Spreading of pathology in neurodegenerative diseases: a focus on human studies

Neuropathological stageing of Alzheimer-related changes.

Braak, H., & Braak, E. (1991) · Acta Neuropathologica · doi:10.1007/bf00308809 · Cited by 16,123

Staging of brain pathology related to sporadic Parkinson’s disease

Braak, H., Tredici, K. D., Rüb, U., de Vos, R. A. I., Jansen Steur, E. N. H., & Braak, E. (2003) · Neurobiology of Aging · doi:10.1016/s0197-4580(02)00065-9 · Cited by 10,777

Amyloid oligomers exacerbate tau pathology in a mouse model of tauopathy

Selenica, M.-L. B., Brownlow, M., Jimenez, J. P., Lee, D. C., Pena, G., Dickey, C. A., Gordon, M. N., & Morgan, D. (2013) · Neurodegenerative Diseases · doi:10.1159/000337230 · Cited by 10,359

Ubiquitinated TDP-43 in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis

Neumann, M., Sampathu, D. M., Kwong, L. K., Truax, A. C., Micsenyi, M. C., Chou, T. T., Bruce, J., Schuck, T., Grossman, M., Clark, C. M., et al. (2006) · Science · doi:10.1126/science.1134108 · Cited by 6,576

Alzheimer's disease: Initial report of the purification and characterization of a novel cerebrovascular amyloid protein

Glenner, G. G., & Wong, C. W. (1984) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(84)80190-4 · Cited by 5,404

Novel Proteinaceous Infectious Particles Cause Scrapie

Prusiner, S. B. (1982) · Science · doi:10.1126/science.6801762 · Cited by 5,221

Soluble protein oligomers in neurodegeneration: lessons from the Alzheimer's amyloid β-peptide

Haass, C., & Selkoe, D. J. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2101 · Cited by 4,744

Imaging brain amyloid in Alzheimer's disease with Pittsburgh Compound‐B

Klunk, W. E., Engler, H., Nordberg, A., Wang, Y., Blomqvist, G., Holt, D. P., Bergström, M., Savitcheva, I., Huang, G., Estrada, S., et al. (2004) · Annals of Neurology · doi:10.1002/ana.20009 · Cited by 4,496

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

Thal, D. R., Rüb, U., Orantes, M., & Braak, H. (2002) · Neurology · doi:10.1212/wnl.58.12.1791 · Cited by 3,490

Staging of Alzheimer disease-associated neurofibrillary pathology using paraffin sections and immunocytochemistry

Braak, H., Alafuzoff, I., Arzberger, T., Kretzschmar, H., & Del Tredici, K. (2006) · Acta Neuropathologica · doi:10.1007/s00401-006-0127-z · Cited by 3,172

In Vitro Approaches for Studying Amyloids and Neurotoxicity

Eid, A., May, S. E., Zawia, N., & Camberg, J. L. (2018) · Methods in pharmacology and toxicology · doi:10.1007/7653_2018_21

Neurodegenerative Disorders

Amin, M. M. (2018) · Advances in medical diagnosis, treatment, and care (AMDTC) book series · doi:10.4018/978-1-5225-5282-6.ch009

ANALYSIS OF ATP-DEPENDENT CHAPERONE PROTEIN INTERACTIONS WITH MISFOLDED PROTEINS, AMYLOIDS, AND AGGREGATED PROTEINS

May, S. E. (2018) · Digital Commons - URI (University of Rhode Island) · doi:10.23860/diss-may-shannon-2018

The postsynaptic protein neurogranin: a new item in the Alzheimer’s disease biomarker toolbox

Kvartsberg, H. (2019) · Gothenburg University Publications Electronic Archive (Gothenburg University)

Characterization of high-density prion protein oligomers in rapid progressive and sporadic Alzheimer’s disease

Shafiq, M. (2019) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-7266

Investigation of the intercellular transmission of α-synuclein, amyloid-β and TDP-43

Sackmann, C. (2019) · Linköping University medical dissertations · doi:10.3384/diss.diva-160318

Understanding and improving the diagnosis of dementia with Lewy bodies

Kane, J. P. M. (2019)

A novel treatment for Parkinson's disease and ALS: Combined cell and gene therapies

Svendsen, S. P., & Svendsen, C. N. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-816475-4.00016-1

Exosomas en la propagación de Enfermedades Neurodegenerativas

Gómez-Chavarı́n, M., & Morales-Gómez, M. R. (2020) · Archivos de Neurociencias · doi:10.31157/an.v23i3.13

Elucidating a Common Mechanism of Proteasome Impairment in Neurodegenerative Disease and its Pharmacological Intervention

Thibaudeau, T. A. (2019) · The Research Repository @ WVU (West Virginia University) · doi:10.33915/etd.3780

Controlling Transgene Expression in the Central Nervous System For MRI-Guided Focused Ultrasound Delivery of Adeno-Associated Virus

Weber‐Adrian, D. (2017) · TSpace (University of Toronto)

[Development in Tissue Clearing Technology and Its Application in Neurodegenerative Diseases].

Gu, P., Shen, J., Zhu, Y. J., Li, J., & Wang, L. (2021) · PubMed Central · doi:10.12182/20210560302

Polyphenols in neuroprotection and brain disorders

Duttaroy, A. K. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-822405-2.00004-9

Age‐related Differences in the Brain–Stomatognathic Axis

Lin, C. (2021) · doi:10.1002/9781119724247.ch7

Misfolded Proteins

Merino, P. (2019) · Wiley eBooks · doi:10.1002/9783527813421.ch9

Notes on Techniques

ten Donkelaar, H. J., Doorduin, J., Catani, M., & van den Heuvel, M. P. (2020) · Springer eBooks · doi:10.1007/978-3-030-41878-6_3

Systematic comparison of the molecular mechanisms underlying the spreading of pathology in different neurodegenerative diseases

Brás, I. C. (2021) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-8891

A felgyorsult fehérje körforgás szerepe a transzlációs hibákkal szembeni alkalmazkodási folyamatokban

Kalapis, D. (2017) · doi:10.14232/phd.3941

Faculty Opinions recommendation of Gut microbiota regulate motor deficits and neuroinflammation in a model of parkinson's disease.

Li, G., & Marlin, M. C. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.727046232.793530050

Alzheimer’s disease

Koychev, I. G., & Gallacher, J. (2020) · doi:10.1093/med/9780198713005.003.0040

Faculty Opinions recommendation of Inflammasome inhibition prevents α-synuclein pathology and dopaminergic neurodegeneration in mice.

Krishnan, Y., & Saminathan, A. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.734317494.793570817

Extracellular Tau Oligomers Induce Disruption of Endogenous Tau Distribution, Invasion of Tau into the Somatodendritic Compartment and Axonal Transport Dysfunction

Swanson, E. C. (2017) · doi:10.18130/v3p643

An investigation into the mechanism of proteasome dysfunction in neurodegenerative disease and the biological impact of proteasome hyperactivation in C. elegans

Anderson, R. T. (2022) · The Research Repository @ WVU (West Virginia University) · doi:10.33915/etd.11619

Dietary Tyrosine intake is associated with Locus Coeruleus, attention and grey matter maintenance: an MRI structural study on 398 healthy individuals of the Berlin Aging Study-IIPreprint

Plini, E. R. G., Melnychuk, M. C., Harkin, A., Dahl, M. J., McAuslan, M. J., Kühn, S., Boyle, R. T., Whelan, R., Andrews, R., Düzel, S., et al. (2023) · Research Square · doi:10.21203/rs.3.rs-3166636/v1

Spatial transcriptomic patterns underlying regional vulnerability to amyloid-β and tau pathologies and their relationships to cognitive dysfunction in Alzheimer’s diseasePreprint

Yu, M., Risacher, S. L., Nho, K. T., Wen, Q., Oblak, A. L., Unverzagt, F. W., Apostolova, L. G., Farlow, M. R., Brosch, J. R., Clark, D. G., et al. (2023) · medRxiv · doi:10.1101/2023.08.12.23294017

A study of work ability and associated factors in aging office workers with non-communicable diseases and musculoskeletal disorders

Rawdeng, S. (2021) · doi:10.58837/chula.the.2021.317

Induced-pluripotent stem cells and neuroproteomics as tools for studying neurodegeneration

Brandão‐Teles, C., Zuccoli, G. S., Vrechi, T. A. D. M., Ramos-da-Silva, L., Santos, A. V. S., Crunfli, F., & Martins‐de‐Souza, D. (2024) · Biochemical Society Transactions · doi:10.1042/bst20230341

Additional file 3 of VCP suppresses proteopathic seeding in neurons

Zhu, J., Pittman, S. K., Dhavale, D. D., French, R. L., Patterson, J. N., Kaleelurrrahuman, M. S., Sun, Y., Vaquer‐Alicea, J., Maggiore, G., Clemen, C. S., et al. (2022) · Figshare · doi:10.6084/m9.figshare.19589268

Additional file 4 of VCP suppresses proteopathic seeding in neurons

Zhu, J., Pittman, S. K., Dhavale, D. D., French, R. L., Patterson, J. N., Kaleelurrrahuman, M. S., Sun, Y., Vaquer‐Alicea, J., Maggiore, G., Clemen, C. S., et al. (2022) · Figshare · doi:10.6084/m9.figshare.19589274

Additional file 2 of VCP suppresses proteopathic seeding in neurons

Zhu, J., Pittman, S. K., Dhavale, D. D., French, R. L., Patterson, J. N., Kaleelurrrahuman, M. S., Sun, Y., Vaquer‐Alicea, J., Maggiore, G., Clemen, C. S., et al. (2022) · Figshare · doi:10.6084/m9.figshare.19589262

Histological study of the effect of curcumin on indomethacin-induced ileitis in adult male albino rats

Abd-Elbaky, R. F., Badr, S. M., Kandeel, S., & Zamzam, A.-E. M. F. (2023) · Tanta Medical Journal · doi:10.4103/tmj.tmj_30_23

Frontotemporal dementia-like disease progression elicited by seeded aggregation and spread of FUSPreprint

Vazquez‐Sanchez, S., Tilkin, B., Gasset-Rosa, F., Zhang, S., Piol, D., McAlonis‐Downes, M., Artates, J. W., Govea-Perez, N., Verresen, Y., Guo, L. E., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.06.03.593639

Protein Metabolism: Critical Factors Implicated in Neurodegenerative Diseases

Singh, J., Sarkar, B., Mukherjee, A., & Mutsuddi, M. (2024) · Springer eBooks · doi:10.1007/978-981-97-4288-2_8

Analysis of Midlife Approaches to Reduce the Risk Factors of Dementia Among Adults in the United Kingdom

Ayandeyi, K., Shaha, S., & Chilaka, M. A. (2024) · Journal of Family Medicine and Health Care · doi:10.11648/j.jfmhc.20241003.14

Global amyloid burden enhances network efficiency of tau propagation in the brain

Lauber, M. V., Bellitti, M., Kapadia, K., Jasodanand, V. H., Au, R., & Kolachalama, V. B. (2024) · Journal of Alzheimer s Disease · doi:10.1177/13872877241294084

Future Directions and Challenges in Enzyme Research for Neurodegenerative Diseases

Rathi, K. M., Pingat, P., & Firdous, S. M. (2024) · Springer eBooks · doi:10.1007/978-981-97-6822-6_10

AI for Discovering the Role of Cognitive and Brain Reserves in Parkinson's Disease Classification

Siviero, I., Pirastru, A., Valè, N., Blasi, V., Menegaz, G., Baglio, F., Galazzo, I. B., & Storti, S. F. (2024) · IEEE International Conference on Metrology for eXtended Reality, Artificial Intelligence and Neural Engineering (MetroXRAINE) · doi:10.1109/metroxraine62247.2024.10796459

Hematological and biochemical evaluation of Rasasindura on Amyloid beta induced Alzheimer’s disease in Sprague Dawley rats

Ajay, H. M., Ravikumar, C., Hemanth Gowda, K., Babu, S., Galib, R., Girish, B. C., Shridhar, N. B., Shiva Kumar, M., & Sarma, M. (2025) · International Journal of Advanced Biochemistry Research · doi:10.33545/26174693.2025.v9.i4sa.4039

Microphysiological engineering of the capillary interface of substantia nigra dopaminergic neurons to study vascular alterations in Parkinson’s DiseasePreprint

Alim, A., Baek, Y., Lee, M., & Paek, J. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.05.14.654131

Application of fMRI to Monitor Motor Rehabilitation

Baglio, F., Bergsland, N., & Blasi, V. (2025) · Neuromethods · doi:10.1007/978-1-0716-4438-6_28

Piperazine Derivatives Attenuate Scopolamine‐Induced Memory Deficits by Modulating Neuroinflammation and Oxidative Stress via the NF‐κB/TNF‐α/COX‐2 Pathway

Fardoos, S., Kaleem, S., Masaud, S. M., Jahan, F., Nadeem, H., Afzal, M., Alrefaei, A. F., Alshehri, E., & Ali, S. (2025) · ChemistrySelect · doi:10.1002/slct.202501590

Proteomic and in silico dissection of MetaAggregates in amyotrophic lateral sclerosis brainsPreprint

Murakami, K., Nguyen, T. H. V., Fujita, N., Nagao, C., Mizuguchi, K., Nishiuchi, T., Sakashita, Y., Noguchi‐Shinohara, M., & Ono, K. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.07.09.663594

Alzheimer’s disease

Koychev, I. G., & Gallacher, J. (2020) · doi:10.1093/med/9780198713005.003.0040_update_001

Glial cell-intrinsic and non-cell autonomous toxicity in a Drosophila C9orf72 neurodegeneration modelPreprint

Hubbard, I., & Dubnau, J. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.07.680869

Additional file 1 of Targeting the glycine-rich domain of TDP-43 with antibodies prevents its aggregation in vitro and reduces neurofilament levels in vivo

Riemenschneider, H., Simonetti, F., Sheth, U., Katona, E., Roth, S., Hutten, S., Farny, D., Michaelsen, M., Nuscher, B., Schmidt, M. K., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26603533

Additional file 1 of VCP suppresses proteopathic seeding in neurons

Zhu, J., Pittman, S. K., Dhavale, D. D., French, R. L., Patterson, J. N., Kaleelurrrahuman, M. S., Sun, Y., Vaquer‐Alicea, J., Maggiore, G., Clemen, C. S., et al. (2022) · Figshare · doi:10.6084/m9.figshare.19589259

Additional file 6 of P62 accumulates through neuroanatomical circuits in response to tauopathy propagation

de Thé, F.-X. B., Lassus, B., Schaler, A. W., Fowler, S. L., Goulbourne, C. N., Jeggo, R., Mannoury la Cour, C., Millan, M. J., & Duff, K. (2021) · Figshare · doi:10.6084/m9.figshare.16921850

Additional file 1 of Pharmacological inhibition of nSMase2 reduces brain exosome release and α-synuclein pathology in a Parkinson’s disease model

Zhu, C., Bilousova, T. V., Focht, S., Jun, M., Elias, C. J., Melnik, M., Chandra, S., Campagna, J. J., Cohn, W., Hatami, A., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14450653

Additional file 2 of Targeting the glycine-rich domain of TDP-43 with antibodies prevents its aggregation in vitro and reduces neurofilament levels in vivo

Riemenschneider, H., Simonetti, F., Sheth, U., Katona, E., Roth, S., Hutten, S., Farny, D., Michaelsen, M., Nuscher, B., Schmidt, M. K., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26603536

Additional file 12 of Impact of APOE genotype on prion-type propagation of tauopathy

Williams, T., Ruiz, A. J., Ruiz, A. M., Vo, Q., Tsering, W., Xu, G., McFarland, K., Giasson, B. I., Sullivan, P. M., Borchelt, D. R., et al. (2022) · Figshare · doi:10.6084/m9.figshare.19619142

Additional file 3 of Targeting the glycine-rich domain of TDP-43 with antibodies prevents its aggregation in vitro and reduces neurofilament levels in vivo

Riemenschneider, H., Simonetti, F., Sheth, U., Katona, E., Roth, S., Hutten, S., Farny, D., Michaelsen, M., Nuscher, B., Schmidt, M. K., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26603539

Additional file 1 of Frontotemporal dementia-like disease progression elicited by seeded aggregation and spread of FUS

Vazquez‐Sanchez, S., Tilkin, B., Gasset-Rosa, F., Zhang, S., Piol, D., McAlonis‐Downes, M., Artates, J. W., Govea-Perez, N., Verresen, Y., Guo, L. E., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26019613

Mechanisms of Dural Involvement in Cerebral Amyloid Angiopathy

Zedde, M., Piazza, F., & Pascarella, R. (2025) · Cells · doi:10.3390/cells15010026

Preparation and application of YFV-17D-derived Anterograde Trans-neuronal Viral Vectors for Neuroscience ResearchPreprint

Panchumarthy, T., Munoz, L., Saleem, U., Le, A.-V., Nelson, I., Li, Y., Xu, X., & Xu, W. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.01.08.698485

Selection for Function in Complex Distributed Pathological Systems

Frédéric Thomas, A., Dujon, A. M., Vaiman, D., Eberl, G., Alix‐Panabières, C., Pujol, P., Újvári, B., Meliani, J., Nedelcu, A. M., & Capp, J. (2026) · Evolutionary Applications · doi:10.1111/eva.70202 · Cited by 1

Volumetric signatures of basal ganglia–thalamo–cortical and cerebello–thalamo–cortical networks in Parkinson's disease and its motor subtypes

Sadeghi, F., Okar, A., Rashedi, R., Gerloff, C. P., Timmann, D., Schulz, R., & Zittel, S. (2026) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2026.1743479

L’olfaction chez le patient gériatrique : constantes et spécificités pathologiques des interactions olfacto-trigéminales dans une population porteuse de synucléopathies

Foguem, C. (2017) · doi:10.70675/57423e96zedabz4b8bz9cfdzac1867a8cfa9

Regulation of neuronal microtubule-based transport by polyglutamylation

Bodakuntla, S. (2019) · theses.fr (ABES) · doi:10.70675/25a5f130z3b63z4663zb3aez400da5d97e80

Unravelling the tangle of motor neuron diseases : insights from neuroimaging and neurophysiology

Querin, G. (2019) · theses.fr (ABES) · doi:10.70675/30ad3e2az5051z4364z9ec1z4b8d1f952b7b

Étude de la composante neuroinflammatoire dans les DFT/SLA

Smeyers, J. (2020) · theses.fr (ABES) · doi:10.70675/219cfa6fz5b3az4198z9deczdfaad3cd784c

Développement et caractérisation de nouveaux modèles murins de maladie à corps de Lewy

Schueller, E. (2020) · theses.fr (ABES) · doi:10.70675/4a313736z3f42z4d92zb1c1ze3cbd7bbe9f6

Développement d’outils pour la caractérisation de la TDP-43 et exploration de marqueurs indirects dans un contexte de dégénérescence lobaire frontotemporale

Escal, J. (2021) · theses.fr (ABES) · doi:10.70675/c8b346f7zb4e3z43e0za63azb407baddab64

Investigation of IAPP fibrillation inhibition by co-chaperonin prefoldin

Törner, R. (2021) · theses.fr (ABES) · doi:10.70675/a82d7207z9aaez4e6bz932fze78c992a067d

Intelligence artificielle et maladies neurologiques : aider le diagnostic et améliorer la compréhension du comportement des réseaux de neurones convolutifs

Mattia, G. M. (2022) · theses.fr (ABES) · doi:10.70675/80dc0355z65a9z470bz9d11zb1ea5cee7492

Implication des sous-populations neuronales du globus pallidus externe dans la physiopathologie de la maladie de Parkinson : Etude optogénétique et comportementale chez le modèle murin

Caballero, S. D. B. (2023) · theses.fr (ABES) · doi:10.70675/1234c979z8052z498cz8e77z12390acdc637

Somatic mutations link focal onset to widespread neurodegeneration in ALS and FTD

(2026) · Nature Genetics · doi:10.1038/s41588-026-02572-4

Residential green spaces and neurodegenerative diseases in middle-aged and older adults: a systematic review and dose-response meta-analysis

Shen, C., Su, J., Liu, L., Li, J., Zhao, X., Wang, Z., Jiang, Y., & Zhao, D. (2026) · Archives of Public Health · doi:10.1186/s13690-026-01957-5

Molecular and Structural Characterization Reveals Divergent Extracellular Vesicle Profiles Between Wild Type and Alzheimer’s Disease Cerebrocortical OrganoidsPreprint

Balistreri, A., Turner, N., Compher, J., Almaraz, M., Prabhavalkar, A., Chittal, S., Labra, S. R., Ezekiel, K., Baal, C., Kwong, C. C., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.05.13.724352

Formation and toxicity of protein misfolded oligomers: Mechanistic insights and therapeutic opportunities in protein aggregation diseases

Neri, L., Anderson, C. A., Fallot, L. B., Mannini, B., & Limbocker, R. (2026) · Elsevier eBooks · doi:10.1016/b978-0-323-99507-8.00045-7

Molecular Dissection of TDP-43 as a Leading Cause of ALS/FTLD

漆谷, 真., Tamaki, Y., & URUSHITANI, M. (n.d.) · Institutional Repositories DataBase (IRDB)

Structures and Dynamics of Tau Assemblies from Solid-State NMR

Mammeri, N. E., & Hong, M. (2026) · Accounts of Chemical Research · doi:10.1021/acs.accounts.6c00208

Associations of local white matter geometry with network efficiency, macrostructural abnormalities, and clinical severity in behavioural variant frontotemporal dementia

Sun, Q., Zhang, Y., Jin, X., Cheng, J., Li, J., Qiu, T., Ren, Z., Li, K., Zhang, H., Initiative, F. T. F. L. D. N., et al. (2026) · Brain Communications · doi:10.1093/braincomms/fcag226

Non-invasive brain stimulation in frontotemporal dementia: syndrome-specific signals and priorities for future trials

Wang, J., Fu, X., Liu, J., & Yang, Y. (2026) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2026.1842455

Characterizing Cutaneous α‐Synuclein Deposition and Seeding Activity in Parkinson's Disease Subtypes

Jin, Y., Yang, T., Liu, M., Luo, H., Yuan, J., Zhang, K., Han, X., Yang, J., & Xu, Y. (2026) · Annals of Clinical and Translational Neurology · doi:10.1002/acn3.70465

Small molecular chaperones regulate protein quality control in neurodegenerative diseases

Rangappa, N., Mishra, A., & Chinnathambi, S. (2026) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2026.06.006

New Insights into Neurodegenerative Diseases: Intercellular Transmission

Xiu-lan, J., Zhao, T.-H., Guo, W., Xue, J., & Yin, D. (2026) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.5c00991

Sequence-encoded conformational biases correlate with self-assembly modes of intrinsically disordered proteins

Kobayashi, R., Yoshida, N., Miyanoiri, Y., Nakamura, H., Ekari, M., Sakamoto, E., Tsutsumi, M., Imamura, K., Kodama, T. S., Tochio, H., et al. (2026) · PNAS Nexus · doi:10.1093/pnasnexus/pgag189 · Cited by 1

Postmortem brain MRI reveals differential associations of subcortical and limbic volumes with cortical thinning and neurodegenerative pathologies

Khandelwal, P., Duong, M. T., Levorse, L. M., Trotman, W., Bahena, A., Lim, S., Denning, A. E., Chung, E. P., Olm, C. A., Radhakrishnan, H., et al. (2026) · Alzheimer s & Dementia · doi:10.1002/alz.71649

Integrative Network Pharmacology and Molecular Docking Analysis Reveals the Multitarget Mechanisms of Pterostilbene in Neurodegenerative Diseases

Rosiak, N., Stojceski, F., Maroni, G., Piontek, B., & Cielecka‐Piontek, J. (2026) · Pharmaceuticals · doi:10.3390/ph19071053

Vesicles of Plant and Fungal Origin Morphology Studying by Cryoelectron Microscopy

Garaeva, L. A., Pichkur, E. A., Putevich, E., Spitsyna, A., Solomina, L. A., Emelianova, S. S., Konevega, А. L., & Shtam, T. A. (2026) · Nanobiotechnology Reports · doi:10.1134/s2635167626602524

Glial cell toxicity in a Drosophila C9orf72 neurodegeneration model

Hubbard, I., & Dubnau, J. (2026) · PLoS Genetics · doi:10.1371/journal.pgen.1011909

Revisiting somatosensory evoked potentials in motor neuron diseases: neurophysiological insights from a large cohort

Iacobelli, V., Vizziello, M., Clementi, L., Anversa, P., Cazzato, D., Grado, A. D., Gallone, A., Izzo, M. G. A., Lanteri, P., Usai, S., et al. (2026) · Clinical Neurophysiology · doi:10.1016/j.clinph.2026.2112372

Targeting Aberrant Protein-Protein Interactions in Cancer and Neurodegenerative Diseases

Ball, T. D. (2025) · Digital Commons - DU (University of Denver) · doi:10.56902/etdcrp.2025.222

Biochemical Analysis of O-GlcNAcylation on α-Synuclein Aggregation, Cytotoxicity and Glycosylation Modification in Fibril-Seeding Neurons

Meng, H., Miao, Y., Ma, Z., & Liu, C.-F. (2026) · IntechOpen eBooks · doi:10.5772/intechopen.1015053

Tau deposition patterns within the medial temporal lobe follow the connectivity of the entorhinal and perirhinal cortex – a combined post-mortem and 7T fMRI studyPreprint

de Bruin, H., Przygodda, X., Wisse, L. E. M., Ravikumar, S., Düzel, E., Pijnenburg, Y. A. L., Yushkevich, P. A., Groot, C., Berron, D., Franzmeier, N., et al. (2026) · Research Square · doi:10.21203/rs.3.rs-10581799/v1

A mechanistically informed framework of hierarchical temporal speech organization for objective differential assessment of motor speech disorders in neurodegenerative diseases

Bruning, K., Heidrick, L., & Rong, P. (2026) · Frontiers in Neuroscience · doi:10.3389/fnins.2026.1907826

Enhancing the glymphatic system as a potential pathway to limit Parkinson disease progression

Ya, Z., & Howitt, J. (2026) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2026.2738182

Altered Kullback-Leibler similarity gradients in cocaine use disorder: Connectome constraints and multiscale biological contextualization

Wang, R., Luo, D., Xu, J., Huang, X., Gong, Q., & Sun, H. (2026) · Journal of Affective Disorders · doi:10.1016/j.jad.2026.122523

Potential Roles of Neuroimaging in Motor Neuron Disease

Kassubek, J., & Müller, H. (2026) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-026-01524-z

Early life social isolation primes flies for more rapid TDP-43 dependent neurodegeneration later in lifePreprint

Murthygowda, S., Huyghue, K., Castillo, B., Gugala, F., Li, W., & Dubnau, J. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.09.23.753732

Sleep and the Gut–Brain Axis: Bidirectional, Converging Mechanisms Linking Brain Health, Neuroinflammation, and Neurodegeneration

Bowler, B., Nasir, A. R., Szewczyk, A., Ocañas, S. R., Unnikrishnan, A., & Nouh, C. D. (2026) · Pathophysiology · doi:10.3390/pathophysiology33040074

New treatments on the horizon for Alzheimer’s and other neurodegenerative diseases

Bailey, H., Layfield, R., & Žerovnik, E. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-34176-2.00003-1

BindingDB Entry 50011128: Design, synthesis and evaluation of flurbiprofen-clioquinol hybrids as multitarget-directed ligands against Alzheimer's disease.

BindingDB (2021) · UC San Diego · doi:10.7270/q24t6nxc

BindingDB Entry 50023417: Effects of Heparan Sulfate Trisaccharide Containing Oleanolic Acid in Attenuating Hyperphosphorylated Tau-Induced Cell Dysfunction Associated with Alzheimer's Disease.

BindingDB (2026) · UC San Diego · doi:10.7270/q2z60tzv

Advanced magnetic resonance imaging in amyotrophic lateral sclerosis: Neuroimaging from the group level to individual subject analysis

Kassubek, J., & Müller, H.-P. (2026) · Advances in magnetic resonance technology and applications · doi:10.1016/b978-0-443-21425-7.01018-6

Endoplasmic Reticulum Autophagy Enhancement Alleviates Synaptic Plasticity Dysfunction and Ameliorates Cognitive Impairment in SAE Mice by Relieving STING ‐Associated Inhibition of PKM2 Activity

Guo, X., Yin, D., Zhang, Z., Zhao, Y., Zhang, Y., Jiang, Y., Zhao, Z., Sun, T., Zhou, F., & Zhang, X. (2026) · CNS Neuroscience & Therapeutics · doi:10.1002/cns.71233

Intercellular Spread of Protein Aggregates in Neurodegenerative Disease

Davis, A. A., Leyns, C. E. G., & Holtzman, D. M. (2018) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-100617-062636 · Cited by 131

Propagation of Pathology through Brain Networks in Neurodegenerative Diseases: From Molecules to Clinical Phenotypes

Agosta, F., Weiler, M., & Filippi, M. (2015) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.12410 · Cited by 56

A critical appraisal of the pathogenic protein spread hypothesis of neurodegeneration

Walsh, D. M., & Selkoe, D. J. (2016) · Nature reviews. Neuroscience · doi:10.1038/nrn.2016.13 · Cited by 301

Prion-like transmission of pathogenic protein aggregates in genetic models of neurodegenerative disease

Pearce, M. M. P. (2017) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2017.03.011 · Cited by 19

Deciphering the prion-like behavior of pathogenic protein aggregates in neurodegenerative diseases

Yoshida, S., & Hasegawa, T. (2022) · Neurochemistry International · doi:10.1016/j.neuint.2022.105307 · Cited by 9