Cortical chemoarchitecture shapes macroscale effective functional connectivity patterns in macaque cerebral cortex

Complex network measures of brain connectivity: Uses and interpretations

Rubinov, M., & Sporns, O. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.10.003 · Cited by 11,522 · see citing works

PRINCIPLES OF NEURAL SCIENCE

Henry, M. A. (1995) · The Journal of the American Dental Association · doi:10.14219/jada.archive.1995.0108 · Cited by 3,454 · see citing works

The Human Connectome: A Structural Description of the Human Brain

Sporns, O., Tononi, G., & Kötter, R. (2005) · PLoS Computational Biology · doi:10.1371/journal.pcbi.0010042 · Cited by 3,260 · see citing works

NEURONAL CIRCUITS OF THE NEOCORTEX

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

Adjusting multiple testing in multilocus analyses using the eigenvalues of a correlation matrix

Li, J., & Ji, L. (2005) · Heredity · doi:10.1038/sj.hdy.6800717 · Cited by 1,458 · see citing works

Resting-state functional connectivity in neuropsychiatric disorders

Greicius, M. (2008) · Current Opinion in Neurology · doi:10.1097/wco.0b013e328306f2c5 · Cited by 1,180 · 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

The anatomical basis of functional localization in the cortex

Passingham, R. E., Stephan, K. E., & Kötter, R. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn893 · Cited by 1,024 · see citing works

Polarity-Sensitive Modulation of Cortical Neurotransmitters by Transcranial Stimulation

Stagg, C. J., Best, J. G., Stephenson, M. C., O’Shea, J., Wylezinska, M., Kincses, Z. T., Morris, P. G., Matthews, P. M., & Johansen‐Berg, H. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4432-08.2009 · Cited by 942 · see citing works

Transcranial magnetic stimulation in cognitive neuroscience–virtual lesion, chronometry, and functional connectivity

Pascual-Leone, A. (2000) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00081-7 · Cited by 923 · 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

A multiple testing correction method for genetic association studies using correlated single nucleotide polymorphisms

Gao, X., Starmer, J., & Martin, E. R. (2008) · Genetic Epidemiology · doi:10.1002/gepi.20310 · Cited by 849 · 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

High-cost, high-capacity backbone for global brain communication

van den Heuvel, M. P., Kahn, R. S., Goñi, J., & Sporns, O. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1203593109 · Cited by 781 · see citing works

Can structure predict function in the human brain?

Honey, C. J., Thivierge, J.-P., & Sporns, O. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.01.071 · Cited by 629 · see citing works

The Role of GABA in Human Motor Learning

Stagg, C. J., Bachtiar, V., & Johansen‐Berg, H. (2011) · Current Biology · doi:10.1016/j.cub.2011.01.069 · Cited by 600 · see citing works

Architectonic parcellation of the temporal operculum in rhesus monkey and its projection pattern

Pandya, D. Ν., & Sanides, F. (1973) · Anatomy and Embryology · doi:10.1007/bf00523634 · Cited by 553 · see citing works

The Neocortex of Macaca mulatta

Romanes, G. (1948) · JAMA · doi:10.1001/jama.1948.02890460089032 · Cited by 551 · see citing works

Functional organization of excitatory synaptic strength in primary visual cortex

Cossell, L., Iacaruso, M. F., Muir, D. R., Houlton, R., Sader, E., Ko, H., Hofer, S. B., & Mrsic‐Flogel, T. D. (2015) · Nature · doi:10.1038/nature14182 · Cited by 529 · see citing works

The Dynamic Synapse

Choquet, D., & Triller, A. (2013) · Neuron · doi:10.1016/j.neuron.2013.10.013 · Cited by 515 · see citing works

Viewpoint: the core and matrix of thalamic organization

Jones, E. G. (1998) · Neuroscience · doi:10.1016/s0306-4522(97)00581-2 · Cited by 504 · see citing works

An anatomical substrate for integration among functional networks in human cortex

van den Heuvel, M. P., & Sporns, O. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.2128-13.2013 · Cited by 404 · see citing works

The specificity of strychnine as a glycine antagonist in the mammalian spinal cord

Curtis, D. R., Duggan, A. W., & Johnston, G. A. R. (1971) · Experimental Brain Research · doi:10.1007/bf00234248 · Cited by 353 · see citing works

Dendritic spines and distributed circuits

Yuste, R. (2011) · Neuron · doi:10.1016/j.neuron.2011.07.024 · Cited by 298 · see citing works

Kainate receptors coming of age: milestones of two decades of research

Contractor, A., Mulle, C., & Swanson, G. T. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2010.12.002 · Cited by 292 · see citing works

Computational analysis of functional connectivity between areas of primate cerebral cortex

Stephan, K. E., Hilgetag, C. C., Burns, G., O’Neill, M. A., Young, M. P., & Kötter, R. (2000) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2000.0552 · Cited by 269 · see citing works

A review of the role of serotonin receptors in psychiatric disorders

Naughton, M., Mulrooney, J. B., & Leonard, B. E. (2000) · Human Psychopharmacology Clinical and Experimental · doi:10.1002/1099-1077(200008)15:6 · Cited by 258 · see citing works

Architectonics of the human cerebral cortex and transmitter receptor fingerprints: reconciling functional neuroanatomy and neurochemistry.

Zilles, K. (2002) · European Neuropsychopharmacology · doi:10.1016/s0924-977x(02)00108-6 · Cited by 244 · see citing works

Mapping of human and macaque sensorimotor areas by integrating architectonic, transmitter receptor, MRI and PET data.

Zilles, K., Gottfried Schlaug, A., Matelli, M., Luppino, G., Schleicher, A., Qü, M., Dabringhaus, A., Seitz, R. J., & Roland, P. E. (1995) · PubMed · Cited by 232 · see citing works

Associations of regional GABA and glutamate with intrinsic and extrinsic neural activity in humans—A review of multimodal imaging studies

Duncan, N. W., Wiebking, C., & Northoff, G. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.07.016 · Cited by 220 · see citing works

Posteromedial cortex glutamate and GABA predict intrinsic functional connectivity of the default mode network

Kapogiannis, D., Reiter, D. A., Willette, A. A., & Mattson, M. P. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2012.09.029 · Cited by 211 · see citing works

Functional Connectivity between Anatomically Unconnected Areas Is Shaped by Collective Network-Level Effects in the Macaque Cortex

Adachi, Y., Osada, T., Sporns, O., Watanabe, T., Matsui, T., Miyamoto, K., & Miyashita, Y. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr234 · Cited by 211 · see citing works

Muscarinic Acetylcholine Receptors (mAChRs) in the Nervous System: Some Functions and Mechanisms

Brown, D. A. (2010) · Journal of Molecular Neuroscience · doi:10.1007/s12031-010-9377-2 · Cited by 193 · see citing works

Baseline GABA concentration and fMRI response

Donahue, M. J., Near, J., Blicher, J. U., & Jezzard, P. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.07.017 · Cited by 174 · see citing works

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

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

Transmitter receptors and functional anatomy of the cerebral cortex

Zilles, K., Palomero‐Gallagher, N., & Schleicher, A. (2004) · Journal of Anatomy · doi:10.1111/j.0021-8782.2004.00357.x · Cited by 159 · see citing works

Cellular and synaptic localization of NMDA and non-NMDA receptor subunits in neocortex: organizational features related to cortical circuitry, function and disease

Huntley, G. W., Vickers, J. C., & Morrison, J. H. (1994) · Trends in Neurosciences · doi:10.1016/0166-2236(94)90158-9 · Cited by 149 · see citing works

The importance of being agranular: a comparative account of visual and motor cortex

Shipp, S. D. (2005) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2005.1630 · Cited by 133 · see citing works

Comparison of diffusion tractography and tract-tracing measures of connectivity strength in rhesus macaque connectome

van den Heuvel, M. P., de Reus, M. A., Feldman Barrett, L., Scholtens, L. H., Coopmans, F. M. T., Schmidt, R., Preuss, T. M., Rilling, J. K., & Li, L. (2015) · Human Brain Mapping · doi:10.1002/hbm.22828 · Cited by 131 · see citing works

Bridging Cytoarchitectonics and Connectomics in Human Cerebral Cortex

van den Heuvel, M. P., Scholtens, L. H., Barrett, L. F., Hilgetag, C. C., & de Reus, M. A. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.2630-15.2015 · Cited by 129 · see citing works

Tumor-suppressor p53 is expressed in proliferating and newly formed neurons of the embryonic and postnatal rat brain: Comparison with expression of the cell cycle regulators p21Waf1/Cip1, p27Kip1, p57Kip2, p16Ink4a, cyclin G1, and the proto-oncogene bax

Campagne, M. V. L., & Gill, R. (1998) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19980727)397:2 · Cited by 127 · see citing works

A predictive model of the cat cortical connectome based on cytoarchitecture and distance

Beul, S. F., Grant, S., & Hilgetag, C. C. (2014) · Brain Structure and Function · doi:10.1007/s00429-014-0849-y · Cited by 104 · see citing works

The effects of strychnine on the inhibition of interneurons by glycine and γ-aminobutyric acid

Davidoff, R. A., Aprison, M. H., & Werman, R. (1969) · International Journal of Neuropharmacology · doi:10.1016/0028-3908(69)90013-6 · Cited by 96 · see citing works

Experimental researches on sensory localization in the cerebral cortex of the monkey (macacus)

de Barenne, D. (1924) · Proceedings of the Royal Society of London Series B Containing Papers of a Biological Character · doi:10.1098/rspb.1924.0026 · Cited by 75 · see citing works

Associated Microscale Spine Density and Macroscale Connectivity Disruptions in Schizophrenia

van den Heuvel, M. P., Scholtens, L. H., de Reus, M. A., & Kahn, R. S. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.10.005 · Cited by 72 · see citing works

Cellular and Molecular Neurophysiology

(2015) · Elsevier eBooks · doi:10.1016/c2011-0-07267-8 · Cited by 69 · see citing works

FUNCTIONAL ORGANIZATION IN THE SENSORY CORTEX OF THE MONKEY (MACACA MULATTA)

de Barenne, J. G. D., & McCulloch, W. S. (1938) · Journal of Neurophysiology · doi:10.1152/jn.1938.1.1.69 · Cited by 59 · see citing works

Multimodal characterisation of cortical areas by multivariate analyses of receptor binding and connectivity data

Kötter, R., Stephan, K. E., Palomero‐Gallagher, N., Geyer, S., Schleicher, A., & Zilles, K. (2001) · Anatomy and Embryology · doi:10.1007/s004290100199 · Cited by 57 · see citing works

The association between cingulate cortex glutamate concentration and delay discounting is mediated by resting state functional connectivity

Schmaal, L., Goudriaan, A. E., van der Meer, J. N., van den Brink, W., & Veltman, D. J. (2012) · Brain and Behavior · doi:10.1002/brb3.74 · Cited by 51 · see citing works

Strychnine-sensitive glycine receptors on pyramidal neurons in layers II/III of the mouse prefrontal cortex are tonically activated

Salling, M. C., & Harrison, N. L. (2014) · Journal of Neurophysiology · doi:10.1152/jn.00714.2013 · Cited by 50 · see citing works

Functional connectivity estimation over large networks at cellular resolution based on electrophysiological recordings and structural prior

Ullo, S., Nieus, T., Sona, D., et al. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00137 · Cited by 41 · see citing works

The Anatomical Segregation of the Frontal Cortex: What Does it Mean for Function?

Amunts, K., & von Cramon, D. Y. (2006) · Cortex · doi:10.1016/s0010-9452(08)70392-7 · Cited by 28 · see citing works

SnapShot: Receptor Dynamics at Plastic Synapses

Kneussel, M., Triller, A., & Choquet, D. (2014) · Cell · doi:10.1016/j.cell.2014.06.002 · Cited by 25 · see citing works

Anatomical Concepts of Brain Connectivity

Kötter, R. (2007) · Understanding complex systems · doi:10.1007/978-3-540-71512-2_5 · Cited by 18 · see citing works

An active inference theory of allostasis and interoception in depression

Barrett, L. F., Quigley, K. S., & Hamilton, P. (2016) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2016.0011 · Cited by 554 · see citing works

Study and Manipulation of Neurotransmitter Function in Humans

Webster, R. A. (2001) · doi:10.1002/0470846577.ch14 · Cited by 1 · see citing works

Neurotransmitter Receptors: Neuroanatomical Localization Through Autoradiography

Murrin, L. C. (1981) · International review of neurobiology · doi:10.1016/s0074-7742(08)60292-5 · Cited by 17 · see citing works

Basic Aspects of Neurotransmitter Function

Leonard, B. E. (2003) · doi:10.1002/0470871482.ch2 · Cited by 2 · see citing works

Prenatal exposure to drugs of abuse in humans: effects on placental neurotransmitter receptors.

Bd, P., Pesavento, D. J., Kussie, P. H., et al. (1985) · PubMed · Cited by 16 · see citing works

Surface Trafficking of Neurotransmitter Receptor: Comparison between Single-Molecule/Quantum Dot Strategies

Groc, L., Lafourcade, M., Heine, M., Renner, M. L., Racine, V., Sibarita, J., Lounis, B., Choquet, D., & Cognet, L. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3349-07.2007 · Cited by 194 · see citing works