The role of prefrontal-hippocampal functional connectivity in schizophrenia-related cognitive dysfunction and the thalamic ventral midline involvement: in vivo and silico evidence
Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic-ecollection
Typ dokumentu časopisecké články, přehledy
PubMed
41293117
PubMed Central
PMC12641012
DOI
10.3389/fnins.2025.1653828
Knihovny.cz E-zdroje
- Klíčová slova
- functional connectivity, hippocampus, in vivo/in silico models, interaction, prefrontal cortex, schizophrenia, thalamus,
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
Schizophrenia (SCZ) is a multiform psychiatric disorder in which impairments of high-order cognitive abilities, such as flexibility, working memory, and decision-making, are considered onset markers. These deficits are associated with dysfunctions in the prefrontal cortex (PFC) and hippocampus (HPC), two brain regions that play crucial roles in higher-order cognitive processes. While the roles of the PFC and HPC in SCZ have been widely studied, the interaction between these regions and their contributions to the observed cognitive deficits, in conjunction with other intermediate structures, refMRI connectivity as a biomarker main poorly understood. This paper primarily aims to create a hypothesis-generating framework in the context of PFC-HPC altered communication and intermediate structures that may contribute to cognitive impairments in psychosis-related conditions. Here, we present several testable hypotheses concerning the role of specific actors (e.g., GABAergic Parvalbumin-positive interneurons, thalamic calcium signaling channels) in the PFC-HPC connectivity. By presenting evidence from in vivo (animal models and human studies) and in silico studies (examining functional connectivity), we desire to reach computational and translational researchers, with the aim of stimulating further planning for new experimental methodologies, both computational and translational, that can provide a broad framework for a more nuanced understanding of maladaptive brain communication in psychosis.
Zobrazit více v PubMed
Abo-Zahhad M., Ahmed S. M., Abbas S. N. (2015). A new EEG acquisition protocol for biometric identification using eye blinking signals. Int. J. Intell. Syst. Appl. 7, 48–54. doi: 10.5815/ijisa.2015.06.05 DOI
Adams R. A., Napier G., Roiser J. P., Mathys C., Gilleen J. (2018). Attractor-like dynamics in belief updating in schizophrenia. J. Neurosci. 38, 9471–9485. doi: 10.1523/JNEUROSCI.3163-17.2018, PMID: PubMed DOI PMC
Aleman A. (2014). Neurocognitive basis of schizophrenia: information processing abnormalities and clues for treatment. Adv. Neurosci. 2014, 1–15. doi: 10.1155/2014/104920 DOI
Alho J., Lahnakoski J. M., Panula J. M., Rikandi E., Mäntylä T., Lindgren M., et al. (2023). Hippocampus-centered network is associated with positive symptom alleviation in patients with first-episode psychosis. Biol. Psychiatry Cognit. Neurosci. Neuroimaging 8, 1197–1206. doi: 10.1016/j.bpsc.2023.06.002, PMID: PubMed DOI
American Psychiatric Association, DSM-5 Task Force (2013). Diagnostic and statistical manual of mental disorders. 5th Edn. New York, NY: American Psychiatric Association. doi: 10.1176/appi.books.9780890425596 DOI
Andrianova L., Banks P. J., Booth C. A., Brady E. S., Margetts-Smith G., Kohli S., et al. (2025). Thalamic nucleus reuniens preferentially targets inhibitory interneurons over pyramidal cells in hippocampal CA1 region. bioRxiv 2:462517. doi: 10.1101/2021.09.30.462517 PubMed DOI PMC
Arguello P. A., Markx S., Gogos J. A., Karayiorgou M. (2010). Development of animal models for schizophrenia. Dis. Model. Mech. 3, 22–26. doi: 10.1242/dmm.003996, PMID: PubMed DOI PMC
Badre D., Wagner A. D. (2004). Selection, integration, and conflict monitoring. Neuron 41, 473–487. doi: 10.1016/s0896-6273(03)00851-1, PMID: PubMed DOI
Asenjo Lobos C., Komossa K., F R.-K. C. H. H. S., Schwarz S., Leucht S. (2010). Clozapine versus other atypical antipsychotics for schizophrenia. Cochrane Database Syst. Rev. 2010:CD006633. doi: 10.1002/14651858.CD006633.pub2, PMID: PubMed DOI PMC
Bai W., Liu Y., Liu A., Xu X., Zheng X., Tian X., et al. (2024). Hippocampal-prefrontal high-gamma flow during performance of a spatial working memory. Brain Res. Bull. 207:110887. doi: 10.1016/j.brainresbull.2024.110887, PMID: PubMed DOI
Bannerman D. M., Rawlins J. N. P., McHugh S. B., Deacon R. M. J., Yee B. K., Bast T., et al. (2004). Regional dissociations within the hippocampus—memory and anxiety. Neurosci. Biobehav. Rev. 28, 273–283. doi: 10.1016/j.neubiorev.2004.03.004, PMID: PubMed DOI
Bar K.-J., Ebert A. (2010). Emil Kraepelin: a pioneer of scientific understanding of psychiatry and psychopharmacology. Indian J. Psychiatry 52:191. doi: 10.4103/0019-5545.64591, PMID: PubMed DOI PMC
Barone J., Rossiter H. E. (2021). Understanding the role of sensorimotor Beta oscillations. Front. Syst. Neurosci. 15:655886. doi: 10.3389/fnsys.2021.655886, PMID: PubMed DOI PMC
Basha D., Azarmehri A., Proulx E., Chauvette S., Ghorbani M., Timofeev I. (2025). The reuniens nucleus of the thalamus facilitates hippocampo-cortical dialogue during sleep. eLife 12:RP90826. doi: 10.7554/eLife.90826, PMID: PubMed DOI PMC
Battaglia D., Brovelli A. (2020). Functional Connectivity and Neuronal Dynamics: Insights from Computational Methods”, The Cognitive Neurosciences, David Poeppel, George R. Mangun, Michael S. Gazzaniga, The MIT Press. doi: 10.7551/mitpress/11442.001.0001 DOI
Bitzenhofer S. H., Pöpplau J. A., Chini M., Marquardt A., Hanganu-Opatz I. L. (2021). A transient developmental increase in prefrontal activity alters network maturation and causes cognitive dysfunction in adult mice. Neuron 109, 1350–1364.e6. doi: 10.1016/j.neuron.2021.02.011, PMID: PubMed DOI PMC
Bolton T. A. W., Van De Ville D., Amico E., Preti M. G., Liégeois R. (2023). The arrow-of-time in neuroimaging time series identifies causal triggers of brain function. Hum. Brain Mapp. 44, 4077–4087. doi: 10.1002/hbm.26331, PMID: PubMed DOI PMC
Braff D. L., Light G. A. (2005). The use of neurophysiological endophenotypes to understand the genetic basis of schizophrenia. Dialogues Clin. Neurosci. 7, 125–135. doi: 10.31887/DCNS.2005.7.2/dlbraff, PMID: PubMed DOI PMC
Brennan C., Proekt A. (2023). Attractor dynamics with activity-dependent plasticity capture human working memory across time scales. Commun. Psychol. 1:28. doi: 10.1038/s44271-023-00027-8, PMID: PubMed DOI PMC
Broeders T. A. A., Linsen F., Louter T. S., Nawijn L., Penninx B. W. J. H., van Tol M. J., et al. (2024). Dynamic reconfigurations of brain networks in depressive and anxiety disorders: the influence of antidepressants. Psychiatry Res. 334:115774. doi: 10.1016/j.psychres.2024.115774, PMID: PubMed DOI
Brunoni A. R., Vanderhasselt M.-A. (2014). Working memory improvement with non-invasive brain stimulation of the dorsolateral prefrontal cortex: A systematic review and meta-analysis. Brain Cogn. 86, 1–9. doi: 10.1016/j.bandc.2014.01.008, PMID: PubMed DOI
Buck S. A., Quincy Erickson-Oberg M., Logan R. W., Freyberg Z. (2022). Relevance of interactions between dopamine and glutamate neurotransmission in schizophrenia. Mol. Psychiatry 27, 3583–3591. doi: 10.1038/s41380-022-01649-w, PMID: PubMed DOI PMC
Bulut T. (2023). Domain-general and domain-specific functional networks of Broca's area underlying language processing. Brain Behav. 13:e3046. doi: 10.1002/brb3.3046, PMID: PubMed DOI PMC
Burgess N., Maguire E. A., O'Keefe J. (2002). The human hippocampus and spatial and episodic memory. Neuron 35, 625–641. doi: 10.1016/s0896-6273(02)00830-9, PMID: PubMed DOI
Cassel J. C., Ferraris M., Quilichini P., Cholvin T., Boch L., Stephan A., et al. (2021). The reuniens and rhomboid nuclei of the thalamus: A crossroads for cognition-relevant information processing? Neurosci. Biobehav. Rev. 126, 338–360. doi: 10.1016/j.neubiorev.2021.03.023, PMID: PubMed DOI
Cassel J. C., Pereira de Vasconcelos A., Loureiro M., Cholvin T., Dalrymple-Alford J. C., Vertes R. P. (2013). The reuniens and rhomboid nuclei: neuroanatomy, electrophysiological characteristics and behavioral implications. Prog. Neurobiol. 111, 34–52. doi: 10.1016/j.pneurobio.2013.08.006, PMID: PubMed DOI PMC
Chari S., Minzenberg M. J., Solomon M., Ragland J. D., Nguyen Q., Carter C. S., et al. (2019). Impaired prefrontal functional connectivity associated with working memory task performance and disorganization despite intact activations in schizophrenia. Psychiatry Res. Neuroimaging 287, 10–18. doi: 10.1016/j.pscychresns.2019.01.013, PMID: PubMed DOI PMC
Choi K.-M., Kim J.-Y., Kim Y.-W., Han J.-W., Im C.-H., Lee S.-H. (2021). Comparative analysis of default mode networks in major psychiatric disorders using resting-state EEG. Sci. Rep. 11:22007. doi: 10.1038/s41598-021-00975-3, PMID: PubMed DOI PMC
Colgin L. L. (2011). Oscillations and hippocampal–prefrontal synchrony. Curr. Opin. Neurobiol. 21, 467–474. doi: 10.1016/j.conb.2011.04.006, PMID: PubMed DOI PMC
Condon E. (2024). Investigating brain network deficits in a rodent schizophrenia model. University of Leicester. Thesis. doi: 10.25392/leicester.data.25650519.v1 DOI
de Bartolomeis A., Barone A., Vellucci L., Mazza B., Austin M. C., Iasevoli F., et al. (2022). Linking inflammation, aberrant glutamate-dopamine interaction, and post-synaptic changes: translational relevance for schizophrenia and antipsychotic treatment: a systematic review. Mol. Neurobiol. 59, 6460–6501. doi: 10.1007/s12035-022-02976-3, PMID: PubMed DOI PMC
de Mooij-van Malsen J. G., Röhrdanz N., Buschhoff A.-S., Schiffelholz T., Sigurdsson T., Wulff P. (2023). Task-specific oscillatory synchronization of prefrontal cortex, nucleus reuniens, and hippocampus during working memory. IScience 26:107532. doi: 10.1016/j.isci.2023.107532, PMID: PubMed DOI PMC
Eichert N., Robinson E. C., Bryant K. L., Jbabdi S., Jenkinson M., Li L., et al. (2020). Cross-species cortical alignment identifies different types of anatomical reorganization in the primate temporal lobe. eLife 9:e53232. doi: 10.7554/eLife.53232, PMID: PubMed DOI PMC
Del Fabro L., Schmidt A., Fortea L., Delvecchio G., D’Agostino A., Radua J., et al. (2021). Functional brain network dysfunctions in subjects at high-risk for psychosis: A meta-analysis of resting-state functional connectivity. Neurosci. Biobehav. Rev. 128, 90–101. doi: 10.1016/j.neubiorev.2021.06.020, PMID: PubMed DOI
Dienel S. J., Fish K. N., Lewis D. A. (2023). The nature of prefrontal cortical GABA neuron alterations in schizophrenia: markedly lower somatostatin and Parvalbumin gene expression without missing neurons. Am. J. Psychiatry 180, 495–507. doi: 10.1176/appi.ajp.20220676, PMID: PubMed DOI PMC
Dolleman-van der Weel M. J., Griffin A. L., Ito H. T., Shapiro M. L., Witter M. P., Vertes R. P., et al. (2019). The nucleus reuniens of the thalamus sits at the nexus of a hippocampus and medial prefrontal cortex circuit enabling memory and behavior. Learning Memory 26, 191–205. doi: 10.1101/lm.048389.118, PMID: PubMed DOI PMC
Dolleman-van der Weel M. J., Witter M. P. (2020). The thalamic midline nucleus reuniens: potential relevance for schizophrenia and epilepsy. Neurosci. Biobehav. Rev. 119, 422–439. doi: 10.1016/j.neubiorev.2020.09.033, PMID: PubMed DOI
Dominicus L. S., Rijn L., Spek R., Podzimek D., Begemann M., de Haan L., et al. (2023). fMRI connectivity as a biomarker of antipsychotic treatment response: a systematic review. Neuroimage Clin. 40:103515. doi: 10.1016/j.nicl.2023.103515, PMID: PubMed DOI PMC
Donati F. L., Mayeli A., Andry B., Sharma K., Janssen S., Krafty R. J., et al. (2024). Prefrontal oscillatory slowing in early-course schizophrenia is associated with worse cognitive performance and negative symptoms: a TMS-EEG study. Biol. Psychiatry Cogn. Neurosci. Neuroimaging 10:13. doi: 10.1016/j.bpsc.2024.07.013 PubMed DOI PMC
Doubovikov E. D., Aksenov D. P. (2025). The diagnostic potential of resting state functional MRI: statistical concerns. NeuroImage 317:121334. doi: 10.1016/j.neuroimage.2025.121334, PMID: PubMed DOI PMC
Druart M., Nosten-Bertrand M., Poll S., Crux S., Nebeling F., Delhaye C., et al. (2021). Elevated expression of complement C4 in the mouse prefrontal cortex causes schizophrenia-associated phenotypes. Mol. Psychiatry 26, 3489–3501. doi: 10.1038/s41380-021-01081-6, PMID: PubMed DOI
Dugré J. R., Dumais A., Tikasz A., Mendrek A., Potvin S. (2021). Functional connectivity abnormalities of the long-axis hippocampal subregions in schizophrenia during episodic memory. NPJ Schizophr. 7:19. doi: 10.1038/s41537-021-00147-2, PMID: PubMed DOI PMC
Fang Z., Dang Y., Ping A., Wang C., Zhao Q., Zhao H., et al. (2025). Human high-order thalamic nuclei gate conscious perception through the thalamofrontal loop. Science 388. doi: 10.1126/science.adr3675, PMID: PubMed DOI
Fanselow M. S., Dong H.-W. (2010). Are the dorsal and ventral Hippocampus functionally distinct structures? Neuron 65, 7–19. doi: 10.1016/j.neuron.2009.11.031, PMID: PubMed DOI PMC
Featherstone R. E., Shimada T., Crown L. M., Melnychenko O., Yi J., Matsumoto M., et al. (2022). Calcium/calmodulin-dependent protein kinase IIα heterozygous knockout mice show electroencephalogram and behavioral changes characteristic of a subpopulation of schizophrenia and intellectual impairment. Neuroscience 499, 104–117. doi: 10.1016/j.neuroscience.2022.07.023, PMID: PubMed DOI
Ferguson B. R., Gao W. J. (2018). PV interneurons: critical regulators of E/I balance for prefrontal cortex-dependent behavior and psychiatric disorders. Front. Neural Circuits 12:37. doi: 10.3389/fncir.2018.00037, PMID: PubMed DOI PMC
Ferraris M., Cassel J. C., Pereira A., Stephan A., Quilichini P. P. (2021). The nucleus reuniens, a thalamic relay for cortico-hippocampal interaction in recent and remote memory consolidation. Neurosci. Biobehav. Rev. 125, 339–354. doi: 10.1016/j.neubiorev.2021.02.025 PubMed DOI
Fitzpatrick R., Stefan M. I. (2022). Validation through collaboration: encouraging team efforts to ensure internal and external validity of computational models of biochemical pathways. Neuroinformatics 20, 277–284. doi: 10.1007/s12021-022-09584-5, PMID: PubMed DOI PMC
Forsingdal A., Jørgensen T. N., Olsen L., Werge T., Didriksen M., Nielsen J. (2019). Can animal models of copy number variants that predispose to schizophrenia elucidate underlying biology? Biol. Psychiatry 85, 13–24. doi: 10.1016/j.biopsych.2018.07.004, PMID: PubMed DOI
Friedman N. P., Robbins T. W. (2021). The role of prefrontal cortex in cognitive control and executive function. Neuropsychopharmacology 47, 72–89. doi: 10.1038/s41386-021-01132-0, PMID: PubMed DOI PMC
Fröhlich E., Salar-Behzadi S. (2014). Toxicological assessment of inhaled nanoparticles: role of in vivo, ex vivo, in vitro, and PubMed DOI PMC
Fu Z., Iraji A., Sui J., Calhoun V. D. (2021). Whole-brain functional network connectivity abnormalities in affective and non-affective early phase psychosis. Front. Neurosci. 15:682110. doi: 10.3389/fnins.2021.682110, PMID: PubMed DOI PMC
Fu Z., Sui J., Turner J. A., Du Y., Assaf M., Pearlson G. D., et al. (2020). Dynamic functional network reconfiguration underlying the pathophysiology of schizophrenia and autism spectrum disorder. Hum. Brain Mapp. 42, 80–94. doi: 10.1002/hbm.25205, PMID: PubMed DOI PMC
Gaebler A. J., Fakour N., Stöhr F., Zweerings J., Taebi A., Suslova M., et al. (2023). Functional connectivity signatures of NMDAR dysfunction in schizophrenia—integrating findings from imaging genetics and pharmaco-fMRI. Transl. Psychiatry 13, 1–12. doi: 10.1038/s41398-023-02344-2 PubMed DOI PMC
Gao W.-J., Yang S.-S., Mack N. R., Chamberlin L. A. (2021). Aberrant maturation and connectivity of prefrontal cortex in schizophrenia—contribution of NMDA receptor development and hypofunction. Mol. Psychiatry 27, 731–743. doi: 10.1038/s41380-021-01196-w, PMID: PubMed DOI PMC
Giraldo-Chica M., Rogers B. P., Damon S. M., Landman B. A., Woodward N. D. (2018). Prefrontal-thalamic anatomical connectivity and executive cognitive function in schizophrenia. Biol. Psychiatry 83, 509–517. doi: 10.1016/j.biopsych.2017.09.022, PMID: PubMed DOI PMC
Godoy L. D., Prizon T., Rossignoli M. T., Leite J. P., Liberato J. L. (2022). Parvalbumin role in epilepsy and psychiatric comorbidities: from mechanism to intervention. Front. Integr. Neurosci. 16:765324. doi: 10.3389/fnint.2022.765324, PMID: PubMed DOI PMC
Goodman J., Packard M. G. (2018). The role of the dorsal striatum in extinction: A memory systems perspective. Neurobiol. Learn. Mem. 150, 48–55. doi: 10.1016/j.nlm.2018.02.028, PMID: PubMed DOI
Grace A. A. (2012). Dopamine system dysregulation by the hippocampus: implications for the pathophysiology and treatment of schizophrenia. Neuropharmacology 62, 1342–1348. doi: 10.1016/j.neuropharm.2011.05.011, PMID: PubMed DOI PMC
Graham K., Spruston N., Bloss E. B. (2021). Hippocampal and thalamic afferents form distinct synaptic microcircuits in the mouse infralimbic frontal cortex. Cell Rep. 37:109837. doi: 10.1016/j.celrep.2021.109837, PMID: PubMed DOI
Greenwood T. A., Shutes-David A., Tsuang D. W. (2019). Endophenotypes in schizophrenia: digging deeper to identify genetic mechanisms. J. Psychiatry Brain Sci. 4:e190005. doi: 10.20900/jpbs.20190005, PMID: PubMed DOI PMC
Haber S. N., Liu H., Seidlitz J., Bullmore E. (2021). Prefrontal connectomics: from anatomy to human imaging. Neuropsychopharmacology 47, 20–40. doi: 10.1038/s41386-021-01156-6, PMID: PubMed DOI PMC
Hallock H. L., Wang A., Griffin A. L. (2016). Ventral midline thalamus is critical for hippocampal-prefrontal synchrony and spatial working memory. J. Neurosci. 36, 8372–8389. doi: 10.1523/JNEUROSCI.0991-16.2016, PMID: PubMed DOI PMC
Hart H., Radua J., Nakao T., Mataix-Cols D., Rubia K. (2013). Meta-analysis of functional magnetic resonance imaging studies of inhibition and attention in attention-deficit/hyperactivity disorder. JAMA Psychiatry 70, 185–198. doi: 10.1001/jamapsychiatry.2013.277, PMID: PubMed DOI
Hollis C., Rapoport J. (2008). “Child and adolescent schizophrenia” in Schizophrenia. eds. Weinberger D., Harrison P.. 3rd ed (London: Blackwell; ), 24–46.
Homayoun H., Moghaddam B. (2007). NMDA receptor hypofunction produces opposite effects on prefrontal cortex interneurons and pyramidal neurons. J. Neurosci. 27, 11496–11500. doi: 10.1523/JNEUROSCI.2213-07.2007, PMID: PubMed DOI PMC
Howes O. D., Shatalina E. (2022). Integrating the neurodevelopmental and dopamine hypotheses of schizophrenia and the role of cortical excitation-inhibition balance. Biol. Psychiatry 92, 501–513. doi: 10.1016/j.biopsych.2022.06.017, PMID: PubMed DOI
Hwang H. C., Kim S. M., Han D. H. (2021). Different facial recognition patterns in schizophrenia and bipolar disorder assessed using a computerized emotional perception test and fMRI. J. Affect. Disord. 279, 83–88. doi: 10.1016/j.jad.2020.09.125 PubMed DOI
Jalilianhasanpour R., Ryan D., Agarwal S., Beheshtian E., Gujar S. K., Pillai J. J., et al. (2021). Dynamic brain connectivity in resting state functional MR imaging. Neuroimaging Clin. N. Am. 31, 81–92. doi: 10.1016/j.nic.2020.09.004, PMID: PubMed DOI
Jayachandran M., Viena T. D., Garcia A., Veliz A. V., Leyva S., Roldan V., et al. (2023). Nucleus reuniens transiently synchronizes memory networks at beta frequencies. Nat. Commun. 14:4326. doi: 10.1038/s41467-023-40044-z, PMID: PubMed DOI PMC
Jia W., Zhu H., Ni Y., Su J., Xu R., Jia H., et al. (2020). Disruptions of frontoparietal control network and default mode network linking the metacognitive deficits with clinical symptoms in schizophrenia. Hum. Brain Mapp. 41, 1445–1458. doi: 10.1002/hbm.24887, PMID: PubMed DOI PMC
Jimenez A. M., Riedel P., Lee J., Reavis E. A., Green M. F. (2019). Linking resting-state networks and social cognition in schizophrenia and bipolar disorder. Hum. Brain Mapp. 40, 4703–4715. doi: 10.1002/hbm.24731, PMID: PubMed DOI PMC
Joyce M. K. P., Marshall L. G., Banik S. L., Wang J., Xiao D., Bunce J. G., et al. (2022). Pathways for memory, cognition and emotional context: hippocampal, Subgenual area 25, and Amygdalar axons show unique interactions in the primate thalamic Reuniens nucleus. J. Neurosci. 42, 1068–1089. doi: 10.1523/JNEUROSCI.1724-21.2021, PMID: PubMed DOI PMC
Kamps F. S., Hendrix C. L., Brennan P. A., Dilks D. D. (2020). Connectivity at the origins of domain specificity in the cortical face and place networks. Proc. Natl. Acad. Sci. USA 117, 6163–6169. doi: 10.1073/pnas.1911359117, PMID: PubMed DOI PMC
Kato S., Bagarinao E., Isoda H., Koyama S., Watanabe H., Maesawa S., et al. (2021). Effects of head motion on the evaluation of age-related brain network changes using resting state functional MRI. MRMS 20, 338–346. doi: 10.2463/mrms.mp.2020-0081, PMID: PubMed DOI PMC
Katsumi Y., Kamona N., Zhang J., Bunce J. G., Hutchinson J. B., Yarossi M., et al. (2021). Functional connectivity gradients as a common neural architecture for predictive processing in the human brain. Commun. Biol. 1:456844. doi: 10.1101/2021.09.01.456844 DOI
Koh W., Kwak H., Cheong E., Lee C. J. (2023). GABA tone regulation and its cognitive functions in the brain. Nat. Rev. Neurosci. 24, 523–539. doi: 10.1038/s41583-023-00724-7, PMID: PubMed DOI
Kozhuharova P., Saviola F., Diaconescu A., Allen P. (2021). High schizotypy traits are associated with reduced hippocampal resting state functional connectivity. Psychiatry Res. Neuroimaging 307:111215. doi: 10.1016/j.pscychresns.2020.111215 PubMed DOI
Krukow P., Jonak K., Grochowski C., Plechawska-Wójcik M., Karakuła-Juchnowicz H. (2020). Resting-state hyperconnectivity within the default mode network impedes the ability to initiate cognitive performance in first-episode schizophrenia patients. Prog. Neuro-Psychopharmacol. Neuro-Psychopharmacol. Biol. Psychiatry, 102:109959. doi: 10.1016/j.pnpbp.2020.109959 PubMed DOI
Kuang J., Kafetzopoulos V., Deth R., Kocsis B. (2023). Dopamine D4 receptor agonist drastically increases delta activity in the thalamic nucleus reuniens: potential role in communication between prefrontal cortex and hippocampus. Int. J. Mol. Sci. 24:15289. doi: 10.3390/ijms242015289 PubMed DOI PMC
Kulhara P., Gupta S. (2010). What is schizophrenia: a neurodevelopmental or neurodegenerative disorder or a combination of both? A critical analysis. Indian J. Psychiatry 52:21. doi: 10.4103/0019-5545.58891, PMID: PubMed DOI PMC
Kurtin D. L., Giunchiglia V., Vohryzek J., Cabral J., Skeldon A. C., Violante I. R. (2023). Moving from phenomenological to predictive modelling: Progress and pitfalls of modelling brain stimulation in-silico. NeuroImage 272:120042. doi: 10.1016/j.neuroimage.2023.120042, PMID: PubMed DOI
Lawrence R. E., Becker I., McGorry P. D. (2024). Schizophrenia and Other Primary Psychotic Disorders. In: Tasman, A., et al. Tasman’s Psychiatry, Cham: Springer. doi: 10.1007/978-3-030-51366-5_104 DOI
Li D., Christ S. E., Cowan N. (2014). Domain-general and domain-specific functional networks in working memory. NeuroImage 102, 646–656. doi: 10.1016/j.neuroimage.2014.08.028, PMID: PubMed DOI PMC
Lipska B. K., Weinberger D. R. (2000). To model a psychiatric disorder in animals: schizophrenia as a reality test. Neuropsychopharmacology 23, 223–239. doi: 10.1016/S0893-133X(00)00137-8, PMID: PubMed DOI
Loh M., Deco G. (2005). Cognitive flexibility and decision-making in a model of conditional visuomotor associations. Eur. J. Neurosci. 22, 2927–2936. doi: 10.1111/j.1460-9568.2005.04505.x, PMID: PubMed DOI
Looijestijn J., Blom J. D., Aleman A., Hoek H. W., Goekoop R. (2015). An integrated network model of psychotic symptoms. Neurosci. Biobehav. Rev. 59, 238–250. doi: 10.1016/j.neubiorev.2015.09.016, PMID: PubMed DOI
Lory P., Nicole S., Monteil A. (2020). Neuronal Cav3 channelopathies: recent progress and perspectives. Pflugers Archiv: Eur. J. Physiol. 472, 831–844. doi: 10.1007/s00424-020-02429-7, PMID: PubMed DOI PMC
Lyttle D., Gereke B. J., Lin K. K., Fellous J. M. (2013). Spatial scale and place field stability in a grid-to-place cell model of the dorsoventral axis of the PubMed DOI PMC
Maheshwari A., Akbar A., Wang M., Marks R. L., Yu K., Park S., et al. (2017). Persistent aberrant cortical phase-amplitude coupling following seizure treatment in absence epilepsy models. J. Physiol. 595, 7249–7260. doi: 10.1113/JP274696, PMID: PubMed DOI PMC
McCutcheon R. A., Keefe R. S. E., McGuire P. K. (2023). Cognitive impairment in schizophrenia: aetiology, pathophysiology, and treatment. Mol. Psychiatry 28, 1902–1918. doi: 10.1038/s41380-023-01949-9, PMID: PubMed DOI PMC
McGrath J., Saha S., Chant D., Welham J. (2008). Schizophrenia: a concise overview of incidence, prevalence, and mortality. Epidemiol. Rev. 30, 67–76. doi: 10.1093/epirev/mxn001, PMID: PubMed DOI
Meyer U., Feldon J. (2012). To poly(I:C) or not to poly(I:C): advancing preclinical schizophrenia research through the use of prenatal immune activation models. Neuropharmacology 62, 1308–1321. doi: 10.1016/j.neuropharm.2011.01.009, PMID: PubMed DOI
Modhej N., Bastanfard A., Teshnehlab M., Raiesdana S. (2022). Computational pattern separation models of dentate gyrus neural subpopulation in the hippocampus. Casp. J. Neurol. Sci. 8, 244–251. doi: 10.32598/cjns.4.31.286.1 DOI
Moser M.-B., Moser E. I. (1998). Distributed encoding and retrieval of spatial memory in the Hippocampus. J. Neurosci. 18, 7535–7542. doi: 10.1523/jneurosci.18-18-07535.1998, PMID: PubMed DOI PMC
Mosolov S. N., Yaltonskaya P. A. (2022). Primary and secondary negative symptoms in schizophrenia. Front. Psych. 12:766692. doi: 10.3389/fpsyt.2021.766692 PubMed DOI PMC
Moura B. M., Rooijen G., Schirmbeck F., Wigman J. T. W., Amelsvoort T., Bartels-Velthuis A. A., et al. (2021). A network of psychopathological, cognitive, and motor symptoms in schizophrenia spectrum disorders. Schizophr. Bull. 47, 915–926. doi: 10.1093/schbul/sbab002 PubMed DOI PMC
Mugan U., Hoffman S. L., Redish A. D. (2024). Environmental complexity modulates information processing and the balance between decision-making systems. Neuron 112, 4096–4114. doi: 10.1016/j.neuron.2024.10.004, PMID: PubMed DOI PMC
Nekovarova T., Fajnerova I., Horacek J., Spaniel F. (2014). Bridging disparate symptoms of schizophrenia: a triple network dysfunction theory. Front. Behav. Neurosci. 8:171. doi: 10.3389/fnbeh.2014.00171, PMID: PubMed DOI PMC
Nitta A., Izuo N., Hamatani K., Inagaki R., Kusui Y., Fu K., et al. (2021). Schizophrenia-like behavioral impairments in mice with suppressed expression of piccolo in the medial prefrontal cortex. J. Pers. Med. 11:607. doi: 10.3390/jpm11070607, PMID: PubMed DOI PMC
Nozari N., Martin R. C. (2024). Is working memory domain-general or domain-specific? Trends Cogn. Sci. 28, 1023–1036. doi: 10.1016/j.tics.2024.06.006, PMID: PubMed DOI PMC
Øie M. G., Sundet K., Haug E., Zeiner P., Klungsøyr O., Rund B. R. (2021). Cognitive performance in early-onset schizophrenia and attention-deficit/hyperactivity disorder: A 25-year follow-up study. Front. Psychol. 11:606365. doi: 10.3389/fpsyg.2020.606365, PMID: PubMed DOI PMC
Onwordi E. C., Whitehurst T., Shatalina E., Mansur A., Arumuham A., Osugo M., et al. (2023). Synaptic terminal density early in the course of schizophrenia: an in vivo UCB-J positron emission tomographic imaging study of synaptic vesicle glycoprotein 2A. Biol. Psychiatry 95:22. doi: 10.1016/j.biopsych.2023.05.022 PubMed DOI PMC
O'Donnell P. (2012). Cortical disinhibition in the neonatal ventral hippocampal lesion model of schizophrenia: new vistas on possible therapeutic approaches. Pharmacol. Ther. 133, 19–25. doi: 10.1016/j.pharmthera.2011.07.005, PMID: PubMed DOI
Padilla-Coreano N., Bolkan S. S., Pierce G. M., Blackman D. R., Hardin W. D., Garcia-Garcia A. L., et al. (2016). Direct ventral hippocampal-prefrontal input is required for anxiety-related neural activity and behavior. Neuron 89, 857–866. doi: 10.1016/j.neuron.2016.01.011, PMID: PubMed DOI PMC
Pafundo D. E., Pretell Annan C. A., Fulginiti N. M., Belforte J. E. (2021). Early NMDA receptor ablation in interneurons causes an activity-dependent E/I imbalance in vivo in prefrontal cortex pyramidal neurons of a mouse model useful for the study of schizophrenia. Schizophr. Bull. 47, 1300–1309. doi: 10.1093/schbul/sbab030, PMID: PubMed DOI PMC
Panzer E., Guimares-Olmo I., Pereira de Vasconcelos A., Stéphan A., Cassel J. C. (2024). In relentless pursuit of the white whale: A role for the ventral midline thalamus in behavioral flexibility and adaption? Neurosci. Biobehav. Rev. 163:105762. doi: 10.1016/j.neubiorev.2024.105762, PMID: PubMed DOI
Papatheodoropoulos C. (2025). Compensatory regulation of excitation/inhibition balance in the ventral hippocampus: insights from fragile X syndrome. Biology 14:363. doi: 10.3390/biology14040363, PMID: PubMed DOI PMC
Parlikar R., Vanteemar S S., Shivakumar V., Narayanaswamy C. J., Rao P. N., Ganesan V. (2021). High definition transcranial direct current stimulation (HD-tDCS): a systematic review on the treatment of neuropsychiatric disorders. Asian J. Psychiatr. 56:102542. doi: 10.1016/j.ajp.2020.102542 PubMed DOI
Patrono E., Černotová D., Svoboda J., Stuchlík A. (2025). Specific parvalbumin-positive optogenetic stimulations in specific brain regions restore navigational flexibility in an acute MK801 mouse model of schizophrenia. Neuroscience. 585, 85–96. doi: 10.1016/j.neuroscience.2025.09.001 PubMed DOI
Patrono E., Hrůzova K., Svoboda J., Stuchlík A. (2023). The role of optogenetic stimulations of parvalbumin-positive interneurons in the prefrontal cortex and the ventral hippocampus on an acute MK-801 model of schizophrenia-like cognitive inflexibility. Schizophr. Res. 252, 198–205. doi: 10.1016/j.schres.2022.12.047, PMID: PubMed DOI
Perez-Reyes E. (2003). Molecular physiology of low-voltage-activated t-type calcium channels. Physiol. Rev. 83, 117–161. doi: 10.1152/physrev.00018.2002, PMID: PubMed DOI
Permyakov E. A., Uversky V. N. (2022). What is parvalbumin for? Biomolecules 12:656. doi: 10.3390/biom12050656, PMID: PubMed DOI PMC
Peterson B. S., Kaur T., Sawardekar S., Colibazzi T., Hao X., Wexler B. E., et al. (2023). Aberrant hippocampus and amygdala morphology associated with cognitive deficits in schizophrenia. Front. Cell. Neurosci. 17:1126577. doi: 10.3389/fncel.2023.1126577, PMID: PubMed DOI PMC
Place R., Farovik A., Brockmann M., Eichenbaum H. (2016). Bidirectional prefrontal-hippocampal interactions support context-guided memory. Nat. Neurosci. 19, 992–994. doi: 10.1038/nn.4327, PMID: PubMed DOI PMC
Pronier É., Morici J. F., Girardeau G. (2023). The role of the hippocampus in the consolidation of emotional memories during sleep. Trends Neurosci. 46, 912–925. doi: 10.1016/j.tins.2023.08.003, PMID: PubMed DOI
Réthelyi J. M., Czobor P., Polgár P., Mersich B., Bálint S., Jekkel E., et al. (2012). General and domain-specific neurocognitive impairments in deficit and non-deficit schizophrenia. Eur. Arch. Psychiatry Clin. Neurosci. 262, 107–115. doi: 10.1007/s00406-011-0224-4, PMID: PubMed DOI
Rojas A. K. P., Linley S. B., Vertes R. P. (2024). Chemogenetic inactivation of the nucleus Reuniens and its projections to the orbital cortex produce deficits on discrete measures of behavioral flexibility in the attentional set-shifting task. Behav. Brain Res. 470:115066. doi: 10.1016/j.bbr.2024.115066, PMID: PubMed DOI
Ruggiero R. N., Rossignoli M. T., Marques D. B., de Sousa B. M., Romcy-Pereira R. N., Lopes-Aguiar C., et al. (2021). Neuromodulation of hippocampal-prefrontal cortical synaptic plasticity and functional connectivity: implications for neuropsychiatric disorders. Front. Cell. Neurosci. 15:732360. doi: 10.3389/fncel.2021.732360, PMID: PubMed DOI PMC
Schlecht M., Jayachandran M., Rasch G. E., Allen T. A. (2022). Dual projecting cells linking thalamic and cortical communication routes between the medial prefrontal cortex and hippocampus. Neurobiol. Learn. Mem. 188:107586. doi: 10.1016/j.nlm.2022.107586, PMID: PubMed DOI PMC
Schäfer J., Reuter T., Karbach J., Leuchter M. (2024). Domain-specific knowledge and domain-general abilities in children's science problem-solving. Br. J. Educ. Psychol. 94, 346–366. doi: 10.1111/bjep.12649, PMID: PubMed DOI
Sendi M. S. E., Zendehrouh E., Ellis C. A., Liang Z., Fu Z., Mathalon D. H., et al. (2021). Aberrant dynamic functional connectivity of default mode network in schizophrenia and links to symptom severity. Fronti. Neural Circuits 15:649417. doi: 10.3389/fncir.2021.649417, PMID: PubMed DOI PMC
Shapiro M. L., Riceberg J. S., Seip-Cammack K., Guise K. G. (2014). Functional Interactions of Prefrontal Cortex and the Hippocampus in Learning and Memory. In: Derdikman, D., Knierim, J. (eds) Space, Time and Memory in the Hippocampal Formation. Vienna: Springer. doi: 10.1007/978-3-7091-1292-2_19 DOI
Sheffield J. M., Barch D. M. (2016). Cognition and resting-state functional connectivity in schizophrenia. Neurosci. Biobehav. Rev. 61, 108–120. doi: 10.1016/j.neubiorev.2015.12.007, PMID: PubMed DOI PMC
Sherif M. A., Neymotin S. A., Lytton W. W. (2020). PubMed DOI PMC
Shin J. D., Jadhav S. P. (2016). Multiple modes of hippocampal–prefrontal interactions in memory-guided behavior. Curr. Opin. Neurobiol. 40, 161–169. doi: 10.1016/j.conb.2016.07.015, PMID: PubMed DOI PMC
Shing N., Walker M. C., Chang P. (2022). The role of aberrant neural oscillations in the hippocampal-medial prefrontal cortex circuit in neurodevelopmental and neurological disorders. Neurobiol. Learn. Mem. 195:107683. doi: 10.1016/j.nlm.2022.107683, PMID: PubMed DOI
Sigurdsson T., Duvarci S. (2016). Hippocampal-prefrontal interactions in cognition, behavior and psychiatric disease. Front. Syst. Neurosci. 9:190. doi: 10.3389/fnsys.2015.00190, PMID: PubMed DOI PMC
Sochan L., Archibald J., Weber A. M. (2025). Does the brain’s E: I balance really shape- Long-range temporal correlations? Lessons learned from 3T MRI. bioRxiv. doi: 10.1101/2025.03.28.645973 DOI
Sohal V. S., Rubenstein J. L. R. (2019). Excitation-inhibition balance as a framework for investigating mechanisms in neuropsychiatric disorders. Mol. Psychiatry 24, 1248–1257. doi: 10.1038/s41380-019-0426-0, PMID: PubMed DOI PMC
Spaniol J., Davidson P. S. R., Kim A. S. N., Han H., Moscovitch M., Grady C. L. (2009). Event-related fMRI studies of episodic encoding and retrieval: Meta-analyses using activation likelihood estimation. Neuropsychologia 47, 1765–1779. doi: 10.1016/j.neuropsychologia.2009.02.028, PMID: PubMed DOI
Speers L. J., Cheyne K. R., Cavani E., Hayward T., Schmidt R., Bilkey D. K. (2021). Hippocampal sequencing mechanisms are disrupted in a maternal immune activation model of schizophrenia risk. J. Neurosci. 41, 6954–6965. doi: 10.1523/jneurosci.0730-21.2021, PMID: PubMed DOI PMC
Spreng R. N., DuPre E., Selarka D., Garcia J., Gojkovic S., Mildner J., et al. (2014). Goal-congruent default network activity facilitates cognitive control. J. Neurosci. 34, 14108–14114. doi: 10.1523/JNEUROSCI.2815-14.2014, PMID: PubMed DOI PMC
Strange B. A., Witter M. P., Lein E. S., Moser E. I. (2014). Functional organization of the hippocampal longitudinal axis. Nat. Rev. Neurosci. 15, 655–669. doi: 10.1038/nrn3785, PMID: PubMed DOI
Summerfield C., Mangels J. A. (2005). Coherent theta-band EEG activity predicts item-context binding during encoding. NeuroImage 24, 692–703. doi: 10.1016/j.neuroimage.2004.09.012, PMID: PubMed DOI
Sylvester A. L., Hensenne E., Ivanov D., Poser B. A., Linden D. E. J., van Amelsvoort T., et al. (2025). Neural excitation/inhibition imbalance and neurodevelopmental pathology in human copy number variant syndromes: a systematic review. J. Neurodev. Disord. 17:31. doi: 10.1186/s11689-025-09614-8, PMID: PubMed DOI PMC
Szczurowska E., Ahuja N., Jiruška P., Kelemen E., Stuchlík A. (2017). Impairment of neural coordination in hippocampal neuronal ensembles after a psychotomimetic dose of dizocilpine. Prog. Neuro-Psychopharmacol. Biol. Psychiatry 81, 275–283. doi: 10.1016/j.pnpbp.2017.09.013 PubMed DOI
Tamminga C. A., Thomas B. P., Chin R., Mihalakos P., Youens K., Wagner A. D., et al. (2012). Hippocampal novelty activations in schizophrenia: disease and medication effects. Schizophr. Res. 138, 157–163. doi: 10.1016/j.schres.2012.03.019, PMID: PubMed DOI
Tatka L. T., Smith L. P., Hellerstein J. L., Sauro H. M. (2023). Adapting modeling and simulation credibility standards to computational systems biology. J. Transl. Med. 21:501. doi: 10.1186/s12967-023-04290-5, PMID: PubMed DOI PMC
Taylor N. L., Whyte C. J., Munn B. R., Chang C., Lizier J. T., Leopold D. A., et al. (2024). Causal evidence for cholinergic stabilization of attractor landscape dynamics. Cell Rep. 43:114359. doi: 10.1016/j.celrep.2024.114359, PMID: PubMed DOI PMC
Thorsen A. L., Johansson K., LÃberg E.-M. (2014). Neurobiology of cognitive remediation therapy for schizophrenia: a systematic review. Front. Psych. 5:103. doi: 10.3389/fpsyt.2014.00103 PubMed DOI PMC
Tseng K. Y., Chambers R. A., Lipska B. K. (2009). The neonatal ventral hippocampal lesion as a heuristic neurodevelopmental model of schizophrenia. Behav. Brain Res. 204, 295–305. doi: 10.1016/j.bbr.2008.11.039, PMID: PubMed DOI PMC
van Bueren N. E. R., van der Ven S. H. G., Hochman S., Sella F., Cohen Kadosh R. (2023). Human neuronal excitation/inhibition balance explains and predicts neurostimulation induced learning benefits. PLoS Biol. 21:e3002193. doi: 10.1371/journal.pbio.3002193, PMID: PubMed DOI PMC
Verma S., Goel T., Tanveer M., Ding W., Sharma R., Murugan R. (2023). Machine learning techniques for the schizophrenia diagnosis: a comprehensive review and future research directions. J. Ambient. Intell. Humaniz. Comput. 14, 4795–4807. doi: 10.1007/s12652-023-04536-6 DOI
Vertes R. P., Hoover W. B., Szigeti-Buck K., Leranth C. (2006). Nucleus reuniens of the midline thalamus: link between the medial prefrontal cortex and the hippocampus. Brain Res. Bullet. 71, 601–609. doi: 10.1016/j.brainresbull.2006.12.002 PubMed DOI PMC
Vertes R. P., Linley S. B., Viena T. D. (2022). “Nucleus Reuniens: circuitry, function, and dysfunction” in Electrophysiological recording techniques. Neuromethods. eds. Vertes R. P., Allen T. (New York, NY: Humana; ).
Viena T. D., Rasch G. E., Silva D., Allen T. A. (2021). Calretinin and calbindin architecture of the midline thalamus associated with prefrontal-hippocampal circuitry. Hippocampus 31, 770–789. doi: 10.1002/hipo.23271, PMID: PubMed DOI PMC
Volk D. W., Lewis D. A. (2005). GABA targets for the treatment of cognitive dysfunction in schizophrenia. Curr. Neuropharmacol. 3, 45–62. doi: 10.2174/1570159052773396, PMID: PubMed DOI PMC
Walsh C., Tait L., Garrido M. G., Brown J. T., Ridler T. (2025). Transient cortical beta-frequency oscillations associated with contextual novelty in high density mouse EEG. Sci. Rep. 15:2897. doi: 10.1038/s41598-025-86008-9, PMID: PubMed DOI PMC
Walther S., Lefebvre S., Conring F., Gangl N., Nadesalingam N., Alexaki D., et al. (2021). Limbic links to paranoia: increased resting-state functional connectivity between amygdala, hippocampus and orbitofrontal cortex in schizophrenia patients with paranoia. Eur. Arch. Psychiatry Clin. Neurosci. 272, 1021–1032. doi: 10.1007/s00406-021-01337-w, PMID: PubMed DOI PMC
Wang C., Furlong T. M., Stratton P. G., Lee C. C. Y., Xu L., Merlin S., et al. (2021). Hippocampus–prefrontal coupling regulates recognition memory for novelty discrimination. J. Neurosci. 41, 9617–9632. doi: 10.1523/JNEUROSCI.1202-21.2021, PMID: PubMed DOI PMC
Wang X., Cheng B., Roberts N., Wang S., Luo Y., Tian F., et al. (2021). Shared and distinct brain fMRI response during performance of working memory tasks in adult patients with schizophrenia and major depressive disorder. Hum. Brain Mapp. 42, 5458–5476. doi: 10.1002/hbm.25618, PMID: PubMed DOI PMC
Wang Y., Jiang Y., Collin G., Liu D., Su W., Xu L., et al. (2021). The effects of antipsychotics on interactions of dynamic functional connectivity in the triple-network in first episode schizophrenia. Schizophr. Res. 236, 29–37. doi: 10.1016/j.schres.2021.07.038, PMID: PubMed DOI
Wang H., Mou S., Pei X., Zhang X., Shen S., Zhang J., et al. (2025). The power spectrum and functional connectivity characteristics of resting-state EEG in patients with generalized anxiety disorder. Sci. Rep. 15:5991. doi: 10.1038/s41598-025-90362-z, PMID: PubMed DOI PMC
Wang Y., Wang X., Wang L., Zheng L., Meng S., Zhu N., et al. (2024). Dynamic prediction of goal location by coordinated representation of prefrontal-hippocampal theta sequences. Current Biol. 34, 1866–1879.e6. doi: 10.1016/j.cub.2024.03.032, PMID: PubMed DOI
Wegrzyn D., Juckel G., Faissner A. (2022). Structural and functional deviations of the hippocampus in schizophrenia and schizophrenia animal models. Int. J. Mol. Sci. 23:5482. doi: 10.3390/ijms23105482, PMID: PubMed DOI PMC
Weiss S., Müller H. M., Rappelsberger P. (2000). Theta synchronization predicts efficient memory encoding of concrete and abstract nouns. Neuroreport 11, 2357–2361. doi: 10.1097/00001756-200008030-00005, PMID: PubMed DOI
Weiss S., Rappelsberger P. (2000). Long-range EEG synchronization during word encoding correlates with successful memory performance. Cogn. Brain Res. 9, 299–312. doi: 10.1016/s0926-6410(00)00011-2, PMID: PubMed DOI
Whitton A. E., Deccy S., Ironside M. L., Kumar P., Beltzer M., Pizzagalli D. A. (2018). Electroencephalography source functional connectivity reveals abnormal high-frequency communication among large-scale functional networks in depression. Biol. Psychiatry Cognitive Neurosci. Neuroimaging 3, 50–58. doi: 10.1016/j.bpsc.2017.07.001, PMID: PubMed DOI PMC
Wiltgen B. J., Zhou M., Cai Y., Balaji J., Karlsson M. G., Parivash S. N., et al. (2010). The hippocampus plays a selective role in the retrieval of detailed contextual memories. Curr. Biol. 20, 1336–1344. doi: 10.1016/j.cub.2010.06.068, PMID: PubMed DOI PMC
Witter M. P., Naber P. A., van Haeften T. W., Machielsen W. C. M., Rombouts S. A. R. B., Barkhof F., et al. (2000). Cortico-hippocampal communication by way of parallel parahippocampal-subicular pathways. Hippocampus 10, 398–410. doi: 10.1002/1098-1063(2000)10:4<398::aid-hipo6>3.0.co;2-k PubMed DOI
Wu Q., Wang X., Wang Y., Long Y.-J., Zhao J.-P., Wu R.-R. (2021). Developments in biological mechanisms and treatments for negative symptoms and cognitive dysfunction of schizophrenia. Neurosci. Bull. 37, 1609–1624. doi: 10.1007/s12264-021-00740-6, PMID: PubMed DOI PMC
Yeh T., Lin Y., Tzeng N., Kao Y., Chung Y., Chang C., et al. (2024). Effects of online high-definition transcranial direct current stimulation over left dorsolateral prefrontal cortex on predominant negative symptoms and EEG functional connectivity in patients with schizophrenia: a randomized, double-blind, controlled trial. Psychiatry Clin. Neurosci. 79, 2–11. doi: 10.1111/pcn.13745, PMID: PubMed DOI
Yoon J. H., Zhang Z., Mormino E., Davidzon G., Minzenberg M. J., Ballon J., et al. (2023). Reductions in synaptic marker SV2A in early-course schizophrenia. J. Psychiatr. Res. 161, 213–217. doi: 10.1016/j.jpsychires.2023.02.026, PMID: PubMed DOI
You W., Luo L., Yao L., Zhao Y., Li Q., Wang Y., et al. (2022). Impaired dynamic functional brain properties and their relationship to symptoms in never treated first-episode patients with schizophrenia. Schizophrenia 8:90. doi: 10.1038/s41537-022-00299-9, PMID: PubMed DOI PMC
Zeng J., Yan J., Cao H., Su Y., Song Y., Luo Y., et al. (2022). Neural substrates of reward anticipation and outcome in schizophrenia: a meta-analysis of fMRI findings in the monetary incentive delay task. Transl. Psychiatry 12:448. doi: 10.1038/s41398-022-02201-8, PMID: PubMed DOI PMC
Zhang W., Guo L., Liu D. (2022). Concurrent interactions between prefrontal cortex and hippocampus during a spatial working memory task. Brain Struct. Funct. 227, 1735–1755. doi: 10.1007/s00429-022-02469-y, PMID: PubMed DOI
Zhang S., Larsen B., Sydnor V. J., Zeng T., An L., Yan X., et al. (2024). In vivo whole-cortex marker of excitation-inhibition ratio indexes cortical maturation and cognitive ability in youth. Proc. Natl. Acad. Sci. USA 121:e2318641121. doi: 10.1073/pnas.2318641121, PMID: PubMed DOI PMC
Zhou L., Pu W., Wang J., Liu H., Wu G., Liu C., et al. (2016). Inefficient DMN suppression in schizophrenia patients with impaired cognitive function but not patients with preserved cognitive function. Sci. Rep. 6:21657. doi: 10.1038/srep21657, PMID: PubMed DOI PMC
Zhu C., Kwok N. T., Chan T. C., Chan G. H., So S. H. (2021). Inflexibility in reasoning: comparisons of cognitive flexibility, explanatory flexibility, and belief flexibility between schizophrenia and major depressive disorder. Front. Psych. 11:609569. doi: 10.3389/fpsyt.2020.609569, PMID: PubMed DOI PMC