The Rat Prefrontostriatal System Analyzed in 3D: Evidence for Multiple Interacting Functional Units

The Rat Brain in Stereotaxic Coordinates

Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585 · see citing works

Measures of the Amount of Ecologic Association Between Species

Dice, L. R. (1945) · Ecology · doi:10.2307/1932409 · Cited by 12,153 · see citing works

Computer visualization of three-dimensional image data using IMOD.

Kremer, J. R., Mastronarde, D., & Mcintosh, J. (1996) · Journal of Structural Biology · doi:10.1006/jsbi.1996.0013 · Cited by 5,770 · see citing works

AChE-stained horizontal sections of the rat brain in stereotaxic coordinates

Paxinos, G., WATSON, C. R. R., & Emson, P. C. (1980) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(80)90021-7 · Cited by 4,497 · see citing works

Functional architecture of basal ganglia circuits: neural substrates of parallel processing

Alexander, G. E., & Crutcher, M. D. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90107-l · Cited by 4,131 · see citing works

The role of the basal ganglia in habit formation

Yin, H. H., & Knowlton, B. J. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1919 · Cited by 2,402 · see citing works

Statistical validation of image segmentation quality based on a spatial overlap index1

Zou, K. H., Warfield, S. K., Bharatha, A., Tempany, C. M., Kaus, M. R., Haker, S. J., Wells, W. M., Jolesz, F. A., & Kikinis, R. (2004) · Academic Radiology · doi:10.1016/s1076-6332(03)00671-8 · Cited by 1,860 · see citing works

Striatonigrostriatal pathways in primates form an ascending spiral from the shell to the dorsolateral striatum

Haber, S. N., Fudge, J. L., & McFarland, N. R. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-06-02369.2000 · Cited by 1,610 · see citing works

Anatomical evidence for cerebellar and basal ganglia involvement in higher cognitive function

Middleton, F. A., & Strick, P. L. (1994) · Science · doi:10.1126/science.7939688 · Cited by 1,356 · see citing works

The organization of the projection from the cerebral cortex to the striatum in the rat

McGeorge, A. J., & Faull, R. L. M. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90128-0 · Cited by 1,345 · see citing works

Putting a spin on the dorsal-ventral divide of the striatum

Voorn, P., Vanderschuren, L. J. M. J., Groenewegen, H. J., Robbins, T. W., & Pennartz, C. M. A. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.06.006 · Cited by 1,188 · see citing works

The Basal Ganglia and Chunking of Action Repertoires

Graybiel, A. M. (1998) · Neurobiology of Learning and Memory · doi:10.1006/nlme.1998.3843 · Cited by 1,042 · see citing works

Do rats have a prefrontal cortex?

Uylings, H. B. M., Groenewegen, H. J., & Kolb, B. (2003) · Behavioural Brain Research · doi:10.1016/j.bbr.2003.09.028 · Cited by 1,013 · see citing works

The medial prefrontal cortex in the rat: evidence for a dorso-ventral distinction based upon functional and anatomical characteristics

Heidbreder, C. A., & Groenewegen, H. J. (2003) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2003.09.003 · Cited by 882 · see citing works

Functions of the frontal cortex of the rat: A comparative review

Kolb, B. E. (1984) · Brain Research Reviews · doi:10.1016/0165-0173(84)90018-3 · Cited by 882 · see citing works

Inhibitory control of neostriatal projection neurons by GABAergic interneurons

Koós, T. Z., & Tepper, J. M. (1999) · Nature Neuroscience · doi:10.1038/8138 · Cited by 851 · see citing works

Topographical organization and relationship with ventral striatal compartments of prefrontal corticostriatal projections in the rat

Berendse, H. W., Graaf, Y. G.-D., & Groenewegen, H. J. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903160305 · Cited by 847 · see citing works

Temporal and spatial dynamics of brain structure changes during extensive learning

Draganski, B., Gaser, C., Kempermann, G., Kuhn, H. G., Winkler, J., Buchel, C., & May, A. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.4628-05.2006 · Cited by 765 · see citing works

The cortico-basal ganglia integrative network: The role of the thalamus

Haber, S. N., & Calzavara, R. (2008) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2008.09.013 · Cited by 721 · see citing works

Reward-related cortical inputs define a large striatal region in primates that interface with associative cortical connections, providing a substrate for incentive-based learning.

Haber, S. N., Kim, K.-S., Mailly, P., & Calzavara, R. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.0271-06.2006 · Cited by 686 · see citing works

The basal ganglia: learning new tricks and loving it

Graybiel, A. M. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.10.006 · Cited by 650 · see citing works

Cortico-striate projections in the rhesus monkey: The organization of certain cortico-caudate connections

Yeterian, E. H., & Hoesen, G. W. V. (1978) · Brain Research · doi:10.1016/0006-8993(78)90059-8 · Cited by 641 · see citing works

Extrinsic connections of the basal ganglia

Parent, A. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90105-j · Cited by 633 · see citing works

The specificity of the ‘nonspecific’ midline and intralaminar thalamic nuclei

Groenewegen, H. J., & Berendse, H. W. (1994) · Trends in Neurosciences · doi:10.1016/0166-2236(94)90074-4 · Cited by 596 · see citing works

The organization of the basal ganglia-thalamocortical circuits: Open interconnected rather than closed segregated

Joel, D., & Weiner, I. (1994) · Neuroscience · doi:10.1016/0306-4522(94)90536-3 · Cited by 430 · see citing works

Organization of the nigrothalamocortical system in the rhesus monkey

Ilinsky, I. A., Jouandet, M. L., & Goldman‐Rakic, P. S. (1985) · Journal of Comparative Neurology · doi:10.1002/cne.902360304 · Cited by 406 · see citing works

Feedforward Inhibition of Projection Neurons by Fast-Spiking GABA Interneurons in the Rat StriatumIn Vivo

Mallet, N. P., Moine, C. L., Charpier, S., & Gonon, F. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.5027-04.2005 · Cited by 380 · see citing works

Potassium currents responsible for inward and outward rectification in rat neostriatal spiny projection neurons

Nisenbaum, E., & Wilson, C. J. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-06-04449.1995 · Cited by 348 · see citing works

Compartmental distribution of ventral striatal neurons projecting to the mesencephalon in the rat

Berendse, H. W., Groenewegen, H. J., & Lohman, A. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-06-02079.1992 · Cited by 230 · see citing works

Dynamics of Synaptic Transmission between Fast-Spiking Interneurons and Striatal Projection Neurons of the Direct and Indirect Pathways

Planert, H., Szydlowski, S. N., Hjorth, J. J. J., Grillner, S. E., & Silberberg, G. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.5139-09.2010 · Cited by 222 · see citing works

Corticostriatal Combinatorics: The Implications of Corticostriatal Axonal Arborizations

Zheng, T., & Wilson, C. J. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00519.2001 · Cited by 205 · see citing works

The orbital cortex in rats topographically projects to central parts of the caudate-putamen complex

Schilman, E. A., Uylings, H. B. M., Graaf, Y. G.-D., Joel, D., & Groenewegen, H. J. (2008) · Neuroscience Letters · doi:10.1016/j.neulet.2007.12.024 · Cited by 187 · see citing works

Forebrain connectivity of the prefrontal cortex in the marmoset monkey (Callithrix jacchus): An anterograde and retrograde tract‐tracing study

Roberts, A., Tomic, D. L., Parkinson, C. H., Roeling, T. A. P., Cutter, D. J., Robbins, T. W., & Everitt, B. J. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21300 · Cited by 181 · see citing works

Relationship between the corticostriatal terminals from areas 9 and 46, and those from area 8A, dorsal and rostral premotor cortex and area 24c: an anatomical substrate for cognition to action

Calzavara, R., Mailly, P., & Haber, S. N. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05825.x · Cited by 170 · see citing works

The associative striatum: Organization of cortical projections to the dorsocentral striatum in rats

Reep, R. L., Cheatwood, J. L., & Corwin, J. V. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10868 · Cited by 125 · see citing works

Intrinsic membrane properties of neostriatal neurons can account for their low level of spontaneous activity

Calabresi, P., Misgeld, U., & Dodt, H. U. (1987) · Neuroscience · doi:10.1016/0306-4522(87)90021-2 · Cited by 107 · see citing works

Cell‐specific spike‐timing‐dependent plasticity in GABAergic and cholinergic interneurons in corticostriatal rat brain slices

Fino, É., Deniau, J., & Venance, L. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2007.144501 · Cited by 105 · see citing works

Double anterograde tracing of outputs from adjacent “barrel columns” of rat somatosensory cortex. Neostriatal projection patterns and terminal ultrastructure

Wright, A. K., Norrie, L., Ingham, C. A., Hutton, E. A. M., & Arbuthnott, G. W. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00186-9 · Cited by 93 · see citing works

Cell cycle kinetics in the embryonic mouse corpus striatum

Bhide, P. G. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19961028)374:4 · Cited by 73 · see citing works

The rat orbital and agranular insular prefrontal cortical areas: a cytoarchitectonic and chemoarchitectonic study

Werd, H. J. J. M. V. D., & Uylings, H. B. M. (2008) · Brain Structure and Function · doi:10.1007/s00429-007-0164-y · Cited by 73 · see citing works

Asymmetric spike-timing dependent plasticity of striatal nitric oxide-synthase interneurons

Fino, É., Paillé, V., Deniau, J., & Venance, L. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.03.015 · Cited by 43 · see citing works

Functional integration across a gradient of corticostriatal channels controls UP state transitions in the dorsal striatum

Kasanetz, F., Riquelme, L. A., Della‐Maggiore, V., O’Donnell, P., & Murer, M. G. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0711113105 · Cited by 41 · see citing works

Anatomical segregation of information processing in the rat substantia nigra pars reticulata.

Deniau, J., & Thierry, A. M. (1997) · PubMed · Cited by 39 · see citing works

Neuroanatomy of Reward: A View from the Ventral Striatum -- Neurobiology of Sensation and Reward

Ja, G. (2011) · Cited by 29 · see citing works

A 3D multi-modal and multi-dimensional digital brain model as a framework for data sharing

Mailly, P., Haber, S. N., Groenewegen, H. J., & Deniau, J. (2009) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2009.12.014 · Cited by 22 · see citing works

A Comparison of Shells Utilized by Hydractinia and Podocoryne

Crowell, S. (1945) · Ecology · doi:10.2307/1930828 · Cited by 20 · see citing works

A mesoscale connectome of the mouse brain

Oh, S. W., Harris, J. A., Ng, L., Winslow, B., Cain, N., Mihalas, S., Wang, Q., Lau, C., Kuan, L., Henry, A. M., et al. (2014) · Nature · doi:10.1038/nature13186 · Cited by 2,612 · see citing works

The mouse cortico-striatal projectome

Hintiryan, H., Foster, N. N., Bowman, I., Bay, M., Song, M. Y., Gou, L., Yamashita, S., Bienkowski, M. S., Zingg, B., Zhu, M., et al. (2016) · Nature Neuroscience · doi:10.1038/nn.4332 · Cited by 541 · see citing works

A comprehensive excitatory input map of the striatum reveals novel functional organization

Hunnicutt, B. J., Jongbloets, B. C., Birdsong, W. T., Gertz, K. J., Zhong, H., & Mao, T. (2016) · eLife · doi:10.7554/elife.19103 · Cited by 536 · see citing works

Behavioral and Neurobiological Mechanisms of Pavlovian and Instrumental Extinction Learning.

Bouton, M., Maren, S., & McNally, G. (2020) · Physiological Reviews · doi:10.1152/physrev.00016.2020 · Cited by 320 · see citing works

Limbic circuitry of the midline thalamus

Vertes, R. P., Linley, S. B., & Hoover, W. B. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.01.014 · Cited by 391 · see citing works

Reassessing Models of Basal Ganglia Function and Dysfunction

Nelson, A., & Kreitzer, A. C. (2014) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071013-013916 · Cited by 339 · see citing works

Circuit-Based Corticostriatal Homologies Between Rat and Primate

Heilbronner, S. R., Rodríguez-Romaguera, J., Quirk, G. J., Groenewegen, H. J., & Haber, S. N. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.05.012 · Cited by 321 · see citing works

A Motivational and Neuropeptidergic Hub: Anatomical and Functional Diversity within the Nucleus Accumbens Shell

Castro, D. C., & Bruchas, M. R. (2019) · Neuron · doi:10.1016/j.neuron.2019.03.003 · Cited by 287 · see citing works

Where is Cingulate Cortex? A Cross-Species View

van Heukelum, S., Mars, R. B., Guthrie, M., Buitelaar, J. K., Beckmann, C. F., Tiesinga, P. H. E., Vogt, B. A., Glennon, J. C., & Havenith, M. N. (2020) · Trends in Neurosciences · doi:10.1016/j.tins.2020.03.007 · Cited by 248 · see citing works

NOW vs LATER brain circuits: implications for obesity and addiction

Volkow, N. D., & Baler, R. D. (2015) · Trends in Neurosciences · doi:10.1016/j.tins.2015.04.002 · Cited by 237 · see citing works

Basal ganglia circuit loops, dopamine and motivation: a review and enquiry

Ikemoto, S., Yang, C., & Tan, A. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.04.018 · Cited by 226 · see citing works

Dopaminergic control of cognitive flexibility in humans and animals

Klanker, M., Feenstra, M., & Denys, D. (2013) · Frontiers in Neuroscience · doi:10.3389/fnins.2013.00201 · Cited by 209 · see citing works

Organization of the connections between claustrum and cortex in the mouse

Wang, Q., Ng, L., Harris, J. A., Feng, D. H., Li, Y., Royall, J. J., Oh, S. W., Bernard, A., Sunkin, S. M., Christof Koch, A., et al. (2016) · The Journal of Comparative Neurology · doi:10.1002/cne.24047 · Cited by 197 · see citing works

Going and stopping: dichotomies in behavioral control by the prefrontal cortex

Gourley, S. L., & Taylor, J. R. (2016) · Nature Neuroscience · doi:10.1038/nn.4275 · Cited by 195 · see citing works

Behavioral and neurophysiological correlates of regret in rat decision-making on a neuroeconomic task

Steiner, A. P., & Redish, A. D. (2014) · Nature Neuroscience · doi:10.1038/nn.3740 · Cited by 171 · 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

Dorsal and ventral streams: the distinct role of striatal subregions in the acquisition and performance of goal-directed actions

Hart, G., Leung, B. K., & Balleine, B. W. (2014) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.11.003 · Cited by 166 · see citing works

Parceling Human Accumbens into Putative Core and Shell Dissociates Encoding of Values for Reward and Pain

Baliki, M. N., Mansour, A. R., Baria, A. T., Huang, L., Berger, S., Fields, H. L., & Apkarian, A. V. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1731-13.2013 · Cited by 146 · see citing works

Afferents to anterior cingulate areas 24a and 24b and midcingulate areas 24a′ and 24b′ in the mouse

Fillinger, C., Yalçın, İ., Barrot, M., & Veinante, P. (2016) · Brain Structure and Function · doi:10.1007/s00429-016-1290-1 · Cited by 139 · see citing works

Unique contributions of parvalbumin and cholinergic interneurons in organizing striatal networks during movement

Gritton, H. J., Howe, W. M., Romano, M. F., DiFeliceantonio, A. G., Kramer, M., Saligrama, V., Bucklin, M. E., Zemel, D., & Han, X. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0341-3 · Cited by 124 · see citing works

Where attention falls: Increased risk of falls from the converging impact of cortical cholinergic and midbrain dopamine loss on striatal function

Sarter, M. F., Albin, R. L., Kucinski, A. J., & Lustig, C. (2014) · Experimental Neurology · doi:10.1016/j.expneurol.2014.04.032 · Cited by 114 · see citing works

Comparative three-dimensional connectome map of motor cortical projections in the mouse brain

Jeong, M., Kim, Y., Kim, J. J., Ferrante, D. D., Mitra, P. P., Osten, P., & Kim, D. (2016) · Scientific Reports · doi:10.1038/srep20072 · Cited by 101 · see citing works

Primate homologs of mouse cortico-striatal circuits

Balsters, J. H., Zerbi, V., Sallet, J., Wenderoth, N., & Mars, R. B. (2020) · eLife · doi:10.7554/elife.53680 · Cited by 98 · see citing works

Efferents of anterior cingulate areas 24a and 24b and midcingulate areas 24aʹ and 24bʹ in the mouse

Fillinger, C., Yalçın, İ., Barrot, M., & Veinante, P. (2017) · Brain Structure and Function · doi:10.1007/s00429-017-1585-x · Cited by 97 · see citing works

Multicolor multiscale brain imaging with chromatic multiphoton serial microscopy

Abdeladim, L., Matho, K. S., Clavreul, S., Mahou, P., Sintès, J.-M., Solinas, X., Arganda‐Carreras, I., Turney, S. G., Lichtman, J. W., Chessel, A., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-09552-9 · Cited by 95 · see citing works

Oscillatory Activity in the Medial Prefrontal Cortex and Nucleus Accumbens Correlates with Impulsivity and Reward Outcome

Donnelly, N. A., Holtzman, T., Rich, P. D., Nevado‐Holgado, A. J., Fernando, A. B. P., Dijck, G. V., Holzhammer, T., Paul, O., Ruther, P., Paulsen, O., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0111300 · Cited by 84 · see citing works

The other side of the histamine H3 receptor

Ellenbroek, B. A., & Ghiabi, B. (2014) · Trends in Neurosciences · doi:10.1016/j.tins.2014.02.007 · Cited by 83 · see citing works

Pyramidal Cell Subtypes and Their Synaptic Connections in Layer 5 of Rat Frontal Cortex

Kawaguchi, Y. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx252 · Cited by 80 · see citing works

Markers of Serotonergic Function in the Orbitofrontal Cortex and Dorsal Raphé Nucleus Predict Individual Variation in Spatial-Discrimination Serial Reversal Learning

Barlow, R. L., Alsiö, J., Jupp, B., Rabinovich, R., Shrestha, S., Roberts, A. C., Robbins, T. W., & Dalley, J. W. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2014.335 · Cited by 77 · see citing works

Connections of the Mouse Orbitofrontal Cortex and Regulation of Goal-Directed Action Selection by Brain-Derived Neurotrophic Factor

Zimmermann, K. S., Yamin, J. A., Rainnie, D. G., Ressler, K. J., & Gourley, S. L. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.10.026 · Cited by 78 · see citing works

Modeling Fall Propensity in Parkinson's Disease: Deficits in the Attentional Control of Complex Movements in Rats with Cortical-Cholinergic and Striatal–Dopaminergic Deafferentation

Kucinski, A. J., Paolone, G., Bradshaw, M., Albin, R. L., & Sarter, M. F. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2545-13.2013 · Cited by 81 · see citing works

Distributed cell assemblies spanning prefrontal cortex and striatum

Oberto, V. J., Boucly, C. J., Gao, H., Todorova, R., Zugaro, M. B., & Wiener, S. I. (2021) · Current Biology · doi:10.1016/j.cub.2021.10.007 · Cited by 74 · see citing works

Reduced Structural Connectivity in Frontostriatal White Matter Tracts in the Associative Loop in Schizophrenia

Levitt, J. J., Nestor, P. G., Levin, L. K., Pelavin, P. E., Lin, P., Kubicki, M. R., McCarley, R. W., Shenton, M. E., & Yogesh Rathi, A. (2017) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2017.16091046 · Cited by 71 · see citing works

Motor cortex can directly drive the globus pallidus neurons in a projection neuron type-dependent manner in the rat

Karube, F., TAKAHASHI, S. Y., Kobayashi, K., & Fujiyama, F. (2019) · eLife · doi:10.7554/elife.49511 · Cited by 63 · see citing works

Differential expression of cytoskeletal regulatory factors in the adolescent prefrontal cortex: Implications for cortical development

Shapiro, L. P., Parsons, R. G., Koleske, A. J., & Gourley, S. L. (2016) · Journal of Neuroscience Research · doi:10.1002/jnr.23960 · Cited by 68 · see citing works

Multiple Dopamine Systems: Weal and Woe of DopaminePreprint

Watabe‐Uchida, M., & Uchida, N. (2018) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2018.83.037648 · Cited by 68 · see citing works

Region-specific and state-dependent action of striatal GABAergic interneurons

Fino, É., Vandecasteele, M., Siaume‐Perez, S., Saudou, F., & Venance, L. (2018) · Nature Communications · doi:10.1038/s41467-018-05847-5 · Cited by 66 · see citing works

Synaptic Wiring of Corticostriatal Circuits in Basal Ganglia: Insights into the Pathogenesis of Neuropsychiatric Disorders

Kuo, H., & Liu, F. (2019) · eNeuro · doi:10.1523/eneuro.0076-19.2019 · Cited by 63 · see citing works

Anatomical Inputs From the Sensory and Value Structures to the Tail of the Rat Striatum

Jiang, H., & Kim, H. F. (2018) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2018.00030 · Cited by 57 · see citing works

Contralateral disconnection of the rat prelimbic cortex and dorsomedial striatum impairs cue-guided behavioral switchingPreprint

Baker, P. M., & Ragozzino, M. E. (2014) · Learning & Memory · doi:10.1101/lm.034819.114 · Cited by 57 · see citing works

An Avoidance-Based Rodent Model of Exposure With Response Prevention Therapy for Obsessive-Compulsive Disorder

Rodríguez-Romaguera, J., Greenberg, B. D., Rasmussen, S. A., & Quirk, G. J. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.02.012 · Cited by 51 · see citing works

Dissociable roles for the ventral and dorsal medial prefrontal cortex in cue-guided risk/reward decision making

van Holstein, M., & Floresco, S. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-019-0557-7 · Cited by 56 · see citing works

Quantitative Imaging of Cholinergic Interneurons Reveals a Distinctive Spatial Organization and a Functional Gradient across the Mouse Striatum

Matamales, M., Götz, J., & Bertran‐Gonzalez, J. (2016) · PLoS ONE · doi:10.1371/journal.pone.0157682 · Cited by 53 · see citing works

A unidirectional but not uniform striatal landscape of dopamine signaling for motivational stimuli

van Elzelingen, W., Goedhoop, J. N., Warnaar, P., Denys, D. A. J. P., Arbab, T., & Willuhn, I. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2117270119 · Cited by 51 · see citing works

Synaptic Cytoskeletal Plasticity in the Prefrontal Cortex Following Psychostimulant Exposure

DePoy, L. M., & Gourley, S. L. (2015) · Traffic · doi:10.1111/tra.12295 · Cited by 51 · see citing works

How contexts promote and prevent relapse to drug seeking

Khoo, S. Y., Gibson, G. D., Prasad, A. A., & McNally, G. P. (2016) · Genes Brain & Behavior · doi:10.1111/gbb.12328 · Cited by 52 · see citing works

Opposing Roles of the Dorsolateral and Dorsomedial Striatum in the Acquisition of Skilled Action Sequencing in Rats

Turner, K. M., Svegborn, A., Langguth, M., McKenzie, C., & Robbins, T. W. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.1907-21.2022 · Cited by 51 · see citing works

Enhancement of fear extinction with deep brain stimulation: evidence for medial orbitofrontal involvement

Rodriguez-Romaguera, J., Do-Monte, F. H., Tanimura, Y., Quirk, G. J., & Haber, S. N. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.20 · Cited by 48 · see citing works

Secretagogin expression delineates functionally-specialized populations of striatal parvalbumin-containing interneurons

Garas, F. N., Shah, R. S., Kormann, E., Doig, N. M., Vinciati, F., Nakamura, K., Dorst, M. C., Smith, Y., Magill, P. J., & Sharott, A. (2016) · eLife · doi:10.7554/elife.16088 · Cited by 48 · see citing works

Prefrontal Corticotropin-Releasing Factor (CRF) Neurons Act Locally to Modulate Frontostriatal Cognition and Circuit Function

Hupalo, S., Martin, A. J., Green, R. K., Devilbiss, D. M., & Berridge, C. W. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2701-18.2019 · Cited by 44 · see citing works

Thalamus

Vertes, R. P., Linley, S. B., Groenewegen, H. J., & Witter, M. P. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-374245-2.00016-4 · Cited by 43 · see citing works

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Delcasso, S., Huh, N., Byeon, J. S., Lee, J., Jung, M. W., & Lee, I. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0622-14.2014 · Cited by 44 · see citing works

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Duan, L. Y., Horst, N. K., Cranmore, S. A. W., Horiguchi, N., Cardinal, R. N., Roberts, A. C., & Robbins, T. W. (2021) · Neuron · doi:10.1016/j.neuron.2021.06.003 · Cited by 41 · see citing works

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Kucinski, A. J., & Sarter, M. F. (2015) · Behavioral Neuroscience · doi:10.1037/bne0000048 · Cited by 41 · see citing works

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Coizet, V., Heilbronner, S. R., Carcenac, C., Mailly, P., Lehman, J. F., Savasta, M., Olivier David, A., Deniau, J., Groenewegen, H. J., & Haber, S. N. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.3304-16.2017 · Cited by 37 · see citing works

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Zimmermann, K. S., Li, C.-C., Rainnie, D. G., Ressler, K. J., & Gourley, S. L. (2018) · Neuropsychopharmacology · doi:10.1038/npp.2017.219 · Cited by 38 · see citing works

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Bryden, D. W., Brockett, A. T., Blume, E., Heatley, K. C., Zhao, A., & Roesch, M. R. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy008 · Cited by 36 · see citing works

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Zimmermann, K. S., Li, C.-C., Rainnie, D. G., Ressler, K. J., & Gourley, S. L. (2018) · Neuropsychopharmacology · doi:10.1038/npp.2017.139 · Cited by 37 · see citing works

Habit learning in hierarchical cortex–basal ganglia loops

Baladron, J., & Hamker, F. H. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14730 · Cited by 31 · see citing works

Neural substrates of habit

Malvaez, M. (2019) · Journal of Neuroscience Research · doi:10.1002/jnr.24552 · Cited by 33 · see citing works

A voxel-based analysis of neurobiological mechanisms in placebo analgesia in rats

Zeng, Y., Hu, D., Yang, W., Hayashinaka, E., Wada, Y., Watanabe, Y., Zeng, Q., & Cui, Y. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.06.009 · Cited by 29 · see citing works

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Green, J. T., & Bouton, M. E. (2021) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2021.107533 · Cited by 32 · see citing works

Nicotinic receptor subtypes differentially modulate glutamate release in the dorsal medial striatum

Howe, W. M., Young, D. A., Bekheet, G., & Kozak, R. (2016) · Neurochemistry International · doi:10.1016/j.neuint.2016.08.009 · Cited by 28 · see citing works

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Janssen, M. L. F., Temel, Y., Delaville, C., Zwartjes, D. G. M., Heida, T., Deurwaerdère, P. D., Visser-Vandewalle, V. E. R. M., & Benazzouz, A. (2016) · Brain Structure and Function · doi:10.1007/s00429-016-1351-5 · Cited by 27 · see citing works

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Avila, C., Kucinski, A. J., & Sarter, M. F. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0220-20.2020 · Cited by 26 · see citing works

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Mair, R. G., Francoeur, M. J., Krell, E. M., & Gibson, B. M. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.928610 · Cited by 32 · see citing works

Neuronal activity of the prefrontal cortex is reduced in rats selectively bred for deficient sensorimotor gating

Alam, M., Angelov, S. D., Stemmler, M., von Wrangel, C., Krauss, J. K., & Schwabe, K. (2014) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2014.08.017 · Cited by 25 · see citing works

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Navailles, S., Guillem, K., Vouillac‐Mendoza, C., & Ahmed, S. H. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu112 · Cited by 22 · see citing works

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Ferbinteanu, J. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1084-20.2020 · Cited by 22 · see citing works

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Baker, P. M., & Ragozzino, M. E. (2013) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.11.006 · Cited by 21 · see citing works

Abnormal neural activation patterns underlying working memory impairment in chronic phencyclidine-treated mice

Arime, Y., & Akiyama, K. (2017) · PLoS ONE · doi:10.1371/journal.pone.0189287 · Cited by 21 · see citing works

NeuroGT: A brain atlas of neurogenic tagging CreER drivers for birthdate-based classification and manipulation of mouse neurons

Hirata, T., Tohsato, Y., Itoga, H., Shioi, G., Kiyonari, H., Oka, S., Fujimori, T., & Onami, S. (2021) · Cell Reports Methods · doi:10.1016/j.crmeth.2021.100012 · Cited by 21 · see citing works

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Braz, B. Y., Galiñanes, G. L., Taravini, I. R. E., Belforte, J. E., & Murer, M. G. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.104 · Cited by 21 · see citing works

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Heilbronner, S. R., Meyer, M. A. A., Choi, E. Y., & Haber, S. N. (2018) · Brain Structure and Function · doi:10.1007/s00429-018-1662-9 · Cited by 21 · see citing works

Neuronal activity in dorsomedial and dorsolateral striatum under the requirement for temporal credit assignment

Her, E. S., Huh, N., Kim, J., & Jung, M. W. (2016) · Scientific Reports · doi:10.1038/srep27056 · Cited by 20 · see citing works

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Sarter, M. F., Avila, C., Kucinski, A. J., & Donovan, E. (2021) · Movement Disorders · doi:10.1002/mds.28532 · Cited by 20 · see citing works

The role of the medial prefrontal cortex in updating reward value and avoiding perseveration

Laskowski, C. S., Williams, R. J., Martens, K. M., Gruber, A. J., Fisher, K. G., & Euston, D. R. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.03.007 · Cited by 23 · see citing works

Structural and molecular heterogeneity of calretinin‐expressing interneurons in the rodent and primate striatum

Garas, F. N., Kormann, E., Shah, R. S., Vinciati, F., Smith, Y., Magill, P. J., & Sharott, A. (2017) · The Journal of Comparative Neurology · doi:10.1002/cne.24373 · Cited by 19 · see citing works

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Shipman, M. L., Johnson, G. C., Bouton, M. E., & Green, J. T. (2019) · eNeuro · doi:10.1523/eneuro.0125-19.2019 · Cited by 20 · see citing works

Dorsomedial striatal contributions to different forms of risk/reward decision making

Schumacher, J. D., van Holstein, M., Bagrodia, V., Bouder, H. B. L., & Floresco, S. (2020) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2020.107369 · Cited by 19 · see citing works

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Davies, D. A., Greba, Q., Selk, J. C., Catton, J. K., Baillie, L. D., Mulligan, S. J., & Howland, J. G. (2017) · Learning & Memory · doi:10.1101/lm.045419.117 · Cited by 19 · see citing works

Dissociable contributions of dorsal and ventral striatal regions on a rodent cost/benefit decision-making task requiring cognitive effort

Silveira, M. M., Tremblay, M., & Winstanley, C. A. (2018) · Neuropharmacology · doi:10.1016/j.neuropharm.2018.04.025 · Cited by 18 · see citing works

Prior cocaine self-administration impairs attention signals in anterior cingulate cortex

Vázquez, D., Pribut, H. J., Burton, A. C., Tennyson, S. S., & Roesch, M. R. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-019-0578-2 · Cited by 18 · see citing works

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Malhotra, S., Cross, R. W. A., Zhang, A., & van der Meer, M. A. A. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.13069 · Cited by 17 · see citing works

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Apetz, N., Kordys, E., Simon, M., Mang, B., Aswendt, M., Wiedermann, D., Neumaier, B., Drzezga, A. E., Timmermann, L., & Endepols, H. (2019) · Disease Models & Mechanisms · doi:10.1242/dmm.039065 · Cited by 17 · see citing works

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Scholl, C., Baladron, J., Vitay, J., & Hamker, F. H. (2022) · Brain Structure and Function · doi:10.1007/s00429-021-02446-x · Cited by 16 · see citing works

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Monko, M. E., & Heilbronner, S. R. (2021) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01699 · Cited by 15 · see citing works

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Maisonneuve, B. G. C., Libralesso, L., Miny, L., Batut, A., Rontard, J., Gleyzes, M., Boudra, B., Viera, J., Debis, D., Larramendy, F., et al. (2022) · Microsystems & Nanoengineering · doi:10.1038/s41378-022-00406-x · Cited by 14 · see citing works

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Groenewegen, H. J., Wouterlood, F. G., & Uylings, H. B. M. (2016) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-802206-1.00021-0 · Cited by 14 · see citing works

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Young, M. K., Conn, K., Das, J., Zou, S., Alexander, S., Burne, T. H. J., & Kesby, J. P. (2022) · Biological Psychiatry Global Open Science · doi:10.1016/j.bpsgos.2022.08.005 · Cited by 13 · see citing works

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Ehinger, Y., Soneja, D., Phamluong, K., Salvi, A., & Dorit Ron, A. (2023) · eNeuro · doi:10.1523/eneuro.0238-21.2023 · Cited by 12 · see citing works

Reduced cortical GABA and glutamate in high schizotypy

Kozhuharova, P., Diaconescu, A. O., & Allen, P. (2021) · Psychopharmacology · doi:10.1007/s00213-021-05867-y · Cited by 12 · see citing works

Mesencephalic dopamine neurons interfacing the shell of nucleus accumbens and the dorsolateral striatum in the rat

Wouterlood, F. G., Engel, A., Daal, M. R. R., Houwen, G., Meinderts, A., Jordá-Siquier, T., Beliën, J. A. M., van Dongen, Y. C., Scheel‐Krüger, J., Thierry, A. M., et al. (2018) · Journal of Neuroscience Research · doi:10.1002/jnr.24242 · Cited by 12 · see citing works

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Gauthier, J. M., Tassin, D. H., Dwoskin, L. P., & Kantak, K. M. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.04.018 · Cited by 12 · see citing works

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Groenewegen, H. J., Voorn, P., & Scheel‐Krüger, J. (2016) · Innovations in cognitive neuroscience · doi:10.1007/978-3-319-42743-0_2 · Cited by 11 · see citing works

Taking Rapid and Intermittent Cocaine Infusions Enhances Both Incentive Motivation for the Drug and Cocaine-induced Gene Regulation in Corticostriatal Regions

Minogianis, E.-A., & Samaha, A. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.05.058 · Cited by 11 · see citing works

Integrative Networks Across Basal Ganglia Circuits

Haber, S. N. (2016) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-802206-1.00027-1 · Cited by 10 · see citing works

Frequency-specific coupling in fronto-parieto-occipital cortical circuits underlie active tactile discrimination

Kunicki, C. B., Moioli, R. C., Pais-Vieira, M., Peres, A. S. C., Morya, E., & Nicolelis, M. A. L. (2019) · Scientific Reports · doi:10.1038/s41598-019-41516-3 · Cited by 10 · see citing works

Orbitofrontal cortex to dorsal striatum circuit is critical for incubation of oxycodone craving after forced abstinence

Lin, H., Olaniran, A., Luo, X., Strauch, J., Burke, M. A. M., Matheson, C. L., & Li, X. (2024) · Addiction Biology · doi:10.1111/adb.13440 · Cited by 9 · see citing works

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Zakiewicz, I. M., Majka, P., Wojcik, D. K., Bjaalie, J. G., & Leergaard, T. B. (2015) · PLoS ONE · doi:10.1371/journal.pone.0137571 · Cited by 8 · see citing works

Longitudinal topography and interdigitation of corticostriatal projections in the rhesus monkey

Selemon, L. D., & Goldman-Rakic, P. S. (1985) · Journal of Neuroscience · doi:10.1523/jneurosci.05-03-00776.1985 · Cited by 1,074 · see citing works

Topographical organization and relationship with ventral striatal compartments of prefrontal corticostriatal projections in the rat

Berendse, H. W., Graaf, Y. G.-D., & Groenewegen, H. J. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903160305 · Cited by 847 · see citing works

Estimates of projection overlap and zones of convergence within frontal-striatal circuits

Averbeck, B. B., Lehman, J., Jacobson, M., & Haber, S. N. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.5806-12.2014 · Cited by 179 · see citing works

Organization of Prefrontal-Striatal Connections

Groenewegen, H. J., Wouterlood, F. G., & Uylings, H. B. M. (2016) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-802206-1.00021-0 · Cited by 14 · see citing works

Prefrontostriatal connections in relation to cortical architectonic organization in rhesus monkeys

Yeterian, E. H., & Pandya, D. N. (1991) · Journal of Comparative Neurology · doi:10.1002/cne.903120105 · Cited by 351 · see citing works