Striatal dopamine, reward, and decision making in schizophrenia

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

Power failure: why small sample size undermines the reliability of neuroscience

Button, K. S., Ioannidis, J. P. A., Mokrysz, C., Nosek, B. A., Flint, J., Robinson, E. S. J., & Munafò, M. R. (2013) · Nature Reviews Neuroscience · doi:10.1038/nrn3475 · Cited by 7,641 · 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

Psychosis as a state of aberrant salience: a framework linking biology, phenomenology and pharmacology in schizophrenia

Kapur, S. (2003) · American Journal of Psychiatry · doi:10.1176/appi.ajp.160.1.13 · Cited by 2,813 · see citing works

The Dopamine Hypothesis of Schizophrenia: Version III--The Final Common Pathway

Howes, O. D., & Kapur, S. (2009) · Schizophrenia Bulletin · doi:10.1093/schbul/sbp006 · Cited by 2,693 · see citing works

Anticipation of Increasing Monetary Reward Selectively Recruits Nucleus Accumbens

Knutson, B., Adams, C. M., Fong, G. W., & Hommer, D. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-16-j0002.2001 · Cited by 2,244 · 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

Model-based influences on humans’ choices and striatal prediction errors

Daw, N. D., Gershman, S. J., Seymour, B., Dayan, P., & Dolan, R. J. (2011) · Neuron · doi:10.1016/j.neuron.2011.02.027 · Cited by 1,779 · see citing works

The environment and schizophrenia

van Os, J., Kenis, G., & Rutten, B. P. F. (2010) · Nature · doi:10.1038/nature09563 · Cited by 1,572 · see citing works

Untitled work

(1995) · PubMed · Cited by 1,320 · see citing works

Single photon emission computerized tomography imaging of amphetamine-induced dopamine release in drug-free schizophrenic subjects

Laruelle, M., Abi-Dargham, A., van Dyck, C. H., Gil, R., D'Souza, C. D., Erdos, J., McCance, E., Rosenblatt, W., Fingado, C., Zoghbi, S. S., et al. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.17.9235 · Cited by 1,291 · see citing works

Dysconnection in schizophrenia: from abnormal synaptic plasticity to failures of self-monitoring

Stephan, K. E., Friston, K. J., & Frith, C. D. (2009) · Schizophrenia Bulletin · doi:10.1093/schbul/sbn176 · Cited by 1,134 · see citing works

Increased baseline occupancy of D ₂ receptors by dopamine in schizophrenia

Abi-Dargham, A., Rodenhiser, J., Printz, D., Zea-Ponce, Y., Gil, R., Kegeles, L. S., Weiss, R., Cooper, T. B., Mann, J. J., Van Heertum, R. L., et al. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.14.8104 · Cited by 1,020 · see citing works

Goals and Habits in the Brain

Dolan, R. J., & Dayan, P. (2013) · Neuron · doi:10.1016/j.neuron.2013.09.007 · Cited by 977 · see citing works

The Nature of Dopamine Dysfunction in Schizophrenia and What This Means for Treatment: Meta-analysis of Imaging Studies

Howes, O. D., Kambeitz, J., Kim, E., Stahl, D., Slifstein, M., Abi-Dargham, A., & Kapur, S. (2012) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2012.169 · Cited by 967 · see citing works

A causal link between prediction errors, dopamine neurons and learning

Steinberg, E. E., Keiflin, R., Boivin, J. R., Witten, I. B., Deisseroth, K. A., & Janak, P. H. (2013) · Nature Neuroscience · doi:10.1038/nn.3413 · Cited by 879 · see citing works

Increased striatal dopamine transmission in schizophrenia: confirmation in a second cohort.

Abi-Dargham, A., Gil, R. B., Krystal, J., Baldwin, R., Seibyl, J., Bowers, M., van Dyck, C., Charney, D., Innis, R., & Laruelle, M. (1998) · American Journal of Psychiatry · doi:10.1176/ajp.155.6.761 · Cited by 860 · see citing works

The Neurodevelopmental Hypothesis of Schizophrenia, Revisited

Fatemi, S. H., & Folsom, T. D. (2009) · Schizophrenia Bulletin · doi:10.1093/schbul/sbn187 · Cited by 860 · see citing works

Synaptic plasticity and dysconnection in schizophrenia

Stephan, K. E., Baldeweg, T., & Friston, K. J. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.10.005 · Cited by 841 · see citing works

Computational psychiatry

Montague, P. R., Dolan, R. J., Friston, K. J., & Dayan, P. (2012) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2011.11.018 · Cited by 809 · see citing works

Elevated Striatal Dopamine Function Linked to Prodromal Signs of Schizophrenia

Howes, O. D., Montgomery, A. J., Asselin, M.-C., Murray, R. M., Valli, I., Tabraham, P., Bramon-Bosch, E., Valmaggia, L., Johns, L., Broome, M., et al. (2009) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2008.514 · Cited by 744 · see citing works

Prefrontal cortex dysfunction during working memory performance in schizophrenia: reconciling discrepant findings

Manoach, D. S. (2003) · Schizophrenia Research · doi:10.1016/s0920-9964(02)00294-3 · Cited by 681 · see citing works

Reduced prefrontal activity predicts exaggerated striatal dopaminergic function in schizophrenia

Meyer-Lindenberg, A., Miletich, R. S., Kohn, P. D., Esposito, G., Carson, R. E., Quarantelli, M., Weinberger, D. R., & Berman, K. F. (2002) · Nature Neuroscience · doi:10.1038/nn804 · Cited by 652 · see citing works

The IMAGEN study: reinforcement-related behaviour in normal brain function and psychopathology

Schumann, G., Loth, E., Banaschewski, T., Barbot, A., Barker, G. J., Büchel, C., Conrod, P., Dalley, J. W., Flor, H., Gallinat, J., et al. (2010) · Molecular Psychiatry · doi:10.1038/mp.2010.4 · Cited by 618 · see citing works

Predicting Schizophrenia Patients’ Real-World Behavior with Specific Neuropsychological and Functional Capacity Measures

Bowie, C. R., Leung, W. W.-M., Reichenberg, A., McClure, M. M., Patterson, T. L., Heaton, R. K., & Harvey, P. D. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2007.05.022 · Cited by 580 · see citing works

Dysfunction of ventral striatal reward prediction in schizophrenia

Juckel, G., Schlagenhauf, F., Koslowski, M., Wüstenberg, T., Villringer, A., Knutson, B., Wrase, J., & Heinz, A. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2005.07.051 · Cited by 578 · see citing works

Imaging Human Mesolimbic Dopamine Transmission with Positron Emission Tomography. Part II: Amphetamine-Induced Dopamine Release in the Functional Subdivisions of the Striatum

Martinez, D., Slifstein, M., Broft, A., Mawlawi, O., Hwang, D.-R., Huang, Y., Cooper, T., Kegeles, L., Zarahn, E., Abi-Dargham, A., et al. (2003) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/01.wcb.0000048520.34839.1a · Cited by 569 · see citing works

Increased Synaptic Dopamine Function in Associative Regions of the Striatum in Schizophrenia

Kegeles, L. S., Abi-Dargham, A., Frankle, W. G., Gil, R., Cooper, T. B., Slifstein, M., Hwang, D.-R., Huang, Y., Haber, S. N., & Laruelle, M. (2010) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2010.10 · Cited by 565 · see citing works

Reward Processing in Schizophrenia: A Deficit in the Representation of Value

Gold, J. M., Waltz, J. A., Prentice, K. J., Morris, S. E., & Heerey, E. A. (2008) · Schizophrenia Bulletin · doi:10.1093/schbul/sbn068 · Cited by 521 · see citing works

Transient and Selective Overexpression of Dopamine D2 Receptors in the Striatum Causes Persistent Abnormalities in Prefrontal Cortex Functioning

Kellendonk, C., Simpson, E. H., Polan, H. J., Malleret, G., Vronskaya, S., Winiger, V., Moore, H., & Kandel, E. R. (2006) · Neuron · doi:10.1016/j.neuron.2006.01.023 · Cited by 520 · see citing works

Model‐Based fMRI and Its Application to Reward Learning and Decision Making

O’Doherty, J. P., Hampton, A. N., & Kim, H. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1390.022 · Cited by 509 · see citing works

Mesolimbic Functional Magnetic Resonance Imaging Activations during Reward Anticipation Correlate with Reward-Related Ventral Striatal Dopamine Release

Schott, B. H., Minuzzi, L., Krebs, R. M., Elmenhorst, D., Lang, M., Winz, O. H., Seidenbecher, C. I., Coenen, H. H., Heinze, H.-J., Zilles, K., et al. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.2058-08.2008 · Cited by 496 · see citing works

Aberrant Hippocampal Activity Underlies the Dopamine Dysregulation in an Animal Model of Schizophrenia

Lodge, D., & Grace, A. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.2847-07.2007 · Cited by 475 · see citing works

The computational neurobiology of learning and reward

Daw, N. D., & Doya, K. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2006.03.006 · Cited by 462 · see citing works

A Review of Reward Processing and Motivational Impairment in Schizophrenia

Strauss, G. P., Waltz, J. A., & Gold, J. M. (2013) · Schizophrenia Bulletin · doi:10.1093/schbul/sbt197 · Cited by 447 · see citing works

Modulation of amphetamine-induced striatal dopamine release by ketamine in humans: implications for schizophrenia.

Kegeles, L., Abi-Dargham, A., Zea-Ponce, Y., Rodenhiser-Hill, J., Mann, J., Heertum, R. V. V., Cooper, T. B., Carlsson, A., & Laruelle, M. (2000) · Biological Psychiatry · doi:10.1016/s0006-3223(00)00976-8 · Cited by 425 · see citing works

How much of reinforcement learning is working memory, not reinforcement learning? A behavioral, computational, and neurogenetic analysis

Collins, A. G. E., & Frank, M. J. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07980.x · Cited by 419 · see citing works

Prefrontal function in schizophrenia: confounds and controversies

Weinberger, D. R., & Berman, K. F. (1996) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.1996.0135 · Cited by 414 · see citing works

Dopaminergic dysfunction in schizophrenia: Salience attribution revisited

Heinz, A., & Schlagenhauf, F. (2010) · Schizophrenia Bulletin · doi:10.1093/schbul/sbq031 · Cited by 412 · see citing works

Deficits in Prefrontal Cortical and Extrastriatal Dopamine Release in Schizophrenia: A Positron Emission Tomographic Functional Magnetic Resonance Imaging Study

Slifstein, M., van de Giessen, E., Van Snellenberg, J., Thompson, J. L., Narendran, R., Gil, R., Hackett, E., Girgis, R., Ojeil, N., Moore, H., et al. (2015) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2014.2414 · Cited by 398 · see citing works

The ubiquity of model-based reinforcement learning

Doll, B. B., Simon, D. A., & Daw, N. D. (2012) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2012.08.003 · Cited by 380 · see citing works

Dopamine Synthesis Capacity in Patients With Treatment-Resistant Schizophrenia

Demjaha, A., Murray, R. M., McGuire, P. K., Kapur, S., & Howes, O. D. (2012) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2012.12010144 · Cited by 351 · see citing works

Dopamine Synthesis Capacity Before Onset of Psychosis: A Prospective [ ¹⁸ F]-DOPA PET Imaging Study

Howes, O. D., Bose, S. K., Turkheimer, F., Valli, I., Egerton, A., Valmaggia, L. R., Murray, R. M., & McGuire, P. (2011) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2011.11010160 · Cited by 343 · see citing works

Hierarchical Prediction Errors in Midbrain and Basal Forebrain during Sensory Learning

Iglesias, S., Mathys, C., Brodersen, K. H., Kasper, L., Piccirelli, M., den Ouden, H. E. M., & Stephan, K. E. (2013) · Neuron · doi:10.1016/j.neuron.2013.09.009 · Cited by 342 · see citing works

Schizophrenia: A Subcortical Neurotransmitter Imbalance Syndrome?

Carlsson, M. L., & Carlsson, A. C. (1990) · Schizophrenia Bulletin · doi:10.1093/schbul/16.3.425 · Cited by 341 · see citing works

Dysfunction of ventral striatal reward prediction in schizophrenic patients treated with typical, not atypical, neuroleptics

Juckel, G., Schlagenhauf, F., Koslowski, M., Filonov, D., Wüstenberg, T., Villringer, A., Knutson, B., Kienast, T., Gallinat, J., Wrase, J., et al. (2006) · Psychopharmacology · doi:10.1007/s00213-006-0405-4 · Cited by 323 · see citing works

Negative Symptoms and the Failure to Represent the Expected Reward Value of Actions

Gold, J. M. (2012) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2011.1269 · Cited by 319 · see citing works

Computational Psychiatry

Wang, X., & Krystal, J. H. (2014) · Neuron · doi:10.1016/j.neuron.2014.10.018 · Cited by 309 · see citing works

Progressive increase in striatal dopamine synthesis capacity as patients develop psychosis: a PET study

Howes, O., Bose, S., Turkheimer, F., Valli, I., Egerton, A., Stahl, D., Valmaggia, L., Allen, P., Murray, R., & McGuire, P. (2011) · Molecular Psychiatry · doi:10.1038/mp.2011.20 · Cited by 292 · see citing works

Dopaminergic dysfunction in alcoholism and schizophrenia—psychopathological and behavioral correlates

Heinz, A. (2002) · European Psychiatry · doi:10.1016/s0924-9338(02)00628-4 · Cited by 270 · see citing works

Do patients with schizophrenia exhibit aberrant salience?

Roiser, J. P., Stephan, K. E., den Ouden, H. E. M., Barnes, T. R. E., Friston, K. J., & Joyce, E. M. (2009) · Psychological Medicine · doi:10.1017/s0033291708003863 · Cited by 262 · see citing works

Computational approaches to psychiatry

Stephan, K. E., & Mathys, C. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.12.007 · Cited by 260 · see citing works

Dissociable Effects of Dopamine and Serotonin on Reversal Learning

den Ouden, H. E. M., Daw, N. D., Fernández, G., Elshout, J. A., Rijpkema, M., Hoogman, M., Franke, B., & Cools, R. (2013) · Neuron · doi:10.1016/j.neuron.2013.08.030 · Cited by 259 · see citing works

Striatal Presynaptic Dopamine in Schizophrenia, Part II: Meta-Analysis of [18F/11C]-DOPA PET Studies

Fusar‐Poli, P., & Meyer‐Lindenberg, A. (2012) · Schizophrenia Bulletin · doi:10.1093/schbul/sbr180 · Cited by 257 · see citing works

Presynaptic Striatal Dopamine Dysfunction in People at Ultra-high Risk for Psychosis: Findings in a Second Cohort

Egerton, A., Chaddock, C. A., Winton-Brown, T. T., Bloomfield, M. A. P., Bhattacharyya, S., Allen, P., McGuire, P. K., & Howes, O. D. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.11.017 · Cited by 253 · see citing works

Striatal dysfunction during reversal learning in unmedicated schizophrenia patients

Schlagenhauf, F., Huys, Q. J. M., Deserno, L., Rapp, M. A., Beck, A., Heinze, H.-J., Dolan, R., & Heinz, A. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2013.11.034 · Cited by 253 · see citing works

On the Plausibility of “The Neurodevelopmental Hypothesis” of Schizophrenia

Weinberger, D. R. (1996) · Neuropsychopharmacology · doi:10.1016/0893-133x(95)00199-n · Cited by 245 · see citing works

Urbanicity, social adversity and psychosis

Heinz, A., Deserno, L., & Reininghaus, U. (2013) · World Psychiatry · doi:10.1002/wps.20056 · Cited by 234 · see citing works

Abnormal Frontostriatal Interactions in People With Prodromal Signs of Psychosis: A Multimodal Imaging Study

Fusar-Poli, P., Howes, O. D., Allen, P., Broome, M., Valli, I., Asselin, M.-C., Grasby, P. M., & McGuire, P. K. (2010) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2010.77 · Cited by 234 · see citing works

Ventral striatal dopamine reflects behavioral and neural signatures of model-based control during sequential decision making

Deserno, L., Huys, Q. J. M., Boehme, R., Buchert, R., Heinze, H.-J., Grace, A. A., Dolan, R. J., Heinz, A., & Schlagenhauf, F. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1417219112 · Cited by 233 · see citing works

The formation of abnormal associations in schizophrenia: Neural and behavioral evidence

Jensen, J., Willeit, M., Zipursky, R. B., Savina, I., Smith, A. J., Menon, M., Crawley, A. P., & Kapur, S. (2008) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301437 · Cited by 225 · see citing works

Alterations of the brain reward system in antipsychotic naïve schizophrenia patients.

Nielsen, M., Rostrup, E., Wulff, S., Bak, N., Lublin, H., Kapur, S., & Glenthøj, B. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.02.007 · Cited by 222 · see citing works

Neural correlates of reward processing in schizophrenia — Relationship to apathy and depression

Simon, J. J., Biller, A., Walther, S., Roesch-Ely, D., Stippich, C., Weisbrod, M., & Kaiser, S. (2009) · Schizophrenia Research · doi:10.1016/j.schres.2009.11.007 · Cited by 222 · see citing works

Working Memory Contributions to Reinforcement Learning Impairments in Schizophrenia

Collins, A. G. E., Brown, J. K., Gold, J. M., Waltz, J. A., & Frank, M. J. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0989-14.2014 · Cited by 214 · see citing works

Reduced prefrontal-parietal effective connectivity and working memory deficits in schizophrenia

Deserno, L., Sterzer, P., Wüstenberg, T., Heinz, A., & Schlagenhauf, F. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.3405-11.2012 · Cited by 214 · see citing works

Neural and Behavioral Correlates of Aberrant Salience in Individuals at Risk for Psychosis

Roiser, J. P., Howes, O. D., Chaddock, C. A., Joyce, E. M., & McGuire, P. (2013) · Schizophrenia Bulletin · doi:10.1093/schbul/sbs147 · Cited by 205 · see citing works

Reward system activation in schizophrenic patients switched from typical neuroleptics to olanzapine

Schlagenhauf, F., Juckel, G., Koslowski, M., Kahnt, T., Knutson, B., Dembler, T., Kienast, T., Gallinat, J., Wrase, J., & Heinz, A. (2008) · Psychopharmacology · doi:10.1007/s00213-007-1016-4 · Cited by 204 · see citing works

Glutamate Modulation of Dopamine Measured in Vivo with Positron Emission Tomography (PET) and 11C-Raclopride in Normal Human Subjects

G Smith, P. D. (1998) · Neuropsychopharmacology · doi:10.1016/s0893-133x(97)00092-4 · Cited by 201 · see citing works

Reward feedback alterations in unmedicated schizophrenia patients: Relevance for delusions

Schlagenhauf, F., Sterzer, P., Schmack, K., Ballmaier, M., Rapp, M., Wrase, J., Juckel, G., Gallinat, J., & Heinz, A. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.12.016 · Cited by 195 · see citing works

Dimensional psychiatry: reward dysfunction and depressive mood across psychiatric disorders

Hägele, C., Schlagenhauf, F., Rapp, M. A., Sterzer, P., Beck, A., Bermpohl, F., Stoy, M., Ströhle, A., Wïttchen, H., Dolan, R. J., et al. (2014) · Psychopharmacology · doi:10.1007/s00213-014-3662-7 · Cited by 191 · see citing works

Patients with Schizophrenia have a Reduced Neural Response to Both Unpredictable and Predictable Primary Reinforcers

Waltz, J. A., Schweitzer, J. B., Gold, J. M., Kurup, P. K., Ross, T. J., Jo Salmeron, B., Rose, E. J., McClure, S. M., & Stein, E. A. (2009) · Neuropsychopharmacology · doi:10.1038/npp.2008.214 · Cited by 186 · see citing works

Neural Correlates of Forward Planning in a Spatial Decision Task in Humans

Simon, D. A., & Daw, N. D. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4647-10.2011 · Cited by 181 · see citing works

The Development of Neural Synchrony and Large-Scale Cortical Networks During Adolescence: Relevance for the Pathophysiology of Schizophrenia and Neurodevelopmental Hypothesis

Uhlhaas, P. J., & Singer, W. (2011) · Schizophrenia Bulletin · doi:10.1093/schbul/sbr034 · Cited by 176 · see citing works

Amphetamine modulates human incentive processing

Knutson, B., Bjork, J. M., Fong, G. W., Hommer, D., Mattay, V. S., & Weinberger, D. R. (2004) · Neuron · doi:10.1016/j.neuron.2004.06.030 · Cited by 174 · see citing works

Dissecting psychiatric spectrum disorders by generative embedding

Brodersen, K. H., Deserno, L., Schlagenhauf, F., Lin, Z., Penny, W. D., Buhmann, J. M., & Stephan, K. E. (2014) · NeuroImage: Clinical · doi:10.1016/j.nicl.2013.11.002 · Cited by 173 · see citing works

Translational perspectives for computational neuroimaging

Stephan, K. E., Iglesias, S., Heinzle, J., & Diaconescu, A. O. (2015) · Neuron · doi:10.1016/j.neuron.2015.07.008 · Cited by 169 · see citing works

Categorical and dimensional approaches to negative symptoms of schizophrenia: Focus on long-term stability and functional outcome

Galderisi, S., Bucci, P., Mucci, A., Kirkpatrick, B. W., Pini, S., Rossi, A., Vita, A., & Maj, M. (2013) · Schizophrenia Research · doi:10.1016/j.schres.2013.03.020 · Cited by 168 · see citing works

Translating the MAM model of psychosis to humans

Modinos, G., Allen, P., Grace, A. A., & McGuire, P. (2015) · Trends in Neurosciences · doi:10.1016/j.tins.2014.12.005 · Cited by 165 · see citing works

Elevated [18F]Fluorodopamine Turnover in Brain of Patients with Schizophrenia: An [18F]Fluorodopa/Positron Emission Tomography Study

Kumakura, Y., Cumming, P., Vernaleken, I., Buchholz, H., Siessmeier, T., Heinz, A., Kienast, T., Bartenstein, P., & Gründer, G. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0805-07.2007 · Cited by 161 · see citing works

Chapter 19 Dopamine, cognitive control, and schizophrenia: the gating model

Braver, T. S., & Cohen, J. D. (1999) · Progress in Brain Research · doi:10.1016/s0079-6123(08)63082-4 · Cited by 159 · see citing works

Neonatal lesions of the medial temporal lobe disrupt prefrontal cortical regulation of striatal dopamine

Saunders, R., Kolachana, B., Bachevalier, J., & Weinberger, D. (1998) · Nature · doi:10.1038/30245 · Cited by 157 · see citing works

Reinforcement and Reversal Learning in First-Episode Psychosis

Murray, G. K., Cheng, F., Clark, L., Barnett, J. H., Blackwell, A. D., Fletcher, P. C., Robbins, T. W., Bullmore, E. T., & Jones, P. B. (2008) · Schizophrenia Bulletin · doi:10.1093/schbul/sbn078 · Cited by 155 · see citing works

Abnormal Responses to Monetary Outcomes in Cortex, but not in the Basal Ganglia, in Schizophrenia

Waltz, J. A., Schweitzer, J. B., Ross, T. J., Kurup, P. K., Salmeron, B. J., Rose, E. J., Gold, J. M., & Stein, E. A. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2010.126 · Cited by 151 · see citing works

Improvement of Brain Reward Abnormalities by Antipsychotic Monotherapy in Schizophrenia

Nielsen, M. Ø., Rostrup, E., Wulff, S., Bak, N. K., Broberg, B. V., Lublin, H., Kapur, S., & Glenthoj, B. Y. (2012) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2012.847 · Cited by 151 · see citing works

Signals in Human Striatum Are Appropriate for Policy Update Rather than Value Prediction

Li, J., & Daw, N. D. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.6316-10.2011 · Cited by 149 · see citing works

Is avolition in schizophrenia associated with a deficit of dorsal caudate activity? A functional magnetic resonance imaging study during reward anticipation and feedback

Mucci, A., Dima, D., Soricelli, A., Volpe, U., Bucci, P., Frangou, S., Prinster, A., Salvatore, M., Galderisi, S., & Maj, M. (2015) · Psychological Medicine · doi:10.1017/s0033291714002943 · Cited by 132 · see citing works

Striatal dopamine synthesis in first-degree relatives of patients with schizophrenia.

Huttunen, J., Heinimaa, M., Svirskis, T., Nyman, M., Kajander, J., Forsback, S., Solin, O., Ilonen, T., Korkeila, J., Ristkari, T., et al. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2007.04.017 · Cited by 128 · see citing works

Schizophrenia: Overview and Dopamine Dysfunction

Abi-Dargham, A. (2014) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.13078tx2c · Cited by 128 · see citing works

Altered reward functions in patients on atypical antipsychotic medication in line with the revised dopamine hypothesis of schizophrenia

Walter, H., Kammerer, H., Frasch, K., Spitzer, M., & Abler, B. (2009) · Psychopharmacology · doi:10.1007/s00213-009-1586-4 · Cited by 127 · see citing works

Striatal Presynaptic Dopamine in Schizophrenia, Part I: Meta-Analysis of Dopamine Active Transporter (DAT) Density

Fusar‐Poli, P., & Meyer‐Lindenberg, A. (2012) · Schizophrenia Bulletin · doi:10.1093/schbul/sbr111 · Cited by 125 · see citing works

The Roles of Reward, Default, and Executive Control Networks in Set-Shifting Impairments in Schizophrenia

Waltz, J. A., Kasanova, Z., Ross, T. J., Salmeron, B. J., McMahon, R. P., Gold, J. M., & Stein, E. A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0057257 · Cited by 122 · see citing works

Alterations in cortical and extrastriatal subcortical dopamine function in schizophrenia: systematic review and meta-analysis of imaging studies

Kambeitz, J., Abi-Dargham, A., Kapur, S., & Howes, O. (2013) · British Journal of Psychiatry · doi:10.1192/bjp.bp.113.132308 · Cited by 115 · see citing works

Midbrain activation during pavlovian conditioning and delusional symptoms in schizophrenia

Romaniuk, L., Honey, G. D., King, J. R. L., Whalley, H. C., McIntosh, A. M., Levita, L., Hughes, M., Johnstone, E. C., Day, M., Lawrie, S. M., et al. (2010) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2010.169 · Cited by 113 · see citing works

Generalization of value in reinforcement learning by humans

Wimmer, G. E., Daw, N. D., & Shohamy, D. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08017.x · Cited by 111 · see citing works

Striatal Response to Reward Anticipation

Grimm, O., Heinz, A., Walter, H., Kirsch, P., Erk, S., Haddad, L., Plichta, M. M., Romanczuk‐Seiferth, N., Pöhland, L., Mohnke, S., et al. (2014) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2014.9 · Cited by 108 · see citing works

Ventral striatal prediction error signaling is associated with dopamine synthesis capacity and fluid intelligence

Schlagenhauf, F., Rapp, M. A., Huys, Q. J. M., Beck, A., Wüstenberg, T., Deserno, L., Buchholz, H., Kalbitzer, J., Buchert, R., Bauer, M., et al. (2012) · Human Brain Mapping · doi:10.1002/hbm.22000 · Cited by 103 · see citing works

Ventral striatal activation during attribution of stimulus saliency and reward anticipation is correlated in unmedicated first episode schizophrenia patients

Esslinger, C., Englisch, S., Inta, D., Rausch, F., Schirmbeck, F. N., Mier, D. U., Kirsch, P., Meyer‐Lindenberg, A., & Zink, M. (2012) · Schizophrenia Research · doi:10.1016/j.schres.2012.06.025 · Cited by 103 · see citing works

Ventral striatal hypoactivation is associated with apathy but not diminished expression in patients with schizophrenia

Kirschner, M., Hager, O. M., Bischof, M., Hartmann-Riemer, M. N., Kluge, A., Seifritz, E., Tobler, P. N., & Kaiser, S. (2016) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.140383 · Cited by 96 · see citing works

Impaired Activation in Cognitive Control Regions Predicts Reversal Learning in Schizophrenia

Culbreth, A. J., Gold, J. M., Cools, R., & Barch, D. M. (2015) · Schizophrenia Bulletin · doi:10.1093/schbul/sbv075 · Cited by 92 · see citing works

Chaotic behavior in dopamine neurodynamics.

King, R., Barchas, J. D., & Huberman, B. A. (1984) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.81.4.1244 · Cited by 91 · see citing works

Reinforcement Learning and Dopamine in Schizophrenia: Dimensions of Symptoms or Specific Features of a Disease Group?

Deserno, L., Boehme, R., Heinz, A., & Schlagenhauf, F. (2013) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2013.00172 · Cited by 89 · see citing works

Aberrant Salience Is Related to Dysfunctional Self-Referential Processing in Psychosis

Pankow, A., Katthagen, T., Diner, S., Deserno, L., Boehme, R., Kathmann, N., Gleich, T., Gaebler, M., Walter, H., Heinz, A., et al. (2015) · Schizophrenia Bulletin · doi:10.1093/schbul/sbv098 · Cited by 86 · see citing works

Working memory as a predictor of negative symptoms and functional outcome in first episode psychosis

González–Ortega, I., Mozos, V. D. L., Echeburúa, E., Mezo, M., Besga, A., de Azúa, S. R., Arrillaga, A. G.-P., Gutiérrez, M., Zorrilla, E. P., & González-Pinto, A. M. (2012) · Psychiatry Research · doi:10.1016/j.psychres.2012.08.025 · Cited by 81 · see citing works

Motivational Deficits in Schizophrenia and the Representation of Expected Value

Waltz, J. A., & Gold, J. M. (2015) · Current topics in behavioral neurosciences · doi:10.1007/7854_2015_385 · Cited by 80 · see citing works

Methamphetamine-Induced Disruption of Frontostriatal Reward Learning Signals: Relation to Psychotic Symptoms

Bernacer, J., Corlett, P. R., Ramachandra, P., McFarlane, B., Turner, D. C., Clark, L., Robbins, T. W., Fletcher, P. C., & Murray, G. K. (2013) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2013.12070978 · Cited by 77 · see citing works

Reward System Dysfunction as a Neural Substrate of Symptom Expression Across the General Population and Patients With Schizophrenia

Simon, J. J., Cordeiro, S. A., Weber, M. D., Friederich, H., Wolf, R. C., Weisbrod, M., & Kaiser, S. (2015) · Schizophrenia Bulletin · doi:10.1093/schbul/sbv067 · Cited by 69 · see citing works

Lateral prefrontal model-based signatures are reduced in healthy individuals with high trait impulsivity

Deserno, L., Wilbertz, T., Reiter, A. M. F., Horstmann, A., Neumann, J., Villringer, A., Heinze, H. –., & Schlagenhauf, F. (2015) · Translational Psychiatry · doi:10.1038/tp.2015.139 · Cited by 62 · see citing works

Prefrontal and striatal glutamate differently relate to striatal dopamine: Potential regulatory mechanisms of striatal presynaptic dopamine function?

Gleich, T., Deserno, L., Lorenz, R. C., Boehme, R., Pankow, A., Buchert, R., Kuhn, S., Heinz, A., Schlagenhauf, F., & Gallinat, J. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0329-15.2015 · Cited by 62 · see citing works

Symptom dimensions are associated with reward processing in unmedicated persons at risk for psychosis

Wotruba, D., Heekeren, K., Michels, L., Buechler, R., Simon, J. J., Theodoridou, A., Kollias, S., Rössler, W., & Kaiser, S. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00382 · Cited by 61 · see citing works

Blockade of NMDA receptors in the prefrontal cortex increases dopamine and acetylcholine release in the nucleus accumbens and motor activity

Arco, A. D., Segovia, G., & Mora, F. (2008) · Psychopharmacology · doi:10.1007/s00213-008-1288-3 · Cited by 60 · see citing works

Striatal dopamine receptors and transporters in monkeys with neonatal temporal limbic damage

Heinz, A., Saunders, R., Kolachana, B., Jones, D., Gorey, J. G., Bachevalier, J., & Weinberger, D. R. (1999) · Synapse · doi:10.1002/(sici)1098-2396(199905)32:2 · Cited by 60 · see citing works

Aberrant Salience Is Related to Reduced Reinforcement Learning Signals and Elevated Dopamine Synthesis Capacity in Healthy Adults

Boehme, R., Deserno, L., Gleich, T., Katthagen, T., Pankow, A., Behr, J., Buchert, R., Roiser, J. P., Heinz, A., & Schlagenhauf, F. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0805-15.2015 · Cited by 52 · see citing works

Altered amygdala activation in schizophrenia patients during emotion processing

Pankow, A., Friedel, E., Sterzer, P., Romanczuk‐Seiferth, N., Walter, H., Heinz, A., & Schlagenhauf, F. (2013) · Schizophrenia Research · doi:10.1016/j.schres.2013.07.015 · Cited by 47 · see citing works

Ketamine increases striatal dopamine release and hyperlocomotion in adult rats after postnatal functional blockade of the prefrontal cortex.

Usun, Y., Eybrard, S., Meyer, F., & Louilot, A. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.08.017 · Cited by 46 · see citing works

General functioning predicts reward and punishment learning in schizophrenia

Somlai, Z., Moustafa, A. A., Kéri, S., Myers, C. E., & Gluck, M. A. (2011) · Schizophrenia Research · doi:10.1016/j.schres.2010.07.028 · Cited by 45 · see citing works

The Effect of Dopamine Agonists on Adaptive and Aberrant Salience in Parkinson's Disease

Nagy, H., Levy-Gigi, E., Somlai, Z., Takáts, A., Bereczki, D., & Kéri, S. (2012) · Neuropsychopharmacology · doi:10.1038/npp.2011.278 · Cited by 42 · see citing works

Schizophrenia: A Computational Reinforcement Learning Perspective

Frank, M. J. (2008) · Schizophrenia Bulletin · doi:10.1093/schbul/sbn123 · Cited by 37 · see citing works

Nature or Nurture? Determining the Heritability of Human Striatal Dopamine Function: an [18F]-DOPA PET Study

Stokes, P. R. A., Shotbolt, P., Mehta, M. A., Turkheimer, E., Benecke, A., Copeland, C., Turkheimer, F. E., Lingford-Hughes, A. R., & Howes, O. D. (2013) · Neuropsychopharmacology · doi:10.1038/npp.2012.207 · Cited by 37 · see citing works

Ketamine Suppresses the Ventral Striatal Response to Reward Anticipation: A Cross-Species Translational Neuroimaging Study

François, J., Grimm, O., Schwarz, A. J., Schweiger, J. I., Haller, L., Risterucci, C., Böhringer, A., Zang, Z., Tost, H., Gilmour, G., et al. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.291 · Cited by 34 · see citing works

Reduced reward-related probability learning in schizophrenia patients

Yılmaz, A., Şimşek, & Gönül, A. S. (2012) · Neuropsychiatric Disease and Treatment · doi:10.2147/ndt.s26243 · Cited by 30 · see citing works

Disruption of Reward Processing in Addiction: An Image-Based Meta-analysis of Functional Magnetic Resonance Imaging Studies

Luijten, M., Schellekens, A. F., Kühn, S., Machielse, M. W. J., & Sescousse, G. (2017) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2016.3084 · Cited by 402 · see citing works

Prefrontal cortical thinning links to negative symptoms in schizophrenia via the ENIGMA consortium

Walton, E., Hibar, D. P., van Erp, T. G. M., Potkin, S. G., Roiz‐Santiáñez, R., Crespo‐Facorro, B., Suárez‐Pinilla, P., van Haren, N. E. M., de Zwarte, S. M. C., Kahn, R. S., et al. (2017) · Psychological Medicine · doi:10.1017/s0033291717001283 · Cited by 168 · see citing works

Integrative Brain Network and Salience Models of Psychopathology and Cognitive Dysfunction in Schizophrenia

Menon, V., Palaniyappan, L. K., & Supekar, K. (2022) · Biological Psychiatry · doi:10.1016/j.biopsych.2022.09.029 · Cited by 161 · see citing works

Recent advancement in nanosensors for neurotransmitters detection: Present and future perspective

Chauhan, N., Soni, S., Agrawal, P., Balhara, Y. P. S., & Jain, U. (2019) · Process Biochemistry · doi:10.1016/j.procbio.2019.12.016 · Cited by 104 · see citing works

Altered Medial Frontal Feedback Learning Signals in Anorexia Nervosa

Bernardoni, F., Geisler, D., King, J. A., Javadi, A., Ritschel, F., Murr, J., Reiter, A. M. F., Roessner, V., Smolka, M. N., Kiebel, S. J., et al. (2017) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.07.024 · Cited by 61 · see citing works

Neurochemistry of Visual Attention

Lockhofen, D. E. L., & Mulert, C. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.643597 · Cited by 62 · see citing works

Free Energy and Virtual Reality in Neuroscience and Psychoanalysis: A Complexity Theory of Dreaming and Mental Disorder

Hopkins, J. (2016) · Frontiers in Psychology · doi:10.3389/fpsyg.2016.00922 · Cited by 53 · see citing works

Functional connectivity of the ventral tegmental area and avolition in subjects with schizophrenia: a resting state functional MRI study

Giordano, G. M., Stanziano, M., Papa, M., Mucci, A., Prinster, A., Soricelli, A., & Galderisi, S. (2018) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2018.03.013 · Cited by 47 · see citing works

Differential neural reward mechanisms in treatment-responsive and treatment-resistant schizophrenia

Vanes, L. D., Mouchlianitis, E. D., Collier, T., Averbeck, B. B., & Shergill, S. S. (2018) · Psychological Medicine · doi:10.1017/s0033291718000041 · Cited by 40 · see citing works

Functional dysconnectivity of the limbic loop of frontostriatal circuits in first‐episode, treatment‐naive schizophrenia

Lin, P., Wang, X., Zhang, B., Kirkpatrick, B. W., Öngür, D., Levitt, J. J., Jovicich, J., Yao, S., & Wang, X. (2017) · Human Brain Mapping · doi:10.1002/hbm.23879 · Cited by 35 · see citing works

Differences in Functional Connectivity Networks Related to the Midbrain Dopaminergic System-Related Area in Various Psychiatric Disorders

Nakamura, Y., Okada, N., Koshiyama, D., Kamiya, K., Abe, O., Kunimatsu, A., Okanoya, K., Kasai, K., & Koike, S. (2019) · Schizophrenia Bulletin · doi:10.1093/schbul/sbz121 · Cited by 31 · see citing works

The “highs and lows” of the human brain on dopaminergics: Evidence from neuropharmacology

Martins, D., Mehta, M. A., & Prata, D. P. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.06.003 · Cited by 29 · see citing works

Computational Psychiatry: From Mechanistic Insights to the Development of New Treatments

Huys, Q. J. M., Maia, T. V., & Paulus, M. P. (2016) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2016.08.001 · Cited by 32 · see citing works

A review of risky decision-making in psychosis-spectrum disorders

Purcell, J. R., Herms, E. N., Morales, J. J., Hetrick, W. P., Wisner, K., & Brown, J. W. (2021) · Clinical Psychology Review · doi:10.1016/j.cpr.2021.102112 · Cited by 28 · see citing works

Analysis of individual differences in neurofeedback training illuminates successful self-regulation of the dopaminergic midbrain

Hellrung, L., Kirschner, M., Sulzer, J. S., Sladky, R., Scharnowski, F., Herdener, M., & Tobler, P. N. (2022) · Communications Biology · doi:10.1038/s42003-022-03756-4 · Cited by 22 · see citing works

Neuronal density and proportion of interneurons in the associative, sensorimotor and limbic human striatum

Lecumberri, A., López‐Janeiro, Á., Corral-Domenge, C., & Bernácer, J. (2017) · Brain Structure and Function · doi:10.1007/s00429-017-1579-8 · Cited by 22 · see citing works

Investigating the Relationship between White Matter Connectivity and Motivational Circuits in Subjects with Deficit Schizophrenia: A Diffusion Tensor Imaging (DTI) Study

Giordano, G. M., Pezzella, P., Quarantelli, M., Bucci, P., Prinster, A., Soricelli, A., Perrottelli, A., Giuliani, L., Fabrazzo, M., & Galderisi, S. (2021) · Journal of Clinical Medicine · doi:10.3390/jcm11010061 · Cited by 20 · see citing works

The Paradox of Delusions

Nicholas Furl, A., Coltheart, M., & McKay, R. (2024) · doi:10.1093/oso/9780198872221.003.0012 · Cited by 18 · see citing works

Computational reinforcement learning, reward (and punishment), and dopamine in psychiatric disorders

Liebenow, B., Jones, R., DiMarco, E. K., Trattner, J. D., Humphries, J. B., Sands, L. P., Spry, K. P., Johnson, C. K., Farkas, E. B., Jiang, A., et al. (2022) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2022.886297 · Cited by 19 · see citing works

fMRI correlates of jumping-to-conclusions in patients with delusions: Connectivity patterns and effects of metacognitive training

Andreou, C., Steinmann, S., Leicht, G., Kolbeck, K., Moritz, S., & Mulert, C. (2018) · NeuroImage Clinical · doi:10.1016/j.nicl.2018.07.004 · Cited by 17 · see citing works

Dopamine, Psychosis, and Symptom Fluctuation: A Narrative Review

Novak, G., & Seeman, M. (2022) · Healthcare · doi:10.3390/healthcare10091713 · Cited by 17 · see citing works

Maternal selenium dietary supplementation alters sociability and reinforcement learning deficits induced by in utero exposure to maternal immune activation in mice

Gillespie, B., Houghton, M. J., Ganio, K., McDevitt, C. A., Bennett, D., Dunn, A. L., Raju, S., Schroeder, A., Hill, R., & Cardoso, B. R. (2023) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2023.12.024 · Cited by 14 · see citing works

Blood‑brain barrier dysfunction in schizophrenia: Mechanisms and implications (Review)

Lv, S., & Luo, C. (2025) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2025.5594 · Cited by 17 · see citing works

Reward, Control & Decision-Making in Cannabis Use Disorder: Insights from Functional MRI

Fatima, H., Howlett, A. C., & Whitlow, C. T. (2019) · British Journal of Radiology · doi:10.1259/bjr.20190165 · Cited by 12 · see citing works

Ventral tegmental area dysfunction affects decision-making in patients with myotonic dystrophy type-1

Serra, L., Scocchia, M., Meola, G., D’Amelio, M., Bruschini, M., Silvestri, G., Petrucci, A., Domenico, C. D., Caltagirone, C., Koch, G., et al. (2020) · Cortex · doi:10.1016/j.cortex.2020.03.022 · Cited by 11 · see citing works

Dopamine D2 −141C Ins/Del and Taq1A polymorphisms, body mass index, and prediction error brain response

Frank, G., Shott, M. E., DeGuzman, M. C., & Smolen, A. (2018) · Translational Psychiatry · doi:10.1038/s41398-018-0147-1 · Cited by 9 · see citing works

Amphetamine disrupts haemodynamic correlates of prediction errors in nucleus accumbens and orbitofrontal cortex

Werlen, E., Shin, S.-L., Gastambide, F., François, J., Tricklebank, M. D., Marston, H. M., Huxter, J. R., Gilmour, G., & Walton, M. E. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-019-0564-8 · Cited by 10 · see citing works

Striatal dopamine D2 binding correlates with locus of control: Preliminary evidence from [11C]raclopride Positron Emission Tomography

Vassena, E., Filip Van Opstal, A., Goethals, I., & Verguts, T. (2019) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2019.09.016 · Cited by 8 · see citing works

Polish Psychiatric Association consensus statement on non-pharmacological methods in the treatment of negative symptoms of schizophrenia

Samochowiec, J., Szulc, A., Bieńkowski, P., Dudek, D., Gałecki, P., Heitzman, J., Wojnar, M., & Wichniak, A. (2021) · Psychiatria Polska · doi:10.12740/pp/onlinefirst/135527 · Cited by 9 · see citing works

Linking haploinsufficiency of the autism- and schizophrenia-associated gene Cyfip1 with striatal-limbic-cortical network dysfunction and cognitive inflexibility

Haddon, J. E., Titherage, D., Heckenast, J. R., Carter, J., Owen, M. J., Hall, J., Wilkinson, L. S., & Jones, M. W. (2024) · Translational Psychiatry · doi:10.1038/s41398-024-02969-x · Cited by 6 · see citing works

High-performance hybrid phase 1T/2H MoS₂ for selective and simultaneous detection of dopamine and uric acid

Thomas, C., S, S., As, A., & R., R. (2025) · Electrochimica Acta · doi:10.1016/j.electacta.2025.147519 · Cited by 6 · see citing works

Cannabis use and hippocampal subfield volumes in males with a first episode of a schizophrenia spectrum disorder and healthy controls

Scheffler, F., du Plessis, S., Asmal, L., Kilian, S., Phahladira, L., Luckhoff, H. K., & Emsley, R. A. (2021) · Schizophrenia Research · doi:10.1016/j.schres.2021.02.017 · Cited by 6 · see citing works

Quantitative analysis of the Golgi impregnated human (neo)striatal neurons: Observation of the morphological characteristics followed by an emphasis on the functional diversity of cells

Krstonošić, B., Milošević, N. T., & Gudović, R. (2022) · Annals of Anatomy - Anatomischer Anzeiger · doi:10.1016/j.aanat.2022.152040 · Cited by 4 · see citing works

Trust and Psychotic Disorders

Lemmers-Jansen, I. L. J., & Fett, A.-K. J. (2021) · Cambridge University Press eBooks · doi:10.1017/9781108770880.022 · Cited by 4 · see citing works

Decreased serum levels of α‐synuclein in patients with schizophrenia and their unaffected siblings

Göverti, D., Büyüklüoğlu, N., Yüksel, R. N., Kaya, H., Yücel, Ç., & Göka, E. (2023) · Early Intervention in Psychiatry · doi:10.1111/eip.13398 · Cited by 4 · see citing works

Activating the dorsomedial and ventral midbrain projections to the striatum differentially impairs goal-directed action in male mice

Conn, K., Zou, S., Das, J., Alexander, S., Burne, T. H. J., & Kesby, J. P. (2023) · Neuropharmacology · doi:10.1016/j.neuropharm.2023.109550 · Cited by 4 · see citing works

Diminished differentiation of rewards in individuals at clinical high-risk for psychosis

Pratt, D. N., Treadway, M. T., Strauss, G. P., & Mittal, V. A. (2024) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-024-01794-z · Cited by 3 · see citing works

For Value or for Worth? Part 2: A Neuroeconomical Thought-Action-Mood-Space Modulated by (Un-)Certainty as Sign- or Goal-tracking

Treviranus, G. R. S. (2017) · Universal Journal of Psychology · doi:10.13189/ujp.2017.050203 · Cited by 1 · see citing works

Individual Variation in Risky Decisions Is Related to Age and Gender but not to Mental Health SymptomsPreprint

Talwar, A., Cormack, F. K., Huys, Q. J. M., & Roiser, J. P. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.07.11.499611 · Cited by 2 · see citing works

EEG-fMRI in Psychiatry

Sammer, G., & Mulert, C. (2022) · Springer eBooks · doi:10.1007/978-3-031-07121-8_20 · Cited by 1 · see citing works

Modeling Decision-Making in Schizophrenia: Associations Between Computationally Derived Risk Propensity and Self-Reported Risk Perception

Herms, E. N., Brown, J. W., Wisner, K., Hetrick, W. P., Zald, D. H., & Purcell, J. R. (2024) · Schizophrenia Bulletin · doi:10.1093/schbul/sbae144 · Cited by 1 · see citing works

Association of the endosomal sorting processes cargo selection and membrane tubulation with human reward system reactivity

Treutlein, J., Krämer, B., Rex‐Haffner, M., Awasthi, S., Ripke, S., Binder, E. B., & Gruber, O. (2025) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-025-02102-z · Cited by 1 · see citing works

Neural Activation During Cognitive Effort-Based Decision Making: Associations With Avolition in Veterans With Schizophrenia and Bipolar Disorder

Leathem, L. D., Patel, P., Barch, D. M., Jimenez, A. M., Moran, E. K., Myers, A. C., Reavis, E. A., Green, M. F., & Wynn, J. K. (2026) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2026.01.007 · Cited by 1 · see citing works

Recent Developments in Electrochemical Sensors for Monitoring Neurotransmitters

Yence, M., Çetinkaya, A., & Özkan, S. A. (2026) · Critical Reviews in Analytical Chemistry · doi:10.1080/10408347.2026.2642802 · Cited by 1 · see citing works

Negative symptoms in the Hierarchical Taxonomy of Psychopathology: Nosology, etiology, and pathophysiology

Williams, T. F., Freilich, C. D., Cowan, H. R., Docherty, A. R., Jonas, K. G., Martin, E. A., & Kotov, R. (2026) · Schizophrenia Research · doi:10.1016/j.schres.2026.05.012 · Cited by 1 · see citing works

Brexpiprazole vs. Aripiprazole in Patients with Schizophrenia with or Without Comorbid Substance Use Disorder: A 12-Month Real-World Naturalistic Study of Efficacy

Lombardozzi, G., Kotzalidis, G. D., Trovini, G., Amici, E., Ceccherelli, A., Albanesi, G., Giovanetti, V., Martinotti, G., & Filippis, S. D. (2026) · Brain Sciences · doi:10.3390/brainsci16070744 · Cited by 1 · see citing works

Association of Unc-51-like Kinase 4 ( ULK4 ) with the reactivity of the extended reward system in response to conditioned stimuli

Treutlein, J., Löhlein, S., Einenkel, K. E., Picotin, R., Diekhof, E. K., & Gruber, O. (2024) · The World Journal of Biological Psychiatry · doi:10.1080/15622975.2024.2393381 · Cited by 1 · see citing works

Multifractal Analysis of Neuronal Morphology in the Human Dorsal Striatum: Age-Related Changes and Spatial Differences

Nedeljković, Z., Krstonošić, B., Milošević, N. T., Stanojlović, O. P., Hrnčić, D., & Rajković, N. (2024) · Fractal and Fractional · doi:10.3390/fractalfract8090514 · Cited by 1 · see citing works

Gene Set-Based Analysis of the Endosomal Sorting Processes Cargo Selection and Membrane Tubulation with Human Reward System ReactivityPreprint

Treutlein, J., Krämer, B., Rex‐Haffner, M., Awasthi, S., Ripke, S., Binder, E. B., & Gruber, O. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.07.18.549434 · Cited by 1 · see citing works

Individual differences in successful self-regulation of the dopaminergic midbrainPreprint

Hellrung, L., Kirschner, M., Sulzer, J. S., Sladky, R., Scharnowski, F., Herdener, M., & Tobler, P. N. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/863639

Neuropathological Level of Trust

Krüeger, F. (2021) · Cambridge University Press eBooks · doi:10.1017/9781108770880.021

Graphene-based nanocomposites for detection of chemical messengers in nervous system

Aziz, A., Iftikhar, T., Ashraf, G., Ajmal, M., Asif, M. H., & Wang, S. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-90553-4.00005-6

Impact of Unc-51 Like Kinase 4 ( ULK4 ) on the Reactivity of the Extended Reward System in Response to Conditioned StimuliPreprint

Treutlein, J., Löhlein, S., Einenkel, K. E., Diekhof, E. K., & Gruber, O. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.15.575326

Avolition predicts variability in optimal risk-taking in early psychosis

Patel, P. K., Thies, M. B., Moyett, A., Arkin, S. C., Currin, D. L., DeRosse, P., & Karlsgodt, K. H. (2025) · Schizophrenia Research · doi:10.1016/j.schres.2025.04.001

Investigation of the role of the LC3 conjugation system in autophagy for human reward system reactivity

Treutlein, J., Krämer, B., & Gruber, O. (2025) · The World Journal of Biological Psychiatry · doi:10.1080/15622975.2025.2522793

Decision-Making Deficits

Bedwell, S. A. (2025) · Cambridge University Press eBooks · doi:10.1017/9781009407946.012

Biochemical Basis of Dopamine and Its Role in Neurofinancial Decision Making

Polat, Y. (2025) · Aksaray Üniversitesi İktisadi ve İdari Bilimler Fakültesi Dergisi · doi:10.52791/aksarayiibd.1708701

The indirect pathway hypothesis of schizophrenia: insights from perinatal asphyxia

Vázquez-Borsetti, P. (2026) · Frontiers in Physiology · doi:10.3389/fphys.2026.1759386

F208. Patients With Schizophrenia Have Reduced Tendency Towards Model-Based Decision Making, Which is not Linked With Ventral Striatal Presynaptic Dopamine as in Healthy Controls

Brandl, F., Sorg, C., Avram, M., Cabello, J., Mustafa, M., Ziegler, S. I., & Wunderlich, K. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2018.02.822

Dopaminergic Circuitry and Risk/Reward Decision Making: Implications for Schizophrenia

Stopper, C. M., & Floresco, S. B. (2015) · Schizophrenia Bulletin · doi:10.1093/schbul/sbu165 · Cited by 51 · see citing works

Negative symptoms, striatal dopamine and model-free reward decision-making in schizophrenia

Brandl, F., Knolle, F., Avram, M., Leucht, C., Yakushev, I., Priller, J., Leucht, S., Ziegler, S., Wunderlich, K., & Sorg, C. (2023) · Brain · doi:10.1093/brain/awac268 · Cited by 24 · see citing works

O5.1. STRIATAL DOPAMINE AND REDUCED REWARD PREDICTION ERROR SIGNALING IN UNMEDICATED SCHIZOPHRENIA PATIENTS

Katthagen, T., Kaminski, J. A., Heinz, A., Buchert, R., & Schlagenhauf, F. (2020) · Schizophrenia Bulletin · doi:10.1093/schbul/sbaa028.024 · Cited by 2 · see citing works

Mesocorticolimbic reinforcement learning of reward representation and value provides an integrated mechanistic account for schizophreniaPreprint

Morita, K., & Kumar, A. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.08.10.669522