Cytoarchitectonic subdivisions of the dorsolateral frontal cortex of the marmoset monkey (Callithrix jacchus), and their projections to dorsal visual areas

Burman, Kathleen J.; Palmer, Susan M.; Gamberini, Michela; Rosa, Marcello G.P.

doi:10.1002/cne.20837

Cited by 107Visual perception and processing mechanismsMotor Control and AdaptationNeural and Behavioral Psychology Studies

Cytoarchitectonic subdivisions of the dorsolateral frontal cortex of the marmoset monkey (Callithrix jacchus), and their projections to dorsal visual areas

Burman, Kathleen J., Palmer, Susan M., Gamberini, Michela, Rosa, Marcello G.P.·2006·The Journal of Comparative Neurology

DOI 10.1002/cne.20837

Open this paper in CoChat — free account

Abstract

We describe the organization of the dorsolateral frontal areas in marmoset monkeys using a combination of architectural methods (Nissl, cytochrome oxidase, and myelin stains) and injections of fluorescent tracers in extrastriate areas (the second visual area [V2], the dorsomedial and dorsoanterior areas [DM, DA], the middle temporal area and middle temporal crescent [MT, MTc], and the posterior parietal cortex [area 7]). Cytoarchitectural field 8 comprises three subdivisions: 8Av, 8Ad, and 8B. The ventrolateral subdivision, 8Av, forms the principal source of frontal projections to the "dorsal stream," having connections with each of the injected visual areas. The cytoarchitectural characteristics of 8Av suggest that this subdivision corresponds to the marmoset's frontal eye field. The intermediate subdivision of area 8 (8Ad) has efferent projections to area 7, while the dorsomedial subdivision (8B) has few or no connections with extrastriate cortex. Area 46, located rostrolateral to area 8Av, has substantial connections with the medial extrastriate areas (DM, DA, and area 7) and with MT, while the cortex lateral to 8Av (area 12/45) projects primarily to MT and to the MTc. The rostromedial prefrontal (area 9) and frontopolar (area 10) regions have very few extrastriate projections. Finally, cells in dorsal area 6 (6d) have sparse projections to DM, MT, and the MTc, as well as strong projections to DA and to area 7. These results illuminate aspects of the evolutionary development of the primate frontal cortex, and serve as a basis for further research into cognitive functions using a marmoset model.

Integrity signals

Registry

Crossref · 10.1002/cne.20837

Cites

84 of 84 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

The homologous cortical area 9L could be unambiguously identified across species upon histological observation, and stereologic counts of cell densities were confined to its borders.
“Therefore, we were able to unambiguously identify this homologous cortical area across species upon histological observation, and our stereologic counts of cell densities were confined to its borders.”
From Evolution of increased glia–neuron ratios in the human frontal cortex (2006) · cites this paper as [43]

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 · see citing works
The updating of the representation of visual space in parietal cortex by intended eye movements
Duhamel, J.-R., Colby, C. L., & Goldberg, M. E. (1992) · Science · doi:10.1126/science.1553535 · Cited by 1,966 · see citing works
AN ANATOMICAL STUDY OF CONVERGING SENSORY PATHWAYS WITHIN THE CEREBRAL CORTEX OF THE MONKEY
Jones, E. G., & Powell, T. P. S. (1970) · Brain · doi:10.1093/brain/93.4.793 · Cited by 1,717 · see citing works
The connections of the middle temporal visual area (MT) and their relationship to a cortical hierarchy in the macaque monkey
Maunsell, J., & van Essen, D. (1983) · The Journal of Neuroscience · doi:10.1523/jneurosci.03-12-02563.1983 · Cited by 1,602 · see citing works
Dissociation in prefrontal cortex of affective and attentional shifts
Dias, R., Robbins, T. W., & Roberts, A. C. (1996) · Nature · doi:10.1038/380069a0 · Cited by 1,527 · see citing works
The functions of the orbitofrontal cortex
Rolls, E. T. (2004) · Brain and Cognition · doi:10.1016/s0278-2626(03)00277-x · Cited by 1,327 · see citing works
Dual streams of auditory afferents target multiple domains in the primate prefrontal cortex
Romanski, L. M., Tian, B., Fritz, J. B., Mishkin, M., Goldman, P. S., & Rauschecker, J. P. (1999) · Nature Neuroscience · doi:10.1038/16056 · Cited by 1,136 · see citing works
Laminar origins and terminations of cortical connections of the occipital lobe in the rhesus monkey
Rockland, K. S., & Pandya, D. Ν. (1979) · Brain Research · doi:10.1016/0006-8993(79)90485-2 · Cited by 1,076 · see citing works
The prefrontal landscape: implications of functional architecture for understanding human mentation and the central executive
Goldman-Rakic, P. S. (1996) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.1996.0129 · Cited by 1,072 · see citing works
Dorsolateral prefrontal cortex: comparative cytoarchitectonic analysis in the human and the macaque brain and corticocortical connection patterns
Petrides, M., & Pandya, D. N. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00518.x · Cited by 1,068 · see citing works
Two different streams form the dorsal visual system: anatomy and functions
Rizzolatti, G., & Matelli, M. (2003) · Experimental Brain Research · doi:10.1007/s00221-003-1588-0 · Cited by 1,068 · see citing works
Intracortical connectivity of architectonic fields in the somatic sensory, motor and parietal cortex of monkeys
Jones, E. G., Coulter, J. D., & Hendry, S. H. C. (1978) · The Journal of Comparative Neurology · doi:10.1002/cne.901810206 · Cited by 975 · see citing works
Cortical connections of visual area MT in the macaque
Ungerleider, L. G., & Desimone, R. (1986) · The Journal of Comparative Neurology · doi:10.1002/cne.902480204 · Cited by 954 · see citing works
Architecture and intrinsic connections of the prefrontal cortex in the rhesus monkey
Barbas, H., & Pandya, D. Ν. (1989) · The Journal of Comparative Neurology · doi:10.1002/cne.902860306 · Cited by 937 · see citing works
Frontal lobe and cognitive development
Fuster, J. M. (2002) · Journal of Neurocytology · doi:10.1023/a:1024190429920 · Cited by 916 · see citing works
Comparative cytoarchitectonic analysis of the human and the macaque ventrolateral prefrontal cortex and corticocortical connection patterns in the monkey
Petrides, M., & Pandya, D. N. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2001.02090.x · Cited by 882 · see citing works
The Prefrontal Cortex: Response Selection or Maintenance Within Working Memory?
Rowe, J. B., Toni, I., Josephs, O., Frackowiak, R. S. J., & Passingham, R. E. (2000) · Science · doi:10.1126/science.288.5471.1656 · Cited by 856 · see citing works
Posterior parietal cortex in rhesus monkey: I. Parcellation of areas based on distinctive limbic and sensory corticocortical connections
Cavada, C., & Goldman-Rakic, P. (1989) · The Journal of comparative neurology · doi:10.1002/cne.902870402 · Cited by 812 · see citing works
A cytoarchitectural study of the prefrontal area of the macaque monkey
Walker, A. E. (1940) · The Journal of Comparative Neurology · doi:10.1002/cne.900730106 · Cited by 803 · see citing works
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 · see citing works
A neural system for human visual working memory
Ungerleider, L. G., Courtney, S. M., & Haxby, J. V. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.3.883 · Cited by 654 · see citing works
Multiarchitectonic and stereotactic atlas of the human thalamus
Morel, A., Magnin, M., & Jeanmonod, D. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19971103)387:4 · Cited by 642 · see citing works
Self-citation
Cognitive Inflexibility After Prefrontal Serotonin Depletion
Clarke, H. F., Dalley, J. W., Crofts, H. S., Robbins, T. W., & Roberts, A. C. (2004) · Science · doi:10.1126/science.1094987 · Cited by 632 · see citing works
Topography of visual cortex connections with frontal eye field in macaque: convergence and segregation of processing streams
Schall, J. D., Morel, A., King, D., & Bullier, J. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-06-04464.1995 · Cited by 625 · see citing works
Connections of inferior temporal areas TEO and TE with parietal and frontal cortex in macaque monkeys.
Webster, M., Bachevalier, J., & Ungerleider, L. G. (1994) · Cerebral Cortex · doi:10.1093/cercor/4.5.470 · Cited by 599 · see citing works
Frontal eye field as defined by intracortical microstimulation in squirrel monkeys, owl monkeys, and macaque monkeys II. cortical connections
Huerta, M. F., Krubitzer, L. A., & Kaas, J. H. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902650304 · Cited by 594 · see citing works
Dorsolateral prefrontal lesions and oculomotor delayed-response performance: evidence for mnemonic "scotomas"
Funahashi, S., Bruce, C. J., & Goldman-Rakic, P. S. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-04-01479.1993 · Cited by 581 · see citing works
Organization of afferent input to subdivisions of area 8 in the rhesus monkey
Barbas, H., & Mesulam, M. M. (1981) · The Journal of Comparative Neurology · doi:10.1002/cne.902000309 · Cited by 541 · see citing works
The relationship of corpus callosum connections to electrical stimulation maps of motor, supplementary motor, and the frontal eye fields in owl monkeys
Gould, H. J., Cusick, C. G., Pons, T. P., & Kaas, J. H. (1986) · The Journal of Comparative Neurology · doi:10.1002/cne.902470303 · Cited by 520 · see citing works
Anatomic organization of basoventral and mediodorsal visual recipient prefrontal regions in the rhesus monkey
Barbas, H. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902760302 · Cited by 515 · see citing works
Macaque monkey retrosplenial cortex: III. Cortical efferents
Kobayashi, Y., & Amaral, D. G. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21346 · Cited by 487 · see citing works
Topographical organization of cortical afferents to extrastriate visual area PO in the macaque: A dual tracer study
Colby, C. L., Gattass, R., Olson, C. R., & Gross, C. G. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902690307 · Cited by 470 · see citing works
Reciprocal inhibitory visual-vestibular interaction. Visual motion stimulation deactivates the parieto-insular vestibular cortex
Brandt, T. (1998) · Brain · doi:10.1093/brain/121.9.1749 · Cited by 462 · cited 1× · see citing works
“Moreover, in both marmosets and humans the cortex in the DM/DA region re- sponds maximally to wide-field moving patterns, such as the background movement experienced during self-motion (Brandt et al., 1998; Lui et al., 2005).”
Background
Updating of the visual representation in monkey striate and extrastriate cortex during saccades
Nakamura, K., & Colby, C. L. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.052379899 · Cited by 438 · see citing works
The prefrontal cortex: categories, concepts and cognition
Miller, E. K., Freedman, D. J., & Wallis, J. D. (2002) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2002.1099 · Cited by 414 · see citing works
Macaque monkey retrosplenial cortex: II. Cortical afferents
Kobayashi, Y., & Amaral, D. G. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10883 · Cited by 378 · see citing works
Topography of projections to posterior cortical areas from the macaque frontal eye fields
Stanton, G. B., Bruce, C. J., & Goldberg, M. E. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903530210 · Cited by 370 · see citing works
Prefrontal connections of the parabelt auditory cortex in macaque monkeys
Hackett, T. A., Stepniewska, I., & Kaas, J. H. (1999) · Brain Research · doi:10.1016/s0006-8993(98)01182-2 · Cited by 343 · see citing works
Role of the medial parieto-occipital cortex in the control of reaching and grasping movements
Galletti, C., Kutz, D. F., Gamberini, M., Breveglieri, R., & Fattori, P. (2003) · Experimental Brain Research · doi:10.1007/s00221-003-1589-z · Cited by 328 · see citing works
Self-citation
Laminar distribution of neurons in extrastriate areas projecting to visual areas V1 and V4 correlates with the hierarchical rank and indicates the operation of a distance rule
Barone, P., Batardiere, A., Knoblauch, K., & Kennedy, H. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-09-03263.2000 · Cited by 300 · see citing works
Cortical connections of MT in four species of primates: Areal, modular, and retinotopic patterns
Krubitzer, L. A., & Kass, J. H. (1990) · Visual Neuroscience · doi:10.1017/s0952523800000213 · Cited by 287 · see citing works
Cortical afferent input to the principals region of the rhesus monkey
Barbas, H., & Mesulam, M. M. (1985) · Neuroscience · doi:10.1016/0306-4522(85)90064-8 · Cited by 286 · see citing works
Prefrontal granular cortex of the rhesus monkey. II. Interhemispheric cortical afferents
Jacobson, S., & Trojanowski, J. Q. (1977) · Brain Research · doi:10.1016/0006-8993(77)90418-8 · Cited by 235 · see citing works
Brain maps, great and small: lessons from comparative studies of primate visual cortical organization
Rosa, M. G. P., & Tweedale, R. (2005) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2005.1626 · Cited by 230 · see citing works
Self-citation
Efferent cortico-cortical projections of the prefrontal cortex in the rhesus monkey
Pandya, D. Ν., Dye, P., & Butters, N. (1971) · Brain Research · doi:10.1016/0006-8993(71)90632-9 · Cited by 220 · see citing works
Differential activity of prefrontal units during right and left delayed response trials
Niki, H. (1974) · Brain Research · doi:10.1016/0006-8993(74)90324-2 · Cited by 220 · see citing works
Subdivisions and connections of auditory cortex in owl monkeys
Morel, A., & Kaas, J. H. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903180104 · Cited by 214 · see citing works
Inhibitory Control and Affective Processing in the Prefrontal Cortex: Neuropsychological Studies in the Common Marmoset
Roberts, A. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.252 · Cited by 211 · see citing works
A visuo‐somatomotor pathway through superior parietal cortex in the macaque monkey: cortical connections of areas V6 and V6A
Shipp, S. D., Blanton, M., & Zeki, S. (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00327.x · Cited by 207 · see citing works
Functional streams in occipito-frontal connections in the monkey
Bullier, J., Schall, J. D., & Morel, A. (1996) · Behavioural Brain Research · doi:10.1016/0166-4328(95)00182-4 · Cited by 201 · see citing works
Working Memory for Location and Time: Activity in Prefrontal Area 46 Relates to Selection Rather than Maintenance in Memory
Rowe, J. B., & Passingham, R. E. (2001) · NeuroImage · doi:10.1006/nimg.2001.0784 · Cited by 199 · see citing works
Spatial coding of odorant features in the glomerular layer of the rat olfactory bulb
Johnson, B. A., Woo, C. C., & Leon, M. (1998) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19980420)393:4 · Cited by 187 · see citing works
Self-citation
Direct visual pathways for reaching movements in the macaque monkey.
Tanné‐Gariépy, J., Boussaoud, D., Boyer-Zeller, N., & Rouiller, E. M. (1995) · PubMed · Cited by 172 · see citing works
Corticocortical input to the smooth and saccadic eye movement subregions of the frontal eye field in Cebus monkeys
Tian, J., & Lynch, J. C. (1996) · Journal of Neurophysiology · doi:10.1152/jn.1996.76.4.2754 · Cited by 143 · see citing works
Lesions of the Orbitofrontal but not Medial Prefrontal Cortex Disrupt Conditioned Reinforcement in Primates
Pears, A., Parkinson, J. A., Hopewell, L. J., Everitt, B. J., & Roberts, A. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-35-11189.2003 · Cited by 136 · see citing works
Direct visual pathways for reaching movements in the macaque monkey
Tanné‐Gariépy, J., Boussaoud, D., Boyer-Zeller, N., & Rouiller, E. M. (1995) · Neuroreport · doi:10.1097/00001756-199512000-00064 · Cited by 125 · see citing works
Cytoarchitectural characteristic of the frontal eye fields in macaque monkeys
Stanton, G. B., Deng, S. ‐., Goldberg, E. M., & McMullen, N. T. (1989) · The Journal of Comparative Neurology · doi:10.1002/cne.902820308 · Cited by 118 · see citing works
The dorsomedial visual area of owl monkeys: Connections, myeloarchitecture, and homologies in other primates
Krubitzer, L. A., & Kaas, J. H. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903340402 · Cited by 115 · see citing works
Early coding of reaching: frontal and parietal association connections of parieto‐occipital cortex
Caminiti, R., Genovesio, A., Marconi, B., Battaglia‐Mayer, A., Onorati, P., Ferraina, S., Mitsuda, T., Giannetti, S., Squatrito, S., Maioli, M. G., et al. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00801.x · Cited by 109 · see citing works
Distribution of a reeler gene-related antigen in the developing cerebellum: An immunohistochemical study with an allogeneic antibody CR-50 on normal and reeler mice
Miyata, T., Nakajima, K., Aruga, J., Takahashi, S., Ikenaka, K., Mikoshiba, K., & Ogawa, M. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19960819)372:2 · Cited by 108 · see citing works
Self-citation
Cortical afferents of visual area MT in the Cebus monkey: Possible homologies between New and old World monkeys
Rosa, M. G. P., Soares, J. G. M., Fiorani, M., & Gattass, R. (1993) · Visual Neuroscience · doi:10.1017/s0952523800006064 · Cited by 105 · see citing works
Self-citation
Visual areas in the dorsal and medial extrastriate cortices of the marmoset
Rosa, M. G. P., & Schmid, L. M. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903590207 · Cited by 94 · see citing works
Self-citation
Oculomotor Areas of the Primate Frontal Lobes: A Transneuronal Transfer of Rabies Virus and [14C]-2-Deoxyglucose Functional Imaging Study
Moschovakis, A. K., Gregoriou, G. G., Ugolini, G., Doldán, M. J., Graf, W. M., Guldin, W. O., Hadjidimitrakis, K., & Savaki, H. E. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1223-04.2004 · Cited by 92 · see citing works
Properties of Delay-Period Neuronal Activity in the Monkey Dorsolateral Prefrontal Cortex During a Spatial Delayed Matching-to-Sample Task
Sawaguchi, T., & Yamane, I. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.82.5.2070 · Cited by 90 · see citing works
Ipsilateral cortical connections of granular frontal cortex in the strepsirhine primate Galago, with comparative comments on anthropoid primates
Preuss, T. M., & Goldman, P. S. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903100404 · Cited by 90 · see citing works
Projections from the superior temporal sulcus to the agranular frontal cortex in the macaque
Luppino, G., Calzavara, R., Rozzi, S., & Matelli, M. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01734.x · Cited by 89 · see citing works
The ipsilateral corticocortical connections of area 7 with the frontal lobe in the monkey
Neal, J., Pearson, R. C. A., & Powell, T. P. S. (1990) · Brain Research · doi:10.1016/0006-8993(90)90305-u · Cited by 82 · see citing works
Evidence for both reaching and grasping activity in the medial parieto‐occipital cortex of the macaque
Fattori, P., Breveglieri, R., Amoroso, K., & Galletti, C. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03697.x · Cited by 79 · see citing works
Resolving the organization of the New World monkey third visual complex: The dorsal extrastriate cortex of the marmoset (Callithrix jacchus)
Rosa, M. G. P., Palmer, S., Gamberini, M., Tweedale, R., Piñon, M. C., & Bourne, J. A. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20412 · Cited by 71 · see citing works
Self-citation
Quantitative analysis of connectivity in the visual cortex: extracting function from structure
Vezoli, J., Falchier, A., Jouve, B., Knoblauch, K., Young, M., & Kennedy, H. (2004) · The Neuroscientist · doi:10.1177/1073858404268478 · Cited by 65 · see citing works
The dorsomedial visual areas in New World and Old World monkeys: homology and function
Rosa, M. G. P., & Tweedale, R. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2000.01414.x · Cited by 63 · see citing works
Self-citation
The neocortex of hapale
Peden, J. K., & von Bonin, G. (1947) · The Journal of Comparative Neurology · doi:10.1002/cne.900860103 · Cited by 62 · see citing works
Cortical streams of visual information processing in primates.
Gattass, R., Rosa, M. G. P., Ap, S., Piñon, M. C., Júnior, M. F. H., & Neuenschwander, S. (1990) · PubMed · Cited by 55 · see citing works
Self-citation
Differential Anterior Prefrontal Activation during the Recognition Stage of a Spatial Working Memory Task
Leung, H.-C., Gore, J. C., & Goldman-Rakic, P. S. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhi051 · Cited by 41 · see citing works
Eye Movements Induced by Electrical Stimulation of the Frontal Eye Fields of Marmosets and Squirrel Monkeys
Blum, B., Kulikowski, J. J., Carden, D. E., & Harwood, D. (2008) · Brain Behavior and Evolution · doi:10.1159/000121613 · Cited by 39 · see citing works
Computer Tomography in Transient Global Amnesia
Ladurner, G., Skvarc, A., & Sager, W. D. (2008) · European Neurology · doi:10.1159/000115451 · Cited by 34 · see citing works
Phenotype of intraadrenal ganglion neurons during postnatal development in rat
Holgert, H., Dagerlind, �., & H�kfelt, T. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19960805)371:4 · Cited by 28 · see citing works
Corticocortical connections between frontal periarcuate regions and visual areas of the superior temporal sulcus and the adjoining inferior parietal lobule in the macaque monkey
Maioli, M. G., Squatrito, S., Dekel, B. G. S., & Sanseverino, E. R. (1998) · Brain Research · doi:10.1016/s0006-8993(98)00025-0 · Cited by 27 · see citing works
Cortical and Subcortical Afferent Connections of the Squirrel Monkey's (Lateral) Premotor Cortex: Evidence for Visual Cortical Afferents
Markowitsch, H. J., Irle, E., & Emmans, D. (1987) · International Journal of Neuroscience · doi:10.3109/00207458708987143 · Cited by 22 · see citing works
Parcellation of the frontal cortex of the New World monkey Callithrix jacchus by eight neurotransmitter-binding sites
Gebhard, R., Zilles, K., Schleicher, A., Everitt, B. J., Robbins, T. W., & Divac, I. (1995) · Anatomy and Embryology · doi:10.1007/bf00186741 · Cited by 20 · see citing works
Untitled work
(2000) · doi:10.1002/1096-9861(20001204)428:1
Untitled work
Nakagawa (1999) · doi:10.1002/(sici)1096-9861(19990830)411:3
Self-citation
Untitled work
Shammah-Lagnado (2000) · doi:10.1002/1096-9861(20000710)422:4
Self-citation
Untitled work
Matelli (1998) · doi:10.1002/(sici)1096-9861(19981221)402:3

Flagged first, then by citations

Sorted by citations

Evolution of increased glia–neuron ratios in the human frontal cortex
Sherwood, C. C., Stimpson, C. D., Raghanti, M. A., Wildman, D. E., Uddin, M., Grossman, L. I., Goodman, M., Redmond, J. C., Bonar, C. J., Erwin, J. M., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0605843103 · Cited by 342 · see citing works
Directional Signals in the Prefrontal Cortex and in Area MT during a Working Memory for Visual Motion Task
Zaksas, D., & Pasternak, T. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3420-06.2006 · Cited by 247 · see citing works
Evolution of prefrontal cortex
Preuss, T. M., & Wise, S. P. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-021-01076-5 · Cited by 245 · see citing works
Differential regulation of fronto-executive function by the monoamines and acetylcholine
Robbins, T., & Roberts, A. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhm066 · Cited by 279 · see citing works
The marmoset monkey as a model for visual neuroscience
Mitchell, J. F., & Leopold, D. A. (2015) · Neuroscience Research · doi:10.1016/j.neures.2015.01.008 · Cited by 231 · see citing works
The nexus between decision making and emotion regulation: A review of convergent neurocognitive substrates
Mitchell, D. G. V. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.10.030 · Cited by 219 · see citing works
Neural Response Properties of Primary, Rostral, and Rostrotemporal Core Fields in the Auditory Cortex of Marmoset Monkeys
Bendor, D., & Wang, X. (2008) · Journal of Neurophysiology · doi:10.1152/jn.00884.2007 · Cited by 185 · see citing works
Forebrain connectivity of the prefrontal cortex in the marmoset monkey (Callithrix jacchus): An anterograde and retrograde tract‐tracing study
Roberts, A., Tomic, D. L., Parkinson, C. H., Roeling, T. A. P., Cutter, D. J., Robbins, T. W., & Everitt, B. J. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21300 · Cited by 181 · see citing works
Cortical connections of the visuomotor parietooccipital area V6Ad of the macaque monkey
Gamberini, M., Passarelli, L., Fattori, P., Zucchelli, M., Bakola, S., Luppino, G., & Galletti, C. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.21980 · Cited by 177 · see citing works
Self-citation
Left, but not right, rostrolateral prefrontal cortex meets a stringent test of the relational integration hypothesis
Bunge, S. A., Helskog, E. H., & Wendelken, C. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.01.064 · Cited by 178 · see citing works
A simpler primate brain: the visual system of the marmoset monkey
Solomon, S. G., & Rosa, M. G. P. (2014) · Frontiers in Neural Circuits · doi:10.3389/fncir.2014.00096 · Cited by 164 · see citing works
Self-citation
Sensitive Period for a Multimodal Response in Human Visual Motion Area MT/MST
Bedny, M., Konkle, T., Pelphrey, K. A., Saxe, R. R., & Pascual‐Leone, Á. (2010) · Current Biology · doi:10.1016/j.cub.2010.09.044 · Cited by 152 · see citing works
Visualizing the entire cortical myelination pattern in marmosets with magnetic resonance imaging
Bock, N. A., Kocharyan, A., Liu, J. V., & Silva, A. C. (2009) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2009.08.022 · Cited by 142 · see citing works
Functional Specialization of Medial Auditory Belt Cortex in the Alert Rhesus Monkey
Kuśmierek, P., & Rauschecker, J. P. (2009) · Journal of Neurophysiology · doi:10.1152/jn.00167.2009 · Cited by 130 · see citing works
A distinct anatomical network of cortical areas for analysis of motion in far peripheral vision
Palmer, S., & Rosa, M. G. P. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.05113.x · Cited by 123 · see citing works
Self-citation
The effect of arousal on the emotional memory network depends on valence
Steinmetz, K. R. M., Addis, D. R., & Kensinger, E. A. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.06.015 · Cited by 121 · see citing works
Of Men and Mice: Modeling the Fragile X Syndrome
Dahlhaus, R. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00041 · Cited by 118 · see citing works
Towards a comprehensive atlas of cortical connections in a primate brain: Mapping tracer injection studies of the common marmoset into a reference digital template
Majka, P., Chaplin, T. A., Yu, H., Tolpygo, A. S., Mitra, P. P., Wojcik, D. K., & Rosa, M. G. P. (2016) · The Journal of Comparative Neurology · doi:10.1002/cne.24023 · Cited by 113 · see citing works
Self-citation
Cortical Connections of Parietal Field PEc in the Macaque: Linking Vision and Somatic Sensation for the Control of Limb Action
Bakola, S., Gamberini, M., Passarelli, L., Fattori, P., & Galletti, C. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhq007 · Cited by 111 · see citing works
Self-citation
Connections of the Dorsomedial Visual Area: Pathways for Early Integration of Dorsal and Ventral Streams in Extrastriate Cortex
Rosa, M. G. P., Palmer, S., Gamberini, M., Burman, K. J., Yu, H., Reser, D. H., Bourne, J. A., Tweedale, R., & Galletti, C. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.0529-09.2009 · Cited by 110 · see citing works
Self-citation
Divergence of rodent and primate medial frontal cortex functional connectivity
Schaeffer, D. J., Hori, Y., Gilbert, K. M., Gati, J. S., Menon, R. S., & Everling, S. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2003181117 · Cited by 107 · see citing works
An Integrated Microcircuit Model of Attentional Processing in the Neocortex
Ardid, S., Wang, X., & Compte, A. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1145-07.2007 · Cited by 105 · see citing works
Cortical Connections of Area V6Av in the Macaque: A Visual-Input Node to the Eye/Hand Coordination System
Passarelli, L., Rosa, M. G. P., Gamberini, M., Bakola, S., Burman, K. J., Fattori, P., & Galletti, C. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4784-10.2011 · Cited by 96 · see citing works
Self-citation
Frontoparietal Functional Connectivity in the Common Marmoset
Ghahremani, M., Hutchison, R. M., Menon, R. S., & Everling, S. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw198 · Cited by 90 · see citing works
Cortical Input to the Frontal Pole of the Marmoset Monkey
Burman, K. J., Reser, D. H., Yu, H., & Rosa, M. G. P. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhq239 · Cited by 92 · see citing works
Self-citation
The Importance of Serotonin for Orbitofrontal Function
Roberts, A. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.12.037 · Cited by 90 · see citing works
Contrasting Patterns of Cortical Input to Architectural Subdivisions of the Area 8 Complex: A Retrograde Tracing Study in Marmoset Monkeys
Reser, D. H., Burman, K. J., Yu, H., Chaplin, T. A., Richardson, K. E., Worthy, K. H., & Rosa, M. G. P. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs177 · Cited by 88 · see citing works
Self-citation
Contributions of frontopolar cortex to judgments about self, others and relations.
Raposo, A., Vicens, L., Clithero, J. A., Dobbins, I., & Huettel, S. A. (2011) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsq033 · Cited by 100 · see citing works
Macroscale cortical organization and a default-like apex transmodal network in the marmoset monkey
Buckner, R. L., & Margulies, D. S. (2019) · Nature Communications · doi:10.1038/s41467-019-09812-8 · Cited by 84 · see citing works
Quantitative Analysis of the Corticocortical Projections to the Middle Temporal Area in the Marmoset Monkey: Evolutionary and Functional Implications
Palmer, S., & Rosa, M. G. P. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhj078 · Cited by 82 · see citing works
Self-citation
Anatomical and physiological definition of the motor cortex of the marmoset monkey
Burman, K. J., Palmer, S., Gamberini, M., Spitzer, M. W., & Rosa, M. G. P. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21580 · Cited by 81 · see citing works
Self-citation
Architectural subdivisions of medial and orbital frontal cortices in the marmoset monkey (Callithrix jacchus)
Burman, K. J., & Rosa, M. G. P. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.21976 · Cited by 77 · see citing works
Self-citation
Microstimulation and architectonics of frontoparietal cortex in common marmosets (Callithrix jacchus)
Burish, M. J., Stepniewska, I., & Kaas, J. H. (2008) · The Journal of Comparative Neurology · doi:10.1002/cne.21596 · Cited by 74 · see citing works
Reconciling Coherent Oscillation with Modulationof Irregular Spiking Activity in Selective Attention:Gamma-Range Synchronization between Sensoryand Executive Cortical Areas
Ardid, S., Wang, X., Gómez-Cabrero, D., & Compte, A. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.4222-09.2010 · Cited by 70 · see citing works
Functional MRI of visual responses in the awake, behaving marmoset
Hung, C.-C., Yen, C. C., Ciuchta, J. L., Papoti, D., Bock, N. A., Leopold, D. A., & Silva, A. C. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.06.090 · Cited by 65 · see citing works
The organization of frontoparietal cortex in the tree shrew (Tupaia belangeri): II. Connectional evidence for a frontal‐posterior parietal network
Remple, M. S., Reed, J. L., Stepniewska, I., Lyon, D. C., & Kaas, J. H. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21226 · Cited by 57 · see citing works
Neuronal Distribution Across the Cerebral Cortex of the Marmoset Monkey (Callithrix jacchus)
Atapour, N., Majka, P., Wolkowicz, I. H., Malamanova, D., Worthy, K. H., & Rosa, M. G. P. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy263 · Cited by 57 · see citing works
Self-citation
A dimensional approach to modeling symptoms of neuropsychiatric disorders in the marmoset monkey
Oikonomidis, L., Santangelo, A. M., Shiba, Y., Clarke, F. H., Robbins, T. W., & Roberts, A. C. (2017) · Developmental Neurobiology · doi:10.1002/dneu.22446 · Cited by 54 · see citing works
Claustrum projections to prefrontal cortex in the capuchin monkey (Cebus apella)
Reser, D. H., Richardson, K. E., Montibeller, M. O., Zhao, S., Chan, J. M., Soares, J. G. M., Chaplin, T. A., Gattass, R., & Rosa, M. G. P. (2014) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2014.00123 · Cited by 54 · see citing works
Self-citation
Patterns of afferent input to the caudal and rostral areas of the dorsal premotor cortex (6DC and 6DR) in the marmoset monkey
Burman, K. J., Bakola, S., Richardson, K. E., Reser, D. H., & Rosa, M. G. P. (2014) · The Journal of Comparative Neurology · doi:10.1002/cne.23633 · Cited by 53 · see citing works
Self-citation
Patterns of cortical input to the primary motor area in the marmoset monkey
Burman, K. J., Bakola, S., Richardson, K. E., Reser, D. H., & Rosa, M. G. P. (2013) · The Journal of Comparative Neurology · doi:10.1002/cne.23447 · Cited by 53 · see citing works
Self-citation
Inhibitory interneurons of the human prefrontal cortex display conserved evolution of the phenotype and related genes
Sherwood, C. C., Raghanti, M. A., Stimpson, C. D., Spocter, M. A., Uddin, M., Boddy, A. M., Wildman, D. E., Bonar, C. J., Lewandowski, A. H., Phillips, K. A., et al. (2009) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2009.1831 · Cited by 51 · see citing works
Connections of the marmoset rostrotemporal auditory area: express pathways for analysis of affective content in hearing
Reser, D. H., Burman, K. J., Richardson, K. E., Spitzer, M. W., & Rosa, M. G. P. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06846.x · Cited by 49 · see citing works
Self-citation
Vocalization Induced CFos Expression in Marmoset Cortex
Miller, C. T., DiMauro, A., Pistorio, A. L., Hendry, S. H. C., & Wang, X. (2010) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2010.00128 · Cited by 49 · see citing works
The cortical motor system of the marmoset monkey (Callithrix jacchus)
Bakola, S., Burman, K. J., & Rosa, M. G. P. (2014) · Neuroscience Research · doi:10.1016/j.neures.2014.11.003 · Cited by 48 · see citing works
Self-citation
Activation of frontal neocortical areas by vocal production in marmosets
Simões, C. S. (2010) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2010.00123 · Cited by 48 · see citing works
Functional and molecular characterization of a non-human primate model of autism spectrum disorder shows similarity with the human disease
Watanabe, S., Kurotani, T., Oga, T., Noguchi, J., Isoda, R., Nakagami, A., Sakai, K., Nakagaki, K., Sumida, K., Hoshino, K., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-25487-6 · Cited by 44 · see citing works
Subcortical projections to the frontal pole in the marmoset monkey
Burman, K. J., Reser, D. H., Richardson, K. E., Heidi, G., Worthy, K. H., & Rosa, M. G. P. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07744.x · Cited by 44 · see citing works
Self-citation
Cortical and thalamic projections to cytoarchitectural areas 6Va and 8C of the marmoset monkey: Connectionally distinct subdivisions of the lateral premotor cortex
Burman, K. J., Bakola, S., Richardson, K. E., Yu, H., Reser, D. H., & Rosa, M. G. P. (2014) · The Journal of Comparative Neurology · doi:10.1002/cne.23734 · Cited by 41 · see citing works
Self-citation
Anatomical and functional neuroimaging in awake, behaving marmosets
Silva, A. C. (2016) · Developmental Neurobiology · doi:10.1002/dneu.22456 · Cited by 43 · see citing works
Looming and receding visual networks in awake marmosets investigated with fMRI
Cléry, J. C., Schaeffer, D. J., Hori, Y., Gilbert, K. M., Hayrynen, L. K., Gati, J. S., Menon, R. S., & Everling, S. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.116815 · Cited by 42 · see citing works
The marmoset as a model system for studying voluntary motor control
Walker, J. D., MacLean, J. N., & Hatsopoulos, N. G. (2016) · Developmental Neurobiology · doi:10.1002/dneu.22461 · Cited by 41 · see citing works
Task-based fMRI of a free-viewing visuo-saccadic network in the marmoset monkey
Schaeffer, D. J., Gilbert, K. M., Hori, Y., Hayrynen, L. K., Johnston, K., Gati, J. S., Menon, R. S., & Everling, S. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.116147 · Cited by 39 · see citing works
Cortical control of object‐specific grasp relies on adjustments of both activity and effective connectivity: a common marmoset study
Tia, B., Takemi, M., Kosugi, A., Castagnola, E., Ansaldo, A., Nakamura, T., Ricci, D., Ushiba, J., Fadiga, L., & Iriki, A. (2017) · The Journal of Physiology · doi:10.1113/jp274629 · Cited by 37 · see citing works
Neural network of social interaction observation in marmosets
Cléry, J. C., Hori, Y., Schaeffer, D. J., Menon, R. S., & Everling, S. (2021) · eLife · doi:10.7554/elife.65012 · Cited by 37 · see citing works
Development of non‐phosphorylated neurofilament protein expression in neurones of the New World monkey dorsolateral frontal cortex
Burman, K. J., Lui, L. L., Rosa, M. G. P., & Bourne, J. A. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05442.x · Cited by 37 · see citing works
Self-citation
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
Critique of Pure Marmoset
Preuss, T. M. (2019) · Brain Behavior and Evolution · doi:10.1159/000500500 · Cited by 35 · see citing works
Unidirectional monosynaptic connections from auditory areas to the primary visual cortex in the marmoset monkey
Rosa, M., Majka, P., Bai, S., Chan, J. M. H., Huo, B.-X., Jermakow, N., Lin, M.-K., Takahashi, Y. S., Wolkowicz, I. H., Worthy, K. H., et al. (2018) · Brain Structure and Function · doi:10.1007/s00429-018-1764-4 · Cited by 34 · see citing works
Self-citation
Visualizing myeloarchitecture with magnetic resonance imaging in primates
Bock, N. A., Hashim, E., Kocharyan, A., & Silva, A. C. (2011) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2011.06000.x · Cited by 34 · see citing works
Functional rostro-caudal gradient in the human posterior lateral frontal cortex
Amiez, C., & Petrides, M. (2017) · Brain Structure and Function · doi:10.1007/s00429-017-1567-z · Cited by 33 · see citing works
Individual differences in behavioral and cardiovascular reactivity to emotive stimuli and their relationship to cognitive flexibility in a primate model of trait anxiety
Shiba, Y., Santangelo, A. M., Braesicke, K., Agustín‐Pavón, C., Cockcroft, G. J., Haggard, M. P., & Roberts, A. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00137 · Cited by 31 · see citing works
Structure and function of the middle temporal visual area (MT) in the marmoset: Comparisons with the macaque monkey
Lui, L. L., & Rosa, M. G. P. (2014) · Neuroscience Research · doi:10.1016/j.neures.2014.09.012 · Cited by 30 · see citing works
Self-citation
The marmoset as a model for investigating the neural basis of social cognition in health and disease
Samandra, R., Haque, Z. Z., Rosa, M. G. P., & Mansouri, F. A. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104692 · Cited by 23 · see citing works
Self-citation
Delay-related activity in marmoset prefrontal cortex
Wong, R. K., Selvanayagam, J., Johnston, K., & Everling, S. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac289 · Cited by 27 · see citing works
Intrinsic functional clustering of anterior cingulate cortex in the common marmoset
Schaeffer, D. J., Gilbert, K. M., Ghahremani, M., Gati, J. S., Menon, R. S., & Everling, S. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.11.005 · Cited by 24 · see citing works
Cortical Afferents of Area 10 in Cebus Monkeys: Implications for the Evolution of the Frontal Pole
Rosa, M. G. P., Soares, J. G. M., Chaplin, T. A., Majka, P., Bakola, S., Phillips, K. A., Reser, D. H., & Gattass, R. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy044 · Cited by 24 · see citing works
Self-citation
Axonal Projections From the Middle Temporal Area in the Common Marmoset
Abe, H., Tani, T., Mashiko, H., Kitamura, N., Hayami, T., Watanabe, S., Sakai, K., Suzuki, W., Mizukami, H., Watakabe, A., et al. (2018) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2018.00089 · Cited by 24 · see citing works
On the Evolution of the Frontal Eye Field: Comparisons of Monkeys, Apes, and Humans
Schall, J. D., Zinke, W., Cosman, J., Schall, M. S., Paré, M., & Pouget, P. (2016) · Evolution of Nervous Systems · doi:10.1016/b978-0-12-804042-3.00130-5 · Cited by 21 · see citing works
Marmosets: a promising model for probing the neural mechanisms underlying complex visual networks such as the frontal–parietal network
D’Souza, J. F., Price, N. S. C., & Hagan, M. A. (2021) · Brain Structure and Function · doi:10.1007/s00429-021-02367-9 · Cited by 20 · see citing works
Anatomical variability, multi-modal coordinate systems, and precision targeting in the marmoset brain
Ose, T., Autio, J. A., Ohno, M., Frey, S., Uematsu, A., Kawasaki, A., Takeda, C., Hori, Y., Nishigori, K., Nakako, T., et al. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.118965 · Cited by 19 · see citing works
Response Disengagement on a Spatial Self-Ordered Sequencing Task: Effects of Regionally Selective Excitotoxic Lesions and Serotonin Depletion within the Prefrontal Cortex
Walker, S. C., Robbins, T. W., & Roberts, A. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.0312-09.2009 · Cited by 20 · see citing works
Neuroanatomy of the Marmoset
Fukushima, M., Ichinohe, N., & Okano, H. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-811829-0.00003-0 · Cited by 18 · see citing works
Age-related plasticity of the axon initial segment of cortical pyramidal cells in marmoset monkeys
Atapour, N., & Rosa, M. G. P. (2017) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2017.05.013 · Cited by 18 · see citing works
Self-citation
Visual responses in the dorsolateral frontal cortex of marmoset monkeys
Feizpour, A., Majka, P., Chaplin, T. A., Rowley, D. P., Yu, H., Zavitz, E., Price, N. S. C., Rosa, M. G. P., & Hagan, M. A. (2020) · Journal of Neurophysiology · doi:10.1152/jn.00581.2020 · Cited by 16 · see citing works
Self-citation
Chronic Implantation of Whole-cortical Electrocorticographic Array in the Common Marmoset
Komatsu, M., Kaneko, T., Okano, H., & Ichinohe, N. (2019) · Journal of Visualized Experiments · doi:10.3791/58980 · Cited by 16 · see citing works
Ketamine treatment upon memory retrieval reduces fear memory in marmoset monkeys
Philippens, I. H. C. H. M., Draaisma, L. R., Baarends, G., Krugers, H. J., & Vermetten, E. H. G. J. M. (2021) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2021.04.004 · Cited by 16 · see citing works
In vivo localization of cortical areas using a 3D computerized atlas of the marmoset brain
Risser, L., Sadoun, A., Mescam, M., Strelnikov, K., Lebreton, S., Boucher, S., Girard, P., Vayssière, N., Rosa, M. G. P., & Fonta, C. (2019) · Brain Structure and Function · doi:10.1007/s00429-019-01869-x · Cited by 13 · see citing works
Self-citation
Development of stereotaxic recording system for awake marmosets (Callithrix jacchus)
Wakabayashi, M., Koketsu, D., Kondo, H., Sato, S., Ohara, K., Polyakova, Z., Chiken, S., Hatanaka, N., & Nambu, A. (2018) · Neuroscience Research · doi:10.1016/j.neures.2018.01.001 · Cited by 12 · see citing works
Marmosets in Auditory Research
Eliades, S. J., & Tsunada, J. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-811829-0.00025-x · Cited by 12 · see citing works
Developmental dynamics of marmoset prefrontal cortical SST and PV interneuron networks highlight primate-specific features
Fin, N. A. S. H., Yip, A., Scott, J. T., Teo, L., Homman‐Ludiye, J., & Bourne, J. A. (2025) · Development · doi:10.1242/dev.204254 · Cited by 13 · see citing works
Higher dopamine D1 receptor expression in prefrontal parvalbumin neurons underlies higher distractibility in marmosets versus macaques
Joyce, M. K. P., Ivanov, T. G., Krienen, F. M., Mitchell, J. F., Ma, S., Inoue, W., Nandy, A. S., Datta, D., Duque, A., Arellano, J. I., et al. (2025) · Communications Biology · doi:10.1038/s42003-025-08297-0 · Cited by 13 · see citing works
Humans and great apes share increased neocortical neuropeptide Y innervation compared to other haplorhine primates
Raghanti, M. A., Edler, M. K., Meindl, R. S., Sudduth, J., Bohush, T., ERWIN, J. M., Stimpson, C. D., Hof, P. R., & Sherwood, C. C. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00101 · Cited by 10 · see citing works
Cytoarchitecture and myeloarchitecture of the entorhinal cortex of the common marmoset monkey ( Callithrix jacchus )
Morais, P. L. A. D. G., de Lima, R. R. M., Ríos-Flórez, J. A., de Melo, T. F. V., Clascá, F., Cavalcante, J. S., Gúzen, F. P., Cavalcanti, J. R. L. D. P., & do Nascimento, E. S. (2019) · The Journal of Comparative Neurology · doi:10.1002/cne.24814 · Cited by 9 · see citing works
Functional Organization of Frontoparietal Cortex in the Marmoset Investigated with Awake Resting-State fMRI
Hori, Y., Cléry, J. C., Schaeffer, D. J., Menon, R. S., & Everling, S. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab328 · Cited by 9 · see citing works
On the Evolution of the Frontal Eye Field: Comparisons of Monkeys, Apes, and Humans
Schall, J. D., Zinke, W., Cosman, J., Schall, M. S., Paré, M., & Pouget, P. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-820584-6.00036-2 · Cited by 9 · see citing works
Positron emission tomography imaging of the social brain of common marmosets
Yokoyama, C., & Onoe, H. (2015) · Neuroscience Research · doi:10.1016/j.neures.2014.12.006 · Cited by 9 · see citing works
Spectral Power in Marmoset Frontal Motor Cortex during Natural Locomotor Behavior
Tia, B., Takemi, M., Kosugi, A., Castagnola, E., Ricci, D., Ushiba, J., Fadiga, L., & Iriki, A. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa275 · Cited by 8 · see citing works
Afferent Connections of Cytoarchitectural Area 6M and Surrounding Cortex in the Marmoset: Putative Homologues of the Supplementary and Pre-supplementary Motor Areas
Bakola, S., Burman, K. J., Bednarek, S., Chan, J. M., Jermakow, N., Worthy, K. H., Majka, P., & Rosa, M. G. P. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab193 · Cited by 7 · see citing works
Self-citation
Monitoring of nonspatial information within working memory in the common marmoset (Callithrix jacchus)
Zlatkina, V., Frey, S., & Petrides, M. (2024) · Cerebral Cortex · doi:10.1093/cercor/bhae444 · Cited by 5 · see citing works
Dopaminergic and Serotonergic Modulation of Two Distinct Forms of Flexible Cognitive Control: Attentional Set‐Shifting and Reversal Learning
Roberts, A. (2007) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195314274.003.0016 · Cited by 5 · see citing works
Functional specialization and distributed processing across marmoset lateral prefrontal subregions
Wong, R. K., Selvanayagam, J., Johnston, K., & Everling, S. (2024) · Cerebral Cortex · doi:10.1093/cercor/bhae407 · Cited by 4 · see citing works
Cortical inputs to the middle temporal visual area in New World owl monkeys
Cerkevich, C. M., Kaas, J. H., & Collins, C. (2014) · Eye and Brain · doi:10.2147/eb.s69713 · Cited by 4 · see citing works
The Marmoset as a Model for Visual Neuroscience
Mitchell, J. F., & Leopold, D. A. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-811829-0.00022-4 · Cited by 3 · see citing works
Developmental dynamics of the prefrontal cortical SST and PV interneuron networks: Insights from the monkey highlight human-specific featuresPreprint
Fin, N. A. S. H., Yip, A., Teo, L., Homman‐Ludiye, J., & Bourne, J. A. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.07.10.602904 · Cited by 3 · see citing works
Brain Morphology Imaging by 3D Microscopy and Fluorescent Nissl Staining
Lazutkin, A. A., Komissarova, N. V., Toptunov, D., & Анохин, К. В. (2013) · Bulletin of Experimental Biology and Medicine · doi:10.1007/s10517-013-2162-9 · Cited by 2 · see citing works
Report Sensitive Period for a Multimodal Response in Human Visual Motion Area MT/MST
Bedny, M., Konkle, T., Pelphrey, K. A., Saxe, R. R., & Pascual‐Leone, Á. (2010) · Cited by 1 · see citing works
Visualizing Myeloarchitecture In Vivo with Magnetic Resonance Imaging in Common Marmosets (Callithrix jacchus)
Bock, N. A., & Silva, A. C. (2013) · Springer eBooks · doi:10.1007/978-3-642-37824-9_8
Marmoset Monkeys of Rostrotemporal Core Fields in the Auditory Cortex Neural Response Properties of Primary, Rostral, and
Wang, X., Kuśmierek, P., Rauschecker, J. P., Griffiths, T. D., Baumann, S., Joly, O., Rees, A., Petkov, C. I., Sun, L. Y., Thiele, A., et al. (2015)
EXPRESSÃO DE GENES IMEDIATOS INDUZIDOS POR VOCALIZAÇÕES EM SAGÜIS-COMUNS (Callithrix jacchus)
Simões, C. S. (2008) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)

Cytoarchitectonic subdivisions of the dorsolateral prefrontal cortex of the marmoset monkey (Callithrix jacchus), and their projections to dorsal extrastriate visual areas
Burman, K., Palmer, S., Rosa, M. G. P., & GAMBERINI, M. (2006) · Archivio istituzionale della ricerca (Alma Mater Studiorum Università di Bologna)
Self-citation
Contrasting Patterns of Cortical Input to Architectural Subdivisions of the Area 8 Complex: A Retrograde Tracing Study in Marmoset Monkeys
Reser, D. H., Burman, K. J., Yu, H., Chaplin, T. A., Richardson, K. E., Worthy, K. H., & Rosa, M. G. P. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs177 · Cited by 88 · see citing works
Self-citation
Architectural subdivisions of medial and orbital frontal cortices in the marmoset monkey (Callithrix jacchus)
Burman, K. J., & Rosa, M. G. P. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.21976 · Cited by 77 · see citing works
Self-citation
Cortical and thalamic projections to cytoarchitectural areas 6Va and 8C of the marmoset monkey: Connectionally distinct subdivisions of the lateral premotor cortex
Burman, K. J., Bakola, S., Richardson, K. E., Yu, H., Reser, D. H., & Rosa, M. G. P. (2014) · The Journal of Comparative Neurology · doi:10.1002/cne.23734 · Cited by 41 · see citing works
Self-citation
Frontal lobe projections to extrastriate visual areas in the marmoset monkey.
Palmer, S., Gamberini, M., & Rosa, M. G. P. (2004) · Archivio istituzionale della ricerca (Alma Mater Studiorum Università di Bologna)
Self-citation

Authors: Burman, K. J., Palmer, S. M., Gamberini, M., & Rosa, M. G. P.
Affiliations: Monash University (AU)
University of Bologna (IT)
Corresponding author: Burman, Kathleen J.
ORCID: Gamberini, Michela
Rosa, Marcello G.P.
Venue: The Journal of Comparative Neurology
Publisher: Wiley
Published: 2006-03-10
Volume: 495
Issue: 2
Pages: 149-172
ISSN: 0021-9967 (ISSN-L)
1096-9861
DOI: 10.1002/cne.20837
OpenAlex: W2169273107
Semantic Scholar: 2960fbabb232d8125041ad1ad89e8b48dd20e5aa
Cited by: 107
References: 84
Citations by year: 2026: 2 · 2025: 2 · 2024: 4 · 2022: 3 · 2021: 7 · 2020: 5 · 2019: 6 · 2018: 11 · 2017: 5 · 2016: 6 · 2015: 4 · 2014: 10 · 2013: 3 · 2012: 1
FWCI: 3.72
Type: journal article
Language: en
Open access: closed
Licence: doi.wiley.com/10.1002/tdm_license_1.1 (tdm, 3462 d)
Locations: The Journal of Comparative Neurology (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
Life Sciences › Neuroscience › Cognitive Neuroscience › Motor Control and Adaptation
Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
Keywords: dorsolateral prefrontal cortex, marmoset monkey, Callithrix jacchus, cytoarchitecture, frontal eye field, dorsal stream, extrastriate visual areas, area 46, area 7, middle temporal area, primate visual cortex, corticocortical connections
MeSH terms: Amidines, Animals, Brain Mapping, Callithrix, Dextrans, Frontal Lobe, Rhodamines, Staining and Labeling, Visual Cortex, Visual Pathways

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Cytoarchitectonic subdivisions of the dorsolateral frontal cortex of the marmoset monkey (Callithrix jacchus), and their projections to dorsal visual areas

Abstract

Integrity signals

Claims the paper makes

Claims other papers make about this one

Cites

Cited by

Related

Record

About these checks