AN ANATOMICAL STUDY OF CONVERGING SENSORY PATHWAYS WITHIN THE CEREBRAL CORTEX OF THE MONKEY

An Integrative Theory of Prefrontal Cortex Function

Miller, E. K., & Cohen, J. D. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.167 · Cited by 12,803

The organization of the human cerebral cortex estimated by intrinsic functional connectivity

Thomas Yeo, B. T., Krienen, F. M., Sepulcre, J., Sabuncu, M. R., Lashkari, D., Hollinshead, M., Roffman, J. L., Smoller, J. W., Zöllei, L., Polimeni, J. R., et al. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00338.2011 · Cited by 9,182

The organization of the human cerebellum estimated by intrinsic functional connectivity

Buckner, R. L., Krienen, F. M., Castellanos, A., Diaz, J. C., & Yeo, B. T. T. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00339.2011 · Cited by 7,304

Where is the semantic system? A critical review and meta-analysis of 120 functional neuroimaging studies

Binder, J. R., Desai, R. H., Graves, W. W., & Conant, L. L. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp055 · Cited by 4,060

The N1 wave of the human electric and magnetic response to sound: A review and an analysis of the component structure

Näätänen, R., & Picton, T. (1987) · Psychophysiology · doi:10.1111/j.1469-8986.1987.tb00311.x · Cited by 3,321

From sensation to cognition

Mesulam, M. (1998) · Brain · doi:10.1093/brain/121.6.1013 · Cited by 3,072

The somatic marker hypothesis and the possible functions of the prefrontal cortex

Damasio, A. R. (1996) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.1996.0125 · Cited by 2,847

Cortical Hubs Revealed by Intrinsic Functional Connectivity: Mapping, Assessment of Stability, and Relation to Alzheimer's Disease

Buckner, R. L., Sepulcre, J., Talukdar, T., Krienen, F. M., Liu, H., Hedden, T., Andrews-Hanna, J. R., Sperling, R. A., & Johnson, K. A. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.5062-08.2009 · Cited by 2,862

Differential contribution of amygdala and hippocampus to cued and contextual fear conditioning.

Phillips, R. G., & LeDoux, J. E. (1992) · Behavioral Neuroscience · doi:10.1037/0735-7044.106.2.274 · Cited by 3,292

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

Funahashi, S., Bruce, C. J., & Goldman-Rakic, P. S. (1989) · Journal of Neurophysiology · doi:10.1152/jn.1989.61.2.331 · Cited by 2,685

The Organization of Networks within the Orbital and Medial Prefrontal Cortex of Rats, Monkeys and Humans

Ongur, D. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.206 · Cited by 2,627

A cortical network for directed attention and unilateral neglect

Mesulam, M. ‐. (1981) · Annals of Neurology · doi:10.1002/ana.410100402 · Cited by 2,498

The neurobiology of semantic memory

Binder, J. R., & Desai, R. H. (2011) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2011.10.001 · Cited by 2,114

Posterior parietal association cortex of the monkey: command functions for operations within extrapersonal space

Mountcastle, V. B., Lynch, J. C., Georgopoulos, A., Sakata, H., & Acuna, C. (1975) · Journal of Neurophysiology · doi:10.1152/jn.1975.38.4.871 · Cited by 2,061

The prefontral cortex and cognitive control

Miller, E. K. (2000) · Nature Reviews Neuroscience · doi:10.1038/35036228 · Cited by 2,016

Circuitry of Primate Prefrontal Cortex and Regulation of Behavior by Representational Memory

Goldman‐Rakic, P. S. (1987) · Comprehensive Physiology · doi:10.1002/cphy.cp010509 · Cited by 1,960

Intrinsic functional connectivity as a tool for human connectomics: theory, properties, and optimization

Van Dijk, K. R. A., Hedden, T., Venkataraman, A., Evans, K. C., Lazar, S. W., & Buckner, R. L. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00783.2009 · Cited by 1,844

Time-locked multiregional retroactivation: a systems-level proposal for the neural substrates of recall and recognition

Damasio, A. R. (1989) · Cognition · doi:10.1016/0010-0277(89)90005-x · Cited by 1,538

Neuronal loss correlates with but exceeds neurofibrillary tangles in Alzheimer's disease

Gómez‐Isla, T., Hollister, R., West, H., Mui, S., Growdon, J. H., Petersen, R. C., Parisi, J. E., & Hyman, B. T. (1997) · Annals of Neurology · doi:10.1002/ana.410410106 · Cited by 1,489

Other minds in the brain: a functional imaging study of “theory of mind” in story comprehension.

Fletcher, P. (1995) · Cognition · doi:10.1016/0010-0277(95)00692-r · Cited by 1,522

Is neocortex essentially multisensory?

GHAZANFAR, A., & SCHROEDER, C. (2006) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2006.04.008 · Cited by 1,463

Cortical pathways to the mammalian amygdala

McDonald, A. J. (1998) · Progress in Neurobiology · doi:10.1016/s0301-0082(98)00003-3 · Cited by 1,303

Individuals with sociopathic behavior caused by frontal damage fail to respond autonomically to social stimuli

DAMASIO, A. (1990) · Behavioural Brain Research · doi:10.1016/0166-4328(90)90144-4 · Cited by 1,275

Segmentation of subcomponents within the superior longitudinal fascicle in humans: A quantitative, in vivo, DT-MRI study.

Makris, N., Kennedy, D. N., McInerney, S., Sorensen, A. G., Wang, R., Caviness, V. S., & Pandya, D. N. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhh186 · Cited by 1,146

Amygdalo‐cortical projections in the monkey ( Macaca fascicularis )

Amaral, D. G., & Price, J. L. (1984) · Journal of Comparative Neurology · doi:10.1002/cne.902300402 · Cited by 1,162

Fiber Pathways of the Brain

Schmahmann, J. D., & Pandya, D. N. (2006) · doi:10.1093/acprof:oso/9780195104233.001.0001 · Cited by 1,157

The functional logic of cortical connections

Zeki, S., & Shipp, S. (1988) · Nature · doi:10.1038/335311a0 · Cited by 1,067

Auditory-Visual Integration during Multimodal Object Recognition in Humans: A Behavioral and Electrophysiological Study

Giard, M. H., & Peronnet, F. (1999) · Journal of Cognitive Neuroscience · doi:10.1162/089892999563544 · Cited by 1,072

Conceptual Processing during the Conscious Resting State: A Functional MRI Study

Binder, J. R., Frost, J. A., Hammeke, T. A., Bellgowan, P. S. F., Rao, S. M., & Cox, R. W. (1999) · Journal of Cognitive Neuroscience · doi:10.1162/089892999563265 · Cited by 1,066

Crossmodal Processing in the Human Brain: Insights from Functional Neuroimaging Studies

Calvert, G. A. (2001) · Cerebral Cortex · doi:10.1093/cercor/11.12.1110 · Cited by 1,012

Anatomical correlates of the distribution of the pathological changes in the neocortex in Alzheimer disease.

Pearson, R. C., Esiri, M. M., Hiorns, R. W., Wilcock, G. K., & Powell, T. P. (1985) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.82.13.4531 · Cited by 987

Evidence from functional magnetic resonance imaging of crossmodal binding in the human heteromodal cortex

Calvert, G. A., Campbell, R., & Brammer, M. J. (2000) · Current Biology · doi:10.1016/s0960-9822(00)00513-3 · Cited by 954

The evolution of distributed association networks in the human brain

Buckner, R. L., & Krienen, F. M. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.09.017 · Cited by 836

The default mode network in cognition: a topographical perspective

Smallwood, J., Bernhardt, B. C., Leech, R., Bzdok, D., Jefferies, E., & Margulies, D. S. (2021) · Nature Reviews Neuroscience · doi:10.1038/s41583-021-00474-4 · Cited by 935

Frontal lobe and cognitive development

Fuster, J. M. (2002) · Journal of Neurocytology · doi:10.1023/a:1024190429920 · Cited by 916

Anatomical evidence of multimodal integration in primate striate cortex

Falchier, A., Clavagnier, S., Barone, P., & Kennedy, H. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-13-05749.2002 · Cited by 892

Organization and functions of cells responsive to faces in the temporal cortex

Perrett, D. I., Hietanen, J. K., Oram, M. W., & Benson, P. J. (1992) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.1992.0003 · Cited by 882

Cingulate cortex of the rhesus monkey: II. Cortical afferents

Vogt, B. A., & Pandya, D. N. (1987) · Journal of Comparative Neurology · doi:10.1002/cne.902620208 · Cited by 854

The orbitofrontal cortex: Neuronal activity in the behaving monkey

Thorpe, S. J., Rolls, E. T., & Maddison, S. (1983) · Experimental Brain Research · doi:10.1007/bf00235545 · Cited by 836

Connectivity-based parcellation of human cingulate cortex and its relation to functional specialization

Beckmann, M., Johansen-Berg, H., & Rushworth, M. F. S. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.3328-08.2009 · Cited by 789

Ventral intraparietal area of the macaque: congruent visual and somatic response properties

Duhamel, J.-R., Colby, C. L., & Goldberg, M. E. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.79.1.126 · Cited by 789

Projections from the amygdaloid complex to the cerebral cortex and thalamus in the rat and cat

Krettek, J. E., & Price, J. L. (1977) · Journal of Comparative Neurology · doi:10.1002/cne.901720408 · Cited by 785

The cerebrocerebellar system

Schmahmann, J. D., & Pandya, D. N. (1997) · International Review of Neurobiology · doi:10.1016/s0074-7742(08)60346-3 · Cited by 774

Voluntary finger movement in man: Cerebral potentials and theory

Deecke, L., Gr�zinger, B., & Kornhuber, H. H. (1976) · Biological Cybernetics · doi:10.1007/bf00336013 · Cited by 757

A description of the amygdaloid complex in the rat and cat with observations on intra‐amygdaloid axonal connections

Krettek, J. E., & Price, J. L. (1978) · Journal of Comparative Neurology · doi:10.1002/cne.901780205 · Cited by 727

Cortical folding patterns and predicting cytoarchitecture

Fischl, B., Rajendran, N., Busa, E., Augustinack, J., Hinds, O., Yeo, B. T. T., Mohlberg, H., Amunts, K., & Zilles, K. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm225 · Cited by 737

Volumetric MRI analysis comparing subjects having attention-deficit hyperactivity disorder with normal controls

Filipek, P. A., Semrud-Clikeman, M., Steingard, R. J., Renshaw, P. F., Kennedy, D. N., & Biederman, J. (1997) · Neurology · doi:10.1212/wnl.48.3.589 · Cited by 732

Architecture and frontal cortical connections of the premotor cortex (area 6) in the rhesus monkey

Barbas, H., & Pandya, D. N. (1987) · Journal of Comparative Neurology · doi:10.1002/cne.902560203 · Cited by 690

Dopamine, schizophrenia, mania, and depression: Toward a unified hypothesis of cortico-striatopallido-thalamic function

Swerdlow, N. R., & Koob, G. F. (1987) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00047488 · Cited by 674

Sensory and premotor connections of the orbital and medial prefrontal cortex of macaque monkeys

Carmichael, S. T., & Price, J. L. (1995) · Journal of Comparative Neurology · doi:10.1002/cne.903630409 · Cited by 678

Connections underlying the synthesis of cognition, memory, and emotion in primate prefrontal cortices

Barbas, H. (2000) · Brain Research Bulletin · doi:10.1016/s0361-9230(99)00245-2 · Cited by 664

Pathways for motion analysis: Cortical connections of the medial superior temporal and fundus of the superior temporal visual areas in the macaque

Boussaoud, D., Ungerleider, L. G., & Desimone, R. (1990) · Journal of Comparative Neurology · doi:10.1002/cne.902960311 · Cited by 634

Visuospatial properties of ventral premotor cortex

Graziano, M. S. A., Hu, X. T., & Gross, C. G. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.77.5.2268 · Cited by 603

Cortical and subcortical afferents to the amygdala of the rhesus monkey (Macaca mulatta)

Aggleton, J. P., Burton, M. J., & Passingham, R. E. (1980) · Brain Research · doi:10.1016/0006-8993(80)90279-6 · Cited by 610

The neuropsychology of 3-D space.

Previc, F. H. (1998) · Psychological Bulletin · doi:10.1037/0033-2909.124.2.123 · Cited by 604

Laminar and regional distributions of neurofibrillary tangles and neuritic plaques in Alzheimer’s disease: a quantitative study of visual and auditory cortices

Lewis, D., Campbell, M., Terry, R., & Morrison, J. (1987) · The Journal of Neuroscience · doi:10.1523/jneurosci.07-06-01799.1987 · Cited by 578

Cortex and memory: emergence of a new paradigm

Fuster, J. M. (2009) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21280 · Cited by 559

Separate neural subsystems within ‘Wernicke's area’

Wise, R. J. S., Scott, S. K., Blank, S. C., Mummery, C. J., Murphy, K., & Warburton, E. A. (2001) · Brain · doi:10.1093/brain/124.1.83 · Cited by 572

Insula of the old world monkey. II: Afferent cortical input and comments on the claustrum

Mufson, E. J., & Mesulam, M. ‐. (1982) · Journal of Comparative Neurology · doi:10.1002/cne.902120103 · Cited by 559

Face-Selective Cells in the Temporal Cortex of Monkeys

Desimone, R. (1991) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1991.3.1.1 · Cited by 565

Dissociable Forms of Inhibitory Control within Prefrontal Cortex with an Analog of the Wisconsin Card Sort Test: Restriction to Novel Situations and Independence from “On-Line” Processing

Dias, R., Robbins, T. W., & Roberts, A. C. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-23-09285.1997 · Cited by 555

Cytoarchitecture and neural afferents of orbitofrontal cortex in the brain of the monkey

Morecraft, R. J., Geula, C., & Mesulam, M. ‐. (1992) · Journal of Comparative Neurology · doi:10.1002/cne.903230304 · Cited by 539

Network memory

Fuster, J. M. (1997) · Trends in Neurosciences · doi:10.1016/s0166-2236(97)01128-4 · Cited by 516

Patterns of cytochrome oxidase activity in the frontal agranular cortex of the macaque monkey

Matelli, M., Luppino, G., & Rizzolatti, G. (1985) · Behavioural Brain Research · doi:10.1016/0166-4328(85)90068-3 · Cited by 519

Afferent properties of periarcuate neurons in macaque monkeys. I. Somatosensory responses

Rizzolatti, G., Scandolara, C., Matelli, M., & Gentilucci, M. (1981) · Behavioural Brain Research · doi:10.1016/0166-4328(81)90052-8 · Cited by 501

Detection of Audio-Visual Integration Sites in Humans by Application of Electrophysiological Criteria to the BOLD Effect

Calvert, G. A., Hansen, P. C., Iversen, S. D., & Brammer, M. J. (2001) · NeuroImage · doi:10.1006/nimg.2001.0812 · Cited by 464

Contrasting Cortical and Subcortical Activations Produced by Attentional-Set Shifting and Reversal Learning in Humans

Rogers, R. D., Andrews, T. C., Grasby, P. M., Brooks, D. J., & Robbins, T. W. (2000) · Journal of Cognitive Neuroscience · doi:10.1162/089892900561931 · Cited by 458

The Contribution of α2-Noradrenergic Mechanisms to Prefrontal Cortical Cognitive Function: Potential Significance for Attention-Deficit Hyperactivity Disorder

Arnsten, A. F. T. (1996) · Archives of General Psychiatry · doi:10.1001/archpsyc.1996.01830050084013 · Cited by 458

Revisiting the role of the prefrontal cortex in the pathophysiology of attention-deficit/hyperactivity disorder.

Halperin, J. M., & Schulz, K. P. (2006) · Psychological Bulletin · doi:10.1037/0033-2909.132.4.560 · Cited by 446

Cortical thinning of the attention and executive function networks in adults with attention-deficit/hyperactivity disorder

Makris, N., Biederman, J., Valera, E. M., Bush, G., Kaiser, J., Kennedy, D. N., Caviness, V. S., Faraone, S. V., & Seidman, L. J. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhl047 · Cited by 450

Understanding brain networks and brain organization

Pessoa, L. (2014) · Physics of Life Reviews · doi:10.1016/j.plrev.2014.03.005 · Cited by 464

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

Midbrain, diencephalic and cortical relationships of the basal nucleus of meynert and associated structures in primates

Jones, E. G., Burton, H., Saper, C. B., & Swanson, L. W. (1976) · Journal of Comparative Neurology · doi:10.1002/cne.901670402 · Cited by 420

The afferent input to the magnocellular division of the mediodorsal thalamic nucleus in the monkey, Macaca fascicularis

Russchen, F. T., Amaral, D. G., & Price, J. L. (1987) · Journal of Comparative Neurology · doi:10.1002/cne.902560202 · Cited by 416

A bimodal map of space: somatosensory receptive fields in the macaque putamen with corresponding visual receptive fields

Graziano, M. A., & Gross, C. (1993) · Experimental Brain Research · doi:10.1007/bf00228820 · Cited by 408

Anatomic organization of basoventral and mediodorsal visual recipient prefrontal regions in the rhesus monkey

Barbas, H. (1988) · Journal of Comparative Neurology · doi:10.1002/cne.902760302 · Cited by 385

Upper processing stages of the perception–action cycle

Fuster, J. M. (2004) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2004.02.004 · Cited by 380

Quantitative analysis of a vulnerable subset of pyramidal neurons in Alzheimer's disease: I. Superior frontal and inferior temporal cortex

Hof, P. R., Morrison, J. H., & Cox, K. (1990) · Journal of Comparative Neurology · doi:10.1002/cne.903010105 · Cited by 365

Anatomical investigation of projections to the basis pontis from posterior parietal association cortices in rhesus monkey

Schmahmann, J. D., & Pandya, D. N. (1989) · Journal of Comparative Neurology · doi:10.1002/cne.902890105 · Cited by 371

The limbic lobe and its output channels: implications for emotional functions and adaptive behavior

Heimer, L., & Van Hoesen, G. W. (2006) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2005.06.006 · Cited by 366

Anatomy of the Prefrontal Cortex

Fuster, J. M. (2008) · The Prefrontal Cortex · doi:10.1016/b978-0-12-373644-4.00002-5 · Cited by 364

Stepwise Connectivity of the Modal Cortex Reveals the Multimodal Organization of the Human Brain

Sepulcre, J., Sabuncu, M. R., Yeo, T. B., Liu, H., & Johnson, K. A. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0759-12.2012 · Cited by 323

Projections to the basis pontis from the superior temporal sulcus and superior temporal region in the rhesus monkey

Schmahmann, J. D., & Pandya, D. N. (1991) · Journal of Comparative Neurology · doi:10.1002/cne.903080209 · Cited by 336

A Synergistic Core for Human Brain Evolution and Cognition

Luppi, A. I., Mediano, P. A. M., Rosas, F. E., Holland, N., Fryer, T. D., O’Brien, J. T., Rowe, J. B., Menon, D. K., Bor, D., & Stamatakis, E. A. (2022) · Nature Neuroscience · doi:10.1038/s41593-022-01070-0 · Cited by 314

Complementary circuits connecting the orbital and medial prefrontal networks with the temporal, insular, and opercular cortex in the macaque monkey

Saleem, K. S., Kondo, H., & Price, J. L. (2008) · Journal of Comparative Neurology · doi:10.1002/cne.21577 · Cited by 315

Spatial maps for the control of movement.

Graziano, M. S., & Gross, C. G. (1998) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(98)80140-2 · Cited by 323

Learning of Sequential Finger Movements in Man: A Combined Kinematic and Positron Emission Tomography (PET) Study

Seitz, R. J., & Roland, P. E. (1992) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1992.tb00862.x · Cited by 321

Sensory-Motor Interaction in the Primate Auditory Cortex During Self-Initiated Vocalizations

Eliades, S. J., & Wang, X. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00627.2002 · Cited by 315

The latency of activation of neurones in the lateral hypothalamus and substantia innominata during feeding in the monkey

Rolls, E. T., Sanghera, M. K., & Roper-Hall, A. (1979) · Brain Research · doi:10.1016/0006-8993(79)90010-6 · Cited by 312

Intrinsic circuit organization of the major layers and sublayers of the dorsolateral prefrontal cortex in the rhesus monkey

Kritzer, M. F., & Goldman‐Rakic, P. S. (1995) · Journal of Comparative Neurology · doi:10.1002/cne.903590109 · Cited by 300

Regional distribution of functions in parietal association area 7 of the monkey

Hyva¨rinen, J. (1981) · Brain Research · doi:10.1016/0006-8993(81)90533-3 · Cited by 292

Parietal inputs to dorsal versus ventral premotor areas in the macaque monkey: Evidence for largely segregated visuomotor pathways

Tanné-Gariépy, J., Rouiller, E. M., & Boussaoud, D. (2002) · Experimental Brain Research · doi:10.1007/s00221-002-1078-9 · Cited by 289

On areas of transition between entorhinal allocortex and temporal isocortex in the human brain. Normal morphology and lamina-specific pathology in Alzheimer's disease

Braak, H., & Braak, E. (1985) · Acta Neuropathologica · doi:10.1007/bf00690836 · Cited by 287

Dimensions of a projection column and architecture of VPM and POm axons in rat vibrissal cortex

Wimmer, V. C., Bruno, R. M., de Kock, C. P. J., Kuner, T., & Sakmann, B. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhq068 · Cited by 263

Redefining the role of limbic areas in cortical processing

Chanes, L., & Barrett, L. F. (2016) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.11.005 · Cited by 259

Cognitive planning in humans: Neuropsychological, neuroanatomical and neuropharmacological perspectives

Owen, A. M. (1997) · Progress in Neurobiology · doi:10.1016/s0301-0082(97)00042-7 · Cited by 251

fMRI reveals language-specific predictive coding during naturalistic sentence comprehension

Shain, C., Blank, I. A., van Schijndel, M., Schuler, W., & Fedorenko, E. (2020) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2019.107307 · Cited by 215

Differential connections of the perirhinal and parahippocampal cortex with the orbital and medial prefrontal networks in macaque monkeys

Kondo, H., Saleem, K. S., & Price, J. L. (2005) · Journal of Comparative Neurology · doi:10.1002/cne.20796 · Cited by 236

Single cell activity in ventral prefrontal cortex of behaving monkeys

Rosenkilde, C. E., Bauer, R. H., & Fuster, J. M. (1981) · Brain Research · doi:10.1016/0006-8993(81)90160-8 · Cited by 233

Frontal granular cortex input to the cingulate (M3), supplementary (M2) and primary (M1) motor cortices in the rhesus monkey

Morecraft, R. J., & van Hoesen, G. W. (1993) · Journal of Comparative Neurology · doi:10.1002/cne.903370411 · Cited by 203