Immediate-Early Genes Modulation by Antipsychotics: Translational Implications for a Putative Gateway to Drug-Induced Long-Term Brain Changes

Imaging brain gene expression profiles by antipsychotics: Region-specific action of amisulpride on postsynaptic density transcripts compared to haloperidol

de Bartolomeis, A., Marmo, F., Buonaguro, E. F., Rossi, R., Tomasetti, C., & Iasevoli, F. (2013) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2012.11.014 · Cited by 38

Differential expression of Homer 1 gene by acute and chronic administration of antipsychotics and dopamine transporter inhibitors in the rat forebrain

Ambesi‐Impiombato, A., Panariello, F., Dell’Aversano, C., Tomasetti, C., Muscettola, G., & de Bartolomeis, A. (2007) · Synapse · doi:10.1002/syn.20385 · Cited by 38

Effects of chronic clozapine administration on markers of arachidonic acid cascade and synaptic integrity in rat brain

Kim, H., Cheon, Y., Modi, H. R., Rapoport, S. I., & Rao, J. S. (2012) · Psychopharmacology · doi:10.1007/s00213-012-2671-7 · Cited by 38

BDNF polymorphisms are associated with schizophrenia onset and positive symptoms

Zhang, X. Y., Chen, D., Tan, Y., Tan, S., Luο, X., Zuo, L., & Soares, J. C. (2015) · Schizophrenia Research · doi:10.1016/j.schres.2015.11.009 · Cited by 38

Complementary activation of hippocampal–cortical subregions and immature neurons following chronic training in single and multiple context versions of the water maze

Snyder, J. S., Clifford, M. A., Jeurling, S. I., & Cameron, H. A. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.06.025 · Cited by 37

Differential expression of IEG mRNA in rat brain following acute treatment with clozapine or haloperidol: a semi-quantitative RT—PCR study

Robbins, M., Critchlow, H., Lloyd, A., Cilia, J., Clarke, J. D. W., Bond, B. C., Jones, D., & Maycox, P. R. (2008) · Journal of Psychopharmacology · doi:10.1177/0269881107081521 · Cited by 37

Novel temporal configurations of stimuli produce discrete changes in immediate‐early gene expression in the rat hippocampus

Amin, E., Pearce, J. M., Brown, M. W., & Aggleton, J. P. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.05131.x · Cited by 36

The dopamine D1 receptor agonist, but not the D2 receptor agonist, induces gene expression of Homer 1a in rat striatum and nucleus accumbens

Yamada, H., Kuroki, T., Nakahara, T., Hashimoto, K., Tsutsumi, T., Hirano, M., & Maeda, H. (2006) · Brain Research · doi:10.1016/j.brainres.2006.11.011 · Cited by 36

NR4A Gene Expression Is Dynamically Regulated in the Ventral Tegmental Area Dopamine Neurons and Is Related to Expression of Dopamine Neurotransmission Genes

Eells, J. B., Wilcots, J., Sisk, S., & Guo‐Ross, S. X. (2011) · Journal of Molecular Neuroscience · doi:10.1007/s12031-011-9642-z · Cited by 36

Contribution of Egr1/zif268 to Activity-Dependent Arc/Arg3.1 Transcription in the Dentate Gyrus and Area CA1 of the Hippocampus

Penke, Z., Chagneau, C., & Laroche, S. (2011) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2011.00048 · Cited by 35

Inverse Regulation of Plasticity-related Immediate Early Genes by Calcineurin in Hippocampal Neurons

Lam, B., Zhang, W., Enticknap, N., Haggis, E., Cader, M. Z., & Chawla, S. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m901121200 · Cited by 35

NMDA and dopamine D1 receptors within NAc-shell regulate IEG proteins expression in reward circuit during cocaine memory reconsolidation

Li, Y., Ge, S., Li, N., Chen, L., Zhang, S., Wang, J., Wu, H., Wang, X., & Wang, X. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.11.063 · Cited by 35

Homer1a protein expression in schizophrenia, bipolar disorder, and major depression

Leber, S. L., Llenos, I. C., Miller, C. L., Dulay, J. R., Haybaeck, J., & Weis, S. (2017) · Journal of Neural Transmission · doi:10.1007/s00702-017-1776-x · Cited by 34

Differential effects of typical and atypical antipsychotic drugs on striosome and matrix compartments of the striatum

Bubser, M., & Deutch, A. Y. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2002.01903.x · Cited by 33

Prolonged exposure to NMDAR antagonist induces cell-type specific changes of glutamatergic receptors in rat prefrontal cortex

Wang, H.-X., & Gao, W. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.11.024 · Cited by 33

Progressive recruitment of cortical and striatal regions by inducible postsynaptic density transcripts after increasing doses of antipsychotics with different receptor profiles: Insights for psychosis treatment

de Bartolomeis, A., Iasevoli, F., Marmo, F., Buonaguro, E. F., Eramo, A., Rossi, R., Avvisati, L., Latte, G., & Tomasetti, C. (2015) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2015.01.003 · Cited by 32

Differential effects of antipsychotics on hippocampal presynaptic protein expressions and recognition memory in a schizophrenia model in mice

Ozdemir, H., Ertuğrul, A., Başar, K., & Saka, E. (2012) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2012.05.009 · Cited by 31

Chronic high-dose haloperidol has qualitatively similar effects to risperidone and clozapine on immediate-early gene and tyrosine hydroxylase expression in the rat locus coeruleus but not medial prefrontal cortex

Verma, V., Lim, E. P., Han, S. P., Nagarajah, R., & Dawe, G. S. (2006) · Neuroscience Research · doi:10.1016/j.neures.2006.09.002 · Cited by 31

Antipsychotic drugs modulate Arc expression in the rat brain

Fumagalli, F., Frasca, A., Racagni, G., & Riva, M. A. (2008) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2008.09.001 · Cited by 31

Basal and stress-induced modulation of activity-regulated cytoskeletal associated protein (Arc) in the rat brain following duloxetine treatment

Molteni, R., Calabrese, F., Mancini, M., Racagni, G., & Riva, M. A. (2008) · Psychopharmacology · doi:10.1007/s00213-008-1276-7 · Cited by 31

Antipsychotic and antidepressant co-treatment: Effects on transcripts of inducible postsynaptic density genes possibly implicated in behavioural disorders

Dell’Aversano, C., Tomasetti, C., Iasevoli, F., & de Bartolomeis, A. (2009) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2009.01.006 · Cited by 30

Presence and induction of Fos B-like immunoreactivity in neural, but not non-neural, cells in adult rat brain

Dragunow, M. (1990) · Brain Research · doi:10.1016/0006-8993(90)91357-m · Cited by 30

Differential effects of acute and chronic treatment with typical and atypical neuroleptics on c-fos mRNA expression in rat forebrain regions using non-radioactive in situ hybridization

Semba, J., Sakai, M. W., Suhara, T., & Akanuma, N. (1999) · Neurochemistry International · doi:10.1016/s0197-0186(99)00009-1 · Cited by 30

Association of a polymorphism in the Homer1 gene with cocaine dependence in an African American population

Dahl, J. P., Kampman, K. M., Oslin, D. W., Weller, A. E., Lohoff, F. W., Ferraro, T. N., Brien, C. P. O., & Berrettini, W. H. (2005) · Psychiatric Genetics · doi:10.1097/00041444-200512000-00010 · Cited by 29

Immediate early gene activation in hippocampus and dorsal striatum: Effects of explicit place and response training

Gill, K. M., Bernstein, I. L., & Mizumori, S. J. Y. (2007) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2006.12.011 · Cited by 29

Repeated aripiprazole treatment regulates Bdnf, Arc and Npas4 expression under basal condition as well as after an acute swim stress in the rat brain

Luoni, A., Fumagalli, F., Racagni, G., & Riva, M. A. (2013) · Pharmacological Research · doi:10.1016/j.phrs.2013.11.008 · Cited by 28

Effect of atypical antipsychotics on phencyclidine-induced expression of arc in rat brain

Nakahara, T., Kuroki, T., Hashimoto, K., Hondo, H., Tsutsumi, T., Motomura, K., Ueki, H., Hirano, M., & Uchimura, H. (2000) · Neuroreport · doi:10.1097/00001756-200002280-00025 · Cited by 28

Transcriptional Mechanisms Underlying Addiction-Related Structural Plasticity

Maze, I. S., & Russo, S. J. (2010) · Molecular Interventions · doi:10.1124/mi.10.4.5 · Cited by 28

Double activity imaging reveals distinct cellular targets of haloperidol, clozapine and dopamine D3 receptor selective RGH-1756

Kovács, K., Csejtei, M., & Laszlovszky, I. (2001) · Neuropharmacology · doi:10.1016/s0028-3908(00)00163-5 · Cited by 28

HOMER1 Promoter Analysis in Parkinson’s Disease: Association Study with Psychotic Symptoms

Luca, V. D., Annesi, G., Marco, E. V. D., de Bartolomeis, A., Nicoletti, G., Pugliese, P., Muscettola, G., Barone, P., & Quattrone, A. (2009) · Neuropsychobiology · doi:10.1159/000230689 · Cited by 27

Identification of Optogenetically Activated Striatal Medium Spiny Neurons by Npas4 Expression

Bepari, A. K., Sano, H., Tamamaki, N., Nambu, A., Tanaka, K. F., & Takebayashi, H. (2012) · PLoS ONE · doi:10.1371/journal.pone.0052783 · Cited by 27

The transcription factor Npas4 contributes to adolescent development of prefrontal inhibitory circuits, and to cognitive and emotional functions: Implications for neuropsychiatric disorders

Shepard, R. M., Heslin, K. A., & Coutellier, L. D. (2016) · Neurobiology of Disease · doi:10.1016/j.nbd.2016.12.012 · Cited by 27

Epigenetic regulation of neuronal immediate early genes is associated with decline in their expression and memory consolidation in scopolamine-induced amnesic mice

Srivas, S., & Thakur, M. K. (2016) · Molecular Neurobiology · doi:10.1007/s12035-016-0047-4 · Cited by 27

Effects of Desmethylclozapine on Fos Protein Expression in the Forebrain: In Vivo Biological Activity of the Clozapine Metabolite

C Young, P. D. (1998) · Neuropsychopharmacology · doi:10.1016/s0893-133x(97)00203-0 · Cited by 26

Temporal and Spatial Transcriptional Fingerprints by Antipsychotic or Propsychotic Drugs in Mouse Brain

Sakuma, K., Komatsu, H., Maruyama, M., Imaichi, S., Habata, Y., & Mori, M. (2015) · PLoS ONE · doi:10.1371/journal.pone.0118510 · Cited by 26

Signaling Pathways Relevant to Cognition-Enhancing Drug Targets

Ménard, C., Gaudreau, P., & Quirion, R. (2015) · Handbook of experimental pharmacology · doi:10.1007/978-3-319-16522-6_3 · Cited by 24

Re-arrangements of gene transcripts at glutamatergic synapses after prolonged treatments with antipsychotics: A putative link with synaptic remodeling

Buonaguro, E. F., Iasevoli, F., Marmo, F., Eramo, A., Latte, G., Avagliano, C., Tomasetti, C., & de Bartolomeis, A. (2017) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2017.02.012 · Cited by 24

The levo enantiomer of amphetamine increases memory consolidation and gene expression in the hippocampus without producing locomotor stimulation

Wiig, K. A., Whitlock, J. R., Epstein, M. H., Carpenter, R. L., & Bear, M. F. (2009) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2009.02.001 · Cited by 24

The PDE10A inhibitor MP-10 and haloperidol produce distinct gene expression profiles in the striatum and influence cataleptic behavior in rodents

Gentzel, R. C., Toolan, D. M., Roberts, R., Koser, A. J., Kandebo, M., Hershey, J. C., Renger, J. J., Uslaner, J. M., & Smith, S. M. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2015.05.024 · Cited by 21

NR4A Orphan Nuclear Receptor Family in Peripheral Blood Eosinophils from Patients with Atopic Dermatitis and Apoptotic Eosinophils in vitro

Kagaya, S., Hashida, R., Ohkura, N., Tsukada, T., Sugita, Y., Terakawa, M., Tsujimoto, G., Katsunuma, T., Akasawa, A., Matsumoto, K., et al. (2005) · International Archives of Allergy and Immunology · doi:10.1159/000085430 · Cited by 21

Postsynaptic density protein transcripts are differentially modulated by minocycline alone or in add-on to haloperidol: Implications for treatment resistant schizophrenia

Buonaguro, E. F., Tomasetti, C., Chiodini, P., Marmo, F., Latte, G., Rossi, R., Avvisati, L., Iasevoli, F., & de Bartolomeis, A. (2016) · Journal of Psychopharmacology · doi:10.1177/0269881116658987 · Cited by 21

Effects of short-term and chronic olanzapine treatment on immediate early gene protein and tyrosine hydroxylase immunoreactivity in the rat locus coeruleus and medial prefrontal cortex

Verma, V., Rasmussen, K., & Dawe, G. S. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.08.010 · Cited by 21

Extracellular signal‐regulated kinases (ERK) and protein kinase C (PKC) activities are involved in the modulation of Nur77 and Nor‐1 expression by dopaminergic drugs

Bourhis, E., Maheux, J., Rouillard, C., & Lévesque, D. (2008) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2008.05455.x · Cited by 20

Chronic vortioxetine treatment in rodents modulates gene expression of neurodevelopmental and plasticity markers

Waller, J. A., Tamm, J. A., Abdourahman, A., Pehrson, A. L., Li, Y., Cajina, M., & Sánchez, C. (2017) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2016.11.014 · Cited by 20

Mice haploinsufficient for Map2k7, a gene involved in neurodevelopment and risk for schizophrenia, show impaired attention, a vigilance decrement deficit and unstable cognitive processing in an attentional task: impact of minocycline

Openshaw, R. L., Thomson, D. M., Penninger, J. M., Pratt, J. A., & MORRIS, B. J. (2016) · Psychopharmacology · doi:10.1007/s00213-016-4463-y · Cited by 20

Chronic treatment with certain antipsychotic drugs preserves upregulation of regulator of G-protein signalling 2 mRNA in rat striatum as opposed to c-fos mRNA

Boutet-Robinet, E. A., Geurts, M., Maloteaux, J., & Pauwels, P. J. (2001) · Neuroscience Letters · doi:10.1016/s0304-3940(01)01923-1 · Cited by 19

Dorsal striatal volumes in never-treated patients with first-episode schizophrenia before and during acute treatment

Emsley, R. A., Asmal, L., du Plessis, S., Chiliza, B., Kidd, M., Carr, J. A., & Vink, M. (2015) · Schizophrenia Research · doi:10.1016/j.schres.2015.09.014 · Cited by 18

Anatomical specificity in the modulation of activity-regulated genes after acute or chronic lurasidone treatment

Luoni, A., da Rocha, F. F., & Riva, M. A. (2013) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2013.12.008 · Cited by 18

Alterations in amphetamine‐stimulated dopamine overflow due to the Nurr1‐null heterozygous genotype and postweaning isolation

Moore, T. M., Brown, T., Cade, M., & Eells, J. B. (2008) · Synapse · doi:10.1002/syn.20550 · Cited by 18

A direct role for c-fos in AP-1-dependent gene transcription.

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MK 801 attenuates c-Fos and c-Jun expression afterin vitroischemia in rat neuronal cell cultures but not in PC 12 cells

Gerlach, R., Beck, M., Zeitschel, U., & Seifert, V. (2002) · Neurological Research · doi:10.1179/016164102101200654 · Cited by 17

Intracellular pathways of antipsychotic combined therapies: Implication for psychiatric disorders treatment

de Bartolomeis, A., Avvisati, L., Iasevoli, F., & Tomasetti, C. (2013) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2013.06.034 · Cited by 17

NR4A2: Effects of an “Orphan” Receptor on Sustained Attention in a Schizophrenic Population

Ancín, I., Cabranes, J. A., Vázquez-Álvarez, B., Santos, J. L., Sánchez‐Morla, E. M., Alaerts, M., Del‐Favero, J., & Barabash, A. (2012) · Schizophrenia Bulletin · doi:10.1093/schbul/sbr176 · Cited by 17

Part II: Functional delivery of a neurotherapeutic gene to neural stem cells using minicircle DNA and nanoparticles: Translational advantages for regenerative neurology

Fernandes, A. R., & Chari, D. M. (2016) · Journal of Controlled Release · doi:10.1016/j.jconrel.2016.06.039 · Cited by 17

Changes in brain functional connectivity after chronic haloperidol in rats: a network analysis

Wheeler, A. L., Creed, M. C., Voineskos, A. N., & Nóbrega, J. N. (2014) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145714000042 · Cited by 15

Switching antipsychotics: Imaging the differential effect on the topography of postsynaptic density transcripts in antipsychotic-naïve vs. antipsychotic-exposed rats

de Bartolomeis, A., Marmo, F., Buonaguro, E. F., Latte, G., Tomasetti, C., & Iasevoli, F. (2016) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2016.04.015 · Cited by 15

Association of the orphan nuclear receptor NR4A1 with tardive dyskinesia

Novak, G., Gallo, A., Zai, C. C. H., Meltzer, H. Y., Lieberman, J. A., Potkin, S. G., Voineskos, A. N., Remington, G. J., Kennedy, J. L., Lévesque, D., et al. (2009) · Psychiatric Genetics · doi:10.1097/ypg.0b013e3283351221 · Cited by 14

Schizophrenia: What’s Arc Got to Do with It?

Managò, F., & Papaleo, F. (2017) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2017.00181 · Cited by 14

Modulation of haloperidol-induced patterns of the transcription factor Nur77 and Nor-1 expression by serotonergic and adrenergic drugs in the mouse brain

Maheux, J., Vuillier, L., Mahfouz, M., Rouillard, C., & Lévesque, D. (2011) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145711000630 · Cited by 13

Roles of Neuronal Activity-Induced Gene Products in Hebbian and Homeostatic Synaptic Plasticity, Tagging, and Capture

Hayashi, Y., Okamoto, K., Bosch, M., & Futai, K. (2012) · Advances in experimental medicine and biology · doi:10.1007/978-3-7091-0932-8_15 · Cited by 13

Injections of an opioid antagonist into the locus coeruleus and periaqueductal gray but not the amygdala precipitates morphine withdrawal in the 7‐day‐old rat

Jones, K. L., & Barr, G. A. (2000) · Synapse · doi:10.1002/1098-2396(200102)39:2 · Cited by 11

Chronic administration of haloperidol and clozapine induces differential effects on the expression of Arc and c-Fos in rat brain

Collins, C. M., Wood, M. D., & Elliott, J. M. (2014) · Journal of Psychopharmacology · doi:10.1177/0269881114536788 · Cited by 11

Schizophrenia-associated Risk and Protective Variants of c-Fos Encoding Gene

Boyajyan, A. S., Zakharyan, R., Atshemyan, S., Chavushyan, A., & Mkrtchyan, G. (2015) · Recent Advances in DNA & Gene Sequences (Formerly Recent Patents on DNA & Gene Sequences) · doi:10.2174/2352092209666150223113334 · Cited by 9

Methamphetamine-induced expression of zif268 mRNA is prevented by haloperidol in mice lacking μ-opioid receptor

Tien, L., Ho, I.-K., & Ma, T. (2010) · NeuroToxicology · doi:10.1016/j.neuro.2010.02.002 · Cited by 7

Increased expression of zif268 mRNA in rat retrosplenial cortex following administration of phencyclidine

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Proteome and pathway effects of chronic haloperidol treatment in mouse hippocampus

Schubert, K. O., Föcking, M., Wynne, K. J., & Cotter, D. (2015) · PROTEOMICS · doi:10.1002/pmic.201500242 · Cited by 6

Acute drug-induced spine changes in the nucleus accumbens are dependent on β-adducin

Engmann, O., Giralt, A., & Girault, J. (2016) · Neuropharmacology · doi:10.1016/j.neuropharm.2016.07.035 · Cited by 6

Untitled work

Jonnal (2000) · doi:10.1002/1096-8628(20001204)96:6

Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder

Gandal, M. J., Zhang, P., Hadjimichael, E., Walker, R. L., Chen, C., Liu, S., Won, H., van Bakel, H., Varghese, M., Wang, Y., et al. (2018) · Science · doi:10.1126/science.aat8127 · Cited by 1,247

Muscarinic acetylcholine receptors for psychotic disorders: bench-side to clinic

Yohn, S. E., Weiden, P. J., Felder, C. C., & Stahl, S. M. (2022) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2022.09.006 · Cited by 113

Clozapine's Multiple Cellular Mechanisms: What Do We Know after More than Fifty Years? a Systematic Review and Critical Assessment of Translational Mechanisms Relevant for Innovative Strategies in Treatment-Resistant Schizophrenia

de Bartolomeis, A., Vellucci, L., Barone, A., Manchia, M., Luca, V. D., Iasevoli, F., & Correll, C. U. (2022) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2022.108236 · Cited by 96

Present and future antipsychotic drugs: A systematic review of the putative mechanisms of action for efficacy and a critical appraisal under a translational perspective

de Bartolomeis, A., Barone, A., Begni, V., & Riva, M. A. (2022) · Pharmacological Research · doi:10.1016/j.phrs.2022.106078 · Cited by 79

Treatment-Resistant to Antipsychotics: A Resistance to Everything? Psychotherapy in Treatment-Resistant Schizophrenia and Nonaffective Psychosis: A 25-Year Systematic Review and Exploratory Meta-Analysis

Polese, D., Fornaro, M., Palermo, M., Luca, V. D., & de Bartolomeis, A. (2019) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2019.00210 · Cited by 78

Differential expression of IEG mRNA in rat brain following acute treatment with clozapine or haloperidol: a semi-quantitative RT—PCR study

Robbins, M., Critchlow, H., Lloyd, A., Cilia, J., Clarke, J. D. W., Bond, B. C., Jones, D., & Maycox, P. R. (2008) · Journal of Psychopharmacology · doi:10.1177/0269881107081521 · Cited by 37

Switching antipsychotics: how and where a prolonged treatment with a typical antipsychotic affects the topography of postsynaptic density gene expression induced by an atypical antipsychotic. Relevance for pychosis treatment.

Marmo, F. (2015) · Università degli Studi di Napoli Federico II · doi:10.6092/unina/fedoa/10507

Temporal and Spatial Transcriptional Fingerprints by Antipsychotic or Propsychotic Drugs in Mouse Brain

Sakuma, K., Komatsu, H., Maruyama, M., Imaichi, S., Habata, Y., & Mori, M. (2015) · PLoS ONE · doi:10.1371/journal.pone.0118510 · Cited by 26

Progressive recruitment of cortical and striatal regions by inducible postsynaptic density transcripts after increasing doses of antipsychotics with different receptor profiles: Insights for psychosis treatment

de Bartolomeis, A., Iasevoli, F., Marmo, F., Buonaguro, E. F., Eramo, A., Rossi, R., Avvisati, L., Latte, G., & Tomasetti, C. (2015) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2015.01.003 · Cited by 32

Re-arrangements of gene transcripts at glutamatergic synapses after prolonged treatments with antipsychotics: A putative link with synaptic remodeling

Buonaguro, E. F., Iasevoli, F., Marmo, F., Eramo, A., Latte, G., Avagliano, C., Tomasetti, C., & de Bartolomeis, A. (2017) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2017.02.012 · Cited by 24