Tipping the Scales: Peptide-Dependent Dysregulation of Neural Circuit Dynamics in Alzheimer’s Disease

Neuropathological stageing of Alzheimer-related changes.

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The Amyloid Hypothesis of Alzheimer’s Disease: Progress and Problems on the Road to Therapeutics

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Tracking pathophysiological processes in Alzheimer's disease: an updated hypothetical model of dynamic biomarkers

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Naturally secreted oligomers of amyloid β protein potently inhibit hippocampal long-term potentiation in vivo

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Amyloid-β protein dimers isolated directly from Alzheimer's brains impair synaptic plasticity and memory

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Abnormal phosphorylation of the microtubule-associated protein tau (tau) in Alzheimer cytoskeletal pathology.

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Phases of Aβ-deposition in the human brain and its relevance for the development of AD

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Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

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Neurofibrillary tangles but not senile plaques parallel duration and severity of Alzheimer's disease

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The Cellular Phase of Alzheimer’s Disease

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Evaluating the Diagnostic Value of Electrovestibulography (EVestG) in Alzheimer’s Patients with Mixed Pathology: A Pilot Study

Dastgheib, Z. A., Lithgow, B., & Moussavi, Z. (2023) · Medicina · doi:10.3390/medicina59122091 · Cited by 4

Virtual neural network-guided optimization of non-invasive brain stimulation in Alzheimer’s disease

Luppi, J. J., Stam, C. J., Scheltens, P., & de Haan, W. (2024) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1011164 · Cited by 4

Co‐activation of Selective Nicotinic Acetylcholine Receptor Subtypes Is Required for Neuroprotection against Alzheimer's Disease

Lee, R., Kim, G., Black, E. R., & Kim, S. (2026) · Advanced Science · doi:10.1002/advs.77858 · Cited by 4

DecGAN: Decoupling Generative Adversarial Network detecting abnormal neural circuits for Alzheimer's diseasePreprint

Pan, J., Lei, B., Wang, S., Wang, B.-C., Liu, Y., & Shen, Y. (2021) · arXiv (Cornell University) · doi:10.48550/arxiv.2110.05712 · Cited by 4

Neuron-like function of the nephron central commandPreprint

Gyarmati, G., Shroff, U. N., Riquier‐Brison, A., Stocker, S. D., Izuhara, A. K., Deepak, S. K., Chen, Y., Biemesderfer, D., James, A. W., Minichiello, L., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.12.06.471478 · Cited by 4

Amyloid-Beta Peptides Trigger Premature Functional and Gene Expression Alterations in Human-Induced Neurons

de Farias, A. R. M., Pelletier, A., Iohan, L. D. C. C., Saha, O., Bonnefond, A., Amouyel, P., Delahaye, F., Lambert, J., & Costa, M. R. (2023) · Biomedicines · doi:10.3390/biomedicines11092564 · Cited by 4

Investigating the neuronal role of the proteasomal ATPase subunit gene PSMC5 in neurodevelopmental proteasomopathies

Küry, S., Stanton, J. E., van Woerden, G. M., Bosc-Rosati, A., Hsieh, T.-C., Bray, L., Oloudé, M., Rosenfelt, C., Scott-Boyer, M. P., Most, V., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-65556-8 · Cited by 3

A Python toolbox for neural circuit parameter inference

Valero, A. O., Rodríguez-González, V., Montobbio, N., Casal, M. A., Tlaie, A., Pelayo, F. J., Morillas, C. A., Poza, J., Gómez, C., & Martínez‐Cañada, P. (2025) · npj Systems Biology and Applications · doi:10.1038/s41540-025-00527-9 · Cited by 3

Hippocampus and amygdala volume and morphology in neurodegenerative disorders with co-morbid epilepsy

Zawar, I., Zhu, S., Quigg, M., Kapur, J., Manning, C. A., & Fletcher, P. T. (2025) · NeuroImage Clinical · doi:10.1016/j.nicl.2025.103830 · Cited by 3

The Interaction between Oligodendrocytes and Aβ in Alzheimer's Disease

Wang, W., Huang, X., Xu, Z., & Yu, C. (2025) · Current Alzheimer Research · doi:10.2174/0115672050401966250625171338 · Cited by 3

Longitudinal functional connectivity during rest and task is differentially related to Alzheimer’s pathology and episodic memory in older adults

Fischer, L., Adams, J. N., Molloy, E. N., Tremblay‐Mercier, J., Remz, J., Binette, A. P., Rajah, M. N., Villeneuve, S., Maaß, A., Poirier, J., et al. (2025) · Scientific Reports · doi:10.1038/s41598-025-21596-0 · Cited by 4

Treadmill exercise prevents the hyperexcitability of pyramidal neurons in medial entorhinal cortex in the 3xTg-AD mouse model of Alzheimer's disease

Chen, H., Cai, J., Wang, A., Su, W., Ji, C., & Zhao, L. (2023) · Experimental Gerontology · doi:10.1016/j.exger.2023.112309 · Cited by 4

The US9-Derived Protein gPTB9TM Modulates APP Processing Without Targeting Secretase Activities

Brandimarti, R., Irollo, E., & Meucci, O. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-03153-2 · Cited by 4

Behaviorally meaningful functional networks mediate the effect of Alzheimer’s pathology on cognition

Ziontz, J., Harrison, T. M., Chen, X., Giorgio, J., Adams, J. N., Wang, Z., Jagust, W. J., & Initiative, A. D. N. (2024) · Cerebral Cortex · doi:10.1093/cercor/bhae134 · Cited by 3

Sex Differences in Magnetoencephalography-Identified Functional Connectivity in the Human Connectome Project Connectomics of Brain Aging and Dementia Cohort

Bruña, R., Maestú, F., López‐Sanz, D., Bagic, A. I., Cohen, A. D., Chang, Y., Cheng, Y., Doman, J. M., Huppert, T., Kim, T., et al. (2021) · Brain Connectivity · doi:10.1089/brain.2021.0059 · Cited by 3

Impairments of spatial memory retrieval via medial mammillary body dysfunction in Alzheimer’s disease model

Huang, D., Long, Y., Yang, Y., Wu, J., Yang, J., Huang, Y., Li, Y., Liu, P., Yuan, M., Song, X., et al. (2025) · Translational Psychiatry · doi:10.1038/s41398-025-03583-1 · Cited by 2

Hippocampal neural circuit mechanisms in Alzheimer's disease revealed by viral-genetic circuit mapping

Ye, Q., Gast, G., Holmes, T. C., & Xu, X. (2025) · Neurobiology of Disease · doi:10.1016/j.nbd.2025.107139 · Cited by 2

The rise and deceleration of neuronal excitability in aging and Alzheimer’s disease: Mechanisms, implications, and therapeutic targets

Delbono, O., Wang, Z., & Messi, M. L. (2025) · Ageing Research Reviews · doi:10.1016/j.arr.2025.102999 · Cited by 3

GABA B Receptor signaling in CA1 Pyramidal Cells is not Regulated by Aging in the APP/PS1 Mouse Model of Amyloid Pathology

Meftah, S., Wilson, M. A., Elliott, J., McLay, L., Dobrovolskis, V., Rosencrans, S., Taylor, L. W., Mugnaini, C., Mostallino, R., Durrant, C. S., et al. (2026) · eNeuro · doi:10.1523/eneuro.0099-23.2025 · Cited by 2

Restoration of gamma center frequency via personalized entrainment marks cognitive preservation in early Alzheimer’s disease

Park, Y., Chae, H., Yoon, E., Kim, Y., Han, J. W., Woo, S. J., Yoo, S., & Kim, K. W. (2026) · GeroScience · doi:10.1007/s11357-026-02235-6 · Cited by 2

Deep cortical layers are more vulnerable in Alzheimer’s disease

Kazmi, S. Z. H., & Wierenga, C. J. (2025) · Neuron · doi:10.1016/j.neuron.2025.06.022 · Cited by 2

Modeling presynaptic inhibition by the amyloid precursor protein demonstrates one potential mechanism for preventing runaway synaptic modification in Alzheimer's disease

Barber, D., Hasselmo, M. E., & Rice, H. C. (2025) · Alzheimer s & Dementia · doi:10.1002/alz.70748 · Cited by 1

Evidence against altered excitatory/inhibitory balance in the posteromedial cortex of young adult APOE E4 carriers: A resting state 1H-MRS study

Costigan, A. G., Umla‐Runge, K., Evans, J., Raybould, R., Graham, K. S., & Lawrence, A. D. (2021) · Neuroimage Reports · doi:10.1016/j.ynirp.2021.100059 · Cited by 2

Altern und neurodegenerative Erkrankungen – warum gehen Nervenzellen verloren?

Klimaschewski, L. P. (2021) · Springer eBooks · doi:10.1007/978-3-662-63392-2_2 · Cited by 2

Homeostatic plasticity of axonal excitable sites in Alzheimer's disease

Quintela-López, T., & Lezmy, J. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1277251 · Cited by 2

A mechanistic model explains oscillatory slowing and neuronal hyperactivity in Alzheimer’s diseasePreprint

Alexandersen, C. G., de Haan, W., Bick, C., & Goriely, A. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.06.20.496731 · Cited by 2

Multimodal brain age estimates relate to Alzheimer disease biomarkers and cognition in early stages: a cross-sectional observational studyPreprint

Millar, P. R., Gordon, B. A., Luckett, P. H., Benzinger, T. L. S., Cruchaga, C., Fagan, A. M., Hassenstab, J. J., Perrin, R. J., Schindler, S. E., Allegri, R., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.08.25.505251 · Cited by 2

Multifunctional Tasks and an Energy Crisis are Crucial Players in Determining the Vulnerability of the Entorhinal Cortex to Early Damage in Alzheimer’s Disease

Sivanesan, S., Howell, M. D., Kaushik, V., Rajadas, J., Pari, S. S., & Goyal, P. (2024) · Current Alzheimer Research · doi:10.2174/0115672050324909240823104209 · Cited by 1

Neuromorphic deviations associated with transcriptomic expression and specific cell type in Alzheimer’s disease

Peng, J., Tang, Q., Li, Y., Liu, L., Biswal, B., & Wang, P. (2025) · Scientific Reports · doi:10.1038/s41598-025-90872-w · Cited by 1

Altered brain network dynamics and functional connectivity in subjective cognitive decline: an edge-centric network study

Wei, X., Zhou, B., Li, J., 徐, 若., & Zhang, W. (2026) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2025.1596537 · Cited by 1

Zinc-binding proteins in Alzheimer’s disease: mechanisms, therapeutic potential, and natural compound interventions

Upadhyay, R., Kar, S., & Sevanan, M. (2026) · Frontiers in Chemical Biology · doi:10.3389/fchbi.2026.1836070 · Cited by 1

ELEMENTARY PATHOPHYSIOLOGY, TREATMENT, RISK FACTOR OF ALZHEIMER’S DISEASE

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Aging and Neurodegenerative Diseases: Why do Nerve Cells Die?

Klimaschewski, L. P. (2022) · Springer eBooks · doi:10.1007/978-3-662-66369-1_2 · Cited by 1

Hippocampal connectivity with retrosplenial cortex drives neocortical tau accumulation and memory functionPreprint

Ziontz, J., Adams, J. N., Harrison, T. M., Baker, S. L., & Jagust, W. J. (2021) · doi:10.21203/rs.3.rs-235539/v1 · Cited by 1

Altered firing output of VIP interneurons and early dysfunctions in CA1 hippocampal circuits in the 3xTg mouse model of Alzheimer’s diseasePreprint

Michaud, F., Francavilla, R., Topolnik, D., Iloun, P., Tamboli, S., Calon, F., & Topolnik, L. (2024) · eLife · doi:10.7554/elife.95412.1 · Cited by 1

Spatial coding defects of hippocampal neural ensemble calcium activities in the 3xTg-AD Alzheimer’s disease mouse modelPreprint

Lin, X., Chen, L., Baglietto‐Vargas, D., Ye, Q., LaFerla, F. M., Nitz, D. A., Holmes, T. C., & Xu, X. (2021) · Research Square · doi:10.21203/rs.3.rs-550358/v1

The Alzheimer’s disease risk gene BIN1 modulates neural network activity via the regulation of L-type calcium channel expression in human-induced neuronsPreprint

Saha, O., de Farias, A. R. M., Pelletier, A., Siedlecki‐Wullich, D., Gadaut, J., Landeira, B. S., Carrier, A., Vreulx, A.-C., Guyot, K., Bonnefond, A., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.01.18.476601

Spectral graph modeling reveals global slowing of neurophysiological network transmission in Alzheimer’s diseasePreprint

Verma, P., Ranasinghe, K. G., Prasad, J., Cai, C., Xie, X., Lerner, H., Mizuiri, D., Miller, B. L., Rankin, K. P., Vossel, K. A., et al. (2023) · Research Square · doi:10.21203/rs.3.rs-2579392/v2

Spectral graph modeling reveals global slowing of neurophysiological network transmission in Alzheimer's diseasePreprint

Verma, P., Ranasinghe, K. G., Prasad, J., Cai, C., Xie, X., Lerner, H., Mizuiri, D., Miller, B. L., Rankin, K., Vossel, K. A., et al. (2023) · Research Square · doi:10.21203/rs.3.rs-2579392/v1

Epileptiforme activiteit bij de ziekte van Alzheimer

Nous, A., Vyver, M. V., & Smolders, I. J. (2023) · Epilepsie periodiek voor professionals · doi:10.54160/epilepsie.13851

Nuevas estrategias farmacológicas en la enfermedad de Alzheimer: la hiperactividad y la neuroinflamación como nuevos blancos potenciales

Lobos, P., More, J., Bruna, B., & Antonello Penna, S. (2023) · Revista Hospital Clínico Universidad de Chile · doi:10.5354/2735-7996.2023.71414

Impaired long-range excitatory time scale predicts abnormal neural oscillations and cognitive deficits in Alzheimer’s diseasePreprint

Verma, P., Ranasinghe, K. G., Prasad, J., Cai, C., Xie, X., Lerner, H., Mizuiri, D., Miller, B. L., Rankin, K. P., Vossel, K. A., et al. (2023) · Research Square · doi:10.21203/rs.3.rs-2579392/v3

Altered firing output of VIP interneurons and early dysfunctions in CA1 hippocampal circuits in the 3xTg mouse model of Alzheimer’s diseasePreprint

Michaud, F., Francavilla, R., Topolnik, D., Iloun, P., Tamboli, S., Calon, F., & Topolnik, L. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.12.575331

Altered firing output of VIP interneurons and early dysfunctions in CA1 hippocampal circuits in the 3xTg mouse model of Alzheimer’s diseasePreprint

Michaud, F., Francavilla, R., Topolnik, D., Iloun, P., Tamboli, S., Calon, F., & Topolnik, L. (2024) · eLife · doi:10.7554/elife.95412.2

Altered firing output of VIP interneurons and early dysfunctions in CA1 hippocampal circuits in the 3xTg mouse model of Alzheimer’s disease

Michaud, F., Francavilla, R., Topolnik, D., Iloun, P., Tamboli, S., Calon, F., & Topolnik, L. (2024) · eLife · doi:10.7554/elife.95412.3

面向神经功能环路解析的全光生理技术

Cheng, 靳. J., & Lingjie, 孔. K. (2024) · Chinese Journal of Lasers · doi:10.3788/cjl240730

Revealing hidden knowledge in amnestic micePreprint

Santi, A., Moore, S., Fogelson, K. A., Wang, A. H., Lawlor, J., Amato, J., Burke, K., Lauer, A. M., & Kuchibhotla, K. V. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.01.09.632026

Evaluating Feature Importance in the Context of Simulation-Based Inference for Cortical Circuit Parameter Estimation

Sandron, A., Valero, A. O., García, J. M., Mancini, G., Pelayo, F. J., Morillas, C. A., Panzeri, S., & Martínez‐Cañada, P. (2025) · Lecture notes in computer science · doi:10.1007/978-981-96-3294-7_35

Predicting cognitive change using functional, structural, and neuropsychological predictors

Décarie-Labbé, L., Mellah, S., Dialahy, I. Z., Bellec, P., Belleville, S., Bocti, C., Calon, F., Chertkow, H. M., Collins, D. L., Cunnane, S. C., et al. (2025) · Brain Communications · doi:10.1093/braincomms/fcaf155

Connectome-guided personalization of optimal tDCS intervention selection in Alzheimer’s diseasePreprint

Luppi, J. J., Koomen, A. P., Stam, C. J., Scheltens, P., & de Haan, W. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.08.18.670847

Additional file 1 of Aη-α and Aη-β peptides impair LTP ex vivo within the low nanomolar range and impact neuronal activity in vivo

Mensch, M., Dunot, J., Yishan, S. M., Harris, S., Blistein, A., Avdiu, A., Pousinha, P. A., Giudici, C., Busche, M. A., Jedlicka, P., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14936338

Additional file 1 of The AppNL-G-F mouse retina is a site for preclinical Alzheimer’s disease diagnosis and research

Vandenabeele, M., Veys, L., Lemmens, S., Hadoux, X., Gelders, G., Masin, L., Serneels, L., Theunis, J., Saito, T., Saido, T. C., et al. (2021) · Figshare · doi:10.6084/m9.figshare.13531796

Additional file 1 of Impaired long-range excitatory time scale predicts abnormal neural oscillations and cognitive deficits in Alzheimer’s disease

Verma, P., Ranasinghe, K. G., Prasad, J., Cai, C., Xie, X., Lerner, H., Mizuiri, D., Miller, B., Rankin, K., Vossel, K. A., et al. (2024) · Figshare · doi:10.6084/m9.figshare.25440916

Functional network phenotypes of mild behavioural impairment: cognitive effects moderated by amyloid

Ng, K. P., Chong, J. S. X., Lussier, F. Z., Therriault, J., Rahmouni, N., Savard, M., Stevenson, J., Pascoal, T. A., Gauthier, S. G., Rosa‐Neto, P., et al. (2026) · Alzheimer s Research & Therapy · doi:10.1186/s13195-026-01980-2 · Cited by 1

A Framework Integrating Spiking Cortical Circuit Modeling and Simulation-Based Inference to Probe Biomarkers of Cortical Dysfunction in Alzheimer’s Disease

Sánchez, M. C., Valero, A. O., García, J. M., Rodríguez-González, V., Montobbio, N., Pelayo, F. J., Morillas, C. A., Poza, J., Gomez, C., & Martínez‐Cañada, P. (2026) · Interdisciplinary Sciences Computational Life Sciences · doi:10.1007/s12539-026-00817-8 · Cited by 1

Selective weakening of population-coupled synaptic activity in vivo in a mouse model of amyloid-beta pathology

Melgosa-Ecenarro, L., Radulescu, C. I., Doostdar, N., Airey, J., Chaloner, F. A., Zabouri, N., Pedretti, G., Osso, F., Perez, L. G., Pilch, K. S., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-69866-3 · Cited by 4

TNFRSF21 Orchestrates Epithelial Keratinization and Tight Junction Integrity in Periodontitis-Associated Oral Mucosal Repair

Zhang, W., Zhang, Y., Sun, Z., Jin, S., Liu, B., Xu, F., Lu, Y., Yang, Y., Wu, M., Sun, W., et al. (2026) · Frontiers in Bioscience-Landmark · doi:10.31083/fbl48371

Connectome-Guided Personalization of Optimal TDCS Intervention Selection in Alzheimer's Disease: A Modeling Study

Luppi, J. J., Koomen, A. P., Stam, C. J., Scheltens, P., & de Haan, W. (2026) · eNeuro · doi:10.1523/eneuro.0407-25.2026

Central sensitization and cognitive vulnerability: a neurobiological framework for central nervous system resilience and brain aging

Hackshaw, K. V. (2026) · Pain Medicine · doi:10.1093/pm/pnag114

Dissecting neuronal circuit function and dysfunction in Alzheimer’s disease mouse models: from conventional calcium imaging analysis to machine learning-based approaches

Gerasimov, E., Fedorov, E., Борисович, Б. И., & Pchitskaya, E. I. (2026) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2026.1930851

Auditory brainstem response deficits precede and are associated with subsequent auditory cortical amyloid burden in male APP/PS1 mice

Luo, Y., Chen, L., Yin, S., Zhang, L., Chen, B., & Wen, H. (2026) · Journal of Alzheimer s Disease · doi:10.1177/13872877261487603

Impairments of neural circuit function in Alzheimer's disease

Busche, M. A., & Konnerth, A. (2016) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2015.0429 · Cited by 360

Brain peptides in Alzheimer’s disease - pathophysiology and therapeutic advances

Pahal, S., Gupta, A., Kumar, V., Singh, P. B. R. P., Kaushik, M., Pahal, V., Atluri, G., & Chaudhary, A. (2026) · Cell and Tissue Research · doi:10.1007/s00441-026-04055-8 · Cited by 3

Mechanismen der Alzheimer-Krankheit

Busche, M. A., Staufenbiel, M., Willem, M., Haass, C., & Förstl, H. (2016) · Der Nervenarzt · doi:10.1007/s00115-015-0041-5 · Cited by 7

Early dysregulation of neuronal activities in models of Alzheimer’s disease

Busche, M. A. (2020) · Alzheimer s & Dementia · doi:10.1002/alz.040406

From Small Peptides to Large Proteins against Alzheimer’sDisease

Picone, P., Sanfilippo, T., Vasto, S., Baldassano, S., Guggino, R., Nuzzo, D., Bulone, D., Biagio, P. L. S., Muscolino, E., Monastero, R., et al. (2022) · Biomolecules · doi:10.3390/biom12101344 · Cited by 16