Structural abnormalities of the cerebral cortex in human chromosomal aberrations: a Golgi study

Synaptic patterns on different cell types in the different laminae of the cat visual cortex. An electron microscope study

Colonnier, M. (1968) · Brain Research · doi:10.1016/0006-8993(68)90234-5 · Cited by 946

Apical dendritic spines of the visual cortex and light deprivation in the mouse

Valverde, P. (1967) · Experimental Brain Research · doi:10.1007/bf00237559 · Cited by 483

Electron Microscopy of Synaptic Contacts on Dendrite Spines of the Cerebral Cortex

Gray, E. G. (1959) · Nature · doi:10.1038/1831592a0 · Cited by 462

The termination of fibres from the cerebral cortex and thalamus upon dendritic spines in the caudate nucleus: a study with the Golgi method

Kemp, J. M., & Powell, T. P. S. (1971) · Philosophical transactions of the Royal Society of London. Series B, Biological sciences · doi:10.1098/rstb.1971.0105 · Cited by 306

Structural changes in the area striata of the mouse after enucleation

Valverde, F. (1968) · Experimental Brain Research · doi:10.1007/bf00235903 · Cited by 286

Prenatal and early postnatal ontogenesis of the human motor cortex: A Golgi study. I. The sequential development of the cortical layers

Marín‐Padilla, M. (1970) · Brain Research · doi:10.1016/0006-8993(70)90037-5 · Cited by 280

The effect of visual deprivation on cortical neurons: A Golgi study

Globus, A., & Scheibel, A. B. (1967) · Experimental Neurology · doi:10.1016/0014-4886(67)90029-5 · Cited by 247

EXPERIMENTAL DEGENERATION IN THE CEREBRAL CORTEX.

Colonnier, M. (1964) · PubMed · Cited by 240

Rate and extent of recovery from dark rearing in the visual cortex of the mouse

Valverde, F. (1971) · Brain Research · doi:10.1016/0006-8993(71)90302-7 · Cited by 235

Double origin of the pericellular baskets of the pyramidal cells of the human motor cortex: A Golgi study

Marín‐Padilla, M. (1972) · Brain Research · doi:10.1016/0006-8993(72)90585-9 · Cited by 193

Developmental sex differences and effect of ovariectomy on the number of cortical pyramidal cell dendritic spines

Muñoz‐Cueto, J. A., García‐Segura, L. M., & Ruiz‐Marcos, A. (1990) · Brain Research · doi:10.1016/0006-8993(90)90577-x · Cited by 60

Microtubule disarray in cortical dendrites and neurobehavioral failure. I. Golgi and electron microscopic studies

Purpura, D. P., Bodick, N. C., Suzuki, K., Rapin, I., & Wurzelmann, S. (1982) · Developmental Brain Research · doi:10.1016/0165-3806(82)90128-6 · Cited by 61

Effect of prenatal exposure to ethanol on the ultrastructure of layer V of mature rat somatosensory cortex

Al-Rabiai, S. D., & Miller, M. W. (1989) · Journal of Neurocytology · doi:10.1007/bf01187226 · Cited by 57

Mouse Models for Down Syndrome-Associated Developmental Cognitive Disabilities

Liu, C., Belichenko, P. V., Zhang, L., Fu, D., Kleschevnikov, A. M., Baldini, A., Antonarakis, S. E., Mobley, W. C., & Yu, Y. E. (2011) · Developmental Neuroscience · doi:10.1159/000329422 · Cited by 57

Neocortical dendritic complexity is controlled during development by NOMA-GAP-dependent inhibition of Cdc42 and activation of cofilinPreprint

Rosário, M., Schuster, S., Jüttner, R., Parthasarathy, S., Tarabykin, V. S., & Birchmeier, W. (2012) · Genes & Development · doi:10.1101/gad.191593.112 · Cited by 53

Dendritic and Synaptic Protection: Is It Enough to Save the Retinal Ganglion Cell Body and Axon?

Morquette, J. B., & Di Polo, A. (2008) · Journal of Neuro-Ophthalmology · doi:10.1097/wno.0b013e318177edf0 · Cited by 51

Fragile x syndrome and autism: from disease model to therapeutic targets

Dölen, G., & Bear, M. F. (2009) · Journal of Neurodevelopmental Disorders · doi:10.1007/s11689-009-9015-x · Cited by 53

9th International workshop on Fragile X syndrome and X-linked mental retardation

Fryns, J., Borghgraef, M., Brown, T. W., Chelly, J., Fisch, G. S., Hamel, B. C. J., Hanauer, A., Lacombe, D., Luo, L., Macpherson, J., et al. (2000) · American Journal of Medical Genetics · doi:10.1002/1096-8628(20001023)94:5 · Cited by 9

Synaptic and Dendritic Development and Mental Defect

Huttenlocher, P. R. (1975) · Elsevier eBooks · doi:10.1016/b978-0-12-139050-1.50013-6 · Cited by 51

Sudden infant death syndrome (SIDS): a preliminary study of reticular dendritic spines in infants with SIDS

Quattrochi, J. J., Baba, N., Liss, L., & Adrion, W. (1980) · Brain Research · doi:10.1016/0006-8993(80)91280-9 · Cited by 50

Transient receptor potential channels as novel effectors of brain-derived neurotrophic factor signaling: Potential implications for Rett syndrome

Amaral, M. D., Chapleau, C. A., & Pozzo‐Miller, L. D. (2006) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2006.09.005 · Cited by 49

Electrophysiological properties of cultured dorsal root ganglion and spinal cord neurons of normal and trisomy 16 fetal mice

Orozco, C. B., SMITH, S. A., Epstein, C. J., & Rapoport, S. I. (1987) · Developmental Brain Research · doi:10.1016/0165-3806(87)90144-1 · Cited by 48

Development of interlaminar astroglial processes in the cerebral cortex of control and Down’s syndrome human cases.

Colombo, J. A., Reisin, H. D., Jones, M., & Bentham, C. (2005) · Experimental Neurology · doi:10.1016/j.expneurol.2004.11.024 · Cited by 48

Experience with prenatal fragile X detection

Jenkins, E. C., Brown, W. T., Brooks, J., Duncan, C. J., Rudelli, R. D., Wisniewski, H. M., & Opitz, J. M. (1984) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320170114 · Cited by 48

Dendritic degeneration and regrowth in the cerebral cortex of patients with Alzheimer's disease

Paula-Barbosa, M. M., Cardoso, R. M., Guimaraes, M. L., & Cruz, C. (1980) · Journal of the Neurological Sciences · doi:10.1016/s0022-510x(80)80014-1 · Cited by 47

Dendritic spine pathology and thrombospondin-1 deficits in Down syndrome

Torres, M. D., Garcı́a, O., Tang, C. G., & Busciglio, J. A. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2017.09.025 · Cited by 49

The Kinesin-3, Unc-104 Regulates Dendrite Morphogenesis and Synaptic Development in Drosophila

Kern, J. V., Zhang, Y. V., Krämer, S., Brenman, J. E., & Rasse, T. M. (2013) · Genetics · doi:10.1534/genetics.113.151639 · Cited by 49

Abnormal maturation of cerebral cortex and behavioral deficit in adult rats after neonatal administration of antibodies to ganglioside

Kasarskis, E. J., Karpiak, S. E., Rapport, M. M., Yu, R. K., & Bass, N. H. (1981) · Developmental Brain Research · doi:10.1016/0165-3806(81)90091-2 · Cited by 46

Intellectual disability: dendritic anomalies and emerging genetic perspectives

Quach, T., Stratton, H. J., Khanna, R., Kolattukudy, P. E., Honnorat, J., Meyer, K., & Duchemin, A. (2020) · Acta Neuropathologica · doi:10.1007/s00401-020-02244-5 · Cited by 47

Synaptic actin stabilization protein loss in Down syndrome and Alzheimer disease

Lauterborn, J. C., Cox, C. D., Chan, S. W., Vanderklish, P. W., Lynch, G., & Gall, C. M. (2020) · Brain Pathology · doi:10.1111/bpa.12779 · Cited by 43

Neurophysiological abnormalities in cultured dorsal root ganglion neurons from the trisomy-16 mouse fetus, a model for Down syndrome

Ault, B., Caviedes, P. A., & Rapoport, S. I. (1989) · Brain Research · doi:10.1016/0006-8993(89)90678-1 · Cited by 42

Dendritic Spines and Development: Towards a Unifying Model of Spinogenesis—A Present Day Review of Cajal's Histological Slides and Drawings

García-López, P., García‐Marín, V., & Freire, M. (2010) · Neural Plasticity · doi:10.1155/2010/769207 · Cited by 47

Regulation of dendrite morphology and excitatory synapse formation by zDHHC15

Shah, B. S., Shimell, J. J., & Bamji, S. X. (2019) · Journal of Cell Science · doi:10.1242/jcs.230052 · Cited by 40

Molecular and Cellular Mechanisms Elucidating Neurocognitive Basis of Functional Impairments Associated With Intellectual Disability in Down Syndrome

Rachidi, M., & Lopes, C. (2010) · American Journal on Intellectual and Developmental Disabilities · doi:10.1352/1944-7558-115.2.83 · Cited by 40

Effects of prenatal ethanol exposure on dendritic spines of layer V pyramidal neurons in the somatosensory cortex of the rat

Galofré, E., Ferrer, I., Fábregues, I., & López-Tejero, D. (1987) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(87)90095-5 · Cited by 37

Quantitative analysis of the spatial distribution of axonal and dendritic terminals of hippocampal pyramidal neurons in immature human brain

Paldino, A. M., & Purpura, D. P. (1979) · Experimental Neurology · doi:10.1016/0014-4886(79)90235-8 · Cited by 37

Elemental characterisation of the pyramidal neuron layer within the rat and mouse hippocampus

Hackett, M. J., Hollings, A. L., Caine, S., Bewer, B., Alaverdashvili, M., Takechi, R., Mamo, J. C. L., Jones, M. W., de Jonge, M. D., Paterson, P. G., et al. (2018) · Metallomics · doi:10.1039/c8mt00230d · Cited by 36

Dendritic Pathology: An Overview of Golgi Studies in Man

Jagadha, V., & Becker, L. E. (1989) · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · doi:10.1017/s0317167100028493 · Cited by 35

The Effect of Epidural Compression on Cerebral Cortex: A Rat Model

Chen, J., Wang, Y., & Tseng, G. (2003) · Journal of Neurotrauma · doi:10.1089/089771503767869999 · Cited by 35

Cytomorphological Alterations in the Aging Animal Brain with Emphasis on Golgi Studies

Mervis, R. F. (1981) · Springer eBooks · doi:10.1007/978-1-4684-3929-8_4 · Cited by 31

Roles for DSCAM and DSCAML1 in Central Nervous System Development and Disease

Montesinos, M. L. (2013) · Advances in neurobiology · doi:10.1007/978-1-4614-8090-7_11 · Cited by 31

Epigenetic regulation of neuronal dendrite and dendritic spine development

Smrt, R. D., & Zhao, X. (2010) · Frontiers in Biology · doi:10.1007/s11515-010-0650-0 · Cited by 35

A study of Golgi preparations from the human lateral geniculate nucleus

Hickey, T. L., & Guillery, R. W. (1981) · The Journal of Comparative Neurology · doi:10.1002/cne.902000407 · Cited by 30

Activity-Dependent Plasticity in Adult Somatic Sensory Cortex

Ebner, F. F., Rema, V., Sachdev, R. N. S., & Symons, F. J. (1997) · Seminars in Neuroscience · doi:10.1006/smns.1997.0105 · Cited by 28

Consequences of trisomy 21 for brain development in Down syndrome

Russo, M. L., Sousa, A. M. M., & Bhattacharyya, A. (2024) · Nature Reviews Neuroscience · doi:10.1038/s41583-024-00866-2 · Cited by 28

Astrocytes regulate neuronal network activity by mediating synapse remodeling

Kim, N., & Chung, W. (2022) · Neuroscience Research · doi:10.1016/j.neures.2022.09.007 · Cited by 31

Effect of hypothyroidism on the size of spines of pyramidal neurons of the cerebral cortex

Berbel, P. J., del Rey, F. E., de Escobar, G. M., & Ruiz‐Marcos, A. (1985) · Brain Research · doi:10.1016/0006-8993(85)90057-5 · Cited by 28

The effect of hyperphenylalaninemia on size and density of synapses in rat neocortex

Nigam, M. P., & Labar, D. (1979) · Brain Research · doi:10.1016/0006-8993(79)90507-9 · Cited by 28

The Effects of Decompression and Exogenous NGF on Compressed Cerebral Cortex

Chen, J., Wang, Y., & Tseng, G. (2004) · Journal of Neurotrauma · doi:10.1089/0897715042441729 · Cited by 27

Down syndrome cell adhesion molecule and its functions in neural development

Zhu, K. Y., Xu, Y., Liu, J., Xu, Q., & Ye, H. (2011) · Neuroscience Bulletin · doi:10.1007/s12264-011-1045-1 · Cited by 27

Down Syndrome

Capone, G. T. (2004) · Infants & Young Children · doi:10.1097/00001163-200401000-00007 · Cited by 29

Ectopic dendrite initiation: CNS pathogenesis as a model of CNS development

Siegel, D. A., Huang, M. K., & Becker, S. F. (2002) · International Journal of Developmental Neuroscience · doi:10.1016/s0736-5748(02)00055-2 · Cited by 26

Actin and Diseases of the Nervous System

Bernstein, B. W., Maloney, M. T., & Bamburg, J. R. (2010) · Advances in neurobiology · doi:10.1007/978-1-4419-7368-9_11 · Cited by 31

Neuronal dysfunction in Down syndrome: Contribution of neuronal models in cell culture

Saud, K., Arriagada, C., Cárdenas, A. M., Shimahara, T., Allen, D. D., Caviedes, R., & Caviedes, P. A. (2006) · Journal of Physiology-Paris · doi:10.1016/j.jphysparis.2005.12.013 · Cited by 26

Ultrastructural pathology of dendritic spines in epitumorous human cerebral cortex

Špaček, J. (1987) · Acta Neuropathologica · doi:10.1007/bf00695505 · Cited by 24

Overexpressed Down Syndrome Cell Adhesion Molecule (DSCAM) Deregulates P21-Activated Kinase (PAK) Activity in an In Vitro Neuronal Model of Down Syndrome: Consequences on Cell Process Formation and Extension

Pérez-Núñez, R., Barraza, N., González‐Jamett, A. M., Cárdenas, A. M., Barnier, J., & Caviedes, P. A. (2016) · Neurotoxicity Research · doi:10.1007/s12640-016-9613-9 · Cited by 26

Expression of the 210 kDa neurofilament subunit in cultured central nervous system from normal and trisomy 16 mice: regulation by interferon

Plioplys, A. V. (1988) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(88)90157-8 · Cited by 25

The role of glycogen synthase kinase-3 signaling in neurodevelopment and fragile X syndrome.

Portis, S. M., Giunta, B. N., Obregon, D. F., & Tan, J. (2012) · Europe PMC (PubMed Central) · Cited by 24

Neurofibrillary changes in the cerebral cortex of a patient with subacute sclerosing panencephalitis (SSPE)

Paula-Barbosa, M. M., Brito, R., Silva, C. A., Faria, R., & Cruz, C. (1979) · Acta Neuropathologica · doi:10.1007/bf00691159 · Cited by 23

Histological maturation of the neocortex in phenylketonuric rats

Cordero, M. E., Trejo, M., Colombo, M., & Aranda, V. (1983) · Early Human Development · doi:10.1016/0378-3782(83)90072-5 · Cited by 24

Regulation of hippocampal excitatory synapses by the Zdhhc5 palmitoyl acyltransferase

Shimell, J. J., Globa, A. K., Sepers, M. D., Wild, A. R., Matin, N., Raymond, L. A., & Bamji, S. X. (2021) · Journal of Cell Science · doi:10.1242/jcs.254276 · Cited by 23

Normal protein composition of synapses in Ts65Dn mice: a mouse model of Down syndrome

Fernandez, F., Trinidad, J. C., Blank, M., Feng, D., Burlingame, A. L., & Garner, C. C. (2009) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2009.06110.x · Cited by 24

Prenatal Exposure to Ethanol Alters Synaptic Activity in Layer V/VI Pyramidal Neurons of the Somatosensory Cortex

Delatour, L. C., Yeh, P. W. L., & Yeh, H. H. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz199 · Cited by 24

Dendritic Spines in Learning and Memory: From First Discoveries to Current Insights

Heck, N., & Santos, M. D. (2023) · Advances in neurobiology · doi:10.1007/978-3-031-36159-3_7 · Cited by 24

Altered intrinsic and network properties of neocortical neurons in the Ts65Dn mouse model of Down syndrome

Cramer, N., Xu, X., Haydar, T. F., & Galdzicki, Z. (2015) · Physiological Reports · doi:10.14814/phy2.12655 · Cited by 22

Normal and Abnormal Human Brain Development

Volpe, J. J. (1977) · Clinics in Perinatology · doi:10.1016/s0095-5108(18)31219-3 · Cited by 22

Basal Dendritic Morphology of Cortical Pyramidal Neurons in Williams Syndrome: Prefrontal Cortex and Beyond

Hrvoj-Mihic, B., Hanson, K. L., Lew, C. H., Stefanacci, L., Jacobs, B., Bellugi, U., & Semendeferi, K. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00419 · Cited by 21

Understanding the genetic mechanisms and cognitive impairments in Down syndrome: towards a holistic approach

Abukhaled, Y., Hatab, K., Awadhalla, M., & Hamdan, H. (2023) · Journal of Neurology · doi:10.1007/s00415-023-11890-0 · Cited by 30

Involvement of the Snk-SPAR pathway in glutamate-induced excitotoxicity in cultured hippocampal neurons

Wu, L., Sun, C., Zhang, Y., Fan, M., Xu, J., Ma, H., & Jian, Z. (2007) · Brain Research · doi:10.1016/j.brainres.2007.06.082 · Cited by 21

Effects of chronic crowding stress on midbrain development: Changes in dendritic spine density and morphology in jewel fish optic tectum

Wesley, B. J., & Coss, R. G. (1982) · Developmental Psychobiology · doi:10.1002/dev.420150508 · Cited by 21

Prenatal methylmercury exposure results in dendritic spine dysgenesis in rats

Stoltenburg, G., & Markwort, S. (1990) · Neurotoxicology and Teratology · doi:10.1016/0892-0362(90)90064-j · Cited by 20

HERC1 Ubiquitin Ligase Is Required for Hippocampal Learning and Memory

Pérez-Villegas, E. M., Pérez-Rodríguez, M., Negrete‐Díaz, J. V., Ruiz, R., Rosa, J. L., de Toledo, G. Á., Moreno, A. R., & Armengol, J. A. (2020) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2020.592797 · Cited by 21

Pitfalls And Hopes in Down Syndrome Therapeutic Approaches: In the Search for Evidence-Based Treatments

Dierssen, M., Ortiz-Abalia, J., Arqué, G., de Lagrán, M. M., & Fillat, C. (2006) · Behavior Genetics · doi:10.1007/s10519-006-9050-2 · Cited by 20

Lisencefalia: Agiria

Ferrer, I., & Fernández‐Álvarez, E. (1977) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(77)90096-x · Cited by 20

Elevated apoptosis in pre-mature neurons differentiated from mouse ES cells containing a single human chromosome 21

Kadota, M., Shirayoshi, Y., & Oshimura, M. (2002) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(02)02686-4 · Cited by 20

Prenatal and postnatal development of lamina IX neurons in the rat thoracic spinal cord

Cummings, J. P., & Stelzner, D. J. (1984) · Experimental Neurology · doi:10.1016/0014-4886(84)90054-2 · Cited by 20

MORPHOLOGICAL CHANGES IN DENDRITIC SPINES ASSOCIATED WITH LONG-TERM

Yuste, R., & Bonhoeffer, T. (2001) · Cited by 19

Neuropathology of sanfilippo syndrome

Ghatak, N. R., Fleming, D., & Hinman, A. (1977) · Annals of Neurology · doi:10.1002/ana.410020214 · Cited by 19

Pathologic axons and synapses in human neuropsychiatric disorders

Gonatas, N. K., & Moss, A. H. (1975) · Human Pathology · doi:10.1016/s0046-8177(75)80042-6 · Cited by 19

Deletion of KIBRA, protein expressed in kidney and brain, increases filopodial-like long dendritic spines in neocortical and hippocampal neurons in vivo and in vitro

Blanqué, A., Repetto, D., Rohlmann, A., Brockhaus, J., Duning, K., Pavenstädt, H. J., Wolff, I., & Missler, M. (2015) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2015.00013 · Cited by 18

Plasticity of dendritic spine formation: A state dependent stochastic process

Berard, D. R., Burgess, J. W., & Coss, R. G. (1981) · International Journal of Neuroscience · doi:10.3109/00207458109043306 · Cited by 18

Long-lasting Behavioral and Neuroanatomical Effects of Postnatal Valproic Acid Treatment

Norton, S. A., Gifford, J. J., Pawlak, A. P., Derbaly, A., Sherman, S. L., Zhang, H., Wagner, G. C., & Kusnecov, A. W. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.02.029 · Cited by 17

Actin-Binding Proteins and Disease

dos Remedios, C. G., & Chhabra, D. (2008) · Springer eBooks · doi:10.1007/978-0-387-71749-4 · Cited by 17

The incidence of ultrastructural abnormalities in the cortex of two retarded human brains (Down's syndrome)

Rees, S. M. (1977) · Acta Neuropathologica · doi:10.1007/bf00684542 · Cited by 17

The cytoarchitecture and soma-dendritic arbors of the pyramidal neurons of aged rat sensorimotor cortex: An intracellular dye injection study

Wang, T., Chen, J., Wang, Y.-J., & Tseng, G. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.10.025 · Cited by 16

Meeting at the crossroads: common mechanisms in Fragile X and Down syndrome

Chang, K. T., Ro, H., Wang, W., & Min, K. (2013) · Trends in Neurosciences · doi:10.1016/j.tins.2013.08.007 · Cited by 17

Publisher's note

Tordjman, S., Cohen, D., Coulon, N., Anderson, G. M., Botbol, M., Canitano, R., & Roubertoux, P. L. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.01.030 · Cited by 19

ABNORMAL PERISOMATIC STRUCTURES IN NON‐PYRAMIDAL NEURONS IN THE CEREBRAL CORTEX IN DOWN'S SYNDROME

Fábregues, I., & FERRERf, I. (1983) · Neuropathology and Applied Neurobiology · doi:10.1111/j.1365-2990.1983.tb00333.x · Cited by 16

Dendritic spine morphology and dynamics in health and disease

Webb, D. J., Lee, S. N., & Zhang, H. (2015) · Cell Health and Cytoskeleton · doi:10.2147/chc.s82214 · Cited by 17

Study of the selectivity of the impregnation of neurons by the Golgi method

Shimono, M., & Tsuji, N. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902590108 · Cited by 15

Spine morphology of neurons in the avian forebrain is affected by rearing conditions

Rollenhagen, A., & Bischof, H. (1994) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(05)80029-9 · Cited by 15

Morphological Features of Human Dendritic Spines

Renner, J., & Rasia‐Filho, A. A. (2023) · Advances in neurobiology · doi:10.1007/978-3-031-36159-3_9 · Cited by 18

Activity-Dependent Structural Plasticity of Dendritic Spines

Chapleau, C. A., & Pozzo‐Miller, L. D. (2008) · Elsevier eBooks · doi:10.1016/b978-012370509-9.00039-5 · Cited by 14

Merging advanced technologies with classical methods to uncover dendritic spine dynamics: A hot spot of synaptic plasticity

Maiti, P., Manna, J., & McDonald, M. P. (2015) · Neuroscience Research · doi:10.1016/j.neures.2015.02.007 · Cited by 16

Role of DSCAM in the Development of Neural Control of Movement and Locomotion

Lemieux, M., Thiry, L., Laflamme, O. D., & Bretzner, F. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22168511 · Cited by 14

A Dual Comparative Approach: Integrating Lines of Evidence from Human Evolutionary Neuroanatomy and Neurodevelopmental Disorders

Hanson, K. L., Hrvoj-Mihić, B., & Semendeferi, K. (2014) · Brain Behavior and Evolution · doi:10.1159/000365409 · Cited by 13

Cognitive and molecular aspects of fragile X

Hinton, V. J., Halperin, J. M., Dobkin, C., Ding, X. H., Brown, W. T., & Miezejeski, C. M. (1995) · Journal of Clinical and Experimental Neuropsychology · doi:10.1080/01688639508405142 · Cited by 13

Electrophysiological analysis of cultured fetal mouse dorsal root ganglion neurons transgenic for human superoxide dismutase-1 a gene in the Down syndrome region of chromosome 21

Ault, B., Caviedes, P. A., Hidalgo, J., Epstein, C. J., & Rapoport, S. I. (1989) · Brain Research · doi:10.1016/0006-8993(89)90988-8 · Cited by 13

Down's syndrome

Plioplys, A. V. (1987) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(87)90263-2 · Cited by 13

Molecular and cellular processes disrupted in the early postnatal Down syndrome prefrontal cortex

Risgaard, R. D., Hanthanan Arachchilage, K., Knaack, S. A., Hosseini, M., Chen, R. J., Kumarage, P., Schmidt, D. K., Huang, X., Sheng, J., Wang, C. J., et al. (2026) · Science · doi:10.1126/science.aea1549 · Cited by 12

Neuroelectric Tuning of Cortical Oscillations by Apical Dendrites in Loop Circuits

LaBerge, D., & Kasevich, R. S. (2017) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2017.00037 · Cited by 14

Trapping in and Escape from Branched Structures of Neuronal Dendrites

Jose, R., Santen, L., & Shaebani, M. R. (2018) · Biophysical Journal · doi:10.1016/j.bpj.2018.09.029 · Cited by 13

Dendritic overgrowth and alterations in laminar phenotypes of neocortical neurons in the newborn with semilobar holoprosencephaly

Judáš, M., Rašin, M., Krušlin, B., Kostović, K., Jukić, D., Petanjek, Z., & Kostović, I. (2003) · Brain and Development · doi:10.1016/s0387-7604(02)00149-3 · Cited by 12

Alzheimer’s disease like neuropathology in Down syndrome cortical organoids

Zhao, H., & Haddad, G. G. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.1050432 · Cited by 12

Local translation of the Down syndrome cell adhesion molecule ( DSCAM ) mRNA in the vertebrate central nervous system

Montesinos, M. L. (2017) · Journal of Neurogenetics · doi:10.1080/01677063.2017.1391250 · Cited by 11

ADF/Cofilin, Actin Dynamics, and Disease

Maloney, M. T., Kinley, A. W., Pak, C. W., & Bamburg, J. R. (2008) · Springer eBooks · doi:10.1007/978-0-387-71749-4_6 · Cited by 10

Central Nervous System

Smith, J. F. (1989) · Springer eBooks · doi:10.1007/978-1-4471-3337-7_4 · Cited by 11

Dendritic arborization in the human fetus and infant with the trisomy 18 syndrome

Jay, V., Chan, F.-W., & Becker, L. E. (1990) · Developmental Brain Research · doi:10.1016/0165-3806(90)90153-p · Cited by 10

Chemogenetic manipulation of astrocyte activity at the synapse— a gateway to manage brain disease

Pereira, M. J., Ayana, R., Holt, M. G., & Arckens, L. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1193130 · Cited by 10

Chronic exposure to caffeine during early development increases dendritic spine and branch formation in midbrain optic tectum

Burgess, J. W., & Monachello, M. P. (1983) · Developmental Brain Research · doi:10.1016/0165-3806(83)90090-1 · Cited by 10

Astrocytes regulate neuronal network activity by mediating synapse remodeling

Kim, N., & Chung, W. (2022) · Neuroscience Research · doi:10.1016/j.neures.2022.09.007 · Cited by 31

The role of astrocyte structural plasticity in regulating neural circuit function and behavior

Lawal, O., Ulloa Severino, F. P., & Eroglu, C. (2022) · Glia · doi:10.1002/glia.24191 · Cited by 142

Emerging roles of astrocytes in neural circuit development

Clarke, L. E., & Barres, B. A. (2013) · Nature Reviews Neuroscience · doi:10.1038/nrn3484 · Cited by 975

Astrocyte-Synapse Structural Plasticity in Neurodegenerative and Neuropsychiatric Diseases

Badia‐Soteras, A., Mak, A., Blok, T. M., Boers-Escuder, C., van den Oever, M. C., Min, R., Smit, A. B., & Verheijen, M. H. G. (2025) · Biological Psychiatry · doi:10.1016/j.biopsych.2025.04.011 · Cited by 21

Role of astrocyte–synapse interactions in CNS disorders

Blanco‐Suárez, E., Caldwell, A. L. M., & Allen, N. J. (2016) · The Journal of Physiology · doi:10.1113/jp270988 · Cited by 234