The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Structural and Functional Analyses of Human Cerebral Cortex Using a Surface-Based Atlas
Open accessAbstract
We have analyzed the geometry, geography, and functional organization of human cerebral cortex using surface reconstructions and cortical flat maps of the left and right hemispheres generated from a digital atlas (the Visible Man). The total surface area of the reconstructed Visible Man neocortex is 1570 cm 2(both hemispheres), ∼70% of which is buried in sulci. By linking the Visible Man cerebrum to the Talairach stereotaxic coordinate space, the locations of activation foci reported in neuroimaging studies can be readily visualized in relation to the cortical surface. The associated spatial uncertainty was empirically shown to have a radius in three dimensions of ∼10 mm. Application of this approach to studies of visual cortex reveals the overall patterns of activation associated with different aspects of visual function and the relationship of these patterns to topographically organized visual areas. Our analysis supports a distinction between an anterior region in ventral occipito-temporal cortex that is selectively involved in form processing and a more posterior region (in or near areas VP and V4v) involved in both form and color processing. Foci associated with motion processing are mainly concentrated in a region along the occipito-temporal junction, the ventral portion of which overlaps with foci also implicated in form processing. Comparisons between flat maps of human and macaque monkey cerebral cortex indicate significant differences as well as many similarities in the relative sizes and positions of cortical regions known or suspected to be homologous in the two species.
Overview
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
Cites
Statistics
Verification
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.
Citations
Cites
Distributed hierarchical processing in the primate cerebral cortex
Felleman, D. J., & Van Essen, D. C. (1991) · Cerebral Cortex · doi:10.1093/cercor/1.1.1 · Cited by 7,783
Motor Areas of the Medial Wall: A Review of Their Location and Functional Activation
Picard, N., & Strick, P. L. (1996) · Cerebral Cortex · doi:10.1093/cercor/6.3.342 · Cited by 1,712
Three-dimensional statistical analysis of sulcal variability in the human brain
Thompson, P. M., Schwartz, C., Lin, R. T., Khan, A. A., & Toga, A. W. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-13-04261.1996 · Cited by 346
Cited by
Cortical Surface-Based Analysis
Dale, A. M., Fischl, B., & Sereno, M. I. (1999) · NeuroImage · doi:10.1006/nimg.1998.0395 · Cited by 10,910
Fischl, B. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.01.021 · Cited by 9,526
Fischl, B., Salat, D. H., Busa, E., Albert, M., Dieterich, M., Haselgrove, C., van der Kouwe, A., Killiany, R., Kennedy, D., Klaveness, S., et al. (2002) · Neuron · doi:10.1016/s0896-6273(02)00569-x · Cited by 8,610
Cortical Surface-Based Analysis
Fischl, B., Sereno, M. I., & Dale, A. M. (1999) · NeuroImage · doi:10.1006/nimg.1998.0396 · Cited by 6,147
Searching for a baseline: Functional imaging and the resting human brain
Gusnard, D. A., & Raichle, M. E. (2001) · Nature Reviews Neuroscience · doi:10.1038/35094500 · Cited by 3,371
Automatic parcellation of human cortical gyri and sulci using standard anatomical nomenclature
Destrieux, C., Fischl, B., Dale, A., & Halgren, E. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.06.010 · Cited by 2,956
A Population-Average, Landmark- and Surface-based (PALS) atlas of human cerebral cortex
Van Essen, D. C. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.06.058 · Cited by 1,151
Self-citationCorbetta, M. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.3.831 · Cited by 995
Architectonic subdivision of the human orbital and medial prefrontal cortex
Öngür, D., Ferry, A. T., & Price, J. L. (2003) · Journal of Comparative Neurology · doi:10.1002/cne.10609 · Cited by 944
Memory's echo: vivid remembering reactivates sensory-specific cortex
Wheeler, M. E., Petersen, S. E., & Buckner, R. L. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.20.11125 · Cited by 865
Allison, T. (1999) · Cerebral Cortex · doi:10.1093/cercor/9.5.415 · Cited by 882
Raznahan, A., Shaw, P., Lalonde, F., Stockman, M., Wallace, G. L., Greenstein, D., Clasen, L., Gogtay, N., & Giedd, J. N. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.0054-11.2011 · Cited by 712
Functional deactivations: Change with age and dementia of the Alzheimer type
Lustig, C., Snyder, A. Z., Bhakta, M., O'Brien, K. C., McAvoy, M., Raichle, M. E., Morris, J. C., & Buckner, R. L. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2235925100 · Cited by 720
An unfolded map of the cerebellar dentate nucleus and its projections to the cerebral cortex
Dum, R. P., & Strick, P. L. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00626.2002 · Cited by 684
Mapping of Contralateral Space in Retinotopic Coordinates by a Parietal Cortical Area in Humans
Sereno, M. I., Pitzalis, S., & Martinez, A. (2001) · Science · doi:10.1126/science.1063695 · Cited by 682
Astafiev, S. V., Shulman, G. L., Stanley, C. M., Snyder, A. Z., Van Essen, D. C., & Corbetta, M. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-11-04689.2003 · Cited by 640
Self-citationDefining functional areas in individual human brains using resting functional connectivity MRI
Cohen, A. L., Fair, D. A., Dosenbach, N. U. F., Miezin, F. M., Dierker, D., Van Essen, D. C., Schlaggar, B. L., & Petersen, S. E. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.01.066 · Cited by 582
Self-citationParcellations and Hemispheric Asymmetries of Human Cerebral Cortex Analyzed on Surface-Based Atlases
Van Essen, D. C., Glasser, M. F., Dierker, D. L., Harwell, J., & Coalson, T. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr291 · Cited by 616
Human brain activity time-locked to perceptual event boundaries
Zacks, J. M., Braver, T. S., Sheridan, M. A., Donaldson, D. I., Snyder, A. Z., Ollinger, J. M., Buckner, R. L., & Raichle, M. E. (2001) · Nature Neuroscience · doi:10.1038/88486 · Cited by 572
Defining the phenotype of schizophrenia: cognitive dysmetria and its neural mechanisms
Andreasen, N. C., Nopoulos, P., O’Leary, D. S., Miller, D. D., Wassink, T., & Flaum, M. (1999) · Biological Psychiatry · doi:10.1016/s0006-3223(99)00152-3 · Cited by 560
Intrinsic functional relations between human cerebral cortex and thalamus
Zhang, D., Snyder, A. Z., Fox, M. D., Sansbury, M. W., Shimony, J. S., & Raichle, M. E. (2008) · Journal of Neurophysiology · doi:10.1152/jn.90463.2008 · Cited by 437
Puce, A. (1999) · Cerebral Cortex · doi:10.1093/cercor/9.5.445 · Cited by 422
The functional logic of cortico-pulvinar connections
Shipp, S. (2003) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.2002.1213 · Cited by 411
A tutorial in connectome analysis: Topological and spatial features of brain networks
Kaiser, M. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.05.025 · Cited by 371
Development of Cortical Surface Area and Gyrification in Attention-Deficit/Hyperactivity Disorder
Shaw, P., Malek, M., Watson, B., Sharp, W., Evans, A., & Greenstein, D. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.01.031 · Cited by 357
Large-scale mirror-symmetry organization of human occipito-temporal object areas
Hasson, U., Harel, M., Levy, I., & Malach, R. (2003) · Neuron · doi:10.1016/s0896-6273(03)00144-2 · Cited by 336
Li, G., Wang, L., Shi, F., Lyall, A. E., Lin, W., Gilmore, J. H., & Shen, D. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.3976-13.2014 · Cited by 251
Simplified intersubject averaging on the cortical surface using SUMA
Argall, B. D., Saad, Z. S., & Beauchamp, M. S. (2006) · Human Brain Mapping · doi:10.1002/hbm.20158 · Cited by 200
Yucel, M., Stuart, G. W., Maruff, P., Velakoulis, D., Crowe, S. F., Savage, G., & Pantelis, C. (2001) · Cerebral Cortex · doi:10.1093/cercor/11.1.17 · Cited by 222
The effects of visual object priming on brain activation before and after recognition
James, T. W., Humphrey, G. K., Gati, J. S., Menon, R. S., & Goodale, M. A. (2000) · Current Biology · doi:10.1016/s0960-9822(00)00655-2 · Cited by 164
Lisdahl, K. M., Wright, N. E., Medina-Kirchner, C., Maple, K. E., & Shollenbarger, S. (2014) · Current Addiction Reports · doi:10.1007/s40429-014-0019-6 · Cited by 160
Receptive fields in human visual cortex mapped with surface electrodes
Yoshor, D., Bosking, W. H., Ghose, G. M., & Maunsell, J. H. R. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhl138 · Cited by 152
Four-dimensional maps of the human somatosensory system
Avanzini, P., Abdollahi, R. O., Sartori, I., Caruana, F., Pelliccia, V., Casaceli, G., Mai, R., Lo Russo, G., Rizzolatti, G., & Orban, G. A. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1601889113 · Cited by 114
Mills, K. L., Bathula, D., Dias, T. G. C., Iyer, S. P., Fenesy, M. C., Musser, E. D., Stevens, C. A., Thurlow, B. L., Carpenter, S. D., Nagel, B. J., et al. (2012) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2012.00002 · Cited by 108
Lee, J. K., Lee, J.-M., Kim, J. S., Kim, I. Y., Evans, A. C., & Kim, S. I. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2005.12.044 · Cited by 108
A cross-validated cytoarchitectonic atlas of the human ventral visual stream
Rosenke, M., Weiner, K. S., Barnett, M. A., Zilles, K., Amunts, K., Goebel, R., & Grill-Spector, K. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2017.02.040 · Cited by 97
Dickson, J., Drury, H., & Van Essen, D. C. (2001) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.2001.0913 · Cited by 54
Self-citationMultiple time courses of somatosensory responses in human cortex
Avanzini, P., Pelliccia, V., Lo Russo, G., Orban, G. A., & Rizzolatti, G. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2017.12.037 · Cited by 49
Assessment of the King-Devick® (KD) test for screening acute mTBI/concussion in warfighters
Walsh, D. V., Capó-Aponte, J. E., Beltran, T., Cole, W. R., Ballard, A., & Dumayas, J. Y. (2016) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2016.09.014 · Cited by 25
Neurophysiological considerations for visual implants
Meikle, S. J., & Wong, Y. T. (2022) · Brain Structure and Function · doi:10.1007/s00429-021-02417-2 · Cited by 15
Fridriksson (2009) · doi:10.1044/1092-4388(2008/06-0197
Metadata
- Authors
- Van Essen, D. C., & Drury, H. A.
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 1997-09-15
- Volume
- 17
- Issue
- 18
- Pages
- 7079-7102
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- OpenAlex
- W2119180809
- Cited by
- 469
- References
- 3
- FWCI
- 13.41
- Type
- journal article
- Language
- en
- Open access
- hybrid
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
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.