Neurons expressing calcium-binding proteins in the prefrontal cortex in schizophrenia

Genome-wide expression analysis reveals dysregulation of myelination-related genes in chronic schizophrenia

Hakak, Y., Walker, J. R., Li, C., Wong, W. H., Davis, K. L., Buxbaum, J. D., Haroutunian, V., & Fienberg, A. A. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.081071198 · Cited by 1,192 · see citing works

Gene expression for glutamic acid decarboxylase is reduced without loss of neurons in prefrontal cortex of schizophrenics.

Akbarian, S. (1995) · Archives of General Psychiatry · doi:10.1001/archpsyc.1995.03950160008002 · Cited by 1,002 · see citing works

Molecular Characterization of Schizophrenia Viewed by Microarray Analysis of Gene Expression in Prefrontal Cortex

Mirnics, K., Middleton, F. A., Marquez, A., Lewis, D. A., & Levitt, P. (2000) · Neuron · doi:10.1016/s0896-6273(00)00085-4 · Cited by 882 · see citing works

Abnormally High Neuronal Density in the Schizophrenic Cortex

Selemon, L. D. (1995) · Archives of General Psychiatry · doi:10.1001/archpsyc.1995.03950220015005 · Cited by 876 · see citing works

Decreased Glutamic Acid Decarboxylase67 Messenger RNA Expression in a Subset of Prefrontal Cortical γ-Aminobutyric Acid Neurons in Subjects With Schizophrenia

Volk, D. W., Austin, M. C., Pierri, J. N., Sampson, A. R., & Lewis, D. A. (2000) · Archives of General Psychiatry · doi:10.1001/archpsyc.57.3.237 · Cited by 697 · see citing works

Parvalbumin-immunoreactive neurons are reduced in the prefrontal cortex of schizophrenics

BEASLEY, C., & REYNOLDS, G. (1997) · Schizophrenia Research · doi:10.1016/s0920-9964(96)00122-3 · Cited by 426 · see citing works

A subclass of prefrontal γ-aminobutyric acid axon terminals are selectively altered in schizophrenia

Woo, T.-U. W., Whitehead, R. E., Melchitzky, D. S., & Lewis, D. A. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.9.5341 · Cited by 410 · see citing works

Cytoarchitectonic Definition of Prefrontal Areas in the Normal Human Cortex: I. Remapping of Areas 9 and 46 using Quantitative Criteria

Rajkowska, G., & Goldman, P. S. (1995) · Cerebral Cortex · doi:10.1093/cercor/5.4.307 · Cited by 392 · see citing works

Selective deficits in prefrontal cortical GABAergic neurons in schizophrenia defined by the presence of calcium-binding proteins

Beasley, C. L., Zhang, Z. J., Patten, I., & Reynolds, G. P. (2002) · Biological Psychiatry · doi:10.1016/s0006-3223(02)01360-4 · Cited by 374 · see citing works

Up-regulation of GABAA receptor binding on neurons of the prefrontal cortex in schizophrenic subjects

Benes, F. M., Vincent, S. L., Marie, A. S., & Khan, Y. (1996) · Neuroscience · doi:10.1016/0306-4522(96)00328-4 · Cited by 274 · see citing works

The density and spatial distribution of gabaergic neurons, labelled using calcium binding proteins, in the anterior cingulate cortex in major depressive disorder, bipolar disorder, and schizophrenia

Cotter, D., Landau, S., Beasley, C. L., Stevenson, R. N., Chana, G., MacMillan, L., & Everall, I. (2002) · Biological Psychiatry · doi:10.1016/s0006-3223(01)01243-4 · Cited by 211 · see citing works

Local circuit neurons of developing and mature macaque prefrontal cortex: Golgi and immunocytochemical characteristics

Lund, J. S., & Lewis, D. A. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903280209 · Cited by 207 · see citing works

Schizophrenia and the parvalbumin-containing class of cortical local circuit neurons

Woo, T., Miller, J. L., & Lewis, D. A. (1997) · American Journal of Psychiatry · doi:10.1176/ajp.154.7.1013 · Cited by 191 · see citing works

Local circuit neurons of the prefrontal cortex in schizophrenia: selective increase in the density of calbindin-immunoreactive neurons

DAVISS, S. R., & Lewis, D. A. (1995) · Psychiatry Research · doi:10.1016/0165-1781(95)02720-3 · Cited by 187 · see citing works

Measurement of GABAergic parameters in the prefrontal cortex in schizophrenia: focus on GABA content, GABAA receptor α-1 subunit messenger RNA and human GABA transporter-1 (hGAT-1) messenger RNA expression

Ohnuma, T., Augood, S. J., Arai, H., McKenna, P. J., & Emson, P. C. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00189-x · Cited by 182 · see citing works

Changes in Serotonin2A and GABAA Receptors in Schizophrenia

Dean, B., Hussain, T., Hayes, W., Scarr, E., Kitsoulis, S., Hill, C., Opeskin, K., & Copolov, D. (1999) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1999.721593.x · Cited by 148 · see citing works

Basal ganglia organization in amphibians: Chemoarchitecture

Marín, Ó., Smeets, W. J. A. J., & González, A. (1998) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19980316)392:3 · Cited by 145 · see citing works

[3H]Muscimol binding sites increased in autopsied brains of chronic schizophrenics

Hanada, S., Mita, T., Nishino, N., & Tanaka, C. (1987) · Life Sciences · doi:10.1016/0024-3205(87)90341-9 · Cited by 140 · see citing works

Neurochemical correlates of cortical GABAergic deficits in schizophrenia: selective losses of calcium binding protein immunoreactivity

Reynolds, G. P., Zhang, Z. J., & Beasley, C. L. (2001) · Brain Research Bulletin · doi:10.1016/s0361-9230(01)00526-3 · Cited by 138 · see citing works

Neuronal calcium-binding proteins and schizophrenia

Eyles, D. W., McGrath, J. J., & Reynolds, G. P. (2002) · Schizophrenia Research · doi:10.1016/s0920-9964(01)00299-7 · Cited by 113 · see citing works

Localisation of tachykinin NK1 and NK3 receptors in the human prefrontal and visual cortex

Tooney, P. A., Au, G. G., & Chahl, L. A. (2000) · Neuroscience Letters · doi:10.1016/s0304-3940(00)00979-4 · Cited by 39 · see citing works

Banking for the future: an Australian experience in brain banking

Sarris, M., Garrick, T. M., Sheedy, D. L., & Harper, C. (2002) · Pathology · doi:10.1080/00313020220131260 · Cited by 34 · see citing works

Cortical parvalbumin interneurons and cognitive dysfunction in schizophrenia

Lewis, D. A., Curley, A. A., Glausier, J. R., & Volk, D. W. (2012) · Trends in Neurosciences · doi:10.1016/j.tins.2011.10.004 · Cited by 1,071 · see citing works

Antipsychotics: mechanisms underlying clinical response and side-effects and novel treatment approaches based on pathophysiology.

Kaar, S., Natesan, S., McCutcheon, R., & Howes, O. (2020) · Neuropharmacology · doi:10.1016/j.neuropharm.2019.107704 · Cited by 348 · see citing works

Expression of Interneuron Markers in the Dorsolateral Prefrontal Cortex of the Developing Human and in Schizophrenia

Fung, S. J., Webster, M. J., Sivagnanasundaram, S., Duncan, C., Elashoff, M., & Weickert, C. S. (2010) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2010.09060784 · Cited by 366 · see citing works

Executive Function, Neural Circuitry, and Genetic Mechanisms in Schizophrenia

Eisenberg, D., & Berman, K. (2009) · Neuropsychopharmacology · doi:10.1038/npp.2009.111 · Cited by 250 · see citing works

Mechanisms underlying dorsolateral prefrontal cortex contributions to cognitive dysfunction in schizophrenia

Smucny, J., Dienel, S. J., Lewis, D. A., & Carter, C. S. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-021-01089-0 · Cited by 231 · see citing works

Reduced Labeling of Parvalbumin Neurons and Perineuronal Nets in the Dorsolateral Prefrontal Cortex of Subjects with Schizophrenia

Enwright, J. F., Sanapala, S., Foglio, A., Berry, R., Fish, K. N., & Lewis, D. A. (2016) · Neuropsychopharmacology · doi:10.1038/npp.2016.24 · Cited by 223 · see citing works

Maternal immune activation leads to selective functional deficits in offspring parvalbumin interneurons

Canetta, S., Bolkan, S., Padilla-Coreano, N., Song, L. J., Sahn, R., Harrison, N. L., Gordon, J. A., Brown, A., & Kellendonk, C. (2016) · Molecular Psychiatry · doi:10.1038/mp.2015.222 · Cited by 201 · see citing works

Pre-frontal parvalbumin interneurons in schizophrenia: a meta-analysis of post-mortem studies

Kaar, S. J., Angelescu, I., Marques, T. R., & Howes, O. D. (2019) · Journal of Neural Transmission · doi:10.1007/s00702-019-02080-2 · Cited by 146 · see citing works

Altered Cortical Expression of GABA-Related Genes in Schizophrenia: Illness Progression vs Developmental Disturbance

Hoftman, G. D., Volk, D. W., Bazmi, H. H., Li, S., Sampson, A. R., & Lewis, D. A. (2013) · Schizophrenia Bulletin · doi:10.1093/schbul/sbt178 · Cited by 146 · see citing works

Bipolar disorder type 1 and schizophrenia are accompanied by decreased density of parvalbumin- and somatostatin-positive interneurons in the parahippocampal region

Wang, A. Y., Lohmann, K. M., Yang, C. K., Zimmerman, E. I., Pantazopoulos, H., Herring, N., Berretta, S., Heckers, S., & Konradi, C. (2011) · Acta Neuropathologica · doi:10.1007/s00401-011-0881-4 · Cited by 135 · see citing works

The neuropathology of schizophrenia: A selective review of past studies and emerging themes in brain structure and cytoarchitecture

Bakhshi, K., & Chance, S. A. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.06.028 · Cited by 128 · see citing works

Alterations of hippocampal and prefrontal GABAergic interneurons in an animal model of psychosis induced by NMDA receptor antagonism

Braun, I., Genius, J., Grunze, H., Bender, A., Möller, H., & Rujescu, D. (2007) · Schizophrenia Research · doi:10.1016/j.schres.2007.05.005 · Cited by 121 · see citing works

Changes in density of calcium‐binding‐protein‐immunoreactive GABAergic neurons in prefrontal cortex in schizophrenia and bipolar disorder

Sakai, T., Oshima, A., Nozaki, Y., Ida, I., Haga, C., Akiyama, H., Nakazato, Y., & Mikuni, M. (2008) · Neuropathology · doi:10.1111/j.1440-1789.2007.00867.x · Cited by 118 · see citing works

Myelination of parvalbumin interneurons: a parsimonious locus of pathophysiological convergence in schizophrenia

Stedehouder, J., & Kushner, S. A. (2016) · Molecular Psychiatry · doi:10.1038/mp.2016.147 · Cited by 113 · see citing works

Altered gene expression in the dorsolateral prefrontal cortex of individuals with schizophrenia

Guillozet-Bongaarts, A. L., Hyde, T. M., Dalley, R. A., Hawrylycz, M., Henry, A. M., Hof, P. R., Hohmann, J. G., Jones, A. R., Kuan, C. L., Royall, J. J., et al. (2013) · Molecular Psychiatry · doi:10.1038/mp.2013.30 · Cited by 114 · see citing works

Prenatal stress and inhibitory neuron systems: implications for neuropsychiatric disorders

Fine, R., Zhang, J., & Stevens, H. E. (2014) · Molecular Psychiatry · doi:10.1038/mp.2014.35 · Cited by 96 · see citing works

Differential protein expression in the prefrontal white matter of human alcoholics: a proteomics study

Alexander, K. L., James, G., Sheedy, D. L., Harper, C., & Matsumoto, I. (2005) · Molecular Psychiatry · doi:10.1038/sj.mp.4001741 · Cited by 93 · see citing works

Cognitive Dysfunction and Prefrontal Cortical Circuit Alterations in Schizophrenia: Developmental Trajectories

Dienel, S. J., Schoonover, K. E., & Lewis, D. A. (2022) · Biological Psychiatry · doi:10.1016/j.biopsych.2022.03.002 · Cited by 81 · see citing works

INVESTIGATING THE NEURODEVELOPMENTAL HYPOTHESIS OF SCHIZOPHRENIA

Rehn, A., & Rees, S. M. (2005) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/j.1440-1681.2005.04257.x · Cited by 76 · see citing works

The Nature of Prefrontal Cortical GABA Neuron Alterations in Schizophrenia: Markedly Lower Somatostatin and Parvalbumin Gene Expression Without Missing Neurons

Dienel, S. J., Fish, K. N., & Lewis, D. A. (2023) · American Journal of Psychiatry · doi:10.1176/appi.ajp.20220676 · Cited by 71 · see citing works

Altered Cortical GABA Neurotransmission in Schizophrenia: Insights into Novel Therapeutic Strategies

Stan, A. D., & Lewis, D. A. (2012) · Current Pharmaceutical Biotechnology · doi:10.2174/138920112800784925 · Cited by 62 · see citing works

Mapping pathologic circuitry in schizophrenia

Glausier, J. R., & Lewis, D. A. (2018) · Handbook of clinical neurology · doi:10.1016/b978-0-444-63639-3.00025-6 · Cited by 52 · see citing works

Impaired Interneuron Development in a Novel Model of Neonatal Brain Injury

Lacaille, H., Vacher, C., Bakalar, D., O’Reilly, J. J., Salzbank, J., & Penn, A. A. (2019) · eNeuro · doi:10.1523/eneuro.0300-18.2019 · Cited by 53 · see citing works

Changes in Calcium-Binding Protein Expression in Human Cortical Contusion Tissue

Buriticá, E., Villamil, L., Guzmán, F., Escobar, M. I., Garcia‐Cairasco, N., & Pimienta, H. J. (2009) · Journal of Neurotrauma · doi:10.1089/neu.2009.0894 · Cited by 50 · see citing works

A “double hit” murine model for schizophrenia shows alterations in the structure and neurochemistry of the medial prefrontal cortex and the hippocampus

Gilabert‐Juan, J., Bellés, M., Sáez-Ibáñez, A. R., Carceller, H., Zamarbide-Forés, S., Moltó, M. D., & Nácher, J. (2013) · Neurobiology of Disease · doi:10.1016/j.nbd.2013.07.008 · Cited by 53 · see citing works

Prefrontal cortical alterations of glutamate and GABA neurotransmission in schizophrenia: Insights for rational biomarker development

Schoonover, K. E., Dienel, S. J., & Lewis, D. A. (2020) · Biomarkers in Neuropsychiatry · doi:10.1016/j.bionps.2020.100015 · Cited by 44 · see citing works

Fine structure analysis of perineuronal nets in the ketamine model of schizophrenia

Kaushik, R., Lipachev, N., Matuszko, G., Kochneva, A., Dvoeglazova, A., Becker, A., Николаевич, П. М., & Dityatev, A. E. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14853 · Cited by 41 · see citing works

Antipsychotics affect multiple calcium calmodulin dependent proteins

Rushlow, W. J., Seah, C. W. T., Sutton, L. P., Bjelica, A., & Rajakumar, N. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.03.011 · Cited by 40 · see citing works

The Importance of Brain Banks for Molecular Neuropathological Research: The New South Wales Tissue Resource Centre Experience

Dedova, I. V., Harding, A. J., Sheedy, D. L., Garrick, T. M., Sundqvist, N., Hunt, C. E., Gillies, J., & Harper, C. G. (2009) · International Journal of Molecular Sciences · doi:10.3390/ijms10010366 · Cited by 38 · see citing works

The cerebral cortex is a substrate of multiple interactions between GABAergic interneurons and oligodendrocyte lineage cells

Benamer, N., Vidal, M., & Angulo, M. C. (2019) · Neuroscience Letters · doi:10.1016/j.neulet.2019.134615 · Cited by 30 · see citing works

Increased white matter neuron density in a rat model of maternal immune activation — Implications for schizophrenia

Duchatel, R. J., Jobling, P., Graham, B. A., Harms, L. R., Michie, P. T., Hodgson, D. M., & Tooney, P. A. (2015) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2015.09.006 · Cited by 29 · see citing works

Altered volume and hemispheric asymmetry of the superficial cortical layers in the schizophrenia planum temporale

Smiley, J. F., Rosoklija, G. B., Mancevski, B., Mann, J. J., Dwork, A. J., & Javitt, D. C. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06838.x · Cited by 28 · see citing works

Exploring causal mechanisms of psychosis risk

Oliver, D., Chesney, E., Cullen, A. E., Davies, C., Englund, A., Gifford, G., Kerins, S., Lalousis, P. A., Logeswaran, Y., Merritt, K., et al. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105699 · Cited by 28 · see citing works

Short-Term Exposure to Enriched Environment in Adult Rats Restores MK-801-Induced Cognitive Deficits and GABAergic Interneuron Immunoreactivity Loss

Murueta‐Goyena, A., Ortuzar, N., Gargiulo, P. Á., Lafuente, J. V., & Bengoetxea, H. (2017) · Molecular Neurobiology · doi:10.1007/s12035-017-0715-z · Cited by 28 · see citing works

Different pattern of changes in calcium binding proteins immunoreactivity in the medial prefrontal cortex of rats exposed to stress models of depression

Zadrożna, M., Nowak, B., Łasoń, M., Wolak, M., Sowa-Kućma, M., Papp, M., Ossowska, G., Pilc, A., & Nowak, G. (2011) · Pharmacological Reports · doi:10.1016/s1734-1140(11)70718-6 · Cited by 27 · see citing works

Pharmacogenetic activation of parvalbumin interneurons in the prefrontal cortex rescues cognitive deficits induced by adolescent MK801 administration

Chamberlin, L. A., Yang, S.-S., McEachern, E., Lucas, J. T. M., McLeod, O. W., Rolland, C. A., Mack, N. R., Ferguson, B. R., & Gao, W. (2023) · Neuropsychopharmacology · doi:10.1038/s41386-023-01576-6 · Cited by 25 · see citing works

Evidence for Decreased Density of Calretinin-Immunopositive Neurons in the Caudate Nucleus in Patients With Schizophrenia

Adorján, I., Sun, B., Feher, V., Tyler, T., Veres, D. S., Chance, S. A., & Szele, F. G. (2020) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2020.581685 · Cited by 24 · see citing works

Adolescent social isolation affects parvalbumin expression in the medial prefrontal cortex in the MAM-E17 model of schizophrenia

Maćkowiak, M., Latusz, J., Głowacka, U., Bator, E., & Bilecki, W. (2018) · Metabolic Brain Disease · doi:10.1007/s11011-018-0359-3 · Cited by 23 · see citing works

Hemispheric comparisons of neuron density in the planum temporale of schizophrenia and nonpsychiatric brains

Smiley, J. F., Rosoklija, G. B., Mancevski, B., Pergolizzi, D., Figarsky, K., Bleiwas, C., Duma, A., Mann, J. J., Javitt, D. C., & Dwork, A. J. (2011) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2010.11.007 · Cited by 22 · see citing works

GABAergic dysfunction in postmortem dorsolateral prefrontal cortex: implications for cognitive deficits in schizophrenia and affective disorders

Hughes, H., Brady, L. J., & Schoonover, K. E. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1440834 · Cited by 20 · see citing works

A Role for the Transcription Factor Nk2 Homeobox 1 in Schizophrenia: Convergent Evidence from Animal and Human Studies

Malt, E. A., Juhasz, K., Malt, U. F., & Naumann, T. (2016) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2016.00059 · Cited by 19 · see citing works

Normative modelling of molecular-based functional circuits captures clinical heterogeneity transdiagnostically in psychiatric patients

Lawn, T., Giacomel, A., Martins, D., Veronese, M., Howard, M. A., Turkheimer, F., & Dipasquale, O. (2024) · Communications Biology · doi:10.1038/s42003-024-06391-3 · Cited by 17 · see citing works

Calretinin and parvalbumin in schizophrenia and affective disorders: a mini-review, a perspective on the evolutionary role of calretinin in schizophrenia, and a preliminary post-mortem study of calretinin in the septal nuclei

Brisch, R., Bielau, H., Saniotis, A., Wolf, R. J., Bogerts, B., Krell, D., Steiner, J. H., Braun, K., Krzyżanowska, M., Krzyżanowski, M., et al. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00393 · Cited by 17 · see citing works

Contributions of Glutamate and GABA Systems to the Neurobiology and Treatment of Schizophrenia

Krystal, J. H., & Moghaddam, B. (2010) · doi:10.1002/9781444327298.ch21 · Cited by 17 · see citing works

Alterations in Prefrontal Cortical Circuitry and Cognitive Dysfunction in Schizophrenia

Lewis, D. A., & Glausier, J. R. (2016) · Nebraska Symposium on Motivation/The Nebraska symposium on motivation · doi:10.1007/978-3-319-30596-7_3 · Cited by 15 · see citing works

Connecting Neurobiological Features with Interregional Dysconnectivity in Social-Cognitive Impairments of Schizophrenia

Adraoui, F. W., Douw, L., Martens, G. J. M., & Maas, D. A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24097680 · Cited by 14 · see citing works

Parvalbumin-containing GABA cells and schizophrenia: experimental model based on targeted gene delivery through adeno-associated viruses

Wołoszynowska-Fraser, M. U., Wulff, P., & Riedel, G. (2017) · Behavioural Pharmacology · doi:10.1097/fbp.0000000000000360 · Cited by 12 · see citing works

No differences in calcium-binding protein immunoreactivity in the posterior cingulate and visual cortex: Schizophrenia and controls

Wheeler, D. G., Dixon, G., & Harper, C. G. (2006) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2005.11.041 · Cited by 12 · see citing works

Cortical interneurons in schizophrenia – cause or effect?

Prkačin, M. V., Banovac, I., Petanjek, Z., & Hladnik, A. (2023) · Croatian Medical Journal · doi:10.3325/cmj.2023.64.110 · Cited by 10 · see citing works

GABAergic and inflammatory changes in the frontal cortex following neonatal PCP plus isolation rearing, as a dual-hit neurodevelopmental model for schizophrenia

Cale, J. A., Chauhan, E. J., Cleaver, J. J., Fusciardi, A. R., McCann, S., Waters, H. C., Žavbi, J., & King, M. V. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-03987-y · Cited by 9 · see citing works

Potential application as screening and drug designing tools of cytoarchitectural deficiencies present in three animal models of schizophrenia

Bellon, A., Pen, G. L., Matricon, J., Jay, T. M., & Krebs, M. (2009) · Expert Opinion on Drug Discovery · doi:10.1517/17460440902762794 · Cited by 7 · see citing works

The effect of deficient muscarinic signaling on commonly reported biochemical effects in schizophrenia and convergence with genetic susceptibility loci in explaining symptom dimensions of psychosis

Vakalopoulos, C. (2014) · Frontiers in Pharmacology · doi:10.3389/fphar.2014.00277 · Cited by 7 · see citing works

Neuroscience Institute of Schizophrenia and Allied Disorders (NISAD): 10 Years of Australia's First Virtual Research Institute

Draganic, D. M., Catts, S. V., & Carr, V. J. (2007) · Australian & New Zealand Journal of Psychiatry · doi:10.1080/00048670601057783 · Cited by 5 · see citing works

Brain abnormalities in schizophrenia

Bogerts, B., Steiner, J. H., & Bernstein, H. (2009) · CRC Press eBooks · doi:10.3109/9781420080063-11 · Cited by 4 · see citing works

Delineating mechanisms underlying parvalbumin neuron impairment in different neurological and neurodegenerative disorders: the emerging role of mitochondrial dysfunction

Olkhova, E. A., Smith, L. A., Dennis, B. H., Ng, Y. S., LeBeau, F. E. N., & Gorman, G. S. (2024) · Biochemical Society Transactions · doi:10.1042/bst20230191 · Cited by 3 · see citing works

Post-traumatic epilepsy: Insights from human cortical contused tissue

Becerra-Hernández, L. V., González-Acosta, C. A., & Buriticá, E. (2025) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2024.110252 · Cited by 3 · see citing works

Gestational MAM (Methylazoxymethanol) Administration: A Promising Animal Model for Psychosis Onset

Pen, G. L., Bellon, A., Krebs, M., & Jay, T. M. (2011) · Neuromethods · doi:10.1007/978-1-61779-157-4_2 · Cited by 3 · see citing works

Normative Modelling of Molecular-based Functional Neurocircuits Captures Clinical Heterogeneity Transdiagnostically in Neuropsychiatric PatientsPreprint

Lawn, T., Giacomel, A., Martins, D., Veronese, M., Howard, M. A., Turkheimer, F., & Dipasquale, O. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.10.21.563428 · Cited by 2 · see citing works

Brain abnormalities in schizophrenia

Bogerts, B., Steiner, J. H., & Bernstein, H. (2009) · Medical psychiatry · doi:10.3109/9781420080063.009 · Cited by 1 · see citing works

Dissecting the cellular mechanisms of NMDA receptor antagonist-induced disruptions to working memory and gamma oscillations

Sokolenko, E. (2019) · Minerva Access (University of Melbourne)

Frontal Cortex

Williams, M. R. (2021) · Springer eBooks · doi:10.1007/978-3-030-68308-5_4

Myelin Matters in Schizophrenia : Neurobiological Insights from Rat Model and Human Studies

Maas, D. A. (2019) · theses.fr (ABES) · doi:10.70675/4ea9aa0azc70cz4bb4zada7z4f82cac02e1c

Impact of PV interneuron - OPC synapse disruption on cognitive functioning

Vidal, M. (2021) · theses.fr (ABES) · doi:10.70675/66c1e527zbd3ez49f6z8736ze9817c27856d

Selective deficits in prefrontal cortical GABAergic neurons in schizophrenia defined by the presence of calcium-binding proteins

Beasley, C. L., Zhang, Z. J., Patten, I., & Reynolds, G. P. (2002) · Biological Psychiatry · doi:10.1016/s0006-3223(02)01360-4 · Cited by 374 · see citing works

Local circuit neurons of the prefrontal cortex in schizophrenia: selective increase in the density of calbindin-immunoreactive neurons

DAVISS, S. R., & Lewis, D. A. (1995) · Psychiatry Research · doi:10.1016/0165-1781(95)02720-3 · Cited by 187 · see citing works

Changes in density of calcium‐binding‐protein‐immunoreactive GABAergic neurons in prefrontal cortex in schizophrenia and bipolar disorder

Sakai, T., Oshima, A., Nozaki, Y., Ida, I., Haga, C., Akiyama, H., Nakazato, Y., & Mikuni, M. (2008) · Neuropathology · doi:10.1111/j.1440-1789.2007.00867.x · Cited by 118 · see citing works

No differences in calcium-binding protein immunoreactivity in the posterior cingulate and visual cortex: Schizophrenia and controls

Wheeler, D. G., Dixon, G., & Harper, C. G. (2006) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2005.11.041 · Cited by 12 · see citing works

Reduced density of calbindin-immunoreactive interneurons in the planum temporale in schizophrenia

Chance, S. A., Walker, M. A., & Crow, T. J. (2005) · Brain Research · doi:10.1016/j.brainres.2005.03.045 · Cited by 58 · see citing works