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

A Mitochondrial Paradigm of Metabolic and Degenerative Diseases, Aging, and Cancer: A Dawn for Evolutionary Medicine

Wallace, D. C. (2005) · Annual Review of Genetics · doi:10.1146/annurev.genet.39.110304.095751 · Cited by 3,185

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

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

Effect of anoxia on ion distribution in the brain

Hansen, A. J. (1985) · Physiological Reviews · doi:10.1152/physrev.1985.65.1.101 · Cited by 1,342

Mitochondria in neuroplasticity and neurological disorders

Mattson, M. P., Gleichmann, M., & Cheng, A. (2008) · Neuron · doi:10.1016/j.neuron.2008.10.010 · Cited by 1,081

Mechanisms of Gamma Oscillations in the Hippocampus of the Behaving Rat

Csicsvari, J., Jamieson, B. G., Wise, K. D., & Buzsáki, G. (2003) · Neuron · doi:10.1016/s0896-6273(02)01169-8 · Cited by 1,031

The neural basis of functional brain imaging signals

Attwell, D., & Iadecola, C. (2002) · Trends in Neurosciences · doi:10.1016/s0166-2236(02)02264-6 · Cited by 957

Integrated analysis of protein composition, tissue diversity, and gene regulation in mouse mitochondria.

Mootha, V. K., Bunkenborg, J., Olsen, J. V., Hjerrild, M., Wisniewski, J. R., Stahl, E., Bolouri, M. S., Ray, H. N., Sihag, S., Kamal, M., et al. (2003) · Cell · doi:10.1016/s0092-8674(03)00926-7 · Cited by 889

Cholinergic induction of network oscillations at 40 Hz in the hippocampus in vitro

Fisahn, A., Pike, F. G., Buhl, E. H., & Paulsen, O. (1998) · Nature · doi:10.1038/28179 · Cited by 884

Mitochondria and neuronal activity

Kann, O., & Kovács, R. (2006) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00222.2006 · Cited by 871

Lights for epilepsy: can photobiomodulation reduce seizures and offer neuroprotection?

Mitrofanis, J., Torres-Martinez, N., & Chabardès, S. (2022) · Neural Regeneration Research · doi:10.4103/1673-5374.360288 · Cited by 15

Event-Associated Oxygen Consumption Rate Increases ca. Five-Fold When Interictal Activity Transforms into Seizure-Like Events In Vitro

Schoknecht, K., Berndt, N., Rösner, J., Heinemann, U., Dreier, J. P., Kovács, R., Friedman, A., & Liotta, A. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18091925 · Cited by 15

Between life and death: the brain twilight zones

Charpier, S. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1156368 · Cited by 15

Parvalbumin as a sex-specific target in Alzheimer’s disease research – A mini-review

Terstege, D. J., & Epp, J. R. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105370 · Cited by 14

The Pathophysiological Underpinnings of Gamma-Band Alterations in Psychiatric Disorders

Palmisano, A., Pandit, S., Smeralda, C. L., Demchenko, I., Rossi, S., Battelli, L., Rivolta, D., Bhat, V., & Santarnecchi, E. (2024) · Life · doi:10.3390/life14050578 · Cited by 17

Dysbindin-1 regulates mitochondrial fission and gamma oscillations

Zhao, J. W., Zhu, H., Duan, K., Petralia, R. S., Wang, Y., Gu, Q., Panja, D., & Li, Z. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01038-9 · Cited by 13

NOSA, an Analytical Toolbox for Multicellular Optical Electrophysiology

Oltmanns, S., Abben, F. S., Ender, A., Aimon, S., Kovacs, R., Sigrist, S. J., Storace, D. A., Geiger, J. R. P., & Raccuglia, D. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00712 · Cited by 13

Altered Postnatal Development of Cortico—Hippocampal Neuronal Electric Activity in Mice Deficient for the Mitochondrial Aspartate—Glutamate Transporter

Gómez‐Galán, M., Makarova, J., Llorente‐Folch, I., Saheki, T., Pardo, B., Satrústegui, J., & Herreras, Ó. (2011) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2011.129 · Cited by 13

Does metabolic failure at the synapse cause Alzheimer’s disease?

Engel, P. A. (2014) · Medical Hypotheses · doi:10.1016/j.mehy.2014.10.013 · Cited by 13

Increased Levels of Reactive Oxygen Species in Brain Slices after Transient Hypoxia Induced By a Reduced Oxygen Supply

Sasaki, T., Awaji, T., Shimada, K., & Sasaki, H. (2018) · Neuropsychiatry · doi:10.4172/neuropsychiatry.1000392 · Cited by 13

Isocitrate supplementation promotes breathing generation, gasping, and autoresuscitation in neonatal mice

Rivera‐Angulo, A., & Peña‐Ortega, F. (2013) · Journal of Neuroscience Research · doi:10.1002/jnr.23330 · Cited by 13

Sevoflurane Effects on Neuronal Energy Metabolism Correlate with Activity States While Mitochondrial Function Remains Intact

Maechler, M., Rösner, J., Wallach, I., Geiger, J. R. P., Spies, C., Liotta, A., & Berndt, N. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23063037 · Cited by 12

Early adenosine release contributes to hypoxia‐induced disruption of stimulus‐induced sharp wave‐ripple complexes in rat hippocampal area CA 3

Jarosch, M. S., Gebhardt, C., Fano, S., Huchzermeyer, C., Haq, R. U., Behrens, C., & Heinemann, U. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.12941 · Cited by 12

Priming of microglia by type II interferon is lasting and resistant to modulation by interleukin-10 in situ

Hemmerich, M., Malorny, N., Lewen, A., Hollnagel, J., Chausse, B., & Kann, O. (2022) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2022.577881 · Cited by 11

A novel mouse model of mitochondrial disease exhibits juvenile-onset severe neurological impairment due to parvalbumin cell mitochondrial dysfunction

Olkhova, E. A., Bradshaw, C., Blain, A., Alvim, D., Turnbull, D. M., LeBeau, F. E. N., Ng, Y., Gorman, G., & Lax, N. (2023) · Communications Biology · doi:10.1038/s42003-023-05238-7 · Cited by 11

Effect of temperature on FAD and NADH-derived signals and neurometabolic coupling in the mouse auditory and motor cortex

Ibrahim, B. A., Wang, H., Lesicko, A. M. H., Bucci, B., Paul, K., & Llano, D. A. (2017) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-017-2037-4 · Cited by 10

Molecular sabotage of hippocampal synaptic plasticity by amyloid-β in Alzheimer's disease: A narrative review

Behroozi, Z., Askarpour, H., & Baghcheghi, Y. (2026) · Journal of Alzheimer s Disease Reports · doi:10.1177/25424823261415807 · Cited by 10

Five energy metabolism pathways show distinct regional distributions and lifespan trajectories in the human brain

Pourmajidian, M., Hansen, J. Y., Shafiei, G., Mišić, B., & Dagher, A. (2026) · PLoS Biology · doi:10.1371/journal.pbio.3003619 · Cited by 11

The use of antioxidant compounds in the treatment of first psychotic episode: Highlights from preclinical studies

Schiavone, S., & Trabace, L. (2018) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.12847 · Cited by 10

Movement-related ERS and connectivity in the gamma frequency decrease with practice

Tatti, E., Cacciola, A., Carrara, F., Luciani, A., Quartarone, A., & Ghilardi, M. F. (2023) · NeuroImage · doi:10.1016/j.neuroimage.2023.120444 · Cited by 10

In situ labeling of non-accommodating interneurons based on metabolic rates

Gotti, G. C., Kikhia, M., Wuntke, V., Hasam‐Henderson, L. A., Wu, B., Geiger, J. R. P., & Kovacs, R. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101798 · Cited by 10

Respiration and rapid eye movement ( REM) sleep substructure: short versus long episodes

Hammer, M., Jung, F., Brankačk, J., Yanovsky, Y., Tort, A. B. L., & Draguhn, A. (2022) · Journal of Sleep Research · doi:10.1111/jsr.13777 · Cited by 8

Lactate Transport via Glial MCT1 and Neuronal MCT2 Is Not Required for Synchronized Synaptic Transmission in Hippocampal Slices Supplied With Glucose

Söder, L., Baeza‐Lehnert, F., Khodaie, B., Elgez, A., Noack, L., Lewen, A., Hallermann, S., Poschet, G., Borges, K., & Kann, O. (2025) · Journal of Neurochemistry · doi:10.1111/jnc.70251 · Cited by 8

TransPhoM-DS Study Grant Report: Rationale and Protocol for Investigating the Efficacy of Low-Power Transcranial Photobiomodulation on Language, Executive Function, Attention, and Memory in Down Syndrome

Vieira, W. F., Coelho, D. R. A., Gersten, M. B., Puerto, A. M. H., Kalli, S., González-Garibay, G., McEachern, K. M., Clancy, J. A., Skotko, B. G., Abbeduto, L., et al. (2024) · Photonics · doi:10.3390/photonics11070670 · Cited by 9

Multiple Kinases Involved in the Nicotinic Modulation of Gamma Oscillations in the Rat Hippocampal CA3 Area

Wang, J., He, X., Guo, F., Cheng, X., Wang, Y., Wang, X., Feng, Z., Vreugdenhil, M., & Lu, C. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00057 · Cited by 8

The Effect of 40-Hz White LED Therapy on Structure–Function of Brain Mitochondrial ATP-Sensitive Ca-Activated Large-Conductance Potassium Channel in Amyloid Beta Toxicity

Nazari, M., Jafari, A., Torabi, N., Vajed-Samiei, T., Ghasemi, R., Fahanik‐Babaei, J., & Eliassi, A. (2022) · Neurotoxicity Research · doi:10.1007/s12640-022-00565-9 · Cited by 8

Increased BOLD Signals Elicited by High Gamma Auditory Stimulation of the Left Auditory Cortex in Acute State Schizophrenia

Kuga, H., Onitsuka, T., Hirano, Y., Nakamura, I., Oribe, N., Mizuhara, H., Kanai, R., Kanba, S., & Ueno, T. (2016) · EBioMedicine · doi:10.1016/j.ebiom.2016.09.008 · Cited by 8

Enhanced brain performance in mice following postnatal stress.

Loizzo, A., Spampinato, S., Campana, G., Vella, S., Fortuna, A., Costa, L., Capasso, A., Monteleone, P., Renzi, P., & Loizzo, S. (2012) · Journal of Endocrinology · doi:10.1530/joe-12-0369 · Cited by 7

Elevated susceptibility to exogenous seizure triggers and impaired interneuron excitability in a mouse model of Leigh syndrome epilepsy

Manning, A. A., Han, V. Z., Stephens, A., Wang, R., Bush, N. E., Bard, M., Ramirez, J., & Kalume, F. K. (2023) · Neurobiology of Disease · doi:10.1016/j.nbd.2023.106288 · Cited by 7

COMPARATIVE EVALUATION OF THE EFFECT OF PSYCHOACTIVE MEDICINES ON HIPPOCAMPAL THETA AND GAMMA RHYTHMS

Fokin, Y. V. (2019) · Journal Biomed · doi:10.33647/2074-5982-15-3-23-32 · Cited by 6

Exogenous AMPA downregulates gamma-frequency network oscillation in CA3 of rat hippocampal slices

Li, C., Li, Z., Xu, S., Jiang, S., Ye, Z.-C., Yu, B., Gong, S., Li, J., Hu, Q., Feng, B., et al. (2023) · Scientific Reports · doi:10.1038/s41598-023-36876-w · Cited by 6

Sporadic and familial subgroups of schizophrenia do not differ on dense array spontaneous gamma oscillatory activity

Tikka, S. K., Yadav, S., Nizamie, S. H., Das, B., Goyal, N., & Tikka, D. L. (2014) · Psychiatry Research · doi:10.1016/j.psychres.2014.08.042 · Cited by 6

Transcriptomic analyses reveal neuronal specificity of Leigh syndrome associated genes

Wahedi, A., Soondram, C., Murphy, A. E., Skene, N., & Rahman, S. (2022) · Journal of Inherited Metabolic Disease · doi:10.1002/jimd.12578 · Cited by 6

Is age-related failure of metabolic reprogramming a principal mediator in idiopathic Parkinson’s disease? Implications for treatment and inverse cancer risk

Engel, P. A. (2016) · Medical Hypotheses · doi:10.1016/j.mehy.2016.05.033 · Cited by 6

Mitochondria and cortical gamma oscillations: food for thought?

Cunningham, M. O., & Chinnery, P. F. (2011) · Brain · doi:10.1093/brain/awq382 · Cited by 6

Psychologically Traumatic Oxidative Stress; A Comprehensive Review of Redox Mechanisms and Related Inflammatory Implications

Karanikas, E. (2025) · Psychopharmacology Bulletin · doi:10.64719/pb.4419 · Cited by 14

Mitochondrial disease manifestations in relation to transcriptome location and function

Jakkamsetti, V., Balasubramaniam, S. R., Grover, N., & Pascual, J. M. (2021) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2021.12.008 · Cited by 5

Nicotinamide as Independent Variable for Intelligence, Fertility, and Health: Origin of Human Creative Explosions?

Williams, A. C., & Hill, L. J. (2019) · International Journal of Tryptophan Research · doi:10.1177/1178646919855944 · Cited by 5

Between Cognitivity and Neuropathies: Neuroimaging of the Effects of GABAergic Modulation of the Hippocampus and Prefrontal Neocortexis by Normalized Brain Electrograms

Karkischenko, N. N., Karkischenko, V. N., Fokin, Y. V., Taboyakova, L. A., Алимкина, О. В., & Борисова, М. М. (2020) · Journal Biomed · doi:10.33647/2074-5982-16-2-12-38 · Cited by 5

From reaction to reflection: A recursive framework for the evolution and structure of intelligence

Trukovich, J. J. (2025) · Biosystems · doi:10.1016/j.biosystems.2025.105549 · Cited by 4

Mechanisms of the Pharmacological Modulation of Obsessive-Compulsive and Cognitive Disorders in Cats Recognized by the Method of Normalizing FFT-Convertible Functions of Electrograms of the Frontal Cortex and Hippocampus

Karkischenko, N. N., Karkischenko, V. N., & Fokin, Y. V. (2020) · Journal Biomed · doi:10.33647/2074-5982-16-1-12-27 · Cited by 4

Decreased BOLD signals elicited by 40-Hz auditory stimulation of the right primary auditory cortex in bipolar disorder: An fMRI study

Okamoto, H., Onitsuka, T., Kuga, H., Oribe, N., Nakayama, N., Fukushima, S., Nakao, T., & Ueno, T. (2022) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2022.833896 · Cited by 4

THE COMPENSATORY ROLE OF CARDIOVASCULAR SYSTEM UNDER ACUTE HYPOXIC HYPOXIA IN HUMAN

Бурых, Э. А., & Si, S. (2014) · Экология человека · doi:10.17816/humeco17220 · Cited by 4

A Novel Approach to Study Coherent γ-Band Oscillations in Hippocampal Brain Sections

Díaz, J. C. R., Jenkins, P. M., Pritchett, D. L., & Jones, K. S. (2023) · eNeuro · doi:10.1523/eneuro.0167-23.2023 · Cited by 4

Any old iron?

Morris, C. M. (2011) · Brain · doi:10.1093/brain/awr056 · Cited by 4

METABOLIC CONTROL OF HIGH-FREQUENCY GAMMA OSCILLATIONS IN THE BRAIN

Анатольевич, П. И., & Karkischenko, N. N. (2019) · Journal Biomed · doi:10.33647/2074-5982-15-2-43-53 · Cited by 4

Native-state proteomics of Parvalbumin interneurons identifies novel molecular signatures and metabolic vulnerabilities to early Alzheimer’s disease pathologyPreprint

Kumar, P., Goettemoeller, A. M., Espinosa‐García, C., Tobin, B. R., Tfaily, A., Nelson, R. S., Natu, A., Dammer, E. B., Santiago, J. V., Malepati, S., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.17.541038 · Cited by 4

Characterization of β-Hydroxybutyrate as a Cell Autonomous Fuel for Active Excitatory and Inhibitory NeuronsPreprint

Bredvik, K. G., Liu, C. C., & Ryan, T. A. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.06.08.598077 · Cited by 4

Neuronal Synaptic Communication and Mitochondrial Energetics in Human Health and Disease

Glausier, J. R. (2025) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-89525-8_5 · Cited by 2

TNF-α and IFN-γ impair neural oscillations and induce neurodegeneration by microglial nitric oxide, metabolic and oxidative stress

Malorny, N., Chausse, B., Khodaie, B., Elgez, A., Söder, L., Lewen, A., Egorov, A. V., & Kann, O. (2026) · Journal of Neuroinflammation · doi:10.1186/s12974-026-03835-x · Cited by 3

Animal Model for Leigh Syndrome

El-Desouky, S., Taalab, Y. M., El‐Gamal, M., Mohamed, W. M. Y., & Salama, M. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-9554-7_27 · Cited by 3

A Vertically‐Stacked Optoelectronic Sensor for Localized Hemodynamics Monitoring

Lee, T.-Y., Jung, J., Park, H., Jung, D., Kim, D. H., Hong, C., Kang, S., Kim, H., Kim, T., & Lee, J. (2025) · Advanced Functional Materials · doi:10.1002/adfm.202504564 · Cited by 2

Associations between infant growth and cognitive development: Insights from EEG functional connectivity and power spectral density

Hartjen, B., Kakon, S. H., Rahman, N., Greaves, G., Xie, W., Tofail, F., Forrester, T., O'Sullivan, J. M., Haque, R., & Nelson, C. A. (2026) · Child Development · doi:10.1093/chidev/aacag006 · Cited by 5

Alteration of perineuronal nets and parvalbumin interneurons in prefrontal cortex and hippocampus, and correlation with blood corticosterone in activity-based anorexia model mice

Nguyen, H. D., Miyazaki, H., Kawai, H., Wang, Z., Sakamoto, S., Takaki, M., & Oohashi, T. (2025) · Neuroscience Research · doi:10.1016/j.neures.2025.104922 · Cited by 2

A primary mechanism for efficacy of the ketogenic diet may be energy repletion at the tripartite synapse

Joshi, S. N., Joshi, A. N., & Joshi, N. D. (2025) · Journal of Neural Engineering · doi:10.1088/1741-2552/adef7f · Cited by 2

Widespread Reductions of Spontaneous Neurophysiological Activity in Leber’s Disease—An Application of EEG Source Current Density Reconstruction

Jonak, K. (2020) · Brain Sciences · doi:10.3390/brainsci10090622 · Cited by 2

Serotonin transporter knockout in rats reduces beta- and gamma-band functional connectivity between the orbitofrontal cortex and amygdala during auditory discrimination

Boillot, M., ter Horst, J., López, J. R., Fazio, I. D., Steens, I. L. M., Cohen, M. X., & Homberg, J. R. (2024) · Cerebral Cortex · doi:10.1093/cercor/bhae334 · Cited by 1

Downregulation of UQCRC1 Expression Leads to Cognitive Decline by Disrupting the Cilia in the Dentate Gyrus

Zhang, J., Liu, T., Long, Z., Wu, Z., Luo, J., Bai, F., Zhou, L., Gong, H., Gong, M., Li, H., et al. (2025) · Neuroscience Bulletin · doi:10.1007/s12264-025-01532-y · Cited by 1

Parvalbumin interneurons under stress: converging mechanisms of vulnerability

Santos‐Silva, T., Godoy, L. D., Guimarães, F. S., & Gomes, F. V. (2026) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyag043 · Cited by 1

Electro-Physiological Approaches to Monitoring Neuro- Degenerative Diseases

Manuel, J., Orozco, C., & Ole, F. (2013) · InTech eBooks · doi:10.5772/55228 · Cited by 1

System Normalized Gamma Oscillations of Brain Structures: Pharmacological Analysis of Neurochemical and Metabolic Processes

Karkischenko, N. N., Fokin, Y. V., & Kharitonov, S. Y. (2024) · Journal Biomed · doi:10.33647/2074-5982-20-2-66-94 · Cited by 1

New Biomedical Approaches in Information and Cognitive Technologies of Psychopathology Modeling

Karkischenko, N. N., Fokin, Y. V., Taboyakova, L. A., Алимкина, О. В., & Борисова, М. М. (2020) · Journal Biomed · doi:10.33647/2074-5982-16-3-35-38 · Cited by 1

Neuroisualization of Pharmaco-EEG Effects of Leutragine by Normalized Cat Brain Electrograms

Fokin, Y. V., Karkischenko, N. N., & Борисова, М. М. (2020) · Journal Biomed · doi:10.33647/2074-5982-16-4-71-82 · Cited by 1

Molecular Genetics of DNA Polymerase Gamma‐associated Neurodegeneration

Tzoulis, C., & Bindoff, L. A. (2016) · Encyclopedia of Life Sciences · doi:10.1002/9780470015902.a0026904 · Cited by 1

The role of oligodendrocytes in higher-order circuit functions

Corona, S. Y. M. (2018) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-7137

Theoretische Untersuchungen zur Kopplung von neuronaler Erregung und neuronalem Energiestoffwechsel

Berndt, N. (2012) · edoc Publication server (Humboldt University of Berlin) · doi:10.18452/16668

Reply: Impaired mitochondrial function abolishes gamma oscillations in the hippocampus through an effect on fast-spiking interneurons

Kann, O., Huchzermeyer, C., Kovacs, R., Wirtz, S., & Schuelke, M. (2011) · Brain · doi:10.1093/brain/awr019

Investigation of Reactive Oxygen Species Management in Biological and Pathological Processes by Fluorescence Imaging

Yin, B. (2015) · D-Scholarship@Pitt (University of Pittsburgh)

THE COMPENSATORY ROLE OF CARDIOVASCULAR SYSTEM UNDER ACUTE HYPOXIC HYPOXIA IN HUMAN

Бурых, Э. А., & Si, S. (2014) · doi:10.33396/1728-0869-2014-7-30-36

Effect of Phencyclidine on Neuregulin Expression, Cortical Interneurons, and Redox Dysregulation

Petronijević, N., & Radonjić, N. V. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-800212-4.00057-1

Modulation of 4-aminopyridine-induced neuronal activity and local pO2 in rat hippocampal slices by changing the flow rate of the superfusion medium

Sydorenko, V., Komarov, O. S., Sushko, B. S., Romanov, A., Isaeva, E., & Isaev, D. S. (2016) · Fìzìologìčnij žurnal · doi:10.15407/fz62.04.003

The role of POLG mutations in human disease

Anagnostou, M. (2018)

Transgene Redoxindikator-Mäuse mit mitochondrialer roGFP1-Expression: Phänotypisierung, neuronales Verteilungsmuster und Sensorfunktionalität

Wagener, K. C. (2017) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-6625

Antibiotic treatment induces activation of microglia and impairment of cholinergic gamma oscillations in the hippocampusPreprint

Çalışkan, G., French, T., Heimesaat, M. M., Dunay, I. R., & Stork, O. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.07.30.454300

Epilepsy

Kovac, S., & Walker, M. C. (2014) · Springer eBooks · doi:10.1007/978-1-4614-5836-4_152

Faculty Opinions recommendation of The role of astrocytes in seizure generation: insights from a novel in vitro seizure model based on mitochondrial dysfunction.

Sisodiya, S. M., & Balestrini, S. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.734937054.793556916

Epilepsy

Kovac, S., & Walker, M. C. (2022) · Springer eBooks · doi:10.1007/978-3-031-15080-7_152

Adolescent stress induces behavioral changes and hippocampal excitatory/inhibitory imbalance: involvement of redox dysregulation and mitochondrial dysfunction

Santos‐Silva, T. (2023) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.17.2023.tde-10112023-160657

In vitro modelling of the neuropathophysiological features of mitochondrial epilepsy

Smith, L. A., Keane, E. B., Connor, K., Chan, F., & Cunningham, M. O. (2025) · Seizure · doi:10.1016/j.seizure.2025.05.005

Gamma-band qEEG biomarkers as trait indicators in depression

Arıkan, M. K., & İlhan, R. (2025) · Journal of Affective Disorders · doi:10.1016/j.jad.2025.120287

Astrocyte-neuron mitochondrial transfer via mitoEVs supports neuronal energy metabolism and is impaired in early Alzheimer’s diseasePreprint

Voorbraeck, L., Alarcón-Gil, J., Giraud, R., Pozzobon, F., Pereira, M. J., Guo, S., Cao, Z., Distefano, K., Forouzanfar, M. H., Wiklander, O. P. B., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.03.09.710050 · Cited by 1

Physiopathologie des comas isoélectriques : de l’EEG au neurone

Carton‐Leclercq, A. (2023) · theses.fr (ABES) · doi:10.70675/7e9150a6z8959z43baza4b4zcaf0222fc163

Brain anoxia : a multiscale and multi structure study

Carrion‐Falgarona, S. (2024) · theses.fr (ABES) · doi:10.70675/0b2670f6z5366z4a56za002z7619042a847c

Mitochondrial turnover at central GABAergic synapses governs vulnerability to epileptic seizuresPreprint

Ndoci, K., Chihab, A. W., Ganesan, K., Jevtic, M., Tofan, K. M., Wani, G. A., Pelzer, P., Soriano-Campos, J. A., Odenthal, F., Sakthivelu, V., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.06.24.734182

The genetic signature of memory encoding along the human hippocampal axisPreprint

Dehnad, M., To, T. V., Moore, H. C., Freelin, A. H., Kulkarni, A., Loer, S. A., Lega, B. C., & Konopka, G. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.06.22.733862

Disrupted metabolic support of intrinsic brain rhythms as a driver of spatiotemporal fragmentation in schizophrenia

Cunha, M. G. (2026) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2026.107007

Cognitive demand as a neurometabolic stress test in diabetes-associated cognitive impairment: from static metabolite pools to dynamic energy responses

Li, M., Ye, M., Xie, H., Gao, T., Kan, W., Chen, Y., Xia, Y., Zhao, Y., & Yuan, A.-H. (2026) · Frontiers in Endocrinology · doi:10.3389/fendo.2026.1991245

Energy demands during gamma oscillations in the hippocampus

Huchzermeyer, C. (2010) · Universitätsbibliothek der FU Berlin Hochschulschriftenstelle u. Dokumentenserver · doi:10.17169/refubium-13329

Impaired mitochondrial function abolishes gamma oscillations in the hippocampus through an effect on fast-spiking interneurons

Whittaker, R. G., Turnbull, D. M., Whittington, M. A., & Cunningham, M. O. (2011) · Brain · doi:10.1093/brain/awr018 · Cited by 74

The Energy Demand of Fast Neuronal Network Oscillations: Insights from Brain Slice Preparations

Kann, O. (2012) · Frontiers in Pharmacology · doi:10.3389/fphar.2011.00090 · Cited by 52

Cellular/Molecular Gamma Oscillations and Spontaneous Network Activity in the Hippocampus Are Highly Sensitive to Decreases in pO 2 and Concomitant Changes in Mitochondrial Redox State

Huchzermeyer, C., Albus, K., Gabriel, H.-J., Otáhal, J., Taubenberger, O., Heinemann, U., Kovács, R., & Kann, O. (2013)

Gamma Oscillations and Spontaneous Network Activity in the Hippocampus Are Highly Sensitive to Decreases in pO2and Concomitant Changes in Mitochondrial Redox State

Huchzermeyer, C., Albus, K., Gabriel, H.-J., Otáhal, J., Taubenberger, N., Heinemann, U., Kovács, R., & Kann, O. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.4105-07.2008 · Cited by 117