reinforcement learning models with behavioral extinction and renewal: implications for addiction, relapse, and problem gambling

Redish, A. D., Jensen, S., Johnson, A., & Kurth-Nelson, Z. (2007) · Psychological Review · doi:10.1037/0033-295x.114.3.784 · Cited by 346 · see citing works

Listening to tailor-made notched music reduces tinnitus loudness and tinnitus-related auditory cortex activity

Okamoto, H., Stracke, H., Stoll, W., & Pantev, C. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0911268107 · Cited by 311 · see citing works

Biased Oxytocinergic Modulation of Midbrain Dopamine Systems

Xiao, L., Priest, M. F., Nasenbeny, J., Lu, T., & Kozorovitskiy, Y. (2017) · Neuron · doi:10.1016/j.neuron.2017.06.003 · Cited by 292 · see citing works

A common framework for perceptual learning

Seitz, A. R., & Dinse, H. R. (2007) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2007.02.004 · Cited by 276 · see citing works

Temporal plasticity in the primary auditory cortex induced by operant perceptual learning

Bao, S., Chang, E. F., Woods, J., & Merzenich, M. M. (2004) · Nature Neuroscience · doi:10.1038/nn1293 · Cited by 265 · see citing works

Coordinated forms of noradrenergic plasticity in the locus coeruleus and primary auditory cortex

Martins, A. R. O., & Froemke, R. C. (2015) · Nature Neuroscience · doi:10.1038/nn.4090 · Cited by 233 · see citing works

Underconnectivity between voice-selective cortex and reward circuitry in children with autism

Abrams, D. A., Lynch, C. J., Cheng, K. M., Phillips, J., Supekar, K., Ryali, S., Uddin, L. Q., & Menon, V. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1302982110 · Cited by 250 · see citing works

A circuit for motor cortical modulation of auditory cortical activity

Nelson, A., Schneider, D. M., Takatoh, J., Sakurai, K., Wang, F., & Mooney, R. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.2275-13.2013 · Cited by 213 · see citing works

From prediction error to psychosis: Ketamine as a pharmacological model of delusions

Corlett, P. R., Honey, G. D., & Fletcher, P. C. (2007) · Journal of Psychopharmacology · doi:10.1177/0269881107077716 · Cited by 227 · see citing works

Brain and cognitive evolution: Forms of modularity and functions of mind.

Geary, D. C., & Huffman, K. J. (2002) · Psychological Bulletin · doi:10.1037/0033-2909.128.5.667 · Cited by 234 · see citing works

Associative representational plasticity in the auditory cortex: a synthesis of two disciplines

Weinberger, N. M. (2007) · Learning & Memory · doi:10.1101/lm.421807 · Cited by 223 · see citing works

Human neural learning depends on reward prediction errors in the blocking paradigm.

Tobler, P. N., O’Doherty, J. P., Dolan, R. J., & Schultz, W. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00762.2005 · Cited by 209 · see citing works

Children, wired: for better and for worse

Bavelier, D., Green, C. S., & Dye, M. W. G. (2010) · Neuron · doi:10.1016/j.neuron.2010.08.035 · Cited by 193 · see citing works

Perceptual learning during action video game playing

Green, C. S., Li, R., & Bavelier, D. (2010) · Topics in Cognitive Science · doi:10.1111/j.1756-8765.2009.01054.x · Cited by 182 · see citing works

Experience-Dependent Adult Cortical Plasticity Requires Cognitive Association between Sensation and Reward

Blake, D. T., Heiser, M. A., Caywood, M., & Merzenich, M. M. (2006) · Neuron · doi:10.1016/j.neuron.2006.08.009 · Cited by 150 · see citing works

Cell-based reporters reveal in vivo dynamics of dopamine and norepinephrine release in murine cortex

Muller, A., Joseph, V., Slesinger, P. A., & Kleinfeld, D. (2014) · Nature Methods · doi:10.1038/nmeth.3151 · Cited by 139 · see citing works

Computational psychiatry: a Rosetta Stone linking the brain to mental illness

Corlett, P. R., & Fletcher, P. C. (2014) · The Lancet Psychiatry · doi:10.1016/s2215-0366(14)70298-6 · Cited by 105 · see citing works

An integrative framework for perceptual disturbances in psychosis

Horga, G., & Abi-Dargham, A. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0234-1 · Cited by 103 · see citing works

Neuroenhancement of love and marriage: the chemicals between us.

Savulescu, J., & Sandberg, A. (2008) · Neuroethics · doi:10.1007/s12152-007-9002-4 · Cited by 111 · see citing works

Improved cortical entrainment to infant communication calls in mothers compared with virgin mice

Liu, R. C., Linden, J. F., & Schreiner, C. E. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04840.x · Cited by 112 · see citing works

Cortical Plasticity, Excitatory–Inhibitory Balance, and Sensory Perception

Carcea, I., & Froemke, R. C. (2013) · Progress in Brain Research · doi:10.1016/b978-0-444-63327-9.00003-5 · Cited by 110 · see citing works

Tracing the Trajectory of Sensory Plasticity across Different Stages of Speech Learning in Adulthood

Reetzke, R., Xie, Z., Llanos, F., & Chandrasekaran, B. (2018) · Current Biology · doi:10.1016/j.cub.2018.03.026 · Cited by 90 · see citing works

Neuroplasticity-based computerized cognitive remediation for treatment-resistant geriatric depression

Morimoto, S. S., Wexler, B. E., Liu, J., Hu, W., Seirup, J., & Alexopoulos, G. S. (2014) · Nature Communications · doi:10.1038/ncomms5579 · Cited by 91 · see citing works

Synaptic dynamism measured over minutes to months: Age-dependent decline in an autonomic ganglion

Gan, W.-B., Kwon, E., Feng, G., Sanes, J. R., & Lichtman, J. W. (2003) · Nature Neuroscience · doi:10.1038/nn1115 · Cited by 84 · see citing works

Storing maternal memories: hypothesizing an interaction of experience and estrogen on sensory cortical plasticity to learn infant cues

Banerjee, S. B., & Liu, R. C. (2013) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2013.07.008 · Cited by 58 · see citing works

Dissecting natural sensory plasticity: hormones and experience in a maternal context

Miranda, J. A., & Liu, R. C. (2009) · Hearing Research · doi:10.1016/j.heares.2009.04.014 · Cited by 52 · see citing works

Norepinephrine Is Necessary for Experience-Dependent Plasticity in the Developing Mouse Auditory Cortex

Shepard, K. N., Liles, L. C., Weinshenker, D., & Liu, R. C. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.0532-14.2015 · Cited by 47 · see citing works

SY02VENTRAL TEGMENTAL AREA DOPAMINE NEURONS AND ETHANOL: THE PUZZLE TO DISENTANGLESY02-1HETEROGENEITY OF ETHANOL RESPONSES IN THE VENTRAL TEGMENTAL AREA

Martí‐Prats, L., Orrico, A., Sánchez-Catalán, M. J., et al. (2015) · Alcohol and Alcoholism · doi:10.1093/alcalc/agv076.05

P352. Ventral Tegmental Area Integrity Measured With 400μm3 MRI in Depression and Anxiety

Morris, L. S., Mehta, M., Ahn, C., et al. (2022) · Biological Psychiatry · doi:10.1016/j.biopsych.2022.02.588

Chronic nicotine treatment decreases neurofilament immunoreactivity in the rat ventral tegmental area

Bunnemann, B., Terron, A., Zantedeschi, V., Pich, E. M., & Chiamulera, C. (2000) · European Journal of Pharmacology · doi:10.1016/s0014-2999(00)00104-7 · Cited by 16 · see citing works

Extracellular dopamine in the rat ventral tegmental area and nucleus accumbens following ventral tegmental infusion of cocaine.

Chen, S.-Y., Burger, R. L., & Reith, M. E. A. (1996) · PubMed · Cited by 11 · see citing works

Release of dopamine in the ventral tegmental area of rat.

Fadda, F., Mr, M., Argiolas, A., et al. (1979) · PubMed