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

Synaptic density in human frontal cortex —Developmental changes and effects of aging

Peter R., H. (1979) · Brain Research · doi:10.1016/0006-8993(79)90349-4 · Cited by 2,645

Morphometric study of human cerebral cortex development

Huttenlocher, P. R. (1990) · Neuropsychologia · doi:10.1016/0028-3932(90)90031-i · Cited by 1,239

Morphological Changes in Dendritic Spines Associated with Long-Term Synaptic Plasticity

Yuste, R., & Bonhoeffer, T. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.1071 · Cited by 1,269

Abnormal dendritic spines in fragile X knockout mice: Maturation and pruning deficits

Comery, T. A., Harris, J. B., Willems, P. J., Oostra, B. A., Irwin, S. A., Weiler, I. J., & Greenough, W. T. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.10.5401 · Cited by 1,046

Dendritic Spines: Cellular Specializations Imparting Both Stability and Flexibility to Synaptic Function

Harris, K. M., & Kater, S. B. (1994) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.17.030194.002013 · Cited by 1,020

Development of Cortical Circuitry and Cognitive Function

Goldman-Rakic, P. S. (1987) · Child Development · doi:10.2307/1130201 · Cited by 655

Dendritic Spine Pathology: Cause or Consequence of Neurological Disorders?

Fiala, J. C., Spacek, J., & Harris, K. M. (2002) · Brain Research Reviews · doi:10.1016/s0165-0173(02)00158-3 · Cited by 811

Synaptogenesis Via Dendritic Filopodia in Developing Hippocampal Area CA1

Fiala, J. C., Feinberg, M., Popov, V., & Harris, K. M. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-21-08900.1998 · Cited by 758

Apoptosis and increased generation of reactive oxygen species in Down's syndrome neurons in vitro

Busciglio, J., & Yankner, B. A. (1995) · Nature · doi:10.1038/378776a0 · Cited by 741

Dendritic Anomalies in Disorders Associated with Mental Retardation

Kaufmann, W. E. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.10.981 · Cited by 746

Genesis of dendritic spines: insights from ultrastructural and imaging studies

Yuste, R., & Bonhoeffer, T. (2004) · Nature reviews. Neuroscience · doi:10.1038/nrn1300 · Cited by 657

Dendritic Spine Structural Anomalies in Fragile-X Mental Retardation Syndrome

Irwin, S. A. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.10.1038 · Cited by 626

Abnormal Development of Dendritic Spines in FMR1 Knock-Out Mice

Nimchinsky, E. A., Oberlander, A. M., & Svoboda, K. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-14-05139.2001 · Cited by 560

Analysis of neocortex in three males with the Fragile X syndrome

Hinton, V. J., Brown, W. T., Wisniewski, K., & Rudelli, R. D. (1991) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320410306 · Cited by 527

Dendritic Spine "Dysgenesis" and Mental Retardation

Purpura, D. P. (1974) · Science · doi:10.1126/science.186.4169.1126 · Cited by 522

From mRNP trafficking to spine dysmorphogenesis: the roots of fragile X syndrome

Bagni, C., & Greenough, W. T. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1667 · Cited by 475

Development of prefrontal cortex

Kolk, S. M., & Rakic, P. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-021-01137-9 · Cited by 378

The dendritic tree and brain disorders

Kulkarni, V. A., & Firestein, B. L. (2012) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2012.03.005 · Cited by 390

Adult fragile X syndrome: Clinico-neuropathologic findings

Rudelli, R. D., Brown, W. T., Wisniewski, K., Jenkins, E. C., Laure-Kamionowska, M., Connell, F., & Wisniewski, H. M. (1985) · Acta Neuropathologica · doi:10.1007/bf00687814 · Cited by 362

Rho GTPases, dendritic structure, and mental retardation

Newey, S. E., Velamoor, V., Govek, E., & Van Aelst, L. (2005) · Journal of Neurobiology · doi:10.1002/neu.20153 · Cited by 351

Delayed Stabilization of Dendritic Spines in Fragile X Mice

Cruz-Martin, A., Crespo, M., & Portera-Cailliau, C. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0577-10.2010 · Cited by 321

Rho proteins, mental retardation and the cellular basis of cognition

Ramakers, G. J. A. (2002) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)02118-4 · Cited by 374

Pyramidal cell abnormalities in the motor cortex of a child with Down's syndrome. A Golgi study

Marin‐Padilla, M. (1976) · Journal of Comparative Neurology · doi:10.1002/cne.901670105 · Cited by 285

Role for metabotropic glutamate receptor 5 (mGluR5) in the pathogenesis of fragile X syndrome

Dölen, G., & Bear, M. F. (2008) · The Journal of Physiology · doi:10.1113/jphysiol.2008.150722 · Cited by 278

Synaptic structural abnormalities in the Ts65Dn mouse model of down syndrome

Belichenko, P. V., Masliah, E., Kleschevnikov, A. M., Villar, A. J., Epstein, C. J., Salehi, A., & Mobley, W. C. (2004) · Journal of Comparative Neurology · doi:10.1002/cne.20337 · Cited by 297

Abnormal neuronal development in the visual cortex of the human fetus and infant with down's syndrome. A quantitative and qualitative golgi study

Takashima, S., Becker, L. E., Armstrong, D. L., & Chan, F. (1981) · Brain Research · doi:10.1016/0006-8993(81)90314-0 · Cited by 307

Dendritic spine pathologies in hippocampal pyramidal neurons from Rett syndrome brain and after expression of Rett-associated MECP2 mutations

Chapleau, C. A., Calfa, G. D., Lane, M. C., Albertson, A. J., Larimore, J. L., Kudo, S., Armstrong, D. L., Percy, A. K., & Pozzo‐Miller, L. D. (2009) · Neurobiology of Disease · doi:10.1016/j.nbd.2009.05.001 · Cited by 264

The neurobiologie consequences of down syndrome

Coyle, J. T., Oster-Granite, M. L., & Gearhart, J. D. (1986) · Brain Research Bulletin · doi:10.1016/0361-9230(86)90074-2 · Cited by 248

Brain-Derived Neurotrophic Factor Rescues Synaptic Plasticity in a Mouse Model of Fragile X Syndrome

Lauterborn, J. C., Rex, C. S., Kramár, E. A., Chen, L. Y., Pandyarajan, V., LYNCH, G. S., & Gall, C. M. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.2624-07.2007 · Cited by 244

The State of Synapses in Fragile X Syndrome

Pfeiffer, B. E., & Huber, K. M. (2009) · The Neuroscientist · doi:10.1177/1073858409333075 · Cited by 216

Synapse formation is regulated by the signaling adaptor GIT1

Zhang, H., Webb, D. J., Asmussen, H., & Horwitz, A. F. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200211002 · Cited by 216

Cortical area and species differences in dendritic spine morphology

Benavides-Piccione, R., Ballesteros-Yáñez, I., DeFelipe, J., & Yuste, R. (2002) · Journal of Neurocytology · doi:10.1023/a:1024134312173 · Cited by 207

A human neurodevelopmental model for Williams syndrome

Chailangkarn, T., Trujillo, C. A., Freitas, B. C., Hrvoj-Mihic, B., Herai, R. H., Yu, D. X., Brown, T. T., Marchetto, M. C., Bardy, C., McHenry, L., et al. (2016) · Nature · doi:10.1038/nature19067 · Cited by 195

Human Models Are Needed for Studying Human Neurodevelopmental Disorders

Zhao, X., & Bhattacharyya, A. (2018) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2018.10.009 · Cited by 192

Dendritic pathology in mental retardation: from molecular genetics to neurobiology

Dierssen, M., & Ramakers, G. J. A. (2006) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2006.00224.x · Cited by 191

Spine distribution along the apical dendrites of the pyramidal neurons in Down's syndrome: A quantitative golgi study

Suetsugu, M., & Mehraein, P. (1980) · Acta Neuropathologica · doi:10.1007/bf00688755 · Cited by 190

Loss of dendritic spines in aging cerebral cortex

Feldman, M. L., & Dowd, C. (1975) · Anatomy and Embryology · doi:10.1007/bf00319848 · Cited by 188

TrkB Signaling Modulates Spine Density and Morphology Independent of Dendrite Structure in Cultured Neonatal Purkinje Cells

Shimada, A., Mason, C. A., & Morrison, M. E. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-21-08559.1998 · Cited by 165

Normal and Aberrant Neuronal Development in the Cerebral Cortex of Human Fetus and Young Infant

Purpura, D. P. (1975) · Elsevier eBooks · doi:10.1016/b978-0-12-139050-1.50014-8 · Cited by 134

Aneuploidy: From a Physiological Mechanism of Variance to Down Syndrome

Dierssen, M., Hérault, Y., & Estivill, X. (2009) · Physiological Reviews · doi:10.1152/physrev.00032.2007 · Cited by 143

Species-specific maturation profiles of human, chimpanzee and bonobo neural cells

Marchetto, M. C., Hrvoj-Mihic, B., Kerman, B. E., Yu, D. X., Vadodaria, K. C., Linker, S. B., Narvaiza, I., Santos, R., Denli, A. M., Mendes, A. P., et al. (2019) · eLife · doi:10.7554/elife.37527 · Cited by 132

Actin in the nervous system

Fifkov/'a, E. (1985) · Brain Research Reviews · doi:10.1016/0165-0173(85)90012-8 · Cited by 130

Brain plasticity and mental processes: Cajal again

DeFelipe, J. (2006) · Nature reviews. Neuroscience · doi:10.1038/nrn2005 · Cited by 135

Plasticity of the dendritic spine

Horner, C. H. (1993) · Progress in Neurobiology · doi:10.1016/0301-0082(93)90002-a · Cited by 125

On dendrites in Down syndrome and DS murine models: a spiny way to learn

Benavides‐Piccione, R. (2004) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2004.08.001 · Cited by 131

Regulation of local translation at the synapse by BDNF

Santos, A. R., Comprido, D., & Duarte, C. B. (2010) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2010.08.004 · Cited by 122

A Role for Thrombospondin-1 Deficits in Astrocyte-Mediated Spine and Synaptic Pathology in Down's Syndrome

Garcia, O., Torres, M., Helguera, P., Coskun, P., & Busciglio, J. (2010) · PLoS ONE · doi:10.1371/journal.pone.0014200 · Cited by 122

Golgi and Cajal: The neuron doctrine and the 100th anniversary of the 1906 Nobel Prize

Glickstein, M. (2006) · Current Biology · doi:10.1016/j.cub.2006.02.053 · Cited by 117

Spine Stems on Tectal Interneurons in Jewel Fish Are Shortened by Social Stimulation

Coss, R. G., & Globus, A. (1978) · Science · doi:10.1126/science.644322 · Cited by 115

Developing cholinergic basal forebrain neurons are sensitive to thyroid hormone

Gould, E., & Ll, B. (1989) · Journal of Neuroscience · doi:10.1523/jneurosci.09-09-03347.1989 · Cited by 114

Brainstem immaturity in sudden infant death syndrome: A quantitative rapid Golgi study of dendritic spines in 95 infants

Quattrochi, J. J., McBride, P. T., & Yates, A. J. (1985) · Brain Research · doi:10.1016/0006-8993(85)90300-2 · Cited by 113

Dendritic changes in the basal nucleus of meynert and in the diagonal band nucleus in Alzheimer's disease—A quantitative Golgi investigation

Arendt, T., Zveuintshva, H. G., & Lkontovich, T. A. (1986) · Neuroscience · doi:10.1016/0306-4522(86)90141-7 · Cited by 112

Structural organization of the cerebral cortex (motor area) in human chromosomal aberrations. A golgi study. I. D1 (13–15) trisomy, patau syndrome

Marín‐Padilla, M. (1974) · Brain Research · doi:10.1016/0006-8993(74)90054-7 · Cited by 111

Mental retardation in Down syndrome: From gene dosage imbalance to molecular and cellular mechanisms

Rachidi, M., & Lopes, C. (2007) · Neuroscience Research · doi:10.1016/j.neures.2007.08.007 · Cited by 117

Down Syndrome: Advances in Molecular Biology and the Neurosciences

Capone, G. T. (2001) · Journal of Developmental & Behavioral Pediatrics · doi:10.1097/00004703-200102000-00007 · Cited by 110

Impaired synaptic development in a maternal immune activation mouse model of neurodevelopmental disorders

Coiro, P., Padmashri, R., Suresh, A., Spartz, E., Pendyala, G., Chou, S., Jung, Y., Meays, B., Roy, S., Gautam, N., et al. (2015) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2015.07.022 · Cited by 105

down syndrome children often have brain with maturation delay, retardation of growth, and cortical dysgenesis.

Wisniewski, K. E. (2005) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320370755 · Cited by 297

Modulation of dendritic spine development and plasticity by BDNF and vesicular trafficking: fundamental roles in neurodevelopmental disorders associated with mental retardation and autism

Chapleau, C. A., Larimore, J. L., Theibert, A. B., & Pozzo‐Miller, L. D. (2009) · Journal of Neurodevelopmental Disorders · doi:10.1007/s11689-009-9027-6 · Cited by 112

The effect of monocular deprivation on dendritic spines in visual cortex of young and adult albino rats: Evidence for a sensitive period

Rothblat, L. A., & Schwartz, M. L. (1979) · Brain Research · doi:10.1016/0006-8993(79)90203-8 · Cited by 103

Amyloid β peptide adversely affects spine number and motility in hippocampal neurons

Shrestha, B. R., Vitolo, O. V., Joshi, P., Lordkipanidze, T. G., Shelanski, M. L., & Dunaevsky, A. (2006) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2006.07.011 · Cited by 106

Intracellular recording and injection study of corticospinal neurons in the rat somatosensory cortex: Effect of prenatal exposure to ethanol

Miller, M. W., Chiaia, N. L., & Rhoades, R. W. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902970107 · Cited by 102

Neurobiology of Down's syndrome

Scott, B. S., Becker, L. E., & Petit, T. L. (1983) · Progress in Neurobiology · doi:10.1016/0301-0082(83)90002-3 · Cited by 103

Deregulated mTOR-mediated translation in intellectual disability

Troca-Marín, J. A., Alves-Sampaio, A., & Montesinos, M. L. (2012) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2012.01.005 · Cited by 109

Changes in morphology of dendritic spines on honeybee calycal interneurons associated with cumulative nursing and foraging experiences

Coss, R. G., Brandon, J. G., & Globus, A. (1980) · Brain Research · doi:10.1016/0006-8993(80)91007-0 · Cited by 101

Opportunities, barriers, and recommendations in Down syndrome research

Hendrix, J. A., Amon, A., Abbeduto, L., Agiovlasitis, S., Alsaied, T., Anderson, H. A., Bain, L. J., Baumer, N., Bhattacharyya, A., Bogunovic, D., et al. (2021) · Translational Science of Rare Diseases · doi:10.3233/trd-200090 · Cited by 117

Brain morphology in Duchenne muscular dystrophy: A Golgi study

Jagadha, V., & Becker, L. E. (1988) · Pediatric Neurology · doi:10.1016/0887-8994(88)90047-1 · Cited by 99

Understanding mental retardation in Down's syndrome using trisomy 16 mouse models

Galdzicki, Z., & Siarey, R. J. (2003) · Genes Brain & Behavior · doi:10.1034/j.1601-183x.2003.00024.x · Cited by 100

Dendritic spine dysgenesis in Rett syndrome

Xu, X., Miller, E. C., & Pozzo‐Miller, L. D. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00097 · Cited by 98

Fetal alcohol syndrome and mental retardation: spine distribution of pyramidal cells in prenatal alcohol-exposed rat cerebral cortex; a Golgi study

Stoltenburg, G., & Spohr, H. L. (1983) · Developmental Brain Research · doi:10.1016/0165-3806(83)90206-7 · Cited by 96

Spine loss and other dendritic abnormalities in epilepsy

Swann, J. W., Al‐Noori, S., Jiang, M., & Lee, C. L. (2000) · Hippocampus · doi:10.1002/1098-1063(2000)10:5 · Cited by 268

Dendritic Spine Pathology in Infants With Severe Protein-Calorie Malnutrition

Benı́tez-Bribiesca, L., la Rosa-Alvarez, I. D., & Mansilla‐Olivares, A. (1999) · PEDIATRICS · doi:10.1542/peds.104.2.e21 · Cited by 93

Oxidative stress and neural dysfunction in Down Syndrome

Iannello, R. C., Crack, P. J., de Haan, J. B., & Kola, I. (1999) · Springer eBooks · doi:10.1007/978-3-7091-6380-1_17 · Cited by 90

Dendritic and synaptic pathology in mental retardation

Huttenlocher, P. R. (1991) · Pediatric Neurology · doi:10.1016/0887-8994(91)90001-2 · Cited by 88

Impaired activity-dependent neural circuit assembly and refinement in autism spectrum disorder genetic models

Doll, C. A., & Broadie, K. S. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00030 · Cited by 86

Dynamics and pathology of dendritic spines

Halpain, S., Spencer, K., & Graber, S. (2005) · Progress in Brain Research · doi:10.1016/s0079-6123(04)47003-4 · Cited by 88

Neuronal effects of experimentally induced hydrocephalus in newborn rats

McAllister, J. P., Maugans, T., Shah, M. V., & Truex, R. C. (1985) · Journal of neurosurgery · doi:10.3171/jns.1985.63.5.0776 · Cited by 88

NMDA-Mediated Regulation of DSCAM Dendritic Local Translation Is Lost in a Mouse Model of Down's Syndrome

Alves-Sampaio, A., Troca-Marín, J. A., & Montesinos, M. L. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.3457-10.2010 · Cited by 88

On the “selectivity” of the Golgi‐Cox method

Pasternak, J. F., & Woolsey, T. A. (1975) · The Journal of Comparative Neurology · doi:10.1002/cne.901600304 · Cited by 86

Rho proteins, mental retardation and the neurobiological basis of intelligence

van Galen, E., & Ramakers, G. J. A. (2004) · Progress in brain research · doi:10.1016/s0079-6123(04)47022-8 · Cited by 87

Abnormal expression of the G‐protein‐activated inwardly rectifying potassium channel 2 (GIRK2) in hippocampus, frontal cortex, and substantia nigra of Ts65Dn mouse: A model of Down syndrome

Harashima, C., Jacobowitz, D. M., Witta, J., Borke, R. C., Best, T. K., Siarey, R. J., & Galdzicki, Z. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20844 · Cited by 82

Correlates across the structural, functional, and molecular phenotypes of fragile X syndrome

Beckel-Mitchener, A. C., & Greenough, W. T. (2004) · Mental Retardation and Developmental Disabilities Research Reviews · doi:10.1002/mrdd.20009 · Cited by 82

The Methods of Golgi

Scheibel, M. E., & Scheibel, A. B. (1978) · Elsevier eBooks · doi:10.1016/b978-0-12-590350-9.50011-2 · Cited by 82

On the cause of mental retardation in Down syndrome: extrapolation from full and segmental trisomy 16 mouse models

Galdzicki, Z., Siarey, R. J., Pearce, R., Stoll, J., & Rapoport, S. I. (2001) · Brain Research Reviews · doi:10.1016/s0926-6410(00)00074-4 · Cited by 84

Prospects for Improving Brain Function in Individuals with Down Syndrome

Costa, A. C. S., & Scott-McKean, J. J. (2013) · CNS Drugs · doi:10.1007/s40263-013-0089-3 · Cited by 83

Synaptic development in the human fetus: A morphometric analysis of normal and Down's syndrome neocortex

Petit, T. L., LeBoutillier, J. C., Alfano, D. P., & Becker, L. E. (1984) · Experimental Neurology · doi:10.1016/0014-4886(84)90041-4 · Cited by 84

Altered network and rescue of human neurons derived from individuals with early-onset genetic epilepsy

Negraes, P. D., Trujillo, C. A., Yu, N., Wu, W., Yao, H., Liang, N., Lautz, J. D., Kwok, E., McClatchy, D. B., Diedrich, J. K., et al. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01104-2 · Cited by 77

The discovery of dendritic spines by Cajal in 1888 and its relevance in the present neuroscience

García-López, P., García‐Marín, V., & Freire, M. (2007) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2007.06.002 · Cited by 83

Dendritic Cytoskeletal Protein Expression in Mental Retardation: An Immunohistochemical Study of the Neocortex in Rett Syndrome

Kaufmann, W. E. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.10.992 · Cited by 75

Pigmentoarchitectonic pathology of the isocortex in juvenile neuronal ceroid-lipofuscinosis: Axonal enlargements in layer IIIab and cell loss in layer V

Braak, H., & Goebel, H. H. (1979) · Acta Neuropathologica · doi:10.1007/bf00684808 · Cited by 75

The Cellular Pathology of Neuronal Ceroid-Lipofuscinosis

Williams, R. S. (1977) · Archives of Neurology · doi:10.1001/archneur.1977.00500170052010 · Cited by 73

Golgi preparations as a tool in neuropathology with particular reference to investigations of the human telencephalic cortex

Braak, H., & Braak, E. (1985) · Progress in Neurobiology · doi:10.1016/0301-0082(85)90001-2 · Cited by 73

Event-related brain potentials during an extended visual recognition memory task depict delayed development of cerebral inhibitory processes among 6-month-old infants with Down syndrome

Karrer, J. H., Karrer, R., Bloom, D., Chaney, L., & Davis, R. (1998) · International Journal of Psychophysiology · doi:10.1016/s0167-8760(98)00015-4 · Cited by 72

Is mental retardation a defect of synapse structure and function?

Chechlacz, M., & Gleeson, J. G. (2003) · Pediatric Neurology · doi:10.1016/s0887-8994(03)00152-8 · Cited by 75

Astrocytes in Neural Circuits: Key Factors in Synaptic Regulation and Potential Targets for Neurodevelopmental Disorders

Liu, X., Ying, J., Wang, X., Zheng, Q., Zhao, T., Yoon, S., Yu, W., Yang, D., Yang, F., & Hua, F. (2021) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.729273 · Cited by 78

Repint of “Reframing autism as a behavioral syndrome and not a specific mental disorder: Implications of genetic and phenotypic heterogeneity”

Tordjman, S., Cohen, D., Anderson, G. M., Botbol, M., Canitano, R., Coulon, N., & Roubertoux, P. L. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.01.014 · Cited by 71

The cellular pathology of microgyria

Williams, R. S., Ferrante, R. J., & Caviness, V. S. (1976) · Acta Neuropathologica · doi:10.1007/bf00685371 · Cited by 66

Neuroanatomical, molecular genetic, and behavioral correlates of fragile X syndrome

Koukoui, S., & Chaudhuri, A. (2006) · Brain Research Reviews · doi:10.1016/j.brainresrev.2006.06.001 · Cited by 65

Neuronal Proliferation, Migration, Organization, and Myelination

Volpe, J. J. (2008) · Elsevier eBooks · doi:10.1016/b978-1-4160-3995-2.10002-0 · Cited by 66

Structural alterations in neurons of aged canine neocortex: A Golgi study

Mervis, R. F. (1978) · Experimental Neurology · doi:10.1016/0014-4886(78)90065-1 · Cited by 65

Cyfip1 Regulates Presynaptic Activity during Development

Hsiao, K., Harony-Nicolas, H., Buxbaum, J. D., Bozdagi-Gunal, O., & Benson, D. L. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.0511-15.2016 · Cited by 64

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

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