Cited by 319Visual perception and processing mechanismsMotor Control and AdaptationSpatial Neglect and Hemispheric Dysfunction

The DOI matches its Crossref record; 75 of the 76 references it cites were found in a registry or an index.

Connections of the medial posterior parietal cortex (area 7m) in the monkey

Open access

Leichnetz, George R.·2001·The Anatomical Record

DOI 10.1002/ar.1082

Open this paper in CoChat — free account Open PDF

Abstract

The afferent and efferent cortical and subcortical connections of the medial posterior parietal cortex (area 7m) were studied in cebus (Cebus apella) and macaque (Macaca fascicularis) monkeys using the retrograde and anterograde capabilities of the horseradish peroxidase (HRP) technique. The principal intraparietal corticocortical connections of area 7m in both cebus and macaque cases were with the ipsilateral medial bank of the intraparietal sulcus (MIP) and adjacent superior parietal lobule (area 5), inferior parietal lobule (area 7a), lateral bank of the IPS (area 7ip), caudal parietal operculum (PGop), dorsal bank of the caudal superior temporal sulcus (visual area MST), and medial prestriate cortex (including visual area PO and caudalmedial lobule). Its principal frontal corticocortical connections were with the prefrontal cortex in the shoulder above the principal sulcus and the cortex in the shoulder above the superior ramus of the arcuate sulcus (SAS), the area purported to contain the smooth eye movement‐related frontal eye field (FEFsem) in the cebus monkey by other investigators. There were moderate connections with the cortex in the rostral bank of the arcuate sulcus (purported to contain the saccade‐related frontal eye field; FEFsac), supplementary eye field (SEF), and rostral dorsal premotor area (PMDr). Area 7m also had major connections with the cingulate cortex (area 23), particularly the ventral bank of the cingulate sulcus. The principal subcortical connections of area 7m were with the dorsal portion of the ventrolateral thalamic (VLc) nucleus, lateral posterior thalamic nucleus, lateral pulvinar, caudal mediodorsal thalamic nucleus and medial pulvinar, central lateral, central superior lateral, and central inferior intralaminar thalamic nuclei, dorsolateral caudate nucleus and putamen, middle region of the claustrum, nucleus of the diagonal band, zona incerta, pregeniculate nucleus, anterior and posterior pretectal nuclei, intermediate layer of the superior colliculus, nucleus of Darkschewitsch and dorsomedial parvicellular red nucleus (macaque cases only), dorsal, dorsolateral and lateral basilar pontine nuclei, nucleus reticularis tegmenti pontis, locus ceruleus, and superior central nucleus. The findings are discussed in terms of the possibility that area 7m contains a “medial parietal eye field” and belongs to a neural network of oculomotor‐related structures that plays a role in the control of eye movement. Anat Rec 263:215–236, 2001. © 2001 Wiley‐Liss, Inc.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Integrity signals

Registry

Crossref · 10.1002/ar.1082

Cites

75 of 75 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Untitled work
(1909) · Cited by 2,575
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 · cited 2×
“Q (Legend on page 228.) heavy connections with LIP where saccadic units have been recorded (Andersen et al., 1990; Lynch et al., 1977; Mountcastle et al., 1975) and that projects to the superior colliculus (Lynch et al., 1985).”
Background
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
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
Primate frontal eye fields. I. Single neurons discharging before saccades
Bruce, C. J., & Goldberg, M. E. (1985) · Journal of Neurophysiology · doi:10.1152/jn.1985.53.3.603 · Cited by 1,415
Posterior parietal cortex in rhesus monkey: II. Evidence for segregated corticocortical networks linking sensory and limbic areas with the frontal lobe
Cavada, C., & Goldman, P. S. (1989) · The Journal of Comparative Neurology · doi:10.1002/cne.902870403 · Cited by 1,140
PREMOTOR AND PARIETAL CORTEX: Corticocortical Connectivity and Combinatorial Computations
Wise, S. P., Boussaoud, D., Johnson, P. B., & Caminiti, R. (1997) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.20.1.25 · Cited by 952
Parietal lobe mechanisms for directed visual attention
Lynch, J. C., Mountcastle, V. B., Talbot, W. H., & Yin, T. C. T. (1977) · Journal of Neurophysiology · doi:10.1152/jn.1977.40.2.362 · Cited by 926
Common cortical and subcortical targets of the dorsolateral prefrontal and posterior parietal cortices in the rhesus monkey: evidence for a distributed neural network subserving spatially guided behavior
Selemon, L. D., & Goldman-Rakic, P. S. (1988) · Journal of Neuroscience · doi:10.1523/jneurosci.08-11-04049.1988 · Cited by 908
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

Show all 76 references

Research works printed but not linked: 6

Donohoe DK, 1996, Chemical composition of the primate zona incerta, Soc Neurosci Abstr, 263, 664
May PJ, 1993, Role of the cerebellum and basal ganglia in voluntary movement, 221
Mesulam M‐M, 1978, Neuroanatomical Techniques, Short Course, 65
Rezak M, 1977, A redefinition of pulvinar subdivisions in the macaque monkey: evidence for three distinct subregions within classically defined lateral pulvinar, Soc Neurosci Abstr, 3, 574
Thier P, 1993, Electrophysiological evidence for a second medial “parietal eye field.”, Soc Neurosci Abstr, 19, 27
Vogt C, 1919, Ergebnisse unserer Hirnforschung. Vierte mitteilung: die physiologische bedeutung der architektonischen rindenreizungen, J Psychol Neurol, 25, 279

Sorted by citations

Items 201–300 of 319

Gaze and smooth pursuit signals interact in parietal area 7m of the behaving monkey
Raffi, M., Squatrito, S., & Maioli, M. G. (2007) · Experimental Brain Research · doi:10.1007/s00221-007-0967-3 · Cited by 15
Changes in Cortical Thickness Are Associated With Cognitive Ability in Postoperative School-Aged Children With Tetralogy of Fallot
Ma, S., Li, Y., Liu, Y., Xu, C., Li, H., Yao, Q., Wang, Y., Yang, Z., Zuo, P., Yang, M., et al. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.00691 · Cited by 14
A direct test of competitive versus cooperative episodic–procedural network dynamics in human memory
Freedberg, M., Reeves, J. A., Fioriti, C. M., Murillo, J., Voss, J. L., & Wassermann, E. M. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhab512 · Cited by 13
Possible rodent equivalent of the posterior cingulate cortex (area 23) interconnects with multimodal cortical and subcortical regions
Xiang, X.-J., Chen, S., Zhang, X., Chen, C., Zhang, S., Cai, H.-R., & Ding, S. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1194299 · Cited by 14
Chapter 3.7 The role of the precuneus in episodic memory
Trimble, M., & Cavanna, A. E. (2008) · Handbook of behavioral neuroscience · doi:10.1016/s1569-7339(08)00220-8 · Cited by 14
The neural mechanism of pure and pseudo-insight problem solving
Wu, C., Tsai, M.-N., & Chen, H. (2019) · Thinking & Reasoning · doi:10.1080/13546783.2019.1663763 · Cited by 14
Thalamic afferents emphasize the different functions of macaque precuneate areas
Gamberini, M., Passarelli, L., Impieri, D., Worthy, K. H., Burman, K. J., Fattori, P., Galletti, C., Rosa, M. G. P., & Bakola, S. (2020) · Brain Structure and Function · doi:10.1007/s00429-020-02045-2 · Cited by 14
Principles of Organization
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0005 · Cited by 14
Metabolic Imaging of Deep Brain Stimulation in Meige Syndrome
Liu, J., Li, L., Li, Y., Wang, Q., Liu, R., & Ding, H. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.848100 · Cited by 13
Distinct connectivity patterns in human medial parietal cortices: Evidence from standardized connectivity map using cortico-cortical evoked potential
Togo, M., Matsumoto, R., Usami, K., Kobayashi, K., Takeyama, H., Nakae, T., Shimotake, A., Kikuchi, T., Yoshida, K., Matsuhashi, M., et al. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119639 · Cited by 12
Cerebral plasticity after contralateral cervical nerve transfer in human by longitudinal PET evaluation
Ma, H., Zheng, M., Lu, Y.-C., Hua, X., & Xu, W.-D. (2017) · Journal of Clinical Neuroscience · doi:10.1016/j.jocn.2017.10.085 · Cited by 13
Multiple parietal pathways are associated with rTMS-induced hippocampal network enhancement and episodic memory changes
Freedberg, M., Cunningham, C. A., Fioriti, C. M., Murillo, J., Reeves, J. A., Taylor, P. A., Sarlls, J. E., & Wassermann, E. M. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118199 · Cited by 13
Performance on the Clock Drawing Task Correlates with fMRI Response to a Visuospatial Task in Alzheimer's Disease
Parks, R. W., Thiyagesh, S. N., Farrow, T. F. D., Ingram, L., Wilkinson, K., Hunter, M. D., Wilkinson, I. D., Young, C., & Woodruff, P. W. R. (2010) · International Journal of Neuroscience · doi:10.3109/00207450903320339 · Cited by 13
Electrophysiological Processes on Motor Imagery Mediate the Association Between Increased Gray Matter Volume and Cognition in Amnestic Mild Cognitive Impairment
Chen, J., Yan, Y., Gu, L., Gao, L., & Zhang, Z. (2019) · Brain Topography · doi:10.1007/s10548-019-00742-8 · Cited by 13
Reticular Formation
Horn, A. K. E., & Adamczyk, C. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-374236-0.10009-4 · Cited by 13
History, citoarchitecture and neurophysiology of human and non human primates' parietal lobe: A review
Aversi‐Ferreira, T. A., de Araújo, M. F. P., Lopes, D. B., & Nishijo, H. (2010) · Dementia & Neuropsychologia · doi:10.1590/s1980-57642010dn40300005 · Cited by 11
Trans-thalamic Pathways: Strong Candidates for Supporting Communication between Functionally Distinct Cortical Areas
Zajzon, B., & Morales-Gregorio, A. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.0656-19.2019 · Cited by 11
Neuro-cognitive aspects of “OM” sound/syllable perception: A functional neuroimaging study
Kumar, U., Guleria, A., & Khetrapal, C. L. (2014) · Cognition & Emotion · doi:10.1080/02699931.2014.917609 · Cited by 11
Corpus Callosum
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0022 · Cited by 11
Electroencephalography reveals lower regional blood perfusion and atrophy of the temporoparietal network associated with memory deficits and hippocampal volume reduction in mild cognitive impairment due to Alzheimer’s disease
Moretti, D. V. (2015) · Neuropsychiatric Disease and Treatment · doi:10.2147/ndt.s78830 · Cited by 10
Stability of cross-sensory input to primary somatosensory cortex across experience
Kato, D. D., & Bruno, R. M. (2024) · Neuron · doi:10.1016/j.neuron.2024.10.020 · Cited by 10
The Developmental Basis of Visuomotor Capabilities and the Causal Nature of Motor Clumsiness to Cognitive and Empathic Dysfunction
Vakalopoulos, C. (2012) · The Cerebellum · doi:10.1007/s12311-012-0416-0 · Cited by 9
Short-latency allocentric control of saccadic eye movements
Chakrabarty, M., Nakano, T., & Kitazawa, S. (2016) · Journal of Neurophysiology · doi:10.1152/jn.00451.2016 · Cited by 9
Chapter 16 - Reticular Formation: Eye Movements, Gaze, and Blinks
Büttner‐Ennever, J. A., & Horn, A. K. E. (2004) · Cited by 9
Understanding early dementia: EEG, MRI, SPECT and memory evaluation
Moretti, D. V. (2015) · Translational Neuroscience · doi:10.1515/tnsci-2015-0005 · Cited by 9
Pontine Reference Frames for the Sensory Guidance of Movement
Tziridis, K., Dicke, P. W., & Thier, P. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhr109 · Cited by 9
Involvement of the claustrum in the cortico-basal ganglia circuitry: connectional study in the non-human primate
Borra, E., Ballestrazzi, G., Biancheri, D., Caminiti, R., & Luppino, G. (2024) · Brain Structure and Function · doi:10.1007/s00429-024-02784-6 · Cited by 8
Neural Correlates of the Perception for Novel Objects
Zhang, H., Liu, J., & Zhang, Q. (2013) · PLoS ONE · doi:10.1371/journal.pone.0062979 · Cited by 8
Histological assessment of optogenetic tools to study fronto-visual and fronto-parietal cortical networks in the rhesus macaque
Fortuna, M. G., Hüer, J., Guo, H., Gruber, J., Gruber-Dujardin, E., Staiger, J. F., Scherberger, H., Treue, S., & Gail, A. (2020) · Scientific Reports · doi:10.1038/s41598-020-67752-6 · Cited by 8
Telencephalon: Hippocampus and Related Structures
(2007) · Springer eBooks · doi:10.1007/978-3-540-34686-9_12 · Cited by 8
Extreme Capsule
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0014 · Cited by 11
Telencephalon: Neocortex
(2007) · Springer eBooks · doi:10.1007/978-3-540-34686-9_15 · Cited by 9
The Bilateral Precuneus as a Potential Neuroimaging Biomarker for Right Temporal Lobe Epilepsy: A Support Vector Machine Analysis
Huang, C., Zhou, Y., Zhong, Y., Wang, X., & Zhang, Y. (2022) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2022.923583 · Cited by 7
Preoperative serum cortisone levels are associated with cognition in preschool-aged children with tetralogy of Fallot after corrective surgery: new evidence from human populations and mice
Ma, S., Liu, Y., Cun, Y.-S., Wang, Q., Fu, M., Wu, K., Cai, X., Cheng, S.-T., Patel, N. D., Da, M., et al. (2023) · World Journal of Pediatrics · doi:10.1007/s12519-023-00754-2 · Cited by 7
Functional MRI in Alzheimer’s Disease
Kivistö, J., Soininen, H. S., & Pihlajamaki, M. M. (2014) · InTech eBooks · doi:10.5772/58264 · Cited by 9
Exploring Executive Functions Using a Distributed Circuit Model
Prasad, J. A. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.0549-18.2018 · Cited by 6
Prior Visual Experience Modulates Learning of Sound Localization Among Blind Individuals
Tao, Q., Chan, C. C. H., Luo, Y., Li, J.-J., Ting, K. H., Lu, Z., Whitfield, S., Wang, J., & Lee, T. M. C. (2017) · Brain Topography · doi:10.1007/s10548-017-0549-z · Cited by 8
Towards an ontology of cognitive processes and their neural substrates: A structural equation modeling approach
Eich, T. S., Parker, D., Gazes, Y., Razlighi, Q. R., Habeck, C. G., & Stern, Y. (2020) · PLoS ONE · doi:10.1371/journal.pone.0228167 · Cited by 7
Temporo-Parietal Brain Network Impairment Is Related To EEG ALPHA3/ALPHA2 Power Ration in Prodormal Alzheimer’s Disease
B, B. G. F. G. (2013) · Journal of Neurology & Neurophysiology · doi:10.4172/2155-9562.1000160 · Cited by 5
Interaction of the dorsolateral prefrontal cortex with the precuneal medial parietal cortex for the monitoring of information in working memory in the macaque monkey
Petrides, M., Lefebvre, S., Novek, J., & Zlatkina, V. (2024) · Cerebral Cortex · doi:10.1093/cercor/bhae315 · Cited by 5
Thalamocortical and corticothalamic connections of multiple functional domains in posterior parietal cortex of galagos
Wang, Q., Stepniewska, I., Liao, C., & Kaas, J. H. (2022) · The Journal of Comparative Neurology · doi:10.1002/cne.25410 · Cited by 4
Belief embodiment through eye movements facilitates memory-guided navigation
Stavropoulos, A., Lakshminarasimhan, K. J., & Angelaki, D. E. (2025) · Nature Communications · doi:10.1038/s41467-025-66080-5 · Cited by 5
The Cerebral Cortex and Complex Cerebral Functions
ten Donkelaar, H. J., Catani, M., van Domburg, P., Eling, P., Küsters, B., & Hori, A. (2020) · Springer eBooks · doi:10.1007/978-3-030-41878-6_15 · Cited by 4
The Effect of Abnormal Regional Homogeneity and Spontaneous Low-Frequency Brain Activity on Lower Cognitive Ability: A Cross-Sectional Study on Postoperative Children With Tetralogy of Fallot
Ma, S., Hu, Y., Liu, Y., Pu, Y., Zuo, P., Hu, Q., Yang, Z., Chen, F., Xie, Z., Cun, Y., et al. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.685372 · Cited by 4
Atrophy and lower regional perfusion of temporo-parietal brain areas are correlated with impairment in memory performances and increase of EEG upper alpha power in prodromal Alzheimer's disease.
Moretti, D. V. (2015) · PubMed Central · Cited by 4
022 Functional connectivity of the posteromedial cortex
Cavanna, A. E., Geminiani, G. C., D’Agata, F., Sacco, K., Duca, S., Bagshaw, A. P., & Cauda, F. (2010) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2010.217554.22 · Cited by 4
Superior Temporal Region
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0007 · Cited by 4
Introduction
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0001 · Cited by 4
Mapping topography and network of brain injury in patients with disorders of consciousness
Arachige, M. L., Seneviratne, U. K., John, N. A., Ma, H., & Phan, T. G. (2023) · Frontiers in Neurology · doi:10.3389/fneur.2023.1027160 · Cited by 3
Inferior Longitudinal Fasciculus
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0018 · Cited by 4
Cingulum Bundle
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0017 · Cited by 3
Uncinate Fasciculus
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0016 · Cited by 4
Extratemporal Resections
Zentner, J. (2020) · Springer eBooks · doi:10.1007/978-3-030-48748-5_7 · Cited by 3
Neural markers for Musical Creativity in Jazz Improvisation and Classical InterpretationPreprint
Rahman, S., Christensen, K., Jensen, H. J., Vuust, P., & Bhattacharya, J. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.02.12.427648 · Cited by 5
Abnormalities of cortical morphology and structural covariance network in the patients with primary trigeminal neuralgia: a preliminary clinical study
Xu, H., Li, J., Wang, Y., Han, W., Li, D., Zhang, M., & Wang, Y. (2025) · Neurological Sciences · doi:10.1007/s10072-025-08360-y · Cited by 2
The association between precuneus cortex thickness and mild behavioral impairment in patients with mild stroke
Liu, Z., Xu, Z., Yan, A., Zhang, P., & Wei, W. (2024) · Brain Imaging and Behavior · doi:10.1007/s11682-024-00955-x · Cited by 2
Fronto-Occipital Fasciculus
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0019 · Cited by 2
White Matter Pathways in Early Neuroscience
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0002 · Cited by 2
Occipital and parietal lobes
Clark, D. L., Boutros, N. N., & Mendez, M. F. (2005) · Cambridge University Press eBooks · doi:10.1017/cbo9780511543661.005 · Cited by 2
Middle Longitudinal Fasciculus
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0015 · Cited by 3
On Bereavement: Studies of Grief in Adult Life by Colin Murray Parkes
Oyebode, J. R. (2014) · The British Journal of Psychiatry · doi:10.1192/bjp.bp.113.143131 · Cited by 2
Sex-Related Variations in the Brain Motor-Network Connectivity at Rest during Puberty
Pacheco, L., González-González, G., & Ortega-Aguilar, A. (2023) · Applied Sciences · doi:10.3390/app131810006 · Cited by 1
Muratoff Bundle (Subcallosal Fasciculus) and the External Capsule
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0020 · Cited by 1
A Functional Neuroimaging Study of Working Memory in Children with Chronic Kidney Disease
Harrell, W. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/vxyj-4z02 · Cited by 1
A case of body lateropulsion to the left in acute cerebral infarction of the right medial parietal lesion
Takamatsu, A., Sakajiri, K., & Nitta, E. (2018) · Rinsho Shinkeigaku · doi:10.5692/clinicalneurol.cn-001172 · Cited by 1
Telencefalo: neocortex
Nieuwenhuys, R., Voogd, J., van Huijzen, C., & Papa, M. (2010) · Springer eBooks · doi:10.1007/978-88-470-1140-3_15 · Cited by 1
The Cerebral Cortex and Complex Cerebral Functions
ten Donkelaar, H. J. (2011) · Springer eBooks · doi:10.1007/978-3-642-19134-3_15 · Cited by 1
Sagittal Stratum
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0025 · Cited by 1
Internal Capsule
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0024 · Cited by 1
Anterior Commissure
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0021 · Cited by 1
More Than the Sum of Its Parts: Visual–Tactile Integration in the Behaving Rat
Nikbakht, N. (2012) · Advances in experimental medicine and biology · doi:10.1007/978-981-99-7611-9_3 · Cited by 1
Surface-Based Morphometry Findings Reveal Structural Alterations of the Brain in Meige Syndrome
Tang, Y., & Liu, R. (2024) · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · doi:10.1017/cjn.2024.326 · Cited by 1
Composite Summary of Cerebral White Matter Fiber Pathways in the Rhesus Monkey
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0027 · Cited by 1
Occipital and parietal lobes
Clark, D. L., Boutros, N. N., & Mendez, M. F. (2010) · Cambridge University Press eBooks · doi:10.1017/cbo9780511776915.006 · Cited by 1
Neuro-ophthalmology: A Short Primer
Schwarz, U. (2005) · Medical radiology · doi:10.1007/3-540-27989-x_3 · Cited by 1
Materials Analyzed
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0003 · Cited by 1
A new cortical parcellation based on systematic review of primate anatomical tracing studies on corticostriatal projectionsPreprint
Dinh, T., Nerland, S., Maximov, I. I., Barth, C., Vernon, A. C., Agartz, I., & Jørgensen, K. N. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.06.20.496804 · Cited by 1
EEG-fMRI signatures of spontaneous brain activity in healthy volunteers and epilepsy patients
Laufs, H. (2014) · UCL Discovery (University College London) · Cited by 1
Neural correlates of intentional actions
Krieghoff, V. (2009) · Max Planck Digital Library · Cited by 1
Gehirn-Computer-Interfaces: Neuroanatomische Korrelate der SCP-Kontrolle
Schumann, B. (2011)
How the brain constructs stable visual representations: Cortical and subcortical mechanisms
Dunn, C. A. (2009)
Using event-related brain potentials to help explain posterior-parietal repetition effects in functional magnetic resonance imaging.
Steele, V. R. (2011) · University of Minnesota Digital Conservancy (University of Minnesota)
Les épilepsies pariétales : cadres nosologiques et sémiologie
Bartoloméi, F. (2015) · Pratique Neurologique - FMC · doi:10.1016/j.praneu.2015.01.004
Finger-Movement-Related Human Brain Activation Gaze and Hand Position Effects on
Sanes, J. N., Bédard, P., Wu, M., Quintero, A., Ichesco, E., Schutt, R., Myers, C., Peltier, S., Merriam, E. P., Gardner, J. L., et al. (2013)
Zur neuronalen Repräsentation bimanuellen Lernens im menschlichen Gehirn: Untersuchungen mit funktioneller Kernspintomographie
Neurologie, A. A., & Weller, M. (2006)
Neural Correlates of Moral Decision-Making in Neural Correlates of Moral Decision-Making in Psychopaths
Psychiatrie, F., & Rupprecht, R. (2011)
Prefrontal cortical modulation of posterior parietal acetylcholine release: a study of glutamatergic and cholinergic mechanisms
Nelson, C. (2004) · OhioLink ETD Center (Ohio Library and Information Network)
Inferior Temporal Region
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0008
Architecture and Nomenclature of Rhesus Monkey Cerebral Hemisphere
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0004
Investigating Higher Order Cognitive Functions in the Dorsal (magnocellular) Stream of Visual Processing
Fortes, M. F., & Merchant, H. (2006) · Springer eBooks · doi:10.1007/0-387-28190-8_13 · Cited by 1
A role for the claustrum in cognitive controlPreprint
Madden, M. B., Stewart, B. W., White, M. G., Krimmel, S. R., Qadir, H., Barrett, F. S., Seminowicz, D. A., & Mathur, B. N. (2022) · doi:10.31234/osf.io/nurv7
Clinical Significance
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0028
Parietal Lobe
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0006
Prefrontal Cortex
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0012
Thalamic Peduncles
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0026
Hippocampal Commissures
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0023
Conclusions
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0029
Occipital Lobe
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0009
Motor Cortex
Schmahmann, J. D., & Pandya, D. Ν. (2006) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195104233.003.0011
Cerebellar Nuclei and the Inferior Olivary Nuclei: Organization and Connections
Voogd, J., Shinoda, Y., Ruigrok, T. J. H., & Sugihara, I. (2020) · Springer eBooks · doi:10.1007/978-3-319-97911-3_19-2

Authors: Leichnetz, G. R.
Affiliations: Virginia Commonwealth University (US)
Corresponding author: Leichnetz, George R.
Venue: The Anatomical Record
Publisher: Wiley
Published: 2001-04-27
Volume: 263
Issue: 2
Pages: 215-236
ISSN: 0003-276X (ISSN-L)
1097-0185
DOI: 10.1002/ar.1082
OpenAlex: W1985804114
Cited by: 318
References: 76
Citations by year: 2026: 2 · 2025: 5 · 2024: 7 · 2023: 11 · 2022: 16 · 2021: 9 · 2020: 19 · 2019: 17 · 2018: 10 · 2017: 14 · 2016: 10 · 2015: 19 · 2014: 19 · 2013: 16 · 2012: 16
FWCI: 1.40
Type: journal article
Language: en
Open access: bronze
doi.org
Licence: onlinelibrary.wiley.com/termsAndConditions#vor (vor)
Locations: The Anatomical Record (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 › Spatial Neglect and Hemispheric Dysfunction
Keywords: corticocortical connections, subcortical connections, intraparietal sulcus, superior parietal lobule, inferior parietal lobule, frontal eye field, supplementary eye field, cingulate cortex, thalamus, superior colliculus, basal ganglia, claustrum, pretectal nuclei, pontine nuclei, Cebus apella, Macaca fascicularis
MeSH terms: Animals, Cebus, Eye Movements, Frontal Lobe, Horseradish Peroxidase, Macaca fascicularis, Neural Pathways, Parietal Lobe, Species Specificity

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

Connections of the medial posterior parietal cortex (area 7m) in the monkey

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks