Mechanisms of Gamma Oscillations

Neuronal Oscillations in Cortical Networks

Buzsáki, G., & Draguhn, A. (2004) · Science · doi:10.1126/science.1099745 · Cited by 6,576

Rhythms of the Brain

Buzsáki, G. (2006) · doi:10.1093/acprof:oso/9780195301069.001.0001 · Cited by 4,873

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

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

Über das Elektrenkephalogramm des Menschen

Berger, H. (1929) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/bf01797193 · Cited by 4,266

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

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

Excitatory and Inhibitory Interactions in Localized Populations of Model Neurons

Wilson, H. R., & Cowan, J. D. (1972) · Biophysical Journal · doi:10.1016/s0006-3495(72)86068-5 · Cited by 3,579

Interneurons of the hippocampus

Freund, T. F., & Buzsáki, G. (1998) · Hippocampus · doi:10.1002/(sici)1098-1063(1996)6:4 · Cited by 3,462

Dynamic predictions: Oscillations and synchrony in top–down processing

Engel, A. K., Fries, P., & Singer, W. (2001) · Nature Reviews Neuroscience · doi:10.1038/35094565 · Cited by 3,454

The gamma rhythm as a guardian of brain health

Ichim, A.-M., Bârzan, H., Moca, V. V., Nagy-Dăbâcan, A., Ciuparu, A., Hapca, A., Vervaeke, K., & Muresan, R. C. (2024) · eLife · doi:10.7554/elife.100238 · Cited by 39

Formation of visual memories controlled by gamma power phase-locked to alpha oscillations

Park, H., Lee, D. S., Kang, E., Kang, H., Hahm, J., Kim, J. S., Chung, C. K., Jiang, H., Groß, J., & Jensen, O. B. (2016) · Scientific Reports · doi:10.1038/srep28092 · Cited by 39

Sleep disruption elevates oxidative stress in parvalbumin-positive cells of the rat cerebral cortex

Harkness, J. H., Bushana, P. N., Todd, R. P., Clegern, W. C., Sorg, B. A., & Wisor, J. P. (2018) · SLEEP · doi:10.1093/sleep/zsy201 · Cited by 39

Differential contributions of subthalamic beta rhythms and 1/f broadband activity to motor symptoms in Parkinson’s disease

Martin, S. L., Iturrate, I., Chavarriaga, R., Leeb, R., Sobolewski, A., Li, A. M., Zaldivar, J., Peciu-Florianu, I., Pralong, É., Jiménez, M. C., et al. (2018) · npj Parkinson s Disease · doi:10.1038/s41531-018-0068-y · Cited by 39

Local and Global Influences of Visual Spatial Selection and Locomotion in Mouse Primary Visual Cortex

McBride, E. G., Lee, S.-Y. J., & Callaway, E. M. (2019) · Current Biology · doi:10.1016/j.cub.2019.03.065 · Cited by 39

Methodological Considerations on the Use of Different Spectral Decomposition Algorithms to Study Hippocampal Rhythms

Zhou, Y., Sheremet, A., Qin, Y. F., Kennedy, J. P., DiCola, N. M., Burke, S. N., & Maurer, A. P. (2019) · eNeuro · doi:10.1523/eneuro.0142-19.2019 · Cited by 39

Movement-related coupling of human subthalamic nucleus spikes to cortical gamma

Fischer, P., Lipski, W. J., Neumann, W., Turner, R. S., Fries, P., Brown, P., & Richardson, R. M. (2020) · eLife · doi:10.7554/elife.51956 · Cited by 39

Excitation-Inhibition Imbalance Leads to Alteration of Neuronal Coherence and Neurovascular Coupling under Acute Stress

Han, K., Lee, M., Lim, H., Jang, M. W., Kwon, J., Lee, C. J., Kim, S., & Suh, M. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1553-20.2020 · Cited by 39

Spike Timing in the Attention Network Predicts Behavioral Outcome Prior to Target Selection

Fiebelkorn, I. C., & Kästner, S. (2020) · Neuron · doi:10.1016/j.neuron.2020.09.039 · Cited by 39

Computation of the electroencephalogram (EEG) from network models of point neurons

Martínez‐Cañada, P., Ness, T. V., Einevoll, G. T., Fellin, T., & Panzeri, S. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1008893 · Cited by 39

Acquiring new memories in neocortex of hippocampal-lesioned mice

Luo, W., Yun, D., Hu, Y., Tian, M., Yang, J., Xu, Y., Tang, Y. C., Zhan, Y., Xie, H. B., & Guan, J. (2022) · Nature Communications · doi:10.1038/s41467-022-29208-5 · Cited by 39

A bibliometric analysis of global research status and trends in neuromodulation techniques in the treatment of autism spectrum disorder

Xiao, L., Huo, X., Wang, Y., Li, W., Li, M., Wang, C., Wang, F., & Sun, T. (2023) · BMC Psychiatry · doi:10.1186/s12888-023-04666-3 · Cited by 39

Time-course of coherence in the human basal ganglia during voluntary movements

Talakoub, O., Neagu, B., Udupa, K., Tsang, E., Chen, R. E., Popović, M. R., & Wong, W. (2016) · Scientific Reports · doi:10.1038/srep34930 · Cited by 39

Spectral specificity of gamma-frequency transcranial alternating current stimulation over motor cortex during sequential movements

Spooner, R. K., & Wilson, T. W. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac423 · Cited by 38

A postnatal molecular switch drives activity-dependent maturation of parvalbumin interneurons

Moissidis, M., Abbasova, L., Selten, M. M., Alis, R., Bernard, C., Domínguez-Canterla, Y., Oozeer, F., Qin, S., Kelly, A., Mòdol, L., et al. (2025) · Cell · doi:10.1016/j.cell.2025.06.029 · Cited by 38

The Suppression of Beta Oscillations in the Primate Supplementary Motor Complex Reflects a Volatile State During the Updating of Action Sequences

Hosaka, R., Nakajima, T., Aihara, K., Yamaguchi, Y., & Mushiake, H. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv163 · Cited by 38

Brain oscillations in perception, timing and action

Gupta, D. S., & Chen, L. (2016) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2016.02.021 · Cited by 38

Altered attentional processing in male and female rats in a prenatal valproic acid exposure model of autism spectrum disorder

Anshu, K., Nair, A. K., Kumaresan, U. D., Kutty, B. M., Srinath, S., & Laxmi, T. R. (2017) · Autism Research · doi:10.1002/aur.1852 · Cited by 38

Physiological Signature of Memory Age in the Prefrontal-Hippocampal Circuit

Makino, Y., Polygalov, D., Bolaños, F., Benucci, A., & McHugh, T. J. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.11.075 · Cited by 38

A neuromechanistic model for rhythmic beat generation

Bose, A., Byrne, Á., & Rinzel, J. (2019) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006450 · Cited by 38

Posterior Alpha and Gamma Oscillations Index Divergent and Superadditive Effects of Cognitive Interference

Wiesman, A. I., & Wilson, T. W. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz214 · Cited by 38

Targeting Gamma‐Related Pathophysiology in Autism Spectrum Disorder Using Transcranial Electrical Stimulation: Opportunities and Challenges

Kayarian, F. B., Jannati, A., Rotenberg, A., & Santarnecchi, E. (2020) · Autism Research · doi:10.1002/aur.2312 · Cited by 38

Network Dysfunction in Comorbid Psychiatric Illnesses and Epilepsy

Colmers, P. L. W., & Maguire, J. L. (2020) · Epiliepsy currents/Epilepsy currents · doi:10.1177/1535759720934787 · Cited by 38

A neural correlate of visual discomfort from flicker

Gentile, C. P., & Aguirre, G. K. (2020) · Journal of Vision · doi:10.1167/jov.20.7.11 · Cited by 38

Assessment of astrocytes as a mediator of memory and learning in rodents

Akther, S., & Hirase, H. (2021) · Glia · doi:10.1002/glia.24099 · Cited by 38

Population spiking and bursting in next-generation neural masses with spike-frequency adaptation

Ferrara, A., Angulo‐García, D., Torcini, A., & Olmi, S. (2023) · Physical review. E · doi:10.1103/physreve.107.024311 · Cited by 38

Interacting Memory Systems—Does EEG Alpha Activity Respond to Semantic Long-Term Memory Access in a Working Memory Task?

Berger, B. E., Omer, S., Minarik, T., Sterr, A., & Sauseng, P. (2014) · Biology · doi:10.3390/biology4010001 · Cited by 38

Superior orientation discrimination and increased peak gamma frequency in autism spectrum conditions.

Dickinson, A. H., Bruyns‐Haylett, M., Smith, R. S., Jones, M., & Milne, E. (2016) · Journal of Abnormal Psychology · doi:10.1037/abn0000148 · Cited by 38

Distinct roles of PV and Sst interneurons in visually induced gamma oscillations

Onorato, I., Τζάνου, Α., Schneider, M., Uran, C., Broggini, A. C., & Vinck, M. A. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115385 · Cited by 37

Interictal network dysfunction and cognitive impairment in epilepsy

Gelinas, J. N., & Khodagholy, D. (2025) · Nature reviews. Neuroscience · doi:10.1038/s41583-025-00924-3 · Cited by 37

Cooperative actions of interneuron families support the hippocampal spatial code

Valero, M., Abad-Perez, P., Gallardo, A., Picco, M., García-Hernandez, R., Brotons‐Mas, J. R., Martínez-Félix, A., Machold, R. P., Rudy, B., & Buzsáki, G. (2025) · Science · doi:10.1126/science.adv5638 · Cited by 37

Impaired recruitment of dopamine neurons during working memory in mice with striatal D2 receptor overexpression

Duvarci, S., Simpson, E. H., Schneider, G., Kandel, E. R., Roeper, J., & Sigurdsson, T. (2018) · Nature Communications · doi:10.1038/s41467-018-05214-4 · Cited by 37

Nucleus Basalis of Meynert Stimulation for Dementia: Theoretical and Technical Considerations

Kumbhare, D., Palys, V., Toms, J., Wickramasinghe, C. S., Amarasinghe, K., Manic, M., Hughes, E., & Holloway, K. L. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00614 · Cited by 37

Miro1-dependent mitochondrial dynamics in parvalbumin interneurons

Kontou, G., Antonoudiou, P., Podpolny, M., Arancibia‐Cárcamo, I. L., Higgs, N., Szulc, B. R., López‐Doménech, G., Salinas, P. C., Mann, E. O., & Kittler, J. T. (2021) · eLife · doi:10.7554/elife.65215 · Cited by 37

Ultra-sparse Connectivity within the Lateral Hypothalamus

Burdakov, D., & Karnani, M. (2020) · Current Biology · doi:10.1016/j.cub.2020.07.061 · Cited by 37

Gamma Oscillations in the Basolateral Amygdala: Localization, Microcircuitry, and Behavioral Correlates

Headley, D. B., Kyriazi, P., Feng, F., Nair, S. S., & Paré, D. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.3159-20.2021 · Cited by 37

The impact of stress on the hippocampal spatial code

Tomar, A., & McHugh, T. J. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2021.11.005 · Cited by 37

Stimulus-specific plasticity of macaque V1 spike rates and gamma

Peter, A., Stauch, B. J., Shapcott, K. A., Kouroupaki, K., Schmiedt, J. T., Klein, L., Klon-Lipok, J., Dowdall, J. R., Schölvinck, M. L., Vinck, M. A., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.110086 · Cited by 37

Sex-specific regulation of inhibition and network activity by local aromatase in the mouse hippocampus

Hernández‐Vivanco, A., Cano-Adamuz, N., Sánchez-Aguilera, A., González‐Alonso, A., Rodríguez-Fernández, A., Azcoitia, Í., de la Prida, L. M., & Méndez, P. (2022) · Nature Communications · doi:10.1038/s41467-022-31635-3 · Cited by 37

Exact low-dimensional description for fast neural oscillations with low firing rates

Clusella, P., & Montbrió, E. (2024) · Physical review. E · doi:10.1103/physreve.109.014229 · Cited by 36

Absence of EEG gamma coherence in a local activated cortical state: a conserved trait of REM sleep

Cavelli, M., Castro‐Zaballa, S., Mondino, A., González, J., Falconi, A., & Torterolo, P. (2017) · Translational Brain Rhythmicity · doi:10.15761/tbr.1000115 · Cited by 36

Optogenetic investigation of the variable neurovascular coupling along the interhemispheric circuits

Iordanova, B. E., Vazquez, A. L., Kozai, T. D. Y., Fukuda, M., & Kim, S. (2018) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x18755225 · Cited by 36

Combined Positive and Negative Feedback Allows Modulation of Neuronal Oscillation Frequency during Sensory Processing

Lee, B., Shin, D., Gross, S. P., & Cho, K. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.10.029 · Cited by 36

Wave Turbulence and Energy Cascade in the Hippocampus

Sheremet, A., Qin, Y. F., Kennedy, J. P., Zhou, Y., & Maurer, A. P. (2019) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2018.00062 · Cited by 36

Modulation of auditory gamma-band responses using transcranial electrical stimulation

Jones, K. T., Johnson, E. L., Tauxe, Z. S., & Rojas, D. C. (2020) · Journal of Neurophysiology · doi:10.1152/jn.00003.2020 · Cited by 36

DNA Methyltransferase 1 (DNMT1) Function Is Implicated in the Age-Related Loss of Cortical Interneurons

Hahn, A., Bayer, C., Pensold, D., Tittelmeier, J., Marx-Blümel, L., González-Bermúdez, L., Linde, J., Groß, J., Salinas, G., Lingner, T., et al. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00639 · Cited by 36

Maternal immune activation targeted to a window of parvalbumin interneuron development improves spatial working memory: Implications for autism

Nakamura, J., Gillespie, B., Gibbons, A. S., Jaehne, E. J., Du, X., Chan, A., Schroeder, A., van den Buuse, M., Sundram, S., & Hill, R. (2020) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2020.10.012 · Cited by 36

Somatostatin Neurons Govern Theta Oscillations Induced by Salient Visual Signals

Huang, P., Xiang, X., Chen, X., & Li, H. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.108415 · Cited by 36

Cortical oscillatory dysrhythmias in visual snow syndrome: a magnetoencephalography study

Hepschke, J. L., Seymour, R. A., He, W., Etchell, A. C., Sowman, P. F., & Fraser, C. L. (2021) · Brain Communications · doi:10.1093/braincomms/fcab296 · Cited by 36

EEG as a translational biomarker and outcome measure in fragile X syndrome

Kenny, A., Wright, D., & Stanfield, A. C. (2022) · Translational Psychiatry · doi:10.1038/s41398-022-01796-2 · Cited by 36

Synaptic Variability and Cortical Gamma Oscillation Power in Schizophrenia

Chung, D. W., Geramita, M. A., & Lewis, D. A. (2022) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2021.21080798 · Cited by 36

Long-Range GABAergic Projections of Cortical Origin in Brain Function

Urrutia-Piñones, J., Morales-Moraga, C., Sanguinetti, N. K., Escobar, A. P., & Chiu, C. Q. (2022) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2022.841869 · Cited by 36

Oscillatory beta/alpha band modulations: A potential biomarker of functional language and motor recovery in chronic stroke?

Ulanov, M., & Юрьевич, Ш. Ю. (2022) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2022.940845 · Cited by 36

Muscarinic excitation of parvalbumin‐positive interneurons contributes to the severity of pilocarpine‐induced seizures

Yi, F., DeCan, E., Stoll, K., Marceau, E., Deisseroth, K. A., & Lawrence, J. J. (2014) · Epilepsia · doi:10.1111/epi.12883 · Cited by 36

Neural repetition suppression in ventral occipito-temporal cortex occurs during conscious and unconscious processing of frequent stimuli

Vidal, J. R., Perrone‐Bertolotti, M., Lévy, J., Palma, L. D., Minotti, L., Kahane, P., Bertrand, O., Antoine Lutz, A., Jerbi, K., & Lachaux, J.-P. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.03.049 · Cited by 36

An enhanced role and expanded developmental origins for gamma‐aminobutyric acidergic interneurons in the human cerebral cortex

Clowry, G. J. (2014) · Journal of Anatomy · doi:10.1111/joa.12198 · Cited by 36

Multichannel brain recordings in behavingDrosophilareveal oscillatory activity and local coherence in response to sensory stimulation and circuit activation

Paulk, A. C., Zhou, Y., Stratton, P. G., Liu, L., & van Swinderen, B. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00414.2013 · Cited by 36

Cross frequency coupling in next generation inhibitory neural mass models

Ceni, A., Olmi, S., Torcini, A., & Angulo‐García, D. (2020) · Chaos An Interdisciplinary Journal of Nonlinear Science · doi:10.1063/1.5125216 · Cited by 36

Physiological features of parvalbumin-expressing GABAergic interneurons contributing to high-frequency oscillations in the cerebral cortex

Milicevic, K. D., Barbeau, B. L., Lovic, D. D., Patel, A. A., Ivanova, V. O., & Antic, S. D. (2023) · Current Research in Neurobiology · doi:10.1016/j.crneur.2023.100121 · Cited by 35

Electroencephalogram monitoring during anesthesia and critical care: a guide for the clinician

Manohar, N., Ferrari, A., Greenblatt, A., Berardino, A., Peixoto, C., Duarte, F., Moaiyeri, Z., Robba, C., Nascimento, F. A., Kreuzer, M., et al. (2024) · Journal of Clinical Monitoring and Computing · doi:10.1007/s10877-024-01250-2 · Cited by 35

Development of modularity in the neural activity of childrenʼs brains

Chen, M., & Deem, M. W. (2015) · Physical Biology · doi:10.1088/1478-3975/12/1/016009 · Cited by 35

Soman‐induced status epilepticus, epileptogenesis, and neuropathology in carboxylesterase knockout mice treated with midazolam

Marrero-Rosado, B. M., Furtado, M. D. A., Schultz, C. R., Stone, M. F., Kundrick, E. R., Walker, K. A., O’Brien, S. W., Du, F., & Lumley, L. A. (2018) · Epilepsia · doi:10.1111/epi.14582 · Cited by 35

A softening laminar electrode for recording single unit activity from the rat hippocampus

Zátonyi, A., Orbán, G., Modi, R., Márton, G., Meszéna, D., Ulbert, I., Pongracz, A., Ecker, M., Voit, W., Joshi‐Imre, A., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-39835-6 · Cited by 35

Effect of spike-timing-dependent plasticity on stochastic burst synchronization in a scale-free neuronal network

Kim, S.-Y., & Lim, W. (2018) · Cognitive Neurodynamics · doi:10.1007/s11571-017-9470-0 · Cited by 35

The breathing brain: The potential of neural oscillations for the understanding of respiratory perception in health and disease

Jelinčić, V., Diest, I. V., Torta, D. M. E., & von Leupoldt, A. (2021) · Psychophysiology · doi:10.1111/psyp.13844 · Cited by 35

Multiscale Network Organization in the Human Brain

Bassett, D. S., & Siebenhühner, F. (2013) · Wiley eBooks · doi:10.1002/9783527671632.ch07 · Cited by 35

Parvalbumin interneurons regulate rehabilitation-induced functional recovery after stroke and identify a rehabilitation drug

Okabe, N., Wei, X., Abumeri, F., Batac, J., Hovanesyan, M., Dai, W., Azarapetian, S., Campagna, J. J., Pilati, N., Marasco, A., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-57860-0 · Cited by 34

Microsaccade-rhythmic modulation of neural synchronization and coding within and across cortical areas V1 and V2

Lowet, E., Gips, B., Roberts, M. J., Weerd, P. D., Jensen, O. B., & van der Eerden, J. P. J. M. (2018) · PLoS Biology · doi:10.1371/journal.pbio.2004132 · Cited by 34

Parametric effects of transcranial alternating current stimulation on multitasking performance

Hsu, W., Zanto, T. P., & Gazzaley, A. H. (2018) · Brain stimulation · doi:10.1016/j.brs.2018.10.010 · Cited by 34

Pharmaco‐electroencephalographic responses in the rat differ between active and inactive locomotor states

Hansen, I. H., Agerskov, C., Arvastson, L., Bastlund, J. F., Sørensen, H. B. D., & Herrik, K. F. (2019) · European Journal of Neuroscience · doi:10.1111/ejn.14373 · Cited by 34

Children with Autism Spectrum Disorder Demonstrate Regionally Specific Altered Resting-State Phase–Amplitude Coupling

Port, R. G., DiPiero, M. A., Ku, M., Liu, S., Blaskey, L. G., Kuschner, E. S., Edgar, J. C., Roberts, T. P. L., & Berman, J. (2019) · Brain Connectivity · doi:10.1089/brain.2018.0653 · Cited by 34

Hippocampal beta oscillations predict mouse object‐location associative memory performance

Iwasaki, S., Sasaki, T., & Ikegaya, Y. (2021) · Hippocampus · doi:10.1002/hipo.23311 · Cited by 34

Brain rhythms control microglial response and cytokine expression via NF-κB signaling

Prichard, A., Garza, K. M., Shridhar, A., He, C. L., Bitarafan, S., Pybus, A. F., Wang, Y., Snyder, E., Goodson, M. C., Franklin, T., et al. (2023) · Science Advances · doi:10.1126/sciadv.adf5672 · Cited by 34

Acute intracerebral treatment with amyloid-beta (1–42) alters the profile of neuronal oscillations that accompany LTP induction and results in impaired LTP in freely behaving rats

Kalweit, A. N., Yang, H., Colitti-Klausnitzer, J., Fülöp, L., BozsÃ, Z., Penke, B., & Manahan‐Vaughan, D. (2015) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2015.00103 · Cited by 34

Cell Assemblies of the Basal Forebrain

Tingley, D., Alexander, A. S., Quinn, L. K., Chiba, A. A., & Nitz, D. A. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.4432-14.2015 · Cited by 34

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 34

Differences in Reperfusion-Induced Mitochondrial Oxidative Stress and Cell Death Between Hippocampal CA1 and CA3 Subfields Are Due to the Mitochondrial Thioredoxin System

Yin, B., Barrionuevo, G., Batinic̈‐Haberle, I., Sandberg, M., & Weber, S. G. (2017) · Antioxidants and Redox Signaling · doi:10.1089/ars.2016.6706 · Cited by 34

From Toxoplasmosis to Schizophrenia via NMDA Dysfunction: Peptide Overlap between Toxoplasma gondii and N-Methyl-d-Aspartate Receptors As a Potential Mechanistic Link

Lucchese, G. (2017) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2017.00037 · Cited by 34

Intracranial high-γ connectivity distinguishes wakefulness from sleep

Mikulan, E., Hesse, E., Sedeño, L., Bekinschtein, T. A., Sigman, M., García, M. D. C., Silva, W., Ciraolo, C. A., García, A. M., & Ibáñez, A. M. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.12.015 · Cited by 34

Synchronization by uncorrelated noise: interacting rhythms in interconnected oscillator networks

Meng, J. H., & Riecke, H. (2018) · Scientific Reports · doi:10.1038/s41598-018-24670-y · Cited by 34

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

Benamer, N., Vidal, M., & Angulo, M. C. (2019) · Neuroscience Letters · doi:10.1016/j.neulet.2019.134615 · Cited by 34

The reuniens and rhomboid nuclei are necessary for contextual fear memory persistence in rats

Quet, É., Majchrzak, M. J., Cosquer, B., Morvan, T., Wolff, M., Cassel, J., de Vasconcelos, A. P., & Stéphan, A. (2020) · Brain Structure and Function · doi:10.1007/s00429-020-02048-z · Cited by 34

Prefrontal PV interneurons facilitate attention and are linked to attentional dysfunction in a mouse model of absence epilepsy

Ferguson, B. R., Glick, C., & Huguenard, J. R. (2023) · eLife · doi:10.7554/elife.78349 · Cited by 33

40 Hz Steady-State Response in Human Auditory Cortex Is Shaped by Gabaergic Neuronal Inhibition

Toso, A., Wermuth, A. P., Arazi, A., Braun, A., Grent-‘t-Jong, T., Uhlhaas, P. J., & Donner, T. H. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.2029-23.2024 · Cited by 33

Exploring causal mechanisms of psychosis risk

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Phase of firing does not reflect temporal order in sequence memory of humans and recurrent neural networks

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