Plasticity of intrinsic neuronal excitability

Homeostatic plasticity in the developing nervous system

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The Spike-Timing Dependence of Plasticity

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The other side of the engram: experience-driven changes in neuronal intrinsic excitability

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Time cells in the hippocampus: a new dimension for mapping memories

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Plasticity in the intrinsic excitability of cortical pyramidal neurons

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Graded persistent activity in entorhinal cortex neurons

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Dendritic Excitability and Synaptic Plasticity

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Compartmentalized dendritic plasticity and input feature storage in neurons

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Hypothalamic control of puberty: from neuronal circuits to mechanisms for its metabolic regulation

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Static magnetic field stimulation enhances shunting inhibition via a SLC26 family Cl−channel, inducing intrinsic plasticity

Sinha, A. S., Shibata, S., Takamatsu, Y., Akita, T., Fukuda, A., & Mima, T. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.1324-22.2024 · Cited by 12

A Novel Ubiquitin Ligase Adaptor PTPRN Suppresses Seizure Susceptibility through Endocytosis of NaV1.2 Sodium Channels

Wang, Y., Yang, H., Li, N., Wang, L., Guo, C., Ma, W., Liu, S., Peng, C., Chen, J., Song, H., et al. (2024) · Advanced Science · doi:10.1002/advs.202400560 · Cited by 11

Conventional measures of intrinsic excitability are poor estimators of neuronal activity under realistic synaptic inputs

Szabó, A., Schlett, K., & Szűcs, A. L. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1009378 · Cited by 12

Nanolayered NbO2-Based Dynamic Memristor for Leaky Integrate and Fire Neuron

Wang, Y., Wang, W., Xu, H., Liu, S., Cao, R., Sun, Y. K., Tong, P., Song, B., & Li, Q. (2024) · ACS Applied Nano Materials · doi:10.1021/acsanm.4c01087 · Cited by 11

Memsensing by surface ion migration within Debye length

Guo, R., Feng, Q., Ma, K., Lee, G., Jamal, M., Zhao, X., Bustillo, K. C., Wan, J., Ritchie, D. S., Shan, L., et al. (2025) · Nature Materials · doi:10.1038/s41563-025-02312-9 · Cited by 11

A second-order adaptive network model for emotion regulation in addictive social media behaviour

Fokker, E. S., Zong, X., & Jan Treur, A. (2021) · Cognitive Systems Research · doi:10.1016/j.cogsys.2021.07.006 · Cited by 11

Removal of Perineuronal Nets Leads to Altered Neuronal Excitability and Synaptic Transmission in Visual Cortex with Distinct Time Courses

Liu, L., Zhang, Y., & Ju, J. (2022) · Neuroscience Letters · doi:10.1016/j.neulet.2022.136763 · Cited by 10

Kallikrein 8: A key sheddase to strengthen and stabilize neural plasticity

Shiosaka, S. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104774 · Cited by 12

Self-Assembled Monolayer and Nanoparticles Coenhanced Fragmented Silver Nanowire Network Memristor

Chen, W., Mou, Z., Xin, Y., Li, H., Wang, T., Chen, Y., Chen, L., Yang, B., Chen, Z., Luo, Y., et al. (2024) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.3c15351 · Cited by 11

Switching In and Out of Sync: A Controlled Adaptive Network Model of Transition Dynamics in the Effects of Interpersonal Synchrony on Affiliation

Hendrikse, S. C. F., Jan Treur, A., Wilderjans, T. F., Dikker, S., & Koole, S. L. (2023) · Studies in computational intelligence · doi:10.1007/978-3-031-21131-7_7 · Cited by 10

Visual activity enhances neuronal excitability in thalamic relay neurons

Duménieu, M., Fronzaroli‐Molinières, L., Naudin, L., Iborra, C., Wakade, A., Zanin, É., Aziz, A., Ankri, N., Incontro, S., Denis, D., et al. (2025) · Science Advances · doi:10.1126/sciadv.adp4627 · Cited by 10

The influence of visual deprivation on the development of the thalamocortical network: Evidence from congenitally blind children and adults

Lin, J., Zhang, L., Guo, R., Jiao, S., Song, X., Feng, S., Wang, K., Li, M., Luo, Y., & Han, Z. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119722 · Cited by 11

Rapid, Activity-Dependent Intrinsic Plasticity in the Developing Zebra Finch Auditory Cortex

Lü, Y., Sciaccotta, F., Kiely, L., Bellanger, B., Erişir, A., & Meliza, C. D. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.0354-23.2023 · Cited by 12

Teaching to Empower: Leveraging the Neuroscience of Now to Help Students Become Self-Regulated Learners

Imad, M. (2022) · Journal of Undergraduate Neuroscience Education · doi:10.59390/wtlq2344 · Cited by 10

Plasticity in the Brainstem: Prenatal and Postnatal Experience Can Alter Laterodorsal Tegmental (LDT) Structure and Function

Kohlmeier, K. A., & Polli, F. S. (2020) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2020.00003 · Cited by 13

Dendritic Kv4.2 potassium channels selectively mediate spatial pattern separation in the dentate gyrus

Oulé, M., Atucha, E., Wells, T. M., Macharadze, T., Sauvage, M. M., Kreutz, M. R., & Lopez‐Rojas, J. (2021) · iScience · doi:10.1016/j.isci.2021.102876 · Cited by 10

Modular arrangement of synaptic and intrinsic homeostatic plasticity within visual cortical circuits

Wen, W., Prada, A. M., & Turrigiano, G. G. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2504775122 · Cited by 12

State-dependent modulation of spiny projection neurons controls levodopa-induced dyskinesia in a mouse model of Parkinson’s disease

Zhai, S., Cui, Q., Wokosin, D. L., Sun, L., Tkatch, T., Crittenden, J. R., Graybiel, A. M., & Surmeier, D. J. (2025) · Science Advances · doi:10.1126/sciadv.adv8224 · Cited by 11

Changes in cerebellar intrinsic neuronal excitability and synaptic plasticity result from eyeblink conditioning

Schreurs, B. G. (2019) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2019.107094 · Cited by 9

Neuronal Spike Shapes (NSS): A straightforward approach to investigate heterogeneity in neuronal excitability states

Martini, L., Amprimo, G., Carlo, S. D., Olmo, G., Ferraris, C., Savino, A., & Bardini, R. (2023) · Computers in Biology and Medicine · doi:10.1016/j.compbiomed.2023.107783 · Cited by 8

Dentate Granule Cells Recruited in the Home Environment Display Distinctive Properties

Pléau, C., Peret, A., Pearlstein, É., Scalfati, T., Vigier, A., Marti, G., Michel, F. J., Marissal, T., & Crépel, V. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.609123 · Cited by 9

Disorder of neuroplasticity aggravates cognitive impairment via neuroinflammation associated with intestinal flora dysbiosis in chronic heart failure

Chen, J., Wei, X., Wu, X.-F., Zhang, Q., Xia, G., Xia, H., Shang, H., & Lin, S. H. (2024) · Aging · doi:10.18632/aging.205960 · Cited by 8

Electromechanically induced membrane restructuring enables learning and memory

Podar, P. T., Bolmatov, D., Kumarage, T., Ashkar, R., Adkisson, A., Ziemer, O. J., Sullivan, V., Mohamed, A. S. I., Najem, J. S., Collier, C. P., et al. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2510664122 · Cited by 8

A Multi-timescale Multi-adaptive Dynamical System Approach for Relationship-Specific and Relationship-Independent Adaptivity in Affiliation and Bonding

Hendrikse, S. C. F., Jan Treur, A., & Koole, S. L. (2025) · Studies in systems, decision and control · doi:10.1007/978-3-031-99968-0_13 · Cited by 8

On the Interplay of Interpersonal Synchrony, Short-Term Affiliation and Long-Term Bonding: A Second-Order Multi-adaptive Neural Agent Model

Hendrikse, S. C. F., Jan Treur, A., Wilderjans, T. F., Dikker, S., & Koole, S. L. (2022) · IFIP advances in information and communication technology · doi:10.1007/978-3-031-08333-4_4 · Cited by 8

Neuronal connectivity, behavioral, and transcriptional alterations associated with the loss of MARK2

Caiola, H., Wu, Q., Li, J., Wang, X., Soni, S., Monahan, K., Wagner, G. C., Pang, Z. P., & Zhang, H. (2024) · The FASEB Journal · doi:10.1096/fj.202400454r · Cited by 8

Intracellular Properties of Deep-Layer Pyramidal Neurons in Frontal Eye Field of Macaque Monkeys

Piette, C., Vandecasteele, M., Bosch‐Bouju, C., Goubard, V., Paillé, V., Cui, Y., Mendes, A., Siaume‐Perez, S., Valtcheva, S., Xu, H., et al. (2021) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2021.725880 · Cited by 8

Neuroligin-3 Regulates Excitatory Synaptic Transmission and EPSP-Spike Coupling in the Dentate Gyrus In Vivo

Muellerleile, J., Vnencak, M., Ippolito, A., Krueger‐Burg, D., Jungenitz, T., Schwarzacher, S. W., & Jedlička, P. (2021) · Molecular Neurobiology · doi:10.1007/s12035-021-02663-9 · Cited by 8

Estrogen signaling in the ventromedial hypothalamus is required for the development of aggression circuitry in male mice

Zha, X., Liu, X.-Y., Wang, L. A., Li, S., Sun, Y.-Z., Lin, J.-K., Yan, J., Gao, M.-T., Zhang, Y., Yang, R., et al. (2025) · Current Biology · doi:10.1016/j.cub.2025.04.076 · Cited by 8

An Integrative Multi-Adaptive Biological-Mental-Environmental Network Architecture for Epigenetic Control and Mental Self-Regulation

Jan Treur, A. (2026) · Studies in systems, decision and control · doi:10.1007/978-3-032-17029-3_4 · Cited by 7

Electroacupuncture modulates cortical excitability in a manner dependent on the parameters used

de Brito, F. X., Luz-Santos, C., Camatti, J. R., da Fonseca, R. J. D. S., Suzarth, G., Moraes, L. M. C., da Silva, M. L., da Silva, J. R. T., Vercelino, R., Sá, K. N., et al. (2021) · Acupuncture in Medicine · doi:10.1177/09645284211057560 · Cited by 7

Electrophysiological properties of layer 2/3 pyramidal neurons in the primary visual cortex of a retinitis pigmentosa mouse model (rd10)

Halfmann, C., Rüland, T., Müller, F. U., Jehasse, K., & Kampa, B. M. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1258773 · Cited by 6

If you please, draw me a neuron — linking evolutionary tinkering with human neuron evolution

Libé‐Philippot, B., Polleux, F., & Vanderhaeghen, P. (2024) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2024.102260 · Cited by 9

Accelerated signal propagation speed in human neocortical dendritesPreprint

Oláh, G., Lákovics, R., Shapira, S., Leibner, Y., Szűcs, A. L., Csajbók, É., Barzó, P., Molnár, G., Segev, I., & Tamás, G. (2024) · eLife · doi:10.7554/elife.93781 · Cited by 10

Heterozygous expression of a Kcnt1 gain-of-function variant has differential effects on somatostatin- and parvalbumin-expressing cortical GABAergic neuronsPreprint

Shore, A. N., Li, K., Safari, M., Qunies, A. M., Spitznagel, B. D., Weaver, C. D., Emmitte, K. A., Frankel, W. N., & Weston, M. C. (2024) · eLife · doi:10.7554/elife.92915.4 · Cited by 9

Rivalling Dynamic Adaptation of Intrinsic Neuronal Plasticity in Dual‐Mode Mott Memristor Electronic Neuron for Spiking Control

Liao, Z., Chen, K., Shih, L., Chen, S. C., Hsu, K., Chen, C., Lin, K., & Chen, J. (2025) · Advanced Functional Materials · doi:10.1002/adfm.202508585 · Cited by 7

Cellular and subcellular specialization enables biology-constrained deep learning

Galloni, A. R., Peddada, A., Chennawar, Y., & Milstein, A. D. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.117159 · Cited by 10

Suppressing Retinal Remodeling to Mitigate Vision Loss in Photoreceptor Degenerative Disorders

Krämer, R. (2023) · Annual Review of Vision Science · doi:10.1146/annurev-vision-112122-020957 · Cited by 9

Compressive sensing of functional connectivity maps from patterned optogenetic stimulation of neuronal ensembles

Navarro, P., & Oweiss, K. G. (2023) · Patterns · doi:10.1016/j.patter.2023.100845 · Cited by 6

Contiguity in perception: origins in cellular associative computations

Hansel, C. (2024) · Trends in Neurosciences · doi:10.1016/j.tins.2024.01.001 · Cited by 6

Differential Modulation of Dopamine D2 Receptor on Somatostatin and Parvalbumin Interneurons in the CA1 Area of the Dorsal Hippocampus

Tuduri, P., Mignon, A., Valjent, E., & Ster, J. (2025) · European Journal of Neuroscience · doi:10.1111/ejn.70176 · Cited by 5

Accelerated signal propagation speed in human neocortical dendrites

Oláh, G., Lákovics, R., Shapira, S., Leibner, Y., Szűcs, A. L., Csajbók, É., Barzó, P., Molnár, G., Segev, I., & Tamás, G. (2025) · eLife · doi:10.1101/2022.09.30.510270 · Cited by 4

Modeling activity-dependent reduction in after hyper-polarization with Hodgkin-Huxley equation of action potential

Talukdar, S., Shrivastava, R., & Ghosh, S. (2019) · Biomedical Physics & Engineering Express · doi:10.1088/2057-1976/ab1a1d · Cited by 5

Accelerated signal propagation speed in human neocortical microcircuitsPreprint

Oláh, G., Lákovics, R., Shapira, S., Leibner, Y., Szűcs, A. L., Csajbók, É., Barzó, P., Molnár, G., Segev, I., & Tamás, G. (2024) · eLife · doi:10.7554/elife.93781.1 · Cited by 5

Metaplasticity and continual learning: mechanisms subserving brain computer interface proficiency

Chueh, S.-Y., Chen, Y., Subramanian, N., Goolsby, B. A., Navarro, P., & Oweiss, K. G. (2025) · Journal of Neural Engineering · doi:10.1088/1741-2552/add37b · Cited by 4

On the Interplay of Epigenetics, ADHD and Digital Media Usage: An Adaptive Dynamical System Modelling Approach

Hinkel, N. L., & Jan Treur, A. (2025) · IFIP advances in information and communication technology · doi:10.1007/978-3-031-96235-6_14 · Cited by 4

Emergence of sparse coding, balance and decorrelation from a biologically-grounded spiking neural network model of learning in the primary visual cortex

Ruslim, M. A., Spencer, M., Hogendoorn, H., Hamish Meffin, A., Lian, Y., & Burkitt, A. N. (2025) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1013644 · Cited by 5

Clinical effects of non-invasive brain stimulation

Hallett, M. (2020) · Swiss Archives of Neurology Psychiatry and Psychotherapy · doi:10.4414/sanp.2020.03154 · Cited by 4

A Novel Neurorehabilitation Approach for Neural Plasticity Overstimulation and Reorganization in Patients with Neurological Disorders

Alashram, A. R., & Annino, G. (2023) · Physikalische Medizin Rehabilitationsmedizin Kurortmedizin · doi:10.1055/a-2004-5836 · Cited by 4

The Role of Cerebellar Intrinsic Neuronal Excitability, Synaptic Plasticity, and Perineuronal Nets in Eyeblink Conditioning

Schreurs, B. G., O’Dell, D. E., & Wang, D. (2024) · Biology · doi:10.3390/biology13030200 · Cited by 4

An integrated in vitro platform and biophysical modeling approach for studying synaptic transmission in isolated neuronal pairs

Amos, G., Vasiliauskaitė, V., Duru, J., Saramago, M. L. A., Schmid, T., Suter, A., Torren, F. C., Küchler, J., Ruff, T., Vörös, J., et al. (2026) · iScience · doi:10.1016/j.isci.2026.115488 · Cited by 3

Afterhyperpolarization amplitude in CA1 pyramidal cells of aged Long-Evans rats characterized for individual differences

Severín, D., Gallagher, M., & Kirkwood, A. (2020) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2020.07.022 · Cited by 4

Echo State Network Optimization: A Systematic Literature ReviewPreprint

Soltani, R., Benmohamed, E., & Ltifi, H. (2022) · Research Square · doi:10.21203/rs.3.rs-1909702/v1 · Cited by 4

LRRC37B Is a Species-Specific Regulator of Voltage-Gated Channels and Excitability in Human Cortical NeuronsPreprint

Libé‐Philippot, B., Lejeune, A., Wierda, K. D. B., Vlaeminck, I., Beckers, S., Gaspariunaite, V., Bilheu, A., Nyitrai, H., Vennekens, K. M., Bird, T. W., et al. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4309022 · Cited by 4

Enhancing Cyber Resilience Securing Governmental Applications for Citizens: Computational Analysis

Babayusuf, Y., Bouma, D., Feteasco, A., van Hekezen, L., Vasov, J., Zwarts, N., Jan Treur, A., & Roelofsma, P. H. M. P. (2025) · Communications in computer and information science · doi:10.1007/978-981-96-1907-8_27 · Cited by 3

Towards dynamic computing: Multi-dynamic neuronal-synaptic transistors for visual intelligence

Xu, C., Zhu, Z., Zeng, H., Xue, J., Yang, Q., & Chen, H. (2025) · Nano Energy · doi:10.1016/j.nanoen.2025.111656 · Cited by 3

Adenosine and Cortical Plasticity

Martínez‐Gallego, I., & Moreno, A. R. (2024) · The Neuroscientist · doi:10.1177/10738584241236773 · Cited by 5

The modulation of cholecystokinin receptor 1 in the NAc core input from VTA on METH-induced CPP acquisition

Wang, J., Zhang, M., Sun, Y., Su, X., Hui, R., Zhang, L., Xie, B., Cong, B., Luo, Y., Wen, D., et al. (2024) · Life Sciences · doi:10.1016/j.lfs.2024.123290 · Cited by 3

Antifragile control systems in neuronal processing: a sensorimotor perspective

Axenie, C. (2025) · Biological Cybernetics · doi:10.1007/s00422-025-01003-7 · Cited by 4

What are memories made of? A survey of neuroscientists on the structural basis of long-term memory

Zeleznikow-Johnston, A., Kendziorra, E., & McKenzie, A. T. (2025) · PLoS ONE · doi:10.1371/journal.pone.0326920 · Cited by 4

From a Multilevel Multi-Timescale Computational Architecture for Synchrony-Induced and Homophily-Induced Attunement to Designing Bonding Bots

Hendrikse, S. C. F., & Jan Treur, A. (2025) · Studies in systems, decision and control · doi:10.1007/978-3-031-99968-0_20 · Cited by 3

Visual Cortical Plasticity: Molecular Mechanisms as Revealed by Induction Paradigms in Rodents

Ribeiro, F. M., Castelo-Branco, M. S., Gonçalves, J., & Martins, J. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054701 · Cited by 3

Distinct Features of Interictal Activity Predict Seizure Localization and Burden in a Mouse Model of Childhood Epilepsy

Tobin, W. F., & Weston, M. C. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.2205-22.2023 · Cited by 4

Perspectives on Social Interaction Science: From a Multilevel Multi-timescale Computational Architecture for Synchrony-Induced and Homophily-Induced Attunement to Designing Bonding Bots

Hendrikse, S. C. F., & Jan Treur, A. (2025) · Lecture notes in networks and systems · doi:10.1007/978-3-031-96759-7_39 · Cited by 3

Intrinsic and Synaptic Dynamics Contribute to Adaptation in the Core of the Avian Central Nucleus of the Inferior Colliculus

Malinowski, S. T., Wolf, J., & Kuenzel, T. (2019) · Frontiers in Neural Circuits · doi:10.3389/fncir.2019.00046 · Cited by 3

Context-Sensitive Control of Adaptation: Self-Modeling Networks for Human Mental Processes Using Mental Models

Bhalwankar, R., van Ments, L., & Jan Treur, A. (2021) · Frontiers in artificial intelligence and applications · doi:10.3233/faia210288 · Cited by 3

Neuronal plasticity at puberty in hypothalamic neurons controlling fertility in female micePreprint

Zhang, Y., Pakulat, L. M., Galliano, E., Colledge, W. H., & Jones, S. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.10.06.616855 · Cited by 3

A Self-Modeling Network Model Addressing Controlled Adaptive Mental Models for Analysis and Support Processes

Jan Treur, A. (2021) · Complex Systems · doi:10.25088/complexsystems.30.4.483 · Cited by 2

Distinct Modulation of I h by Synaptic Potentiation in Excitatory and Inhibitory Neurons

Herstel, L. J., & Wierenga, C. J. (2024) · eNeuro · doi:10.1523/eneuro.0185-24.2024 · Cited by 2

β-adrenergic receptor-induced E-S potentiation in the dorsal and ventral hippocampus

Trompoukis, G., Miliou, A., & Papatheodoropoulos, C. (2024) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2024.1511485 · Cited by 3

Computational models of learning and synaptic plasticity

Tyulmankov, D. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-15754-7.00078-x · Cited by 3

Non-synaptic plasticity enables memory-dependent local learning

Romain, F., Baronig, M., Unger, F., & Legenstein, R. A. (2025) · PLoS ONE · doi:10.1371/journal.pone.0313331 · Cited by 3

Burst firing represents learned composite stimuli in primary sensory cortices

Jia, H., Wang, M., Pakan, J. M. P., Li, S. C., & Chen, X. (2025) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2025.103039 · Cited by 3

Memory retention in pyramidal neurons: a unified model of energy-based homo and heterosynaptic plasticity with homeostasis

Chen, H., Xie, L., Wang, Y., & Zhang, H. (2020) · Cognitive Neurodynamics · doi:10.1007/s11571-020-09652-z · Cited by 2

A Model of the Early Visual System Based on Parallel Spike-Sequence Detection, Showing Orientation Selectivity

Santos‐Mayo, A., Moratti, S., de Echegaray, J., & Susi, G. (2021) · Biology · doi:10.3390/biology10080801 · Cited by 3

Memory destabilization during reconsolidation: a consequence of homeostatic plasticity?Preprint

Amorim, F. E., Chapot, R. L., Moulin, T. C., Lee, J. L. C., & Amaral, O. B. (2021) · Learning & Memory · doi:10.1101/lm.053418.121 · Cited by 3

Getting seniors back on their bicycle; a pretest-posttest case-control study on the improvement of bicycle balance controlPreprint

Maris, E. (2024) · medRxiv · doi:10.1101/2024.04.17.24305755 · Cited by 2

Heterozygous expression of a Kcnt1 gain-of-function variant has differential effects on SST- and PV-expressing cortical GABAergic neuronsPreprint

Shore, A. N., Li, K., Safari, M., Qunies, A. M., Spitznagel, B. D., Weaver, C. D., Emmitte, K. A., Frankel, W. N., & Weston, M. C. (2024) · eLife · doi:10.7554/elife.92915.3 · Cited by 2

Accelerated signal propagation speed in human neocortical dendritesPreprint

Oláh, G., Lákovics, R., Shapira, S., Leibner, Y., Szűcs, A. L., Csajbók, É., Barzó, P., Molnár, G., Segev, I., & Tamás, G. (2025) · eLife · doi:10.7554/elife.93781.2 · Cited by 2

A bibliometric analysis of synaptic plasticity and epilepsy from 2003 to 2023

Li, X., Sun, H., Chen, Z., Meng, H., & Zhang, D. (2025) · Frontiers in Neurology · doi:10.3389/fneur.2025.1533268 · Cited by 1

Modeling Musical Perception

Sawicki, J. (2025) · Current research in systematic musicology · doi:10.1007/978-3-031-97003-0_5 · Cited by 1

Gain modulation of probabilistic selection without synaptic relearning

Ersöz, E. K., Chossat, P., & Lavigne, F. (2025) · PLoS ONE · doi:10.1371/journal.pone.0333350 · Cited by 4

Temporal dynamics of Purkinje cell-intrinsic excitability governs cerebellar systems consolidation

Seo, J., Kim, Y. G., Lee, Y., & Kim, S. J. (2025) · iScience · doi:10.1016/j.isci.2025.113760 · Cited by 5

Neuronal plasticity at puberty in mouse hypothalamic Kiss1 neurons that control fertility

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Input-Specific Organization of Intrinsic Excitability Expands Coding Capacity of Fast-Spiking Auditory Neurons

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Intrinsic Plasticity Underlies the Malleability of Neural Network Heterogeneity

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Heterozygous expression of a Kcnt1 gain-of-function variant has differential effects on SST- and PV-expressing cortical GABAergic neuronsPreprint

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Plasticity of neuronal excitability: Hebbian rules beyond the synapse.

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