Physical Processes in Biological Neuronal Networks During Epileptic Seizures: An Overview of Models

Authors

DOI:

https://doi.org/10.20535/ibb.2026.10.2.349634

Keywords:

electroencephalography, ictal transition, synthetic calibration data, phenomenological dynamics, Epileptor‑2, bifurcation mechanisms, multiscale connectome, feature extraction, classifier calibration, transfer validation

Abstract

Abstract: This review summarizes approaches to epileptic seizure detection and forecasting from electroencephalo-graphic and intracranial electroencephalographic signals, with emphasis on physically grounded modelling of neurons and neuronal networks. The topic is relevant because modern machine-learning and deep-learning methods often achieve high classification performance, but their practical use is limited by cross-patient variability, scarcity of la-belled data, dependence on preprocessing, false-alarm control and insufficient interpretability of informative features. The paper systematizes the main model classes used in computational epileptology: low-dimensional phenomenologi-cal models, biophysical models of single neurons and membrane processes, network and multiscale frameworks, ma-chine-learning approaches, and high-order numerical schemes for large-scale simulations. It is shown that biophysical and multiscale models provide deeper insight into ionic, synaptic and network mechanisms of epileptiform activity, but require many parameters and substantial computational resources. In contrast, phenomenological models, espe-cially Epileptor and Epileptor-2, offer a rational compromise between simulation speed, parameter controllability and the ability to reproduce transitions between normal, ictal and post-ictal regimes. We argue that such models should not be considered a replacement for real EEG/iEEG recordings, but rather a controlled source of synthetic signals for fea-ture calibration, classifier robustness testing and analysis of the physical origin of informative signal characteristics. Model-generated signals are therefore positioned as an intermediate layer between experimental recordings and ma-chine-learning algorithms. This approach may improve the reproducibility of studies, increase the interpretability of diagnostic features and provide a basis for further development of compact systems for epileptic seizure detection and forecasting.

References

Thijs RD, Surges R, O'Brien TJ, Sander JW. Epilepsy in adults. Lancet. 2019;393(10172):689-701. DOI: 10.1016/S0140-6736(18)32596-0.

Alotaiby TN, Alshebeili SA, Alshawi T, Ahmad I, El-Samie FEA. EEG seizure detection and prediction algorithms: a survey. EURASIP J Adv Signal Process. 2014;2014:183. DOI: 10.1186/1687-6180-2014-183.

Kwan P, Brodie MJ. Early identification of refractory epilepsy. N Engl J Med. 2000;342(5):314-319. DOI: 10.1056/NEJM200002033420503.

Mula M, Sander JW. Psychosocial aspects of epilepsy: a wider approach. BJPsych Open. 2016;2(4):270-274. DOI: 10.1192/bjpo.bp.115.002345.

World Health Organization. Epilepsy: a public health imperative. Geneva: World Health Organization; 2019. 146 p.

Tejada J, Costa KM, Bertti P, Garcia-Cairasco N. The epilepsies: complex challenges needing complex solutions. Epilepsy Behav. 2013;26(3):212-228. DOI: 10.1016/j.yebeh.2012.09.029.

Borhade RR, Bairagi VK, Nagmode MS, Borhade RH. Epileptic Seizure Prediction Using Electroencephalogram Signals. 1st ed. Boca Raton: Chapman & Hall/CRC; 2024. 154 p. ISBN: 9781032714394.

Carmo AS, Abreu M, Baptista MF, et al. Automated algorithms for seizure forecast: a systematic review and meta-analysis. J Neurol. 2024;271:6573-6587. DOI: 10.1007/s00415-024-12655-z.

Costa G, Teixeira C, Pinto MF. Comparison between epileptic seizure prediction and forecasting based on machine learning. Sci Rep. 2024;14:5653. DOI: 10.1038/s41598-024-56019-z.

Segal G, Feigin VL, Delanty N, et al. Utilizing risk-controlling prediction calibration to reduce false alarm rates in epileptic seizure predic-tion. Front Neurosci. 2023;17:1184990. DOI: 10.3389/fnins.2023.1184990.

Batista J, Pinto MF, Tavares M, Lopes F, Oliveira A, Teixeira C. EEG epilepsy seizure prediction: the post-processing stage as a chronology. Sci Rep. 2024;14:407. DOI: 10.1038/s41598-023-50609-z.

Zhang Z, Li X, Chen Y, et al. Efficient and generalizable cross-patient epileptic seizure detection through a spiking neural network. Front Neurosci. 2024;17:1303564. DOI: 10.3389/fnins.2023.1303564.

Shafiezadeh S, Duma GM, Pozza M, Testolin A. A systematic review of cross-patient approaches for EEG epileptic seizure prediction. J Neu-ral Eng. 2024;21(6):061004. DOI: 10.1088/1741-2552/ad9682.

Kostas D, Aroca-Ouellette S, Rudzicz F. BENDR: using transformers and a contrastive self-supervised learning task to learn from massive amounts of EEG data. Front Hum Neurosci. 2021;15:653659. DOI: 10.3389/fnhum.2021.653659.

Wan Z, Yang R, Huang M, Zeng N, Liu X. A review on transfer learning in EEG signal analysis. Neurocomputing. 2021;421:1-14. DOI: 10.1016/j.neucom.2020.09.017.

Rafiei MH, Gauthier LV, Adeli H, Takabi D. Self-supervised learning for electroencephalography. IEEE Trans Neural Netw Learn Syst. 2024;35(2):1457-1471. DOI: 10.1109/TNNLS.2022.3190448.

Zhang Y, Yu Y, Li H, Wu A, Chen X, Liu J, Zeng LL, Hu D. DMAE-EEG: a pretraining framework for EEG spatiotemporal representation learn-ing. IEEE Trans Neural Netw Learn Syst. 2025;36(10):17664-17678. DOI: 10.1109/TNNLS.2025.3581991.

Mormann F, Andrzejak RG, Elger CE, Lehnertz K. Seizure prediction: the long and winding road. Brain. 2007;130(Pt 2):314-333. DOI: 10.1093/brain/awm241.

Wong KT, Tadel F, Artoni F, et al. EEG datasets for seizure detection and prediction - a review. Epilepsia Open. 2023;8(2):1-16. DOI: 10.1002/epi4.12704.

Horwitz B, Banerjee A. A role for neural modeling in the study of brain disorders. Front Syst Neurosci. 2012;6:13. DOI: 10.3389/fnsys.2012.00013.

Traub RD, Wong RK, Miles R, Michelson H. A model of a CA3 hippocampal pyramidal neuron incorporating voltage-clamp data on intrinsic conductances. J Neurophysiol. 1991;66(2):635-650. DOI: 10.1152/jn.1991.66.2.635.

Jirsa VK, Stacey WC, Quilichini PP, Ivanov AI, Bernard C. On the nature of seizure dynamics. Brain. 2014;137(Pt 8):2210-2230. DOI: 10.1093/brain/awu133.

Case MJ, Morgan RJ, Schneider CJ, Soltesz I. Computer modeling of epilepsy. In: Noebels JL, Avoli M, Rogawski MA, Olsen RW, Delgado-Escueta AV, editors. Jasper's Basic Mechanisms of the Epilepsies. 4th ed. Bethesda (MD): National Center for Biotechnology Information; 2012. Available from: https://www.ncbi.nlm.nih.gov/books/NBK98156/.

Proix T, Bartolomei F, Chauvel P, Bernard C, Jirsa VK. Virtual epileptic patient: personalized whole-brain modeling. Brain. 2017;140(3):641-654. DOI: 10.1093/brain/awx004.

Lang S, Momi D, Vetkas A, Santyr B, Yang AZ, Kalia SK, et al. Computational modeling of whole-brain dynamics: a review of neurosurgical applications. J Neurosurg. 2024;140(1):218-230. DOI: 10.3171/2023.5.JNS23250.

Gleichgerrcht E, Munsell B, Bhatia S, Vandergrift WA III, Rorden C, McDonald C, et al. Deep learning applied to whole-brain connectome to determine seizure control after epilepsy surgery. Epilepsia. 2018;59(9):1643-1654. doi:10.1111/epi.14528.

Stefanescu RA, Shivakeshavan RG, Talathi SS. Computational models of epilepsy. Seizure. 2012;21(10):748-759. DOI: 10.1016/j.seizure.2012.08.012.

van Gils S, van Drongelen W. Epilepsy: computational models. In: Jaeger D, Jung R, editors. Encyclopedia of Computational Neuroscience. New York: Springer; 2022. p. 1330-1344. DOI: 10.1007/978-1-0716-1006-0_504.

Bernard C, Naze S, Proix T, Jirsa VK. Modern concepts of seizure modeling. Int Rev Neurobiol. 2014;114:121-153. DOI: 10.1016/B978-0-12-418693-4.00006-6.

Wendling F, Koksal-Ersoz E, Al-Harrach M, Yochum M, Merlet I, Ruffini G, et al. Multiscale neuro-inspired models for interpretation of EEG signals in patients with epilepsy. Clin Neurophysiol. 2024;161:198-210. DOI: 10.1016/j.clinph.2024.03.006.

Depannemaecker D, Ezzati A, Wang HE, Jirsa V, Bernard C. From phenomenological to biophysical models of seizures. Neurobiol Dis. 2023;182:106131. DOI: 10.1016/j.nbd.2023.106131.

Sip V, Guye M, Bartolomei F, Jirsa V. Computational modeling of seizure spread on a cortical surface. J Comput Neurosci. 2022;50:141-159. DOI: 10.1007/s10827-021-00802-8.

Gleichgerrcht E, Dumitru M, Hartmann DA, Munsell BC, Kuzniecky R, Bonilha L, Sameni R. Seizure forecasting using machine learning models trained by seizure diaries. Physiol Meas. 2022;43(12):125006. DOI: 10.1088/1361-6579/aca6ca.

Najafi T, Jaafar R, Remli R, Zaidi AW, Chellappan K. The role of brain signal processing and neuronal modelling in epilepsy - a review. J Kejuruteraan. 2021;33(4):801-815. DOI: 10.17576/jkukm-2021-33(4)-03.

Rigney G, Lennon M, Holderrieth P. The use of computational models in the management and prognosis of refractory epilepsy: a critical evaluation. Seizure. 2021;91:295-304. DOI: 10.1016/j.seizure.2021.06.006.

Wendling F. Computational models of epileptic activity: a bridge between observation and pathophysiological interpretation. Expert Rev Neurother. 2008;8(6):889-896. DOI: 10.1586/14737175.8.6.889.

Lytton WW. Computer modeling of epilepsy: opportunities for drug discovery. Drug Discov Today Dis Models. 2016;19:23-30. DOI: 10.1016/j.ddmod.2017.02.007.

Hashemi M, Vattikonda AN, Sip V, et al. The Bayesian virtual epileptic patient: a probabilistic framework designed to infer the hidden vari-ables of epilepsy. NeuroImage. 2020;217:116839. DOI: 10.1016/j.neuroimage.2020.116839.

Vattikonda AN, Hashemi M, Sip V, Woodman MM, Bartolomei F, Jirsa VK. Identifying spatio-temporal seizure propagation patterns in epi-lepsy using Bayesian inference. Commun Biol. 2021;4:1244. DOI: 10.1038/s42003-021-02751-5.

Lopes da Silva FH. The impact of EEG/MEG signal processing and modeling in the diagnostic and management of epilepsy. IEEE Rev Bio-med Eng. 2008;1:143-156. DOI: 10.1109/RBME.2008.2008246.

Lytton WW. Computer modelling of epilepsy. Nat Rev Neurosci. 2008;9(8):626-637. DOI: 10.1038/nrn2416.

Batarchuk V, Sudakov O. Design of wearable EEG device for seizures early detection. Int J Electron Telecommun. 2021;67(2):187-192. DOI: 10.24425/ijet.2021.135963.

Sudakov O, Kriukova G, Natarov R, Gaidar V, Maximyuk O, Radchenko S, et al. Distributed system for sampling and analysis of electroencephalograms. In: Proceedings of the 9th IEEE International Conference on Intelligent Data Acquisition and Advanced Computing Systems: Technology and Applications (IDAACS); 2017. Vol. 1. p. 306-310. DOI: 10.1109/IDAACS.2017.8095095.

Mathe M, Mididoddi P, Battula TK. Artifact removal methods in EEG recordings: a review. Proc Eng Technol Innov. 2021;20:35-56. DOI: 10.46604/peti.2021.7653.

Banerjee S, Jirsa V. A review of epileptic markers: from ion channels, astrocytes, synaptic imbalance to whole brain network dynamics. Ex-plor Neurosci. 2024;3:213-230. DOI: 10.37349/en.2024.00047.

Edoho M, Mooney C, Wei L. AI-based electroencephalogram analysis in rodent models of epilepsy: a systematic review. Appl Sci (Basel). 2024;14(11):4594. DOI: 10.3390/app14114594.

Shayegh F, Amir Fattahi R, Sadri S, Ansari-Asl K. A brief survey of computational models of normal and epileptic EEG signals: a guideline to model-based seizure prediction. J Med Signals Sens. 2011;1(1):62-72. DOI: 10.4103/2228-7477.83521.

Glomb K, Cabral J, Cattani A, Mazzoni A, Raj A, Franceschiello B. Computational models in electroencephalography. Brain Topogr. 2022;35(1):21-39. DOI: 10.1007/s10548-021-00828-2

Pidvalnyi I, Sudakov O, Natarov R, et al. Classification of epileptic seizures by simple machine learning techniques: application to animals' electroencephalography signals. IEEE Access. 2025;13:8951-8962. DOI: 10.1109/ACCESS.2025.3527866.

Maistrenko V, Sudakov O, Maistrenko Y. Spiral wave chimeras for coupled oscillators with inertia. Eur Phys J Spec Top. 2020;229(12):2327-2340. DOI: 10.1140/epjst/e2020-900279-x.

Maistrenko Y, Sudakov O, Osiv O, Maistrenko V. Chimera states in three dimensions. New J Phys. 2015;17(7):073037. DOI: 10.1088/1367-2630/17/7/073037.

Maistrenko V, Sudakov O, Osiv O. Chimera and solitary states in 3D oscillator networks with inertia. Chaos. 2020;30(6):063113. DOI: 10.1063/5.0005281.

Maistrenko V, Sudakov O, Sliusar I. Scroll ring chimera states in oscillatory networks. J Phys Commun. 2021;5(8):085001. DOI: 10.1088/2399-6528/ac1750.

Sudakov O, Maistrenko V. Parallelization of network dynamics computations in heterogeneous distributed environment. IEEE Trans Paral-lel Distrib Syst. 2025;36(10):2030-2044. DOI: 10.1109/TPDS.2025.3593154

Wang HE. Virtual brain twins: from basic neuroscience to clinical use. Natl Sci Rev. 2024;11(5):nwae079. DOI: 10.1093/nsr/nwae079.

El Houssaini K, Bernard C, Jirsa VK. The Epileptor model: a systematic mathematical analysis linked to the dynamics of seizures, refracto-ry status epilepticus, and depolarization block. eNeuro. 2020;7(2):ENEURO.0485-19.2020. DOI: 10.1523/ENEURO.0485-19.2020

Proix T, Bartolomei F, Guye M, Jirsa VK. Predicting the spatiotemporal diversity of seizure propagation and termination in human focal epilepsy. Nat Commun. 2018;9(1):1088. doi:10.1038/s41467-018-02973-y

Montgomery RM. Exploring seizure dynamics: a computational model of epilepsy. ResearchGate; 2024. DOI: 10.20944/preprints202404.1557.v1

Shokooh LA, Lesage F, Nguyen DK. Computational modeling of seizure onset patterns to underpin their underlying mechanisms. medRxiv. 2023:2023.02.16.23286033. DOI: 10.1101/2023.02.16.23286033.

Kini LG, Bernabei JM, Mikhail F, Hadar PN, Shah P, Khambhati AN, et al. Virtual resection predicts surgical outcome for drug-resistant epilepsy. Brain. 2019;142(12):3892-3905. doi:10.1093/brain/awz303

Wang HF, Scholly J, Triebkorn P, Sip V, Medina Villalon S, Woodman MM, et al. VEP atlas: an anatomic and functional human brain atlas dedicated to epilepsy patients. J Neurosci Methods. 2021;348:108983. DOI: 10.1016/j.jneumeth.2020.108983.

Bressloff PC. Single neuron modeling. In: Bressloff PC, editor. Stochastic Processes in Cell Biology. Lecture Notes on Mathematical Model-ling in the Life Sciences. New York: Springer; 2014. p. 3-62. DOI: 10.1007/978-1-4614-8866-8_1.

Ahn S, Jun SB, Lee HW, Lee S. Computational modeling of epileptiform activities in medial temporal lobe epilepsy combined with in vitro experiments. J Comput Neurosci. 2016;40(3):295-313. DOI: 10.1007/s10827-016-0614-8.

Najafi T, Jaafar R, Remli R, Zaidi WAW, Chellappan K. A computational model to determine membrane ionic conductance using electroen-cephalography in epilepsy. Phys Sci Forum. 2023;5(1):45. DOI: 10.3390/psf2022005045.

Hamill OP, Marty A, Neher E, Sakmann B, Sigworth FJ. Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches. Pflugers Arch. 1981;391(2):85-100. DOI: 10.1007/BF00656997.

Gandolfi D, Boiani GM, Bigiani A, Mapelli J. Modeling neurotransmission: computational tools to investigate neurological disorders. Int J Mol Sci. 2021;22(9):4565. DOI: 10.3390/ijms22094565.

Lazarewicz MT, Migliore M, Ascoli GA. A new bursting model of CA3 pyramidal cell physiology suggests multiple locations for spike initi-ation. Biosystems. 2003;67(1-3):129-137. DOI: 10.1016/S0303-2647(02)00071-0.

Markram H, Muller E, Ramaswamy S, Reimann MW, Abdellah M, Sanchez CA, et al. Reconstruction and simulation of neocortical microcircuitry. Cell. 2015;163(2):456-492. DOI: 10.1016/j.cell.2015.09.029.

Breakspear M. Dynamic models of large-scale brain activity. Nat Neurosci. 2017;20(3):340-352. DOI: 10.1038/nn.4497.

Woldman W, Terry JR. Multilevel computational modelling in epilepsy: classical studies and recent advances. In: Validating Neuro-Computational Models of Neurological and Psychiatric Disorders. Cham: Springer International Publishing; 2015. p. 161-188. DOI: 10.1007/978-3-319-20037-8_7.

Naze S, Bernard C, Jirsa V. Computational modeling of seizure dynamics using coupled neuronal networks: factors shaping epileptiform ac-tivity. PLoS Comput Biol. 2015;11(5):e1004209. DOI: 10.1371/journal.pcbi.1004209.

Karoly PJ, Kuhlmann L, Soudry D, Grayden DB, Cook MJ, Freestone DR. Seizure pathways: a model-based investigation. PLoS Comput Biol. 2018;14(10):e1006403. DOI: 10.1371/journal.pcbi.1006403.

Junges L, Lopes MA, Terry JR, Goodfellow M. The role that choice of model plays in predictions for epilepsy surgery. Sci Rep. 2019;9(1):7351. doi:10.1038/s41598-019-43871-7

Cosandier-Rimele D, Merlet I, Bartolomei F, Badier JM, Wendling F. Computational modeling of epileptic activity: from cortical sources to EEG signals. J Clin Neurophysiol. 2010;27(6):465-470. DOI: 10.1097/WNP.0b013e3182005dcd.

Wendling F, Benquet P, Bartolomei F, Jirsa V. Computational models of epileptiform activity. J Neurosci Methods. 2016;260:233-251. DOI: 10.1016/j.jneumeth.2015.03.027.

Jirsa VK, Depannemaecker D, Proix T, et al. Epileptor-2: dynamical inhibition during seizure progression. Proc Natl Acad Sci U S A. 2023;120(37):e2301241120. DOI: 10.1073/pnas.2301241120.

Richardson MP. Large scale brain models of epilepsy: dynamics meets connectomics. J Neurol Neurosurg Psychiatry. 2012;83(12):1238-1240. DOI: 10.1136/jnnp-2011-301944.

Taylor PN, Kaiser M, Dauwels J. Structural connectivity based whole brain modelling in epilepsy. J Neurosci Methods. 2014;236:51-57. DOI: 10.1016/j.jneumeth.2014.08.010.

Sinha N, Dauwels J, Kaiser M, Cash SS, Westover MB, Wang Y, et al. Computer modelling of connectivity change suggests epileptogenesis mechanisms in idiopathic generalised epilepsy. Neuroimage Clin. 2019;21:101655. DOI: 10.1016/j.nicl.2019.101655.

Maliia MD, Koksal-Ersoz E, Benard A, Calas T, Nica A, Denoyer Y, et al. Localization of the epileptogenic network from scalp EEG using a patient-specific whole-brain model. Netw Neurosci. 2025;9(1):18-37. DOI: 10.1162/netn_a_00418.

Miltiadous A, Tzimourta KD, Tzallas AT, et al. Machine learning algorithms for epilepsy detection based on published EEG databases: a systematic review. IEEE Access. 2023;11:130112-130130. DOI: 10.1109/ACCESS.2022.3232563.

Farooq MS, Zulfiqar A, Riaz S. Epileptic seizure detection using machine learning: taxonomy, opportunities, and challenges. Diagnostics (Basel). 2023;13(6):1058. DOI: 10.3390/diagnostics13061058.

Habashi AG, Azab AM, Eldawlatly S, Aly GM, et al. Generative adversarial networks in EEG analysis: an overview. J Neuroeng Rehabil. 2023;20:40. DOI: 10.1186/s12984-023-01169-w.

Martins FM, Gonzalez Suarez VM, Villar Flecha JR, Garcia Lopez B. Data augmentation effects on highly imbalanced EEG datasets for auto-matic detection of photoparoxysmal responses. Sensors (Basel). 2023;23(4):2312. DOI: 10.3390/s23042312.

Zhang X, Dong S, Shen Q, Zhou J, Min J. Deep extreme learning machine with knowledge augmentation for EEG seizure signal recognition. Front Neuroinform. 2023;17:1205529. DOI: 10.3389/fninf.2023.1205529.

Shah V, von Weltin E, Lopez S, McHugh JR, Veloso L, Golmohammadi M, et al. The Temple University Hospital Seizure Detection Corpus. Front Neuroinform. 2018;12:83. DOI: 10.3389/fninf.2018.00083.

Obeid I, Picone J. The Temple University Hospital EEG Data Corpus. Front Neurosci. 2016;10:196. DOI: 10.3389/fnins.2016.00196.

Guttag J. CHB-MIT Scalp EEG Database (version 1.0.0). PhysioNet. 2010. DOI: 10.13026/C2K01R.

Klatt J, Feldwisch-Drentrup H, Ihle M, et al. The EPILEPSIAE database: an extensive electroencephalography database of epilepsy patients. Epilepsia. 2012;53(9):1669-1676. DOI: 10.1111/j.1528-1167.2012.03564.x.

Brinkmann BH, Wagenaar J, Abbot D, et al. Crowdsourcing reproducible seizure forecasting in human and canine epilepsy. Brain. 2016;139(6):1713-1722. DOI: 10.1093/brain/aww045.

Andrzejak RG, Lehnertz K, Mormann F, Rieke C, David P, Elger CE. Indications of nonlinear deterministic and finite-dimensional structures in time series of brain electrical activity: dependence on recording region and brain state. Phys Rev E. 2001;64(6 Pt 1):061907. DOI: 10.1103/PhysRevE.64.061907.

Kingma DP, Ba J. Adam: a method for stochastic optimization. In: Proceedings of the 3rd International Conference on Learning Representa-tions (ICLR); 2015. arXiv:1412.6980.

Zhu R, Pan W, Liu J, Shang J. Epileptic seizure prediction via multidimensional transformer and recurrent neural network fusion. J Transl Med. 2024;22(1):895. DOI: 10.1186/s12967-024-05678-7.

Liu X, Li C, Lou X, Kong H, Li X, Li Z, et al. Epileptic seizure prediction based on EEG using pseudo-three-dimensional CNN. Front Neuroin-form. 2024;18:1354436. DOI: 10.3389/fninf.2024.1354436.

Li Z, Hwang K, Li K, Wu J, Ji T. Graph-generative neural network for EEG-based epileptic seizure detection via discovery of dynamic brain functional connectivity. Sci Rep. 2022;12:18998. DOI: 10.1038/s41598-022-23656-1.

Dallmer Zerbe I, Khambhati AN, Davis KA, et al. Computational modeling allows unsupervised classification of epileptic brain states across species. Sci Rep. 2023;13:14063. DOI: 10.1038/s41598-023-39867-z.

Kashyap N, Tripathi M, Bhattacharya S, Pandey S. Unsupervised pre-ictal state identification in human EEG using variational auto-encoders. Front Neurosci. 2022;16:1045732. DOI: 10.3389/fnins.2022.1045732.

Dubcek T, Levenstein D, Buzsaki G, et al. Personalized identification, prediction, and stimulation of neural oscillations via data-driven models of epileptic network dynamics. arXiv. 2023:2310.13480. DOI: 10.48550/arXiv.2310.13480.

Weiss SA, Banks GP, McKhann GM, et al. Localizing epileptogenic regions using high-frequency oscillations and machine learning. Biomark Med. 2019;13(5):409-418. DOI: 10.2217/bmm-2018-0335.

Li Z, Zhao B, Hu W, et al. Machine learning-based classification of physiological and pathological high-frequency oscillations recorded by stereoelectroencephalography. Seizure. 2023;113:58-65. DOI: 10.1016/j.seizure.2023.11.005.

Monsoor T, Zhang Y, Daida A, et al. Optimizing detection and deep learning-based classification of pathological high-frequency oscillations in epilepsy. Clin Neurophysiol. 2023;154:129-140. DOI: 10.1016/j.clinph.2023.07.012.

Gabeff V, Teijeiro T, Zapater M, Cammoun L, Rheims S, Ryvlin P, et al. Interpreting deep learning models for epileptic seizure detection on EEG signals. Artif Intell Med. 2021;117:102084. doi:10.1016/j.artmed.2021.102084

Saglio CBL, Pagani S, Corti M, Antonietti PF. A high-order discontinuous Galerkin method for the numerical modeling of epileptic seizures. arXiv. 2024:2401.14310. DOI: 10.48550/arXiv.2401.14310.

Proix T, Jirsa VK, Bartolomei F, Guye M, Truccolo W. How do parcellation size and short-range connectivity affect dynamics in large-scale brain network models? Neuroimage. 2016;142:135-149. doi:10.1016/j.neuroimage.2016.06.016.

Hesthaven JS, Warburton T. Nodal Discontinuous Galerkin Methods: Algorithms, Analysis, and Applications. New York (NY): Springer; 2008. DOI: 10.1007/978-0-387-72067-8.

van der Vlag MA, Hernando JB, Woodman MM, et al. RateML: a code generation tool for brain network models. Front Netw Physiol. 2022;2:826345. DOI: 10.3389/fnetp.2022.826345.

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2026-07-01

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1.
Pidvalnyi I, Sudakov O. Physical Processes in Biological Neuronal Networks During Epileptic Seizures: An Overview of Models. Innov Biosyst Bioeng [Internet]. 2026Jul.1 [cited 2026Jul.4];10(2):17-32. Available from: https://ibb.kpi.ua/article/view/349634