Oscillations and Neuronal Dynamics in Schizophrenia: The Search for Basic Symptoms and Translational Opportunities

Uhlhaas, Peter J.; Singer, Wolf

doi:10.1016/j.biopsych.2014.11.019

Cited by 243Neural dynamics and brain functionSchizophrenia research and treatmentNeuroscience and Neuropharmacology Research

Oscillations and Neuronal Dynamics in Schizophrenia: The Search for Basic Symptoms and Translational Opportunities

Uhlhaas, Peter J., Singer, Wolf·2015·Biological Psychiatry

DOI 10.1016/j.biopsych.2014.11.019

Open this paper in CoChat — free account

Abstract

A considerable body of work over the last 10 years combining noninvasive electrophysiology (electroencephalography/magnetoencephalography) in patient populations with preclinical research has contributed to the conceptualization of schizophrenia as a disorder associated with aberrant neural dynamics and disturbances in excitation/inhibition balance. This complements previous research that has largely focused on the identification of abnormalities in circumscribed brain regions and on disturbances of dopaminergic mechanisms as a cause of positive symptoms and executive deficits. In the current review, we provide an update on studies focusing on aberrant neural dynamics. First, we discuss the role of rhythmic activity in neural dynamics and in the coordination of distributed neuronal activity into organized neural states. This is followed by an overview on the current evidence for impaired neural oscillations and synchrony in schizophrenia and associated abnormalities in gamma-aminobutyric acidergic and glutamatergic neurotransmission. Finally, we discuss the distinction between fundamental symptoms, which are reflected in cognitive deficits, and psychotic, accessory symptoms, the latter likely constituting a compensatory response for aberrant neuronal dynamics.

Integrity signals

Registry

Crossref · 10.1016/j.biopsych.2014.11.019

Cites

113 of 113 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Parvalbumin- and perineuronal-net-mediated alterations are likely to contribute to dysfunction of the layer 3 parvalbumin-pyramidal cell local circuitry that generates gamma oscillations and thus to the neural basis for impairments in dorsolateral prefrontal cortex gamma oscillations seen during cognitive tasks in individuals with schizophrenia.
“Through a variety of mechanisms, PV and PNN-mediated alterations are likely to contribute to dysfunction of the layer 3 PV-PC local circuitry that generates γ-oscillations (Gonzalez-Burgos et al, 2015) and thus to the neural basis for the impairments in DLPFC γ-oscillations seen during cognitive tasks in individuals with schizophrenia (Uhlhaas and Singer, 2015).”
From Reduced Labeling of Parvalbumin Neurons and Perineuronal Nets in the Dorsolateral Prefrontal Cortex of Subjects with Schizophrenia (2016) · cites this paper as Uhlhaas and Singer, 2015

Complex brain networks: graph theoretical analysis of structural and functional systems
Bullmore, E., & Sporns, O. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2575 · Cited by 11,820 · see citing works
Effectiveness of Antipsychotic Drugs in Patients with Chronic Schizophrenia
Lieberman, J. A., Stroup, T. S., McEvoy, J. P., Swartz, M. S., Rosenheck, R. A., Perkins, D. O., Keefe, R. S. E., Davis, S. M., Davis, C. E., Lebowitz, B. D., et al. (2005) · New England Journal of Medicine · doi:10.1056/nejmoa051688 · Cited by 5,892 · see citing works
Rhythms of the Brain
Buzsáki, G. (2006) · doi:10.1093/acprof:oso/9780195301069.001.0001 · Cited by 4,873 · see citing works
The brainweb: phase synchronization and large-scale integration
Varela, F., Lachaux, J.-P., Rodriguez, E., & Martinerie, J. (2001) · Nature Reviews Neuroscience · doi:10.1038/35067550 · Cited by 4,761 · see citing works
Synaptic Modifications in Cultured Hippocampal Neurons: Dependence on Spike Timing, Synaptic Strength, and Postsynaptic Cell Type
Bi, G.-Q., & Poo, M.-M. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-24-10464.1998 · Cited by 4,744 · see citing works
Dementia Praecox or the Group of Schizophrenias
(1951) · Journal of the American Medical Association · doi:10.1001/jama.1951.02920270079043 · Cited by 4,407 · see citing works
A mechanism for cognitive dynamics: neuronal communication through neuronal coherence.
Fries, P. (2005) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2005.08.011 · Cited by 4,284 · see citing works
Oscillatory responses in cat visual cortex exhibit inter-columnar synchronization which reflects global stimulus properties
Gray, C. M., König, P., Engel, A. K., & Singer, W. (1989) · Nature · doi:10.1038/338334a0 · Cited by 4,183 · see citing works
Self-citation
Regulation of Synaptic Efficacy by Coincidence of Postsynaptic APs and EPSPs
Markram, H., Lübke, J., Frotscher, M., & Sakmann, B. (1997) · Science · doi:10.1126/science.275.5297.213 · Cited by 3,832 · see citing works
What are the functional consequences of neurocognitive deficits in schizophrenia?
(1996) · American Journal of Psychiatry · doi:10.1176/ajp.153.3.321 · Cited by 3,516 · see citing works
Psychosis as a state of aberrant salience: a framework linking biology, phenomenology and pharmacology in schizophrenia
Kapur, S. (2003) · American Journal of Psychiatry · doi:10.1176/appi.ajp.160.1.13 · Cited by 2,813 · see citing works
Mechanisms of Gamma Oscillations
Buzsáki, G., & Wang, X.-J. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062111-150444 · Cited by 2,796 · see citing works
High Gamma Power Is Phase-Locked to Theta Oscillations in Human Neocortex
Canolty, R. T., Edwards, E., Dalal, S. S., Soltani, M., Nagarajan, S. S., Kirsch, H. E., Berger, M. S., Barbaro, N. M., & Knight, R. T. (2006) · Science · doi:10.1126/science.1128115 · Cited by 2,650 · see citing works
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
Cortical inhibitory neurons and schizophrenia
Lewis, D. A., Hashimoto, T., & Volk, D. W. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1648 · Cited by 2,297 · 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
Self-citation
Physiologic Dysfunction of Dorsolateral Prefrontal Cortex in Schizophrenia
Weinberger, D. R. (1986) · Archives of General Psychiatry · doi:10.1001/archpsyc.1986.01800020020004 · Cited by 2,019 · see citing works
Neurophysiological and Computational Principles of Cortical Rhythms in Cognition
Wang, X.-J. (2010) · Physiological Reviews · doi:10.1152/physrev.00035.2008 · Cited by 1,939 · see citing works
Rethinking schizophrenia
Insel, T. R. (2010) · Nature · doi:10.1038/nature09552 · Cited by 1,783 · see citing works
Synchronized oscillations in interneuron networks driven by metabotropic glutamate receptor activation
Whittington, M. A., Traub, R. D., & Jefferys, J. G. R. (1995) · Nature · doi:10.1038/373612a0 · Cited by 1,613 · see citing works
Gamma Oscillation by Synaptic Inhibition in a Hippocampal Interneuronal Network Model
Wang, X., & Buzsáki, G. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-20-06402.1996 · Cited by 1,571 · see citing works
Different frequencies for different scales of cortical integration: from local gamma to long range alpha/theta synchronization
von Stein, A., & Sarnthein, J. (2000) · International Journal of Psychophysiology · doi:10.1016/s0167-8760(00)00172-0 · Cited by 1,553 · see citing works
Synchronization of neuronal activity in hippocampus by individual GABAergic interneurons
Cobb, S. R., Buhl, E. H., Halasy, K., Paulsen, O., & Somogyi, P. (1995) · Nature · doi:10.1038/378075a0 · Cited by 1,498 · see citing works
The Psychosis High-Risk State: A Comprehensive State-of-the-Art Review
Fusar-Poli, P., Borgwardt, S., Bechdolf, A., Addington, J., Riecher-Rössler, A., Schultze-Lutter, F., Keshavan, M., Wood, S., Ruhrmann, S., Seidman, L. J., et al. (2013) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2013.269 · Cited by 1,483 · see citing works
Modulation of Neuronal Interactions Through Neuronal Synchronization
Womelsdorf, T., Schoffelen, J.-M., Oostenveld, R., Singer, W., Desimone, R., Engel, A. K., & Fries, P. (2007) · Science · doi:10.1126/science.1139597 · Cited by 1,367 · see citing works
Self-citation
Spectral fingerprints of large-scale neuronal interactions
Siegel, M., Donner, T. H., & Engel, A. K. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3137 · Cited by 1,295 · see citing works
High-frequency, long-range coupling between prefrontal and visual cortex during attention
Gregoriou, G. G., Gotts, S. J., Zhou, H., & Desimone, R. (2009) · Science · doi:10.1126/science.1171402 · Cited by 1,194 · see citing works
Visuomotor integration is associated with zero time-lag synchronization among cortical areas
Roelfsema, P. R., Engel, A. K., König, P., & Singer, W. (1997) · Nature · doi:10.1038/385157a0 · Cited by 1,136 · see citing works
Self-citation
Dopamine neurons report an error in the temporal prediction of reward during learning
Hollerman, J. R., & Schultz, W. (1998) · Nature Neuroscience · doi:10.1038/1124 · Cited by 1,103 · see citing works
Cross-frequency coupling between neuronal oscillations
Jensen, O., & Colgin, L. L. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2007.05.003 · Cited by 991 · see citing works
Long-term Antipsychotic Treatment and Brain Volumes
Ho, B., Andreasen, N. C., Ziebell, S., Pierson, R. K., & Magnotta, V. A. (2011) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2010.199 · Cited by 975 · see citing works
Interhemispheric Synchronization of Oscillatory Neuronal Responses in Cat Visual Cortex
Engel, A. K., Peter König, B., Kreiter, A. K., & Singer, W. (1991) · Science · doi:10.1126/science.252.5009.1177 · Cited by 914 · see citing works
Self-citation
Attentional stimulus selection through selective synchronization between monkey visual areas
Bosman, C. A., Schoffelen, J.-M., Brunet, N., Oostenveld, R., Bastos, A. M., Womelsdorf, T., Rubehn, B., Stieglitz, T., De Weerd, P., & Fries, P. (2012) · Neuron · doi:10.1016/j.neuron.2012.06.037 · Cited by 720 · see citing works
The metastable brain
Tognoli, E., & Kelso, J. A. S. (2014) · Neuron · doi:10.1016/j.neuron.2013.12.022 · Cited by 718 · see citing works
Schizophrenia, neuroimaging and connectomics
Fornito, A., Zalesky, A., Pantelis, C., & Bullmore, E. T. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.12.090 · Cited by 716 · see citing works
Impaired hippocampal–prefrontal synchrony in a genetic mouse model of schizophrenia
Sigurdsson, T., Stark, K. L., Karayiorgou, M., Gogos, J. A., & Gordon, J. A. (2010) · Nature · doi:10.1038/nature08855 · Cited by 702 · see citing works
Development and plasticity of cortical processing architectures
Singer, W. (1995) · Science · doi:10.1126/science.270.5237.758 · Cited by 669 · see citing works
Self-citation
Gamma frequency-range abnormalities to auditory stimulation in schizophrenia
Kwon, J. S., O'Donnell, B. F., Wallenstein, G. V., Greene, R. W., Hirayasu, Y., Nestor, P. G., Hasselmo, M. E., Potts, G. F., Shenton, M. E., & McCarley, R. W. (1999) · Archives of General Psychiatry · doi:10.1001/archpsyc.56.11.1001 · Cited by 654 · see citing works
Abnormal neural synchrony in schizophrenia
Spencer, K. M., Nestor, P. G., Niznikiewicz, M. A., Salisbury, D. F., Shenton, M. E., & McCarley, R. W. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-19-07407.2003 · Cited by 624 · see citing works
Untangling cross-frequency coupling in neuroscience
Aru, J., Aru, J., Priesemann, V., Wibral, M., Lana, L., Pipa, G., Singer, W., & Vicente, R. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.08.002 · Cited by 612 · see citing works
Self-citation
Oscillatory synchronization in large-scale cortical networks predicts perception
Hipp, J. F., Engel, A. K., & Siegel, M. (2011) · Neuron · doi:10.1016/j.neuron.2010.12.027 · Cited by 599 · 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
Self-citation
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 Hypofunction, Parvalbumin-Positive Neurons, and Cortical Gamma Oscillations in Schizophrenia
Gonzalez-Burgos, G., & Lewis, D. A. (2012) · Schizophrenia Bulletin · doi:10.1093/schbul/sbs010 · Cited by 478 · see citing works
Complementary Roles of Cholecystokinin- and Parvalbumin-Expressing GABAergic Neurons in Hippocampal Network Oscillations
Klausberger, T., Marton, L. F., O'Neill, J., Huck, J. H. J., Dalezios, Y., Fuentealba, P., Suen, W. Y., Papp, E., Kaneko, T., Watanabe, M., et al. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.3269-05.2005 · Cited by 469 · 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
Conserved regional patterns of GABA-related transcript expression in the neocortex of subjects with schizophrenia
Hashimoto, T., Bazmi, H. H., Mirnics, K., Wu, Q., Sampson, A. R., & Lewis, D. A. (2008) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2007.07081223 · Cited by 457 · see citing works
An oscillatory mechanism for prioritizing salient unattended stimuli
Jensen, O. B., Bonnefond, M., & Rufin Vanrullen, A. (2012) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2012.03.002 · Cited by 449 · see citing works
Rapid Neocortical Dynamics: Cellular and Network Mechanisms
Haider, B., & McCormick, D. A. (2009) · Neuron · doi:10.1016/j.neuron.2009.04.008 · Cited by 441 · see citing works
Synchronous Oscillatory Neural Ensembles for Rules in the Prefrontal Cortex
Buschman, T. J., Denovellis, E. L., Diogo, C., Bullock, D. H., & Miller, E. K. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.029 · Cited by 428 · see citing works
Content-Specific Fronto-Parietal Synchronization During Visual Working Memory
Salazar, R. F., Dotson, N. M., Bressler, S. L., & Gray, C. M. (2012) · Science · doi:10.1126/science.1224000 · Cited by 420 · see citing works
N-methyl-d-aspartate (NMDA) receptor dysfunction or dysregulation: The final common pathway on the road to schizophrenia?
Kantrowitz, J. T., & Javitt, D. C. (2010) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2010.04.006 · Cited by 397 · see citing works
SYNCHRONOUS ACTIVITY IN THE VISUAL SYSTEM
Usrey, W. M., & Reid, R. C. (1999) · Annual Review of Physiology · doi:10.1146/annurev.physiol.61.1.435 · Cited by 369 · see citing works
The development of neural synchrony reflects late maturation and restructuring of functional networks in humans
Uhlhaas, P. J., Roux, F., Singer, W., Haenschel, C., Sireteanu, R., & Rodriguez, E. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0900390106 · Cited by 356 · see citing works
Self-citation
Schizotaxia Revisited
Meehl, P. E. (1989) · Archives of General Psychiatry · doi:10.1001/archpsyc.1989.01810100077015 · Cited by 352 · see citing works
Dynamic circuit motifs underlying rhythmic gain control, gating and integration
Womelsdorf, T., Valiante, T. A., Sahin, N. T., Miller, K. J., & Tiesinga, P. (2014) · Nature Neuroscience · doi:10.1038/nn.3764 · Cited by 341 · see citing works
Dynamical relaying can yield zero time lag neuronal synchrony despite long conduction delays
Vicente, R., Gollo, L. L., Mirasso, C. R., Fischer, I., & Pipa, G. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0809353105 · Cited by 341 · see citing works
Dopamine Modulation of Prefrontal Cortical Interneurons Changes during Adolescence
Tseng, K.-Y., & O'Donnell, P. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhl034 · Cited by 339 · see citing works
Long-range-projecting GABAergic neurons modulate inhibition in hippocampus and entorhinal cortex
Melzer, S., Michael, M., Caputi, A., Eliava, M., Fuchs, E. C., Whittington, M. A., & Monyer, H. (2012) · Science · doi:10.1126/science.1217139 · Cited by 333 · see citing works
Gamma Power Is Phase-Locked to Posterior Alpha Activity
Osipova, D. V., Hermes, D., & Jensen, O. B. (2008) · PLoS ONE · doi:10.1371/journal.pone.0003990 · Cited by 329 · see citing works
Postnatal maturation of the dopaminergic innervation of monkey prefrontal and motor cortices: A tyrosine hydroxylase immunohistochemical analysis
Rosenberg, D. R., & Lewis, D. A. (1995) · Journal of Comparative Neurology · doi:10.1002/cne.903580306 · Cited by 319 · see citing works
N-Methyl d-Aspartate Receptor Antagonists Ketamine and MK-801 Induce Wake-Related Aberrant γ Oscillations in the Rat Neocortex
Pinault, D. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2007.10.006 · Cited by 315 · see citing works
Subjective Symptoms of Schizophrenia in Research and the Clinic: The Basic Symptom Concept
Schultze-Lutter, F. (2008) · Schizophrenia Bulletin · doi:10.1093/schbul/sbn139 · Cited by 315 · see citing works
Postnatal development of monoamine content and synthesis in the cerebral cortex of rhesus monkeys
Goldman‐Rakic, P. S., & Brown, R. M. (1982) · Developmental Brain Research · doi:10.1016/0165-3806(82)90146-8 · Cited by 283 · see citing works
Gamma and delta neural oscillations and association with clinical symptoms under subanesthetic ketamine
Hong, L. E., Summerfelt, A., Buchanan, R. W., O'Donnell, P., Thaker, G. K., Weiler, M. A., & Lahti, A. C. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2009.168 · Cited by 274 · see citing works
The assessment of neuropsychological functioning in schizophrenia
Reichenberg, A. (2010) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2010.12.3/areichenberg · Cited by 270 · see citing works
A Disappearing Heritage: The Clinical Core of Schizophrenia
Parnas, J. (2011) · Schizophrenia Bulletin · doi:10.1093/schbul/sbr081 · Cited by 270 · see citing works
Neurocognitive growth charting in psychosis spectrum youths.
Gur, R., Calkins, M., Satterthwaite, T., Ruparel, K., Bilker, W., Moore, T. M., Savitt, A. P., Hakonarson, H., & Gur, R. E. (2014) · JAMA psychiatry · doi:10.1001/jamapsychiatry.2013.4190 · Cited by 247 · see citing works
Effect of Bitopertin, a Glycine Reuptake Inhibitor, on Negative Symptoms of Schizophrenia
Umbricht, D., Alberati, D., Martin‐Facklam, M., Borroni, E., Youssef, E. A., Ostland, M., Wallace, T. L., Knoflach, F., Dorflinger, E. E., Wettstein, J. G., et al. (2014) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2014.163 · Cited by 234 · see citing works
Perceptual Organization in Schizophrenia Spectrum Disorders: Empirical Research and Theoretical Implications.
Uhlhaas, P. J., & Silverstein, S. M. (2005) · Psychological Bulletin · doi:10.1037/0033-2909.131.4.618 · Cited by 233 · see citing works
Self-citation
Cognitive Behavioral Therapy for Subjects at Ultrahigh Risk for Developing Psychosis: A Randomized Controlled Clinical Trial
van der Gaag, M., Nieman, D. H., Rietdijk, J., Dragt, S., Ising, H. K., Klaassen, R. M. C., Koeter, M., Cuijpers, P., Wunderink, L., & Linszen, D. H. (2012) · Schizophrenia Bulletin · doi:10.1093/schbul/sbs105 · Cited by 209 · 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
A Class of GABAergic Neurons in the Prefrontal Cortex Sends Long-Range Projections to the Nucleus Accumbens and Elicits Acute Avoidance Behavior
Lee, A. T., Vogt, D. L., Rubenstein, J. L. R., & Sohal, V. S. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1157-14.2014 · Cited by 202 · see citing works
A new look at gamma? High- (>60 Hz) γ-band activity in cortical networks: Function, mechanisms and impairment
Uhlhaas, P. J., Pipa, G., Neuenschwander, S., Wibral, M., & Singer, W. (2010) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2010.10.004 · Cited by 198 · see citing works
Self-citation
Cell Type-Specific Development of NMDA Receptors in the Interneurons of Rat Prefrontal Cortex
Wang, H.-X., & Gao, W. (2009) · Neuropsychopharmacology · doi:10.1038/npp.2009.20 · Cited by 198 · see citing works
Basic Symptoms and the Prediction of First-Episode Psychosis
Schultze‐Lutter, F., Ruhrmann, S., Fusar‐Poli, P., Bechdolf, A., SCHIMMELMANN, B. G., & Klosterkötter, J. (2012) · Current Pharmaceutical Design · doi:10.2174/138161212799316064 · Cited by 185 · see citing works
Hierarchical Organization of Gamma and Theta Oscillatory Dynamics in Schizophrenia
Kirihara, K., Rissling, A. J., Swerdlow, N. R., BRAFF, D. L., & Light, G. A. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.01.016 · Cited by 184 · see citing works
Event-related theta oscillations during working memory tasks in patients with schizophrenia and healthy controls
Schmiedt‐Fehr, C., Brand, A., Hildebrandt, H., & Basar-Eroglu, C. (2005) · Cognitive Brain Research · doi:10.1016/j.cogbrainres.2005.09.015 · Cited by 181 · see citing works
The Development of Neural Synchrony and Large-Scale Cortical Networks During Adolescence: Relevance for the Pathophysiology of Schizophrenia and Neurodevelopmental Hypothesis
Uhlhaas, P. J., & Singer, W. (2011) · Schizophrenia Bulletin · doi:10.1093/schbul/sbr034 · Cited by 176 · see citing works
Self-citation
A randomized clinical trial of MK-0777 for the treatment of cognitive impairments in people with schizophrenia
Buchanan, R. W., Keefe, R. S. E., Lieberman, J. A., Barch, D. M., Csernansky, J. G., Goff, D. C., Gold, J. M., Green, M. F., Jarskog, L. F., Javitt, D. C., et al. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.09.052 · Cited by 172 · see citing works
The Phase of Thalamic Alpha Activity Modulates Cortical Gamma-Band Activity: Evidence from Resting-State MEG Recordings
Roux, F., Wibral, M., Singer, W., Aru, J., & Uhlhaas, P. J. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.5778-12.2013 · Cited by 169 · see citing works
Self-citation
Reduced Natural Oscillatory Frequency of Frontal Thalamocortical Circuits in Schizophrenia
Ferrarelli, F., Sarasso, S., Bodien, Y. G., Riedner, B. A., Peterson, M. J., Bellesi, M., Massimini, M., Postle, B. R., & Tononi, G. (2012) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2012.147 · Cited by 163 · see citing works
Region-Specific Changes in Gamma and Beta2 Rhythms in NMDA Receptor Dysfunction Models of Schizophrenia
Roopun, A. K., Cunningham, M. O., Racca, C., Alter, K., Traub, R. D., & Whittington, M. A. (2008) · Schizophrenia Bulletin · doi:10.1093/schbul/sbn059 · Cited by 163 · see citing works
The role of negative symptoms and cognitive dysfunction in schizophrenia outcome
Tamminga, C. A., Buchanan, R. W., & Gold, J. M. (1998) · International Clinical Psychopharmacology · doi:10.1097/00004850-199803003-00004 · Cited by 162 · see citing works
Baseline gamma power during auditory steady-state stimulation in schizophrenia
M. Spencer, K. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2011.00190 · Cited by 155 · see citing works
Protracted Developmental Trajectories of GABAA Receptor α1 and α2 Subunit Expression in Primate Prefrontal Cortex
Hashimoto, T., Nguyen, Q. L., Rotaru, D., Keenan, T., Arion, D., Beneyto, M., Gonzalez-Burgos, G., & Lewis, D. A. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.01.004 · Cited by 151 · see citing works
Abnormalities of Neuronal Oscillations and Temporal Integration to Low- and High-Frequency Auditory Stimulation in Schizophrenia
Hamm, J. P., Gilmore, C. S., Natalie, P., Sponheim, S. R., & Clementz, B. A. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.11.021 · Cited by 150 · see citing works
Schizophrenia and epilepsy: Is there a shared susceptibility?
Cascella, N. G., Schretlen, D. J., & Sawa, A. (2009) · Neuroscience Research · doi:10.1016/j.neures.2009.01.002 · Cited by 146 · see citing works
Deficits in high- (>60 Hz) gamma-band oscillations during visual processing in schizophrenia
Grützner, C., Wibral, M., Sun, L., Rivolta, D., Singer, W., Maurer, K., & Uhlhaas, P. J. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00088 · Cited by 140 · see citing works
Self-citation
Early Recognition and Disease Prediction in the At-Risk Mental States for Psychosis Using Neurocognitive Pattern Classification
Koutsouleris, N., Davatzikos, C. A., Ronald Bottlender, A., Patschurek‐Kliche, K., Scheuerecker, J., Decker, P., Christian Gaser, B., Möller, H., & Meisenzahl, E. M. (2011) · Schizophrenia Bulletin · doi:10.1093/schbul/sbr037 · Cited by 132 · see citing works
Acute D2 receptor blockade induces rapid, reversible remodeling in human cortical-striatal circuits
Tost, H., Braus, D. F., Hakimi, S., Ruf, M., Vollmert, C., Höhn, F., & Meyer‐Lindenberg, A. (2010) · Nature Neuroscience · doi:10.1038/nn.2572 · Cited by 127 · see citing works
Early Cognitive Experience Prevents Adult Deficits in a Neurodevelopmental Schizophrenia Model
Lee, H., Dvorak, D., Kao, H.-Y., Duffy, Á. M., Scharfman, H. E., & Fenton, A. A. (2012) · Neuron · doi:10.1016/j.neuron.2012.06.016 · Cited by 122 · see citing works
Magnetoencephalographic gamma power reduction in patients with schizophrenia during resting condition
Rutter, L. A., Carver, F. W., Holroyd, T., Nadar, S. R., Mitchell-Francis, J., Apud, J. A., Weinberger, D. R., & Coppola, R. (2009) · Human Brain Mapping · doi:10.1002/hbm.20746 · Cited by 116 · 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
Evidence for dysregulated high-frequency oscillations during sensory processing in medication-naïve, first episode schizophrenia
Sun, L., Castellanos, N., Grützner, C., Koethe, D., Rivolta, D., Wibral, M., Kranaster, L., Singer, W., Leweke, M. F., & Uhlhaas, P. J. (2013) · Schizophrenia Research · doi:10.1016/j.schres.2013.08.023 · Cited by 96 · see citing works
Self-citation
The functional consequences of cortical circuit abnormalities on gamma oscillations in schizophrenia: insights from computational modeling
Spencer, K. (2009) · Frontiers in Human Neuroscience · doi:10.3389/neuro.09.033.2009 · Cited by 96 · see citing works
Hyperdopaminergia and NMDA Receptor Hypofunction Disrupt Neural Phase Signaling
Dzirasa, K., Ramsey, A. J., Takahashi, D. Y., Stapleton, J. R., Potes, J. M., Williams, J. K., Gainetdinov, R. R., Sameshima, K., Caron, M. G., & Nicolelis, M. A. L. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.1773-09.2009 · Cited by 95 · see citing works
NMDA antagonists recreate signal-to-noise ratio and timing perturbations present in schizophrenia
Saunders, J. A., Gandal, M. J., & Siegel, S. J. (2012) · Neurobiology of Disease · doi:10.1016/j.nbd.2011.12.049 · Cited by 89 · see citing works
Frontal areas contribute to reduced global coordination of resting-state gamma activities in drug-naïve patients with schizophrenia
Kikuchi, M., Hashimoto, T., Nagasawa, T., Hirosawa, T., Minabe, Y., Yoshimura, M., Strik, W., Dierks, T., & Koenig, T. (2011) · Schizophrenia Research · doi:10.1016/j.schres.2011.06.003 · Cited by 74 · see citing works
Prior Antipsychotic Drug Treatment Prevents Response to Novel Antipsychotic Agent in the Methylazoxymethanol Acetate Model of Schizophrenia
Gill, K. M., Cook, J. M., Poe, M. M., & Grace, A. A. (2014) · Schizophrenia Bulletin · doi:10.1093/schbul/sbt236 · Cited by 73 · see citing works
Altered Glutamatergic and GABAergic Mechanisms in the Cingulate Cortex of the Schizophrenic Brain
Benes, F. M. (1995) · Archives of General Psychiatry · doi:10.1001/archpsyc.1995.03950240033007 · Cited by 72 · see citing works
Reduced gamma-band coherence to distorted feedback during speech when what you say is not what you hear
Ford, J. M., GRAY, M., Faustman, W. O., Heinks, T., & Mathalon, D. H. (2005) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2005.03.002 · Cited by 71 · see citing works
Dopamine D4 Receptor Activation Increases Hippocampal Gamma Oscillations by Enhancing Synchronization of Fast-Spiking Interneurons
Andersson, R., Johnston, A. D., & Fisahn, A. (2012) · PLoS ONE · doi:10.1371/journal.pone.0040906 · Cited by 58 · see citing works
Alterations of the early auditory evoked gamma-band response in first-degree relatives of patients with schizophrenia: Hints to a new intermediate phenotype
Leicht, G., Karch, S., Karamatskos, E., Giegling, I., Möller, H., Hegerl, U., Pogarell, O. M., Rujescu, D., & Mulert, C. (2010) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2010.10.002 · Cited by 56 · see citing works
Are oscillatory brain responses generally reduced in schizophrenia during long sustained attentional processing?
Başar‐Eroğlu, C., Schmiedt‐Fehr, C., Mathes, B., Zimmermann, J., & Brand, A. (2008) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2008.07.004 · Cited by 53 · see citing works
Monoamines block kainate‐ and carbachol‐induced γ‐oscillations but augment stimulus‐induced γ‐oscillations in rat hippocampus in vitro
Wójtowicz, A. M., van den Boom, L., Chakrabarty, A., Maggio, N., Haq, R. U., Behrens, C., & Heinemann, U. (2009) · Hippocampus · doi:10.1002/hipo.20508 · Cited by 52 · see citing works
Untangling cross-frequency coupling in neurosciencePreprint
Aru, J., Aru, J., Priesemann, V., et al. (2014) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/005926 · Cited by 41 · see citing works
Appraisals and responses to experimental symptom analogues in clinical and nonclinical individuals with psychotic experiences
Ward, T. A., Gaynor, K. J., Hunter, M. D., Woodruff, P. W. R., Garety, P. A., & Peters, E. R. (2014) · Schizophrenia Bulletin · doi:10.1093/schbul/sbt094 · Cited by 38 · see citing works
Serotonergic modulation of carbachol-induced rhythmic activity in hippocampal slices
KRAUSE, M., & JIA, Y. (2005) · Neuropharmacology · doi:10.1016/j.neuropharm.2004.10.011 · Cited by 30 · see citing works
Dynamics of alpha oscillations elucidate facial affect recognition in schizophrenia
Popov, T. G., Rockstroh, B. S., Popova, P., Carolus, A. M., & Miller, G. A. (2013) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-013-0194-2 · Cited by 25 · see citing works
Stabilization of visual responses through cholinergic activation
Rodríguez, R., Kallenbach, U., Singer, W., & Munk, M. H. J. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.10.059 · Cited by 21 · see citing works
Self-citation
Circuits and brain rhythms in schizophrenia: a wealth of convergent targets
Whittington, M. A., Roopun, A. K., Traub, R. D., & Davies, C. H. (2011) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2011.04.010 · Cited by 17 · see citing works
[Basic schizophrenic disorders].
Süllwold, L., & Huber, G. (1986) · PubMed · Cited by 17 · see citing works

Flagged first, then by citations

Sorted by citations

Social cognition in schizophrenia
Green, M. F., Horan, W. P., & Lee, J. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn4005 · Cited by 1,159 · see citing works
Altering the course of schizophrenia: progress and perspectives
Millan, M. J., Andrieux, A., Bartzokis, G., Cadenhead, K., Dazzan, P., Fusar-Poli, P., Gallinat, J., Giedd, J., Grayson, D. R., Heinrichs, M., et al. (2016) · Nature Reviews Drug Discovery · doi:10.1038/nrd.2016.28 · Cited by 516 · see citing works
Self-citation
Prefrontal Cortex and Social Cognition in Mouse and Man
Bicks, L. K., Koike, H., Akbarian, S., & Morishita, H. (2015) · Frontiers in Psychology · doi:10.3389/fpsyg.2015.01805 · Cited by 491 · see citing works
White matter and cognition: making the connection
Filley, C. M., & Fields, R. D. (2016) · Journal of Neurophysiology · doi:10.1152/jn.00221.2016 · Cited by 445 · see citing works
Oscillatory Dynamics of Prefrontal Cognitive Control
Helfrich, R. F., & Knight, R. T. (2016) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2016.09.007 · Cited by 307 · see citing works
Searching for Cross-Diagnostic Convergence: Neural Mechanisms Governing Excitation and Inhibition Balance in Schizophrenia and Autism Spectrum Disorders
Foss‐Feig, J. H., Adkinson, B. D., Ji, J. L., Yang, G., Srihari, V. H., McPartland, J. C., Krystal, J. H., Murray, J. D., & Anticevic, A. (2017) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.03.005 · Cited by 310 · see citing works
The 40-Hz Auditory Steady-State Response in Patients With Schizophrenia: A Meta-analysis
Thuné, H., Recasens, M., & Uhlhaas, P. J. (2016) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2016.2619 · Cited by 292 · see citing works
Self-citation
Prefrontal Cortex Development in Health and Disease: Lessons from Rodents and Humans
Chini, M., & Hanganu-Opatz, I. L. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2020.10.017 · Cited by 253 · see citing works
Two distinct neuroanatomical subtypes of schizophrenia revealed using machine learning
Chand, G. B., Dwyer, D., Erus, G., Sotiras, A., Varol, E., Srinivasan, D., Doshi, J. J., Pomponio, R., Pigoni, A., Dazzan, P., et al. (2020) · Brain · doi:10.1093/brain/awaa025 · Cited by 271 · see citing works
Integrating the Neurodevelopmental and Dopamine Hypotheses of Schizophrenia and the Role of Cortical Excitation-Inhibition Balance.
Howes, O., & Shatalina, E. (2022) · Biological Psychiatry · doi:10.1016/j.biopsych.2022.06.017 · Cited by 233 · 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
Electrophysiological Brain Connectivity: Theory and Implementation
He, B., Laura Astolfi, A., Valdes-Sosa, P. A., Marinazzo, D., Palva, S., Bénar, C., Michel, C. M., & Koenig, T. W. (2019) · IEEE Transactions on Biomedical Engineering · doi:10.1109/tbme.2019.2913928 · Cited by 236 · see citing works
Lasting EEG/MEG Aftereffects of Rhythmic Transcranial Brain Stimulation: Level of Control Over Oscillatory Network Activity
Veniero, D., Vossen, A. Y., Groß, J., & Thut, G. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00477 · Cited by 202 · see citing works
Impaired Tuning of Neural Ensembles and the Pathophysiology of Schizophrenia: A Translational and Computational Neuroscience Perspective
Krystal, J. H., Anticevic, A., Yang, G., Dragoi, G., Driesen, N. R., Wang, X., & Murray, J. D. (2017) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.01.004 · Cited by 195 · see citing works
Hippocampal Non-Theta-Contingent Eyeblink Classical Conditioning: A Model System for Neurobiological Dysfunction
Cicchese, J. J., & Berry, S. D. (2016) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2016.00001 · Cited by 172 · see citing works
Long-Lasting Rescue of Network and Cognitive Dysfunction in a Genetic Schizophrenia Model
Mukherjee, A., Carvalho, F., Eliez, S., & Caroni, P. (2019) · Cell · doi:10.1016/j.cell.2019.07.023 · Cited by 169 · see citing works
Acetylcholine Release in Prefrontal Cortex Promotes Gamma Oscillations and Theta–Gamma Coupling during Cue Detection
Howe, W. M., Gritton, H. J., Lusk, N. A., Roberts, E. A., Hetrick, V. L., Berke, J. D., & Sarter, M. F. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.2737-16.2017 · Cited by 147 · see citing works
Targeting Muscarinic Acetylcholine Receptors for the Treatment of Psychiatric and Neurological Disorders
Moran, S. P., Maksymetz, J., & Conn, P. J. (2019) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2019.10.007 · Cited by 137 · see citing works
The Role of Alpha Oscillations among the Main Neuropsychiatric Disorders in the Adult and Developing Human Brain: Evidence from the Last 10 Years of Research
Ippolito, G., Bertaccini, R., Tarasi, L., di Gregorio, F., Trajković, J., Battaglia, S., & Romei, V. (2022) · Biomedicines · doi:10.3390/biomedicines10123189 · Cited by 114 · see citing works
Current findings and perspectives on aberrant neural oscillations in schizophrenia
Hirano, Y., & Uhlhaas, P. J. (2021) · Psychiatry and Clinical Neurosciences · doi:10.1111/pcn.13300 · Cited by 121 · see citing works
Self-citation
Memristor‐Based Intelligent Human‐Like Neural Computing
Wang, S., Song, L., Chen, W., Wang, G., Hao, E., Li, C., Hu, Y., Pan, Y., Nathan, A., Hu, G., et al. (2022) · Advanced Electronic Materials · doi:10.1002/aelm.202200877 · Cited by 121 · see citing works
Energy deficit in parvalbumin neurons leads to circuit dysfunction, impaired sensory gating and social disability.
Inan, M., Zhao, M., Manuszak, M., Karakaya, C., Rajadhyaksha, A. M., Pickel, V. M., Schwartz, T. H., Goldstein, P. A., & Manfredi, G. (2016) · Neurobiology of Disease · doi:10.1016/j.nbd.2016.04.004 · Cited by 118 · see citing works
Examining and Modulating Neural Circuits in Psychiatric Disorders With Transcranial Magnetic Stimulation and Electroencephalography: Present Practices and Future Developments
Ferrarelli, F., & Phillips, M. L. (2021) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2020.20071050 · Cited by 119 · see citing works
Myelination of parvalbumin interneurons: a parsimonious locus of pathophysiological convergence in schizophrenia
Stedehouder, J., & Kushner, S. A. (2016) · Molecular Psychiatry · doi:10.1038/mp.2016.147 · Cited by 113 · see citing works
Mismatch negativity as a biomarker of theta band oscillatory dysfunction in schizophrenia
Javitt, D. C., Lee, M., Kantrowitz, J. T., & Martı́nez, A. (2017) · Schizophrenia Research · doi:10.1016/j.schres.2017.06.023 · Cited by 112 · see citing works
Long-Range Attention Networks: Circuit Motifs Underlying Endogenously Controlled Stimulus Selection
Womelsdorf, T., & Everling, S. (2015) · Trends in Neurosciences · doi:10.1016/j.tins.2015.08.009 · Cited by 100 · see citing works
Synchronizing Brain Rhythms to Improve Cognition
Grover, S., Nguyen, J. A., & Reinhart, R. M. G. (2020) · Annual Review of Medicine · doi:10.1146/annurev-med-060619-022857 · Cited by 96 · see citing works
Cross-hemispheric gamma synchrony between prefrontal parvalbumin interneurons supports behavioral adaptation during rule shift learning
Cho, K. K. A., Davidson, T. J., Bouvier, G., Marshall, J. D., Schnitzer, M. J., & Sohal, V. S. (2020) · Nature Neuroscience · doi:10.1038/s41593-020-0647-1 · Cited by 101 · see citing works
Converging models of schizophrenia – Network alterations of prefrontal cortex underlying cognitive impairments
Sakurai, T., Gamo, N. J., Hikida, T., Kim, S.-H., Murai, T., Tomoda, T., & Sawa, A. (2015) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2015.09.010 · Cited by 96 · see citing works
Revisiting the Basic Symptom Concept: Toward Translating Risk Symptoms for Psychosis into Neurobiological Targets
Schultze‐Lutter, F., Debbané, M., Theodoridou, A., Wood, S. J., Raballo, A., Michel, C., Schmidt, S. J., Kindler, J., Ruhrmann, S., & Uhlhaas, P. J. (2016) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2016.00009 · Cited by 94 · see citing works
Self-citation
On the Role of Theory and Modeling in Neuroscience
Levenstein, D., Alvarez, V. A., Amarasingham, A., Azab, H., Chen, Z. S., Gerkin, R. C., Hasenstaub, A. R., Iyer, R., Jolivet, R., Marzen, S., et al. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.1179-22.2022 · Cited by 96 · see citing works
The self and its prolonged intrinsic neural timescale in schizophrenia
Northoff, G., Sandsten, K. E., Nordgaard, J., Kjaer, T. W., & Parnas, J. (2021) · Schizophrenia Bulletin · doi:10.1093/schbul/sbaa083 · Cited by 91 · see citing works
Emerging evidence for astrocyte dysfunction in schizophrenia
Figueiredo, E. C. D. O., Calì, C., Petrelli, F., & Bezzi, P. (2022) · Glia · doi:10.1002/glia.24221 · Cited by 85 · see citing works
Increased MRI-based cortical grey/white-matter contrast in sensory and motor regions in schizophrenia and bipolar disorder
Jørgensen, K., Nerland, S., Norbom, L., Doan, N. T., Nesvåg, R., Mørch-Johnsen, L., Haukvik, U., Melle, I., Andreassen, O., Westlye, L., et al. (2016) · Psychological Medicine · doi:10.1017/s0033291716000593 · Cited by 82 · see citing works
Animal models of gene–environment interaction in schizophrenia: A dimensional perspective
Ayhan, Y., McFarland, R., & Pletnikov, M. V. (2015) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2015.10.002 · Cited by 81 · see citing works
Network Asynchrony Underlying Increased Broadband Gamma Power
Guyon, N., Zacharias, L. R., de Oliveira, E. F., Kim, H., Leite, J. P., Lopes‐Aguiar, C., & Carlén, M. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.2250-20.2021 · Cited by 80 · see citing works
Neural circuit dysfunction in schizophrenia: Insights from animal models
Sigurdsson, T. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.06.059 · Cited by 71 · see citing works
Predictive waves in the autism-schizophrenia continuum: A novel biobehavioral model
Tarasi, L., Trajkovic, J., Diciotti, S., di Pellegrino, G., Ferri, F., Ursino, M., & Romei, V. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.11.006 · Cited by 69 · see citing works
How to Link Brain and Experience? Spatiotemporal Psychopathology of the Lived Body
Northoff, G., & Stanghellini, G. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00172 · Cited by 74 · see citing works
Clinical applications of EEG power spectra aperiodic component analysis: A mini-review
Pani, S. M., Saba, L., & Fraschini, M. (2022) · Clinical Neurophysiology · doi:10.1016/j.clinph.2022.08.010 · Cited by 74 · see citing works
Aberrant maturation and connectivity of prefrontal cortex in schizophrenia—contribution of NMDA receptor development and hypofunction
Gao, W., Yang, S.-S., Mack, N. R., & Chamberlin, L. A. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01196-w · Cited by 70 · see citing works
It’s All in the Rhythm: The Role of Cannabinoids in Neural Oscillations and Psychosis
Skosnik, P. D., Cortes-Briones, J., & Hajós, M. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.12.011 · Cited by 71 · see citing works
Hierarchical Pathways from Sensory Processing to Cognitive, Clinical, and Functional Impairments in Schizophrenia
Koshiyama, D., Thomas, M. L., Miyakoshi, M., Joshi, Y. B., Molina, J. L., Tanaka‐Koshiyama, K., Sprock, J., BRAFF, D. L., Swerdlow, N. R., & Light, G. A. (2020) · Schizophrenia Bulletin · doi:10.1093/schbul/sbaa116 · Cited by 68 · see citing works
Whole-Brain Source-Reconstructed MEG-Data Reveal Reduced Long-Range Synchronization in Chronic Schizophrenia
Hirvonen, J., Wibral, M., Palva, J. M., Singer, W., Uhlhaas, P. J., & Palva, S. (2017) · eNeuro · doi:10.1523/eneuro.0338-17.2017 · Cited by 67 · see citing works
Self-citation
Resolving and Rescuing Developmental Miswiring in a Mouse Model of Cognitive Impairment
Chini, M., Pöpplau, J. A., Lindemann, C., Carol-Perdiguer, L., Hnida, M., Oberlander, V. C., Xu, X., Ahlbeck, J., Bitzenhofer, S. H., Mulert, C., et al. (2019) · Neuron · doi:10.1016/j.neuron.2019.09.042 · Cited by 68 · see citing works
Language deficits in schizophrenia and autism as related oscillatory connectomopathies: An evolutionary account
Murphy, E., & Benítez‐Burraco, A. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.07.029 · Cited by 64 · see citing works
A comprehensive analysis of auditory event-related potentials and network oscillations in an NMDA receptor antagonist mouse model using a novel wireless recording technology
Schuelert, N., Dorner‐Ciossek, C., Brendel, M., & Rosenbrock, H. (2018) · Physiological Reports · doi:10.14814/phy2.13782 · Cited by 58 · see citing works
Disruption of Conscious Access in Schizophrenia
Berkovitch, L., Dehaene, S., & Gaillard, R. (2017) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2017.08.006 · Cited by 60 · see citing works
Spindle activity orchestrates plasticity during development and sleep
Lindemann, C., Ahlbeck, J., Bitzenhofer, S. H., & Hanganu-Opatz, I. L. (2016) · Neural Plasticity · doi:10.1155/2016/5787423 · Cited by 59 · see citing works
40-Hz Auditory Steady-State Responses in Schizophrenia: Toward a Mechanistic Biomarker for Circuit Dysfunctions and Early Detection and Diagnosis
Grent-‘t-Jong, T., Brickwedde, M., Metzner, C., & Uhlhaas, P. J. (2023) · Biological Psychiatry · doi:10.1016/j.biopsych.2023.03.026 · Cited by 57 · see citing works
Self-citation
Impaired Midline Theta Power and Connectivity During Proactive Cognitive Control in Schizophrenia
Ryman, S. G., Cavanagh, J. F., Wertz, C. J., Shaff, N. A., Dodd, A. B., Stevens, B., Ling, J. M., Yeo, R. A., Hanlon, F. M., Bustillo, J., et al. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2018.04.021 · Cited by 56 · see citing works
22q11.2 Deletion Syndrome Is Associated With Impaired Auditory Steady-State Gamma Response
Larsen, K. M., Pellegrino, G., Birknow, M. R., Kjær, T. N., Baaré, W. F. C., Didriksen, M., Olsen, L., Werge, T. M., Mørup, M., & Siebner, H. R. (2017) · Schizophrenia Bulletin · doi:10.1093/schbul/sbx058 · Cited by 54 · see citing works
Human NMDAR autoantibodies disrupt excitatory-inhibitory balance, leading to hippocampal network hypersynchrony
Ceangă, M., Rahmati, V., Haselmann, H., Schmidl, L., Hunter, D., Brauer, A.-K., Liebscher, S., Kreye, J., Prüß, H., Groc, L., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113166 · Cited by 54 · see citing works
Bridging the Gap between Genes and Language Deficits in Schizophrenia: An Oscillopathic Approach
Murphy, E., & Benítez‐Burraco, A. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00422 · Cited by 52 · see citing works
Non-Invasive Brain Stimulation Does Not Improve Working Memory in Schizophrenia: A Meta-Analysis of Randomised Controlled Trials
Sloan, N. P., Byrne, L. K., Enticott, P. G., & Lum, J. A. G. (2020) · Neuropsychology Review · doi:10.1007/s11065-020-09454-4 · Cited by 52 · see citing works
Impaired hippocampal-dependent memory and reduced parvalbumin-positive interneurons in a ketamine mouse model of schizophrenia
Koh, M. T., Shao, Y., Sherwood, A., & Smith, D. R. (2016) · Schizophrenia Research · doi:10.1016/j.schres.2016.01.023 · Cited by 51 · see citing works
Glutamatergic Deficits in Schizophrenia – Biomarkers and Pharmacological Interventions within the Ketamine Model
Haaf, M., Leicht, G., Ćurić, S., & Mulert, C. (2018) · Current Pharmaceutical Biotechnology · doi:10.2174/1389201019666180620112528 · Cited by 51 · see citing works
Blocking NMDAR Disrupts Spike Timing and Decouples Monkey Prefrontal Circuits: Implications for Activity-Dependent Disconnection in Schizophrenia
Zick, J. L., Blackman, R. K., Crowe, D. A., Amirikian, B., DeNicola, A. L., Netoff, T. I., & Chafee, M. V. (2018) · Neuron · doi:10.1016/j.neuron.2018.05.010 · Cited by 50 · see citing works
The Physiology of Homeoprotein Transduction
Nardo, A. A. D., Fuchs, J., Joshi, R. L., Moya, K. L., & Prochiantz, A. (2018) · Physiological Reviews · doi:10.1152/physrev.00018.2017 · Cited by 41 · see citing works
The dynamics of disordered dialogue: Prefrontal, hippocampal and thalamic miscommunication underlying working memory deficits in schizophrenia
Kupferschmidt, D. A., & Gordon, J. A. (2018) · Brain and Neuroscience Advances · doi:10.1177/2398212818771821 · Cited by 44 · see citing works
A developmental redox dysregulation leads to spatio-temporal deficit of parvalbumin neuron circuitry in a schizophrenia mouse model
Cabungcal, J.-H., Steullet, P., Kraftsik, R., Cuénod, M., & Kim, Q. (2019) · Schizophrenia Research · doi:10.1016/j.schres.2019.02.017 · Cited by 45 · see citing works
Altered self-recognition in patients with schizophrenia
Sandsten, K. E., Nordgaard, J., Kjaer, T. W., Gallese, V., Ardizzi, M., Ferroni, F., Petersen, J., & Parnas, J. (2020) · Schizophrenia Research · doi:10.1016/j.schres.2020.01.022 · Cited by 44 · see citing works
Resolving the Delusion Paradox
Petrovic, P., & Sterzer, P. (2023) · Schizophrenia bulletin · doi:10.1093/schbul/sbad084 · Cited by 37 · see citing works
Investigating the neurobiology of schizophrenia and other major psychiatric disorders with Transcranial Magnetic Stimulation
Kaskie, R. E., & Ferrarelli, F. (2017) · Schizophrenia Research · doi:10.1016/j.schres.2017.04.045 · Cited by 43 · see citing works
Developmental trajectories of brain maturation and behavior: Relevance to major mental illnesses
Lockhart, S., Sawa, A., & Niwa, M. (2018) · Journal of Pharmacological Sciences · doi:10.1016/j.jphs.2018.04.008 · Cited by 45 · see citing works
The interhemispheric miscommunication theory of auditory verbal hallucinations in schizophrenia
Steinmann, S., Leicht, G., & Mulert, C. (2019) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2019.02.002 · Cited by 43 · see citing works
Loss of Parvalbumin in the Hippocampus of MAM Schizophrenia Model Rats Is Attenuated by Peripubertal Diazepam
Du, Y., & Grace, A. A. (2016) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyw065 · Cited by 43 · see citing works
Interneuron epigenomes during the critical period of cortical plasticity: Implications for schizophrenia
Morishita, H., Kundakovic, M., Bicks, L., Mitchell, A., & Akbarian, S. (2015) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2015.03.005 · Cited by 42 · see citing works
High-sucrose diets contribute to brain angiopathy with impaired glucose uptake and psychosis-related higher brain dysfunctions in mice
Hirai, S., Miwa, H., Tanaka, T., Toriumi, K., Kunii, Y., Shimbo, H., Sakamoto, T., Hino, M., Izumi, R., Nagaoka, A., et al. (2021) · Science Advances · doi:10.1126/sciadv.abl6077 · Cited by 41 · see citing works
Reduced auditory evoked gamma-band response and schizophrenia-like clinical symptoms under subanesthetic ketamine
Ćurić, S., Leicht, G., Thiebes, S., Andreou, C., Polomac, N., Eichler, I.-C., Eichler, L., Zöllner, C., Gallinat, J., Steinmann, S., et al. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-019-0328-5 · Cited by 40 · see citing works
What Can Transcranial Alternating Current Stimulation Tell Us About Brain Oscillations?
Herrmann, C. S., & Strüber, D. (2017) · Current Behavioral Neuroscience Reports · doi:10.1007/s40473-017-0114-9 · Cited by 40 · see citing works
Impaired conscious access and abnormal attentional amplification in schizophrenia
Berkovitch, L., Cul, A. D., Maheu, M., & Dehaene, S. (2018) · NeuroImage Clinical · doi:10.1016/j.nicl.2018.03.010 · Cited by 39 · see citing works
Cannabinoids and Vanilloids in Schizophrenia: Neurophysiological Evidence and Directions for Basic Research
Ruggiero, R. N., Rossignoli, M. T., Ross, J. B. D., Hallak, J. E. C., Leite, J. P., & Bueno-Júnior, L. S. (2017) · Frontiers in Pharmacology · doi:10.3389/fphar.2017.00399 · Cited by 37 · see citing works
Activation of Functional Brain Networks in Children With Psychogenic Non-epileptic Seizures
Radmanesh, M., Jalili, M., & Kozlowska, K. (2020) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2020.00339 · Cited by 35 · see citing works
State-dependent alterations in sleep/wake architecture elicited by the M4 PAM VU0467154 – Relation to antipsychotic-like drug effects
Gould, R. W., Nedelcovych, M. T., Gong, X., Tsai, E., Bubser, M., Bridges, T. M., Wood, M. R., Duggan, M. E., Brandon, N. J., Dunlop, J., et al. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2015.11.016 · Cited by 35 · see citing works
Auditory verbal hallucinations related to altered long-range synchrony of gamma-band oscillations
Steinmann, S., Leicht, G., Andreou, C., Polomac, N., & Mulert, C. (2017) · Scientific Reports · doi:10.1038/s41598-017-09253-7 · Cited by 35 · see citing works
Beta/Gamma Oscillations and Event-Related Potentials Indicate Aberrant Multisensory Processing in Schizophrenia
Balz, J., Romero, Y. R., KEIL, J. E., Krebber, M., Niedeggen, M., Gallinat, J., & Senkowski, D. (2016) · Frontiers in Psychology · doi:10.3389/fpsyg.2016.01896 · Cited by 34 · see citing works
Altered avalanche dynamics in a developmental NMDAR hypofunction model of cognitive impairment
Seshadri, S., Klaus, A., Winkowski, D. E., Kanold, P. O., & Plenz, D. (2018) · Translational Psychiatry · doi:10.1038/s41398-017-0060-z · Cited by 34 · see citing works
Abnormal functional connectivity of high-frequency rhythms in drug-naïve schizophrenia
Takahashi, T., Goto, T., Nobukawa, S., Tanaka, Y., Kikuchi, M., Higashima, M., & Wada, Y. (2017) · Clinical Neurophysiology · doi:10.1016/j.clinph.2017.11.004 · Cited by 34 · see citing works
Disorganization and cognitive impairment in schizophrenia: New insights from electrophysiological findings
Vignapiano, A., Koenig, T. W., Mucci, A., Giordano, G. M., Amodio, A., Altamura, M., Bellomo, A., Brugnoli, R., Corrivetti, G., Lorenzo, G. D., et al. (2019) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2019.03.008 · Cited by 33 · see citing works
Disturbances of novel object exploration and recognition in a chronic ketamine mouse model of schizophrenia
Hauser, M. J., Isbrandt, D., & Roeper, J. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.06.013 · Cited by 33 · see citing works
Rhythmicity of neuronal oscillations delineates their cortical and spectral architecture
Myrov, V. O., Siebenhühner, F., Juvonen, J. J., Arnulfo, G., Palva, S., & Palva, J. M. (2024) · Communications Biology · doi:10.1038/s42003-024-06083-y · Cited by 31 · see citing works
Top–Down Control of Alpha Phase Adjustment in Anticipation of Temporally Predictable Visual Stimuli
Solís‐Vivanco, R., Jensen, O. B., & Bonnefond, M. (2018) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01280 · Cited by 32 · see citing works
Brain Oscillatory Correlates of Altered Executive Functioning in Positive and Negative Symptomatic Schizophrenia Patients and Healthy Controls
Berger, B. E., Minarik, T., Griesmayr, B., Stelzig-Schöler, R., Aichhorn, W., & Sauseng, P. (2016) · Frontiers in Psychology · doi:10.3389/fpsyg.2016.00705 · Cited by 32 · see citing works
Atypical antipsychotics normalize low-gamma evoked oscillations in patients with schizophrenia
Alegre, M., Molero, P., Valencia, M., Mayner, G., Ortuño, F., & Artieda, J. (2016) · Psychiatry Research · doi:10.1016/j.psychres.2016.11.030 · Cited by 33 · see citing works
Electrophysiological assessment methodology of sensory processing dysfunction in schizophrenia and dementia of the Alzheimer type
Danjou, P., Viardot, G., Maurice, D., Garcés, P., Wams, E. J., Phillips, K. G., Bertaina‐Anglade, V., McCarthy, A. P., & Pemberton, D. J. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.09.004 · Cited by 31 · see citing works
Predictive Processing: A Circuit Approach to Psychosis
Keller, G. B., & Sterzer, P. (2024) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-100223-121214 · Cited by 47 · see citing works
Clinical utility and prospective of TMS–EEG: Updated review from an international expert group
Ziemann, U., Bai, Y., Baumer, F. M., Beck, M. M., Belardinelli, P., Belvisi, D., Bender, S., Bergmann, T. O., Bortoletto, M., Casarotto, S., et al. (2026) · Clinical Neurophysiology · doi:10.1016/j.clinph.2025.2111487 · Cited by 35 · see citing works
Abnormalities in the evoked frontal oscillatory activity of first-episode psychosis: A TMS/EEG study
Ferrarelli, F., Kaskie, R. E., Graziano, B., Reis, C. C., & Casali, A. G. (2018) · Schizophrenia Research · doi:10.1016/j.schres.2018.11.008 · Cited by 31 · see citing works
Multimodal Fingerprints of Resting State Networks as assessed by Simultaneous Trimodal MR-PET-EEG Imaging
Shah, N. J., Arrubla, J., Rajkumar, R., Farrher, E., Mauler, J., Kops, E. R., Tellmann, L., Scheins, J. J., Boers, F., Dammers, J., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-05484-w · Cited by 30 · see citing works
Neural and neuronal discoordination in schizophrenia: from ensembles through networks to symptoms
Krajcovic, B., Fajnerova, I., Horacek, J., Kelemen, E., Kubik, S., Svoboda, J., & Stuchlik, A. (2019) · Acta Physiologica · doi:10.1111/apha.13282 · Cited by 29 · see citing works
Methylphenidate Attenuates the Cognitive and Mood Alterations Observed inMbnl2Knockout Mice and Reduces Microglia Overexpression
Ramon‐Duaso, C., Gener, T., Consegal, M., Fernández-Avilés, C., Gallego, J., Castarlenas, L., Swanson, M. S., de la Torre, R., Maldonado, R. J., Puig, M. V., et al. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy164 · Cited by 29 · see citing works
Neural network dynamics underlying gamma synchronization deficits in schizophrenia
Koshiyama, D., Miyakoshi, M., Joshi, Y. B., Molina, J. L., Tanaka‐Koshiyama, K., Sprock, J., BRAFF, D. L., Swerdlow, N. R., & Light, G. A. (2020) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2020.110224 · Cited by 29 · see citing works
The novel antipsychotic cariprazine stabilizes gamma oscillations in rat hippocampal slices
Meier, M. A., Lemercier, C. E., Kulisch, C., Kiss, B., Lendvai, B., Adham, N., & Gerevich, Z. (2019) · British Journal of Pharmacology · doi:10.1111/bph.14923 · Cited by 30 · see citing works
Dopamine Is Signaled by Mid-frequency Oscillations and Boosts Output Layers Visual Information in Visual Cortex
Zaldivar, D., Goense, J. B. M., Lowe, S., Logothetis, N. K., & Panzeri, S. (2018) · Current Biology · doi:10.1016/j.cub.2017.12.006 · Cited by 28 · see citing works
Positive and Negative Symptoms in Schizophrenia Relate to Distinct Oscillatory Signatures of Sensory Gating
KEIL, J. E., Romero, Y. R., Balz, J., Henjes, M. S., & Senkowski, D. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00104 · Cited by 28 · see citing works
Cannabinoid–glutamate interactions and neural oscillations: implications for psychosis
Sherif, M. A., Cortes-Briones, J., Ranganathan, M., & Skosnik, P. D. (2017) · European Journal of Neuroscience · doi:10.1111/ejn.13800 · Cited by 27 · see citing works
Cognitive Pragmatic Rehabilitation Program in Schizophrenia: A Single Case fMRI Study
Gabbatore, I., Bosco, F. M., Geda, E., Gastaldo, L., Duca, S., Costa, T., Bara, B. G., & Sacco, K. (2017) · Neural Plasticity · doi:10.1155/2017/1612078 · Cited by 27 · see citing works
Low protein-induced intrauterine growth restriction as a risk factor for schizophrenia phenotype in a rat model: assessing the role of oxidative stress and neuroinflammation interaction
Allgäuer, L., Cabungcal, J.-H., Yzydorczyk, C., Kim, Q., & Dwir, D. (2023) · Translational Psychiatry · doi:10.1038/s41398-023-02322-8 · Cited by 26 · see citing works
Odor-Induced Neuronal Rhythms in the Olfactory Bulb Are Profoundly Modified in ob/ob Obese Mice
Chelminski, Y., Magnan, C., Luquet, S. H., Everard, A., Meunier, N., Gurden, H., & Martin, C. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00002 · Cited by 25 · see citing works

Current findings and perspectives on aberrant neural oscillations in schizophrenia
Hirano, Y., & Uhlhaas, P. J. (2021) · Psychiatry and Clinical Neurosciences · doi:10.1111/pcn.13300 · Cited by 121 · see citing works
Self-citation
Neural Synchrony in Schizophrenia
Ford, J. M., & Mathalon, D. H. (2008) · Schizophrenia Bulletin · doi:10.1093/schbul/sbn090 · Cited by 41 · see citing works
High-frequency oscillations and the neurobiology of schizophrenia
Uhlhaas, P. J., & Singer, W. (2013) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2013.15.3/puhlhaas · Cited by 196 · see citing works
Self-citation
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
Self-citation
Neural Synchrony in Schizophrenia: From Networks to New Treatments
Ford, J. M., Krystal, J. H., & Mathalon, D. H. (2007) · Schizophrenia Bulletin · doi:10.1093/schbul/sbm062 · Cited by 112 · see citing works

Authors: Uhlhaas, P. J., & Singer, W.
Affiliations: University of Glasgow (GB)
Goethe University Frankfurt (DE)
Corresponding author: Uhlhaas, Peter J.
ORCID: Uhlhaas, Peter J.
Singer, Wolf
Venue: Biological Psychiatry
Publisher: Elsevier BV
Published: 2015-06
Volume: 77
Issue: 12
Pages: 1001-1009
ISSN: 0006-3223 (ISSN-L)
DOI: 10.1016/j.biopsych.2014.11.019
OpenAlex: W2032378986
Cited by: 243
References: 113
Citations by year: 2026: 15 · 2025: 19 · 2024: 14 · 2023: 26 · 2022: 14 · 2021: 24 · 2020: 22 · 2019: 23 · 2018: 24 · 2017: 22 · 2016: 28 · 2015: 12
FWCI: 1.99
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Biological Psychiatry (publishedVersion)
PubMed (publishedVersion)
ENLIGHTEN (Jurnal Bimbingan dan Konseling Islam) (submittedVersion)
Max Planck Digital Library (submittedVersion)
MPG.PuRe (Max Planck Society) (submittedVersion)
Funders: Medical Research Council (MR/N003403/1)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Keywords: schizophrenia, neural oscillations, neural dynamics, excitation-inhibition balance, neuronal synchronization, GABAergic neurotransmission, glutamatergic neurotransmission, psychotic symptoms, cognitive impairment, neural states, translational research
MeSH terms: Animals, Brain, Electroencephalography, Humans, Nerve Net, Neural Inhibition, Schizophrenia, Translational Research, Biomedical, Brain Waves

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Oscillations and Neuronal Dynamics in Schizophrenia: The Search for Basic Symptoms and Translational Opportunities

Abstract

Integrity signals

Claims the paper makes

Claims other papers make about this one

Cites

Cited by

Related

Record

About these checks