Morphology of Microglia Across Contexts of Health and Disease

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

A Unique Microglia Type Associated with Restricting Development of Alzheimer’s Disease

Keren-Shaul, H., Spinrad, A., Weiner, A., Matcovitch-Natan, O., Dvir-Szternfeld, R., Ulland, T. K., David, E., Baruch, K., Lara-Astaiso, D., Toth, B., et al. (2017) · Cell · doi:10.1016/j.cell.2017.05.018 · Cited by 5,493

The M1 and M2 paradigm of macrophage activation: Time for reassessment

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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

jvenn: an interactive Venn diagram viewer

Bardou, P., Mariette, J., Escudié, F., Djemiel, C., & Klopp, C. (2014) · BMC Bioinformatics · doi:10.1186/1471-2105-15-293 · Cited by 2,506

Heterogeneity in the distribution and morphology of microglia in the normal adult mouse brain

Lawson, L. J., Perry, V. H., Dri, P., & Gordon, S. (1990) · Neuroscience · doi:10.1016/0306-4522(90)90229-w · Cited by 2,045

How neuroinflammation contributes to neurodegeneration

Ransohoff, R. M. (2016) · Science · doi:10.1126/science.aag2590 · Cited by 1,967

New tools for studying microglia in the mouse and human CNS

Bennett, M. L., Bennett, F. C., Liddelow, S. A., Ajami, B., Zamanian, J. L., Fernhoff, N. B., Mulinyawe, S. B., Bohlen, C. J., Adil, A., Tucker, A., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1525528113 · Cited by 1,804

Integrated Systems Approach Identifies Genetic Nodes and Networks in Late-Onset Alzheimer’s Disease

Zhang, B., Gaiteri, C., Bodea, L.-G., Wang, Z., McElwee, J., Podtelezhnikov, A. A., Zhang, C., Xie, T., Tran, L., Dobrin, R., et al. (2013) · Cell · doi:10.1016/j.cell.2013.03.030 · Cited by 1,657

Microglia Shape Adult Hippocampal Neurogenesis through Apoptosis-Coupled Phagocytosis

Sierra, A., Encinas, J. M., Deudero, J. J. P., Chancey, J. H., Enikolopov, G., Overstreet-Wadiche, L. S., Tsirka, S. E., & Maletic-Savatic, M. (2010) · Cell Stem Cell · doi:10.1016/j.stem.2010.08.014 · Cited by 1,622

Microglial interactions with synapses are modulated by visual experience

Tremblay, M.-È., Lowery, R. L., & Majewska, A. K. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000527 · Cited by 1,542

Soluble Amyloid β Peptide Concentration as a Predictor of Synaptic Change in Alzheimer's Disease

Lue, L.-F., Kuo, Y.-M., Roher, A. E., Brachova, L., Shen, Y., Sue, L., Beach, T., Kurth, J. H., Rydel, R. E., & Rogers, J. (1999) · The American Journal of Pathology · doi:10.1016/s0002-9440(10)65184-x · Cited by 1,530

Microglial priming in neurodegenerative disease

Perry, V. H., & Holmes, C. (2014) · Nature Reviews Neurology · doi:10.1038/nrneurol.2014.38 · Cited by 1,127

Cytology & cellular pathology of the nervous system

Penfield, W. G. (1965) · Medical Entomology and Zoology · Cited by 1,035

Alzheimer’s Disease Risk Gene CD33 Inhibits Microglial Uptake of Amyloid Beta

Griciuc, A., Serrano-Pozo, A., Parrado, A. R., Lesinski, A. N., Asselin, C. N., Mullin, K., Hooli, B., Choi, S. H., Hyman, B. T., & Tanzi, R. E. (2013) · Neuron · doi:10.1016/j.neuron.2013.04.014 · Cited by 1,004

Review: Activation patterns of microglia and their identification in the human brain

Boche, D., Perry, V. H., & Nicoll, J. A. R. (2012) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12011 · Cited by 955

CNS immune privilege: hiding in plain sight

Carson, M. J., Doose, J. M., Melchior, B., Schmid, C. D., & Ploix, C. C. (2006) · Immunological Reviews · doi:10.1111/j.1600-065x.2006.00441.x · Cited by 838

Review: microglia of the aged brain: primed to be activated and resistant to regulation

Norden, D. M., & Godbout, J. P. (2013) · Neuropathology and Applied Neurobiology · doi:10.1111/j.1365-2990.2012.01306.x · Cited by 792

Dystrophic (senescent) rather than activated microglial cells are associated with tau pathology and likely precede neurodegeneration in Alzheimer’s disease

Streit, W. J., Braak, H., Xue, Q.-S., & Bechmann, I. (2009) · Acta Neuropathologica · doi:10.1007/s00401-009-0556-6 · Cited by 727

Changing face of microglia

Graeber, M. B. (2010) · Science · doi:10.1126/science.1190929 · Cited by 608

Age-related myelin degradation burdens the clearance function of microglia during aging

Safaiyan, S., Kannaiyan, N., Snaidero, N., Brioschi, S., Biber, K., Yona, S., Edinger, A. L., Jung, S., Rossner, M. J., & Simons, M. (2016) · Nature Neuroscience · doi:10.1038/nn.4325 · Cited by 604

TAM receptors regulate multiple features of microglial physiology

Fourgeaud, L., Través, P. G., Tufail, Y., Leal-Bailey, H., Lew, E. D., Burrola, P. G., Callaway, P., Zagórska, A., Rothlin, C. V., Nimmerjahn, A., et al. (2016) · Nature · doi:10.1038/nature17630 · Cited by 600

Immune phenotypes of microglia in human neurodegenerative disease: challenges to detecting microglial polarization in human brains

Walker, D. G., & Lue, L.-F. (2015) · Alzheimer's Research & Therapy · doi:10.1186/s13195-015-0139-9 · Cited by 562

Microglia across the lifespan: from origin to function in brain development, plasticity and cognition

Tay, T. L., Savage, J. C., Hui, C. W., Bisht, K., & Tremblay, M. (2017) · The Journal of Physiology · doi:10.1113/jp272134 · Cited by 562

Microglia contribute to normal myelinogenesis and to oligodendrocyte progenitor maintenance during adulthood

Hagemeyer, N., Hanft, K.-M., Akriditou, M.-A., Unger, N., Park, E. S., Stanley, E. R., Staszewski, O., Dimou, L., & Prinz, M. (2017) · Acta Neuropathologica · doi:10.1007/s00401-017-1747-1 · Cited by 558

Modulating inflammatory monocytes with a unique microRNA gene signature ameliorates murine ALS

Butovsky, O., Siddiqui, S., Gabriely, G., Lanser, A. J., Dake, B., Murugaiyan, G., Doykan, C. E., Wu, P. M., Gali, R. R., Iyer, L. K., et al. (2012) · Journal of Clinical Investigation · doi:10.1172/jci62636 · Cited by 481

Microglial Ramification, Surveillance, and Interleukin-1β Release Are Regulated by the Two-Pore Domain K+ Channel THIK-1

Madry, C., Kyrargyri, V., Arancibia-Cárcamo, I. L., Jolivet, R., Kohsaka, S., Bryan, R. M., & Attwell, D. (2018) · Neuron · doi:10.1016/j.neuron.2017.12.002 · Cited by 464

Dark microglia: A new phenotype predominantly associated with pathological states

Bisht, K., Sharma, K. P., Lecours, C., Gabriela Sánchez, M., El Hajj, H., Milior, G., Olmos‐Alonso, A., Gómez‐Nicola, D., Luheshi, G., Vallières, L., et al. (2016) · Glia · doi:10.1002/glia.22966 · Cited by 421

Chronic Stress Induced Remodeling of the Prefrontal Cortex: Structural Re-Organization of Microglia and the Inhibitory Effect of Minocycline

Hinwood, M., Tynan, R. J., Charnley, J. L., Beynon, S. B., Day, T. A., & Walker, F. R. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs151 · Cited by 336

Evidence for synaptic stripping by cortical microglia

Trapp, B. D., Wujek, J. R., Criste, G. A., Jalabi, W., Yin, X., Kidd, G. J., Stohlman, S. A., & Ransohoff, R. M. (2006) · Glia · doi:10.1002/glia.20462 · Cited by 331

Microglial pathology

Streit, W. J., Xue, Q.-S., Tischer, J., & Bechmann, I. (2014) · Acta Neuropathologica Communications · doi:10.1186/s40478-014-0142-6 · Cited by 317

Effects of aging and sensory loss on glial cells in mouse visual and auditory cortices

Tremblay, M., Zettel, M. L., Ison, J. R., Allen, P. D., & Majewska, A. K. (2012) · Glia · doi:10.1002/glia.22287 · Cited by 309

Neuroprotective function for ramified microglia in hippocampal excitotoxicity

Vinet, J., van Weering, H. R., Heinrich, A., Kälin, R. E., Wegner, A., Brouwer, N., Heppner, F. L., van Rooijen, N., Boddeke, H. W., & Biber, K. (2012) · Journal of Neuroinflammation · doi:10.1186/1742-2094-9-27 · Cited by 274

The “Big‐Bang” for modern glial biology: Translation and comments on Pío del Río‐Hortega 1919 series of papers on microglia

Sierra, A., de Castro, F., del Río‐Hortega, J., Rafael Iglesias‐Rozas, J., Garrosa, M., & Kettenmann, H. (2016) · Glia · doi:10.1002/glia.23046 · Cited by 266

Microglial and Astroglial Reactions to Ischemic and Kainic Acid-Induced Lesions of the Adult Rat Hippocampus

Jørgensen, M. B., Finsen, B. R., Jensen, M. B., Castellano, B., Diemer, N. H., & Zimmer, J. (1993) · Experimental Neurology · doi:10.1006/exnr.1993.1041 · Cited by 264

Disease-related microglia heterogeneity in the hippocampus of Alzheimer’s disease, dementia with Lewy bodies, and hippocampal sclerosis of aging

Bachstetter, A. D., Van Eldik, L. J., Schmitt, F. A., Neltner, J. H., Ighodaro, E. T., Webster, S. J., Patel, E., Abner, E. L., Kryscio, R. J., & Nelson, P. T. (2015) · Acta Neuropathologica Communications · doi:10.1186/s40478-015-0209-z · Cited by 258

Altered microglia morphology and higher resilience to stress-induced depression-like behavior in CX3CR1-deficient mice

Hellwig, S., Brioschi, S., Dieni, S., Frings, L., Masuch, A., Blank, T., & Biber, K. (2016) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2015.11.008 · Cited by 252

Microglia show altered morphology and reduced arborization in human brain during aging and Alzheimer's disease

Davies, D. S., Ma, J., Jegathees, T., & Goldsbury, C. (2017) · Brain Pathology · doi:10.1111/bpa.12456 · Cited by 251

Cytology and Cellular Pathology of the Nervous System.

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Human-to-mouse prion-like propagation of mutant huntingtin protein

Jeon, I., Cicchetti, F., Cisbani, G., Lee, S., Li, E., Bae, J., Lee, N., Li, L., Im, W., Kim, M., et al. (2016) · Acta Neuropathologica · doi:10.1007/s00401-016-1582-9 · Cited by 197

Insulin‐like growth factor type 1 receptor signaling in the cells of oligodendrocyte lineage is required for normal in vivo oligodendrocyte development and myelination

Zeger, M., Popken, G., Zhang, J., Xuan, S., Lu, Q. R., Schwab, M. H., Nave, K., Rowitch, D. H., D’Ercole, A. J., & Ye, P. (2006) · Glia · doi:10.1002/glia.20469 · Cited by 194

Rod microglia: elongation, alignment, and coupling to form trains across the somatosensory cortex after experimental diffuse brain injury

Ziebell, J. M., Taylor, S. E., Cao, T., Harrison, J. L., & Lifshitz, J. (2012) · Journal of Neuroinflammation · doi:10.1186/1742-2094-9-247 · Cited by 182

Activation of microglia in the brains of humans with heart disease and hypercholesterolemic rabbits

Streit, W. J., & Sparks, D. L. (1997) · Journal of Molecular Medicine · doi:10.1007/s001090050097 · Cited by 170

Prenatal Immune Challenge in Mice Leads to Partly Sex-Dependent Behavioral, Microglial, and Molecular Abnormalities Associated with Schizophrenia

Hui, C. W., St-Pierre, A., Hajj, H. E., Remy, Y., Hébert, S. S., Luheshi, G. N., Srivastava, L. K., & Tremblay, M. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00013 · Cited by 166

Bipolar/rod-shaped microglia are proliferating microglia with distinct M1/M2 phenotypes

Tam, W. Y., & Ma, C. H. E. (2014) · Scientific Reports · doi:10.1038/srep07279 · Cited by 158

Transitory macrophages in the white matter of the developing visual cortex. II. Development and relations with axonal pathways

Innocenti, G. M., Clarke, S., & Koppel, H. (1983) · Developmental Brain Research · doi:10.1016/0165-3806(83)90201-8 · Cited by 150

Rod Microglia: A Morphological Definition

Taylor, S. E., Morganti-Kossmann, M. C., Lifshitz, J., & Ziebell, J. M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0097096 · Cited by 149

Priming of microglia in a DNA-repair deficient model of accelerated aging

Raj, D. D. A., Jaarsma, D., Holtman, I. R., Olah, M., Ferreira, F. M., Schaafsma, W., Brouwer, N., Meijer, M., de Waard, M. C., van der Pluijm, I., et al. (2014) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2014.03.025 · Cited by 148

Shape descriptors of the “never resting” microglia in three different acute brain injury models in mice

Zanier, E. R., Fumagalli, S., Perego, C., Pischiutta, F., & De Simoni, M.-G. (2015) · Intensive Care Medicine Experimental · doi:10.1186/s40635-015-0039-0 · Cited by 147

Axon Initial Segment–Associated Microglia

Baalman, K., Marin, M. A., Ho, T., Godoy, M. I., Cherian, L., Robertson, C., & Rasband, M. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3751-14.2015 · Cited by 129

Microglia activation and phagocytosis: relationship with aging and cognitive impairment in the rhesus monkey

Shobin, E., Bowley, M. P., Estrada, L. I., Heyworth, N. C., Orczykowski, M. E., Eldridge, S. A., Calderazzo, S. M., Mortazavi, F., Moore, T. L., & Rosene, D. L. (2017) · GeroScience · doi:10.1007/s11357-017-9965-y · Cited by 126

Soman-induced seizures rapidly activate astrocytes and microglia in discrete brain regions

Zimmer, L. A., Ennis, M. J., & Shipley, M. T. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19970224)378:4 · Cited by 124

Transcriptome analysis of amoeboid and ramified microglia isolated from the corpus callosum of rat brain

Rangarajan, P., Jiang, B., Baby, N., Manivannan, J., Jayapal, M., Lu, J., Tay, S. S. W., Ling, E., & Dheen, S. T. (2012) · BMC Neuroscience · doi:10.1186/1471-2202-13-64 · Cited by 121

Inhomogeneous distribution of Iba‐1 characterizes microglial pathology in Alzheimer's disease

Tischer, J., Krueger, M., Mueller, W. C., Staszewski, O., Prinz, M., Streit, W. J., & Bechmann, I. (2016) · Glia · doi:10.1002/glia.23024 · Cited by 121

Increased expression of the chemokines CXCL1 and MIP-1α by resident brain cells precedes neutrophil infiltration in the brain following prolonged soman-induced status epilepticus in rats

Johnson, E. A., Dao, T. L., Guignet, M. A., Geddes, C. E., Koemeter-Cox, A., & Kan, R. K. (2011) · Journal of Neuroinflammation · doi:10.1186/1742-2094-8-41 · Cited by 119

Fluoxetine treatment affects the inflammatory response and microglial function according to the quality of the living environment

Alboni, S., Poggini, S., Garofalo, S., Milior, G., Hajj, H. E., Lecours, C., Girard, I., Gagnon, S., Boisjoly‐Villeneuve, S., Brunello, N., et al. (2016) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2016.07.155 · Cited by 114

High resolution dissection of reactive glial nets in Alzheimer’s disease

Bouvier, D. S., Jones, E. V., Quesseveur, G., Davoli, M. A., A. Ferreira, T., Quirion, R., Mechawar, N., & Murai, K. K. (2016) · Scientific Reports · doi:10.1038/srep24544 · Cited by 111

Morphological and Phagocytic Profile of Microglia in the Developing Rat Cerebellum

Perez‐Pouchoulen, M., VanRyzin, J. W., & McCarthy, M. M. (2015) · eNeuro · doi:10.1523/eneuro.0036-15.2015 · Cited by 100

Spatial arrangement of microglia in the mouse hippocampus: A stereological study in comparison with astrocytes

Jinno, S., Fleischer, F., Eckel, S., Schmidt, V., & Kosaka, T. (2007) · Glia · doi:10.1002/glia.20552 · Cited by 98

A Brief History of Microglial Ultrastructure: Distinctive Features, Phenotypes, and Functions Discovered Over the Past 60 Years by Electron Microscopy

Savage, J. C., Picard, K., Ibáñez, F. G., & Tremblay, M. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00803 · Cited by 96

Rod-shaped microglia morphology is associated with aging in 2 human autopsy series

Bachstetter, A. D., Ighodaro, E. T., Hassoun, Y., Aldeiri, D., Neltner, J. H., Patel, E., Abner, E. L., & Nelson, P. T. (2017) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2016.12.028 · Cited by 89

Formation of multinucleated giant cells and microglial degeneration in rats expressing a mutant Cu/Zn superoxide dismutase gene

Fendrick, S. E., Xue, Q., & Streit, W. J. (2007) · Journal of Neuroinflammation · doi:10.1186/1742-2094-4-9 · Cited by 88

Resting Microglial Motility Is Independent of Synaptic Plasticity in Mammalian Brain

Wu, L., & Zhuo, M. (2008) · Journal of Neurophysiology · doi:10.1152/jn.01210.2007 · Cited by 81

An MRI study of age-related white and gray matter volume changes in the rhesus monkey

Wisco, J. J., Killiany, R., Guttmann, C. R. G., Warfield, S. K., Moss, M. B., & Rosene, D. L. (2007) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2007.03.022 · Cited by 79

Increased activation of Iba1+ microglia in pediatric epilepsy patients with Rasmussen's encephalitis compared with cortical dysplasia and tuberous sclerosis complex

Wirenfeldt, M., Clare, R., Tung, S., Bottini, A. R., Mathern, G., & Vinters, H. (2009) · Neurobiology of Disease · doi:10.1016/j.nbd.2009.02.015 · Cited by 73

Age-related changes in the hippocampus (loss of synaptophysin and glial–synaptic interaction) are modified by systemic treatment with an NCAM-derived peptide, FGL

Ojo, B., Rezaie, P., Gabbott, P. L. A., Davies, H. A., Colyer, F. M., Cowley, T. R., Lynch, M. A., & Stewart, M. G. (2011) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2011.09.013 · Cited by 61

Nonfunctional mutant Wrn protein leads to neurological deficits, neuronal stress, microglial alteration, and immune imbalance in a mouse model of Werner syndrome

Hui, C. W., St‐Pierre, M., Detuncq, J., Aumailley, L., Dubois, M.-J., Couture, V., Skuk, D., Marette, A., Tremblay, J. P., Lebel, M., et al. (2018) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2018.06.007 · Cited by 47

A lysosome-specific two-photon phosphorescent binuclear cyclometalated platinum(ii) probe for in vivo imaging of live neurons

Ho, Y., Au, N. P. B., Wong, K., Chan, C. T., Kwok, W., Law, G., Tang, K.-K., Wong, W., Ma, C. H. E., & Lam, M. H. (2014) · Chemical Communications · doi:10.1039/c3cc48934e · Cited by 41

Differences in Origin of Reactive Microglia in Bone Marrow Chimeric Mouse and Rat After Transient Global Ischemia

Lambertsen, K. L., Deierborg, T., Gregersen, R., Clausen, B. H., Wirenfeldt, M., Nielsen, H. H., Dalmau, I., Diemer, N. H., Dagnæs‐Hansen, F., Johansen, F. F., et al. (2011) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e31821db3aa · Cited by 39

Microglia: An Intrinsic Component of the Proliferative Zones in the Fetal Rhesus Monkey (Macaca mulatta) Cerebral Cortex

Barger, N., Keiter, J. A., Kreutz, A., Krishnamurthy, A., Weidenthaler, C., Martínez‐Cerdeño, V., Tarantal, A. F., & Noctor, S. C. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy145 · Cited by 38

Microglia: Senescence Impairs Clearance of Myelin Debris

Thériault, P., & Rivest, S. (2016) · Current Biology · doi:10.1016/j.cub.2016.06.066 · Cited by 37

Satellite microglia show spontaneous electrical activity that is uncorrelated with activity of the attached neuron

Wogram, E., Wendt, S., Matyash, M., Pivneva, T. A., Draguhn, A., & Kettenmann, H. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13256 · Cited by 33

Ultrastructure of microglia-synapse interactions in the HIV-1 Tat-injected murine central nervous system

Tremblay, M., Marker, D. F., Puccini, J. M., Muly, E. C., Lu, S., & Gelbard, H. A. (2013) · Communicative & Integrative Biology · doi:10.4161/cib.27670 · Cited by 28

The Importance of Inter-Species Variation in Traumatic Brain Injury-Induced Alterations of Microglial-Axonal Interactions

Gorse, K. M., & Lafrenaye, A. D. (2018) · Frontiers in Neurology · doi:10.3389/fneur.2018.00778 · Cited by 22

Gitter cells and their relationship to macrophages in the developing cerebellum

Das, G. D. (1976) · Virchows Archiv B Cell Pathology Including Molecular Pathology · doi:10.1007/bf02890348 · Cited by 18

Three-Dimensional Nanostructure of an Intact Microglia Cell

Bolasco, G., Weinhard, L., Boissonnet, T., Neujahr, R., & Gross, C. T. (2018) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2018.00105 · Cited by 17

Microglial response to murine leukemia virus-induced encephalopathy is a good indicator of neuronal perturbations

Xue, Q., Yang, C., Hoffman, P. M., & Streit, W. J. (2010) · Brain Research · doi:10.1016/j.brainres.2009.12.089 · Cited by 13

Microglia Detection by Enzymatic Histochemistry

Almolda, B., González, B., & Castellano, B. (2013) · Methods in molecular biology · doi:10.1007/978-1-62703-520-0_22 · Cited by 7

Microglia states and nomenclature: A field at its crossroads

Paolicelli, R. C., Sierra, A., Stevens, B., Tremblay, M.-E., Aguzzi, A., Ajami, B., Amit, I., Audinat, E., Bechmann, I., Bennett, M., et al. (2022) · Neuron · doi:10.1016/j.neuron.2022.10.020 · Cited by 1,973

Microglia in neurodegenerative diseases: mechanism and potential therapeutic targets

Gao, C., Jiang, J., Tan, Y., & Chen, S. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01588-0 · Cited by 1,616

Neuropathobiology of COVID-19: The Role for Glia

Tremblay, M.-E., Madore, C., Bordeleau, M., Tian, L., & Verkhratsky, A. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.592214 · Cited by 159

Microglial morphometric analysis: so many options, so little consistency

Reddaway, J., Richardson, P., Bevan, R. J., Stoneman, J., & Palombo, M. (2023) · Frontiers in Neuroinformatics · doi:10.3389/fninf.2023.1211188 · Cited by 131

Plasticity of microglia

Augusto‐Oliveira, M., Arrifano, G. D. P., Delage, C. I., Tremblay, M., Lopez, M. E. C., & Verkhratsky, A. (2021) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.12797 · Cited by 114

Microglial dynamics during brain development

Tsuruta, F., & Okajima, T. (2018) · Neural Regeneration Research · doi:10.4103/1673-5374.226386 · Cited by 22

Quantitative Morphological Comparison of Microglia in Normal and Alzheimer's Disease Model Brains

Zhong, Z. (2025) · Journal of Clinical Medicine Research · doi:10.32629/jcmr.v6i3.4437

Morphological diversity of microglia: Implications for learning, environmental adaptation, ageing, sex differences and neuropathology

Augusto‐Oliveira, M., Arrifano, G. D. P., Leal-Nazaré, C. G., Chaves-Filho, A. J. M., Santos-Sacramento, L., Lopes-Araújo, A., Tremblay, M., & Lopez, M. E. C. (2025) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2025.106091 · Cited by 28

Microglial morphology in the somatosensory cortex across lifespan. A quantitative study

Godeanu, S., Clarke, D., Stopper, L., Deftu, A., Popa‐Wagner, A., Bălşeanu, T. A., Scheller, A., & Cătălin, B. (2023) · Developmental Dynamics · doi:10.1002/dvdy.582 · Cited by 15

Microglia morphology in the physiological and diseased brain : from fixed tissue to in vivo conditions

Stopper, L., Bălşeanu, T. A., Cătălin, B., Rogoveanu, O. C., Mogoantă, L., & Scheller, A. (2018) · PubMed · doi:10.22028/d291-39556 · Cited by 23