Targeting Oxidative Stress and Aberrant Critical Period Plasticity in the Developmental Trajectory to Schizophrenia

Parvalbumin neurons and gamma rhythms enhance cortical circuit performance

Sohal, V. S., Zhang, F., Yizhar, O., & Deisseroth, K. (2009) · Nature · doi:10.1038/nature07991 · Cited by 2,606 · see citing works

Driving fast-spiking cells induces gamma rhythm and controls sensory responses

Cardin, J. A., Carlén, M., Meletis, K., Knoblich, U., Zhang, F., Deisseroth, K., Tsai, L.-H., & Moore, C. I. (2009) · Nature · doi:10.1038/nature08002 · Cited by 2,603 · see citing works

Critical period plasticity in local cortical circuits

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

Abnormal neural oscillations and synchrony in schizophrenia

Uhlhaas, P. J., & Singer, W. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2774 · Cited by 2,120 · see citing works

Synaptic mechanisms of synchronized gamma oscillations in inhibitory interneuron networks

Bartos, M., Vida, I., & Jonas, P. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2044 · Cited by 2,070 · see citing works

Rethinking schizophrenia

Insel, T. R. (2010) · Nature · doi:10.1038/nature09552 · Cited by 1,783 · see citing works

Synaptic Energy Use and Supply

Harris, J. J., Jolivet, R., & Attwell, D. (2012) · Neuron · doi:10.1016/j.neuron.2012.08.019 · Cited by 1,747 · see citing works

Metabolism and functions of glutathione in brain

Dringen, R. (2000) · Progress in Neurobiology · doi:10.1016/s0301-0082(99)00060-x · Cited by 1,702 · see citing works

Radical-free biology of oxidative stress

Jones, D. P. (2008) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00283.2008 · Cited by 1,213 · see citing works

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

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

The gamma cycle.

Fries, P., Nikolić, D., & Singer, W. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.05.005 · Cited by 1,044 · see citing works

Circuit-based framework for understanding neurotransmitter and risk gene interactions in schizophrenia

Lisman, J. E., Coyle, J. T., Green, R. W., Javitt, D. C., Benes, F. M., Heckers, S., & Grace, A. A. (2008) · Trends in Neurosciences · doi:10.1016/j.tins.2008.02.005 · Cited by 1,010 · see citing works

Oligodendrocyte dysfunction in schizophrenia and bipolar disorder.

Tkachev, D., Mimmack, M., Ryan, M. M., Wayland, M., Freeman, T., Jones, P., Starkey, M., Webster, M., Yolken, R., & Bahn, S. (2003) · The Lancet · doi:10.1016/s0140-6736(03)14289-4 · Cited by 940 · see citing works

Oligodendrocytes: biology and pathology

Bradl, M., & Lassmann, H. (2010) · Acta Neuropathologica · doi:10.1007/s00401-009-0601-5 · Cited by 933 · see citing works

Local GABA Circuit Control of Experience-Dependent Plasticity in Developing Visual Cortex

Hensch, T. K., Fagiolini, M., Mataga, N., Stryker, M. P., Baekkeskov, S., & Kash, S. F. (1998) · Science · doi:10.1126/science.282.5393.1504 · Cited by 910 · see citing works

Long-Chain ω-3 Fatty Acids for Indicated Prevention of Psychotic Disorders: A Randomized, Placebo-Controlled Trial

Amminger, G. P., Schäfer, M. R., Papageorgiou, K., Klier, C. M., Cotton, S. M., Harrigan, S. M., Mackinnon, A., McGorry, P. D., & Berger, G. E. (2010) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2009.192 · Cited by 896 · see citing works

Sulforaphane inhibits extracellular, intracellular, and antibiotic-resistant strains of Helicobacter pylori and prevents benzo[ a ]pyrene-induced stomach tumors

Fahey, J. W., Haristoy, X., Dolan, P. M., Kensler, T. W., Scholtus, I., Stephenson, K. K., Talalay, P., & Lozniewski, A. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.112203099 · Cited by 794 · see citing works

White Matter Changes in Schizophrenia: Evidence for Myelin-Related Dysfunction

Davis, K. L., Stewart, D. G., Friedman, J. I., Buchsbaum, M., Harvey, P. D., Hof, P. R., Buxbaum, J., & Haroutunian, V. (2003) · Archives of General Psychiatry · doi:10.1001/archpsyc.60.5.443 · Cited by 793 · see citing works

Omega-3 Fatty Acids: Evidence Basis for Treatment and Future Research in Psychiatry

Freeman, M. P., Hibbeln, J. R., Wisner, K. L., Davis, J. M., Mischoulon, D., Peet, M., Keck, P. E., Marangell, L. B., Richardson, A. J., Lake, J., et al. (2006) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.v67n1217 · Cited by 709 · see citing works

Parvalbumin-expressing basket-cell network plasticity induced by experience regulates adult learning

Donato, F., Rompani, S. B., & Caroni, P. (2013) · Nature · doi:10.1038/nature12866 · Cited by 703 · see citing works

A critical role for NMDA receptors in parvalbumin interneurons for gamma rhythm induction and behavior

Carlén, M., Meletis, K., Siegle, J. H., Cardin, J. A., Futai, K., Vierling-Claassen, D., Rühlmann, C., Jones, S. R., Deisseroth, K., Sheng, M., et al. (2012) · Molecular Psychiatry · doi:10.1038/mp.2011.31 · Cited by 669 · see citing works

Balancing Plasticity/Stability Across Brain Development

Takesian, A. E., & Hensch, T. K. (2013) · Progress in Brain Research · doi:10.1016/b978-0-444-63327-9.00001-1 · Cited by 667 · see citing works

The environment and susceptibility to schizophrenia

Brown, A. S. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2010.09.003 · Cited by 664 · see citing works

Oligodendroglial density in the prefrontal cortex in schizophrenia and mood disorders: a study from the Stanley Neuropathology Consortium

Uranova, N. A., Vostrikov, V. M., Orlovskaya, D. D., & Rachmanova, V. I. (2004) · Schizophrenia Research · doi:10.1016/s0920-9964(03)00181-6 · Cited by 659 · see citing works

Parvalbumin-expressing interneurons linearly transform cortical responses to visual stimuli

Atallah, B. V., Bruns, W., Carandini, M., & Scanziani, M. (2012) · Neuron · doi:10.1016/j.neuron.2011.12.013 · Cited by 612 · see citing works

Decreased levels of glutathione, the major brain antioxidant, in post-mortem prefrontal cortex from patients with psychiatric disorders

Gawryluk, J. W., Wang, J.-F., Andreazza, A. C., Shao, L., & Young, L. T. (2011) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145710000805 · Cited by 594 · see citing works

Removing brakes on adult brain plasticity: From molecular to behavioral interventions

Bavelier, D., Levi, D. M., Li, R. W., Dan, Y., & Hensch, T. K. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4812-10.2010 · Cited by 589 · see citing works

Ketamine-Induced Loss of Phenotype of Fast-Spiking Interneurons Is Mediated by NADPH-Oxidase

Behrens, M. M., Ali, S. S., Dao, D. N., Lucero, J., Shekhtman, G., Quick, K. L., & Dugan, L. L. (2007) · Science · doi:10.1126/science.1148045 · Cited by 585 · see citing works

Ketamine-Induced Deficits in Auditory and Visual Context-Dependent Processing in Healthy Volunteers

Umbricht, D., Schmid, L., Koller, R., Vollenweider, F. X., Hell, D., & Javitt, D. C. (2000) · Archives of General Psychiatry · doi:10.1001/archpsyc.57.12.1139 · Cited by 583 · see citing works

Sulforaphane, a Dietary Component of Broccoli/Broccoli Sprouts, Inhibits Breast Cancer Stem Cells

Li, Y., Zhang, T., Körkaya, H., Liu, S., Lee, H.-F., Newman, B. W., Yu, Y., Clouthier, S. G., Schwartz, S. J., Wicha, M. S., et al. (2010) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-09-2937 · Cited by 561 · see citing works

N-Acetyl Cysteine as a Glutathione Precursor for Schizophrenia—A Double-Blind, Randomized, Placebo-Controlled Trial

Berk, M., Copolov, D., Dean, O., Lu, K., Jeavons, S., Schapkaitz, I., Anderson-Hunt, M., Judd, F., Katz, F., Katz, P., et al. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.03.004 · Cited by 552 · see citing works

Schizophrenia: glutathione deficit in cerebrospinal fluid and prefrontal cortex in vivo

Do, K. Q., Trabesinger, A. H., Kirsten‐Krüger, M., Lauer, C. J., Dydak, U., Hell, D., Holsboer, F., Boesiger, P., & Cuénod, M. (2000) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2000.00229.x · Cited by 540 · see citing works

Recruitment of Parvalbumin-Positive Interneurons Determines Hippocampal Function and Associated Behavior

Fuchs, E. C., Zivkovic, A. R., Cunningham, M. O., Middleton, S., LeBeau, F. E. N., Bannerman, D. M., Rozov, A., Whittington, M. A., Traub, R. D., Rawlins, J. N. P., et al. (2007) · Neuron · doi:10.1016/j.neuron.2007.01.031 · Cited by 532 · see citing works

Neural synchrony and the development of cortical networks

Uhlhaas, P. J., Roux, F., Rodriguez, E., Rotarska-Jagiela, A., & Singer, W. (2010) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2009.12.002 · Cited by 532 · see citing works

Circadian clock proteins regulate neuronal redox homeostasis and neurodegeneration

Musiek, E. S., Lim, M. M., Yang, G., Bauer, A. Q., Qi, L., Lee, Y., Roh, J. H., Ortiz-Gonzalez, X., Dearborn, J. T., Culver, J. P., et al. (2013) · Journal of Clinical Investigation · doi:10.1172/jci70317 · Cited by 524 · see citing works

Perineuronal nets protect fast-spiking interneurons against oxidative stress

Cabungcal, J.-H., Steullet, P., Morishita, H., Kraftsik, R., Cuenod, M., Hensch, T. K., & Do, K. Q. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1300454110 · Cited by 512 · see citing works

Neuronal Dynamics and Neuropsychiatric Disorders: Toward a Translational Paradigm for Dysfunctional Large-Scale Networks

Uhlhaas, P. J., & Singer, W. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.004 · Cited by 512 · see citing works

PirB is a Functional Receptor for Myelin Inhibitors of Axonal Regeneration

Atwal, J. K., Pinkston-Gosse, J., Syken, J., Stawicki, S. S., Wu, Y., Shatz, C. J., & Tessier‐Lavigne, M. (2008) · Science · doi:10.1126/science.1161151 · Cited by 503 · see citing works

Control of cortical GABA circuitry development by Nrg1 and ErbB4 signalling

Fazzari, P., Paternain, A. V., Valiente, M., Pla, R., Luján, R., Lloyd, K., Lerma, J., Marín, O., & Rico, B. (2010) · Nature · doi:10.1038/nature08928 · Cited by 501 · see citing works

Invited Review Free radicals and the pathobiology of brain dopamine systems

Cadet, J. L., & Brannock, C. (1998) · Neurochemistry International · doi:10.1016/s0197-0186(97)00031-4 · Cited by 499 · see citing works

A Loss of Parvalbumin-Containing Interneurons Is Associated with Diminished Oscillatory Activity in an Animal Model of Schizophrenia

Lodge, D. J., Behrens, M. M., & Grace, A. A. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.5419-08.2009 · Cited by 488 · see citing works

NMDA Receptor Ablation on Parvalbumin-Positive Interneurons Impairs Hippocampal Synchrony, Spatial Representations, and Working Memory

Korotkova, T., Fuchs, E. C., Ponomarenko, A., von Engelhardt, J., & Monyer, H. (2010) · Neuron · doi:10.1016/j.neuron.2010.09.017 · Cited by 480 · see citing works

A selective decrease in the relative density of parvalbumin-immunoreactive neurons in the hippocampus in schizophrenia

Zhang, Z. J., & Reynolds, G. P. (2002) · Schizophrenia Research · doi:10.1016/s0920-9964(01)00188-8 · Cited by 460 · see citing works

The antioxidants α‐lipoic acid and <i>N</i> ‐acetylcysteine reverse memory impairment and brain oxidative stress in aged SAMP8 mice

Farr, S. A., Poon, H. F., Dogrukol‐Ak, D., Drake, J., Banks, W. A., Eyerman, E., Butterfield, D. A., & Morley, J. E. (2003) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2003.01580.x · Cited by 459 · see citing works

Adult brain and behavioral pathological markers of prenatal immune challenge during early/middle and late fetal development in mice

Meyer, U., Nyffeler, M., Yee, B. K., Knuesel, I., & Feldon, J. (2008) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2007.09.012 · Cited by 457 · see citing works

NgR1 and NgR3 are receptors for chondroitin sulfate proteoglycans

Dickendesher, T. L., Baldwin, K. T., Mironova, Y. A., Koriyama, Y., Raiker, S. J., Askew, K. L., Wood, A., Geoffroy, C. G., Zheng, B., Liepmann, C. D., et al. (2012) · Nature Neuroscience · doi:10.1038/nn.3070 · Cited by 449 · see citing works

The promise of N-acetylcysteine in neuropsychiatry

Berk, M., Malhi, G. S., Gray, L. J., & Dean, O. M. (2013) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2013.01.001 · Cited by 434 · see citing works

Dominant-negative DISC1 transgenic mice display schizophrenia-associated phenotypes detected by measures translatable to humans

Hikida, T., Jaaro-Peled, H., Seshadri, S., Oishi, K., Hookway, C., Kong, S., Wu, D., Xue, R., Andradé, M., Tankou, S. K., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0704774104 · Cited by 417 · see citing works

Hippocampal theta rhythm and its coupling with gamma oscillations require fast inhibition onto parvalbumin-positive interneurons

Wulff, P., Ponomarenko, A. A., Bartos, M., Korotkova, T. M., Fuchs, E. C., Bähner, F., Both, M., Tort, A. B. L., Kopell, N. J., Wisden, W., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0813176106 · Cited by 400 · see citing works

Otx2 Binding to Perineuronal Nets Persistently Regulates Plasticity in the Mature Visual Cortex

Beurdeley, M., Spatazza, J., Lee, H. H. C., Sugiyama, S., Bernard, C., Di Nardo, A. A., Hensch, T. K., & Prochiantz, A. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0394-12.2012 · Cited by 398 · see citing works

Glutathione Precursor, N-Acetyl-Cysteine, Improves Mismatch Negativity in Schizophrenia Patients

Lavoie, S., Murray, M. M., Deppen, P., Knyazeva, M. G., Berk, M., Boulat, O., Bovet, P., Bush, A. I., Conus, P., Copolov, D., et al. (2008) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301624 · Cited by 371 · see citing works

Lynx1, a Cholinergic Brake, Limits Plasticity in Adult Visual Cortex

Morishita, H., Miwa, J. M., Heintz, N., & Hensch, T. K. (2010) · Science · doi:10.1126/science.1195320 · Cited by 365 · see citing works

Persistent cortical plasticity by upregulation of chondroitin 6-sulfation

Miyata, S., Komatsu, Y., Yoshimura, Y., Taya, C., & Kitagawa, H. (2012) · Nature Neuroscience · doi:10.1038/nn.3023 · Cited by 365 · see citing works

Linking oligodendrocyte and myelin dysfunction to neurocircuitry abnormalities in schizophrenia

Takahashi, N., Sakurai, T., Davis, K. L., & Buxbaum, J. D. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2010.09.004 · Cited by 337 · see citing works

Diffusion Tensor Imaging in Schizophrenia

Kanaan, R., Kim, J.-S., Kaufmann, W. E., Pearlson, G. D., Barker, G. J., & McGuire, P. K. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.05.015 · Cited by 332 · see citing works

Gamma-Band Activity in Human Prefrontal Cortex Codes for the Number of Relevant Items Maintained in Working Memory

Roux, F., Wibral, M., Mohr, H. M., Singer, W., & Uhlhaas, P. J. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0421-12.2012 · Cited by 322 · see citing works

Altered glutathione redox state in schizophrenia.

Yao, J. K., Leonard, S., & Reddy, R. (2006) · Disease Markers · doi:10.1155/2006/248387 · Cited by 321 · see citing works

Protective effect of sulforaphane against oxidative stress: Recent advances

Guerrero-Beltrán, C. E., Calderón‐Oliver, M., Pedraza‐Chaverrí, J., & Chirino, Y. I. (2010) · Experimental and Toxicologic Pathology · doi:10.1016/j.etp.2010.11.005 · Cited by 320 · see citing works

Neuregulin 1 regulates pyramidal neuron activity via ErbB4 in parvalbumin-positive interneurons

Wen, L., Lu, Y.-S., Zhu, X.-H., Li, X.-M., Woo, R., Chen, Y., Yin, D., Lai, C., Terry, A. V., Vazdarjanova, A. I., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0910302107 · Cited by 302 · see citing works

Extracellular Matrix-Glial Abnormalities in the Amygdala and Entorhinal Cortex of Subjects Diagnosed With Schizophrenia

Pantazopoulos, H., Woo, T.-U. W., Lim, M. P., Lange, N., & Berretta, S. (2010) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2009.196 · Cited by 296 · see citing works

Highly energized inhibitory interneurons are a central element for information processing in cortical networks.

Kann, O., Papageorgiou, I. E., & Draguhn, A. (2014) · Journal of Cerebral Blood Flow &amp; Metabolism · doi:10.1038/jcbfm.2014.104 · Cited by 295 · see citing works

Glutathione peroxidase-catalase cooperativity is required for resistance to hydrogen peroxide by mature rat oligodendrocytes

Baud, O., Greene, A. E., Li, J., Wang, H., Volpe, J. J., & Rosenberg, P. A. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.3989-03.2004 · Cited by 292 · see citing works

Developmental Pattern of Perineuronal Nets in the Human Prefrontal Cortex and Their Deficit in Schizophrenia

Mauney, S. A., Athanas, K. M., Pantazopoulos, H., Shaskan, N., Passeri, E., Berretta, S., & Woo, T.-U. W. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.05.007 · Cited by 291 · see citing works

Antioxidants, Redox Signaling, and Pathophysiology in Schizophrenia: An Integrative View

Yao, J. K., & Keshavan, M. S. (2011) · Antioxidants &amp; Redox Signaling · doi:10.1089/ars.2010.3603 · Cited by 285 · see citing works

Review of functional and anatomical brain connectivity findings in schizophrenia

Fitzsimmons, J., Kubicki, M., & Shenton, M. E. (2013) · Current Opinion in Psychiatry · doi:10.1097/yco.0b013e32835d9e6a · Cited by 277 · see citing works

System xc− and Thioredoxin Reductase 1 Cooperatively Rescue Glutathione Deficiency

Mandal, P. K., Seiler, A., Perisic, T., Kölle, P., Banjac Canak, A., Förster, H., Weiss, N., Kremmer, E., Lieberman, M. W., Bannai, S., et al. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.121327 · Cited by 269 · see citing works

Electrophysiological evidence of corollary discharge dysfunction in schizophrenia during talking and thinking

Ford, J. M., & Mathalon, D. H. (2004) · Journal of Psychiatric Research · doi:10.1016/s0022-3956(03)00095-5 · Cited by 266 · see citing works

Redox dysregulation, neuroinflammation, and NMDA receptor hypofunction: A “central hub” in schizophrenia pathophysiology?

Steullet, P., Cabungcal, J. H., Monin, A., Dwir, D., O'Donnell, P., Cuenod, M., & Do, K. Q. (2016) · Schizophrenia Research · doi:10.1016/j.schres.2014.06.021 · Cited by 262 · see citing works

Parvalbumin-Containing Fast-Spiking Basket Cells Generate the Field Potential Oscillations Induced by Cholinergic Receptor Activation in the Hippocampus

Gulyás, A. I., Szabo, G. G., Ulbert, I., Holderith, N. B., Monyer, H., Erdélyi, F., Szabó, G., Freund, T. F., & Hájos, N. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.4104-10.2010 · Cited by 257 · see citing works

Disordered Self in the Schizophrenia Spectrum

Parnas, J., & Henriksen, M. G. (2014) · Harvard Review of Psychiatry · doi:10.1097/hrp.0000000000000040 · Cited by 239 · see citing works

White matter alterations in early stages of schizophrenia: a systematic review of diffusion tensor imaging studies

Samartzis, L., Dima, D., Fusar‐Poli, P., & Kyriakopoulos, M. (2014) · Journal of Neuroimaging · doi:10.1111/j.1552-6569.2012.00779.x · Cited by 236 · see citing works

Deficit of perineuronal oligodendrocytes in the prefrontal cortex in schizophrenia and mood disorders

Vostrikov, V. M., Uranova, N. A., & Orlovskaya, D. D. (2007) · Schizophrenia Research · doi:10.1016/j.schres.2007.04.014 · Cited by 233 · see citing works

Essential polyunsaturated fatty acid and lipid peroxide levels in never-medicated and medicated schizophrenia patients

Arvindakshan, M., Sitasawad, S. L., Debsikdar, V. B., Ghate, M. R., Evans, D. R., Horrobin, D. F., Bennett, C. N., Ranjekar, P. K., & Mahadik, S. P. (2002) · Biological Psychiatry · doi:10.1016/s0006-3223(02)01443-9 · Cited by 232 · see citing works

Early-Life Insults Impair Parvalbumin Interneurons via Oxidative Stress: Reversal by N-Acetylcysteine

Cabungcal, J.-H., Steullet, P., Kraftsik, R., Cuenod, M., & Do, K. Q. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.09.020 · Cited by 232 · see citing works

Gap junctions among dendrites of cortical GABAergic neurons establish a dense and widespread intercolumnar network

Fukuda, T., Kosaka, T., Singer, W., & Galuske, R. A. W. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.4076-05.2006 · Cited by 209 · see citing works

Involvement of NOX2 in the Development of Behavioral and Pathologic Alterations in Isolated Rats

Schiavone, S., Sorce, S., Dubois-Dauphin, M., Jaquet, V., Colaianna, M., Zotti, M., Cuomo, V., Trabace, L., & Krause, K.-H. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.04.033 · Cited by 208 · see citing works

Sulforaphane mobilizes cellular defenses that protect skin against damage by UV radiation

Talalay, P., Fahey, J. W., Healy, Z. R., Wehage, S. L., Benedict, A. L., Min, C., & Dinkova‐Kostova, A. T. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0708710104 · Cited by 208 · see citing works

Juvenile Antioxidant Treatment Prevents Adult Deficits in a Developmental Model of Schizophrenia

Cabungcal, J.-H., Counotte, D. S., Lewis, E. M., Tejeda, H. A., Piantadosi, P., Pollock, C., Calhoon, G. G., Sullivan, E. M., Presgraves, E., Kil, J., et al. (2014) · Neuron · doi:10.1016/j.neuron.2014.07.028 · Cited by 204 · see citing works

Redox Dysregulation Affects the Ventral But Not Dorsal Hippocampus: Impairment of Parvalbumin Neurons, Gamma Oscillations, and Related Behaviors

Steullet, P., Cabungcal, J.-H., Kulak, A., Kraftsik, R., Chen, Y., Dalton, T. P., Cuenod, M., & Do, K. Q. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.3857-09.2010 · Cited by 202 · see citing works

Molecular and Cellular Evidence for an Oligodendrocyte Abnormality in Schizophrenia

Hof, P. R., Haroutunian, V., Copland, C., Davis, K. L., & Buxbaum, J. D. (2002) · Neurochemical Research · doi:10.1023/a:1020981510759 · Cited by 199 · see citing works

Gamma oscillations in the hippocampus require high complex I gene expression and strong functional performance of mitochondria

Kann, O., Huchzermeyer, C., Kovács, R., Wirtz, S., & Schuelke, M. (2011) · Brain · doi:10.1093/brain/awq333 · Cited by 189 · see citing works

Myelin-associated mRNA and protein expression deficits in the anterior cingulate cortex and hippocampus in elderly schizophrenia patients

Dracheva, S. M., Davis, K. L., Chin, B., Woo, D. A., Schmeidler, J., & Haroutunian, V. H. (2005) · Neurobiology of Disease · doi:10.1016/j.nbd.2005.08.012 · Cited by 178 · see citing works

Ultrastructural Alterations of Myelinated Fibers and Oligodendrocytes in the Prefrontal Cortex in Schizophrenia: A Postmortem Morphometric Study

Uranova, N. A., Vikhreva, O. V., Rachmanova, V. I., & Orlovskaya, D. D. (2011) · Schizophrenia Research and Treatment · doi:10.1155/2011/325789 · Cited by 177 · see citing works

Oligodendrogenesis in the normal and pathological central nervous system

Waly, B. E., Macchi, M., Cayre, M., & Durbec, P. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00145 · Cited by 176 · see citing works

Choroid-Plexus-Derived Otx2 Homeoprotein Constrains Adult Cortical Plasticity

Spatazza, J., Lee, H. H. C., Di Nardo, A. A., Tibaldi, L., Joliot, A., Hensch, T. K., & Prochiantz, A. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.05.014 · Cited by 176 · see citing works

Sulforaphane destabilizes the androgen receptor in prostate cancer cells by inactivating histone deacetylase 6

Gibbs, A., Schwartzman, J. A., Deng, V., & Alumkal, J. J. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0908908106 · Cited by 174 · see citing works

Schizophrenic autism: clinical phenomenology and pathogenetic implications.

Parnas, J., Bovet, P., & Zahavi, D. (2002) · Europe PMC (PubMed Central) · Cited by 159 · see citing works

Dysfunctional long-term potentiation-like plasticity in schizophrenia revealed by transcranial direct current stimulation

Hasan, A., Nitsche, M. A., Rein, B., Schneider-Axmann, T., Guse, B., Gruber, O., Falkai, P., & Wobrock, T. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.05.017 · Cited by 156 · see citing works

N-Acetylcysteine as an Adjunct to Risperidone for Treatment of Negative Symptoms in Patients With Chronic Schizophrenia: A Randomized, Double-Blind, Placebo-Controlled Study

Farokhnia, M., Azarkolah, A., Adinehfar, F., Khodaie-Ardakani, M.-R., Hosseini, S.-M.-R., Yekehtaz, H., Tabrizi, M., Rezaei, F., Salehi, B., Sadeghi, S.-M.-H., et al. (2013) · Clinical Neuropharmacology · doi:10.1097/wnf.0000000000000001 · Cited by 155 · see citing works

Oligodendroglial alterations and the role of microglia in white matter injury: relevance to schizophrenia

Chew, L.-J., Fusar-Poli, P., & Schmitz, T. (2013) · Developmental Neuroscience · doi:10.1159/000346157 · Cited by 154 · see citing works

Redox sensing: orthogonal control in cell cycle and apoptosis signalling

Jones, D. P. (2010) · Journal of Internal Medicine · doi:10.1111/j.1365-2796.2010.02268.x · Cited by 153 · see citing works

Diffusion tensor imaging in schizophrenia

Kyriakopoulos, M., Bargiotas, T., Barker, G. J., & Frangou, S. (2008) · European Psychiatry · doi:10.1016/j.eurpsy.2007.12.004 · Cited by 153 · see citing works

Valproate reopens critical-period learning of absolute pitch

Gervain, J., Vines, B. W., Chen, L. M., Seo, R. J., Hensch, T. K., Werker, J. F., & Young, A. H. (2013) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2013.00102 · Cited by 151 · see citing works

Deficits in parvalbumin and calbindin immunoreactive cells in the hippocampus of isolation reared rats

Harte, M., Powell, S. B., Swerdlow, N. R., Geyer, M. A., & Reynolds, G. P. (2007) · Journal of Neural Transmission · doi:10.1007/s00702-007-0627-6 · Cited by 146 · see citing works

Adolescent Onset of Cortical Disinhibition in Schizophrenia: Insights From Animal Models

O'Donnell, P. (2011) · Schizophrenia Bulletin · doi:10.1093/schbul/sbr028 · Cited by 145 · see citing works

A Neonatal Ventral Hippocampal Lesion Causes Functional Deficits in Adult Prefrontal Cortical Interneurons

Tseng, K. Y., Lewis, B. L., Hashimoto, T., Sesack, S. R., Kloc, M., Lewis, D. A., & O'Donnell, P. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4166-08.2008 · Cited by 144 · see citing works

Schizophrenia, myelination, and delayed corollary discharges: a hypothesis

Whitford, T. J., Ford, J. M., Mathalon, D. H., Kubicki, M., & Shenton, M. E. (2012) · Schizophrenia Bulletin · doi:10.1093/schbul/sbq105 · Cited by 140 · 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

Dysfunctional neural plasticity in patients with schizophrenia

Daskalakis, Z. J., Christensen, B. K., Fitzgerald, P. B., & Chen, R. (2008) · Archives of General Psychiatry · doi:10.1001/archpsyc.65.4.378 · Cited by 130 · see citing works

Decrease in parvalbumin‐expressing neurons in the hippocampus and increased phencyclidine‐induced locomotor activity in the rat methylazoxymethanol (MAM) model of schizophrenia

Penschuck, S., Flagstad, P., Didriksen, M., Leist, M., & Michael-Titus, A. T. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04536.x · Cited by 127 · see citing works

Redox Dysregulation in the Pathophysiology of Schizophrenia and Bipolar Disorder: Insights from Animal Models

Kulak, A., Steullet, P., Cabungcal, J.-H., Werge, T., Ingason, A., Cuenod, M., & Do, K. Q. (2013) · Antioxidants &amp; Redox Signaling · doi:10.1089/ars.2012.4858 · Cited by 124 · see citing works

N-acetylcysteine normalizes neurochemical changes in the glutathione-deficient schizophrenia mouse model during development

das Neves Duarte, J. M., Kulak, A., Gholam-Razaee, M. M., Cuenod, M., Gruetter, R., & Do, K. Q. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.07.035 · Cited by 124 · see citing works

Nonsteroidal Anti-Inflammatory Treatment Prevents Delayed Effects of Early Life Stress in Rats

Brenhouse, H. C., & Andersen, S. L. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.05.006 · Cited by 123 · see citing works

BSABS - Bonner Skala für die Beurteilung von Basissymptomen

Gross, G. (1987) · Springer eBooks · Cited by 119 · see citing works

Predictions, perception, and a sense of self

Picard, F., & Friston, K. J. (2014) · Neurology · doi:10.1212/wnl.0000000000000798 · Cited by 118 · see citing works

The contributions of excitotoxicity, glutathione depletion and DNA repair in chemically induced injury to neurones: exemplified with toxic effects on cerebellar granule cells

Fonnum, F., & Lock, E. A. (2003) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2003.02211.x · Cited by 117 · see citing works

Glutathione deficit impairs myelin maturation: relevance for white matter integrity in schizophrenia patients

Monin, A., Baumann, P. S., Griffa, A., Xin, L., Mekle, R., Fournier, M., Butticaz, C., Klaey, M., Cabungcal, J. H., Steullet, P., et al. (2015) · Molecular Psychiatry · doi:10.1038/mp.2014.88 · Cited by 113 · see citing works

Psychosocial stress is associated with in vivo dopamine release in human ventromedial prefrontal cortex: A positron emission tomography study using [18F]fallypride

Lataster, J., Collip, D., Ceccarini, J., Haas, D., Booij, L., van Os, J., Pruessner, J., Van Laere, K., & Myin-Germeys, I. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.07.030 · Cited by 109 · see citing works

Tracing the development of psychosis and its prevention: what can be learned from animal models

Piontkewitz, Y., Arad, M., & Weiner, I. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.04.019 · Cited by 108 · see citing works

Peripubertal Diazepam Administration Prevents the Emergence of Dopamine System Hyperresponsivity in the MAM Developmental Disruption Model of Schizophrenia

Du, Y., & Grace, A. A. (2013) · Neuropsychopharmacology · doi:10.1038/npp.2013.101 · Cited by 105 · see citing works

Parvalbumin Deficiency and GABAergic Dysfunction in Mice Lacking PGC-1α

Lucas, E. K., Markwardt, S. J., Gupta, S., Meador‐Woodruff, J. H., Lin, J. D., Overstreet‐Wadiche, L., & Cowell, R. M. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0698-10.2010 · Cited by 104 · see citing works

Prenatal stress delays inhibitory neuron progenitor migration in the developing neocortex

Stevens, H. E., Su, T., Yanagawa, Y., & Vaccarino, F. M. (2012) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2012.07.011 · Cited by 104 · see citing works

Redox State as a Central Modulator of Precursor Cell Function

Noble, M., Smith, J., Power, J., & Mayer-Pröschel, M. (2003) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2003.tb07481.x · Cited by 104 · see citing works

Dysbindin-1 mutant mice implicate reduced fast-phasic inhibition as a final common disease mechanism in schizophrenia

Carlson, G. C., Talbot, K., Halene, T. B., Gandal, M. J., Kazi, H. A., Schlosser, L., Phung, Q. H., Gur, R. E., Arnold, S. E., & Siegel, S. J. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1109625108 · Cited by 103 · see citing works

Synaptic plasticity, neural circuits, and the emerging role of altered short-term information processing in schizophrenia

Crabtree, G. W., & Gogos, J. A. (2014) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2014.00028 · Cited by 102 · see citing works

Abnormal Indices of Cell Cycle Activity in Schizophrenia and their Potential Association with Oligodendrocytes

Katsel, P., Davis, K. L., Li, C., Tan, W., Greenstein, E., Hoffman, L. B., & Haroutunian, V. H. (2008) · Neuropsychopharmacology · doi:10.1038/npp.2008.19 · Cited by 102 · see citing works

Critical period for acoustic preference in mice

Yang, E.-J., Lin, E. W., & Hensch, T. K. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1200705109 · Cited by 102 · see citing works

Transcranial magnetic stimulation: A neuroscientific probe of cortical function in schizophrenia

McClintock, S. M., Freitas, C., Oberman, L., Lisanby, S. H., & Pascual-Leone, A. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.02.031 · Cited by 101 · see citing works

Correlations between peripheral polyunsaturated fatty acid content and in vivo membrane phospholipid metabolites

Yao, J. K., Stanley, J. A., Reddy, R. D., Keshavan, M. S., & Pettegrew, J. W. (2002) · Biological Psychiatry · doi:10.1016/s0006-3223(02)01397-5 · Cited by 100 · see citing works

Clock Genes Control Cortical Critical Period Timing

Kobayashi, Y., Ye, Z., & Hensch, T. K. (2015) · Neuron · doi:10.1016/j.neuron.2015.02.036 · Cited by 99 · see citing works

N-acetyl Cysteine Treatment Rescues Cognitive Deficits Induced by Mitochondrial Dysfunction in G72/G30 Transgenic Mice

Otte, D.-M., Sommersberg, B., Kudin, A., Guerrero, C., Albayram, Ö., Filiou, M. D., Frisch, P., Yilmaz, Ö., Drews, E., Turck, C. W., et al. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2011.109 · Cited by 97 · see citing works

Epigenetic treatments of adult rats promote recovery from visual acuity deficits induced by long‐term monocular deprivation

Silingardi, D., Scali, M., Belluomini, G., & Pizzorusso, T. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07261.x · Cited by 96 · see citing works

Glutathione deficit during development induces anomalies in the rat anterior cingulate GABAergic neurons: Relevance to schizophrenia

Cabungcal, J.-H., Nicolas, D., Kraftsik, R., Cuénod, M., Do, K. Q., & Hornung, J.-P. (2006) · Neurobiology of Disease · doi:10.1016/j.nbd.2006.01.003 · Cited by 96 · see citing works

Lipopolysaccharide-induced peroxisomal dysfunction exacerbates cerebral white matter injury: attenuation by N-acetyl cysteine

Paintlia, M. K., Paintlia, A. S., Contreras, M. A., Singh, I., & Singh, A. K. (2008) · Experimental Neurology · doi:10.1016/j.expneurol.2007.12.011 · Cited by 93 · see citing works

Prolonged Period of Cortical Plasticity upon Redox Dysregulation in Fast-Spiking Interneurons

Morishita, H., Cabungcal, J.-H., Chen, Y., Do, K. Q., & Hensch, T. K. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.12.026 · Cited by 92 · see citing works

Blocking PirB up-regulates spines and functional synapses to unlock visual cortical plasticity and facilitate recovery from amblyopia

Bochner, D., Sapp, R. W., Steinmetz, J. D., Zhang, S., Lee, H., Djurisic, M. R., Syken, J., Dan, Y., & Shatz, C. J. (2014) · Science Translational Medicine · doi:10.1126/scitranslmed.3010157 · Cited by 92 · see citing works

Behavioral phenotyping of glutathione-deficient mice: Relevance to schizophrenia and bipolar disorder

Kulak, A., Cuenod, M., & Do, K. Q. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.10.020 · Cited by 90 · see citing works

Chemically Diverse Toxicants Converge on Fyn and c-Cbl to Disrupt Precursor Cell Function

Li, Z., Dong, T., Pröschel, C., & Noble, M. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050035 · Cited by 90 · see citing works

Temporal Dynamics of Parvalbumin-Expressing Axo-axonic and Basket Cells in the Rat Medial Prefrontal Cortex<i>In Vivo</i>

Massi, L., Lagler, M., Hartwich, K., Borhegyi, Z., Somogyi, P., & Klausberger, T. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.3475-12.2012 · Cited by 88 · see citing works

Hypoxia-Induced Developmental Delays of Inhibitory Interneurons Are Reversed by Environmental Enrichment in the Postnatal Mouse Forebrain

Komitova, M., Xenos, D., Salmaso, N., May Tran, K., Brand, T., Schwartz, M. L., Ment, L., & Vaccarino, F. M. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.5286-12.2013 · Cited by 88 · see citing works

Role of Endogenous Glutathione in the Oxidation of Dopamine

Rabinovic, A. D., & Hastings, T. G. (1998) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1998.71052071.x · Cited by 82 · see citing works

Glutathione precursor N-acetyl-cysteine modulates EEG synchronization in schizophrenia patients: a double-blind, randomized, placebo-controlled trial

Carmeli, C., Knyazeva, M. G., Cuénod, M., & Do, K. Q. (2012) · PLoS ONE · doi:10.1371/journal.pone.0029341 · Cited by 81 · see citing works

Mouse resident microglia: Isolation and characterization of immunoregulatory properties with naïve CD4 and CD8 T‐cells

Havenith, C. E. G., Askew, D., & Walker, W. S. G. (1998) · Glia · doi:10.1002/(sici)1098-1136(199804)22:4 · Cited by 80 · see citing works

Prefrontal membrane phospholipid metabolism of child and adolescent offspring at risk for schizophrenia or schizoaffective disorder: an in vivo 31P MRS study

Keshavan, M. S., Stanley, J. A., Montrose, D. M., Minshew, N. J., & Pettegrew, J. W. (2003) · Molecular Psychiatry · doi:10.1038/sj.mp.4001325 · Cited by 76 · see citing works

Omega-3 prevents behavior response and brain oxidative damage in the ketamine model of schizophrenia

Zugno, A. I., Chipindo, H. L., Volpato, A. M., Budni, J., Steckert, A. V., de Oliveira, M. B., Heylmann, A. S., Silveira, F. D. R., Mastella, G. A., Maravai, S. G., et al. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.11.049 · Cited by 74 · see citing works

Beneficial effects of<i>N-</i>acetylcysteine in treatment resistant schizophrenia

Bulut, M., Savas, H. A., Altindag, A., Virit, O., & Dalkilic, A. (2009) · The World Journal of Biological Psychiatry · doi:10.1080/15622970903144004 · Cited by 73 · see citing works

Schizophrenia-associated reduction of neuronal and oligodendrocyte numbers in the anterior principal thalamic nucleus

Byne, W. M., KIDKARDNEE, S., TATUSOV, A., Yiannoulos, G., Buchsbaum, M. S., & HAROUTUNIAN, V. (2006) · Schizophrenia Research · doi:10.1016/j.schres.2006.03.029 · Cited by 73 · see citing works

Plasticity of Binocularity and Visual Acuity Are Differentially Limited by Nogo Receptor

Stephany, C.-É., Chan, L. L.-H., Parivash, S. N., Dorton, H. M., Piechowicz, M., Qiu, S., & McGee, A. W. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0545-14.2014 · Cited by 71 · see citing works

Deletion of selenoprotein P results in impaired function of parvalbumin interneurons and alterations in fear learning and sensorimotor gating

Pitts, M. W., Raman, A. V., Hashimoto, A. C., Todorovic, C., Nichols, R. A., & Berry, M. J. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.02.017 · Cited by 67 · see citing works

Load Dependence of β and γ Oscillations Predicts Individual Capacity of Visual Attention

Rouhinen, S., Panula, J. M., Palva, J. M., & Palva, S. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1666-13.2013 · Cited by 66 · see citing works

Electrophysiological assessment of auditory stimulus-specific plasticity in schizophrenia

Mears, R. P., & Spencer, K. M. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.12.016 · Cited by 64 · see citing works

A fundamental role for hippocampal parvalbumin in the dopamine hyperfunction associated with schizophrenia

Boley, A. M., Perez, S. M., & Lodge, D. J. (2014) · Schizophrenia Research · doi:10.1016/j.schres.2014.05.005 · Cited by 63 · see citing works

Neonatal lipopolysaccharide induces pathological changes in parvalbumin immunoreactivity in the hippocampus of the rat

Jenkins, T. A., Harte, M. K., Stenson, G., & Reynolds, G. P. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2009.07.014 · Cited by 61 · see citing works

Corresponding decrease in neuronal markers signals progressive parvalbumin neuron loss in MAM schizophrenia model

Gill, K. M., & Grace, A. A. (2014) · The International Journal of Neuropsychopharmacology · doi:10.1017/s146114571400056x · Cited by 60 · see citing works

Carbonic Anhydrase in Oligodendrocytes and Myelin in the Central Nervous Systema

Cammer, W. (1984) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1984.tb12376.x · Cited by 57 · see citing works

Bimodal Distribution of Polyunsaturated Fatty Acids in Schizophrenia Suggests Two Endophenotypes of the Disorder

Bentsen, H., Solberg, D. K., Refsum, H., Gran, J. M., Bøhmer, T., Torjesen, P. A., Halvorsen, O., & Lingjærde, O. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.02.011 · Cited by 56 · see citing works

Effects of the Antioxidant Sulforaphane on Hyperlocomotion and Prepulse Inhibition Deficits in Mice after Phencyclidine Administration

Shirai, Y., Fujita, Y., & Hashimoto, K. (2012) · Clinical Psychopharmacology and Neuroscience · doi:10.9758/cpn.2012.10.2.94 · Cited by 54 · see citing works

Early-Life Iron Deficiency Anemia Alters the Development and Long-Term Expression of Parvalbumin and Perineuronal Nets in the Rat Hippocampus

Callahan, L. S. N., Thibert, K. A., Wobken, J. D., & Georgieff, M. (2013) · Developmental Neuroscience · doi:10.1159/000354178 · Cited by 52 · see citing works

Age-Related Increase in the Number of Oligodendrocytes Is Dysregulated in Schizophrenia and Mood Disorders

Vm, V., & Uranova, N. A. (2011) · Schizophrenia Research and Treatment · doi:10.1155/2011/174689 · Cited by 51 · see citing works

N-acetyl cysteine reverses social isolation rearing induced changes in cortico-striatal monoamines in rats

Möller, M., du Preez, J. L., Viljoen, F. P., Berk, M., & Harvey, B. H. (2013) · Metabolic Brain Disease · doi:10.1007/s11011-013-9433-z · Cited by 48 · see citing works

Impaired GABAergic neurotransmission in schizophrenia underlies impairments in cortical gamma band oscillations

McNally, J. M., McCarley, R. W., & Brown, R. E. (2013) · Current Psychiatry Reports · doi:10.1007/s11920-012-0346-z · Cited by 47 · see citing works

Perceptual training strongly improves visual motion perception in schizophrenia

Norton, D. J., McBain, R. K., Öngür, D., & Chen, Y. (2011) · Brain and Cognition · doi:10.1016/j.bandc.2011.08.003 · Cited by 39 · see citing works

Development of GABA and calcium binding proteins immunoreactivity in the rat hippocampus following neonatal anoxia

Dell’Anna, E., Geloso, M. C., Magarelli, M., & Molinari, M. (1996) · Neuroscience Letters · doi:10.1016/0304-3940(96)12733-6 · Cited by 38 · see citing works

Quercetin and Omega 3 Ameliorate Oxidative Stress Induced by Aluminium Chloride in the Brain

Ali, H. A., Afifi, M., Abdelazim, A. M., et al. (2014) · Journal of Molecular Neuroscience · doi:10.1007/s12031-014-0232-8 · Cited by 34 · see citing works

Faster perceptual learning through excitotoxic neurodegeneration

Beste, C., Wascher, E., Dinse, H. R., & Saft, C. (2012) · Current Biology · doi:10.1016/j.cub.2012.08.012 · Cited by 33 · see citing works

Is Prophylactic Psychiatry around the Corner? Combating Adolescent Oxidative Stress for Adult Psychosis and Schizophrenia

Sawa, A., & Seidman, L. J. (2014) · Neuron · doi:10.1016/j.neuron.2014.08.028 · Cited by 31 · see citing works

Expression of Fyn, a non-receptor tyrosine kinase in prefrontal cortex from patients with schizophrenia and its correlation with clinical onset

Ohnuma, T., Kato, H., Arai, H., McKenna, P. J., & Emson, P. C. (2003) · Molecular Brain Research · doi:10.1016/s0169-328x(03)00051-2 · Cited by 29 · see citing works

Does dantrolene influence central dopamine and serotonin metabolism in the neuroleptic malignant syndrome? A retrospective study

Nisijima, K., & Ishiguro, T. (1993) · Biological Psychiatry · doi:10.1016/0006-3223(93)90277-k · Cited by 24 · see citing works

Sulforaphane protects SK‐N‐SH cells against antipsychotic‐induced oxidative stress

Mas, S., Gassó, P., Trias, G., Bernardo, M., & Lafuente, A. (2011) · Fundamental and Clinical Pharmacology · doi:10.1111/j.1472-8206.2011.00988.x · Cited by 22 · see citing works

Reduction in phencyclidine induced sensorimotor gating deficits in the rat following increased system xc − activity in the medial prefrontal cortex

Lutgen, V., Qualmann, K. J., Resch, J. M., Kong, L., Choi, S., & Baker, D. L. (2012) · Psychopharmacology · doi:10.1007/s00213-012-2926-3 · Cited by 16 · see citing works

Glutathione Deficit and Redox Dysregulation in Animal Models of Schizophrenia

Steullet, P., Cabungcal, J.-H., Kulak, A., Cuénod, M., Schenk, F., & Kim, Q. (2011) · Neuromethods · doi:10.1007/978-1-61779-157-4_7 · Cited by 4 · see citing works

(Li+)ghting the Way for a Treatment for Cognitive Impairments in Fragile X Syndrome

Bhattacharya, A., & Klann, E. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.11.017 · Cited by 1 · see citing works

Prospective and Mutual Influences of Reward Processing and Emotional Disorders in a Longitudinal Study of the Adolescent Offspring of Depressed Parents: The EPAD Cohort

Rice, F. J. (2014) · UCL Discovery (University College London) · doi:10.1016/j.biopsych.2014.03.015

Prevention and early intervention in youth mental health: is it time for a multidisciplinary and trans-diagnostic model for care?

Colizzi, M., Lasalvia, A., & Ruggeri, M. (2020) · International Journal of Mental Health Systems · doi:10.1186/s13033-020-00356-9 · Cited by 727 · see citing works

Biological embedding of childhood adversity: from physiological mechanisms to clinical implications

Berens, A. E., Jensen, S. K. G., & Nelson, C. A. (2017) · BMC Medicine · doi:10.1186/s12916-017-0895-4 · Cited by 657 · see citing works

The roles of perineuronal nets and the perinodal extracellular matrix in neuronal function

Fawcett, J. W., Oohashi, T., & Pizzorusso, T. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0196-3 · Cited by 589 · see citing works

Improving outcomes of first‐episode psychosis: an overview

Fusar‐Poli, P., McGorry, P. D., & Kane, J. M. (2017) · World Psychiatry · doi:10.1002/wps.20446 · Cited by 575 · see citing works

Critical period regulation across multiple timescales

Reh, R. K., Dias, B. G., Nelson, C. A., Kaufer, D., Werker, J. F., Kolb, B., Levine, J. D., & Hensch, T. K. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1820836117 · Cited by 492 · see citing works

Oxidative stress-driven parvalbumin interneuron impairment as a common mechanism in models of schizophrenia

Steullet, P., Cabungcal, J.-H., Coyle, J., Didriksen, M., Gill, K., Grace, A. A., Hensch, T. K., LaMantia, A.-S., Lindemann, L., Maynard, T. M., et al. (2017) · Molecular Psychiatry · doi:10.1038/mp.2017.47 · Cited by 360 · 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

The P2X7 Receptor: Central Hub of Brain Diseases

Andrejew, R., Oliveira-Giacomelli, Á., Ribeiro, D. E., Glaser, T., Arnaud-Sampaio, V. F., Lameu, C., & Ulrich, H. (2020) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2020.00124 · Cited by 162 · see citing works

Transcriptome alterations of prefrontal cortical parvalbumin neurons in schizophrenia

Enwright III, J. F., Huo, Z., Arion, D., Corradi, J. P., Tseng, G., & Lewis, D. A. (2018) · Molecular Psychiatry · doi:10.1038/mp.2017.216 · Cited by 109 · see citing works

The pathophysiological impact of stress on the dopamine system is dependent on the state of the critical period of vulnerability

Gomes, F. V., Zhu, X., & Grace, A. A. (2020) · Molecular Psychiatry · doi:10.1038/s41380-019-0514-1 · Cited by 91 · see citing works

Age-dependent and region-specific alteration of parvalbumin neurons and perineuronal nets in the mouse cerebral cortex

Ueno, H., Takao, K., Suemitsu, S., Murakami, S., Kitamura, N., Wani, K., Okamoto, M., Aoki, S., & Ishihara, T. (2018) · Neurochemistry International · doi:10.1016/j.neuint.2017.11.001 · Cited by 72 · see citing works

New Targets for Prevention of Schizophrenia: Is It Time for Interventions in the Premorbid Phase?

Seidman, L. J., & Nordentoft, M. (2015) · Schizophrenia Bulletin · doi:10.1093/schbul/sbv050 · Cited by 65 · see citing works

Schizophrenia Synaptic Pathology and Antipsychotic Treatment in the Framework of Oxidative and Mitochondrial Dysfunction: Translational Highlights for the Clinics and Treatment

De Simone, G., Mazza, B., Vellucci, L., Barone, A., Ciccarelli, M., & de Bartolomeis, A. (2023) · Antioxidants · doi:10.3390/antiox12040975 · Cited by 49 · see citing works

Genome-Wide Target Analyses of Otx2 Homeoprotein in Postnatal Cortex

Sakai, A., Nakato, R., Ling, Y., Hou, X., Hara, N., Iijima, T., Yanagawa, Y., Kuwano, R., Okuda, S., Shirahige, K., et al. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00307 · Cited by 30 · see citing works

Early Destruction of the Extracellular Matrix around Parvalbumin-Immunoreactive Interneurons in Creutzfeldt-Jakob Disease

Belichenko, P. V., Judith Miklossy, A., Belser, B., Budka, H., & Celio, M. R. (1999) · Neurobiology of Disease · doi:10.1006/nbdi.1999.0245 · Cited by 83 · see citing works

Alteration of parvalbumin expression and perineuronal nets formation in the cerebral cortex of aged mice

Ueno, H., Fujii, K., Takao, K., Suemitsu, S., Murakami, S., Kitamura, N., Wani, K., Matsumoto, Y., Okamoto, M., & Ishihara, T. (2019) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2018.12.008 · Cited by 18 · see citing works

Phosphacan immunoreactivity is associated with perineuronal nets around parvalbumin-expressing neurones

Haunsø, A., Celio, M. R., Margolis, R. K., & Menoud, P.-A. (1999) · Brain Research · doi:10.1016/s0006-8993(99)01596-6 · Cited by 52 · see citing works

P4-397 Zwitterionic compounds promote conformationally and morphologically unique changes in the Aβ peptide

McLaughlin, R. W., Kong, X., Wu, X., et al. (2004) · Neurobiology of Aging · doi:10.1016/s0197-4580(04)81954-7

THE PROTEOGLYCAN DSD‐1‐PG OCCURS IN PERINEURONAL NETS AROUND PARVALBUMIN‐IMMUNOREACTIVE INTERNEURONS OF THE RAT CEREBRAL CORTEX

Wintergerst, E. S., Faissner, A., & Celio, M. R. (1996) · International Journal of Developmental Neuroscience · doi:10.1016/0736-5748(96)00011-1 · Cited by 46 · see citing works