Factors modulating neural reactivity to drug cues in addiction: a survey of human neuroimaging studies
Open accessAbstract
Human neuroimaging studies suggest that neural cue reactivity is strongly associated with indices of drug use, including addiction severity and treatment success. However, little is known about factors that modulate cue reactivity. The goal of this review, in which we survey published fMRI and PET studies on drug cue reactivity in cocaine, alcohol, and tobacco cigarette users, is to highlight major factors that modulate brain reactivity to drug cues. First, we describe cue reactivity paradigms used in neuroimaging research and outline the brain circuits that underlie cue reactivity. We then discuss major factors that have been shown to modulate cue reactivity and review specific evidence as well as outstanding questions related to each factor. Building on previous model-building reviews on the topic, we then outline a simplified model that includes the key modulatory factors and a tentative ranking of their relative impact. We conclude with a discussion of outstanding challenges and future research directions, which can inform future neuroimaging studies as well as the design of treatment and prevention programs.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In humans, cue-induced craving involves activation of circuits similar to those in animals, with drug-associated and non-drug addiction cues activating the prefrontal cortex, including dorsolateral prefrontal cortex, anterior cingulate gyrus, and medial orbitofrontal cortex.
“In humans, cue-induced craving appears to involve activation of similar circuits, in which cues that are associated with drugs and elements of non-drug addictions produce activation of the prefrontal cortex, including the dorsolateral prefrontal cortex, anterior cingulate gyrus, and medial orbitofrontal cortex.101–105”
From Neurobiology of addiction: a neurocircuitry analysis (2016) · cites this paper as [105]
Split into 2 atoms — 1 confirmed, 1 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Experimental — accuracy not yet measuredThe Go system could drive craving and engage habits via the basal ganglia.
“The Go system could drive craving and engage habits via the basal ganglia.105,127”
From Neurobiology of addiction: a neurocircuitry analysis (2016) · cites this paper as [105]
In drug-dependent humans, drug cues consistently increase BOLD responses in the STR, BLA, VTA, PFC, hippocampus, and NAc.
“In drug-dependent humans, drug cues consistently increase BOLD responses in the STR, BLA, VTA, PFC, hippocampus, and NAc (Grusser et al., 2004, Jasinska et al., 2014, Lukas et al., 2013, Maas et al., 1998).”
From Sensitive periods of substance abuse: Early risk for the transition to dependence (2017) · cites this paper as Jasinska et al., 2014
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
A neural substrate of prediction and reward
Schultz, W., Dayan, P., & Montague, P. R. (1997) · Science · doi:10.1126/science.275.5306.1593 · Cited by 9,388 · see citing works
Dissociable intrinsic connectivity networks for salience processing and executive control
Seeley, W. W., Menon, V., Schatzberg, A. F., Keller, J., Glover, G. H., Kenna, H., Reiss, A. L., & Greicius, M. D. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5587-06.2007 · Cited by 7,426 · see citing works
The neural basis of drug craving: An incentive-sensitization theory of addiction
Robinson, T. (1993) · Brain Research Reviews · doi:10.1016/0165-0173(93)90013-p · Cited by 7,346 · see citing works
Saliency, switching, attention and control: a network model of insula function
Menon, V., & Uddin, L. Q. (2010) · Brain Structure and Function · doi:10.1007/s00429-010-0262-0 · Cited by 5,592 · see citing works
Neural systems of reinforcement for drug addiction: from actions to habits to compulsion
Everitt, B. J., & Robbins, T. W. (2005) · Nature Neuroscience · doi:10.1038/nn1579 · Cited by 3,785 · see citing works
The reward circuit: linking primate anatomy and human imaging
Haber, S. N., & Knutson, B. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2009.129 · Cited by 3,718 · see citing works
Sridharan, D., Levitin, D. J., & Menon, V. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0800005105 · Cited by 2,892 · see citing works
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
NEURAL MECHANISMS OF ADDICTION: The Role of Reward-Related Learning and Memory
Hyman, S. E., Malenka, R. C., & Nestler, E. J. (2006) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.29.051605.113009 · Cited by 2,647 · see citing works
Interoception: the sense of the physiological condition of the body
(Bud) Craig, A. (2003) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(03)00090-4 · Cited by 2,556 · see citing works
Decision making, impulse control and loss of willpower to resist drugs: a neurocognitive perspective
Bechara, A. (2005) · Nature Neuroscience · doi:10.1038/nn1584 · Cited by 2,149 · cited 2× · see citing works
“Consistent with this view, recent theories of drug addiction stress the contribution of impaired cognitive control or executive function in addictive behaviors and in the progression from controlled, recreational drug use to drug abuse and drug dependence (Bechara, 2005; Feil et al., 2010; Goldstein and Volkow, 2011;…”
BackgroundThe integration of negative affect, pain and cognitive control in the cingulate cortex
Shackman, A. J., Salomons, T. V., Slagter, H. A., Fox, A. S., Winter, J. J., & Davidson, R. J. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn2994 · Cited by 2,082 · see citing works
Action Observation and Acquired Motor Skills: An fMRI Study with Expert Dancers
Calvo‐Merino, B., Glaser, D. E., Grèzes, J., Passingham, R. E., & Haggard, P. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhi007 · Cited by 1,991 · see citing works
Chronic stress, drug use, and vulnerability to addiction
Sinha, R. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1441.030 · Cited by 1,904 · see citing works
A Core System for the Implementation of Task Sets
Dosenbach, N. U. F., Visscher, K. M., Palmer, E. D., Miezin, F. M., Wenger, K. K., Kang, H. C., Burgund, E. D., Grimes, A. L., Schlaggar, B. L., & Petersen, S. E. (2006) · Neuron · doi:10.1016/j.neuron.2006.04.031 · Cited by 1,772 · see citing works
A cognitive model of drug urges and drug-use behavior: role of automatic and nonautomatic processes
Tiffany, S. T. (1990) · Psychological Review · doi:10.1037/0033-295x.97.2.147 · Cited by 1,554 · see citing works
Jentsch, J. D., & Taylor, J. R. (1999) · Psychopharmacology · doi:10.1007/pl00005483 · Cited by 1,545 · see citing works
Limbic Activation During Cue-Induced Cocaine Craving
Childress, A. R., Mozley, P. D., McElgin, W., Fitzgerald, J., Reivich, M., & O’Brien, C. P. (1999) · American Journal of Psychiatry · doi:10.1176/ajp.156.1.11 · Cited by 1,513 · see citing works
Multiple dopamine functions at different time courses
Schultz, W. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.28.061604.135722 · Cited by 1,415 · see citing works
Is there a common molecular pathway for addiction?
Nestler, E. J. (2005) · Nature Neuroscience · doi:10.1038/nn1578 · Cited by 1,388 · see citing works
Attentional bias in addictive behaviors: A review of its development, causes, and consequences
FIELD, M., & COX, W. (2008) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2008.03.030 · Cited by 1,376 · see citing works
Phasic Firing in Dopaminergic Neurons Is Sufficient for Behavioral Conditioning
Tsai, H.-C., Zhang, F., Adamantidis, A., Stuber, G. D., Bonci, A., de Lecea, L., & Deisseroth, K. (2009) · Science · doi:10.1126/science.1168878 · Cited by 1,266 · see citing works
Representation of Manipulable Man-Made Objects in the Dorsal Stream
Chao, L. L., & Martin, A. D. (2000) · NeuroImage · doi:10.1006/nimg.2000.0635 · Cited by 1,233 · see citing works
Cocaine cues and dopamine in dorsal striatum: mechanism of craving in cocaine addiction
Volkow, N. D., Wang, G.-J., Telang, F., Fowler, J. S., Logan, J., Childress, A.-R., Jayne, M., Ma, Y., & Wong, C. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1544-06.2006 · Cited by 1,164 · see citing works
Seeing or Doing? Influence of Visual and Motor Familiarity in Action Observation
Calvo‐Merino, B., Grèzes, J., Glaser, D. E., Passingham, R. E., & Haggard, P. (2006) · Current Biology · doi:10.1016/j.cub.2006.07.065 · Cited by 1,141 · see citing works
A Role for Brain Stress Systems in Addiction
Koob, G. F. (2008) · Neuron · doi:10.1016/j.neuron.2008.06.012 · Cited by 1,056 · see citing works
Schultz, W. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.03.007 · Cited by 1,028 · see citing works
Garavan, H. (2002) · NeuroImage · doi:10.1006/nimg.2002.1326 · Cited by 988 · 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
Self-citationThe 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
Liu, X., Hairston, J., Schrier, M., & Fan, J. (2011) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.12.012 · Cited by 916 · see citing works
Interference resolution: Insights from a meta-analysis of neuroimaging tasks
NEE, D. E., WAGER, T. D., & JONIDES, J. (2007) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/cabn.7.1.1 · Cited by 798 · see citing works
Kelley, A. E. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.016 · Cited by 773 · see citing works
Drug craving and addiction: integrating psychological and neuropsychopharmacological approaches
Franken, I. H. A. (2003) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/s0278-5846(03)00081-2 · Cited by 765 · see citing works
Drug Addiction as a Pathology of Staged Neuroplasticity
Kalivas, P. W., & O’Brien, C. P. (2007) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301564 · Cited by 735 · see citing works
Synaptic mechanisms underlie nicotine-induced excitability of brain reward areas
Mansvelder, H. D., Keath, J. R., & McGehee, D. S. (2002) · Neuron · doi:10.1016/s0896-6273(02)00625-6 · Cited by 701 · see citing works
The neural bases of complex tool use in humans
Johnson-Frey, S. H. (2003) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2003.12.002 · Cited by 697 · see citing works
Belin, D., & Everitt, B. J. (2008) · Neuron · doi:10.1016/j.neuron.2007.12.019 · Cited by 697 · see citing works
Prefrontal–striatal pathway underlies cognitive regulation of craving
Kober, H., Mende-Siedlecki, P., Kross, E. F., Weber, J., Mischel, W., Hart, C. L., & Ochsner, K. N. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1007779107 · Cited by 695 · see citing works
Nicotine preferentially stimulates dopamine release in the limbic system of freely moving rats
Imperato, A., Mulas, A., & Di Chiara, G. (1986) · European Journal of Pharmacology · doi:10.1016/0014-2999(86)90629-1 · Cited by 693 · see citing works
Gr�sser, S. M., Wrase, J., Klein, S., Hermann, D., Smolka, M. N., Ruf, M., Weber-Fahr, W., Flor, H., Mann, K., Braus, D. F., et al. (2004) · Psychopharmacology · doi:10.1007/s00213-004-1828-4 · Cited by 598 · see citing works
A new perspective on the role of the orbitofrontal cortex in adaptive behaviour
Schoenbaum, G., Roesch, M. R., Stalnaker, T. A., & Takahashi, Y. K. (2009) · Nature reviews. Neuroscience · doi:10.1038/nrn2753 · Cited by 585 · see citing works
Schacht, J. P., Anton, R. F., & Myrick, H. (2013) · Addiction Biology · doi:10.1111/j.1369-1600.2012.00464.x · Cited by 583 · see citing works
Dopamine: a potential substrate for synaptic plasticity and memory mechanisms
Jay, T. M. (2003) · Progress in Neurobiology · doi:10.1016/s0301-0082(03)00085-6 · Cited by 576 · see citing works
A distributed left hemisphere network active during planning of everyday tool use skills
Johnson-Frey, S. H., Newman-Norlund, R., & Grafton, S. T. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhh169 · Cited by 558 · 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
Clarke, P. B. S., & Pert, A. (1985) · Brain Research · doi:10.1016/0006-8993(85)90456-1 · Cited by 527 · see citing works
Myrick, H., Anton, R. F., Li, X., Henderson, S., Drobes, D., Voronin, K., & George, M. S. (2004) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300295 · Cited by 521 · see citing works
Belin, D., Jonkman, S., Dickinson, A., Robbins, T. W., & Everitt, B. J. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.09.027 · Cited by 520 · 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 · cited 9× · see citing works
“…including the insula (Bonson et al., 2002; Kilts et al., 2001; Wang et al., 1999), ACC (Maas et al., 1998), OFC (Bonson et al., 2002), DLPFC (Bonson et al., 2002; Grant et al., 1996; Kilts et al., 2001; Maas et al., 1998), DS (Volkow et al., 2006), amygdala (Bonson et al., 2002; Grant et…”
BackgroundInfluentialDifferential control over cocaine-seeking behavior by nucleus accumbens core and shell
Ito, R., Robbins, T. W., & Everitt, B. J. (2004) · Nature Neuroscience · doi:10.1038/nn1217 · Cited by 501 · see citing works
Orbitofrontal cortex, decision-making and drug addiction
Schoenbaum, G., Roesch, M. R., & Stalnaker, T. A. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2005.12.006 · Cited by 499 · see citing works
SINHA, R., & LI, C. ‐. R. (2007) · Drug and Alcohol Review · doi:10.1080/09595230601036960 · Cited by 497 · see citing works
Resting state functional connectivity in addiction: Lessons learned and a road ahead
Sutherland, M. T., McHugh, M. J., Pariyadath, V., & Stein, E. A. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.01.117 · Cited by 495 · see citing works
Self-citationDoes visual perception of object afford action? Evidence from a neuroimaging study
Grèzes, J., & Decety, J. (2002) · Neuropsychologia · doi:10.1016/s0028-3932(01)00089-6 · Cited by 488 · see citing works
Common and unique components of response inhibition revealed by fMRI
Wager, T. D., Sylvester, C.-Y. C., Lacey, S. C., Nee, D. E., Franklin, M., & Jonides, J. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.01.054 · Cited by 486 · see citing works
Dysfunction of reward processing correlates with alcohol craving in detoxified alcoholics
Wrase, J., Schlagenhauf, F., Kienast, T., Wüstenberg, T., Bermpohl, F., Kahnt, T., Beck, A., Ströhle, A., Juckel, G., Knutson, B. D., et al. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2006.11.043 · Cited by 480 · see citing works
Kühn, S., & Gallinat, J. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07590.x · Cited by 474 · see citing works
Food and drug cues activate similar brain regions: A meta-analysis of functional MRI studies
Tang, D., Fellows, L. K., Small, D. M., & Dagher, A. (2012) · Physiology & Behavior · doi:10.1016/j.physbeh.2012.03.009 · Cited by 457 · see citing works
Cortical Networks Related to Human Use of Tools
Lewis, J. W. (2006) · The Neuroscientist · doi:10.1177/1073858406288327 · Cited by 450 · see citing works
Drug Addiction and the Memory Systems of the Brain
Robbins, T. W., Ersche, K. D., & Everitt, B. J. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1441.020 · Cited by 447 · see citing works
Ito, R., Dalley, J. W., Howes, S. R., Robbins, T. W., & Everitt, B. J. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-19-07489.2000 · Cited by 441 · see citing works
Functional Magnetic Resonance Imaging of Human Brain Activation During Cue-Induced Cocaine Craving
Maas, L. C., Lukas, S. E., Kaufman, M. J., Weiss, R. D., Daniels, S. L., Rogers, V. W., Kukes, T. J., & Renshaw, P. F. (1998) · American Journal of Psychiatry · doi:10.1176/ajp.155.1.124 · Cited by 434 · see citing works
Due, D. L., Huettel, S. A., HALL, W. G., & Rubin, D. C. (2002) · American Journal of Psychiatry · doi:10.1176/appi.ajp.159.6.954 · Cited by 429 · see citing works
Brain metabolic changes during cigarette craving
Brody, A. L., Mandelkern, M. A., London, E. D., Childress, A. R., Lee, G. S., Bota, R. G., Ho, M. L., Saxena, S., Baxter, L. R., Madsen, D., et al. (2002) · Archives of General Psychiatry · doi:10.1001/archpsyc.59.12.1162 · Cited by 425 · see citing works
Functional Magnetic Resonance Imaging of Cocaine Craving
Wexler, B. E., Gottschalk, C. H., Fulbright, R. K., Prohovnik, I., Lacadie, C. M., Rounsaville, B. J., & Gore, J. C. (2001) · American Journal of Psychiatry · doi:10.1176/appi.ajp.158.1.86 · Cited by 420 · see citing works
Janes, A. C., Pizzagalli, D. A., Richardt, S., Frederick, B. D., Chuzi, S., Pachas, G., Culhane, M. A., Holmes, A. J., Fava, M., Evins, A. E., et al. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.12.034 · Cited by 416 · 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
Prelude to Passion: Limbic Activation by “Unseen” Drug and Sexual Cues
Childress, A. R., Ehrman, R. N., Wang, Z., Li, Y., Sciortino, N., Hakun, J. G., Jens, W., Suh, J. J., Listerud, J., Marquez, K., et al. (2008) · PLoS ONE · doi:10.1371/journal.pone.0001506 · Cited by 395 · see citing works
Neural substrates of smoking cue reactivity: A meta-analysis of fMRI studies
Engelmann, J. M., Versace, F., Robinson, J. D., Minnix, J. A., Lam, C. Y., Cui, Y., Brown, V. L., & Cinciripini, P. M. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.12.024 · Cited by 394 · see citing works
Involvement of the dorsal striatum in cue-controlled cocaine seeking
Vanderschuren, L. J. M. J., Di Ciano, P., & Everitt, B. J. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.0925-05.2005 · Cited by 393 · see citing works
George, M. S., Anton, R. F., Bloomer, C., Tenebäck, C. C., Drobes, D. J., Lorberbaum, J. P., Nahas, Z. H., & Vincent, D. J. (2001) · Archives of General Psychiatry · doi:10.1001/archpsyc.58.4.345 · Cited by 382 · see citing works
Neural Response to Alcohol Stimuli in Adolescents With Alcohol Use Disorder
Tapert, S. F., Cheung, E. H., Brown, G. G., Frank, L. R., Paulus, M. P., Schweinsburg, A. D., Meloy, M. J., & Brown, S. A. (2003) · Archives of General Psychiatry · doi:10.1001/archpsyc.60.7.727 · Cited by 372 · see citing works
Wooltorton, J. R. A., Pidoplichko, V. I., Broide, R. S., & Dani, J. A. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-08-03176.2003 · Cited by 363 · see citing works
Franklin, T. R., wang, Z., Wang, J., Sciortino, N., Harper, D., Li, Y., Ehrman, R., Kampman, K. M., O’Brien, C. P., Detre, J. A., et al. (2007) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301371 · Cited by 359 · see citing works
Vollstädt‐Klein, S., Wichert, S., Rabinstein, J., Bühler, M., Klein, O., Ende, G., Hermann, D., & Mann, K. (2010) · Addiction · doi:10.1111/j.1360-0443.2010.03022.x · Cited by 357 · see citing works
Objects automatically potentiate action: an fMRI study of implicit processing
Grèzes, J., Tucker, M., Armony, J. L., Ellis, R., & Passingham, R. E. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02695.x · Cited by 357 · see citing works
Value-Based Modulations in Human Visual Cortex
Serences, J. T. (2008) · Neuron · doi:10.1016/j.neuron.2008.10.051 · Cited by 353 · see citing works
Feil, J., Sheppard, D., Fitzgerald, P. B., Yücel, M., Lubman, D. I., & Bradshaw, J. L. (2010) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.03.001 · Cited by 342 · see citing works
Regional brain metabolic activation during craving elicited by recall of previous drug experiences
Wang, G.-J., Volkow, N. D., Fowler, J. S., Cervany, P., Hitzemann, R. J., Pappas, N. R., Wong, C. T., & Felder, C. (1999) · Life Sciences · doi:10.1016/s0024-3205(98)00619-5 · Cited by 336 · see citing works
Goudriaan, A. E., De Ruiter, M. B., Van Den Brink, W., Oosterlaan, J., & Veltman, D. J. (2010) · Addiction Biology · doi:10.1111/j.1369-1600.2010.00242.x · Cited by 327 · see citing works
McBride, D., Barrett, S. P., Kelly, J. T., Aw, A., & Dagher, A. (2006) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301075 · Cited by 323 · see citing works
Subcortical Correlates of Craving in Recently Abstinent Alcoholic Patients
Schneider, F. W., Habel, U., Wagner, M., Franke, P. E., Salloum, J. B., Shah, N. J., Toni, I., Sulzbach, C., Hönig, K., Maier, W., et al. (2001) · American Journal of Psychiatry · doi:10.1176/appi.ajp.158.7.1075 · Cited by 319 · see citing works
Chase, H. W., Eickhoff, S. B., Laird, A. R., & Hogarth, L. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.05.025 · Cited by 316 · see citing works
Neural Substrates of Resisting Craving During Cigarette Cue Exposure
Brody, A. L., Mandelkern, M. A., Olmstead, R. E., Jou, J., Tiongson, E., Allen, V., Scheibal, D., London, E. D., Monterosso, J. R., Tiffany, S. T., et al. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2006.10.026 · Cited by 312 · see citing works
Increased Occupancy of Dopamine Receptors in Human Striatum during Cue-Elicited Cocaine Craving
Wong, D. F., Kuwabara, H., Schretlen, D. J., Bonson, K. R., Zhou, Y., Nandi, A., Brašić, J. R., Kimes, A. S., Maris, M. A., Kumar, A., et al. (2006) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301194 · Cited by 311 · see citing works
Cue-Induced Brain Activity Changes and Relapse in Cocaine-Dependent Patients
Kosten, T. R., Scanley, B. E., Tucker, K. A., Oliveto, A. H., Prince, C. N., Sinha, R., Potenza, M. N., Skudlarski, P., & Wexler, B. E. (2005) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300851 · Cited by 306 · see citing works
Neural representations of graspable objects: are tools special?
Creem-Regehr, S. H., & Lee, J. N. (2004) · Cognitive Brain Research · doi:10.1016/j.cogbrainres.2004.10.006 · Cited by 295 · see citing works
Ciano, P. D. (2001) · Neuropsychopharmacology · doi:10.1016/s0893-133x(01)00235-4 · Cited by 287 · see citing works
Calabresi, P., Lacey, M. G., & North, R. A. (1989) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.1989.tb16873.x · Cited by 285 · see citing works
Cognitive control of drug craving inhibits brain reward regions in cocaine abusers
Volkow, N. D., Fowler, J. S., Wang, G.-J., Telang, F., Logan, J., Jayne, M., Ma, Y., Pradhan, K., Wong, C., & Swanson, J. M. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.10.088 · Cited by 283 · see citing works
Mindful attention reduces neural and self-reported cue-induced craving in smokers
Westbrook, C., Creswell, J. D., Tabibnia, G., Julson, E., Kober, H., & Tindle, H. A. (2013) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsr076 · Cited by 278 · see citing works
David, S. P., Munafo, M. R., Johansen‐Berg, H., Smith, S. M., Rogers, R. D., Matthews, P. M., & Walton, R. T. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.04.028 · Cited by 275 · see citing works
Exposure to the Taste of Alcohol Elicits Activation of the Mesocorticolimbic Neurocircuitry
Filbey, F. M., Claus, E., Audette, A. R., Niculescu, M., Banich, M. T., Tanabe, J., Du, Y. P., & Hutchison, K. E. (2008) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301513 · Cited by 270 · see citing works
Beck, A., Wüstenberg, T., Genauck, A., Wrase, J., Schlagenhauf, F., Smolka, M. N., Mann, K. F., & Heinz, A. (2012) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2011.2026 · Cited by 269 · see citing works
Marijuana craving in the brain
Filbey, F. M., Schacht, J. P., Myers, U. S., Chavez, R. S., & Hutchison, K. E. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0903863106 · Cited by 265 · see citing works
Myrick, H., Anton, R. F., Li, X., Henderson, S., Randall, P. K., & Voronin, K. (2008) · Archives of General Psychiatry · doi:10.1001/archpsyc.65.4.466 · Cited by 258 · see citing works
Hayashi, T., Ko, J. H., Strafella, A. P., & Dagher, A. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1212185110 · Cited by 251 · see citing works
Identifying Neurobiological Phenotypes Associated with Alcohol Use Disorder Severity
Claus, E. D., Ewing, S. W. F., Filbey, F. M., Sabbineni, A., & Hutchison, K. E. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2011.99 · Cited by 249 · see citing works
McClernon, F. J., Kozink, R. V., Lutz, A. M., & Rose, J. E. (2009) · Psychopharmacology · doi:10.1007/s00213-008-1436-9 · Cited by 244 · see citing works
Buxbaum, L. J., Kyle, K. M., Grossman, M., & Coslett, H. B. (2007) · Cortex · doi:10.1016/s0010-9452(08)70466-0 · Cited by 239 · see citing works
Smolka, M. N., Bühler, M., Klein, S., Zimmermann, U., Mann, K., Heinz, A., & Braus, D. F. (2006) · Psychopharmacology · doi:10.1007/s00213-005-0080-x · Cited by 230 · see citing works
Volkow, N. D., Wang, G.-J., Telang, F., Fowler, J. S., Logan, J., Childress, A.-R., Jayne, M., Ma, Y., & Wong, C. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2007.09.059 · Cited by 224 · see citing works
McClernon, F. J., Hiott, F. B., Huettel, S. A., & Rose, J. E. (2005) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300780 · Cited by 216 · see citing works
fMRI BOLD response to alcohol stimuli in alcohol dependent young women
Tapert, S. F., Brown, G. G., Baratta, M. V., & Brown, S. A. (2003) · Addictive Behaviors · doi:10.1016/j.addbeh.2003.07.003 · Cited by 211 · see citing works
The impact of orbitofrontal dysfunction on cocaine addiction
Lucantonio, F., Stalnaker, T. A., Shaham, Y., Niv, Y., & Schoenbaum, G. M. (2012) · Nature Neuroscience · doi:10.1038/nn.3014 · Cited by 210 · see citing works
Effects of cue-exposure treatment on neural cue reactivity in alcohol dependence: a randomized trial
Vollstädt-Klein, S., Loeber, S., Kirsch, M., Bach, P., Richter, A., Bühler, M., von der Goltz, C., Hermann, D., Mann, K., & Kiefer, F. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.12.016 · Cited by 202 · see citing works
McClernon, F. J., Kozink, R. V., & Rose, J. E. (2008) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301618 · Cited by 202 · see citing works
Nicotine Enhances Visuospatial Attention by Deactivating Areas of the Resting Brain Default Network
Hahn, B., Ross, T. J., Yang, Y., Kim, I., Huestis, M. A., & Stein, E. A. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5129-06.2007 · Cited by 199 · see citing works
Self-citationSex differences in neural responses to stress and alcohol context cues
Seo, D., Jia, Z., Lacadie, C., Tsou, K. A., Bergquist, K. L., & Sinha, R. (2010) · Human Brain Mapping · doi:10.1002/hbm.21165 · Cited by 199 · see citing works
Alcohol-associated stimuli activate the ventral striatum in abstinent alcoholics
Braus, D. F., Wrase, J., Grüsser, S. M., Hermann, D., Ruf, M., Flor, H., Mann, K. F., & Heinz, A. (2001) · Journal of Neural Transmission · doi:10.1007/s007020170038 · Cited by 192 · see citing works
A review of the effects of perceived drug use opportunity on self-reported urge.
Wertz, J. M., & Sayette, M. A. (2001) · Experimental and Clinical Psychopharmacology · doi:10.1037/1064-1297.9.1.3 · Cited by 192 · see citing works
Development of alcohol-associated cues and cue-induced brain activation in alcoholics
Wrase, J., Grüsser, S. M., Vollstädt‐Klein, S., Diener, C., Hermann, D., Flor, H., Mann, K. F., Braus, D. F., & Heinz, A. (2002) · European Psychiatry · doi:10.1016/s0924-9338(02)00676-4 · Cited by 192 · see citing works
Anterior cingulate cortex hypoactivations to an emotionally salient task in cocaine addiction
Goldstein, R. Z., Nelly Alia-klein, A., Tomasi, D. G., Honorio, J., Maloney, T., Woicik, P. A., Wang, R., Telang, F., & Volkow, N. D. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0900491106 · Cited by 191 · see citing works
Effects of Varenicline on Smoking Cue–Triggered Neural and Craving Responses
Franklin, T. R., Wang, Z., Suh, J. J., Hazan, R., Cruz, J., Li, Y., Goldman, M., Detre, J. A., O’Brien, C. P., & Childress, A. R. (2011) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2010.190 · Cited by 162 · see citing works
Ihssen, N., Cox, W. M., Wiggett, A., Fadardi, J. S., & Linden, D. E. J. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhq220 · Cited by 157 · see citing works
Neural responses associated with cue‐reactivity in frequent cannabis users
Cousijn, J., Goudriaan, A. E., Ridderinkhof, K. R., van den Brink, W., Veltman, D. J., & Wiers, R. W. H. J. (2012) · Addiction Biology · doi:10.1111/j.1369-1600.2011.00417.x · Cited by 154 · see citing works
Instructed smoking expectancy modulates cue‐elicited neural activity: A preliminary study
Wilson, S. J., Sayette, M. A., Delgado, M. R., & Fiez, J. A. (2005) · Nicotine & Tobacco Research · doi:10.1080/14622200500185520 · Cited by 143 · see citing works
Enhanced cue reactivity and fronto-striatal functional connectivity in cocaine use disorders
Wilcox, C. E., Teshiba, T. M., Merideth, F. L., Ling, J. M., & Mayer, A. R. (2011) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2011.01.009 · Cited by 132 · see citing works
Neural correlates of craving and resisting craving for tobacco in nicotine dependent smokers
Hartwell, K. J., Johnson, K. A., Li, X., Myrick, H., LeMatty, T., George, M. S., & Brady, K. T. (2011) · Addiction Biology · doi:10.1111/j.1369-1600.2011.00340.x · Cited by 129 · see citing works
Functional neuroimaging studies in addiction: Multisensory drug stimuli and neural cue reactivity
Yalachkov, Y., Kaiser, J., & Naumer, M. J. (2011) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2011.12.004 · Cited by 118 · see citing works
Self-citationSensory and motor aspects of addiction
Yalachkov, Y., Kaiser, J., & Naumer, M. J. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2009.09.015 · Cited by 117 · see citing works
Self-citationBrain substrates of craving to alcohol cues in subjects with alcohol use disorder
Park, M., Sohn, J., Ra, J. S., Kim, S. H., Sohn, S., & Sparacio, R. (2007) · Alcohol and Alcoholism · doi:10.1093/alcalc/agl117 · Cited by 111 · see citing works
Neurobiological substrate of smoking-related attentional bias
Luijten, M., Veltman, D. J., van den Brink, W., Hester, R., Field, M., Smits, M., & Franken, I. H. A. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.09.064 · Cited by 110 · see citing works
Marhe, R., Luijten, M., van de Wetering, B. J. M., Smits, M., & Franken, I. H. A. (2013) · Neuropsychopharmacology · doi:10.1038/npp.2013.7 · Cited by 108 · see citing works
Effects of smoking opportunity on attentional bias in smokers.
Wertz, J. M., & Sayette, M. A. (2001) · Psychology of Addictive Behaviors · doi:10.1037/0893-164x.15.3.268 · Cited by 106 · see citing works
Immunohistochemical localization of a neuronal nicotinic acetylcholine receptor in mammalian brain.
Deutch, A. Y., Holliday, J., Roth, R. H., Chun, L. L. Y., & Hawrot, E. (1987) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.84.23.8697 · Cited by 102 · see citing works
Brain Regions Related to Tool Use and Action Knowledge Reflect Nicotine Dependence
Yalachkov, Y., Kaiser, J., & Naumer, M. J. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4891-08.2009 · Cited by 100 · see citing works
Self-citationDavid, S. P., Munafo, M. R., Johansen‐Berg, H., MacKillop, J. M., Sweet, L. H., Cohen, R. A., NIAURA, R. S., Rogers, R. D., Matthews, P. M., & Walton, R. T. (2007) · Brain Imaging and Behavior · doi:10.1007/s11682-007-9004-1 · Cited by 97 · see citing works
Anatomical differences and network characteristics underlying smoking cue reactivity
Zhang, X., Salmeron, B. J., Ross, T. J., Gu, H., Geng, X., Yang, Y., & Stein, E. A. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.07.063 · Cited by 95 · see citing works
Self-citationVollstädt‐Klein, S., Kobiella, A., Fauth‐Bühler, M., Graf, C., Fehr, C., Mann, K. F., & Smolka, M. N. (2010) · Addiction Biology · doi:10.1111/j.1369-1600.2010.00207.x · Cited by 88 · see citing works
Bringing the real world into the laboratory: Personal smoking and nonsmoking environments
Conklin, C. A., Perkins, K. A., Robin, N., McClernon, F. J., & Salkeld, R. P. (2010) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2010.03.017 · Cited by 87 · see citing works
The Role of Dorsal Anterior Cingulate Cortex in the Regulation of Craving by Reappraisal in Smokers
Zhao, L., Tian, J., Wang, W., Qin, W., Shi, J., Li, Q., Yuan, K., Dong, M., Yang, W.-C., Wang, Y., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0043598 · Cited by 81 · see citing works
An acute psychosocial stress enhances the neural response to smoking cues
Dagher, A., Tannenbaum, B., Hayashi, T., Pruessner, J. C., & McBride, D. (2009) · Brain Research · doi:10.1016/j.brainres.2009.07.048 · Cited by 80 · see citing works
Dager, A. D., Anderson, B. M., Stevens, M. C. G., Pulido, C., Rosen, R., Jiantonio‐Kelly, R. E., Sisante, J.-F. V., Raskin, S. A., Tennen, H. A., Austad, C. S., et al. (2012) · Alcoholism Clinical and Experimental Research · doi:10.1111/j.1530-0277.2012.01879.x · Cited by 80 · see citing works
Spontaneous Action Representation in Smokers when Watching Movie Characters Smoke
Wagner, D. D., Cin, S. D., Sargent, J. D., Kelley, W. M., & Heatherton, T. F. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.5174-10.2011 · Cited by 80 · see citing works
Stability of fMRI striatal response to alcohol cues: A hierarchical linear modeling approach
Schacht, J. P., Anton, R. F., Randall, P. K., Li, X., Henderson, S., & Myrick, H. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.02.004 · Cited by 77 · see citing works
Wilson, S. J., Creswell, K. G., Sayette, M. A., & Fiez, J. A. (2012) · Addictive Behaviors · doi:10.1016/j.addbeh.2012.03.020 · Cited by 68 · see citing works
Brain activation to cocaine cues and motivation/treatment status
Prisciandaro, J. J., McRae‐Clark, A. L., Myrick, H., Henderson, S., & Brady, K. T. (2012) · Addiction Biology · doi:10.1111/j.1369-1600.2012.00446.x · Cited by 67 · see citing works
Cue reactivity in cocaine-dependent subjects: effects of cue type and cue modality
Johnson, B. A., Chen, Y. R., Schmitz, J. M., Bordnick, P. S., & Shafer, A. (1998) · Addictive Behaviors · doi:10.1016/s0306-4603(97)00014-2 · Cited by 59 · see citing works
Fauth‐Bühler, M., Vollstädt‐Klein, S., Klemen, J., & Smolka, M. N. (2008) · Behavioral and Brain Functions · doi:10.1186/1744-9081-4-30 · Cited by 57 · see citing works
Differential brain response to alcohol cue distractors across stages of alcohol dependence
Fryer, S. L., Jørgensen, K. W., Yetter, E., Daurignac, E. C., Watson, T. D., Shanbhag, H., Krystal, J. H., & Mathalon, D. H. (2012) · Biological Psychology · doi:10.1016/j.biopsycho.2012.10.004 · Cited by 56 · see citing works
Reid, M. S., Flammino, F., Starosta, A., Palamar, J. J., & Franck, J. (2006) · Journal of Neural Transmission · doi:10.1007/s00702-005-0439-5 · Cited by 47 · see citing works
Wray, J. M., Godleski, S. A., & Tiffany, S. T. (2011) · Psychology of Addictive Behaviors · doi:10.1037/a0023687 · Cited by 46 · see citing works
Shadel, W. G., NIAURA, R. S., & Abrams, D. B. (2001) · Journal of Behavior Therapy and Experimental Psychiatry · doi:10.1016/s0005-7916(01)00035-0 · Cited by 42 · see citing works
Ewing, S. W. F., Filbey, F. M., Chandler, L. D., & Hutchison, K. E. (2009) · Alcoholism Clinical and Experimental Research · doi:10.1111/j.1530-0277.2009.01104.x · Cited by 38 · see citing works
Sensory modality of smoking cues modulates neural cue reactivity
Yalachkov, Y., Kaiser, J., Görres, A., Seehaus, A., & Naumer, M. J. (2012) · Psychopharmacology · doi:10.1007/s00213-012-2830-x · Cited by 34 · see citing works
Self-citationMasked smoking‐related images modulate brain activity in smokers
Zhang, X., Chen, X., Yu, Y., Sun, D., Ma, N., He, S., Hu, X. P., & Zhang, D. (2008) · Human Brain Mapping · doi:10.1002/hbm.20552 · Cited by 30 · see citing works
Haemodynamic responses to sensory stimulation are enhanced following acute cocaine administration
Devonshire, I. M., Berwick, J., Jones, M., Martindale, J., Johnston, D., Overton, P. G., & Mayhew, J. E. W. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2004.03.042 · Cited by 29 · see citing works
Cocaine preferentially enhances sensory processing in the upper layers of the primary sensory cortex
Devonshire, I. M., Mayhew, J. E. W., & Overton, P. G. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.01.070 · Cited by 29 · see citing works
Involvement of action-related brain regions in nicotine addiction
Yalachkov, Y., & Naumer, M. J. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00195.2011 · Cited by 26 · see citing works
Self-citationEric Artiges, A., Ricalens, E., Berthoz, S., Krebs, M., Penttilä, J., Trichard, C., & Martinot, J. (2009) · Addiction Biology · doi:10.1111/j.1369-1600.2009.00167.x · Cited by 23 · see citing works
(2011) · Wiley eBooks · doi:10.1002/9781119998938 · Cited by 19 · see citing works
Flagged first, then by citations
Research works printed but not linked: 2
- Everitt BJ Robbins TW Neural systems of reinforcement for drug addiction: from actions to habits to compulsion Nat Neurosci 2005b 8 1481 1489 16251991
- Janes AC Pizzagalli DA Richardt S deB Frederick B Chuzi S Pachas G Culhane MA Holmes AJ Fava M Evins AE Kaufman MJ Brain reactivity to smoking cues prior to smoking cessation predicts ability to maintain tobacco abstinence Biol Psychiatry 2010b 67 722 729 20172508 PMC2954596
Cited by
Sorted by citations
Neurobiology of addiction: a neurocircuitry analysis
Koob, G. F., & Volkow, N. D. (2016) · The Lancet Psychiatry · doi:10.1016/s2215-0366(16)00104-8 · Cited by 3,698 · see citing works
The brain on drugs: from reward to addiction
Volkow, N. D., & Morales, M. (2015) · Cell · doi:10.1016/j.cell.2015.07.046 · Cited by 1,306 · see citing works
Sensitive periods of substance abuse: Early risk for the transition to dependence
Jordan, C. J., & Andersen, S. L. (2017) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2016.10.004 · Cited by 455 · see citing works
Addictions neuroclinical assessment: a neuroscience-based framework for addictive disorders
Kwako, L. E., Momenan, R., Litten, R. Z., Koob, G. F., & Goldman, D. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.10.024 · Cited by 395 · see citing works
Addiction and Stress: An Allostatic View
Koob, G. F., & Schulkin, J. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.09.008 · Cited by 315 · see citing works
Basolateral amygdala and stress-induced hyperexcitability affect motivated behaviors and addiction
Sharp, B. M. (2017) · Translational Psychiatry · doi:10.1038/tp.2017.161 · Cited by 244 · see citing works
Cue-reactivity in behavioral addictions: a meta-analysis and methodological considerations
Starcke, K., Antons, S., Trotzke, P., & Brand, M. (2018) · Journal of Behavioral Addictions · doi:10.1556/2006.7.2018.39 · Cited by 180 · see citing works
Zhang, J.-T., Yao, Y.-W., Potenza, M. N., Xia, C.-C., Lan, J., Liu, L., Wang, L.-J., Liu, B., Ma, S.-S., & Fang, X.-Y. (2016) · NeuroImage: Clinical · doi:10.1016/j.nicl.2016.09.004 · Cited by 177 · see citing works
Biomarkers in Substance Use Disorders
Volkow, N. D., Koob, G., & Baler, R. (2015) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.5b00067 · Cited by 141 · see citing works
21st century neurobehavioral theories of decision making in addiction: Review and evaluation
Bickel, W. K., Mellis, A. M., Snider, S. E., Athamneh, L. N., Stein, J. S., & Pope, D. A. (2018) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2017.09.009 · Cited by 134 · see citing works
Xiao, P., Dai, Z., Zhong, J., Zhu, Y., Shi, H., & Pan, P. (2015) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2015.05.030 · Cited by 120 · see citing works
Altered appetitive conditioning and neural connectivity in subjects with compulsive sexual behavior
Klucken, T., Wehrum-Osinsky, S., Schweckendiek, J., Kruse, O., & Stark, R. (2016) · The Journal of Sexual Medicine · doi:10.1016/j.jsxm.2016.01.013 · Cited by 110 · see citing works
Müller, U., Sturm, V., Voges, J., Heinze, H.-J., Galazky, I., Büntjen, L., Heldmann, M., Frodl, T., Steiner, J., & Bogerts, B. (2016) · Pharmacopsychiatry · doi:10.1055/s-0042-104507 · Cited by 108 · see citing works
Froeliger, B., Mathew, A. R., McConnell, P. A., Eichberg, C., Saladin, M. E., Carpenter, M. J., & Garland, E. L. (2017) · Evidence-Based Complementary and Alternative Medicine · doi:10.1155/2017/7018014 · Cited by 83 · see citing works
Zhou, X., Zimmermann, K., Xin, F., Zhao, W., Derckx, R. T., Sassmannshausen, A., Scheele, D., Hurlemann, R., Weber, B., Kendrick, K. M., et al. (2019) · Biological Psychiatry: Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2019.04.006 · Cited by 77 · see citing works
Herremans, S. C., Van Schuerbeek, P., De Raedt, R., Matthys, F., Buyl, R., De Mey, J., & Baeken, C. (2015) · PLOS ONE · doi:10.1371/journal.pone.0136182 · Cited by 78 · see citing works
Kober, H., Brewer, J. A., Height, K. L., & Sinha, R. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2016.09.042 · Cited by 75 · see citing works
A meta-analysis of cue reactivity in tobacco cigarette smokers
Betts, J. M., Dowd, A. N., Forney, M., Hetelekides, E., & Tiffany, S. T. (2021) · Nicotine & Tobacco Research · doi:10.1093/ntr/ntaa147 · Cited by 72 · see citing works
Cocaine cue-induced dopamine release in the human prefrontal cortex
Milella, M. S., Fotros, A., Gravel, P., Casey, K. F., Larcher, K., Verhaeghe, J. A. J., Cox, S. M. L., Reader, A. J., Dagher, A., Benkelfat, C., et al. (2016) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.150207 · Cited by 56 · see citing works
Brand, M., Rumpf, H.-J., Demetrovics, Z., King, D. L., Potenza, M. N., & Wegmann, E. (2019) · Current Addiction Reports · doi:10.1007/s40429-019-00258-y · Cited by 53 · see citing works
A Biopsychosocial Overview of the Opioid Crisis: Considering Nutrition and Gastrointestinal Health
Wiss, D. A. (2019) · Frontiers in Public Health · doi:10.3389/fpubh.2019.00193 · Cited by 41 · see citing works
Psychedelic-Assisted Therapy for Substance Use Disorders and Potential Mechanisms of Action
Rieser, N. M., Herdener, M., & Preller, K. H. (2021) · Current Topics in Behavioral Neurosciences · doi:10.1007/7854_2021_284 · Cited by 37 · see citing works
Kearney-Ramos, T. E., Dowdle, L. T., Mithoefer, O. J., Devries, W., George, M. S., & Hanlon, C. A. (2019) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2019.00317 · Cited by 37 · see citing works
Tsamitros (2022) · doi:10.1007/s00115-022-01378-z · Cited by 16 · see citing works
Moeller, S. J., Kundu, P., Bachi, K., Maloney, T., Malaker, P., Parvaz, M. A., Alia-Klein, N., London, E. D., & Goldstein, R. Z. (2020) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2020.107930 · Cited by 14 · see citing works
Lowen, S. B., Rohan, M. L., Gillis, T. E., Thompson, B. S., Wellons, C. B. W., & Andersen, S. L. (2015) · NeuroImage: Clinical · doi:10.1016/j.nicl.2015.06.012 · Cited by 11 · see citing works
Addressing altered anticipation as a transdiagnostic target through computational psychiatry
Sepúlveda, P., Aitsahalia, I., Kumar, K., Atkin, T., & Iigaya, K. (2025) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2025.02.014 · Cited by 3 · see citing works
- Authors
- Jasinska, A. J., Stein, E. A., Kaiser, J., Naumer, M. J., & Yalachkov, Y.
- Affiliations
- National Institute on Drug Abuse (US)
- Goethe University Frankfurt (DE)
- Corresponding author
- Jasinska, Agnes J.
- Yalachkov, Yavor
- Venue
- Neuroscience & Biobehavioral Reviews
- Publisher
- Elsevier BV
- Published
- 2014-01
- Volume
- 38
- Pages
- 1-16
- ISSN
- 0149-7634 (ISSN-L)
- PMC
- PMC3913480
- OpenAlex
- W2020327987
- Cited by
- 513
- References
- 154
- Citations by year
- 2026: 20 · 2025: 29 · 2024: 30 · 2023: 38 · 2022: 39 · 2021: 44 · 2020: 64 · 2019: 42 · 2018: 48 · 2017: 45 · 2016: 50 · 2015: 42 · 2014: 21 · 2013: 1
- FWCI
- 3.86
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Neuroscience & Biobehavioral Reviews (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (Z99 DA999999)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Health Sciences › Medicine › Epidemiology › Substance Abuse Treatment and Outcomes
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Keywords
- drug cue reactivity, addiction, cocaine use, alcohol consumption, smoking, brain circuits, addiction severity, treatment outcomes
- MeSH terms
- Brain, Brain Mapping, Cues, Humans, Models, Neurological, Behavior, Addictive, Substance-Related Disorders
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review