Serotonergic neurons signal reward and punishment on multiple timescales

A neural substrate of prediction and reward

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Millisecond-timescale, genetically targeted optical control of neural activity

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The origin of extracellular fields and currents — EEG, ECoG, LFP and spikes

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Channelrhodopsin-2, a directly light-gated cation-selective membrane channel

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Driving fast-spiking cells induces gamma rhythm and controls sensory responses

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Structure and function of the brain serotonin system

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Distribution of serotonin-immunoreactivity in the central nervous system of the rat-cell bodies and terminals

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An autoradiographic analysis of the differential ascending projections of the dorsal and median raphe nuclei in the rat

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Two types of dopamine neuron distinctly convey positive and negative motivational signals

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Neuron-type-specific signals for reward and punishment in the ventral tegmental area

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Impact of distinct neurotransmitter release modes on neuronal signaling

Zhang, K. J., Monteggia, L. M., & Kavalali, E. T. (2025) · Molecular Psychiatry · doi:10.1038/s41380-025-03373-7 · Cited by 22

Striatal Serotonin Release Signals Reward Value

Spring, M. G., & Nautiyal, K. M. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.0602-24.2024 · Cited by 13

Synaptic Interactions Between Serotonergic and Dopaminergic Systems in Parkinson’s Disease

Marino, G., Campanelli, F., Natale, G., Carluccio, M. D., Servillo, F., Ghiglieri, V., & Calabresi, P. (2025) · Current Neuropharmacology · doi:10.2174/011570159x336597241217062042 · Cited by 14

Dopamine and serotonin signals for reward across time scales

Cohen, J. Y. (2015) · Science · doi:10.1126/science.aad3003 · Cited by 14

Social Dominance Representations in the Human Brain

Ligneul, R., & Dreher, J. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-805308-9.00017-8 · Cited by 15

Global Transcriptome Changes That Accompany Alterations in Serotonin Levels inCaenorhabditis elegans

Cruz-Corchado, J., Ooi, F. K., Das, S., & Prahlad, V. (2020) · G3 Genes Genomes Genetics · doi:10.1534/g3.120.401088 · Cited by 13

Medial Prefrontal Cortex Serotonin Input Regulates Cognitive Flexibility in MicePreprint

Morgan, A. A., Alves, N. D., Stevens, G. S., Yeasmin, T. T., MacKay, A. S., Power, S. K., Sargin, D., Hanna, C., Adib, A., Ziolkowski-Blake, A., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.03.30.534775 · Cited by 16

A single oral dose of citalopram increases interoceptive insight in healthy volunteers

Livermore, J. J. A., Holmes, C. L., Moga, G., Adamatzky, K., Critchley, H., Garfinkel, S. N., & Campbell-Meiklejohn, D. K. (2022) · Psychopharmacology · doi:10.1007/s00213-022-06115-7 · Cited by 17

Dorsal raphe neurons integrate the values of reward amount, delay, and uncertainty in multi-attribute decision-making

Feng, Y.-Y., Bromberg-Martin, E. S., & Monosov, I. E. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114341 · Cited by 18

Systematic Analysis of Transmitter Coexpression Reveals Organizing Principles of Local Interneuron Heterogeneity

Lizbinski, K. M., Marsat, G., & Dacks, A. M. (2018) · eNeuro · doi:10.1523/eneuro.0212-18.2018 · Cited by 15

Serotonin and the neurobiology of anxious states

Lawther, A. J., Hale, M. W., & Lowry, C. A. (2020) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-444-64125-0.00029-3 · Cited by 17

A distributed subcortical circuit linked to instrumental information-seeking about threat

Trier, H. A., Khalighinejad, N., Hamilton, S., Harbison, C., Priestley, L., Laubach, M., Klein-Flügge, M., Scholl, J., & Rushworth, M. F. S. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2410955121 · Cited by 12

Coding principles and mechanisms of serotonergic transmission modes

Zhang, Y., Zhang, P., Shin, M., Chang, Y., Abbott, S. B. G., Venton, B. J., & Zhu, J. (2025) · Molecular Psychiatry · doi:10.1038/s41380-025-02930-4 · Cited by 14

Serotonin distribution in the brain of the plainfin midshipman: Substrates for vocal‐acoustic modulation and a reevaluation of the serotonergic system in teleost fishes

Timothy, M., & Forlano, P. M. (2020) · The Journal of Comparative Neurology · doi:10.1002/cne.24938 · Cited by 11

Neural activity of orbitofrontal cortex contributes to control of waiting

Xiao, X., Deng, H., Lei, W. I., Huang, Y., & Wang, Z. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13320 · Cited by 12

Prior Activation of 5-HT7 Receptors Modulates the Conditioned Place Preference With Methylphenidate

Carbone, C., Russo, S. L. M. L., Lacivita, E., Frank, A., Alleva, E., Stark, H., Saso, L., Leopoldo, M., & Adriani, W. (2019) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2019.00208 · Cited by 11

Serotonin predictively encodes valuePreprint

Harkin, E. F., Grossman, C. D., Cohen, J. Y., Béïque, J.-C., & Naud, R. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.09.19.558526 · Cited by 11

Implications of Kynurenine Pathway Metabolism for the Immune System, Hypothalamic–Pituitary–Adrenal Axis, and Neurotransmission in Alcohol Use Disorder

Osuch, B., Misztal, T., Pałatyńska, K., & Tomaszewska-Zaremba, D. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25094845 · Cited by 10

Parvalbumin-expressing basal forebrain neurons mediate learning from negative experience

Hegedüs, P., Király, B., Schlingloff, D., Lyakhova, V., Velencei, A., Szabó, Í., Mayer, M. I., Zelenak, Z., Nyíri, G., & Hangya, B. (2024) · Nature Communications · doi:10.1038/s41467-024-48755-7 · Cited by 14

Two eARCHT3.0 Lines for Optogenetic Silencing of Dopaminergic and Serotonergic Neurons

Krol, A., López-Huerta, V. G., Corey, T. E. C., Deisseroth, K. A., Ting, J. T., & Feng, G. (2019) · Frontiers in Neural Circuits · doi:10.3389/fncir.2019.00004 · Cited by 10

Dorsal Raphe Nucleus Serotoninergic Neurons Mediate Morphine Rewarding Effect and Conditioned Place Preference

Fu, B., Yao, J.-Q., Lu, C., Wang, B., Li, Z., Huang, M., Tian, T., Peng, H., & Liu, S. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2021.10.031 · Cited by 10

Reduced serotonergic transmission alters sensitivity to cost and reward via 5-HT1A and 5-HT1B receptors in monkeys

Hori, Y., Mimura, K., Nagai, Y., Hori, Y., Kumata, K., Zhang, M., Suhara, T., Higuchi, M., & Minamimoto, T. (2024) · PLoS Biology · doi:10.1371/journal.pbio.3002445 · Cited by 9

Pavlovian-instrumental interactions in active avoidance: The bark of neutral trials

Lloyd, K., & Dayan, P. (2018) · Brain Research · doi:10.1016/j.brainres.2018.10.011 · Cited by 9

Learning fast and slow: deviations from the matching law can reflect an optimal strategy under uncertaintyPreprint

Iigaya, K., Ahmadian, Y., Sugrue, L. P., Corrado, G. S., Loewenstein, Y., Newsome, W. T., & Fusi, S. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/141309 · Cited by 11

Forebrain dopamine value signals arise independently from midbrain dopamine cell firingPreprint

Mohebi, A., Pettibone, J. R., Hamid, A., Wong, J. T., Kennedy, R. T., & Berke, J. D. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/334060 · Cited by 10

Effects of reward history on decision-making and movement vigorPreprint

Sukumar, S., Shadmehr, R., & Ahmed, A. A. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.07.22.453376 · Cited by 10

Global and compartmentalized serotonergic control of sensorimotor integration underlying motor adaptationPreprint

Haruvi, R., Barbara, R., Shainer, I., Rosenberg, A. M., Moshe, L., Malamud, D., Toledano, J., Braun, D., Baier, H., & Kawashima, T. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.15.613094 · Cited by 16

Serotonin neurons in mating female mice are activated by male ejaculation

Troconis, E. L., Seo, C., Guru, A., & Warden, M. R. (2023) · Current Biology · doi:10.1016/j.cub.2023.09.071 · Cited by 10

Neural correlates of object identity and reward outcome in the sensory cortical-hippocampal hierarchy: coding of motivational information in perirhinal cortex

Fiorilli, J., Marchesi, P., Ruikes, T. R., Veld, G. H. I. ’., Buckton, R., Duque-Quintero, M., Reiten, I., Bjaalie, J. G., & Pennartz, C. M. A. (2024) · Cerebral Cortex · doi:10.1093/cercor/bhae002 · Cited by 10

Aggression modulator: Understanding the multifaceted role of the dorsal raphe nucleus

Mitsui, K., & Takahashi, A. (2024) · BioEssays · doi:10.1002/bies.202300213 · Cited by 9

DORSAL RAPHE NUCLEUS CONTROLS MOTIVATIONAL STATE TRANSITIONS IN MONKEYSPreprint

Priestley, L., Chiew, M., Shahdloo, M., Mahmoodi, A., Cheng, X., Cleveland, R. O., Rushworth, M. F. S., & Khalighinejad, N. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.02.13.580224 · Cited by 9

The Role of Dorsal Raphe Nucleus Serotonergic Systems in Emotional Learning and Memory in Male BALB/c Mice

Payet, J. M., Stevens, L., Russo, A. M., Jaehne, E. J., van den Buuse, M., Kent, S., Lowry, C. A., Baratta, M. V., & Hale, M. W. (2023) · Neuroscience · doi:10.1016/j.neuroscience.2023.10.003 · Cited by 9

The selective serotonin reuptake inhibitor sertraline alters learning from aversive reinforcements in patients with depression: evidence from a randomized controlled trial

Malamud, J., Lewis, G., Moutoussis, M., Duffy, L., Bone, J. K., Srinivasan, R., Lewis, G., & Huys, Q. J. M. (2024) · Psychological Medicine · doi:10.1017/s0033291724000837 · Cited by 8

Neural Representation of Costs and Rewards in Decision Making

Chen, Y. (2021) · Brain Sciences · doi:10.3390/brainsci11081096 · Cited by 9

Adenosine Monophosphate-activated Protein Kinase (AMPK) in serotonin neurons mediates select behaviors during protracted withdrawal from morphine in mice

Eacret, D., Noreck, J., & Blendy, J. A. (2021) · Behavioural Brain Research · doi:10.1016/j.bbr.2021.113688 · Cited by 7

Dorsal Raphe 5-HT Neurons Utilize, But Do Not Generate, Negative Aversive Prediction Errors

Walker, R. A., Suthard, R. L., Perison, T. N., Sheehan, N. M., Dwyer, C. C., Lee, J. K., Enabulele, E. K., Ray, M. H., & McDannald, M. A. (2022) · eNeuro · doi:10.1523/eneuro.0132-21.2022 · Cited by 11

Serotonergic control of GABAergic inhibition in the lateral amygdala

Yamamoto, R., Furuyama, T., Sugai, T., Ono, M., Paré, D., & Kato, N. (2019) · Journal of Neurophysiology · doi:10.1152/jn.00500.2019 · Cited by 8

Serotonergic reinforcement of a complete swallowing circuit

Schoofs, A., Miroschnikow, A., Schlegel, P., Zinke, I., Schneider-Mizell, C. M., Cardona, A., & Pankratz, M. J. (2023) · doi:10.1101/2023.05.26.542464 · Cited by 7

Functional Diversity of Serotonin Neurons in the Dorsal and Median Raphe Nuclei in Emotional Responses

Ohmura, Y., & Nagayasu, K. (2025) · Neuropsychopharmacology Reports · doi:10.1002/npr2.70015 · Cited by 8

Neural signaling mechanisms in depression: bridging classical monoamine hypotheses, animal models, and emerging antidepressant strategies

Yamamoto, M., Hirakata, H., & Toda, K. (2026) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2026.1777975 · Cited by 11

Interactive effects of incentive value and valence on the performance of discrete action sequences

Adkins, T. J., Gary, B. S., & Lee, T. G. (2021) · Scientific Reports · doi:10.1038/s41598-021-88286-5 · Cited by 7

Anatomical, Physiological, and Functional Heterogeneity of the Dorsal Raphe Serotonin SystemPreprint

Ren, J., Friedmann, D., Xiong, J., Liu, C. D., DeLoach, K. E., Chen, R., Pu, A., Sun, Y., Weissbourd, B., Neve, R. L., et al. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/257378 · Cited by 7

Exploring the effects of adolescent social isolation stress on the serotonin system and ethanol-motivated behaviors

McElroy, B. D., Li, C., McCloskey, N. S., Alberici, A. R., & Kirby, L. G. (2025) · Psychopharmacology · doi:10.1007/s00213-025-06749-3 · Cited by 6

Erasing “bad memories”: reversing aberrant synaptic plasticity as therapy for neurological and psychiatric disorders

Shi, Z., Wen, K., Sammudin, N. H., LoRocco, N. C., & Zhuang, X. (2025) · Molecular Psychiatry · doi:10.1038/s41380-025-03013-0 · Cited by 7

Perinatal serotonin signalling dynamically influences the development of cortical GABAergic circuits with consequences for lifelong sensory encoding

Ocana-Santero, G., Warming, H., Munday, V., MacKay, H. A., Gibeily, C., Hemingway, C., Stacey, J. A., Saha, A., Lazarte, I. P., Bachetta, A., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-59659-5 · Cited by 7

A self-adjusting, progressive shock strength procedure to investigate resistance to punishment: Characterization in male and female rats

Desmercieres, S., Lardeux, V., Longueville, J.-E., Hanna, M., Panlilio, L. V., Thiriet, N., & Solinas, M. (2022) · Neuropharmacology · doi:10.1016/j.neuropharm.2022.109261 · Cited by 6

Distinct spatiotemporal brainstem pathways of outcome valence during reward- and punishment-based learning

Carvalheiro, J., & Philiastides, M. G. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113589 · Cited by 11

Regulation of stress-induced sleep perturbations by dorsal raphe VGLUT3 neurons in male mice

Henderson, F. J., Dumas, S., Gangarossa, G., Bernard, V., Pujol, M., Poirel, O., Pietrancosta, N., Mestikawy, S. E., Daumas, S., & Fabre, V. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114411 · Cited by 8

Slow motion

Uchida, N., & Cohen, J. Y. (2017) · eLife · doi:10.7554/elife.24792 · Cited by 6

Lesions of lateral habenula attenuate win-stay but not lose-shift responses in a competitive choice task

Thapa, R., Donovan, C. H., Wong, S. A., Sutherland, R. J., & Gruber, A. J. (2018) · Neuroscience Letters · doi:10.1016/j.neulet.2018.10.056 · Cited by 6

Serotonin neurobiology in cocaine use disorder

Cunningham, K. A., Howell, L. L., & Anastasio, N. C. (2020) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-444-64125-0.00040-2 · Cited by 6

Serotonin system function, organization, and feedback

Commons, K. G. (2020) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-444-64125-0.00003-7 · Cited by 6

Dorsal raphe serotonergic neurons regulate behavior on multiple timescales

Cohen, J. Y., & Grossman, C. D. (2020) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-444-64125-0.00030-x · Cited by 6

Serotonin Subsystems Modulate Diverse and Opposite Behavioral Functions

Garcia‐García, Á. L., & Soiza‐Reilly, M. (2018) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.8b00534 · Cited by 6

Neuron-type specificity of dorsal raphe projections to ventral tegmental areaPreprint

Chang, A. J., Wang, L., Lucantonio, F., Adams, M., Lemire, A. L., Dudman, J. T., & Cohen, J. Y. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.01.06.425641 · Cited by 8

Spiking activity in the visual thalamus is coupled to pupil dynamics across temporal scalesPreprint

Crombie, D., Spacek, M. A., Leibold, C., & Busse, L. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.04.30.442134 · Cited by 6

Dorsal raphe neurons signal integrated value during multi-attribute decision-makingPreprint

Feng, Y.-Y., Bromberg-Martin, E. S., & Monosov, I. E. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.08.17.553745 · Cited by 6

Early-life polystyrene nanoplastics exposure impairs pathogen avoidance behavior associated with intestine-derived insulin-like neuropeptide (ins-11) and serotonin signaling in Caenorhabditis elegans

Yu, C., Yen, P.-L., Kuo, Y.-H., Lin, T.-A., & Liao, V. H. (2024) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2024.117347 · Cited by 5

Neuromodulatory signaling contributing to the encoding of aversion

Wu, C.-H., Camelot, L., Lecca, S., & Mameli, M. (2025) · Trends in Neurosciences · doi:10.1016/j.tins.2025.04.003 · Cited by 6

Dynamic decision making and value computations in medial frontal cortex

Bari, B. A., & Cohen, J. Y. (2021) · International review of neurobiology · doi:10.1016/bs.irn.2020.12.001 · Cited by 6

Complementary roles of serotonin and dopamine in model-based learning

Taira, M., & Sharpe, M. J. (2024) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2024.101464 · Cited by 7

Homeostatic mechanisms may shape the type and duration of oscillatory modulation

Peterson, E. J., & Voytek, B. (2020) · Journal of Neurophysiology · doi:10.1152/jn.00119.2020 · Cited by 6

5-HT2C receptor perturbation has bidirectional influence over instrumental vigour and restraint

Härmson, O., Grima, L. L., Panayi, M. C., Husain, M., & Walton, M. E. (2021) · Psychopharmacology · doi:10.1007/s00213-021-05992-8 · Cited by 4

5-HT and α-m-5-HT attenuate excitatory synaptic transmissions onto the lateral amygdala principal neurons via presynaptic 5-HT1B receptors

Yamamoto, R., Ito, T., Furuyama, T., Ono, M., & Kato, N. (2022) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2022.07.076 · Cited by 5

Illuminating complexity in serotonin neurons of the dorsal raphe nucleus

Baruni, J., & Luo, L. (2022) · Neuron · doi:10.1016/j.neuron.2022.07.013 · Cited by 5

Serotonergic Effects on InteroceptionPreprint

Livermore, J. J. A., Holmes, C. L., Moga, G., Adamatzky, K., Critchley, H., Garfinkel, S. N., & Campbell-Meiklejohn, D. K. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.08.28.262550 · Cited by 5

Computational Psychiatry

Rutledge, R. B., & Adams, R. A. (2017) · Wiley eBooks · doi:10.1002/9781119159193.ch3 · Cited by 6

The Serotonergic System and Its Role in Thermoregulation

Negoita, A., Amuzescu, B. P., Mihailescu, D. F., & Bordea, C. (2025) · Physiologia · doi:10.3390/physiologia5040037 · Cited by 4

Toward a Brain-Inspired Theory of Artificial Learning

Thivierge, J., Giraud, É., & Lynn, M. B. (2023) · Cognitive Computation · doi:10.1007/s12559-023-10121-y · Cited by 4

GABAergic miR-34a regulates Dorsal Raphè inhibitory transmission in response to aversive, but not rewarding, stimuli

Ielpo, D., Guzzo, S. M., Porcheddu, G. F., Viscomi, M. T., Catale, C., Reverte, I., Cabib, S., Cifani, C., Antonucci, G., Ventura, R., et al. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2301730120 · Cited by 3

Ultraslow serotonin oscillations in the hippocampus delineate substates across NREM and waking

Cooper, C., Parthier, D., Sibille, J., Tukker, J., Tritsch, N. X., & Schmitz, D. (2025) · eLife · doi:10.7554/elife.101105.3 · Cited by 5

Serotonergic modulation of local network processing in V1 mirrors previously reported signatures of local network modulation by spatial attention

Patel, A., Kawaguchi, K., Seillier, L., & Nienborg, H. (2023) · European Journal of Neuroscience · doi:10.1111/ejn.15953 · Cited by 5

Serotonergic modulation of basolateral amygdala nucleus in the extinction of reward-driven learning: The role of 5-HT bioavailability and 5-HT1A receptor

Pereyra, A. E., Mininni, C. J., & Zanutto, B. S. (2021) · Behavioural Brain Research · doi:10.1016/j.bbr.2021.113161 · Cited by 5

Transmitter Co-Expression Reveals Key Organizational Principles of Local Interneuron Heterogeneity in the Olfactory SystemPreprint

Lizbinski, K. M., Marsat, G., & Dacks, A. M. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/167403 · Cited by 4

Emotional Intelligence And Decision-Making As Predictors Of Antisocial Behavior

Sample, M. (2017) · Digital Commons - Andrews University (Andrews University) · doi:10.32597/dissertations/1632 · Cited by 4

Firing patterns of serotonin neurons underlying cognitive flexibilityPreprint

Matias, S., Lottem, E., Dugué, G. P., & Mainen, Z. F. (2016) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/059758 · Cited by 5

Nonlinear computation by a habenula-driven recurrent inhibitory network in the raphePreprint

Lynn, M. B., Geddes, S. D., Chahrour, M. A., Maillé, S., Caya-Bissonnette, L., Harkin, E. F., Harvey‐Girard, E., Haj‐Dahmane, S., Naud, R., & Béïque, J.-C. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.08.31.506056 · Cited by 5

Serotonin drives choice-independent reconfiguration of distributed neural activityPreprint

Meijer, G. T., Catarino, J. A., Freitas-Silva, L., Laranjeira, I. C., & Mainen, Z. F. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.08.01.668048 · Cited by 6

Rethinking Predictive Processing

Furutachi, S., & Hofer, S. B. (2026) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-102124-031410 · Cited by 3

Neurofeedback, Biofeedback, and Basic Learning Theory: Revisiting the 2011 Conceptual Framework

Kerson, C. R., Sherlin, L. H., & Davelaar, E. J. (2025) · Applied Psychophysiology and Biofeedback · doi:10.1007/s10484-025-09756-4 · Cited by 4

Serotonin-endocannabinoid crosstalk selectively regulates inhibitory GABAergic inputs in the medial prefrontal cortex

Meza, R. C., Morales-Weil, K., Ancatén-González, C., Escobar, A. P., Alcaino, A., Sanguinetti, N. K., Delpire, E. J., Moya, P. R., Chiu, C. Q., Fuenzalida, M., et al. (2026) · Neuropsychopharmacology · doi:10.1038/s41386-026-02364-8 · Cited by 3

Transcriptional Regulation of the Human 5-HT1A Receptor Gene by Lithium: Role of Deaf1 and GSK3β

Harkin, E. F., Nasrallah, G., François, B. L., & Albert, P. R. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242115620 · Cited by 3

Increased c-Fos immunoreactivity in anxiety-related brain regions following paroxetine discontinuation

Collins, H. M., Gullino, L. S., Fuller, C., Pinacho, R., Bannerman, D. M., & Sharp, T. (2025) · Neuropharmacology · doi:10.1016/j.neuropharm.2025.110541 · Cited by 3

Serotonergic inhibition of responding for conditioned but not primary reinforcers

McDevitt, R. A., Marino, R. A. M., Tejeda, H. A., & Bonci, A. (2021) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2021.173186 · Cited by 3

Tonic activity in lateral habenula neurons promotes disengagement from reward-seeking behaviorPreprint

Sleezer, B. J., Post, R. J., Bulkin, D. A., Ebitz, R. B., Lee, V., Han, K. J., & Warden, M. R. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.01.15.426914 · Cited by 3

Opposing Contributions of GABAergic and Glutamatergic Ventral Pallidal Neurons to Motivational BehavioursPreprint

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