Striatal dopamine transporter availability in unmedicated bipolar disorder: Striatal DAT in unmedicated bipolar disorder

A rating scale for depression

Hamilton, M. (1960) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp.23.1.56 · Cited by 32,817 · see citing works

A Rating Scale for Mania: Reliability, Validity and Sensitivity

Young, R. C., Biggs, J. T., Ziegler, V. E., & Meyer, D. A. (1978) · British Journal of Psychiatry · doi:10.1192/bjp.133.5.429 · Cited by 8,744 · see citing works

Voxel-Based Morphometry—The Methods

Ashburner, J., & Friston, K. J. (2000) · NeuroImage · doi:10.1006/nimg.2000.0582 · Cited by 8,676 · see citing works

Basal ganglia-thalamocortical circuits: parallel substrates for motor, oculomotor, "prefrontal" and "limbic" functions.

Alexander, G. E., Crutcher, M. D., & DeLong, M. R. (1990) · PubMed · Cited by 2,422 · see citing works

Chapter 6 Basal ganglia-thalamocortical circuits: Parallel substrates for motor, oculomotor, “prefrontal” and “limbic” functions

(1991) · Progress in Brain Research · doi:10.1016/s0079-6123(08)62678-3 · Cited by 1,961 · see citing works

Consensus Nomenclature for <i>in vivo</i> Imaging of Reversibly Binding Radioligands

Innis, R. B., Cunningham, V. J., Delforge, J., Fujita, M., Gjedde, A., Gunn, R. N., Holden, J., Houle, S., Huang, S.-C., Ichise, M., et al. (2007) · Journal of Cerebral Blood Flow &amp; Metabolism · doi:10.1038/sj.jcbfm.9600493 · Cited by 1,955 · see citing works

The Biochemical Basis of Neuropharmacology.

(1974) · Annals of Internal Medicine · doi:10.7326/0003-4819-81-4-575_2 · Cited by 1,882 · see citing works

Neuropsychological Function in Schizophrenia

Saykin, A. J. (1991) · Archives of General Psychiatry · doi:10.1001/archpsyc.1991.01810310036007 · Cited by 1,160 · see citing works

Depression in Parkinson's disease: loss of dopamine and noradrenaline innervation in the limbic system

Rémy, P., Doder, M., Lees, A. J., Turjanski, N., & Brooks, D. J. (2005) · Brain · doi:10.1093/brain/awh445 · Cited by 1,046 · see citing works

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

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

The functional neuroanatomy of bipolar disorder: a review of neuroimaging findings

Strakowski, S. M., DelBello, M. P., & Adler, C. M. (2005) · Molecular Psychiatry · doi:10.1038/sj.mp.4001585 · Cited by 818 · see citing works

Linearized Reference Tissue Parametric Imaging Methods: Application to [ 11 C]DASB Positron Emission Tomography Studies of the Serotonin Transporter in Human Brain

Ichise, M., Liow, J., Lu, J., Takano, A., Modell, K. J., Toyama, H., Suhara, T., Suzuki, K., Innis, R. B., & Carson, R. E. (2003) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/01.wcb.0000085441.37552.ca · Cited by 651 · see citing works

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

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

Imaging Human Mesolimbic Dopamine Transmission with Positron Emission Tomography: I. Accuracy and Precision of D ₂ Receptor Parameter Measurements in Ventral Striatum

Mawlawi, O., Martinez, D., Slifstein, M., Broft, A., Chatterjee, R., Hwang, D.-R., Huang, Y., Simpson, N., Ngo, K., Van Heertum, R., et al. (2001) · Journal of Cerebral Blood Flow &amp; Metabolism · doi:10.1097/00004647-200109000-00002 · Cited by 525 · see citing works

Subcortical and temporal structures in affective disorder and schizophrenia: A magnetic resonance imaging study

Swayze, V. W., Andreasen, N. C., Alliger, R. J., Yuh, W. T. C., & Ehrhardt, J. C. (1992) · Biological Psychiatry · doi:10.1016/0006-3223(92)90046-3 · Cited by 403 · see citing works

The Biochemical Basis of Neuropharmacology

Faden, A. I. (1992) · Archives of Neurology · doi:10.1001/archneur.1992.00530350019005 · Cited by 320 · see citing works

Striatal dopamine transporters and cognitive functioning in healthy men and women

Mozley, L. H., Gur, R. C., Mozley, P. D., & Gur, R. E. (2001) · American Journal of Psychiatry · doi:10.1176/appi.ajp.158.9.1492 · Cited by 314 · see citing works

Impulsivity: a link between bipolar disorder and substance abuse

Swann, A. C., Dougherty, D. M., Pazzaglia, P. J., Pham, M., & Moeller, F. G. (2004) · Bipolar Disorders · doi:10.1111/j.1399-5618.2004.00110.x · Cited by 292 · see citing works

The role of dopamine in bipolar disorder

Cousins, D. A., Butts, K. A., & Young, A. H. (2009) · Bipolar Disorders · doi:10.1111/j.1399-5618.2009.00760.x · Cited by 286 · see citing works

Imaging dopamine transmission in schizophrenia. A review and meta-analysis.

Laruelle, M. (1998) · PubMed · Cited by 280 · see citing works

Basal ganglia volumes and white matter hyperintensities in patients with bipolar disorder

Aylward, E., Roberts-Twillie, J. V., Barta, P. E., Kumar, A. J., Harris, G. J., Geer, M. J., Peyser, C. E., & Pearlson, G. D. (1994) · American Journal of Psychiatry · doi:10.1176/ajp.151.5.687 · Cited by 273 · see citing works

Lower dopamine transporter binding potential in striatum during depression

Meyer, J. H., Krüger, S., Wilson, A. A., Christensen, B. K., Goulding, V. S., Schaffer, A., Minifie, C., Houle, S., Hussey, D., & Kennedy, S. H. (2001) · Neuroreport · doi:10.1097/00001756-200112210-00052 · Cited by 269 · see citing works

Age-Related Decline in Dopamine Transporters: Analysis of Striatal Subregions, Nonlinear Effects, and Hemispheric Asymmetries

van Dyck, C. H., Seibyl, J. P., Malison, R. T., Laruelle, M. A., Zoghbi, S. S., Baldwin, R. M., & Innis, R. B. (2002) · American Journal of Geriatric Psychiatry · doi:10.1097/00019442-200201000-00005 · Cited by 251 · see citing works

Sex differences in [123I]β‐CIT SPECT measures of dopamine and serotonin transporter availability in healthy smokers and nonsmokers

Staley, J. K., Krishnan‐Sarin, S., Zoghbi, S. S., Tamagnan, G. D., Fujita, M., Seibyl, J. P., Maciejewski, P. K., O’Malley, S. S., & Innis, R. B. (2001) · Synapse · doi:10.1002/syn.1084 · Cited by 245 · see citing works

Setting the stage: from prodrome to treatment resistance in bipolar disorder

Berk, M., Conus, P., Lucas, N., Hallam, K. T., Malhi, G. S., Dodd, S., Yatham, L. N., Yung, A. R., & McGorry, P. D. (2007) · Bipolar Disorders · doi:10.1111/j.1399-5618.2007.00484.x · Cited by 239 · see citing works

Frontostriatal Abnormalities in Adolescents With Bipolar Disorder: Preliminary Observations From Functional MRI

Blumberg, H. P., Martin, A., Kaufman, J., Leung, H.-C., Skudlarski, P., Lacadie, C., Fulbright, R. K., Gore, J. C., Charney, D. S., Krystal, J. H., et al. (2003) · American Journal of Psychiatry · doi:10.1176/appi.ajp.160.7.1345 · Cited by 235 · see citing works

In Vivo D2 Dopamine Receptor Density in Psychotic and Nonpsychotic Patients With Bipolar Disorder

Pearlson, G. D. (1995) · Archives of General Psychiatry · doi:10.1001/archpsyc.1995.03950180057008 · Cited by 235 · see citing works

Age-related decline in striatal dopamine transporter binding with iodine-123-beta-CITSPECT.

van Dyck, C. H., Seibyl, J. P., Malison, R. T., Laruelle, M. A., Wallace, E. A., Zoghbi, S. S., Zea‐Ponce, Y., Baldwin, R. M., Charney, D. S., & Hoffer, P. B. (1995) · PubMed · Cited by 226 · see citing works

Brain SPECT Imaging of Amphetamine-Induced Dopamine Release in Euthymic Bipolar Disorder Patients

Anand, A., Verhoeff, P., Seneca, N., Zoghbi, S. S., Seibyl, J. P., Charney, D. S., & Innis, R. B. (2000) · American Journal of Psychiatry · doi:10.1176/appi.ajp.157.7.1108 · Cited by 222 · see citing works

Cortical abnormalities in bipolar disorder investigated with MRI and voxel-based morphometry

Nugent, A. C., Milham, M. P., Bain, E. E., Mah, L., Cannon, D. M., Marrett, S., Zarate, C. A., Pine, D. S., Price, J. L., & Drevets, W. C. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2005.09.029 · Cited by 206 · see citing works

Decreased dopamine transporters with age in healthy human subjects

Volkow, N. D., Fowler, J. S., Wang, G., Logan, J., Schlyer, D. J., MacGregor, R. R., Hitzemann, R., & Wolf, A. P. (1994) · Annals of Neurology · doi:10.1002/ana.410360218 · Cited by 205 · see citing works

Fronto-thalamo-striatal gray and white matter volumes and anisotropy of their connections in bipolar spectrum illnesses

Haznedar, M. M., Roversi, F., Pallanti, S., Rossi, N. B., Schnur, D. B., LiCalzi, E. M., Tang, C. Y., Hof, P. R., Hollander, E., & Buchsbaum, M. S. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.01.002 · Cited by 202 · see citing works

Hallucinations, sleep fragmentation, and altered dream phenomena in Parkinson's disease

Pappert, E. J., Goetz, C. G., Niederman, F. G., Raman, R., & Leurgans, S. E. (1999) · Movement Disorders · doi:10.1002/1531-8257(199901)14:1 · Cited by 180 · see citing works

Neuropsychological function in schizophrenia

Nyman, H. (2002) · European Psychiatry · doi:10.1016/s0924-9338(02)80803-3 · Cited by 166 · see citing works

D1 dopamine receptor binding in mood disorders measured by positron emission tomography

Suhara, T., Nakayama, K., Inoue, O., Fukuda, H., Shimizu, M., Mori, A., & Tateno, Y. (1992) · Psychopharmacology · doi:10.1007/bf02253582 · Cited by 163 · see citing works

Stabilization of Mood From Below Versus Above Baseline in Bipolar Disorder: A New Nomenclature

Ketter, T., & Calabrese, J. R. (2002) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.v63n0210 · Cited by 161 · see citing works

Tyrosine Hydroxylase- and Dopamine Transporter-Immunoreactive Axons in the Primate Cerebellum Evidence for a Lobular- and Laminar-Specific Dopamine Innervation

Melchitzky, D. S. (2000) · Neuropsychopharmacology · doi:10.1016/s0893-133x(99)00139-6 · Cited by 146 · see citing works

A dopaminergic mechanism in mania

Gerner, R. H., Post, R. M., & Bunney, W. E. (1976) · American Journal of Psychiatry · doi:10.1176/ajp.133.10.1177 · Cited by 144 · see citing works

PET Study of [¹⁸F]6-Fluoro-<scp>l</scp>-Dopa Uptake in Neuroleptic- and Mood-Stabilizer-Naive First-Episode Nonpsychotic Mania: Effects of Treatment With Divalproex Sodium

Yatham, L. N., Liddle, P. F., Shiah, I.-S., Lam, R. W., Ngan, E., Scarrow, G., Imperial, M., Stoessl, J., Sossi, V., & Ruth, T. J. (2002) · American Journal of Psychiatry · doi:10.1176/appi.ajp.159.5.768 · Cited by 122 · see citing works

Dopamine D2 Receptor Density and Personal Detachment in Healthy Subjects

Breier, A. F., Kestler, L. J., Adler, C. M., Elman, I., Wiesenfeld, N., Malhotra, A. K., & Pickar, D. (1998) · American Journal of Psychiatry · doi:10.1176/ajp.155.10.1440 · Cited by 119 · see citing works

Quantification of Neuroreceptors in the Living Human Brain: IV. Effect of Aging and Elevations of D ₂ -Like Receptors in Schizophrenia and Bipolar Illness

Wong, D. F., Pearlson, G. D., Tune, L. E., Young, L. T., Meltzer, C. C., Dannals, R. F., Ravert, H. T., Reith, J., Kuhar, M. J., & Gjedde, A. (1997) · Journal of Cerebral Blood Flow &amp; Metabolism · doi:10.1097/00004647-199703000-00010 · Cited by 118 · see citing works

Basal Ganglia Shape Alterations in Bipolar Disorder

Hwang, J., Lyoo, I. K., Dager, S. R., Friedman, S. D., Oh, J. S., Lee, J., Kim, S. J., Dünner, D. L., & Renshaw, P. F. (2006) · American Journal of Psychiatry · doi:10.1176/appi.ajp.163.2.276 · Cited by 111 · see citing works

Anatomical MRI study of basal ganglia in bipolar disorder patients

Brambilla, P., Harenski, K. A., Nicoletti, M., Mallinger, A. G., Frank, E., Kupfer, D. J., Keshavan, M. S., & Soares, J. C. (2001) · Psychiatry Research Neuroimaging · doi:10.1016/s0925-4927(01)00073-7 · Cited by 109 · see citing works

PET imaging of dopamine transporter and drug craving during methadone maintenance treatment and after prolonged abstinence in heroin users

Shi, J., Zhao, L.-Y., Copersino, M. L., Fang, Y.-X., Chen, Y., Tian, J., Deng, Y., Shuai, Y., Jin, J., & Lu, L. (2008) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2007.09.042 · Cited by 108 · see citing works

Computational neuroanatomy: new perspectives for neuroradiology.

Good, C. D., Ashburner, J., & Frackowiak, R. S. J. (2001) · PubMed · Cited by 104 · see citing works

Dopamine transporter availability in medication free and in bupropion treated depression: A 99mTc-TRODAT-1 SPECT study

Árgyelán, M., Szabó, Z., Kanyó, B., Tanács, A., Kovács, Z. Z. A., Janka, Z., & Pávics, L. (2005) · Journal of Affective Disorders · doi:10.1016/j.jad.2005.08.016 · Cited by 98 · see citing works

Striatal structure and function in mood disorders: a comprehensive review

Marchand, W. R., & Yurgelun‐Todd, D. (2010) · Bipolar Disorders · doi:10.1111/j.1399-5618.2010.00874.x · Cited by 91 · see citing works

Regional analysis of age‐related decline in dopamine transporters and dopamine D2‐like receptors in human striatum

Ishibashi, K., Ishii, K., Oda, K., Kawasaki, K., Mizusawa, H., & Ishiwata, K. (2008) · Synapse · doi:10.1002/syn.20603 · Cited by 89 · see citing works

A Preliminary Study of Dopamine Transporter Binding in Bipolar and Unipolar Depressed Patients and Healthy Controls

Amsterdam, J. D., & Newberg, A. B. (2007) · Neuropsychobiology · doi:10.1159/000106476 · Cited by 84 · see citing works

Striatal dopaminergic denervation and gait in healthy adults

Cham, R., Studenski, S. A., Perera, S., & Bohnen, N. I. (2007) · Experimental Brain Research · doi:10.1007/s00221-007-1161-3 · Cited by 72 · see citing works

in vivo Presynaptic and Postsynaptic Striatal Dopamine Functions in Idiopathic Normal Pressure Hydrocephalus

Ouchi, Y., Nakayama, T., Kanno, T., Yoshikawa, E., Shinke, T., & Torizuka, T. (2006) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/sj.jcbfm.9600389 · Cited by 64 · see citing works

A dopamine transporter mutation associated with bipolar affective disorder causes inhibition of transporter cell surface expression

Horschitz, S., Hummerich, R., Lau, T., Rietschel, M., & Schloss, P. D. (2005) · Molecular Psychiatry · doi:10.1038/sj.mp.4001730 · Cited by 64 · see citing works

Higher striatal dopamine transporters in euthymic patients with bipolar disorder: a SPECT study with [ ^99m Tc] TRODAT‐1

Chang, T. T., Yeh, T. L., Chiu, N. T., Chen, P. S., Huang, H. Y., Yang, Y. K., Lee, I. H., & Lu, R. B. (2010) · Bipolar Disorders · doi:10.1111/j.1399-5618.2009.00771.x · Cited by 63 · see citing works

Euphorigenic doses of cocaine reduce [123I]β-CIT SPECT measures of dopamine transporter availability in human cocaine addicts

Malison, R. T., Best, S. E., McCance, E. F., Laruelle, M. A., Baldwin, R. M., Seibyl, J. P., Price, L. H., Kosten, T. R., Innis, R. B., Hoffer, P. B., et al. (1995) · Psychopharmacology · doi:10.1007/bf02246266 · Cited by 58 · see citing works

Age-Related Decline in Dopamine Transporters: Analysis of Striatal Subregions, Nonlinear Effects, and Hemispheric Asymmetries

van Dyck, C. H. (2002) · American Journal of Geriatric Psychiatry · doi:10.1176/appi.ajgp.10.1.36 · Cited by 53 · see citing works

Human brain monoamine oxidase type B: mechanism of deamination as probed by steady-state methods

Pearce, L. B., & Roth, J. A. (1985) · Biochemistry · doi:10.1021/bi00329a003 · Cited by 39 · see citing works

Dopamine transporter density in schizophrenic subjects with and without tardive dyskinesia

Yoder, K. K., Hutchins, G. D., Morris, E. D., Brashear, A., Wang, C., & Shekhar, A. (2004) · Schizophrenia Research · doi:10.1016/j.schres.2004.03.015 · Cited by 34 · see citing works

No association between particular DRD3 and DAT gene polymorphisms and manic-depressive illness in a Spanish sample

Gómez‐Casero, E., de Castro, I. P., Sáiz‐Ruiz, J., Llinares, C., & Fernández‐Piqueras, J. (1996) · Psychiatric Genetics · doi:10.1097/00041444-199624000-00007 · Cited by 30 · see citing works

Test–retest variability of [11C]raclopride‐binding potential in nontreatment‐seeking alcoholics

Yoder, K. K., Albrecht, D., Kareken, D. A., Federici, L. M., Perry, K. M., Patton, E. A., Zheng, Q., Mock, B. H., O’Connor, S., & Herring, C. M. (2010) · Synapse · doi:10.1002/syn.20874 · Cited by 25 · see citing works

A Second Generation Catecholamine Hypothesis

Bunney, W. E., & GARLAND, B. L. (1982) · Pharmacopsychiatry · doi:10.1055/s-2007-1019521 · Cited by 24 · see citing works

Unchanged striatal dopamine transporter availability in narcolepsy: a PET studywith [11 C]-CFT

Rinne, J. O., Hublin, C., Någren, K., Helenius, H. Y. M., & Partinen, M. (2003) · Acta Neurologica Scandinavica · doi:10.1034/j.1600-0404.2003.00175.x · Cited by 18 · see citing works

Evaluation of the effect of drugs on dopamine metabolism in the rat superior cervical ganglion by HPLC with electrochemical detection

Westerink, B. H. C., & van Oene, J. C. (1980) · European Journal of Pharmacology · doi:10.1016/0014-2999(80)90210-1 · Cited by 16 · see citing works

Inhibition of rat and mouse brain monoamine oxidases by (+)-amphetamine

Green, A. L. (1971) · Biochemical Journal · doi:10.1042/bj1210037p · Cited by 16 · see citing works

Association study of 5′‐UTR polymorphisms of the human dopamine transporter gene with manic depression

Stöber, G., Sprandel, J., Schmidt, F., Faul, T., Jabs, B. E., & Knapp, M. (2006) · Bipolar Disorders · doi:10.1111/j.1399-5618.2006.00352.x · Cited by 11 · see citing works

Dopamine transporter binding in rat striatum: a comparison of [O-methyl-11C]β-CFT and [N-methyl-11C]β-CFT

Yoder, K. K., Hutchins, G. D., Mock, B. H., Fei, X., Winkle, W. L., Gitter, B. D., Territo, P. R., & Zheng, Q. (2009) · Nuclear Medicine and Biology · doi:10.1016/j.nucmedbio.2008.10.007 · Cited by 10 · see citing works

Effects of imipramine, nomifensine and d-amphetamine on type B monoamine oxidase, cyclic AMP phosphodiesterase and dopamine-.BETA.-hydroxylase.

Izumi, H., TOGASHI, O., Hayakari, M., Hayashi, S., & Ozawa, H. (1976) · The Tohoku Journal of Experimental Medicine · doi:10.1620/tjem.118.223 · Cited by 3 · see citing works

Reward processing dysfunction in major depression, bipolar disorder and schizophrenia

Whitton, A. E., Treadway, M. T., & Pizzagalli, D. A. (2014) · Current Opinion in Psychiatry · doi:10.1097/yco.0000000000000122 · Cited by 740 · see citing works

The dopamine hypothesis of bipolar affective disorder: the state of the art and implications for treatment

Ashok, A. H., Marques, T. R., Jauhar, S., Nour, M. M., Goodwin, G. M., Young, A. H., & Howes, O. D. (2017) · Molecular Psychiatry · doi:10.1038/mp.2017.16 · Cited by 546 · see citing works

Is there a “metabolic-mood syndrome”? A review of the relationship between obesity and mood disorders

Mansur, R. B., Brietzke, E. M., & McIntyre, R. S. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.12.017 · Cited by 325 · see citing works

SLC6 transporters: Structure, function, regulation, disease association and therapeutics

Pramod, A. B., Foster, J. D., Carvelli, L., & Henry, L. K. (2013) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2012.07.002 · Cited by 317 · see citing works

Reward circuitry dysfunction in psychiatric and neurodevelopmental disorders and genetic syndromes: animal models and clinical findings

Dichter, G. S., Damiano, C. A., & Allen, J. A. (2012) · Journal of Neurodevelopmental Disorders · doi:10.1186/1866-1955-4-19 · Cited by 299 · see citing works

Biological hypotheses and biomarkers of bipolar disorder

Sigitova, E., Fišar, Z., Hroudová, J., Cikánková, T., & Raboch, J. (2016) · Psychiatry and Clinical Neurosciences · doi:10.1111/pcn.12476 · Cited by 247 · see citing works

Neurobiology of Chronic Stress-Related Psychiatric Disorders: Evidence from Molecular Imaging Studies

Davis, M. T., Holmes, S. E., Pietrzak, R. H., & Esterlis, I. (2017) · Chronic Stress · doi:10.1177/2470547017710916 · Cited by 176 · see citing works

Neuroreceptor imaging in depression

Savitz, J. B., & Drevets, W. C. (2012) · Neurobiology of Disease · doi:10.1016/j.nbd.2012.06.001 · Cited by 165 · see citing works

A model of the mitochondrial basis of bipolar disorder

Morris, G., Walder, K., McGee, S. L., Dean, O. M., Tye, S. J., Maes, M., & Berk, M. (2017) · Neuroscience &amp; Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.01.014 · Cited by 162 · see citing works

The role of mitochondria in mood disorders: from physiology to pathophysiology and to treatment

Giménez-Palomo, A., Dodd, S., Anmella, G., Carvalho, A. F., Scaini, G., Quevedo, J., Pacchiarotti, I., Vieta, E., & Berk, M. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2021.546801 · Cited by 140 · see citing works

Animal models of bipolar mania: The past, present and future

Logan, R. W., & McClung, C. A. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2015.08.041 · Cited by 136 · see citing works

Obesity in Bipolar Disorder: An Overview

McElroy, S. L., & Keck, P. E. (2012) · Current Psychiatry Reports · doi:10.1007/s11920-012-0313-8 · Cited by 124 · see citing works

Animal models for bipolar disorder: from bedside to the cage

Beyer, D. K. E., & Freund, N. (2017) · International Journal of Bipolar Disorders · doi:10.1186/s40345-017-0104-6 · Cited by 110 · see citing works

The catecholaminergic–cholinergic balance hypothesis of bipolar disorder revisited

van Enkhuizen, J., Janowsky, D. S., Olivier, B., Minassian, A., Perry, W., Young, J. W., & Geyer, M. A. (2014) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2014.05.063 · Cited by 106 · see citing works

Reduced Dopamine Transporter Functioning Induces High-Reward Risk-Preference Consistent with Bipolar Disorder

van Enkhuizen, J., Henry, B. L., Minassian, A., Perry, W., Milienne-Petiot, M., Higa, K. K., Geyer, M. A., & Young, J. W. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2014.170 · Cited by 94 · see citing works

Mice with reduced DAT levels recreate seasonal-induced switching between states in bipolar disorder

Young, J. W., Cope, Z. A., Romoli, B., Schrurs, E., Joosen, A., van Enkhuizen, J., Sharp, R. F., & Dulcis, D. (2018) · Neuropsychopharmacology · doi:10.1038/s41386-018-0031-y · Cited by 81 · see citing works

Circadian Mechanisms Underlying Reward-Related Neurophysiology and Synaptic Plasticity

Parekh, P. K., & McClung, C. A. (2016) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2015.00187 · Cited by 75 · see citing works

Drugs related to monoamine oxidase activity

Fišar, Z. (2016) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2016.02.012 · Cited by 72 · see citing works

Investigating the mechanism(s) underlying switching between states in bipolar disorder

Young, J. W., & Dulcis, D. (2015) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2015.03.019 · Cited by 68 · see citing works

Dopamine transporter (DAT) knockdown in the nucleus accumbens improves anxiety- and depression-related behaviors in adult mice

Bahí, A., & Dreyer, J. (2018) · Behavioural Brain Research · doi:10.1016/j.bbr.2018.10.028 · Cited by 67 · see citing works

Transcriptome sequencing implicates dorsal striatum-specific gene network, immune response and energy metabolism pathways in bipolar disorder

Pacifico, R., & Davis, R. L. (2017) · Molecular Psychiatry · doi:10.1038/mp.2016.94 · Cited by 61 · see citing works

Differential effects of dopamine transporter inhibitors in the rodent Iowa gambling task

van Enkhuizen, J., Geyer, M. A., & Young, J. W. (2012) · Psychopharmacology · doi:10.1007/s00213-012-2854-2 · Cited by 64 · see citing works

Chronic valproate attenuates some, but not all, facets of mania-like behaviour in mice

van Enkhuizen, J., Geyer, M. A., Kooistra, K., & Young, J. W. (2012) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145712001198 · Cited by 56 · see citing works

Altered GluA1 (Gria1) Function and Accumbal Synaptic Plasticity in the ClockΔ19 Model of Bipolar Mania

Parekh, P. K., Becker-Krail, D., Sundaravelu, P., Ishigaki, S., Okado, H., Sobue, G., Huang, Y., & McClung, C. A. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.06.022 · Cited by 48 · see citing works

Dopamine depletion attenuates some behavioral abnormalities in a hyperdopaminergic mouse model of bipolar disorder

van Enkhuizen, J., Geyer, M. A., Halberstadt, A. L., Zhuang, X., & Young, J. W. (2013) · Journal of Affective Disorders · doi:10.1016/j.jad.2013.08.041 · Cited by 48 · see citing works

Modeling neurodevelopmental cognitive deficits in tasks with cross‐species translational validity

Cope, Z. A., Powell, S. B., & Young, J. W. (2015) · Genes Brain & Behavior · doi:10.1111/gbb.12268 · Cited by 45 · see citing works

The emerging role of dopamine–glutamate interaction and of the postsynaptic density in bipolar disorder pathophysiology: Implications for treatment

de Bartolomeis, A., Buonaguro, E. F., Iasevoli, F., & Tomasetti, C. (2014) · Journal of Psychopharmacology · doi:10.1177/0269881114523864 · Cited by 44 · see citing works

Amphetamine increases activity but not exploration in humans and mice

Minassian, A., Young, J. W., Cope, Z. A., Henry, B. L., Geyer, M. A., & Perry, W. (2015) · Psychopharmacology · doi:10.1007/s00213-015-4098-4 · Cited by 44 · see citing works

Modeling bipolar disorder in mice by increasing acetylcholine or dopamine: chronic lithium treats most, but not all features

van Enkhuizen, J., Milienne-Petiot, M., Geyer, M. A., & Young, J. W. (2015) · Psychopharmacology · doi:10.1007/s00213-015-4000-4 · Cited by 44 · see citing works

Causal Link between n-3 Polyunsaturated Fatty Acid Deficiency and Motivation Deficits

Ducrocq, F., Walle, R., Contini, A., Oummadi, A., Caraballo, B., van der Veldt, S., Boyer, M.-L., Aby, F., Tolentino‐Cortez, T., Helbling, J., et al. (2019) · Cell Metabolism · doi:10.1016/j.cmet.2020.02.012 · Cited by 42 · see citing works

The effects of reduced dopamine transporter function and chronic lithium on motivation, probabilistic learning, and neurochemistry in mice: Modeling bipolar mania

Milienne-Petiot, M., Kesby, J. P., Graves, M., van Enkhuizen, J., Semenova, S., Minassian, A., Markou, A., Geyer, M. A., & Young, J. W. (2016) · Neuropharmacology · doi:10.1016/j.neuropharm.2016.07.030 · Cited by 39 · see citing works

The Neurobiology of Bipolar Disorder

Young, A. H., & Juruena, M. F. (2020) · Current topics in behavioral neurosciences · doi:10.1007/7854_2020_179 · Cited by 39 · see citing works

Inhibitory deficits in euthymic bipolar disorder patients assessed in the human behavioral pattern monitor

Henry, B. L., Minassian, A., Patt, V. M., Hua, J. P. Y., Young, J. W., Geyer, M. A., & Perry, W. (2013) · Journal of Affective Disorders · doi:10.1016/j.jad.2013.05.020 · Cited by 38 · see citing works

Investigating the underlying mechanisms of aberrant behaviors in bipolar disorder from patients to models

van Enkhuizen, J., Geyer, M. A., Minassian, A., Perry, W., Henry, B. L., & Young, J. W. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.08.008 · Cited by 31 · see citing works

Expression of dopamine signaling genes in the post-mortem brain of individuals with mental illnesses is moderated by body mass index and mediated by insulin signaling genes

Mansur, R. B., Fries, G. R., Subramaniapillai, M., Frangou, S., Felice, F. G. D., Rasgon, N., McEwen, B. S., Brietzke, E. M., & McIntyre, R. S. (2018) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2018.10.020 · Cited by 33 · see citing works

The relationship between the dopaminergic system and depressive symptoms in cervical dystonia

Zoons, E., Tijssen, M. A. J., Dreissen, Y. E. M., Speelman, J. D., Smit, M., & Booij, J. (2017) · European Journal of Nuclear Medicine and Molecular Imaging · doi:10.1007/s00259-017-3664-x · Cited by 31 · see citing works

The emerging neuroimmune hypothesis of bipolar disorder: An updated overview of neuroimmune and microglial findings

Filho, A. J. M. C., Eyres, C., Blöbaum, L., Landwehr, A., & Tremblay, M. (2024) · Journal of Neurochemistry · doi:10.1111/jnc.16098 · Cited by 30 · see citing works

Dopamine dysfunction in depression: application of texture analysis to dopamine transporter single-photon emission computed tomography imaging

Tamura, T., Sugihara, G., Okita, K., Mukai, Y., Matsuda, H., Shiwaku, H., Takagi, S., Daisaki, H., Tateishi, U., & Takahashi, H. (2022) · Translational Psychiatry · doi:10.1038/s41398-022-02080-z · Cited by 29 · see citing works

Significance of protein kinase C in the neuropsychotoxicity induced by methamphetamine-like psychostimulants

Shin, E., Dang, D.-K., Hwang, Y. G., Tran, H., Sharma, N., Jeong, J. H., Jang, C., Nah, S.-Y., Nabeshima, T., Yoneda, Y., et al. (2019) · Neurochemistry International · doi:10.1016/j.neuint.2019.01.014 · Cited by 26 · see citing works

Failure of activation of striatum during the performance of executive function tasks in adult patients with bipolar disorder

Tian, F., Diao, W., Yang, X., Wang, X., Roberts, N., Feng, C., & Jia, Z. (2019) · Psychological Medicine · doi:10.1017/s0033291719000473 · Cited by 25 · see citing works

Research Domain Criteria versus DSM V: How does this debate affect attempts to model corticostriatal dysfunction in animals?

Young, J. W., Winstanley, C. A., Brady, A. M., & Hall, F. S. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.10.029 · Cited by 24 · see citing works

Evaluation of Neurotransmitter Alterations in Four Distinct Brain Regions After Rapid Eye Movement Sleep Deprivation (REMSD) Induced Mania-Like Behaviour in Swiss Albino Mice

Siddique, S. A., Tamilselvan, T., Vishnupriya, M., & Balamurugan, E. (2018) · Neurochemical Research · doi:10.1007/s11064-018-2533-8 · Cited by 24 · see citing works

Dopamine transporter knockdown mice in the behavioral pattern monitor: A robust, reproducible model for mania-relevant behaviors

Kwiatkowski, M. A., Hellemann, G., Sugar, C. A., Cope, Z. A., Minassian, A., Perry, W., Geyer, M. A., & Young, J. W. (2017) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2017.12.007 · Cited by 22 · see citing works

GBR 12909 administration as an animal model of bipolar mania: time course of behavioral, brain oxidative alterations and effect of mood stabilizing drugs

Queiroz, A. I. G., de Araújo, M. M., Araújo, T. D. S., de Souza, G. C., Cavalcante, L. M., Machado, M. D. J. S., de Lucena, D. F., Quevedo, J., & Macêdo, D. S. (2015) · Metabolic Brain Disease · doi:10.1007/s11011-015-9697-6 · Cited by 22 · see citing works

The development of delusion revisited: A transdiagnostic framework

Poletti, M., & Sambataro, F. (2013) · Psychiatry Research · doi:10.1016/j.psychres.2013.07.032 · Cited by 20 · see citing works

The influence of dopamine‐related genes on perceptual stability

Schmack, K., Sekutowicz, M., Rössler, H., Brandl, E. J., Müller, D. J., & Sterzer, P. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12339 · Cited by 21 · see citing works

Association of CACNA1C with bipolar disorder among the Pakistani population

Khalid, M., Driessen, T. M., Lee, J. S., Tejwani, L., Rasool, A., Saqlain, M., Shaiq, P. A., Hanif, M., Nawaz, A., DeWan, A. T., et al. (2018) · Gene · doi:10.1016/j.gene.2018.04.061 · Cited by 20 · see citing works

Altered brain activation during reward anticipation in bipolar disorder

Long, X.-P., Wang, X.-L., Tian, F.-F., Cao, Y., Xie, H.-S., & Jia, Z. (2022) · Translational Psychiatry · doi:10.1038/s41398-022-02075-w · Cited by 15 · see citing works

Intracellular Signaling Cascades in Bipolar Disorder

Jones, G. H., Rong, C., Shariq, A. S., Mishra, A. P., & Machado‐Vieira, R. (2020) · Current topics in behavioral neurosciences · doi:10.1007/7854_2020_157 · Cited by 18 · see citing works

Changes in striatal dopamine transporters in bipolar disorder and valproate treatment

Hsueh, Y., Lin, C.-Y., Chiu, N.-T., Yang, Y. K., Chen, P. S., & Chang, H. H. (2021) · European Psychiatry · doi:10.1192/j.eurpsy.2021.1 · Cited by 17 · see citing works

Biological Psychiatry and Psychopharmacology

Fountoulakis, K. N., Nimatoudis, I., & Stahl, S. M. (2019) · Springer eBooks · doi:10.1007/978-3-030-18323-3_13 · Cited by 17 · see citing works

Motor Transitions’ Peculiarity of Heterozygous DAT Rats When Offspring of an Unconventional KOxWT Mating

Carbone, C., Brancato, A., Adinolfi, A., Russo, S. L. M. L., Alleva, E., Cannizzaro, C., & Adriani, W. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.03.005 · Cited by 16 · see citing works

Translational cognitive systems: focus on attention

Roberts, B. Z., & Young, J. W. (2022) · Emerging Topics in Life Sciences · doi:10.1042/etls20220009 · Cited by 14 · see citing works

Assessing positive and negative valence systems to refine animal models of bipolar disorders: the example of GBR 12909-induced manic phenotype

Bigot, M., Vicq, É., Lledo, P., Alonso, M., & Henry, C. (2022) · Scientific Reports · doi:10.1038/s41598-022-10965-8 · Cited by 13 · see citing works

Sleep and Memory Consolidation Dysfunction in Psychiatric Disorders: Evidence for the Involvement of Extracellular Matrix Molecules

Gisabella, B., Babu, J., Valeri, J., Rexrode, L., & Pantazopoulos, H. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.646678 · Cited by 13 · see citing works

Different pharmacokinetics of lithium orotate inform why it is more potent, effective, and less toxic than lithium carbonate in a mouse model of mania

Pacholko, A. G., & Bekar, L. K. (2023) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2023.06.012 · Cited by 14 · see citing works

Advances in brain and religion studies: a review and synthesis of recent representative studies

McNamara, P., & Grafman, J. H. (2024) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2024.1495565 · Cited by 12 · see citing works

Longitudinal changes in the dopamine transporter and cognition in suicide attempters with charcoal burning

Yang, K., Wang, S.-J., Hsieh, W.-C., Lirng, J.-F., Yang, C., Deng, J., Lin, C.-L., & Chou, Y.-H. (2014) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2014.12.002 · Cited by 12 · see citing works

Molecular Imaging of Depressive Disorders

Ruhé, H., Visser, A. K. D., Frokjaer, V., Haarman, B., Klein, H., & Booij, J. (2020) · PET and SPECT in Psychiatry · doi:10.1007/978-3-642-40384-2_5 · Cited by 2 · see citing works

Manic symptom severity correlates with COMT activity in the striatum: A post-mortem study

Bortolato, M., Walss‐Bass, C., Thompson, P. M., & Moskovitz, J. (2016) · The World Journal of Biological Psychiatry · doi:10.1080/15622975.2016.1208844 · Cited by 10 · see citing works

Biomarker potential of hsa-miR-145-5p in peripheral whole blood of manic bipolar I patients

Tekin, S., Erdal, M. E., Aşoğlu, M., Ay, Ö. İ., Ay, M. E., & Yılmaz, Ş. G. (2022) · Brazilian Journal of Psychiatry · doi:10.47626/1516-4446-2021-2260 · Cited by 10 · see citing works

Chronic nicotine, but not suramin or resveratrol, partially remediates the mania-like profile of dopamine transporter knockdown mice

Kwiatkowski, M. A., Roberts, B. Z., van Enkhuizen, J., Ji, B., Zhou, X., & Young, J. W. (2020) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2020.11.004 · Cited by 9 · see citing works

Is SARS-CoV-2 a Risk Factor of Bipolar Disorder?—A Narrative Review

Lorkiewicz, P., & Waszkiewicz, N. (2022) · Journal of Clinical Medicine · doi:10.3390/jcm11206060 · Cited by 8 · see citing works

Microstructural changes of the nucleus accumbens due to increase of estradiol level during menstrual cycle contribute to recurrent manic episodes—A single case study

Matsuoka, K., Yasuno, F., Inoue, M., Yamamoto, A., Kudo, T., Kitamura, S., Okada, K., Kiuchi, K., Kosaka, J., Iida, H., et al. (2013) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2013.11.006 · Cited by 6 · see citing works

Altered levels of dopamine transporter in the frontal pole and the striatum in mood disorders: A postmortem study

Sekiguchi, H., Pavey, G., & Dean, B. (2022) · Journal of Affective Disorders · doi:10.1016/j.jad.2022.09.065 · Cited by 6 · see citing works

Chronic cannabis use in people with bipolar disorder is associated with comparable decision-making and functional outcome to healthy participants

Miranda, A. H., Roberts, B. Z., Holloway, B. M., Peek, E. M., Rosberg, H., Ayoub, S. M., Piomelli, D., Jung, K., Barnes, S. A., Rossi, S. S., et al. (2025) · Translational Psychiatry · doi:10.1038/s41398-025-03718-4 · Cited by 5 · see citing works

Catecholamine depletion in first-degree relatives of individuals with mood disorders: An [18F]fluorodeoxyglucose positron emission tomography study

Savitz, J. B., Nugent, A. C., Bellgowan, P. S. F., Wright, N., Tinsley, R., Zarate, C. A., Herscovitch, P., & Drevets, W. C. (2013) · NeuroImage Clinical · doi:10.1016/j.nicl.2013.02.004 · Cited by 4 · see citing works

Mania Risk is Associated with Dominance Behavior in an Interpersonal Negotiation Task

Fulford, D., Sinclair, S., John, O. P., & Johnson, S. L. (2014) · Journal of Experimental Psychopathology · doi:10.5127/jep.040513 · Cited by 4 · see citing works

An Overview of Machine Learning Applications in Mood Disorders

Topolski, N., Jeong, S. H., & Mwangi, B. (2021) · Cambridge University Press eBooks · doi:10.1017/9781108623018.017 · Cited by 4 · see citing works

Chronic antipsychotic treatment exerts limited effects on the mania-like behavior of dopamine transporter knockdown mice

Cope, Z. A., Kenton, J. A., Minassian, A., Martin, M. V., Perry, W., Bundgaard, C., Arnt, J., van Enkhuizen, J., Geyer, M. A., & Young, J. W. (2021) · Behavioural Brain Research · doi:10.1016/j.bbr.2021.113167 · Cited by 4 · see citing works

Molecular Imaging of Depressive Disorders

Ruhé, H. G., Frøkjær, V. G., Haarman, B. C. M., Jacobs, G. E., & Booij, J. (2020) · Springer eBooks · doi:10.1007/978-3-030-57231-0_4 · Cited by 3 · see citing works

Neuroanatomic and Functional Neuroimaging Findings

Díaz, A. P., Bauer, I. E., Sanches, M., & Soares, J. C. (2020) · Current topics in behavioral neurosciences · doi:10.1007/7854_2020_174 · Cited by 4 · see citing works

Omega-3 fatty acids supplementation with lithium and aripiprazole for improving the balance of circulating hormones and brain neurotransmitters in manic mice model

Arunagiri, P., Balamurugan, E., Murugesan, S., & Mackraj, I. (2017) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-017-1460-6 · Cited by 4 · see citing works

Biomarkers for bipolar disorder: current insights

Scola, G., Duong, A., & Syed, B. (2015) · Current Biomarker Findings · doi:10.2147/cbf.s79138 · Cited by 4 · see citing works

Dopamine release during psychological stress in euthymic bipolar I disorder: a Positron Emission Tomography study with [11C]raclopride

Saraf, G., Pinto, J. V., Cahn, A. J., White, A. G., Shahinfard, E., Vafai, N. M., Sossi, V., & Yatham, L. N. (2021) · Journal of Affective Disorders · doi:10.1016/j.jad.2021.08.022 · Cited by 3 · see citing works

Bipolar Disorders

Haarman, B. C. M., der Lek, R. F. R., Ruhé, H. G., de Groot, J. C., Nolen, W. A., & Doorduin, J. (2014) · Springer eBooks · doi:10.1007/978-3-642-40384-2_9 · Cited by 3 · see citing works

Mood Disorders

(2021) · Cambridge University Press eBooks · doi:10.1017/9781108623018 · Cited by 3 · see citing works

Genetic animal models for psychiatric disorders

Zhou, Y., Samsom, J., & Wong, A. H. C. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-819602-1.00015-2 · Cited by 4 · see citing works

Subchronic amphetamine decreases hyperactivity, anti-social behaviour and anhedonia in dopamine transporter knockout rats: role of prefrontal glutamate

Sadighi, M., Foka, K., Mottarlini, F., van den Burg, E. H., Taddini, S., Leo, D., Sanna, F., Caffino, L., Fumagalli, F., & Homberg, J. R. (2025) · Neuropharmacology · doi:10.1016/j.neuropharm.2025.110597 · Cited by 3 · see citing works

Neuroimaging Studies of Effects of Psychotherapy in Depression

Bauer, I. E., & Meyer, T. D. (2021) · Cambridge University Press eBooks · doi:10.1017/9781108623018.021 · Cited by 2 · see citing works

Anti‐manic effect of deep brain stimulation of the ventral tegmental area in an animal model of mania induced by methamphetamine

Varela, R. B., Boschen, S. L., Yates, N. J., Houghton, T., Blaha, C. D., Lee, K. H., Bennet, K. E., Kouzani, A. Z., Berk, M., Quevedo, J., et al. (2024) · Bipolar Disorders · doi:10.1111/bdi.13423 · Cited by 2 · see citing works

Alterations of striatal phosphodiesterase 10 A and their association with recurrence rate in bipolar I disorder

Sano, Y., Yamamoto, Y., Kubota, M., Moriguchi, S., Matsuoka, K., Kurose, S., Tagai, K., Endo, H., Yamagata, B., Suzuki, H., et al. (2024) · Translational Psychiatry · doi:10.1038/s41398-024-03107-3 · Cited by 2 · see citing works

Mood Disorders and Severe Obesity: A Case Study

Amodeo, G., Subramaniapillai, M., Mansur, R. B., & McIntyre, R. S. (2016) · Springer eBooks · doi:10.1007/978-3-319-42536-8_9 · Cited by 2 · see citing works

Electrophysiological Biomarkers for Mood Disorders

Ramakrishnan, N., Murphy, N., Selvaraj, S., & Cho, R. Y. (2021) · Cambridge University Press eBooks · doi:10.1017/9781108623018.015 · Cited by 2 · see citing works

Animal Models for Mania

Schmerder, K., & Freund, N. (2022) · Neuromethods · doi:10.1007/978-1-0716-2748-8_13 · Cited by 2 · see citing works

Striatal Dopamine Transporter Availability is Associated with Sleep Disturbance among Patients with Bipolar I Disorder: A Single-photon Emission Computed Tomography Study Using [99mTc] TRODAT-1

Lu, T., Lin, S., Tseng, H., Yang, Y. K., Chiu, N.-T., & Chen, P. S. (2022) · Clinical Psychopharmacology and Neuroscience · doi:10.9758/cpn.2022.20.4.768 · Cited by 2 · see citing works

Neuroimaging Studies of Bipolar Depression: Therapeutic Implications

Savitz, J. B., Morris, H. M., & Drevets, W. C. (2016) · Milestones in drug therapy · doi:10.1007/978-3-319-31689-5_8 · Cited by 2 · see citing works

Polydipsia as a Precursor of Manic Episode in Bipolar Affective Disorder Patients with Alcohol Use Disorder

Ceylan, M. E., Ünsalver, B. Ö., & Evrensel, A. (2018) · Clinical Psychopharmacology and Neuroscience · doi:10.9758/cpn.2018.16.1.114 · Cited by 1 · see citing works

Trace amine-associated receptor 1 (TAAR1) activation reduced mania-relevant hyperexploration and risky decision-making in dopamine transporter knockdown mice

Munir, T. Y., Roberts, B. Z., & Young, J. W. (2025) · Journal of Psychopharmacology · doi:10.1177/02698811251364394 · Cited by 1 · see citing works

Bipolar Disorder: Diagnosis, Neuroanatomical and Biochemical Background

Kristina, R., & Duds, B. (2012) · InTech eBooks · doi:10.5772/33467 · Cited by 1 · see citing works

Addictive Drugs and Synaptic Plasticity

Vicente, J., Flores, G., Sihra, T. S., & Rodriguez-Moreno, A. (2012) · InTech eBooks · doi:10.5772/33299 · Cited by 1 · see citing works

Neuroradiological Imaging Studies in Bipolar Disorder

Kara, K., Akarsu, S., & Verim, S. (2012) · Psikiyatride Guncel Yaklasimlar - Current Approaches in Psychiatry · doi:10.5455/cap.20130501 · Cited by 1 · see citing works

Bipolar Bozuklukta Nörogörüntüleme Neuroimaging in Bipolar Disorder

Kara, K., Verim, S., & Akarsu, S. (2013) · Cited by 1 · see citing works

The evolution of animal models for bipolar disorder

Valvassori, S. S., Gava, F. F., Cararo, J. H., & Quevedo, J. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819182-8.00009-0 · Cited by 1 · see citing works

Aetiopathogenesis of Bipolar Disorder

Fountoulakis, K. N. (2014) · Springer eBooks · doi:10.1007/978-3-642-37216-2_13 · Cited by 1 · see citing works

An assessment of the catecholamine hypothesis of bipolar disorder

Charney, A. W., Sayed, S., & Charney, D. S. (2016) · Cambridge University Press eBooks · doi:10.1017/cbo9781107477278.004 · Cited by 1 · see citing works

[Microcirculation end effect of detralex in patients with chronic venous insufficiency of the lower extremities].

Sirotin, B. Z., & Жмеренецкий, К. В. (2003) · PubMed · Cited by 1 · see citing works

Brain Imaging and the Mechanisms of Antidepressant Action

Godlewska, B. R., Selvaraj, S., & Cowen, P. J. (2021) · Cambridge University Press eBooks · doi:10.1017/9781108623018.020 · Cited by 1 · see citing works

Effects of Lithium on Brain Structure in Bipolar Disorder

Kaur, J., Kafantaris, V., & Szeszko, P. R. (2021) · Cambridge University Press eBooks · doi:10.1017/9781108623018.018 · Cited by 1 · see citing works

Functional Connectome in Bipolar Disorder

Cha, J., & Anand, A. (2021) · Cambridge University Press eBooks · doi:10.1017/9781108623018.008 · Cited by 1 · see citing works

Higher striatal dopamine transporters in euthymic patients with bipolar disorder: a SPECT study with [ ^99m Tc] TRODAT‐1

Chang, T. T., Yeh, T. L., Chiu, N. T., Chen, P. S., Huang, H. Y., Yang, Y. K., Lee, I. H., & Lu, R. B. (2010) · Bipolar Disorders · doi:10.1111/j.1399-5618.2009.00771.x · Cited by 63 · see citing works

A Preliminary Study of Dopamine Transporter Binding in Bipolar and Unipolar Depressed Patients and Healthy Controls

Amsterdam, J. D., & Newberg, A. B. (2007) · Neuropsychobiology · doi:10.1159/000106476 · Cited by 84 · see citing works

235. State-dependent associations between striatal dopamine transporter availability and large-scale brain network in bipolar disorder

Huang, M.-H., Zhu, J.-D., Tu, P.-C., Chan, Y.-L., Mao, W.-C., & Su, T.-P. (2026) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyag040.208

A Positron Emission Tomography Study of Dopamine Transporter Density in Patients With Bipolar Disorder With Current Mania and Those With Recently Remitted Mania

Yatham, L. N., Liddle, P. F., Gonzalez, M., Saraf, G., Vafai, N. M., Lam, R. W. M., & Sossi, V. (2022) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2022.3541 · Cited by 26 · see citing works

State-dependent associations between striatal dopamine transporter availability and large-scale functional networks in bipolar disorder: An exploratory multimodal imaging study

Huang, M., Zhu, J., Tu, P., Chan, Y. E., Mao, W., & Su, T. (2026) · Asian Journal of Psychiatry · doi:10.1016/j.ajp.2026.105137