New insights on the role of microglia in synaptic pruning in health and disease

Copper-Zinc Superoxide Dismutase (SOD1) Is Released by Microglial Cells and Confers Neuroprotection against 6-OHDA Neurotoxicity

Polazzi, E., Mengoni, I., Caprini, M., Peña‐Altamira, E., Kurtys, E., & Monti, B. (2012) · Neurosignals · doi:10.1159/000337115 · Cited by 9,023

Resting microglial cells are highly dynamic surveillants of brain parenchyma in vivo

Nimmerjahn, A., Kirchhoff, F., & Helmchen, F. (2005) · Science · doi:10.1126/science.1110647 · Cited by 5,827

Fate Mapping Analysis Reveals That Adult Microglia Derive from Primitive Macrophages

Ginhoux, F., Greter, M., Leboeuf, M., Nandi, S., See, P., Gokhan, S., Mehler, M. F., Conway, S. J., Ng, L. G., Stanley, E. R., et al. (2010) · Science · doi:10.1126/science.1194637 · Cited by 5,175

Physical basis of cognitive alterations in alzheimer's disease: Synapse loss is the major correlate of cognitive impairment

Terry, R. D., Masliah, E., Salmon, D. P., Butters, N., DeTeresa, R., Hill, R., Hansen, L. A., & Katzman, R. (1991) · Annals of Neurology · doi:10.1002/ana.410300410 · Cited by 4,397

Meta-Analysis of 74,046 Individuals Identifies 11 New Susceptibility Loci for Alzheimer’s Disease

(EADI), E. A. D. I., Lambert, J.-C., (GERAD), G. A. E. R. I. A. D., Alzheimer's Disease Genetic Consortium (ADGC), (CHARGE), C. F. H. A. A. R. I. G. E., Ibrahim-Verbaas, C. A., Harold, D., Naj, A. C., Sims, R., Bellenguez, C., et al. (2013) · Nature Genetics · doi:10.1038/ng.2802 · Cited by 4,336

Synaptic Pruning by Microglia Is Necessary for Normal Brain Development

Paolicelli, R. C., Bolasco, G., Pagani, F., Maggi, L., Scianni, M., Panzanelli, P., Giustetto, M., Ferreira, T. A., Guiducci, E., Dumas, L., et al. (2011) · Science · doi:10.1126/science.1202529 · Cited by 4,244

Microglia Sculpt Postnatal Neural Circuits in an Activity and Complement-Dependent Manner

Schafer, D. P., Lehrman, E. K., Kautzman, A. G., Koyama, R., Mardinly, A. R., Yamasaki, R., Ransohoff, R. M., Greenberg, M. E., Barres, B. A., & Stevens, B. (2012) · Neuron · doi:10.1016/j.neuron.2012.03.026 · Cited by 4,089

ATP mediates rapid microglial response to local brain injury in vivo

Davalos, D., Grutzendler, J., Yang, G., Kim, J. V., Zuo, Y., Jung, S., Littman, D. R., Dustin, M. L., & Gan, W.-B. (2005) · Nature Neuroscience · doi:10.1038/nn1472 · Cited by 3,913

Microglia: Active sensor and versatile effector cells in the normal and pathologic brain

Hanisch, U.-K., & Kettenmann, H. (2007) · Nature Neuroscience · doi:10.1038/nn1997 · Cited by 3,676

Characterization of striatal phenotypes in heterozygous Disc1 mutant mice, a model of haploinsufficiency

Baskaran, R., Lai, C.-C., Li, W.-Y., Tuan, L., Wang, C.-C., Lee, L., Liu, C.-M., Hwu, H., & Lee, L.-J. (2019) · The Journal of comparative neurology · doi:10.1002/cne.24813 · Cited by 4

Intra-cellular accumulation of amyloid is a marker of selective neuronal vulnerability in Alzheimer’s diseasePreprint

Caramello, A., Fancy, N. N., Tournerie, C., Eklund, M., Chau, V. M. N., Adair, E., Papageorgopoulou, M., Jackson, J., Hardy, J., & Matthews, P. M. (2023) · medRxiv · doi:10.1101/2023.11.23.23298911 · Cited by 6

From engrams to schemas

Szcześniak, K., & Řeřicha, V. (2024) · Lingua · doi:10.1016/j.lingua.2024.103788 · Cited by 5

Microglial MS4A4A Protects against Epileptic Seizures in Alzheimer's Disease

Jiang, M., Li, Q., Chen, J., Li, R., Yao, J., Hu, Y., Zhang, H., Cai, L., Luo, M., Sun, Y., et al. (2025) · Advanced Science · doi:10.1002/advs.202417733 · Cited by 6

NRF2 deficiency is associated with synaptic alterations and ether-linked phospholipid imbalance in the hippocampus

Carnicero-Senabre, D., Barata, M. A., Jiménez-Villegas, J., Almeida, C. G., Cuadrado, A., & Rojo, A. I. (2025) · Redox Biology · doi:10.1016/j.redox.2025.103853 · Cited by 5

Microglia depletion improves hippocampal circuit function after mild traumatic brain injury in male mice

Delcy, S. A. S., Farrugia, A. M., Nieves, I. A. D., O’Brien, C. A., Bennett, F. C., & Cohen, A. S. (2025) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2025.106178 · Cited by 5

Evolving insights into the identity and function of dark microglia

Flury, A. G., St‐Pierre, M., Ayata, P., & Tremblay, M. (2025) · Trends in Neurosciences · doi:10.1016/j.tins.2025.11.002 · Cited by 7

Proposed key characteristics of neurotoxic chemicals

Lein, P. J., Bowman, A. B., Cao, Z., Carson, M. J., Eskenazi, B., Fritsche, E., Harry, G. J., Härtung, T., Pessah, I. N., Slikker, W., et al. (2025) · NeuroToxicology · doi:10.1016/j.neuro.2025.103370 · Cited by 6

Frontiers and future perspectives of neuroimmunology

Qi, H., Duan, S., Xu, Y., & Zhang, H. (2022) · Fundamental Research · doi:10.1016/j.fmre.2022.10.002 · Cited by 5

Pathogenic mechanisms of human immunodeficiency virus (HIV)-associated pain

Liu, X., & Tang, S. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02294-7 · Cited by 5

Microglia Activation in the Midbrain of the Human Neonate: The Effect of Perinatal Hypoxic-Ischemic Injury

Panayotacopoulou, M. T., Papageorgiou, I. E., Pagida, M. A., Katsogridaki, A. E., Chrysanthou‐Piterou, M., Valous, N. A., Halama, N., Patsouris, E., & Konstantinidou, A. E. (2022) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nlab135 · Cited by 5

Prognostic Signature Development on the Basis of Macrophage Phagocytosis‐Mediated Oxidative Phosphorylation in Bladder Cancer

Qu, G., Xu, Y., Lu, Z., Nie, H.-B., Tang, C., Hou, J. Y., & Wen, X. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/4754935 · Cited by 5

Progressive Voxel‐Wise Homotopic Connectivity from childhood to adulthood: Age‐related functional asymmetry in resting‐state functional magnetic resonance imaging

Tarchi, L., Damiani, S., La‐Torraca‐Vittori, P., Frick, A., Castellini, G., Politi, P., Fusar‐Poli, P., & Ricca, V. (2023) · Developmental Psychobiology · doi:10.1002/dev.22366 · Cited by 5

Bone marrow-derived myeloid cells transiently colonize the brain during postnatal development and interact with glutamatergic synapses

Carrier, M., Robert, M.-È., St-Pierre, M.-K., Ibáñez, F. G., Gonçalves de Andrade, E., Laroche, A., Picard, K., Vecchiarelli, H. A., Savage, J. C., Boilard, É., et al. (2024) · iScience · doi:10.1016/j.isci.2024.110037 · Cited by 5

Effects of Multisession Anodal Electrical Stimulation of the Auditory Cortex on Temporary Noise-Induced Hearing Loss in the Rat

Díaz, I., Colmenárez-Raga, A. C., Pérez‐González, D., Carmona-Barrón, V. G., Plaza, I., & Merchán, M. Á. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.642047 · Cited by 5

Pathogenetical and Neurophysiological Features of Patients with Autism Spectrum Disorder: Phenomena and Diagnoses

Jin, Y., Choi, J., Lee, S.-H., Kim, J. W., & Hong, Y. (2019) · Journal of Clinical Medicine · doi:10.3390/jcm8101588 · Cited by 5

Long-term cellular and molecular signatures of pregnancy in the adult and ageing brainPreprint

Duarte‐Guterman, P., Richard, J. E., Lieblich, S. E., Eid, R., Lamers, Y., & Galea, L. A. M. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.02.24.529879 · Cited by 5

Opposing roles of microglial and macrophagic C3ar1 signaling in stress-induced synaptic and behavioral changes

Tripathi, A., Bartosh, A., Jose, D. A., Mata, J., Hussein, U. K., Laezza, F., Zhao, Z., & Pillai, A. (2025) · Molecular Psychiatry · doi:10.1038/s41380-025-03097-8 · Cited by 4

The Effects of Dietary Intervention and Macrophage-Activating Factor Supplementation on Cognitive Function in Elderly Users of Outpatient Rehabilitation

Uchiyama‐Tanaka, Y., Yamakage, H., & Inui, T. (2024) · Nutrients · doi:10.3390/nu16132078 · Cited by 5

Sensitive periods for exposure to indoor air pollutants and psychosocial factors in association with symptoms of psychopathology at school-age in a South African birth cohort

Christensen, G. M., Marcus, M., Vanker, A., Eick, S. M., Malcolm‐Smith, S., Smith, A. D. A. C., Dunn, E. C., Suglia, S. F., Chang, H. H., Zar, H. J., et al. (2025) · Environmental Pollution · doi:10.1016/j.envpol.2025.125975 · Cited by 4

Microglial heterogeneity and complement component 3 elimination within emerging multisensory midbrain compartments during an early critical period

Carroll, J. B., Hamidi, S., & Gabriele, M. L. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.1072667 · Cited by 4

The Brain-Gut-Microbiome Axis

Aderbal, S., Ana, M., Sabrá Filho, A., Sabrá, S., Bandeira, T. L., Bandeira, I. M., & Werber-Bandeira, L. (2022) · International Journal of Psychiatry Research · doi:10.33425/2641-4317.1147 · Cited by 4

Segregation of Multimodal Inputs Into Discrete Midbrain Compartments During an Early Critical Period

Weakley, J. M., Kavusak, E. K., Carroll, J. B., & Gabriele, M. L. (2022) · Frontiers in Neural Circuits · doi:10.3389/fncir.2022.882485 · Cited by 5

Neurofibromatosis type 1-dependent alterations in mouse microglia function are not cell-intrinsic

Logiacco, F., Grzegorzek, L. C., Cordell, E., Popp, O., Mertins, P., Gutmann, D. H., Kettenmann, H., & Semtner, M. (2023) · Acta Neuropathologica Communications · doi:10.1186/s40478-023-01525-w · Cited by 4

Ultrastructural characterization of dark microglia during aging in a mouse model of Alzheimer’s disease pathology and in human post-mortem brain samplesPreprint

St‐Pierre, M., Carrier, M., Ibáñez, F. G., Šimončičová, E., Wallman, M., Vallières, L., Parent, M., & Tremblay, M. (2022) · Research Square · doi:10.21203/rs.3.rs-1751270/v1 · Cited by 4

Factors Affecting Macro-Structural Development in the Cerebral Cortex: The Potential Role of Tissue Removal Through Pruning and Apoptosis

Levman, J. E. D. (2025) · Biology · doi:10.3390/biology14121651 · Cited by 3

Viral modulation of synaptic pruning: implications for neuropathology and brain function

Aliakbari, S., Asadi, S., Sayyah, M., Naderi, N., Salarvandian, S., Khodagholi, F., & Pourbadie, H. G. (2026) · Journal of Virology · doi:10.1128/jvi.01684-25 · Cited by 4

Liquid-liquid phase separation of RBM33 facilitates hippocampus aging by inducing microglial senescence by activating CDKN1A

Yang, X., Lin, W., Zhong, S., Wang, Q., Zhang, Y., Zhang, Y., & Yu, A. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.142986 · Cited by 3

Troubles du neurodéveloppement : mécanismes

Gressèns, P. (2020) · Contraste · doi:10.3917/cont.051.0011 · Cited by 3

Lytic Cell Death in Specific Microglial Subsets Is Required for Preventing Atypical Behavior in Mice

Chuang, H.-C., Nichols, E. K., Rauch, I., Chang, W.-C., Misra, R., Lin, P. M., Kitaoka, M., Vance, R. E., & Saijo, K. (2021) · eNeuro · doi:10.1523/eneuro.0342-20.2020 · Cited by 3

A correlational study between microstructural, macrostructural and functional age-related changes in the human visual cortex

Malakshan, S. R., Daneshvarfard, F., & Moghaddam, H. A. (2023) · PLoS ONE · doi:10.1371/journal.pone.0266206 · Cited by 3

Chitosan-Based Biomaterials for Tissue Engineering of Glial Cells

Hamdan, Y. A., Oudadesse, H., Laadraoui, J., Smimih, K., Kabdy, H., Elouali, S., Eladlani, N., & Rhazi, M. (2023) · Advances in bioinformatics and biomedical engineering book series · doi:10.4018/978-1-6684-9675-6.ch021 · Cited by 6

Prenatal Immune Challenge Differentiates the Effect of Aripiprazole and Risperidone on CD200–CD200R and CX3CL1–CX3CR1 Dyads and Microglial Polarization: A Study in Organotypic Cortical Cultures

Chamera, K., Curzytek, K., Kamińska, K., Leśkiewicz, M., & Basta‐Kaim, A. (2024) · Life · doi:10.3390/life14060721 · Cited by 4

The meal Maketh the Microglia: Why studying microglial phagocytosis is critical to stroke research

Morrison, V. E., & Bix, G. J. (2023) · Neurochemistry International · doi:10.1016/j.neuint.2023.105488 · Cited by 3

Translational profiling of microglia reveals artifacts of cell sortingPreprint

Kang, S. S., Baker, K. E., Wang, X., Kocher, J.-P., & Fryer, J. D. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/135566 · Cited by 4

RiboTag-Seq Reveals a Compensatory cAMP Responsive Gene Network in Striatal Microglia Induced by Morphine WithdrawalPreprint

Coffey, K. R., Lesiak, A. J., Marx, R. G., Vo, E. K., Garden, G. A., & Neumaier, J. F. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.02.10.942953 · Cited by 3

Sex, not estrous cycle stage, drives differences in the microglial transcriptome in the 5xFAD mouse model of amyloidosisPreprint

Rodriguez, L. C., Noyes-Martel, N., Becker, J. D., Majewska, A. K., & O’Banion, M. K. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.28.646050 · Cited by 3

A human pluripotent stem cell triculture platform to elucidate microglial regulation of retinal ganglion cells in neuroinflammation

Harkin, J., Gomes, C., Afify, R. A. A., Patil, S. V., Hetzer, S. M., Tutrow, K. D., Peña, K. H., Baker, A., Lavekar, S. S., Huang, K.-C., et al. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2522958123 · Cited by 3

Some Basics on Innate Neuroimmunology for Nonspecialists

Konsman, J. P. (2025) · NeuroImmunoModulation · doi:10.1159/000550200 · Cited by 2

Microglial senescence and epigenetic reprogramming in alzheimer's disease: An immunometabolic perspective

Ma, J., Yang, B., Jiang, X., Wang, L., Wei, W., Cao, Y., & Li, H. (2026) · Experimental Gerontology · doi:10.1016/j.exger.2026.113177 · Cited by 4

Functional Medicine

Hudson, T. R. (2020) · Physical Medicine and Rehabilitation Clinics of North America · doi:10.1016/j.pmr.2020.07.011 · Cited by 2

The Multi-Omics Landscape and Clinical Relevance of the Immunological Signature of Phagocytosis Regulators: Implications for Risk Classification and Frontline Therapies in Skin Cutaneous Melanoma

Xing, J., Guo, L., Jia, Z., Li, Y., & Han, Y. (2022) · Cancers · doi:10.3390/cancers14153582 · Cited by 2

Protocol to assess engulfment and degradation of synaptosomes by murine microglia in vitro

Matera, A., Compagnion, A., & Paolicelli, R. C. (2025) · STAR Protocols · doi:10.1016/j.xpro.2025.103936 · Cited by 3

Neural tissue microphysiological systems in the era of patient-derived pluripotent stem cells

Mungenast, A. E., Aron, R., White, J. D., Tardiff, D. F., & Raja, W. K. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-813671-3.00009-8 · Cited by 2

Assessing amyloid-β, tau, and glial features in Lothian Birth Cohort 1936 participants post-mortem

Tzioras, M., Easter, J., Harris, S. E., McKenzie, C.-A., Smith, C., Deary, I. J., Henstridge, C. M., & Spires‐Jones, T. L. (2017) · Matters · doi:10.19185/matters.201708000003 · Cited by 2

Sex differences in microglia as a risk factor for Alzheimer’s disease

Delage, C. I., Rendina, D. N., Malacon, K. E., Tremblay, M., & Bilbo, S. D. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819344-0.00008-9 · Cited by 2

Normal development of the brain: a survey of joint structural–functional brain studies

Namiranian, R., Malakshan, S. R., Moghaddam, H. A., Khadem, A. A., & Jafari, R. (2022) · Reviews in the Neurosciences · doi:10.1515/revneuro-2022-0017 · Cited by 4

Bioinformatics analyses and experimental validation of the role of phagocytosis in low‐grade glioma

Fei, M., Lu, C., Feng, B., Sun, J., Wang, J., Sun, F., & Dong, B. (2023) · Environmental Toxicology · doi:10.1002/tox.24095 · Cited by 2

Behavioral stress and antidepressant treatments altered hippocampal expression of Nogo signal-related proteins in rats

Nibuya, M., Kezuka, D., Kanno, Y., Wakamatsu, S., & Suzuki, E. (2023) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2023.12.019 · Cited by 3

Loss of TREM2 reduces hyperactivation of progranulin deficient microglia but not lysosomal pathologyPreprint

Reifschneider, A., Robinson, S., van Lengerich, B., Gnörich, J. S., Logan, T., Heindl, S., Vogt, M. A., Weidinger, E., Riedl, L., Wind-Mark, K., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.07.08.451574 · Cited by 2

Human iPSC-derived Microglia Cells Integrated into Mouse Retina and Recapitulated Features of Endogenous Microglia CellsPreprint

Ma, W., Zhao, L., Xu, B., Fariss, R. N., Redmond, T. M., Zou, J., Wong, W. T., & Li, W. (2023) · eLife · doi:10.7554/elife.90695.1 · Cited by 2

Human iPSC-derived Microglial Cells Integrated into Mouse Retina and Recapitulated Features of Endogenous MicrogliaPreprint

Ma, W., Zhao, L., Xu, B., Fariss, R. N., Redmond, T. M., Zou, J., Wong, W. T., & Li, W. (2024) · eLife · doi:10.7554/elife.90695.2 · Cited by 2

Short Polysialic Acid Counteracts Age-Related Synaptic and Cognitive DeficitsPreprint

Frroku, L., Jia, S., Aleshin, S. E., Makesh, S., Böhm, K., Alo, A., Fiebig, T., Gerardy‐Schahn, R., Fendt, M., Thiesler, H., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.13.643031 · Cited by 2

Surface translocation of Kir2.1 channel induces IL-1β secretion in microglia

Maejima, Y., Horita, S., Yokota, S., Yamachi, M., Shimizu, M., Ono, T., Yu, Z., Tomita, H., & Shimomura, K. (2022) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2022.103734 · Cited by 1

Advances of the risk factors, immune and inflammation, therapy in postpartum post-traumatic stress disorder

Yang, B., Li, Z., Xu, X., & Miao, Z. (2024) · Brain Behavior and Immunity Integrative · doi:10.1016/j.bbii.2024.100086 · Cited by 1

Long-term Individual and Joint Exposure to Multiple Ambient Air Pollutants Associated with Progression Trajectory of Neuropsychiatric Multimorbidity: Multi-state Transition Analysis

Chen, D., Zhang, Y., Zhou, Y. F., & Liang, Z. (2025) · International Journal of Environmental Research · doi:10.1007/s41742-025-00747-1 · Cited by 1

Functional Diversity of Two Novel Embryonic Microglial Subpopulations and Their Developmental Trajectories in Developing Mouse Brains

Cheng, S. M., Ho, C., Chen, S., Huang, Y.-T., Mao, P., Lin, T., Chen, J., Sun, H. S., Hwang, D., & Chu, C. (2025) · Glia · doi:10.1002/glia.70064 · Cited by 3

Effects of Quantitative and Qualitative Visual Feedback on Motor Learning in Male Novices During a Badminton Underhand-Clear Striking Task

Suh, D., & Jeong, J. (2025) · Journal of Motor Behavior · doi:10.1080/00222895.2025.2550373 · Cited by 3

Visualising the Knowledge Structure of Microglia in Alzheimer’s Disease: A CiteSpace Analysis

Wang, Q., Zhang, X. C., Wang, D., Jiang, X., Zhou, Y., Zhang, T., Yang, X., Liu, L.-Z., & Li, Q. (2025) · Journal of Multidisciplinary Healthcare · doi:10.2147/jmdh.s521350 · Cited by 1

Multi-level expression profiling of cardiac and musculoskeletal Schwann cells in young and old mice

Haider, S., Stefanovska, D., Sassu, E., Domisch, C., Hoßfeld, M., Iaconianni, P., Perez‐Feliz, S., Schneider‐Warme, F., Kohl, P. K., Preißl, S., et al. (2025) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2025.10.001 · Cited by 1

Sox10 glial-neuron nuclear communication mediates anti-apoptosis neuroprotection after ischaemic stroke

Huang, M., Huang, X., Chen, Y., Zhang, Z., Wang, J., Yin, Q., Liu, J., Xie, F., Huang, W., Yuan, F., et al. (2026) · Stroke and Vascular Neurology · doi:10.1136/svn-2025-004934 · Cited by 1

Mechanisms and management of pegylated interferon-α toxicity in chronic hepatitis B

Zhu, L., Peng, F., Pi, D., & Lu, J. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1801043 · Cited by 1

Partners in plasticity: serotonergic glial interactions in brain circuit remodeling

Miller, V. K., & Broadie, K. (2026) · Frontiers in Neuroscience · doi:10.3389/fnins.2026.1782246 · Cited by 1

Targeting HIF-1α rescues microglial efferocytosis via the SLC7A11–TAM pathway to ameliorate Sepsis-associated encephalopathy

Wang, S., Chen, Y., Sun, Z., Zeng, Y., Wang, G., Lin, Q., Chen, C., & He, H. (2026) · International Immunopharmacology · doi:10.1016/j.intimp.2026.116623 · Cited by 1

Persisting Region‐Specific Microglia Activation and Synaptic Imbalance During Remission in a DSS ‐Induced Colitis Model

Morton, L., Villafuerte, L. E., Garza, A. P., Lindemann, N., Wider-Eberspächer, E., Bruder, D., & Dunay, I. R. (2026) · Glia · doi:10.1002/glia.70208 · Cited by 1

Molecular Mechanisms of Synaptic Plasticity and Memory and Their Dysfunction in Alzheimer's Disease ☆

Stephens, G. S., You, J. C., Fu, C.-H., & Chin, J. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21126-7 · Cited by 1

Molecular alterations contributing to brain aging

Martín‐Segura, A., & Benvegnù, S. (2019) · Journal of Neuroscience Research · doi:10.1002/jnr.24523 · Cited by 1

BIOQUÍMICA MITOCONDRIAL E ESTRESSE OXIDATIVO NO TRANSTORNO BIPOLAR: NOVOS HORIZONTES

Cyrino, L. A. R., de Lima, D. D., Ullmann, O. M., Maia, T. P., & Sardo, A. C. (2020) · Revista Contexto & Saúde · doi:10.21527/2176-7114.2020.39.6-18 · Cited by 1

Microglial Engulfment of Multisensory Terminals in the Midbrain Inferior Colliculus During an Early Critical Period

Moran, E. R., & Gabriele, M. L. (2025) · The Journal of Comparative Neurology · doi:10.1002/cne.70033 · Cited by 1

Microglia are required for developmental specification of AgRP innervation in the hypothalamus of offspring exposed to maternal high-fat diet during lactation

Mendoza-Romero, H. N., Biddinger, J. E., Bedenbaugh, M. N., & Simerly, R. B. (2025) · eLife · doi:10.7554/elife.101391.3 · Cited by 1

Microglia are not brain macrophages?

Zhelezov, M., & Tonchev, A. B. (2018) · Biomedical Reviews · doi:10.14748/bmr.v29.5855 · Cited by 1

Re-Expression of Thrombospondin-1 in the Thalamocortical Whisker Circuit after Experimental Diffuse Traumatic Brain Injury: Potential Role in Mediating Synaptogenesis?

Ogle, S. B. (2016) · UA Campus Repository (The University of Arizona) · Cited by 1

Pyruvate Kinase Isoenzyme M2 Impairs Cognition in Systemic Lupus Erythematosus by Promoting Microglial Synaptic Pruning via β-Catenin Signaling PathwayPreprint

Lu, L., Wang, H., Liu, X., Tan, L., Qiao, X., Ni, J., Sun, Y., Liang, J., Hou, Y., & Dou, H. (2020) · Research Square · doi:10.21203/rs.3.rs-126756/v1 · Cited by 1

Shadow imaging for panoptical visualization of living brain tissuePreprint

Dembitskaya, Y., Boyce, A. K. J., Idziak, A., Langeroudi, A. P., Bourdellès, G. L., Girard, J., Arizono, M., Ducros, M. G., Sato-Fitoussi, M., Otxoa-de-Amezaga, A., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.11.03.511028 · Cited by 1

Investigating chondroitin sulphate proteoglycans as a therapeutic target for Parkinson's disease

Fletcher, E. J. R. (2017) · Research Portal (King's College London)

Microglia subtype and brain functions

Tanabe, S., & Muramatsu, R. (2019) · Folia Pharmacologica Japonica · doi:10.1254/fpj.153.199

Metabolic reprogramming supports microglial survival and immune function

York, E. M. (2021) · cIRcle (University of British Columbia) · doi:10.14288/1.0379730

Microglia depletion disrupts normal functional development of adult-born neurons in the olfactory bulbPreprint

Wallace, J. L., Lord, J. S., Dissing‐Olesen, L., Stevens, B., & Murthy, V. N. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/714337

Terapia génica anti-inflamatoria en el abordaje de la neurodegeneración dopaminérgica motora

Lockhart, E. F. (2020) · El Servicio de Difusión de la Creación Intelectual (National University of La Plata) · doi:10.35537/10915/97168

Brain-engrafted macrophages provide protection against therapeutic irradiation and secondary concussive injuryPreprint

Feng, X., Frias, E. S., Paladini, M. S., Chen, D., Boosalis, Z., Becker, M., Gupta, S., Liu, S., Gupta, N., & Rosi, S. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/794354

Role of Extracellular Vesicles in Neuroinflammatory Progression and Mitochondrial Functional Alterations

Russell, A. E. (2019) · The Research Repository @ WVU (West Virginia University) · doi:10.33915/etd.3947

In vitro human stem cell–mediated central nervous system platforms

Coleman, M. D., Grainger, A. I., Parri, H. R., & Hill, E. J. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-85764-2.00003-x

Dancing with Glia: The Role of Astrocytes, Microglia and Oligodendrocytes and their Relation with Neurons in Neuroinflammation and Aging

Bellini, M. J. (2020) · Open Access Journal of Biomedical Science · doi:10.38125/oajbs.000238

The development of microfluidic assays for functional neural network communication studies & CNS drug discovery

MacKerron, C. (2020)

White matter integrity of the frontal brain and its relevance for catatonia and executive function

Arinrad, S. (2021) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-8974

The multi-omics landscape and clinical relevance of the immunological signature of phagocytosis regulators: Implications for risk classification and frontline therapies in skin cutaneous melanomaPreprint

Xing, J., Jia, Z., Li, Y., & Han, Y. (2022) · Research Square · doi:10.21203/rs.3.rs-1615209/v1

Faculty Opinions recommendation of Noninflammatory changes of microglia are sufficient to cause epilepsy.

Wu, L., & Eyo, U. B. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.732725584.793546013

Genome-Wide Approaches to Defining Macrophage Identity and Function

Fonseca, G. J., Seidman, J. S., & Glass, C. K. (2017) · ASM Press eBooks · doi:10.1128/9781555819194.ch30

Faculty Opinions recommendation of Sensory lesioning induces microglial synapse elimination via ADAM10 and fractalkine signaling.

Kano, M. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.735998030.793570314

Assessing amyloid-β, tau, and glial features in Lothian Birth Cohort 1936 participants post-mortem

Tzioras, M., Henstridge, C. M., & Spires‐Jones, T. L. (2018) · doi:10.26226/morressier.5b31ec592afeeb001345aa88

The multi-omics landscape and clinical relevance of the immunological signature of phagocytosis regulators: Implications for risk classification and frontline therapies in skin cutaneous melanomaPreprint

Xing, J., Jia, Z., Li, Y., & Han, Y. (2022) · Research Square · doi:10.21203/rs.3.rs-1615209/v2

Using Computational Methods and 3D Volume EM Reconstructions to Examine Interactions Between Microglia and Oligodendrocyte Precursor Cells in Mouse Cortex

Buchanan, J., Schardt, J., Collman, F., Smith, S. J., Bergles, D. E., Glatzer, J. C., Seung, H. S., Reid, R. C., & da Costa, N. M. (2022) · Microscopy and Microanalysis · doi:10.1017/s1431927622005682

Endocannabinoids and sex differences in the developing social behavior network

McCarthy, M. M., Marquardt, A. E., & VanRyzin, J. W. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-823490-7.00006-x

Antioxidants as Adjuncts to Conventional Therapies Against Oxidative Stress

Ahmed, A., Saleem, M. A., Afzaal, M., Ali, S. W., Nadeem, M., & Majeed, N. (2023) · Food bioactive ingredients · doi:10.1007/978-3-031-41188-5_9

Bone Marrow-Derived Myeloid Cells Colonize the Brain Parenchyma During Postnatal Development and Interact with Synapses in Mice Under Normal Physiological ConditionsPreprint

Carrier, M., Robert, M.-È., St‐Pierre, M., Ibáñez, F. G., de Andrade, E. G., Savage, J. C., Desjardins, M., & Tremblay, M. (2023) · SSRN Electronic Journal · doi:10.2139/ssrn.4608531

Pathogenesis of HIV-associated pain

Liu, X., & Tang, S. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-99744-7.00035-3

The molecular signature of Rett syndrome

Sangani, N. B. (2024) · Research Publications (Maastricht University) · doi:10.26481/dis.20240702ns

Reviewer #2 (Public Review): Human iPSC-derived Microglial Cells Integrated into Mouse Retina and Recapitulated Features of Endogenous Microglia

Ma, W., Zhao, L., Xu, B., et al. (2024) · eLife · doi:10.7554/elife.90695.2.sa1

eLife Assessment: Human iPSC-derived Microglial Cells Integrated into Mouse Retina and Recapitulated Features of Endogenous Microglia

Liu, X. (2024) · eLife · doi:10.7554/elife.90695.2.sa3

Reviewer #1 (Public Review): Human iPSC-derived Microglial Cells Integrated into Mouse Retina and Recapitulated Features of Endogenous Microglia

Ma, W., Zhao, L., Xu, B., et al. (2024) · eLife · doi:10.7554/elife.90695.2.sa2

Microglia-Mediated Synapse Loss in Alzheimer's Disease

Rajendran, L., & Paolicelli, R. C. (2018) · The Journal of Neuroscience · doi:10.1523/jneurosci.1136-17.2017 · Cited by 355

Targeting Microglia-Synapse Interactions in Alzheimer’s Disease

Piccioni, G., Mango, D., Saidi, A., Corbo, M., & Nisticò, R. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22052342 · Cited by 64

Contributions of Microglia to Structural Synaptic Plasticity

Kim, K. H., Son, S. M., & Mook‐Jung, I. (2013) · Journal of Experimental Neuroscience · doi:10.4137/jen.s11269 · Cited by 25

A role for astrocytes and microglia in synapse loss in Alzheimer’s disease

Tzioras, M., Daniels, M. J. D., Davies, C., Hooley, M., He, X., Dando, O., Hardingham, G. E., McColl, B. W., & Spires‐Jones, T. L. (2021) · Alzheimer s & Dementia · doi:10.1002/alz.052532 · Cited by 3

Microglia and Network Redundancy Loss in Early Alzheimer's Disease

Kim, Y. (2026) · Oxford Journal of Student Scholarship · doi:10.65161/recgnhabkfsxeh1ul