Neural responses to acute cocaine administration in the human brain detected by fMRI

AFNI: Software for analysis and visualization of functional magnetic resonance neuroimages

Cox, R. W. (1996) · Computers and Biomedical Research · doi:10.1006/cbmr.1996.0014 · Cited by 10,913 · see citing works

Neurophysiological investigation of the basis of the fMRI signal

Logothetis, N. K., Pauls, J., Augath, M., Trinath, T., & Oeltermann, A. (2001) · Nature · doi:10.1038/35084005 · Cited by 6,542 · see citing works

Predictive reward signal of dopamine neurons

Schultz, W. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.1.1 · Cited by 4,564 · see citing works

Improved assessment of significant activation in functional magnetic resonance imaging (fMRI): use of a cluster-size threshold

Forman, S. D., Cohen, J. D., Fitzgerald, M., Eddy, W. F., Mintun, M. A., & Noll, D. C. (1995) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910330508 · Cited by 3,202 · see citing works

Drug Addiction and Its Underlying Neurobiological Basis: Neuroimaging Evidence for the Involvement of the Frontal Cortex

Goldstein, R. Z., & Volkow, N. D. (2002) · American Journal of Psychiatry · doi:10.1176/appi.ajp.159.10.1642 · Cited by 2,667 · see citing works

The Organization of Networks within the Orbital and Medial Prefrontal Cortex of Rats, Monkeys and Humans

Ongur, D. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.206 · Cited by 2,627 · see citing works

Emotion and motivation: the role of the amygdala, ventral striatum, and prefrontal cortex

Cardinal, R. N., Parkinson, J. A., Hall, J., & Everitt, B. J. (2002) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(02)00007-6 · Cited by 2,129 · see citing works

Cellular and molecular mechanisms of drug dependence

Koob, G. F., & Bloom, F. E. (1988) · Science · doi:10.1126/science.2903550 · Cited by 2,070 · see citing works

The Biochemical Basis of Neuropharmacology.

(1974) · Annals of Internal Medicine · doi:10.7326/0003-4819-81-4-575_2 · Cited by 1,882 · see citing works

The Orbitofrontal Cortex and Reward

Rolls, E. T. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.284 · Cited by 1,595 · see citing works

Impulsivity resulting from frontostriatal dysfunction in drug abuse: implications for the control of behavior by reward-related stimuli

Jentsch, J. D., & Taylor, J. R. (1999) · Psychopharmacology · doi:10.1007/pl00005483 · Cited by 1,545 · see citing works

Addiction

Robinson, T. E., & Berridge, K. C. (2003) · Annual Review of Psychology · doi:10.1146/annurev.psych.54.101601.145237 · Cited by 1,509 · see citing works

Correction for geometric distortion in echo planar images from B0 field variations

Jezzard, P., & Balaban, R. S. (1995) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910340111 · Cited by 1,428 · see citing works

Relative reward preference in primate orbitofrontal cortex

Tremblay, L., & Schultz, W. (1999) · Nature · doi:10.1038/19525 · Cited by 1,314 · see citing works

Acute effects of cocaine on human brain activity and emotion

Breiter, H. C., Gollub, R. L., Weisskoff, R. M., Kennedy, D. N., Makris, N., Berke, J. D., Goodman, J. M., Kantor, H. L., Gastfriend, D. R., Riorden, J. P., et al. (1997) · Neuron · doi:10.1016/s0896-6273(00)80374-8 · Cited by 1,270 · see citing works

Addiction, a disease of compulsion and drive: involvement of the orbitofrontal cortex

Volkow, N. D. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.318 · Cited by 1,240 · 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

Anterior prefrontal cortex: insights into function from anatomy and neuroimaging

Ramnani, N., & Owen, A. M. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1343 · Cited by 1,170 · see citing works

Subsecond dopamine release promotes cocaine seeking

Phillips, P. E. M., Stuber, G. D., Heien, M. L. A. V., Wightman, R. M., & Carelli, R. M. (2003) · Nature · doi:10.1038/nature01476 · Cited by 1,113 · see citing works

Cocaine and Other Stimulants

Gawin, F. H., & Ellinwood, E. H. (1988) · New England Journal of Medicine · doi:10.1056/nejm198805053181806 · Cited by 965 · see citing works

Reward processing in primate orbitofrontal cortex and basal ganglia

Schultz, W. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.272 · Cited by 942 · see citing works

Activation of memory circuits during cue-elicited cocaine craving.

Grant, S., London, E. D., Newlin, D. B., Villemagne, V. L., Liu, X., Contoreggi, C., Phillips, R. L., Kimes, A. S., & Margolin, A. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.21.12040 · Cited by 936 · see citing works

Cue-induced cocaine craving: neuroanatomical specificity for drug users and drug stimuli

Garavan, H., Pankiewicz, J., Bloom, A., Cho, J.-K., Sperry, L., Ross, T. J., Salmeron, B. J., Risinger, R., Kelley, D., & Stein, E. A. (2000) · American Journal of Psychiatry · doi:10.1176/appi.ajp.157.11.1789 · Cited by 931 · see citing works

Dopaminergic modulation of neuronal excitability in the striatum and nucleus accumbens

Nicola, S. M., Surmeier, D. J., & Malenka, R. C. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.185 · Cited by 931 · see citing works

The addicted human brain: insights from imaging studies

Volkow, N. D., Fowler, J. S., & Wang, G.-J. (2003) · Journal of Clinical Investigation · doi:10.1172/jci18533 · Cited by 916 · see citing works

The circuitry mediating cocaine-induced reinstatement of drug-seeking behavior

McFarland, K., & Kalivas, P. W. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-21-08655.2001 · Cited by 905 · see citing works

Brain Reward Circuitry

Wise, R. A. (2002) · Neuron · doi:10.1016/s0896-6273(02)00965-0 · Cited by 881 · see citing works

Orbitofrontal cortex and basolateral amygdala encode expected outcomes during learning

Schoenbaum, G. M., Chiba, A. A., & Gallagher, M. (1998) · Nature Neuroscience · doi:10.1038/407 · Cited by 849 · see citing works

Memory and Addiction

Kelley, A. E. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.016 · Cited by 773 · see citing works

Drug-activation of brain reward pathways

Wise, R. A. (1998) · Drug and Alcohol Dependence · doi:10.1016/s0376-8716(98)00063-5 · Cited by 684 · see citing works

Relationship between subjective effects of cocaine and dopamine transporter occupancy

Volkow, N. D., Wang, G., Fischman, M. W., Foltin, R. W., Fowler, J. S., Abumrad, N. N., Vitkun, S. A., Logan, J., Gatley, S. J., Pappas, N. R., et al. (1997) · Nature · doi:10.1038/386827a0 · Cited by 646 · see citing works

Dissociating valence of outcome from behavioral control in human orbital and ventral prefrontal cortices

O'Doherty, J., Critchley, H., Deichmann, R., & Dolan, R. J. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-21-07931.2003 · Cited by 611 · 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 activity related to drug craving in cocaine addiction

Kilts, C. D., Schweitzer, J. B., Quinn, C. K., Gross, R. E., Faber, T. L., Muhammad, F., Ely, T. D., Hoffman, J. M., & Drexler, K. P. G. (2001) · Archives of General Psychiatry · doi:10.1001/archpsyc.58.4.334 · Cited by 556 · see citing works

Susceptibility-Induced Loss of Signal: Comparing PET and fMRI on a Semantic Task

Devlin, J. T., Russell, R. P., Davis, M. H., Price, C. J., Wilson, J. L., Moss, H. E., Matthews, P. M., & TYLER, L. K. (2000) · NeuroImage · doi:10.1006/nimg.2000.0595 · Cited by 439 · see citing works

Prefrontal responses to drug cues: a neurocognitive analysis

Wilson, S. J., Sayette, M. A., & Fiez, J. A. (2004) · Nature Neuroscience · doi:10.1038/nn1200 · Cited by 408 · see citing works

The Biochemical Basis of Neuropharmacology

Jellinger, K. A. (2003) · European Journal of Neurology · doi:10.1046/j.1468-1331.2003.00586.x · Cited by 372 · see citing works

Orbitofrontal Cortex and Human Drug Abuse: Functional Imaging

London, E. D. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.334 · Cited by 360 · see citing works

Neurobiology of cocaine abuse

Woolverton, W. L., & Johnson, K. M. (1992) · Trends in Pharmacological Sciences · doi:10.1016/0165-6147(92)90063-c · Cited by 355 · see citing works

Drug addiction as dopamine-dependent associative learning disorder

Chiara, G. D. (1999) · European Journal of Pharmacology · doi:10.1016/s0014-2999(99)00372-6 · Cited by 317 · see citing works

Cocaine-Induced Redoppuction of Glucose Utilization in Human Brain

London, E. D. (1990) · Archives of General Psychiatry · doi:10.1001/archpsyc.1990.01810180067010 · Cited by 305 · see citing works

Neurotransmitter systems of the medial prefrontal cortex: potential role in sensitization to psychostimulants

Steketee, J. (2003) · Brain Research Reviews · doi:10.1016/s0165-0173(02)00233-3 · Cited by 293 · see citing works

Functional Magnetic Resonance Imaging of Brain Reward Circuitry in the Human

BREITER, H. C., & Rosen, B. R. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb09287.x · Cited by 231 · see citing works

Brain Function and Neurophysiological Correlates of Signals Used in Functional Neuroimaging

Lauritzen, M., & Gold, L. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-10-03972.2003 · Cited by 187 · see citing works

Cocaine Activation Discriminates Dopaminergic Projections by Temporal Response: An fMRI Study in Rat

Marota, J. J. A., Mandeville, J. B., Weisskoff, R. M., Moskowitz, M. A., Rosen, B. R., & Kosofsky, B. E. (2000) · NeuroImage · doi:10.1006/nimg.1999.0520 · Cited by 163 · see citing works

Functional MRI of the Human Amygdala?

Merboldt, K., Fransson, P., Bruhn, H., & Frahm, J. (2001) · NeuroImage · doi:10.1006/nimg.2001.0802 · Cited by 162 · see citing works

The dopamine-containing neuron: maestro or simple musician in the orchestra of addiction?

Bonci, A., Bernardi, G., Grillner, P., & Mercuri, N. B. (2003) · Trends in Pharmacological Sciences · doi:10.1016/s0165-6147(03)00068-3 · Cited by 160 · see citing works

Excitatory and inhibitory effects of dopamine on neuronal activity of the caudate nucleus neurons in vitro

Akaike, A., Ohno, Y., Sasa, M., & Takaori, S. (1987) · Brain Research · doi:10.1016/0006-8993(87)90094-1 · Cited by 154 · see citing works

Diffusion imaging of the spinal cord in vivo: Estimation of the principal diffusivities and application to multiple sclerosis

Clark, C. A., Werring, D. J., & Miller, D. H. (2000) · Magnetic Resonance in Medicine · doi:10.1002/(sici)1522-2594(200001)43:1 · Cited by 150 · see citing works

Self‐Administration of Cocaine by Humans: A Laboratory Perspective

Fischman, M. W., & Foltin, R. W. (2007) · Novartis Foundation symposium · doi:10.1002/9780470514245.ch10 · Cited by 127 · see citing works

Cocaine alters cerebral metabolism within the ventral striatum and limbic cortex of monkeys

Huston-Lyons, D., Friedman, D. P., Nader, M. A., & Porrino, L. J. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-03-01230.1996 · Cited by 120 · see citing works

Cocaine Decreases Cortical Cerebral Blood Flow but Does Not Obscure Regional Activation in Functional Magnetic Resonance Imaging in Human Subjects

Gollub, R. L., Breiter, H. C., Kantor, H. L., Kennedy, D. N., Gastfriend, D. R., Mathew, R. T., Makris, N., Guimarães, A. R., Riorden, J., Campbell, T., et al. (1998) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-199807000-00003 · Cited by 120 · see citing works

Selective alterations in cerebral metabolism within the mesocorticolimbic dopaminergic system produced by acute cocaine administration in rats

Porrino, L. J. (1988) · Neuropsychopharmacology · doi:10.1016/0893-133x(88)90002-4 · Cited by 117 · see citing works

Correlation of acute cocaine-induced changes in local cerebral blood flow with subjective effects

Pearlson, G. D., Jeffery, P. J., Harris, G. J., Ross, C. A., Fischman, M. W., & Camargo, E. E. (1993) · American Journal of Psychiatry · doi:10.1176/ajp.150.3.495 · Cited by 103 · see citing works

Metabolic Mapping of the Effects of Cocaine during the Initial Phases of Self-Administration in the Nonhuman Primate

Porrino, L. J., Huston-Lyons, D., Miller, M. D., Smith, H. R., Friedman, D. P., Daunais, J. B., & Nader, M. A. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-17-07687.2002 · Cited by 89 · see citing works

Acute cocaine effects on absolute cerebral blood flow

Wallace, E. A., Wisniewski, G., Zubal, G. I., vanDyck, C., Pfau, S. E., Smith, E. O., Rosen, M. I., Sullivan, M. C., Woods, S. W., & Kosten, T. R. (1996) · Psychopharmacology · doi:10.1007/s002130050104 · Cited by 77 · see citing works

Episodic Memory Meets Working Memory in the Frontal Lobe: Functional Neuroimaging Studies of Encoding and Retrieval

Lee, A. C. H., Robbins, T. W., & Owen, A. M. (2000) · Critical Reviews in Neurobiology · doi:10.1615/critrevneurobiol.v14.i3-4.10 · Cited by 70 · see citing works

A critique of the use of the Kolmogorov‐Smirnov (KS) statistic for the analysis of BOLD fMRI data

Aguirre, G. K., Zarahn, E., & D’Esposito, M. (1998) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910390322 · Cited by 69 · see citing works

Characterization of effects of mean arterial blood pressure induced by cocaine and cocaine methiodide on BOLD signals in rat brain

Luo, F. R., Wu, G., Li, Z., & Li, S. (2003) · Magnetic Resonance in Medicine · doi:10.1002/mrm.10366 · Cited by 63 · see citing works

Cocaine-induced brain activation determined by positron emission tomography neuroimaging in conscious rhesus monkeys

Howell, L. L., Hoffman, J. M., Votaw, J. R., Landrum, A. M., Wilcox, K. M., & Lindsey, K. P. (2001) · Psychopharmacology · doi:10.1007/s002130100911 · Cited by 62 · see citing works

Cocaine : scientific and social dimensions

Bock, G., & Whelan, J. (1992) · Cited by 39 · see citing works

Multiecho segmented EPI with z‐shimmed background gradient compensation (MESBAC) pulse sequence for fMRI

Li, Z., Wu, G., Zhao, X., Luo, F. R., & Li, S. (2002) · Magnetic Resonance in Medicine · doi:10.1002/mrm.10219 · Cited by 29 · see citing works

Effects of lesions of the nucleus basalis magnocellularis on the acquisition of cocaine self-administration in rats

Robledo, P., Weissenborn, R., Robbins, T. W., & Everitt, B. J. (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00204.x · Cited by 16 · see citing works

Cocaine: Scientific and Social Dimensions (Ciba Foundation Symposium 166)

Nunes, E. V. (1994) · Journal of Neuropsychiatry · doi:10.1176/jnp.6.2.195 · Cited by 13 · see citing works

The Scientific Exegesis of Desire

Gawin, F. H. (2001) · Archives of General Psychiatry · doi:10.1001/archpsyc.58.4.342 · Cited by 7 · see citing works

High-resolution intersubject averaging and a coordinate system for the cortical surface

Fischl, B., Sereno, M. I., Tootell, R. B. H., & Dale, A. M. (1999) · Human Brain Mapping · doi:10.1002/(sici)1097-0193(1999)8:4

Dysfunction of the prefrontal cortex in addiction: neuroimaging findings and clinical implications

Goldstein, R. Z., & Volkow, N. D. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn3119 · Cited by 2,749 · see citing works

Why ritualized behavior? Precaution Systems and action parsing in developmental, pathological and cultural rituals

Boyer, P., & Liénard, P. (2006) · Behavioral and Brain Sciences · doi:10.1017/s0140525x06009332 · Cited by 601 · see citing works

Addiction circuitry in the human brain

Volkow, N. D., Wang, G.-J., Fowler, J. S., & Tomasi, D. (2012) · Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev-pharmtox-010611-134625 · Cited by 592 · see citing works

Altered Expression of Genes Involved in Inflammation and Apoptosis in Frontal Cortex in Major Depression

Shelton, R. C., Claiborne, J., Sidoryk-Wegrzynowicz, M., Reddy, R., Aschner, M., Lewis, D. A., & Mirnics, K. (2011) · Molecular Psychiatry · doi:10.1038/mp.2010.52 · Cited by 511 · see citing works

Brain basis of early parent–infant interactions: psychology, physiology, and <i>in vivo</i> functional neuroimaging studies

Swain, J. E., Lorberbaum, J. P., Kose, S., & Strathearn, L. (2007) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.2007.01731.x · Cited by 499 · see citing works

What’s in a smile? Maternal brain responses to infant facial cues

Strathearn, L., Li, J., Fonagy, P., & Montague, P. R. (2008) · Pediatrics · doi:10.1542/peds.2007-1566 · Cited by 460 · see citing works

Linking nucleus accumbens dopamine and blood oxygenation

Knutson, B., & Gibbs, S. E. B. (2007) · Psychopharmacology · doi:10.1007/s00213-006-0686-7 · Cited by 337 · see citing works

The maternal brain and its plasticity in humans

Kim, P., Strathearn, L., & Swain, J. E. (2016) · Hormones and Behavior · doi:10.1016/j.yhbeh.2015.08.001 · Cited by 278 · see citing works

Maternal brain response to own baby‐cry is affected by cesarean section delivery

Swain, J. E., Tasgin, E., Mayes, L. C., Feldman, R., Todd Constable, R., & Leckman, J. F. (2008) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.2008.01963.x · Cited by 206 · see citing works

Neuroimaging for drug addiction and related behaviors

Parvaz, M. A., Alia-Klein, N., Woicik, P. A., Volkow, N. D., & Goldstein, R. Z. (2011) · Reviews in the Neurosciences · doi:10.1515/rns.2011.055 · Cited by 151 · see citing works

Craving correlates with mesolimbic responses to heroin-related cues in short-term abstinence from heroin: an event-related fMRI study

Li, Q., Wang, Y., Zhang, Y., Li, W., Yang, W., Zhu, J., Wu, N., Chang, H., Zheng, Y., Qin, W., et al. (2012) · Brain Research · doi:10.1016/j.brainres.2012.06.024 · Cited by 133 · see citing works

Amygdala and bed nucleus of the stria terminalis circuitry: Implications for addiction-related behaviors

Stamatakis, A. M., Sparta, D. R., Jennings, J. H., McElligott, Z. A., Decot, H., & Stuber, G. D. (2014) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.05.046 · Cited by 132 · see citing works

Probing the frontostriatal loops involved in executive and limbic processing via interleaved TMS and functional MRI at two prefrontal locations: a pilot study

Hanlon, C. A., Canterberry, M., Taylor, J. J., DeVries, W., Li, X., Brown, T. R., & George, M. S. (2013) · PLoS ONE · doi:10.1371/journal.pone.0067917 · Cited by 80 · see citing works

Pharmacological modulation of functional connectivity: the correlation structure underlying the phMRI response to d-amphetamine modified by selective dopamine D3 receptor antagonist SB277011A

Schwarz, A. J., Gozzi, A., Reese, T., Heidbreder, C. A., & Bifone, A. (2007) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2007.02.017 · Cited by 68 · see citing works

Repeated cocaine exposure decreases dopamine D₂‐like receptor modulation of Ca²⁺homeostasis in rat nucleus accumbens neurons

Perez, M. F., Ford, K. A., Goussakov, I., Stutzmann, G. E., & Hu, X. (2011) · Synapse · doi:10.1002/syn.20831 · Cited by 40 · see citing works

Faculty Opinions recommendation of Distinct roles of rodent orbitofrontal and medial prefrontal cortex in decision making.

Frank, M. J. (2010) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.3286956.2972054

Distinct Roles of Rodent Orbitofrontal and Medial Prefrontal Cortex in Decision Making

Sul, J. H., Kim, H., Huh, N., Lee, D., & Jung, M. W. (2010) · Neuron · doi:10.1016/j.neuron.2010.03.033 · Cited by 372 · see citing works

Inhibitory Control and Affective Processing in the Prefrontal Cortex: Neuropsychological Studies in the Common Marmoset

Roberts, A. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.252 · Cited by 211 · see citing works

The distinct role of orbitofrontal and medial prefrontal cortex in encoding impulsive choices in an animal model of attention deficit hyperactivity disorder

Cao, A., Hong, D., Che, C., Yu, X., Cai, Z., Yang, X., Zhang, D., & Yu, P. (2023) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.1039288 · Cited by 2 · see citing works

Orbitofrontal cortex and its contribution to decision-making.

Wallis, J. D. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.30.051606.094334 · Cited by 938 · see citing works