Pyramidal Cells of the Frontal Lobe: All the More Spinous to Think With

Mnemonic coding of visual space in the monkey's dorsolateral prefrontal cortex

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Dendritic organization in the neurons of the visual and motor cortices of the cat.

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Neuron Activity Related to Short-Term Memory

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Dissociation of object and spatial processing domains in primate prefrontal cortex.

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Dual streams of auditory afferents target multiple domains in the primate prefrontal cortex

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The prefrontal landscape: implications of functional architecture for understanding human mentation and the central executive

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Unit activity in prefrontal cortex during delayed-response performance: neuronal correlates of transient memory.

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The pyramidal neuron of the cerebral cortex: Morphological and chemical characteristics of the synaptic inputs

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Prefrontal cortical unit activity and delayed alternation performance in monkeys.

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Integration of diverse information in working memory within the frontal lobe

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Comparison of Intrinsic Connectivity in Different Areas of Macaque Monkey Cerebral Cortex

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Areal Segregation of Face-Processing Neurons in Prefrontal Cortex

Scalaidhe, S. P., Wilson, F. A. W., & Goldman, P. S. (1997) · Science · doi:10.1126/science.278.5340.1135 · Cited by 346 · see citing works

The role of prefrontal cortex in working memory: examining the contents of consciousness

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Morphological variations in the dendritic spines of the neocortex

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Synchronous development of pyramidal neuron dendritic spines and parvalbumin-immunoreactive chandelier neuron axon terminals in layer III of monkey prefrontal cortex

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The occipitoparietal pathway of the macaque monkey: comparison of pyramidal cell morphology in layer III of functionally related cortical visual areas

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Morphological variation of layer III pyramidal neurones in the occipitotemporal pathway of the macaque monkey visual cortex

Elston, G. N. (1998) · Cerebral Cortex · doi:10.1093/cercor/8.3.278 · Cited by 161 · see citing works

Immunocytochemical localization of cannabinoid CB1 receptor and fatty acid amide hydrolase in rat retina

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Plasticity of the dendritic spine

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Ipsilateral cortical connections of granular frontal cortex in the strepsirhine primate Galago, with comparative comments on anthropoid primates

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Comparison of Dendritic Fields of Layer III Pyramidal Neurons in Striate and Extrastriate Visual Areas of the Marmoset: a Lucifer Yellow Intracellular Injection Study

Elston, G. N., Rosa, M. G. P., & Calord, M. B. (1996) · Cerebral Cortex · doi:10.1093/cercor/6.6.807 · Cited by 57 · see citing works

The Prefrontal Landscape: Implications of Functional Architecture for Understanding Human Mentation and the Central Executive

Goldman-Rakic, P. S. (2003) · The MIT Press eBooks · doi:10.7551/mitpress/2834.003.0032 · Cited by 48 · see citing works

Untitled work

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Experimental and theoretical approaches to conscious processing

Dehaene, S., & Changeux, J.-P. (2011) · Neuron · doi:10.1016/j.neuron.2011.03.018 · Cited by 2,573 · see citing works

NEURONAL CIRCUITS OF THE NEOCORTEX

Douglas, R. J., & Martin, K. A. C. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144152 · Cited by 1,886 · see citing works

Structure and function of dendritic spines

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Similar patterns of cortical expansion during human development and evolution

Hill, J., Inder, T., Neil, J., Dierker, D., Harwell, J., & Van Essen, D. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1001229107 · Cited by 811 · see citing works

Working Memory 2.0

Miller, E. K., Lundqvist, M., & Bastos, A. M. (2018) · Neuron · doi:10.1016/j.neuron.2018.09.023 · Cited by 797 · see citing works

Neuromodulation of thought: flexibilities and vulnerabilities in prefrontal cortical network synapses

Arnsten, A. F. T., Wang, M. J., & Paspalas, C. D. (2012) · Neuron · doi:10.1016/j.neuron.2012.08.038 · Cited by 538 · see citing works

Cortex, Cognition and the Cell: New Insights into the Pyramidal Neuron and Prefrontal Function

Elston, G. N. (2003) · Cerebral Cortex · doi:10.1093/cercor/bhg093 · Cited by 440 · see citing works

Neuronal Mechanisms of Cortical Alpha Oscillations in Awake-Behaving Macaques

Bollimunta, A., Chen, Y., Schroeder, C. E., & Ding, M. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.2699-08.2008 · Cited by 434 · see citing works

Regional Dendritic and Spine Variation in Human Cerebral Cortex: a Quantitative Golgi Study

Jacobs, B. (2001) · Cerebral Cortex · doi:10.1093/cercor/11.6.558 · Cited by 423 · see citing works

Transcriptomic and morphophysiological evidence for a specialized human cortical GABAergic cell type

Boldog, E., Bakken, T. E., Hodge, R. D., Novotny, M., Aevermann, B. D., Baka, J., Bordé, S., Close, J. L., Diez-Fuertes, F., Ding, S.-L., et al. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0205-2 · Cited by 291 · see citing works

Geometry and structural plasticity of synaptic connectivity

Stepanyants, A., Hof, P. R., & Chklovskii, D. B. (2002) · Neuron · doi:10.1016/s0896-6273(02)00652-9 · Cited by 312 · see citing works

Quantitative assessment of prefrontal cortex in humans relative to nonhuman primates

Donahue, C. J., Glasser, M. F., Preuss, T. M., Rilling, J. K., & Van Essen, D. C. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1721653115 · Cited by 301 · see citing works

Evidence for reduced experience-dependent dendritic spine plasticity in the aging prefrontal cortex

Bloss, E. B., Janssen, W. G., Ohm, D. T., Yuk, F. J., Wadsworth, S., Saardi, K. M., McEwen, B. S., & Morrison, J. H. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.0839-11.2011 · Cited by 219 · see citing works

Rethinking schizophrenia in the context of normal neurodevelopment

Catts, V. S., Fung, S. J., Long, L. E., Joshi, D., Vercammen, A., Allen, K. M., Fillman, S. G., Rothmond, D. A., Sinclair, D., Tiwari, Y., et al. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00060 · Cited by 206 · see citing works

Linking macroscale graph analytical organization to microscale neuroarchitectonics in the macaque connectome

Scholtens, L. H., Schmidt, R., de Reus, M. A., & van den Heuvel, M. P. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.0752-14.2014 · Cited by 160 · see citing works

Specializations of the granular prefrontal cortex of primates: Implications for cognitive processing

Elston, G. N., Benavides‐Piccione, R., Elston, A., Zietsch, B., Defelipe, J., Manger, P., Casagrande, V., & Kaas, J. H. (2006) · The Anatomical Record Part A: Discoveries in Molecular, Cellular, and Evolutionary Biology · doi:10.1002/ar.a.20278 · Cited by 167 · see citing works

Repetitive transcranial magnetic stimulation of dorsolateral prefrontal cortex increases tolerance to human experimental pain

Graff-Guerrero, A., González-Olvera, J., Fresán, A., Gómez-Martín, D., Carlos Méndez-Núñez, J., & Pellicer, F. (2005) · Cognitive Brain Research · doi:10.1016/j.cogbrainres.2005.05.002 · Cited by 154 · see citing works

Density and morphology of dendritic spines in mouse neocortex.

Ballesteros-Yáñez, I., Benavides-Piccione, R., Elston, G. N., Yuste, R., & DeFelipe, J. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2005.11.038 · Cited by 143 · see citing works

SLC25A12 expression is associated with neurite outgrowth and is upregulated in the prefrontal cortex of autistic subjects

Lepagnol-Bestel, A.-M., Maussion, G., Boda, B., Cardona, A., Iwayama, Y., Delezoide, A.-L., Moalic, J.-M., Muller, D., Dean, B., Yoshikawa, T., et al. (2008) · Molecular Psychiatry · doi:10.1038/sj.mp.4002120 · Cited by 93 · see citing works

Regional Dendritic Variation in Neonatal Human Cortex: A Quantitative Golgi Study

Travis, K., Ford, K., & Jacobs, B. (2005) · Developmental Neuroscience · doi:10.1159/000086707 · Cited by 89 · see citing works

Targeting Prefrontal Cortical Systems for Drug Development: Potential Therapies for Cognitive Disorders

Arnsten, A. F. T., & Wang, M. (2016) · Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev-pharmtox-010715-103617 · Cited by 50 · see citing works

Analysis of synaptic gene expression in the neocortex of primates reveals evolutionary changes in glutamatergic neurotransmission

Muntané, G., Horvath, J. E., Hof, P. R., Ely, J. J., Hopkins, W. D., Raghanti, M. A., Lewandowski, A. H., Wray, G. A., & Sherwood, C. C. (2015) · Cerebral Cortex · doi:10.1093/cercor/bht354 · Cited by 36 · see citing works

Parallel Development of Chromatin Patterns, Neuron Morphology, and Connections: Potential for Disruption in Autism

García-Cabezas, M. Á., Barbas, H., & Zikopoulos, B. (2018) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2018.00070 · Cited by 30 · see citing works

Faculty Opinions recommendation of Representation of time by neurons in the posterior parietal cortex of the macaque.

Angelaki, D. E. (2003) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1013275.191853

Neuronal representation of visual saliency in the macaque posterior parietal cortex

Tanaka, T., Fujimoto, A., & Ogawa, T. (2009) · Neuroscience Research · doi:10.1016/j.neures.2009.09.1037

Author response: Neuronal representation of saccadic error in macaque posterior parietal cortex (PPC)

Zhou, Y., Liu, Y., Lu, H. D., et al. (2016) · doi:10.7554/elife.10912.019

Decision letter: Neuronal representation of saccadic error in macaque posterior parietal cortex (PPC)

(2015) · doi:10.7554/elife.10912.018

2101 Connections between area 24 and the parietal cortex in macaque monkeys

Arikuni, T., Sako, H., & Murata, A. (1993) · Neuroscience Research Supplements · doi:10.1016/s0921-8696(05)81312-x