Rethinking psychopharmacotherapy: the role of treatment context and brain plasticity in antidepressant and antipsychotic interventions.

Emotion circuits in the brain

LeDoux, J. E. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.155 · Cited by 8,444 · see citing works

Requirement of hippocampal neurogenesis for the behavioral effects of antidepressants

Santarelli, L., Saxe, M., Gross, C., Surget, A., Battaglia, F., Dulawa, S., Weisstaub, N., Lee, J., Duman, R., Arancio, O., et al. (2003) · Science · doi:10.1126/science.1083328 · Cited by 4,321 · see citing works

Chronic antidepressant treatment increases neurogenesis in adult rat hippocampus

Malberg, J. E., Eisch, A. J., Nestler, E. J., & Duman, R. S. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-24-09104.2000 · Cited by 3,111 · see citing works

Selective publication of antidepressant trials and its influence on apparent efficacy

Turner, E. H., Matthews, A. M., Linardatos, E., Tell, R. A., & Rosenthal, R. (2008) · New England Journal of Medicine · doi:10.1056/nejmsa065779 · Cited by 2,435 · see citing works

Maximizing exposure therapy: An inhibitory learning approach

Craske, M. G., Treanor, M., Conway, C. C., Zbozinek, T., & Vervliet, B. (2014) · Behaviour Research and Therapy · doi:10.1016/j.brat.2014.04.006 · Cited by 2,339 · see citing works

Critical period plasticity in local cortical circuits

Hensch, T. K. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1787 · Cited by 2,323 · see citing works

Exercise for depression

Cooney, G. M., Dwan, K., Greig, C. A., Lawlor, D. A., Rimer, J., Waugh, F. R., McMurdo, M., & Mead, G. E. (2013) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd004366.pub6 · Cited by 1,834 · see citing works

Plasticity in gray and white: neuroimaging changes in brain structure during learning

Zatorre, R. J., Fields, R. D., & Johansen-Berg, H. (2012) · Nature Neuroscience · doi:10.1038/nn.3045 · Cited by 1,685 · see citing works

Synaptic Dysfunction in Depression: Potential Therapeutic Targets

Duman, R. S., & Aghajanian, G. K. (2012) · Science · doi:10.1126/science.1222939 · Cited by 1,651 · see citing works

Plasticity of ocular dominance columns in monkey striate cortex

Hubel, D. H., Wiesel, T. N., LeVay, S., Barlow, H. B., & Gaze, R. M. (1977) · Philosophical transactions of the Royal Society of London. Series B, Biological sciences · doi:10.1098/rstb.1977.0050 · Cited by 1,642 · see citing works

The contextual brain: implications for fear conditioning, extinction and psychopathology

Maren, S., Phan, K. L., & Liberzon, I. (2013) · Nature Reviews Neuroscience · doi:10.1038/nrn3492 · Cited by 1,547 · see citing works

The prevalence and distribution of major depression in a national community sample: the National Comorbidity Survey

(1994) · American Journal of Psychiatry · doi:10.1176/ajp.151.7.979 · Cited by 1,485 · see citing works

Identification of a Common Neurobiological Substrate for Mental Illness

Goodkind, M., Eickhoff, S. B., Oathes, D. J., Jiang, Y., Chang, A., Jones-Hagata, L. B., Ortega, B. N., Zaiko, Y. V., Roach, E. L., Korgaonkar, M. S., et al. (2015) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2014.2206 · Cited by 1,404 · see citing works

Placebo Response in Studies of Major Depression: Variable, Substantial, and Growing

Walsh, B. T., Seidman, S. N., Sysko, R., & Gould, M. (2002) · JAMA · doi:10.1001/jama.287.14.1840 · Cited by 1,109 · see citing works

Eye tracking of attention in the affective disorders: a meta-analytic review and synthesis

Armstrong, T., & Olatunji, B. O. (2012) · Clinical Psychology Review · doi:10.1016/j.cpr.2012.09.004 · Cited by 1,049 · see citing works

Expectation and Dopamine Release: Mechanism of the Placebo Effect in Parkinson's Disease

de la Fuente‐Fernández, R., Ruth, T. J., Sossi, V., Schulzer, M., Calne, D. B., & Stoessl, A. J. (2001) · Science · doi:10.1126/science.1060937 · Cited by 991 · see citing works

Long-term Antipsychotic Treatment and Brain Volumes

Ho, B., Andreasen, N. C., Ziebell, S., Pierson, R. K., & Magnotta, V. A. (2011) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2010.199 · Cited by 975 · see citing works

Cardiovascular disease and diabetes in people with severe mental illness position statement from the European Psychiatric Association (EPA), supported by the European Association for the Study of Diabetes (EASD) and the European Society of Cardiology (ESC)

De Hert, M., Dekker, J. M., Wood, D., Kahl, K. G., Holt, R. I. G., & Möller, H.-J. (2009) · European Psychiatry · doi:10.1016/j.eurpsy.2009.01.005 · Cited by 951 · see citing works

Exercise for depression

Cooney, G. M., Dwan, K., Greig, C. A., Lawlor, D. A., Rimer, J., Waugh, F. R., McMurdo, M., & Mead, G. E. (2014) · Advances in Psychiatric Treatment · doi:10.1192/apt.20.1.2 · Cited by 895 · see citing works

The antidepressant fluoxetine restores plasticity in the adult visual cortex

Vetencourt, J. F. M., Sale, A., Viegi, A., Baroncelli, L., De Pasquale, R., F. O'Leary, O., Castrén, E., & Maffei, L. (2008) · Science · doi:10.1126/science.1150516 · Cited by 890 · see citing works

Expectation in perceptual decision making: neural and computational mechanisms

Summerfield, C., & de Lange, F. P. (2014) · Nature Reviews Neuroscience · doi:10.1038/nrn3838 · Cited by 832 · see citing works

Early-Life Blockade of the 5-HT Transporter Alters Emotional Behavior in Adult Mice

Ansorge, M. S., Zhou, M., Lira, A., Hen, R., & Gingrich, J. A. (2004) · Science · doi:10.1126/science.1101678 · Cited by 817 · see citing works

Facilitation of Conditioned Fear Extinction by Systemic Administration or Intra-Amygdala Infusions of d-Cycloserine as Assessed with Fear-Potentiated Startle in Rats

Walker, D. L., Ressler, K. J., Lu, K.-T., & Davis, M. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-06-02343.2002 · Cited by 815 · see citing works

Cell Proliferation in Adult Hippocampus is Decreased by Inescapable Stress: Reversal by Fluoxetine Treatment

Malberg, J. E., & Duman, R. S. (2003) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300234 · Cited by 815 · see citing works

Neurobiological Mechanisms of the Placebo Effect

Benedetti, F., Mayberg, H., Wager, T., Stohler, C., & Zubieta, J. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.3458-05.2005 · Cited by 771 · see citing works

Perineuronal Nets Protect Fear Memories from Erasure

Gogolla, N., Caroni, P., Lüthi, A., & Herry, C. (2009) · Science · doi:10.1126/science.1174146 · Cited by 760 · see citing works

The Functional Neuroanatomy of the Placebo Effect

Mayberg, H. S., Silva, J. A., Brannan, S., Tekell, J. L., Mahurin, R. K., McGinnis, S. M., & Jerabek, P. A. (2002) · American Journal of Psychiatry · doi:10.1176/appi.ajp.159.5.728 · Cited by 718 · see citing works

Marble burying reflects a repetitive and perseverative behavior more than novelty-induced anxiety

Thomas, A., Burant, A., Bui, N., Graham, D., Yuva-Paylor, L. A., & Paylor, R. (2009) · Psychopharmacology · doi:10.1007/s00213-009-1466-y · Cited by 698 · see citing works

The placebo response in medicine: minimize, maximize or personalize?

Enck, P., Bingel, U., Schedlowski, M., & Rief, W. (2013) · Nature Reviews Drug Discovery · doi:10.1038/nrd3923 · Cited by 671 · see citing works

A meta-analysis of the magnitude of biased attention in depression

Peckham, A. D., McHugh, R. K., & Otto, M. W. (2010) · Depression and Anxiety · doi:10.1002/da.20755 · Cited by 647 · see citing works

Linking Molecules to Mood: New Insight Into the Biology of Depression

Krishnan, V., & Nestler, E. J. (2010) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2009.10030434 · Cited by 643 · see citing works

Twenty-five year mortality of a community cohort with schizophrenia

Brown, S., Kim, M., Mitchell, C., & Inskip, H. (2010) · British Journal of Psychiatry · doi:10.1192/bjp.bp.109.067512 · Cited by 601 · see citing works

Reboxetine for acute treatment of major depression: systematic review and meta-analysis of published and unpublished placebo and selective serotonin reuptake inhibitor controlled trials

Eyding, D., Lelgemann, M., Grouven, U., Härter, M. C., Kromp, M., Kaiser, T., Kerekeş, M., Gerken, M., & Wieseler, B. (2010) · BMJ · doi:10.1136/bmj.c4737 · Cited by 591 · see citing works

Is mood chemistry?

Castrén, E. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1629 · Cited by 563 · see citing works

BDNF in schizophrenia, depression and corresponding animal models

Angelucci, F., Brené, S., & Mathé, A. A. (2005) · Molecular Psychiatry · doi:10.1038/sj.mp.4001637 · Cited by 548 · see citing works

Progressive brain changes in schizophrenia related to antipsychotic treatment? A meta-analysis of longitudinal MRI studies

Fusar-Poli, P., Smieskova, R., Kempton, M. J., Ho, B. C., Andreasen, N. C., & Borgwardt, S. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.06.001 · Cited by 512 · see citing works

Listening to Prozac but hearing placebo: A meta-analysis of antidepressant medication.

Kirsch, I., & Sapirstein, G. (1998) · Prevention & Treatment · doi:10.1037/1522-3736.1.1.12a · Cited by 509 · see citing works

How effective are second-generation antipsychotic drugs? A meta-analysis of placebo-controlled trials.

Leucht, S., Arbter, D., Engel, R. R., Kissling, W., & Davis, J. M. (2009) · Molecular Psychiatry · doi:10.1038/sj.mp.4002136 · Cited by 489 · see citing works

Mechanism of Action of Atypical Antipsychotic Drugs and the Neurobiology of Schizophrenia

Horáček, J., Bubeníková‐Valešová, V., Kopeček, M., Páleníček, T., Dockery, C. A., Mohr, P., & Höschl, C. (2006) · CNS Drugs · doi:10.2165/00023210-200620050-00004 · Cited by 462 · see citing works

Induction of Fear Extinction with Hippocampal-Infralimbic BDNF

Peters, J., Dieppa-Perea, L. M., Melendez, L. M., & Quirk, G. J. (2010) · Science · doi:10.1126/science.1186909 · Cited by 462 · see citing works

Placebo in emotional processing—induced expectations of anxiety relief activate a generalized modulatory network

Petrovic, P., Dietrich, T., Fransson, P., Andersson, J., Carlsson, K., & Ingvar, M. (2005) · Neuron · doi:10.1016/j.neuron.2005.05.023 · Cited by 437 · see citing works

Spontaneous improvement in randomised clinical trials: meta-analysis of three-armed trials comparing no treatment, placebo and active intervention

Krogsbøll, L. T., Hróbjartsson, A., & Gøtzsche, P. C. (2009) · BMC Medical Research Methodology · doi:10.1186/1471-2288-9-1 · Cited by 435 · see citing works

Overgeneral autobiographical memory as a predictor of the course of depression: A meta-analysis

Sumner, J. A., Griffith, J. W., & Mineka, S. (2010) · Behaviour Research and Therapy · doi:10.1016/j.brat.2010.03.013 · Cited by 414 · see citing works

Chronic Social Stress Inhibits Cell Proliferation in the Adult Medial Prefrontal Cortex: Hemispheric Asymmetry and Reversal by Fluoxetine Treatment

Czéh, B., Keuker, J. I. H., Ryguła, R., Abumaria, N., Hiemke, C., Domenici, E., & Fuchs, E. (2006) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301275 · Cited by 397 · see citing works

Changes in Brain Function of Depressed Subjects During Treatment With Placebo

Leuchter, A. F., Cook, I. A., Witte, E. A., Morgan, M. L., & Abrams, M. (2002) · American Journal of Psychiatry · doi:10.1176/appi.ajp.159.1.122 · Cited by 394 · see citing works

Chronic olanzapine or fluoxetine administration increases cell proliferation in hippocampus and prefrontal cortex of adult rat

Kodama, M., Fujioka, T., & Duman, R. S. (2004) · Biological Psychiatry · doi:10.1016/j.biopsych.2004.07.008 · Cited by 387 · see citing works

Fear erasure in mice requires synergy between antidepressant drugs and extinction training

Karpova, N. N., Pickenhagen, A., Lindholm, J., Tiraboschi, E., Kulesskaya, N., Ágústsdóttir, A., Antila, H., Popova, D., Akamine, Y., Sullivan, R., et al. (2011) · Science · doi:10.1126/science.1214592 · Cited by 382 · see citing works

Antidepressants versus placebo for depression in primary care

Arroll, B., Elley, C. R., Fishman, T., Goodyear‐Smith, F., Kenealy, T. W., Blashki, G. A., Kerse, N. M., & MacGillivray, S. A. (2009) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd007954 · Cited by 353 · see citing works

Meta-analysis of the placebo response in antidepressant trials.

Rief, W., Nestoriuc, Y., Weiss, S., Welzel, E., Barsky, A. J., & Hofmann, S. G. (2009) · Journal of Affective Disorders · doi:10.1016/j.jad.2009.01.029 · Cited by 346 · see citing works

Neural mechanisms of social risk for psychiatric disorders

Meyer‐Lindenberg, A., & Tost, H. (2012) · Nature Neuroscience · doi:10.1038/nn.3083 · Cited by 342 · see citing works

Active placebos versus antidepressants for depression

Moncrieff, J., Wessely, S., & Hardy, R. (2004) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd003012.pub2 · Cited by 342 · see citing works

Antipsychotic Treatment and Functional Connectivity of the Striatum in First-Episode Schizophrenia

Sarpal, D. K., Robinson, D. G., Lencz, T., Árgyelán, M., Ikuta, T., Karlsgodt, K. H., Gallego, J. A., Kane, J. M., Szeszko, P. R., & Malhotra, A. K. (2014) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2014.1734 · Cited by 328 · see citing works

Physical exercise-induced hippocampal neurogenesis and antidepressant effects are mediated by the adipocyte hormone adiponectin

Yau, S. Y., Li, A., Hoo, R. L. C., Ching, Y. P., Christie, B. R., Lee, T. M. C., Xu, A., & So, K.-F. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1415219111 · Cited by 326 · see citing works

Selective Reinforcement Learning Deficits in Schizophrenia Support Predictions from Computational Models of Striatal-Cortical Dysfunction

Waltz, J. A., Frank, M. J., Robinson, B. M., & Gold, J. M. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2006.09.042 · Cited by 326 · see citing works

Adult neuroplasticity: more than 40 years of research

Fuchs, E., & Flügge, G. (2014) · Neural Plasticity · doi:10.1155/2014/541870 · Cited by 325 · see citing works

Neuro-bio-behavioral mechanisms of placebo and nocebo responses: implications for clinical trials and clinical practice

Schedlowski, M., Enck, P., Rief, W., & Bingel, U. (2015) · Pharmacological Reviews · doi:10.1124/pr.114.009423 · Cited by 323 · see citing works

Agomelatine, a new antidepressant, induces regional changes in hippocampal neurogenesis

Banasr, M., Soumier, A., Hery, M., Mocaër, E., & Daszuta, A. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.11.025 · Cited by 318 · see citing works

Adult Neurogenesis: Beyond Learning and Memory

Cameron, H. A., & Glover, L. R. (2014) · Annual Review of Psychology · doi:10.1146/annurev-psych-010814-015006 · Cited by 302 · see citing works

Maintenance treatment with antipsychotic drugs for schizophrenia

Leucht, S., Tardy, M., Komossa, K., Heres, S., Kissling, W., & Davis, J. M. (2012) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd008016.pub2 · Cited by 287 · see citing works

Selected Pregnancy and Delivery Outcomes After Exposure to Antidepressant Medication: A Systematic Review and Meta-analysis

Ross, L. E., Grigoriadis, S., Mamisashvili, L., VonderPorten, E. H., Roerecke, M., Rehm, J., Dennis, C.-L., Koren, G., Steiner, M., Mousmanis, P., et al. (2013) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2013.684 · Cited by 268 · see citing works

The effect of physical activity on the brain derived neurotrophic factor: from animal to human studies.

Zoladz, J. A., & Pilc, A. (2010) · PubMed · Cited by 268 · see citing works

A Model of Placebo Response in Antidepressant Clinical Trials

Rutherford, B. R., & Roose, S. P. (2013) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2012.12040474 · Cited by 268 · see citing works

New perspectives on the neurodevelopmental effects of SSRIs

Homberg, J. R., Schubert, D., & Gaspar, P. (2009) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2009.11.003 · Cited by 266 · see citing works

Lack of parvalbumin in mice leads to behavioral deficits relevant to all human autism core symptoms and related neural morphofunctional abnormalities

Wöhr, M., Orduz, D., Gregory, P., Moreno, H., Khan, U., Vörckel, K. J., Wolfer, D. P., Welzl, H., Gall, D., Schiffmann, S. N., et al. (2015) · Translational Psychiatry · doi:10.1038/tp.2015.19 · Cited by 258 · see citing works

Long-Term Plasticity of Visually Evoked Potentials in Humans is Altered in Major Depression

Normann, C., Schmitz, D., Fürmaier, A., Döing, C., & Bach, M. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2006.10.006 · Cited by 243 · see citing works

The neurogenesis hypothesis of affective and anxiety disorders: Are we mistaking the scaffolding for the building?

Petrik, D., Lagace, D. C., & Eisch, A. J. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.09.003 · Cited by 241 · see citing works

Expectancies as core features of mental disorders

Rief, W., Glombiewski, J. A., Gollwitzer, M., Schubö, A., Schwarting, R. K. W., & Thorwart, A. (2015) · Current Opinion in Psychiatry · doi:10.1097/yco.0000000000000184 · Cited by 235 · see citing works

Atypical neuroleptics stimulate neurogenesis in adult rat brain

Wakade, C. G., Mahadik, S. P., Waller, J. L., & Chiu, F. (2002) · Journal of Neuroscience Research · doi:10.1002/jnr.10281 · Cited by 230 · see citing works

Placebo effects in psychiatry: mediators and moderators

Weimer, K., Colloca, L., & Enck, P. (2015) · The Lancet Psychiatry · doi:10.1016/s2215-0366(14)00092-3 · Cited by 222 · see citing works

Reversal of hippocampal neuronal maturation by serotonergic antidepressants

Kobayashi, K., Ikeda, Y., Sakai, A., Yamasaki, N., Haneda, E., Miyakawa, T., & Suzuki, H. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0912690107 · Cited by 212 · see citing works

Repeated social defeat-induced depression-like behavioral and biological alterations in rats: involvement of cholecystokinin

Becker, C., Zeau, B., Rivat, C., Blugeot, A., Hamon, M., & Benoliel, J. J. (2007) · Molecular Psychiatry · doi:10.1038/sj.mp.4002097 · Cited by 211 · see citing works

A link between serotonin-related gene polymorphisms, amygdala activity, and placebo-induced relief from social anxiety

Furmark, T., Appel, L., Henningsson, S., Åhs, F., Faria, V., Linnman, C., Pissiota, A., Frans, Ö., Bani, M., Bettica, P., et al. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.2534-08.2008 · Cited by 210 · see citing works

Differences in Adverse Effect Reporting in Placebo Groups in SSRI and Tricyclic Antidepressant Trials: A Systematic Review and Meta-Analysis

Rief, W., Nestoriuc, Y., von Lilienfeld-Toal, A., Dogan, I., Schreiber, F., Hofmann, S. G., Barsky, A. J., & Avorn, J. (2009) · Drug Safety · doi:10.2165/11316580-000000000-00000 · Cited by 202 · see citing works

Prenatal exposure to antidepressants and depressed maternal mood alter trajectory of infant speech perception

Weikum, W., Oberlander, T. F., Hensch, T. K., & Werker, J. F. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1121263109 · Cited by 201 · see citing works

Neuronal network plasticity and recovery from depression

Castrén, E. (2013) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2013.1 · Cited by 190 · see citing works

Does Inclusion of a Placebo Arm Influence Response to Active Antidepressant Treatment in Randomized Controlled Trials?

Sinyor, M., LEVITT, A. J., Cheung, A. H., Schaffer, A., Kiss, A., Dowlati, Y., & Lanctôt, K. L. (2010) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.08r04516blu · Cited by 189 · see citing works

Effects of Chronic Haloperidol and Clozapine Treatment on Neurogenesis in the Adult Rat Hippocampus

Halim, N. D., Weickert, C. S., McClintock, B., Weinberger, D. R., & Lipska, B. K. (2004) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300422 · Cited by 189 · see citing works

Combined Prolonged Exposure Therapy and Paroxetine for PTSD Related to the World Trade Center Attack: A Randomized Controlled Trial

Schneier, F. R., Neria, Y., Pavlicová, M., Hembree, E. A., Suh, E. J., Amsel, L., & Marshall, R. D. (2011) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2011.11020321 · Cited by 187 · see citing works

Enhancement of cognitive function in models of brain disease through environmental enrichment and physical activity.

Pang, T., & Hannan, A. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.06.029 · Cited by 182 · see citing works

Effect of chronic antipsychotic treatment on brain structure: a serial magnetic resonance imaging study with ex vivo and postmortem confirmation

Vernon, A. C., Natesan, S., Modo, M., & Kapur, S. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.11.010 · Cited by 173 · see citing works

Glucocorticoids Orchestrate Divergent Effects on Mood through Adult Neurogenesis

Lehmann, M. L., Brachman, R. A., Martinowich, K., Schloesser, R. J., & Herkenham, M. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.3878-12.2013 · Cited by 168 · see citing works

Exercise for Depression

Cooney, G., Dwan, K., & Mead, G. (2014) · JAMA · doi:10.1001/jama.2014.4930 · Cited by 168 · see citing works

Sustained and “Sleeper” Effects of Group Metacognitive Training for Schizophrenia

Moritz, S., Veckenstedt, R., Andreou, C., Bohn, F., Hottenrott, B., Leighton, L., Köther, U., Woodward, T. S., Treszl, A., Menon, M., et al. (2014) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2014.1038 · Cited by 165 · see citing works

Effects of Antipsychotic Drugs on Neurogenesis in the Forebrain of the Adult Rat

Wang, H.-D., Dunnavant, F. D., Jarman, T., & Deutch, A. Y. (2004) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300449 · Cited by 162 · see citing works

Effects of working memory training on functional connectivity and cerebral blood flow during rest

Takeuchi, H., Taki, Y., Nouchi, R., Hashizume, H., Sekiguchi, A., Kotozaki, Y., Nakagawa, S., Miyauchi, C. M., Sassa, Y., & Kawashima, R. (2013) · Cortex · doi:10.1016/j.cortex.2012.09.007 · Cited by 162 · see citing works

Short-Term Dynamic Psychotherapy Versus Pharmacotherapy for Major Depressive Disorder: A Randomized, Placebo-Controlled Trial

Barber, J. P., Barrett, M. S., Gallop, R., Rynn, M. A., & Rickels, K. (2012) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.11m06831 · Cited by 157 · see citing works

Haloperidol versus placebo for schizophrenia

Adams, C. E., Bergman, H., Irving, C. B., & Lawrie, S. M. (2013) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd003082.pub3 · Cited by 157 · see citing works

Placebo Response in Antipsychotic Clinical Trials

Rutherford, B. R., Pott, E., Tandler, J. M., Wall, M. M., Roose, S. P., & Lieberman, J. A. (2014) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2014.1319 · Cited by 152 · see citing works

Association Between Placebo-Activated Neural Systems and Antidepressant Responses

Peciña, M., Bohnert, A. M., Sikora, M., Avery, E. T., Langenecker, S. A., Mickey, B. J., & Zubieta, J. (2015) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2015.1335 · Cited by 152 · see citing works

The prospective long-term course of adult depression in general practice and the community. A systematic literature review

Steinert, C., Hofmann, M., Kruse, J., & Leichsenring, F. (2013) · Journal of Affective Disorders · doi:10.1016/j.jad.2013.10.017 · Cited by 148 · see citing works

Changes of brain morphometry in first-episode, drug-naive, non-late-life adult patients with major depression: an optimized voxel-based morphometry study

Zou, K., Deng, W., Li, T., Zhang, B., Jiang, L., Huang, C., Sun, X., & Sun, X. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.09.014 · Cited by 141 · see citing works

Reduced Stress-Sensitivity or Increased Reward Experience: The Psychological Mechanism of Response to Antidepressant Medication

Wichers, M. C., Barge-Schaapveld, D. Q. C. M., Nicolson, N. A., Peeters, F., de Vries, M., Mengelers, R., & van Os, J. (2009) · Neuropsychopharmacology · doi:10.1038/npp.2008.66 · Cited by 139 · see citing works

Inhibition of adult hippocampal neurogenesis disrupts contextual learning but spares spatial working memory, long-term conditional rule retention and spatial reversal

Hernández‐Rabaza, V., Llorens-Martı́n, M., Velázquez-Sánchez, C., Ferragud, A., Arcusa, A., Gumus, H. G., Gómez‐Pinedo, U., Pérez‐Villalba, A., Roselló, J., Trejo, J. L., et al. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.11.054 · Cited by 138 · see citing works

Mechanisms Involved in Placebo and Nocebo Responses and Implications for Drug Trials

Rief, W., Bingel, U., Schedlowski, M., & Enck, P. (2011) · Clinical Pharmacology & Therapeutics · doi:10.1038/clpt.2011.204 · Cited by 133 · see citing works

Neuroplasticity in Depressed Individuals Compared with Healthy Controls

Player, M. J., Taylor, J. L., Weickert, C. S., Alonzo, A., Sachdev, P., Martin, D., Mitchell, P. B., & Loo, C. K. (2013) · Neuropsychopharmacology · doi:10.1038/npp.2013.126 · Cited by 127 · see citing works

Utilizing placebo mechanisms for dose reduction in pharmacotherapy

Doering, B. K., & Rief, W. (2012) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2011.12.001 · Cited by 125 · see citing works

Active placebos versus antidepressants for depression (Review)

Moncrieff, J., Wessely, S. C., & Hardy, R. (2004) · UCL Discovery (University College London) · Cited by 125 · see citing works

Contrasting Effects of Haloperidol and Lithium on Rodent Brain Structure: A Magnetic Resonance Imaging Study with Postmortem Confirmation

Vernon, A. C., Natesan, S., Crum, W. R., Cooper, J. D., Modo, M., Williams, S., & Kapur, S. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.12.004 · Cited by 124 · see citing works

Monoamine Oxidase A and Catechol-O-Methyltransferase Functional Polymorphisms and the Placebo Response in Major Depressive Disorder

Leuchter, A. F., McCracken, J. T., Hunter, A. M., Cook, I. A., & Alpert, J. E. (2009) · Journal of Clinical Psychopharmacology · doi:10.1097/jcp.0b013e3181ac4aaf · Cited by 122 · see citing works

Modeling Social Influences on Human Health

Karelina, K., & DeVries, A. C. (2011) · Psychosomatic Medicine · doi:10.1097/psy.0b013e3182002116 · Cited by 115 · see citing works

Quetiapine reverses the suppression of hippocampal neurogenesis caused by repeated restraint stress

Luo, C., Xu, H., & Li, X. (2005) · Brain Research · doi:10.1016/j.brainres.2005.09.043 · Cited by 114 · see citing works

Trajectories of Depression Severity in Clinical Trials of Duloxetine

Gueorguieva, R. V. (2011) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2011.132 · Cited by 114 · see citing works

d -Cycloserine vs Placebo as Adjunct to Cognitive Behavioral Therapy for Obsessive-Compulsive Disorder and Interaction With Antidepressants

Andersson, E., Hedman‐Lagerlöf, E., Enander, J., Djurfeldt, D. R., Ljótsson, B., Červenka, S., Isung, J., Svanborg, C., Mataix‐Cols, D., Kaldo, V., et al. (2015) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2015.0546 · Cited by 109 · see citing works

Stress coping stimulates hippocampal neurogenesis in adult monkeys

Lyons, D. M., Buckmaster, P. S., Lee, A. G., Wu, C., Mitra, R., Duffey, L. M., Buckmaster, C. L., Her, S., Patel, P. D., & Schatzberg, A. F. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0914568107 · Cited by 109 · see citing works

Striatal Volume Changes in the Rat Following Long-term Administration of Typical and Atypical Antipsychotic Drugs

Andersson, C. (2002) · Neuropsychopharmacology · doi:10.1016/s0893-133x(02)00287-7 · Cited by 105 · see citing works

Individual Differences in Psychotic Effects of Ketamine Are Predicted by Brain Function Measured under Placebo

Honey, G. D., Corlett, P. R., Absalom, A. R., Lee, M., Pomarol‐Clotet, E., Murray, G. K., McKenna, P. J., Bullmore, E. T., Menon, D. K., & Fletcher, P. C. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0910-08.2008 · Cited by 102 · see citing works

Antidepressant Treatment Outcome Depends on the Quality of the Living Environment: A Pre-Clinical Investigation in Mice

Branchi, I., Santarelli, S., Capoccia, S., Poggini, S., D’Andrea, I., Cirulli, F., & Alleva, E. (2013) · PLoS ONE · doi:10.1371/journal.pone.0062226 · Cited by 102 · see citing works

Genetic Strain Differences in Learned Fear Inhibition Associated with Variation in Neuroendocrine, Autonomic, and Amygdala Dendritic Phenotypes

Camp, M., MacPherson, K. P., Lederle, L. I., Graybeal, C., Gaburro, S., DeBrouse, L., Ihne, J. L., Bravo, J. A., O’Connor, R. M., Ciocchi, S., et al. (2012) · Neuropsychopharmacology · doi:10.1038/npp.2011.340 · Cited by 101 · see citing works

Striatal enlargement in rats chronically treated with neuroleptic

Chakos, M., Shirakawa, O., Lieberman, J. A., Lee, H., Bilder, R. M., & Tamminga, C. A. (1998) · Biological Psychiatry · doi:10.1016/s0006-3223(98)00029-8 · Cited by 100 · see citing works

The hidden effects of blinded, placebo-controlled randomized trials: An experimental investigation

Rief, W., & Glombiewski, J. A. (2012) · Pain · doi:10.1016/j.pain.2012.09.007 · Cited by 98 · see citing works

Moving from efficacy to effectiveness in cognitive behavioral therapy for psychosis: A randomized clinical practice trial.

Lincoln, T. M., Ziegler, M., Mehl, S., Kesting, M.-L., Lüllmann, E., Westermann, S., & Rief, W. (2012) · Journal of Consulting and Clinical Psychology · doi:10.1037/a0028665 · Cited by 97 · see citing works

Chronic Haloperidol Promotes Corticostriatal Long-Term Potentiation by Targeting Dopamine D2L Receptors

Centonze, D., Usiello, A., Costa, C., Picconi, B., Erbs, E., Bernardi, G., Borrelli, E., & Calabresi, P. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1274-04.2004 · Cited by 96 · see citing works

The scientific and ethical basis for placebo-controlled trials in depression and schizophrenia: an FDA perspective

LAUGHREN, T. P. (2001) · European Psychiatry · doi:10.1016/s0924-9338(01)00600-9 · Cited by 93 · see citing works

Role of pill-taking, expectation and therapeutic alliance in the placebo response in clinical trials for major depression

Leuchter, A. F., Hunter, A. M., Tartter, M. A., & Cook, I. A. (2014) · The British Journal of Psychiatry · doi:10.1192/bjp.bp.113.140343 · Cited by 87 · see citing works

Increased responsiveness of dopamine to atypical, but not typical antipsychotics in the medial prefrontal cortex of rats reared in isolation

Heidbreder, C. A., Foxton, R. H., Cilia, J., Hughes, Z. A., Shah, A. J., Atkins, A. R., Hunter, J. A., Hagan, J. J., & Jones, D. N. C. (2001) · Psychopharmacology · doi:10.1007/s002130100760 · Cited by 84 · see citing works

Mind matters: placebo enhances reward learning in Parkinson's disease

Schmidt, L., Braun, E. K., Wager, T. D., & Shohamy, D. (2014) · Nature Neuroscience · doi:10.1038/nn.3842 · Cited by 84 · see citing works

Environmental Enrichment Induces Behavioral Recovery and Enhanced Hippocampal Cell Proliferation in an Antidepressant-Resistant Animal Model for PTSD

Hendriksen, H., Prins, J., Olivier, B., & Oosting, R. S. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011943 · Cited by 77 · see citing works

Delayed BDNF alterations in the prefrontal cortex of rats exposed to prenatal stress: Preventive effect of lurasidone treatment during adolescence

Luoni, A., Berry, A., Calabrese, F., Capoccia, S., Bellisario, V., Gass, P., Cirulli, F., & Riva, M. A. (2014) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2013.12.010 · Cited by 74 · see citing works

Morphometric study of synaptic patterns in the rat caudate nucleus and hippocampus under haloperidol treatment

Uranova, N. A., Orlovskaya, D. D., Apel, K., et al. (1991) · Synapse · doi:10.1002/syn.890070402 · Cited by 69 · see citing works

Mechanisms and therapeutic implications of the placebo effect in neurological and psychiatric conditions.

Murray, D. K., & Stoessl, A. (2013) · Pharmacology and Therapeutics · doi:10.1016/j.pharmthera.2013.07.009 · Cited by 67 · see citing works

Post-extinction fluoxetine treatment prevents stress-induced reemergence of extinguished fear

Deschaux, O., Zheng, X., Lavigne, J., Nachon, O., Cleren, C., Moreau, J.-L., & Garcia, R. (2013) · Psychopharmacology · doi:10.1007/s00213-012-2806-x · Cited by 62 · see citing works

Synaptic rearrangements in medial prefrontal cortex of haloperidol-treated rats

Benes, F. M., Paskevich, P. A., Davidson, J., et al. (1985) · Brain Research · doi:10.1016/0006-8993(85)90353-1 · Cited by 61 · see citing works

Synaptic Plasticity in the Rat Striatum following Chronic Haloperidol Treatment

Kerns, J. M., Sierens, D. K., Kao, L. C., et al. (1992) · Clinical Neuropharmacology · doi:10.1097/00002826-199212000-00006 · Cited by 61 · see citing works

Hippocampal volume and cell proliferation after acute and chronic clozapine or haloperidol treatment

Schmitt, A., Weber, S., Jatzko, A., Braus, D. F., & Henn, F. A. (2004) · Journal of Neural Transmission · doi:10.1007/s00702-003-0070-2 · Cited by 60 · see citing works

Amitriptyline versus placebo for major depressive disorder

Leucht, C., Huhn, M., & Leucht, S. (2012) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd009138.pub2 · Cited by 60 · see citing works

Fluoxetine Exposure during Adolescence Alters Responses to Aversive Stimuli in Adulthood

Iñiguez, S. D., Parise, L. F., Warren, B. L., Riggs, L. M., Parise, E. M., Vialou, V., Wright, K. N., Dayrit, G., Nieto, S. J., Wilkinson, M. B., et al. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.5725-12.2014 · Cited by 59 · see citing works

Adult neurogenesis is reduced in the dorsal hippocampus of rats displaying learned helplessness behavior

Ho, Y., & Wang, S. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.08.062 · Cited by 57 · see citing works

Chronic treatment with fluoxetine prevents the return of extinguished auditory-cued conditioned fear

Deschaux, O., Spennato, G., Moreau, J., & Garcia, R. (2010) · Psychopharmacology · doi:10.1007/s00213-010-2134-y · Cited by 57 · see citing works

Assessment of adverse effects in clinical studies of antipsychotic medication: survey of methods used

Pope, A., Adams, C. E., Paton, C., Weaver, T. D., & Barnes, T. R. E. (2010) · The British Journal of Psychiatry · doi:10.1192/bjp.bp.109.070961 · Cited by 57 · see citing works

Amitriptyline versus placebo for major depressive disorder

Leucht, C., Huhn, M., & Leucht, S. (2011) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd009138 · Cited by 57 · see citing works

Antipsychotic-associated neuronal changes in the brain: Toxic, therapeutic, or irrelevant to the long-term outcome of schizophrenia?

Dean, C. E. (2005) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2005.08.019 · Cited by 56 · see citing works

Schizophrenia, antipsychotics and risk of hip fracture: A population-based analysis

Sørensen, H. J., Jensen, S. O. W., & Nielsen, J. (2013) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2013.04.002 · Cited by 54 · see citing works

Physical Skill Training Increases the Number of Surviving New Cells in the Adult Hippocampus

Curlik, D. M., Maeng, L. Y., Agarwal, P. R., & Shors, T. J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0055850 · Cited by 53 · see citing works

Listening to Prozac but hearing placebo: A meta-analysis of antidepressant medication.

Sapirstein, G. (1998) · Prevention & Treatment · doi:10.1037//1522-3736.1.0002a · Cited by 53 · see citing works

Early exposure to haloperidol or olanzapine induces long‐term alterations of dendritic form

Frost, D. O., Page, S. C., Carroll, C., & Kolb, B. E. (2009) · Synapse · doi:10.1002/syn.20715 · Cited by 52 · see citing works

Long-Term Antidepressant Use and the Risk of Type 2 Diabetes Mellitus

Wu, C., Gau, S. S., & Lai, M. (2014) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.13m08421 · Cited by 46 · see citing works

A neurocomputational account of catalepsy sensitization induced by D2 receptor blockade in rats: context dependency, extinction, and renewal

Wiecki, T. V., Riedinger, K., von Ameln-Mayerhofer, A., Schmidt, W., & Frank, M. J. (2009) · Psychopharmacology · doi:10.1007/s00213-008-1457-4 · Cited by 46 · see citing works

Context-dependent catalepsy intensification is due to classical conditioning and sensitization

Amtage, J., & Schmidt, W. (2003) · Behavioural Pharmacology · doi:10.1097/00008877-200311000-00009 · Cited by 45 · see citing works

Nonpharmacological bases of drug tolerance and dependence

Hinson, R. E., & Siegel, S. (1982) · Journal of Psychosomatic Research · doi:10.1016/0022-3999(82)90089-7 · Cited by 45 · see citing works

Exercise affects memory acquisition, anxiety-like symptoms and activity of membrane-bound enzyme in brain of rats fed with different dietary fats: impairments of trans fat.

Teixeira, A. M., Pase, C. S., Boufleur, N., Roversi, K., Barcelos, R. C. S., Benvegnú, D. M., Segat, H. J., Dias, V. T., Reckziegel, P., Trevizol, F., et al. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.08.055 · Cited by 44 · see citing works

Haloperidol conditioned catalepsy in rats: a possible role for D1-like receptors

Banasikowski, T. J., & Beninger, R. J. (2011) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145711001696 · Cited by 41 · see citing works

Catalepsy intensifies context-dependently irrespective of whether it is induced by intermittent or chronic dopamine deficiency

Klein, A., & Schmidt, W. (2003) · Behavioural Pharmacology · doi:10.1097/00008877-200302000-00005 · Cited by 41 · see citing works

Psychotropic medication use among adolescents: United States, 2005-2010.

Jonas, B. S., Gu, Q., & Albertorio‐Diaz, J. R. (2013) · PubMed · Cited by 40 · see citing works

A follow-up fMRI study of a transferable placebo anxiolytic effect.

Zhang, W., Qin, S., Guo, J., & Luo, J. (2011) · Psychophysiology · doi:10.1111/j.1469-8986.2011.01178.x · Cited by 39 · see citing works

Treatment with olanzapine increases cell proliferation in the subventricular zone and prefrontal cortex

Green, W., Patil, P. G., Marsden, C. A., Bennett, G. W., & Wigmore, P. M. (2006) · Brain Research · doi:10.1016/j.brainres.2005.11.047 · Cited by 38 · see citing works

Amygdala-frontal couplings characterizing SSRI and placebo response in social anxiety disorder

Faria, V., Åhs, F., Appel, L., Linnman, C., Bani, M., Bettica, P., Pich, E. M., Fredrikson, M., & Furmark, T. (2014) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145714000352 · Cited by 37 · see citing works

Dopaminergic modulation of the reward system in schizophrenia: A placebo-controlled dopamine depletion fMRI study

Alves, F. D. S., Bakker, G., Schmitz, N., Abeling, N. G. G. M., Hasler, G., van der Meer, J. N., Nederveen, A. J., de Haan, L., LINSZEN, D. H., & van Amelsvoort, T. (2013) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2013.06.008 · Cited by 36 · see citing works

Facilitation of Serotonin Signaling by SSRIs is Attenuated by Social Isolation

Dankoski, E. C., Agster, K. L., Fox, M. E., Moy, S. S., & Wightman, R. M. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2014.162 · Cited by 36 · see citing works

Prenatal Antidepressant Exposure: Clinical and Preclinical Findings

Bourke, C. H., Stowe, Z. N., & Owens, M. J. (2014) · Pharmacological Reviews · doi:10.1124/pr.111.005207 · Cited by 36 · see citing works

Rethinking mental disorders: The role of learning and brain plasticity

Morris, S. E., Rumsey, J. M., & Cuthbert, B. N. (2014) · Restorative Neurology and Neuroscience · doi:10.3233/rnn-139015 · Cited by 35 · see citing works

Effects of sertraline on behavioral alterations caused by environmental enrichment and social isolation

Yildirim, E. O., Erol, K., & Ulupınar, E. (2012) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2011.12.017 · Cited by 35 · see citing works

Haloperidol modulates midbrain-prefrontal functional connectivity in the rat brain

Gass, N., Schwarz, A. J., Sartorius, A., Cleppien, D., Zheng, L., Schenker, E., Risterucci, C., Meyer‐Lindenberg, A., & Weber‐Fahr, W. (2012) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2012.10.013 · Cited by 35 · see citing works

Neuroimaging and plasticity in schizophrenia

Meyer-Lindenberg, A., & Tost, H. (2014) · Restorative Neurology and Neuroscience · doi:10.3233/rnn-139014 · Cited by 33 · see citing works

The effects of isolated and enriched housing conditions on baseline and drug-induced behavioural responses in the male rat

Simpson, J., & Kelly, J. P. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.06.015 · Cited by 32 · see citing works

Contextual and behavioral control of antipsychotic sensitization induced by haloperidol and olanzapine

Zhang, C., & Li, M. (2011) · Behavioural Pharmacology · doi:10.1097/fbp.0b013e32834ecac4 · Cited by 31 · see citing works

Influence of enrichment on behavioral and neurogenic effects of antidepressants in Wistar rats submitted to repeated forced swim test

Possamai, F., dos Santos, J., Walber, T., Marcon, J. C., dos Santos, T. S., & de Oliveira, C. L. (2014) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2014.10.017 · Cited by 31 · see citing works

Antidepressants differentially modify the extinction of an aversive memory task in female rats

Melo, T. G., Izídio, G. S., Ferreira, L. S., Sousa, D. S., Macêdo, P. T., Cabral, A., Ribeiro, A. M., & Silva, R. H. (2012) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2012.01.012 · Cited by 30 · see citing works

Combination of fluoxetine and extinction treatments forms a unique synaptic protein profile that correlates with long-term fear reduction in adult mice

Popova, D., Ágústsdóttir, A., Lindholm, J., Mazulis, U., Akamine, Y., Castrén, E., & Karpova, N. N. (2014) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2014.04.002 · Cited by 26 · see citing works

Effects of chronic exercise and treatment with the antipsychotic drug olanzapine on hippocampal volume in adult female rats.

Barr, A. M., Wu, C. H., Wong, C., Hercher, C., Töpfer, E., Boyda, H. N., Procyshyn, R. M., Honer, W. G., & Beasley, C. L. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.10.010 · Cited by 26 · see citing works

Catatonic Behavior Induced by Haloperidol, Increased by Retesting and Elicited without Drug in Rats

Moreira, L. F. D. S., Pinheiro, M. D. C. C., & Masur, J. (2008) · Pharmacology · doi:10.1159/000137716 · Cited by 25 · see citing works

Physical exercise down-regulated locomotor side effects induced by haloperidol treatment in Wistar rats.

Baptista, P. P. A., de Senna, P. N., Paim, M. F., Saur, L., Blank, M., do Nascimento, P., Ilha, J., Vianna, M. R. M., Mestriner, R. G., Achaval, M., et al. (2013) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2012.12.020 · Cited by 23 · see citing works

Effect of early life housing manipulation on baseline and drug-induced behavioural responses on neurochemistry in the male rat

Simpson, J., Bree, D., & Kelly, J. P. (2012) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2012.02.008 · Cited by 23 · see citing works

Effects of antipsychotic D2 antagonists on long-term potentiation in animals and implications for human studies

Price, R., Salavati, B., Graff‐Guerrero, A., Blumberger, D. M., Mulsant, B. H., Daskalakis, Z. J., & Rajji, T. K. (2014) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2014.05.001 · Cited by 22 · see citing works

Drug Approval and Drug Effectiveness

Spielmans, G. I., & Kirsch, I. (2013) · Annual Review of Clinical Psychology · doi:10.1146/annurev-clinpsy-050212-185533 · Cited by 21 · see citing works

Chronic Fluoxetine Treatment Suppresses Plasticity (Long-Term Potentiation) in the Mature Rodent Primary Auditory Cortex In Vivo

Dringenberg, H. C., Day, L. R. B., & Choi, D. H. (2014) · Neural Plasticity · doi:10.1155/2014/571285 · Cited by 18 · see citing works

A novel application of the Intent to Attend assessment to reduce bias due to missing data in a randomized controlled clinical trial

Rabideau, D. J., Nierenberg, A. A., Sylvia, L. G., Friedman, E. S., Bowden, C. L., Thase, M. E., Ketter, T. A., Ostacher, M. J., Reilly-Harrington, N. A., Iosifescu, D. V., et al. (2014) · Clinical Trials · doi:10.1177/1740774514531096 · Cited by 17 · see citing works

Synaptic plasticity in rat medial prefrontal cortex under chronic haloperidol treatment produced behavioral sensitization.

Klinzova, A. J., Uranova, N. A., Haselhorst, U., et al. (1990) · PubMed · Cited by 11 · see citing works

The placebo response in pain and depression in search of a common pathway

Wernicke, J. (2009) · Frontiers in Bioscience-Scholar · doi:10.2741/s49 · Cited by 9 · see citing works

The role of NMDA and AMPA/Kainate receptors in the consolidation of catalepsy sensitization

Riedinger, K., Kulak, A., Schmidt, W., et al. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.11.055 · Cited by 9 · see citing works

Desvenlafaxine May Accelerate Neuronal Maturation in the Dentate Gyri of Adult Male Rats

Asokan, A., Ball, A. R., Laird, C. D., Hermer, L., & Ormerod, B. K. (2014) · PLoS ONE · doi:10.1371/journal.pone.0098530 · Cited by 8 · see citing works

Effect of environmental cues on the behavioral efficacy of haloperidol, olanzapine, and clozapine in rats

Sun, T., Liu, X., & Li, M. (2014) · Behavioural Pharmacology · doi:10.1097/fbp.0000000000000047 · Cited by 6 · see citing works

Psychobiological mechanisms of placebo and nocebo effects: pathways to improve treatments and reduce side effects

Petrie, K. J., & Rief, W. (2019) · Annual Review of Psychology · doi:10.1146/annurev-psych-010418-102907 · Cited by 309 · see citing works

Preoperative optimization of patient expectations improves long-term outcome in heart surgery patients: results of the randomized controlled PSY-HEART trial

Rief, W., Shedden-Mora, M. C., Laferton, J. A. C., Auer, C., Petrie, K. J., Salzmann, S., Schedlowski, M., & Moosdorf, R. (2017) · BMC Medicine · doi:10.1186/s12916-016-0767-3 · Cited by 261 · see citing works

Aerobic Exercise as a Tool to Improve Hippocampal Plasticity and Function in Humans: Practical Implications for Mental Health Treatment

Kandola, A., Hendrikse, J., Lucassen, P. J., & Yücel, M. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00373 · Cited by 155 · see citing works

Molecular Mechanisms of Psilocybin and Implications for the Treatment of Depression

Ling, S., Ceban, F., Lui, L. M. W., Lee, Y., Teopiz, K. M., Rodrigues, N. B., Lipsitz, O., Gill, H., Subramaniapillai, M., Mansur, R. B., et al. (2022) · CNS Drugs · doi:10.1007/s40263-021-00877-y · Cited by 127 · see citing works

Using different expectation mechanisms to optimize treatment of patients with medical conditions: a systematic review

Kube, T., Glombiewski, J. A., & Rief, W. (2018) · Psychosomatic Medicine · doi:10.1097/psy.0000000000000596 · Cited by 62 · see citing works

Μελέτη της πολυπαραγοντικής αναλγησίας στο μετεγχειρητικό πόνο μετά από λαπαροσκοπική χολοκυστεκτομή

Κοτσόβολης, Γ. (2014) · doi:10.12681/eadd/34564

Conditioned Placebo Analgesia Persists When Subjects Know They Are Receiving a Placebo

Schafer, S. M., Colloca, L., & Wager, T. D. (2015) · The Journal of Pain · doi:10.1016/j.jpain.2014.12.008 · Cited by 117 · see citing works

A comparison of placebo effects in clinical analgesic trials versus studies of placebo analgesia

Vase, L., Riley, J. L., & Price, D. D. (2002) · Pain · doi:10.1016/s0304-3959(02)00205-1 · Cited by 434 · see citing works

(404) Use of a placebo run-in in clinical trials in patients with FM does not impact the response to pregabalin

Pauer, L., Brown, P. B., Clair, A. G., et al. (2015) · Journal of Pain · doi:10.1016/j.jpain.2015.01.323

Gender Differences in Placebo Analgesia: Event-Related Potentials and Emotional Modulation

Aslaksen, P. M., Bystad, M. K., Vambheim, S. M., & Flaten, M. A. (2011) · Psychosomatic Medicine · doi:10.1097/psy.0b013e3182080d73 · Cited by 111 · see citing works