Toward a Genetic Dissection of Cortical Circuits in the Mouse

Multiplex Genome Engineering Using CRISPR/Cas Systems

Cong, L., Ran, F. A., Cox, D., Lin, S., Barretto, R., Habib, N., Hsu, P. D., Wu, X., Jiang, W., Marraffini, L. A., et al. (2013) · Science · doi:10.1126/science.1231143 · Cited by 15,339 · see citing works

Green fluorescent protein as a marker for gene expression

Chalfie, M., Tu, Y., Euskirchen, G., Ward, W. W., & Prasher, D. C. (1994) · Science · doi:10.1126/science.8303295 · Cited by 6,802 · see citing works

Receptive fields of single neurones in the cat's striate cortex

Hubel, D. H., & Wiesel, T. N. (1959) · The Journal of Physiology · doi:10.1113/jphysiol.1959.sp006308 · Cited by 4,653 · see citing works

Mutations affecting segment number and polarity in Drosophila

Nüsslein‐Volhard, C., & Wieschaus, E. F. (1980) · Nature · doi:10.1038/287795a0 · Cited by 4,370 · see citing works

The Molecular Biology of Axon Guidance

Tessier‐Lavigne, M., & Goodman, C. S. (1996) · Science · doi:10.1126/science.274.5290.1123 · Cited by 3,295 · see citing works

Specification of Cerebral Cortical Areas

Rakic, P. (1988) · Science · doi:10.1126/science.3291116 · Cited by 3,127 · see citing works

An anatomically comprehensive atlas of the adult human brain transcriptome

Hawrylycz, M. J., Lein, E. S., Guillozet-Bongaarts, A. L., Shen, E. H., Ng, L., Miller, J. A., van de Lagemaat, L. N., Smith, K. A., Ebbert, A., Riley, Z. L., et al. (2012) · Nature · doi:10.1038/nature11405 · Cited by 3,083 · see citing works

Interneurons of the neocortical inhibitory system

Markram, H., Toledo-Rodriguez, M., Wang, Y., Gupta, A., Silberberg, G., & Wu, C. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1519 · Cited by 2,954 · see citing works

Mechanisms of Gamma Oscillations

Buzsáki, G., & Wang, X.-J. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062111-150444 · Cited by 2,796 · see citing works

Driving fast-spiking cells induces gamma rhythm and controls sensory responses

Cardin, J. A., Carlén, M., Meletis, K., Knoblich, U., Zhang, F., Deisseroth, K., Tsai, L.-H., & Moore, C. I. (2009) · Nature · doi:10.1038/nature08002 · Cited by 2,603 · see citing works

Mosaic Analysis with a Repressible Cell Marker for Studies of Gene Function in Neuronal Morphogenesis

Lee, T., & Luo, L. (1999) · Neuron · doi:10.1016/s0896-6273(00)80701-1 · Cited by 2,540 · see citing works

The Glial Nature of Embryonic and Adult Neural Stem Cells

Kriegstein, A., & Alvarez-Buylla, A. (2009) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.051508.135600 · Cited by 2,475 · see citing works

MODALITY AND TOPOGRAPHIC PROPERTIES OF SINGLE NEURONS OF CAT'S SOMATIC SENSORY CORTEX

Mountcastle, V. B. (1957) · Journal of Neurophysiology · doi:10.1152/jn.1957.20.4.408 · Cited by 2,411 · see citing works

Cortical neurons arise in symmetric and asymmetric division zones and migrate through specific phases

Noctor, S. C., Martínez-Cerdeño, V., Ivic, L., & Kriegstein, A. R. (2004) · Nature Neuroscience · doi:10.1038/nn1172 · Cited by 2,229 · see citing works

Neuronal specification in the spinal cord: inductive signals and transcriptional codes

Jessell, T. M. (2000) · Nature Reviews Genetics · doi:10.1038/35049541 · Cited by 2,089 · see citing works

Synaptic mechanisms of synchronized gamma oscillations in inhibitory interneuron networks

Bartos, M., Vida, I., & Jonas, P. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2044 · Cited by 2,070 · see citing works

Neuronal Diversity and Temporal Dynamics: The Unity of Hippocampal Circuit Operations

Klausberger, T., & Somogyi, P. (2008) · Science · doi:10.1126/science.1149381 · Cited by 2,050 · see citing works

Neurons derived from radial glial cells establish radial units in neocortex

Noctor, S. C., Flint, A. C., Weissman, T. A., Dammerman, R. S., & Kriegstein, A. R. (2001) · Nature · doi:10.1038/35055553 · Cited by 2,016 · 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

A resource of Cre driver lines for genetic targeting of GABAergic neurons in cerebral cortex

Taniguchi, H., He, M., Wu, P., Kim, S., Paik, R., Sugino, K., Kvitsani, D., Fu, Y., Lu, J., Lin, Y., et al. (2011) · Neuron · doi:10.1016/j.neuron.2011.07.026 · Cited by 1,828 · see citing works

How Inhibition Shapes Cortical Activity

Isaacson, J. S., & Scanziani, M. (2011) · Neuron · doi:10.1016/j.neuron.2011.09.027 · Cited by 1,678 · see citing works

Neuronal subtype specification in the cerebral cortex

Molyneaux, B. J., Arlotta, P., Menezes, J. R. L., & Macklis, J. D. (2007) · Nature reviews. Neuroscience · doi:10.1038/nrn2151 · Cited by 1,632 · see citing works

Evolution of the neocortex: a perspective from developmental biology

Rakic, P. (2009) · Nature reviews. Neuroscience · doi:10.1038/nrn2719 · Cited by 1,565 · see citing works

Autoradiographic Study of Cell Migration during Histogenesis of Cerebral Cortex in the Mouse

ANGEVINE, J. B., & SIDMAN, R. L. (1961) · Nature · doi:10.1038/192766b0 · Cited by 1,530 · see citing works

Petilla terminology: nomenclature of features of GABAergic interneurons of the cerebral cortex

The Petilla Interneuron Nomenclature Group (PING) (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2402 · Cited by 1,491 · see citing works

Interneuron Migration from Basal Forebrain to Neocortex: Dependence on <i>Dlx</i> Genes

Anderson, S. A., Eisenstat, D. D., Shi, L., & Rubenstein, J. L. R. (1997) · Science · doi:10.1126/science.278.5337.474 · Cited by 1,462 · see citing works

A GAL4-Driver Line Resource for Drosophila Neurobiology

Jenett, A., Rubin, G. M., Ngo, T.-T. B., Shepherd, D., Murphy, C., Dionne, H., Pfeiffer, B. D., Cavallaro, A., Hall, D., Jeter, J., et al. (2012) · Cell Reports · doi:10.1016/j.celrep.2012.09.011 · Cited by 1,449 · see citing works

Three groups of interneurons account for nearly 100% of neocortical GABAergic neurons

Rudy, B., Fishell, G., Lee, S., & Hjerling‐Leffler, J. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20853 · Cited by 1,420 · see citing works

Neurogenic radial glia in the outer subventricular zone of human neocortex

Hansen, D. V., Lui, J. H., Parker, P. R. L., & Kriegstein, A. R. (2010) · Nature · doi:10.1038/nature08845 · Cited by 1,388 · see citing works

Inhibition of inhibition in visual cortex: the logic of connections between molecularly distinct interneurons

Pfeffer, C. K., Xue, M., He, M., Huang, Z. J., & Scanziani, M. (2013) · Nature Neuroscience · doi:10.1038/nn.3446 · Cited by 1,353 · see citing works

Development and Evolution of the Human Neocortex

Lui, J. H., Hansen, D. V., & Kriegstein, A. R. (2011) · Cell · doi:10.1016/j.cell.2011.06.030 · Cited by 1,342 · see citing works

The Blue Brain Project

Markram, H. (2006) · Nature reviews. Neuroscience · doi:10.1038/nrn1848 · Cited by 1,191 · see citing works

Jasper's Basic Mechanisms of the Epilepsies

(2012) · Oxford University Press eBooks · doi:10.1093/med/9780199746545.001.0001 · Cited by 1,157 · see citing works

Neuronal Subtype-Specific Genes that Control Corticospinal Motor Neuron Development In Vivo

Arlotta, P., Molyneaux, B. J., Chen, J., Inoue, J., Kominami, R., & Macklis, J. D. (2005) · Neuron · doi:10.1016/j.neuron.2004.12.036 · Cited by 1,157 · see citing works

Cortical interneurons that specialize in disinhibitory control

Pi, H.-J., Hangya, B., Kvitsiani, D., Sanders, J. I., Huang, Z. J., & Kepecs, A. (2013) · Nature · doi:10.1038/nature12676 · Cited by 1,136 · see citing works

Interneuron cell types are fit to function

Kepecs, A., & Fishell, G. (2014) · Nature · doi:10.1038/nature12983 · Cited by 1,110 · see citing works

A long, remarkable journey: Tangential migration in the telencephalon

Marín, Ó., & Rubenstein, J. L. R. (2001) · Nature reviews. Neuroscience · doi:10.1038/35097509 · Cited by 1,050 · see citing works

Neurons arise in the basal neuroepithelium of the early mammalian telencephalon: A major site of neurogenesis

Haubensak, W. E., Attardo, A., Denk, W. T., & Huttner, W. Β. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0308600100 · Cited by 1,004 · see citing works

A Cortical Circuit for Gain Control by Behavioral State

Fu, Y., Tucciarone, J. M., Espinosa, J. S., Sheng, N., Darcy, D. P., Nicoll, R. A., Huang, Z. J., & Stryker, M. P. (2014) · Cell · doi:10.1016/j.cell.2014.01.050 · Cited by 937 · see citing works

Biological Pattern Generation: The Cellular and Computational Logic of Networks in Motion

Grillner, S. E. (2006) · Neuron · doi:10.1016/j.neuron.2006.11.008 · Cited by 920 · see citing works

Molecular logic of neocortical projection neuron specification, development and diversity

Greig, L. C., Woodworth, M. B., Galazo, M. J., Padmanabhan, H., & Macklis, J. D. (2013) · Nature Reviews Neuroscience · doi:10.1038/nrn3586 · Cited by 863 · see citing works

Salient features of synaptic organisation in the cerebral cortex1Published on the World Wide Web on 3 March 1998.1

Somogyi, P., Tamás, G., Luján, R., & Buhl, E. H. (1998) · Brain Research Reviews · doi:10.1016/s0165-0173(97)00061-1 · Cited by 860 · see citing works

The motor infrastructure: from ion channels to neuronal networks

Grillner, S. E. (2003) · Nature reviews. Neuroscience · doi:10.1038/nrn1137 · Cited by 839 · see citing works

New insights into the classification and nomenclature of cortical GABAergic interneurons

DeFelipe, J., López-Cruz, P. L., Benavides-Piccione, R., Bielza, C., Larrañaga, P., Anderson, S., Burkhalter, A., Cauli, B., Fairén, A., Feldmeyer, D., et al. (2013) · Nature Reviews Neuroscience · doi:10.1038/nrn3444 · Cited by 833 · see citing works

Circuits controlling vertebrate locomotion: moving in a new direction

Goulding, M. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2608 · Cited by 777 · see citing works

Three-Dimensional Reconstruction of Brain-wide Wiring Networks in Drosophila at Single-Cell Resolution

Chiang, A.-S., Lin, C.-Y., Chuang, C.-C., Chang, H.-M., Hsieh, C.-H., Yeh, C.-W., Shih, C.-T., Wu, J.-J., Wang, G.-T., Chen, Y.-C., et al. (2011) · Current Biology · doi:10.1016/j.cub.2010.11.056 · Cited by 767 · see citing works

A disinhibitory circuit mediates motor integration in the somatosensory cortex

Lee, S., Kruglikov, I., Huang, Z. J., Fishell, G., & Rudy, B. (2013) · Nature Neuroscience · doi:10.1038/nn.3544 · Cited by 758 · see citing works

Patterns of neural stem and progenitor cell division may underlie evolutionary cortical expansion

Kriegstein, A., Noctor, S., & Martínez-Cerdeño, V. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn2008 · Cited by 738 · see citing works

Permanent genetic access to transiently active neurons via TRAP: targeted recombination in active populations

Guenthner, C. J., Miyamichi, K., Yang, H. H., Heller, H. C., & Luo, L. (2013) · Neuron · doi:10.1016/j.neuron.2013.03.025 · Cited by 705 · see citing works

A neural circuit for spatial summation in visual cortex

Adesnik, H., Bruns, W., Taniguchi, H., Huang, Z. J., & Scanziani, M. (2012) · Nature · doi:10.1038/nature11526 · Cited by 702 · see citing works

Developmental genetics of vertebrate glial–cell specification

Rowitch, D., & Kriegstein, A. (2010) · Nature · doi:10.1038/nature09611 · Cited by 685 · see citing works

BEHAVIORAL MUTANTS OF Drosophila ISOLATED BY COUNTERCURRENT DISTRIBUTION

Benzer, S. (1967) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.58.3.1112 · Cited by 679 · see citing works

Patterning and plasticity of the cerebral cortex

Sur, M., & Rubenstein, J. L. R. (2005) · Science · doi:10.1126/science.1112070 · Cited by 677 · see citing works

GENSAT BAC cre-recombinase driver lines to study the functional organization of cerebral cortical and basal ganglia circuits

Gerfen, C. R., Paletzki, R., & Heintz, N. (2013) · Neuron · doi:10.1016/j.neuron.2013.10.016 · Cited by 647 · see citing works

Excitatory cortical neurons form fine-scale functional networks

Yoshimura, Y., Dantzker, J. L. M., & Callaway, E. M. (2005) · Nature · doi:10.1038/nature03252 · Cited by 601 · see citing works

The largest group of superficial neocortical GABAergic interneurons expresses ionotropic serotonin receptors

Lee, S., Hjerling-Leffler, J., Zagha, E., Fishell, G., & Rudy, B. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.1869-10.2010 · Cited by 600 · see citing works

Area Patterning of the Mammalian Cortex

O’Leary, D. D. M., Chou, S., & Sahara, S. (2007) · Neuron · doi:10.1016/j.neuron.2007.10.010 · Cited by 574 · see citing works

Fate mapping Nkx2.1‐lineage cells in the mouse telencephalon

Xu, Q., Tam, M., & Anderson, S. A. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21529 · Cited by 560 · see citing works

Delineation of multiple subpallial progenitor domains by the combinatorial expression of transcriptional codes

Flames, N., Pla, R., Gelman, D. M., Rubenstein, J. L. R., Puelles, L., & Marín, O. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.2750-07.2007 · Cited by 560 · see citing works

The caudal ganglionic eminence is a source of distinct cortical and subcortical cell populations

Nery, S., Fishell, G., & Corbin, J. G. (2002) · Nature Neuroscience · doi:10.1038/nn971 · Cited by 558 · see citing works

Targeting cells with single vectors using multiple-feature Boolean logic

Fenno, L. E., Mattis, J., Ramakrishnan, C., Hyun, M., Lee, S. Y., He, M., Tucciarone, J., Selimbeyoglu, A., Berndt, A., Grosenick, L., et al. (2014) · Nature Methods · doi:10.1038/nmeth.2996 · Cited by 557 · see citing works

A specific ‘axo-axonal’ interneuron in the visual cortex of the rat

Somogyi, P. (1977) · Brain Research · doi:10.1016/0006-8993(77)90808-3 · Cited by 530 · see citing works

Interneuron Diversity series: Circuit complexity and axon wiring economy of cortical interneurons

Buzsáki, G., Geisler, C. E., Henze, D. A., & Wang, X. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.02.007 · Cited by 483 · see citing works

Precursor Diversity and Complexity of Lineage Relationships in the Outer Subventricular Zone of the Primate

Betizeau, M., Cortay, V., Patti, D., Pfister, S., Gautier, E., Bellemin-Ménard, A., Afanassieff, M., Huissoud, C., Douglas, R. J., Kennedy, H., et al. (2013) · Neuron · doi:10.1016/j.neuron.2013.09.032 · Cited by 462 · see citing works

Immunochemical characterization of inhibitory mouse cortical neurons: Three chemically distinct classes of inhibitory cells

Xu, X., Roby, K. D., & Callaway, E. M. (2010) · Journal of Comparative Neurology · doi:10.1002/cne.22229 · Cited by 429 · see citing works

Spatial genetic patterning of the embryonic neuroepithelium generates GABAergic interneuron diversity in the adult cortex

Fogarty, M., Grist, M., Gelman, D., Marín, O., Pachnis, V., & Kessaris, N. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.1629-07.2007 · Cited by 412 · see citing works

Physiologically Distinct Temporal Cohorts of Cortical Interneurons Arise from Telencephalic <i>Olig2</i> -Expressing Precursors

Miyoshi, G., Butt, S. J. B., Takebayashi, H., & Fishell, G. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.1807-07.2007 · Cited by 400 · see citing works

Development, specification, and diversity of callosal projection neurons

Fame, R. M., MacDonald, J. L., & Macklis, J. D. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2010.10.002 · Cited by 381 · see citing works

Measured motion: searching for simplicity in spinal locomotor networks

Grillner, S. E., & Jessell, T. M. (2009) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2009.10.011 · Cited by 380 · see citing works

The genetics of early telencephalon patterning: some assembly required

Hébert, J. M., & Fishell, G. (2008) · Nature reviews. Neuroscience · doi:10.1038/nrn2463 · Cited by 377 · see citing works

Multiple distinct subtypes of GABAergic neurons in mouse visual cortex identified by triple immunostaining

Gonchar, Y. (2008) · Frontiers in Neuroanatomy · doi:10.3389/neuro.05.003.2007 · Cited by 369 · see citing works

Neocortical Somatostatin-Expressing GABAergic Interneurons Disinhibit the Thalamorecipient Layer 4

Xu, H., Jeong, H.-Y., Tremblay, R., & Rudy, B. (2013) · Neuron · doi:10.1016/j.neuron.2012.11.004 · Cited by 366 · see citing works

Temporal fate specification and neural progenitor competence during development

Kohwi, M., & Doe, C. Q. (2013) · Nature reviews. Neuroscience · doi:10.1038/nrn3618 · Cited by 366 · see citing works

Intracortical circuits of pyramidal neurons reflect their long-range axonal targets

Brown, S. P., & Hestrin, S. (2009) · Nature · doi:10.1038/nature07658 · Cited by 357 · see citing works

Physiology of the Nervous System

Fulton, J. F. (1939) · Science · doi:10.1126/science.90.2327.110.a · Cited by 355 · see citing works

SnapShot: spinal cord development

Alaynick, W. A., Jessell, T. M., & Pfaff, S. L. (2011) · Cell · doi:10.1016/j.cell.2011.06.038 · Cited by 338 · see citing works

Fate-Restricted Neural Progenitors in the Mammalian Cerebral Cortex

Franco, S. J., Gil, C., Martínez‐Garay, I., Espinosa, A., Harkins-Perry, S. R., Ramos, C., & Müller, U. (2012) · Science · doi:10.1126/science.1223616 · Cited by 334 · see citing works

Motor Circuits in Action: Specification, Connectivity, and Function

Arber, S. (2012) · Neuron · doi:10.1016/j.neuron.2012.05.011 · Cited by 303 · see citing works

Genetic Dissection of the Drosophila Nervous System by Means of Mosaics

Hotta, Y., & Benzer, S. (1970) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.67.3.1156 · Cited by 293 · see citing works

A Blueprint for the Spatiotemporal Origins of Mouse Hippocampal Interneuron Diversity

Tricoire, L., Pelkey, K. A., Erkkila, B. E., Jeffries, B. W., Yuan, X., & McBain, C. J. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.0323-11.2011 · Cited by 292 · see citing works

In VivoLabeling of Parvalbumin-Positive Interneurons and Analysis of Electrical Coupling in Identified Neurons

Meyer, A. H., Katona, I., Blatow, M., Rozov, A. V., & Monyer, H. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-16-07055.2002 · Cited by 286 · see citing works

Development of GABA innervation in the cerebral and cerebellar cortices

Huang, Z. J., Cristo, G. D., & Ango, F. (2007) · Nature reviews. Neuroscience · doi:10.1038/nrn2188 · Cited by 281 · see citing works

The spatial and temporal origin of chandelier cells in mouse neocortex

Taniguchi, H., Lu, J., & Huang, Z. J. (2013) · Science · doi:10.1126/science.1227622 · Cited by 278 · see citing works

The Subthalamic Nucleus Is One of Multiple Innervation Sites for Long-Range Corticofugal Axons: A Single-Axon Tracing Study in the Rat

Kita, T., & Kita, H. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.5717-11.2012 · Cited by 276 · see citing works

Decision by division: making cortical maps

RAKIC, P. T., Ayoub, A. E., Breunig, J. J., & Dominguez, M. H. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2009.01.007 · Cited by 272 · see citing works

Interneuron Diversity series: Fast in, fast out – temporal and spatial signal processing in hippocampal interneurons

Jónás, P., Bischofberger, J., Fricker, D., & Miles, R. (2003) · Trends in Neurosciences · doi:10.1016/j.tins.2003.10.010 · Cited by 266 · see citing works

A High-Resolution Enhancer Atlas of the Developing Telencephalon

Visel, A., Taher, L., Girgis, H., May, D., Golonzhka, O., Hoch, R. V., McKinsey, G. L., Pattabiraman, K., Silberberg, S. N., Blow, M. J., et al. (2013) · Cell · doi:10.1016/j.cell.2012.12.041 · Cited by 257 · see citing works

The Magnificent Compromise: Cortical Field Evolution in Mammals

Krubitzer, L. A. (2007) · Neuron · doi:10.1016/j.neuron.2007.10.002 · Cited by 256 · see citing works

Alteration of Neuronal Firing Properties afterIn VivoExperience in a FosGFP Transgenic Mouse

Barth, A. L., Gerkin, R. C., & Dean, K. L. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.4737-03.2004 · Cited by 255 · see citing works

Developmental origins of central norepinephrine neuron diversity

Robertson, S. D., Plummer, N. W., de Marchena, J., & Jensen, P. (2013) · Nature Neuroscience · doi:10.1038/nn.3458 · Cited by 249 · see citing works

Sequences and consequences

Brenner, S. (2010) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2009.0221 · Cited by 244 · see citing works

Contributions of the 12 Neuron Classes in the Fly Lamina to Motion Vision

Tuthill, J. C., Nern, A., Holtz, S. L., Rubin, G. M., & Reiser, M. B. (2013) · Neuron · doi:10.1016/j.neuron.2013.05.024 · Cited by 239 · see citing works

Synaptic Computation and Sensory Processing in Neocortical Layer 2/3

Petersen, C. C. H., & Crochet, S. (2013) · Neuron · doi:10.1016/j.neuron.2013.03.020 · Cited by 239 · see citing works

Selective Coexpression of Multiple Chemical Markers Defines Discrete Populations of Neocortical GABAergic Neurons

Kubota, Y., Shigematsu, N., Karube, F., Sekigawa, A., Kato, S., Yamaguchi, N., Hirai, Y., Morishima, M., & Kawaguchi, Y. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhq252 · Cited by 235 · see citing works

Mechanisms of Inhibition within the Telencephalon: “Where the Wild Things Are”

Fishell, G., & Rudy, B. (2011) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-061010-113717 · Cited by 233 · see citing works

Demonstration of long‐range GABAergic connections distributed throughout the mouse neocortex

Tomioka, R., Okamoto, K., Furuta, T., Fujiyama, F., Iwasato, T., Yanagawa, Y., Obata, K., Kaneko, T., & Tamamaki, N. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.03989.x · Cited by 223 · see citing works

Role of emergent neural activity in visual map development

Ackman, J. B., & Crair, M. C. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.11.011 · Cited by 219 · see citing works

Mapping the face in the somatosensory brainstem

Erzurumlu, R., Murakami, Y., & Rijli, F. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2804 · Cited by 213 · see citing works

Genetic Approaches to Neural Circuits in the Mouse

Josh Huang, Z., & Zeng, H. (2013) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062012-170307 · Cited by 200 · see citing works

Novel Subtype-Specific Genes Identify Distinct Subpopulations of Callosal Projection Neurons

Molyneaux, B. J., Arlotta, P., Fame, R. M., MacDonald, J. L., MacQuarrie, K. L., & Macklis, J. D. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.6108-08.2009 · Cited by 198 · see citing works

Expression from a Dlx Gene Enhancer Marks Adult Mouse Cortical GABAergic Neurons

Stühmer, T. (2002) · Cerebral Cortex · doi:10.1093/cercor/12.1.75 · Cited by 198 · see citing works

Structural neurobiology: missing link to a mechanistic understanding of neural computation

Denk, W. T., Briggman, K. L., & Helmstaedter, M. N. (2012) · Nature reviews. Neuroscience · doi:10.1038/nrn3169 · Cited by 192 · see citing works

Microcircuits in action – from CPGs to neocortex

Grillner, S. E., Markram, H., Schutter, E. D., Silberberg, G., & LeBeau, F. E. N. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2005.08.003 · Cited by 187 · see citing works

Integration of GABAergic interneurons into cortical cell assemblies: lessons from embryos and adults

Bartolini, G., Ciceri, G., & Marín, O. (2013) · Neuron · doi:10.1016/j.neuron.2013.08.014 · Cited by 185 · see citing works

The Role of Organizers in Patterning the Nervous System

Kiecker, C. M., & Lumsden, A. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062111-150543 · Cited by 185 · see citing works

Hierarchical Connectivity and Connection-Specific Dynamics in the Corticospinal–Corticostriatal Microcircuit in Mouse Motor Cortex

Kiritani, T., Wickersham, I. R., Seung, H. S., & Shepherd, G. M. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.4759-11.2012 · Cited by 184 · see citing works

Dlx1&amp;2 and Mash1 Transcription Factors Control MGE and CGE Patterning and Differentiation through Parallel and Overlapping Pathways

Long, J. E., Cobos, I., Potter, G. B., & Rubenstein, J. L. R. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp045 · Cited by 178 · see citing works

Membrane Potential Dynamics of Neocortical Projection Neurons Driving Target-Specific Signals

Yamashita, T., Pala, A., Pedrido, L., Kremer, Y., Welker, E., & Petersen, C. C. H. (2013) · Neuron · doi:10.1016/j.neuron.2013.10.059 · Cited by 172 · see citing works

Fezf2 Expression Identifies a Multipotent Progenitor for Neocortical Projection Neurons, Astrocytes, and Oligodendrocytes

Guo, C., Eckler, M. J., McKenna, W. L., McKinsey, G. L., Rubenstein, J. L. R., & Chen, B. (2013) · Neuron · doi:10.1016/j.neuron.2013.09.037 · Cited by 170 · see citing works

Clonal Development and Organization of the Adult Drosophila Central Brain

Yu, H.-H., Awasaki, T., Schroeder, M. D., Long, F., Yang, J. S., He, Y., Ding, P., Kao, J.-C., Wu, G. Y.-Y., Peng, H., et al. (2013) · Current Biology · doi:10.1016/j.cub.2013.02.057 · Cited by 163 · see citing works

Cell-Type Specific Properties of Pyramidal Neurons in Neocortex Underlying a Layout that Is Modifiable Depending on the Cortical Area

Groh, A., Meyer, H. S., Schmidt, E. F., Heintz, N., Sakmann, B. J., & Krieger, P. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp152 · Cited by 162 · see citing works

Spatial and temporal bias in the mitotic origins of somatostatin- and parvalbumin-expressing interneuron subgroups and the chandelier subtype in the medial ganglionic eminence

Inan, M., Welagen, J., & Anderson, S. A. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr148 · Cited by 161 · see citing works

Twin-spot MARCM to reveal the developmental origin and identity of neurons

Yu, H., Chen, C., Shi, L., Huang, Y., & Lee, T. (2009) · Nature Neuroscience · doi:10.1038/nn.2345 · Cited by 159 · see citing works

Temporal redistribution of inhibition over neuronal subcellular domains underlies state-dependent rhythmic change of excitability in the hippocampus

Somogyi, P., Katona, L., Klausberger, T., Lasztóczi, B., & Viney, T. J. (2013) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2012.0518 · Cited by 158 · see citing works

Clonal production and organization of inhibitory interneurons in the neocortex

Brown, K. N., Chen, S., Han, Z., Lu, C.-H., Tan, X., Zhang, X.-J., Ding, L., Lopez-Cruz, A., Saur, D., Anderson, S. A., et al. (2011) · Science · doi:10.1126/science.1208884 · Cited by 152 · see citing works

Laminar and Columnar Development of Barrel Cortex Relies on Thalamocortical Neurotransmission

Li, H., Fertuzinhos, S., Mohns, E. J., Hnasko, T. S., Verhage, M., Edwards, R. H., Šestan, N., & Crair, M. C. (2013) · Neuron · doi:10.1016/j.neuron.2013.06.043 · Cited by 150 · see citing works

Ascl1 genetics reveals insights into cerebellum local circuit assembly

Sudarov, A., Turnbull, R. K., Kim, E. J., Lebel-Potter, M., Guillemot, F., & Joyner, A. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.0479-11.2011 · Cited by 148 · see citing works

A Complete Developmental Sequence of a Drosophila Neuronal Lineage as Revealed by Twin-Spot MARCM

Yu, H.-H., Kao, C.-F., He, Y., Ding, P., Kao, J.-C., & Lee, T. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000461 · Cited by 146 · see citing works

Reverse engineering the mouse brain

O’Connor, D. H., Huber, D., & Svoboda, K. (2009) · Nature · doi:10.1038/nature08539 · Cited by 137 · see citing works

Linking Genetically Defined Neurons to Behavior through a Broadly Applicable Silencing Allele

Kim, J. C., Cook, M. N., Carey, M. R., Shen, C., Regehr, W. G., & Dymecki, S. M. (2009) · Neuron · doi:10.1016/j.neuron.2009.07.010 · Cited by 134 · see citing works

Correlated gene expression and target specificity demonstrate excitatory projection neuron diversity

Sorensen, S. A., Bernard, A., Menon, V., Royall, J. J., Glattfelder, K. J., Desta, T., Hirokawa, K., Mortrud, M., Miller, J. A., Zeng, H., et al. (2015) · Cerebral Cortex · doi:10.1093/cercor/bht243 · Cited by 131 · see citing works

Three-dimensional axon morphologies of individual layer 5 neurons indicate cell type-specific intracortical pathways for whisker motion and touch

Oberlaender, M., Boudewijns, Z. S. R. M., Kleele, T., Mansvelder, H. D., Sakmann, B. J., & de Kock, C. P. J. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1100647108 · Cited by 128 · see citing works

Textura del sistema nervioso del hombre y de los vertebrados : estudios sobre el plan estructural y composición histológica de los centros nerviosos adicionados de consideraciones fisiológicas fundadas en los nuevos descubrimientos. Volumen III

y Cajal, S. R. (1904) · Institutional Repository of the University of Granada (University of Granada) · Cited by 127 · see citing works

Genetic programs controlling cortical interneuron fate

Kessaris, N., Magno, L., Rubin, A. N., & Oliveira, M. G. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.12.012 · Cited by 122 · see citing works

A Cortico-Hippocampal Learning Rule Shapes Inhibitory Microcircuit Activity to Enhance Hippocampal Information Flow

Basu, J., Srinivas, K. V., Cheung, S. K., Taniguchi, H., Huang, Z. J., & Siegelbaum, S. A. (2013) · Neuron · doi:10.1016/j.neuron.2013.07.001 · Cited by 122 · see citing works

Twenty-five years of cell cycle genetics.

Hartwell, L. H. (1991) · Genetics · doi:10.1093/genetics/129.4.975 · Cited by 108 · see citing works

Sonic hedgehog functions through dynamic changes in temporal competence in the developing forebrain

Sousa, V. H., & Fishell, G. (2010) · Current Opinion in Genetics &amp; Development · doi:10.1016/j.gde.2010.04.008 · Cited by 106 · see citing works

Motor-Circuit Communication Matrix from Spinal Cord to Brainstem Neurons Revealed by Developmental Origin

Pivetta, C., Esposito, M. S., Sigrist, M., & Arber, S. (2014) · Cell · doi:10.1016/j.cell.2013.12.014 · Cited by 106 · see citing works

Transcriptional Regulation of Enhancers Active in Protodomains of the Developing Cerebral Cortex

Pattabiraman, K., Golonzhka, O., Lindtner, S., Nord, A. S., Taher, L., Hoch, R. V., Silberberg, S. N., Zhang, D., Chen, B., Zeng, H., et al. (2014) · Neuron · doi:10.1016/j.neuron.2014.04.014 · Cited by 99 · see citing works

Characterization of Type I and Type II nNOS-Expressing Interneurons in the Barrel Cortex of Mouse

Perrenoud, Q., Geoffroy, H., Gauthier, B., Rancillac, A., Alfonsi, F., Kessaris, N., Rossier, J., Vitalis, T., & Gallopin, T. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00036 · Cited by 99 · see citing works

Unsere Korperform Und Das Physiologische Problem Ihrer Entstehung: Briefe an Einen Befreundeten Naturforscher

His, W. (2011) · doi:10.5962/bhl.title.28860 · Cited by 98 · see citing works

Anatomy of the soul as reflected in the cerebral hemispheres: Neural circuits underlying voluntary control of basic motivated behaviors

Swanson, L. W. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20733 · Cited by 98 · see citing works

Reconstruction of an average cortical column in silico

Helmstaedter, M. N., de Kock, C. P. J., Feldmeyer, D., Bruno, R. M., & Sakmann, B. J. (2007) · Brain Research Reviews · doi:10.1016/j.brainresrev.2007.07.011 · Cited by 85 · see citing works

Motor Neurons and the Sense of Place

Jessell, T. M., Sürmeli, G., & Kelly, J. S. (2011) · Neuron · doi:10.1016/j.neuron.2011.10.021 · Cited by 74 · see citing works

Specialized Cortical Subnetworks Differentially Connect Frontal Cortex to Parahippocampal Areas

Hirai, Y., Morishima, M., Karube, F., & Kawaguchi, Y. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.2810-11.2012 · Cited by 73 · see citing works

Chondroitin sulfate proteoglycan expression pattern in hippocampal development: Potential regulation of axon tract formation

Wilson, M. T., & Snow, D. M. (2000) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20000828)424:3 · Cited by 72 · see citing works

SnapShot: Cortical Development

Woodworth, M. B., Greig, L. C., Kriegstein, A. R., & Macklis, J. D. (2012) · Cell · doi:10.1016/j.cell.2012.10.004 · Cited by 71 · see citing works

Linking Cell Fate, Trajectory Choice, and Target Selection: Genetic Analysis of Sema-2b in Olfactory Axon Targeting

Joo, W. J., Sweeney, L. B., Liang, L., & Luo, L. (2013) · Neuron · doi:10.1016/j.neuron.2013.03.022 · Cited by 58 · see citing works

Patterning and Cell Type Specification in the Developing CNS and PNS

Rubenstein, J. L. R., & RAKIC, P. T. (2013) · Elsevier eBooks · doi:10.1016/c2011-0-07685-8 · Cited by 56 · see citing works

The (Not Necessarily) Convoluted Role of Basal Radial Glia in Cortical Neurogenesis

Hevner, R. F., & Haydar, T. F. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr336 · Cited by 56 · see citing works

Generating neuronal diversity in the Drosophila central nervous system

Lin, S., & Lee, T. (2011) · Developmental Dynamics · doi:10.1002/dvdy.22739 · Cited by 53 · see citing works

Edging toward Entelechy in Motor Control

Miri, A., Azim, E., & Jessell, T. M. (2013) · Neuron · doi:10.1016/j.neuron.2013.10.049 · Cited by 31 · see citing works

Megascience Efforts and the Brain

Grillner, S. (2014) · Neuron · doi:10.1016/j.neuron.2014.05.045 · Cited by 31 · see citing works

The Generation of Cortical Interneurons

Gelman, D. M., Marín, Ó., & Rubenstein, J. L. R. (2012) · Oxford University Press eBooks · doi:10.1093/med/9780199746545.003.0061 · Cited by 28 · see citing works

Untangling the cortex: Advances in understanding specification and differentiation of corticospinal motor neurons

Shoemaker, L. D., & Arlotta, P. (2010) · BioEssays · doi:10.1002/bies.200900114 · Cited by 25 · see citing works

The generation of cortical interneurons

Rubenstein, J. L. R. (2010) · Epilepsia · doi:10.1111/j.1528-1167.2010.02854.x · Cited by 24 · see citing works

Behavioral architecture of the cortical sheet

Douglas, R. J., & Martin, K. A. C. (2012) · Current Biology · doi:10.1016/j.cub.2012.11.017 · Cited by 23 · see citing works

Morphogens, Patterning Centers, and their Mechanisms of Action

Grove, E. A., & Monuki, E. S. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397265-1.00019-8 · Cited by 16 · see citing works

Genetic Labeling of Neuronal Subsets through Enhancer Trapping in Mice

Kelsch, W., Stolfi, A., & Lois, C. (2012) · PLoS ONE · doi:10.1371/journal.pone.0038593 · Cited by 13 · see citing works

The Generation of Cortical Interneurons

Batista‐Brito, R., & Fishell, G. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397265-1.00071-x · Cited by 8 · see citing works

GABAergic Interneurons in the Neocortex: From Cellular Properties to Circuits

Tremblay, R., Lee, S., & Rudy, B. (2016) · Neuron · doi:10.1016/j.neuron.2016.06.033 · Cited by 2,033 · see citing works

Adult mouse cortical cell taxonomy revealed by single cell transcriptomics

Tasic, B., Menon, V., Nguyen, T. N., Kim, T. K., Jarsky, T., Yao, Z., Levi, B., Gray, L. T., Sorensen, S. A., Dolbeare, T., et al. (2016) · Nature Neuroscience · doi:10.1038/nn.4216 · Cited by 1,714 · see citing works

The neocortical circuit: themes and variations

Harris, K. D., & Shepherd, G. M. G. (2015) · Nature Neuroscience · doi:10.1038/nn.3917 · Cited by 1,215 · see citing works

Architectonic Mapping of the Human Brain beyond Brodmann

Amunts, K., & Zilles, K. (2015) · Neuron · doi:10.1016/j.neuron.2015.12.001 · Cited by 533 · see citing works

Transcriptional Architecture of Synaptic Communication Delineates GABAergic Neuron Identity

Paul, A., Crow, M., Raudales, R., He, M., Gillis, J., & Huang, Z. J. (2017) · Cell · doi:10.1016/j.cell.2017.08.032 · Cited by 421 · see citing works

Astrocytes, neurons, synapses: a tripartite view on cortical circuit development

Farhy-Tselnicker, I., & Allen, N. J. (2018) · Neural Development · doi:10.1186/s13064-018-0104-y · Cited by 396 · see citing works

Closed-Loop and Activity-Guided Optogenetic Control

Grosenick, L., Marshel, J. H., & Deisseroth, K. A. (2015) · Neuron · doi:10.1016/j.neuron.2015.03.034 · Cited by 384 · see citing works

High-throughput mapping of single-neuron projections by sequencing of barcoded RNA

Kebschull, J. M., Garcia da Silva, P., Reid, A. P., Peikon, I. D., Albeanu, D. F., & Zador, A. M. (2016) · Neuron · doi:10.1016/j.neuron.2016.07.036 · Cited by 376 · see citing works

High-throughput dual-colour precision imaging for brain-wide connectome with cytoarchitectonic landmarks at the cellular level

Gong, H., Xu, D., Yuan, J., Li, X., Guo, C., Peng, J., Li, Y., Schwarz, L. A., Li, A., Hu, B., et al. (2016) · Nature Communications · doi:10.1038/ncomms12142 · Cited by 368 · see citing works

Strategies and Tools for Combinatorial Targeting of GABAergic Neurons in Mouse Cerebral Cortex

He, M., Tucciarone, J., Lee, S., Nigro, M. J., Kim, Y., Levine, J. M., Kelly, S. M., Krugikov, I., Wu, P., Chen, Y., et al. (2016) · Neuron · doi:10.1016/j.neuron.2016.08.021 · Cited by 339 · see citing works

The diversity of GABAergic neurons and neural communication elements

Huang, Z. J., & Paul, A. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0195-4 · Cited by 201 · see citing works

Whole-Brain Profiling of Cells and Circuits in Mammals by Tissue Clearing and Light-Sheet Microscopy

Ueda, H. R., Dodt, H., Osten, P., Economo, M. N., Chandrashekar, J. V., & Keller, P. (2020) · Neuron · doi:10.1016/j.neuron.2020.03.004 · Cited by 223 · see citing works

An atlas of gene regulatory elements in adult mouse cerebrum

Li, Y. E., Preissl, S., Hou, X., Zhang, Z., Zhang, K., Qiu, Y., Poirion, O. B., Li, B., Chiou, J., Liu, H., et al. (2021) · Nature · doi:10.1038/s41586-021-03604-1 · Cited by 185 · see citing works

Neuronal circuits in barrel cortex for whisker sensory perception

Staiger, J. F., & Petersen, C. C. H. (2021) · Physiological Reviews · doi:10.1152/physrev.00019.2019 · Cited by 165 · see citing works

Genetic dissection of the glutamatergic neuron system in cerebral cortex

Matho, K. S., Huilgol, D., Galbavy, W., He, M., Kim, G., An, X., Lu, J., Wu, P., Di Bella, D. J., Shetty, A. S., et al. (2021) · Nature · doi:10.1038/s41586-021-03955-9 · Cited by 155 · see citing works

Immature excitatory neurons develop during adolescence in the human amygdala

Sorrells, S. F., Paredes, M. F., Velmeshev, D., Herranz‐Pérez, V., Sandoval, K., Mayer, S., Chang, E. F., Insausti, R., Kriegstein, A. R., Rubenstein, J. L. R., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-10765-1 · Cited by 145 · see citing works

Inhibitory Interneurons and their Circuit Motifs in the Many Layers of the Barrel Cortex

Feldmeyer, D., Qi, G., Emmenegger, V., & Staiger, J. F. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.05.027 · Cited by 134 · see citing works

Inhibitory Circuits in Cortical Layer 5

Naka, A., & Adesnik, H. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00035 · Cited by 130 · see citing works

Cortical and Striatal Circuits in Huntington’s Disease

Blumenstock, S., & Dudanova, I. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00082 · Cited by 118 · see citing works

Dynamics of a disinhibitory prefrontal microcircuit in controlling social competition

Zhang, C., Zhu, H. L., Ni, Z., Xin, Q., Zhou, T., Wu, R., Gao, G., Gao, Z., Ma, H., Li, H., et al. (2021) · Neuron · doi:10.1016/j.neuron.2021.10.034 · Cited by 123 · see citing works

Chrna2-Martinotti cells synchronize layer 5 type A pyramidal cells via rebound excitation

Hilscher, M. M., Leão, R. N., Edwards, S. J., Leão, K. E., & Kullander, K. (2017) · PLoS Biology · doi:10.1371/journal.pbio.2001392 · Cited by 118 · see citing works

Selective inhibitory control of pyramidal neuron ensembles and cortical subnetworks by chandelier cells

Lu, J., Tucciarone, J., Padilla-Coreano, N., He, M., Gordon, J. A., & Huang, Z. J. (2017) · Nature Neuroscience · doi:10.1038/nn.4624 · Cited by 118 · see citing works

Expanding the power of recombinase-based labeling to uncover cellular diversity

Plummer, N. W., Evsyukova, I. Y., Robertson, S. D., de Marchena, J., Tucker, C. J., & Jensen, P. (2015) · Development · doi:10.1242/dev.129981 · Cited by 108 · see citing works

Area-specific development of distinct projection neuron subclasses is regulated by postnatal epigenetic modifications

Harb, K., Magrinelli, E., Nicolas, C. S., Lukianets, N., Frangeul, L., Piétri, M., Sun, T., Sandoz, G., Grammont, F., Jabaudon, D., et al. (2016) · eLife · doi:10.7554/elife.09531 · Cited by 109 · see citing works

“Braking” the Prefrontal Cortex: The Role of Glucocorticoids and Interneurons in Stress Adaptation and Pathology

McKlveen, J. M., Moloney, R. D., Scheimann, J. R., Myers, B., & Herman, J. P. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2019.04.032 · Cited by 109 · see citing works

Facing the challenge of mammalian neural microcircuits: taking a few breaths may help

Feldman, J. L., & Kam, K. (2014) · The Journal of Physiology · doi:10.1113/jphysiol.2014.277632 · Cited by 97 · see citing works

Optogenetic activation of neocortical neurons in vivo with a sapphire-based micro-scale LED probe

McAlinden, N., Gu, E., Dawson, M. D., Sakata, S., & Mathieson, K. (2015) · Frontiers in Neural Circuits · doi:10.3389/fncir.2015.00025 · Cited by 87 · see citing works

Human pallial MGE-type GABAergic interneuron cell therapy for chronic focal epilepsy

Bershteyn, M., Bröer, S., Parekh, M. B., Maury, Y., Havlicek, S., Kriks, S., Fuentealba, L. C., Lee, S., Zhou, R., Subramanyam, G., et al. (2023) · Cell stem cell · doi:10.1016/j.stem.2023.08.013 · Cited by 75 · see citing works

Cell-type-specific recruitment of GABAergic interneurons in the primary somatosensory cortex by long-range inputs

Naskar, S., Qi, J., Pereira, F., Gerfen, C. R., & Lee, S. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.108774 · Cited by 72 · see citing works

Marked Diversity of Unique Cortical Enhancers Enables Neuron-Specific Tools by Enhancer-Driven Gene Expression

Blankvoort, S., Witter, M. P., Noonan, J., Cotney, J., & Kentros, C. (2018) · Current Biology · doi:10.1016/j.cub.2018.05.015 · Cited by 72 · see citing works

Transcriptomic and anatomic parcellation of 5-HT3AR expressing cortical interneuron subtypes revealed by single-cell RNA sequencing

Frazer, S., Prados, J., Niquille, M., Cadilhac, C., Markopoulos, F., Gomez, L., Tomasello, U., Telley, L., Holtmaat, A., Jabaudon, D., et al. (2017) · Nature Communications · doi:10.1038/ncomms14219 · Cited by 72 · see citing works

Precision in the development of neocortical architecture: From progenitors to cortical networks

Kast, R. J., & Levitt, P. R. (2019) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2019.01.003 · Cited by 70 · see citing works

Channelrhodopsin-Assisted Patching: In Vivo Recording of Genetically and Morphologically Identified Neurons throughout the Brain

Muñoz, W., Tremblay, R., & Rudy, B. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.11.042 · Cited by 65 · see citing works

Conservation and divergence of related neuronal lineages in the Drosophila central brain

Lee, Y.-J., Yang, C.-P., Miyares, R. L., Huang, Y.-F., He, Y., Ren, Q., Chen, H.-M., Kawase, T., Ito, M., Otsuna, H., et al. (2020) · eLife · doi:10.7554/elife.53518 · Cited by 60 · see citing works

Parvalbumin-positive interneurons regulate cortical sensory plasticity in adulthood and development through shared mechanisms

Rupert, D. D., & Shea, S. D. (2022) · Frontiers in Neural Circuits · doi:10.3389/fncir.2022.886629 · Cited by 58 · see citing works

CaMKIIα Promoter-Controlled Circuit Manipulations Target Both Pyramidal Cells and Inhibitory Interneurons in Cortical Networks

Veres, J. M., Andrási, T., Nagy-Pál, P., & Hájos, N. (2023) · eNeuro · doi:10.1523/eneuro.0070-23.2023 · Cited by 58 · see citing works

5-HT6 Receptor: A New Player Controlling the Development of Neural Circuits

Dayer, A. G., Jacobshagen, M., Chaumont‐Dubel, S., & Marin, P. (2015) · ACS Chemical Neuroscience · doi:10.1021/cn500326z · Cited by 58 · see citing works

Neurogliaform cortical interneurons derive from cells in the preoptic area

Niquille, M., Limoni, G., Markopoulos, F., Cadilhac, C., Prados, J., Holtmaat, A., & Dayer, A. (2018) · eLife · doi:10.7554/elife.32017 · Cited by 55 · see citing works

Estrogen receptor alpha is required in GABAergic, but not glutamatergic, neurons to masculinize behavior

Wu, M. V., & Tollkühn, J. (2017) · Hormones and Behavior · doi:10.1016/j.yhbeh.2017.07.001 · Cited by 55 · see citing works

Multiscale Model of Primary Motor Cortex Circuits Predicts in vivo Cell Type-Specific, Behavioral State-Dependent Dynamics

Durá-Bernal, S., Neymotin, S. A., Suter, B. A., Dacre, J., Moreira, J. V. S., Urdapilleta, E., Schiemann, J. M., Duguid, I., Shepherd, G. M., & Lytton, W. W. (2022) · Cell Reports · doi:10.1016/j.celrep.2023.112574 · Cited by 46 · see citing works

Single-axon level morphological analysis of corticofugal projection neurons in mouse barrel field

Guo, C., Peng, J., Zhang, Y., Li, A., Li, Y., Yuan, J., Xu, X., Ren, M., Gong, H., & Chen, S. (2017) · Scientific Reports · doi:10.1038/s41598-017-03000-8 · Cited by 47 · see citing works

Molecular and spatial profiling of the paraventricular nucleus of the thalamus

Gao, C., Gohel, C., Leng, Y., Ma, J., Goldman, D. A., Levine, A. J., & Penzo, M. A. (2023) · eLife · doi:10.7554/elife.81818 · Cited by 45 · see citing works

Rabies Virus Pseudotyped with CVS-N2C Glycoprotein as a Powerful Tool for Retrograde Neuronal Network Tracing

Zhu, X., Lin, K., Liu, Q., Yue, X., Mi, H., Huang, X., He, X., Wu, R., Zheng, D., Wei, D., et al. (2019) · Neuroscience Bulletin · doi:10.1007/s12264-019-00423-3 · Cited by 46 · see citing works

Molecular, spatial and projection diversity of neurons in primary motor cortex revealed by in situ single-cell transcriptomics

Zhang, M., Eichhorn, S. W., Zingg, B., Yao, Z., Zeng, H., Dong, H., & Zhuang, X. (2020) · doi:10.1101/2020.06.04.105700 · Cited by 44 · see citing works

A corticoamygdalar pathway controls reward devaluation and depression using dynamic inhibition code

Yuan, Z., Qi, Z., Wang, R., Cui, Y., An, S., Wu, G., Feng, Q., Lin, R., Dai, R., Li, A., et al. (2023) · Neuron · doi:10.1016/j.neuron.2023.08.022 · Cited by 45 · see citing works

How many markers are needed to robustly determine a cell's type?

Fischer, S., & Gillis, J. A. (2021) · iScience · doi:10.1016/j.isci.2021.103292 · Cited by 43 · see citing works

Genetically encoded fluorescent sensors for imaging neuronal dynamics in vivo

Day‐Cooney, J., Dalangin, R., Zhong, H., & Mao, T. (2022) · Journal of Neurochemistry · doi:10.1111/jnc.15608 · Cited by 42 · see citing works

Intersectional monosynaptic tracing for dissecting subtype-specific organization of GABAergic interneuron inputs

Yetman, M. J., Washburn, E. K., Hyun, J. H., Osakada, F., Hayano, Y., Zeng, H., Callaway, E. M., Kwon, H., & Taniguchi, H. (2019) · Nature Neuroscience · doi:10.1038/s41593-018-0322-y · Cited by 41 · see citing works

The diversity and specificity of functional connectivity across spatial and temporal scales

Engel, T. A., Schölvinck, M. L., & Lewis, C. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118692 · Cited by 39 · see citing works

Cerebral Cortical Circuitry Formation Requires Functional Glycine Receptors

Morelli, G., Ávila, A., Ravanidis, S., Aourz, N., Neve, R. L., Smolders, I. J., Harvey, R. J., Rigo, J., Nguyen, L., & Brône, B. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw025 · Cited by 39 · see citing works

Visible rodent brain-wide networks at single-neuron resolution

Yuan, J., Gong, H., Li, A., Li, X., Chen, S., Zeng, S., & Luo, Q. (2015) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2015.00070 · Cited by 37 · see citing works

Transient Cell-intrinsic Activity Regulates the Migration and Laminar Positioning of Cortical Projection Neurons

Hurni, N., Kolodziejczak, M., Tomasello, U., Badia, J., Jacobshagen, M., Prados, J., & Dayer, A. G. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx059 · Cited by 38 · see citing works

Distribution Patterns of Three Molecularly Defined Classes of GABAergic Neurons Across Columnar Compartments in Mouse Barrel Cortex

Almási, Z., Dávid, C., Witte, M., & Staiger, J. F. (2019) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2019.00045 · Cited by 37 · see citing works

Cortical glutamatergic projection neuron types contribute to distinct functional subnetworks

Mohan, H., An, X., Xu, X. H., Kondo, H., Zhao, S., Matho, K. S., Wang, B., Musall, S., Mitra, P. P., & Huang, Z. J. (2023) · Nature Neuroscience · doi:10.1038/s41593-022-01244-w · Cited by 37 · see citing works

Genetic approaches to access cell types in mammalian nervous systems

He, M., & Huang, Z. J. (2018) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2018.02.003 · Cited by 33 · see citing works

Parallel processing of working memory and temporal information by distinct types of cortical projection neurons

Bae, J. W., Jeong, H., Yoon, Y. J., Bae, C., Lee, H., Paik, S., & Jung, M. W. (2021) · Nature Communications · doi:10.1038/s41467-021-24565-z · Cited by 34 · see citing works

Hyperexcitability of the local cortical circuit in mouse models of tuberous sclerosis complex

Zhao, J.-P., & Yoshii, A. (2019) · Molecular Brain · doi:10.1186/s13041-019-0427-6 · Cited by 33 · see citing works

Multimodal cortical neuronal cell type classification

Mao, X., & Staiger, J. F. (2024) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-024-02923-2 · Cited by 34 · see citing works

Regulation of Synapse Development byVgatDeletion from ErbB4-Positive Interneurons

Lin, T. W., Tan, Z., Barik, A., Yin, D., Brudvik, E., Wang, H., Xiong, W., & Mei, L. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.0669-17.2018 · Cited by 33 · see citing works

Early-life serotonin dysregulation affects the migration and positioning of cortical interneuron subtypes

Frazer, S., Otomo, K., & Dayer, A. G. (2015) · Translational Psychiatry · doi:10.1038/tp.2015.147 · Cited by 32 · see citing works

A platform for stereological quantitative analysis of the brain-wide distribution of type-specific neurons

Zhang, C., Yan, C., Ren, M., Li, A., Quan, T., Gong, H., & Yuan, J. (2017) · Scientific Reports · doi:10.1038/s41598-017-14699-w · Cited by 28 · see citing works

Whole Brain Mapping of Long-Range Direct Input to Glutamatergic and GABAergic Neurons in Motor Cortex

Luo, P., Li, A., Zheng, Y., Han, Y., Tian, J., Xu, Z., Gong, H., & Li, X. (2019) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2019.00044 · Cited by 29 · see citing works

An Atlas of Gene Regulatory Elements in Adult Mouse Cerebrum

Li, Y. E., Preissl, S., Hou, X., Zhang, Z., Zhang, K., Fang, R., Qiu, Y., Poirion, O., Li, B., Liu, H., et al. (2020) · doi:10.1101/2020.05.10.087585 · Cited by 187 · see citing works

In search of a periodic table of the neurons: Axonal‐dendritic circuitry as the organizing principle

Ascoli, G. A., & Wheeler, D. W. (2016) · BioEssays · doi:10.1002/bies.201600067 · Cited by 27 · see citing works

Developmental Markers Expressed in Neocortical Layers Are Differentially Exhibited in Olfactory Cortex

Brunjes, P. C., & Osterberg, S. K. (2015) · PLoS ONE · doi:10.1371/journal.pone.0138541 · Cited by 26 · see citing works

Distinct in vivo Dynamics of Excitatory Synapses Onto Cortical Pyramidal Neurons and Inhibitory Interneurons

Melander, J. B., Nayebi, A., Jongbloets, B. C., Fortin, D. A., Qin, M., Ganguli, S., Mao, T., & Zhong, H. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109972 · Cited by 27 · see citing works

Regional Cellular Environment Shapes Phenotypic Variations of Hippocampal and Neocortical Chandelier Cells

Ishino, Y., Yetman, M. J., Sossi, S. M., Steinecke, A., Hayano, Y., & Taniguchi, H. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0047-17.2017 · Cited by 25 · see citing works

A subpopulation of cortical VIP-expressing interneurons with highly dynamic spines

Georgiou, C., Kehayas, V., Lee, K. S., Brandalise, F., Sahlender, D. A., Blanc, J., Knott, G. W., & Holtmaat, A. J. D. G. (2022) · Communications Biology · doi:10.1038/s42003-022-03278-z · Cited by 23 · see citing works

Altered somatosensory cortex neuronal activity in a rat model of Parkinson's disease and levodopa-induced dyskinesias

Alam, M., Rumpel, R., Jin, X., von Wrangel, C., Tschirner, S. K., Krauss, J. K., Grothe, C., Ratzka, A., & Schwabe, K. (2017) · Experimental Neurology · doi:10.1016/j.expneurol.2017.04.011 · Cited by 23 · see citing works

Ectopic clustering of Cajal–Retzius and subplate cells is an initial pathological feature in Pomgnt2-knockout mice, a model of dystroglycanopathy

Nakagawa, N., Yagi, H., Kato, K., Takematsu, H., & Oka, S. (2015) · Scientific Reports · doi:10.1038/srep11163 · Cited by 22 · see citing works

Neurogenic to Gliogenic Fate Transition Perturbed by Loss of HMGB2

Bronstein, R. D., Kyle, J., Abraham, A. B., & Tsirka, S. E. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00153 · Cited by 22 · see citing works

Genetic dissection of glutamatergic neuron subpopulations and developmental trajectories in the cerebral cortex

Matho, K. S., Huilgol, D., Galbavy, W., He, M., Kim, G., An, X., Lu, J., Wu, P., Di Bella, D. J., Shetty, A. S., et al. (2020) · doi:10.1101/2020.04.22.054064 · Cited by 20 · see citing works

Dissecting executive control circuits with neuron types

Kamigaki, T. (2018) · Neuroscience Research · doi:10.1016/j.neures.2018.07.004 · Cited by 21 · see citing works

A novel technology for in vivo detection of cell type-specific neural connection with AQP1-encoding rAAV2-retro vector and metal-free MRI

Zheng, N., Li, M., Wu, Y., Kaewborisuth, C., Li, Z., Gui, Z., Wu, J., Cai, A., Lin, K., Su, K., et al. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119402 · Cited by 19 · see citing works

Enhancer-Driven Gene Expression (EDGE) enables the generation of cell type specific tools for the analysis of neural circuits

Blankvoort, S., Descamps, L. A. L., & Kentros, C. G. (2020) · Neuroscience Research · doi:10.1016/j.neures.2020.01.009 · Cited by 19 · see citing works

Learning-related congruent and incongruent changes of excitation and inhibition in distinct cortical areas

Esmaeili, V., Oryshchuk, A., Asri, R., Tamura, K., Foustoukos, G., Liu, Y., Guiet, R., Crochet, S., & Petersen, C. C. H. (2022) · PLoS Biology · doi:10.1371/journal.pbio.3001667 · Cited by 19 · see citing works

Vibrissa Sensory Neurons: Linking Distinct Morphology to Specific Physiology and Function

Takatoh, J., Prevosto, V., & Wang, F. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.06.033 · Cited by 18 · see citing works

Molecular expression profiles of morphologically defined hippocampal neuron types: Empirical evidence and relational inferences

White, C. M., Rees, C. L., Wheeler, D. W., Hamilton, D. J., & Ascoli, G. A. (2019) · Hippocampus · doi:10.1002/hipo.23165 · Cited by 20 · see citing works

Advances in Spatial Omics Technologies

Hui, T., Zhou, J., Yao, M., Xie, Y., & Zeng, H. (2025) · Small Methods · doi:10.1002/smtd.202401171 · Cited by 18 · see citing works

Genetic Feedback Regulation of Frontal Cortical Neuronal Ensembles Through Activity-Dependent Arc Expression and Dopaminergic Input

Mastwal, S. S., Cao, V. Y., & Wang, K. H. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00100 · Cited by 15 · see citing works

Dynamics of neocortical networks: connectivity beyond the canonical microcircuit

Luhmann, H. J. (2023) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-023-02830-y · Cited by 17 · see citing works

A cortical circuit for orchestrating oromanual food manipulationPreprint

An, X., Li, Y., Matho, K. S., Mohan, H., Xu, X. H., Whishaw, I. Q., Kepecs, Á., & Huang, Z. J. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.12.03.518964 · Cited by 23 · see citing works

Orderly specification and precise laminar deployment of mouse cortical projection neuron types through intermediate progenitors

Huilgol, D., Levine, J. M., Galbavy, W., Wang, B., & Huang, Z. J. (2025) · Developmental Cell · doi:10.1016/j.devcel.2025.02.009 · Cited by 15 · see citing works

Excitatory and Inhibitory Synaptic Placement and Functional Implications

Villa, K. L., & Nedivi, E. (2016) · Springer eBooks · doi:10.1007/978-4-431-56050-0_18 · Cited by 15 · see citing works

DeepBouton: Automated Identification of Single-Neuron Axonal Boutons at the Brain-Wide Scale

Cheng, S., Wang, X., Liu, Y., Su, L., Quan, T., Li, N., Yin, F.-F., Xiong, F., Liu, X., Luo, Q., et al. (2019) · Frontiers in Neuroinformatics · doi:10.3389/fninf.2019.00025 · Cited by 15 · see citing works

Cxcr4 and Ackr3 regulate allocation of caudal ganglionic eminence-derived interneurons to superficial cortical layers

Venkataramanappa, S., Saaber, F., Abe, P., Schütz, D., Kumar, P. A., & Stumm, R. K. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111157 · Cited by 14 · see citing works

Multiscale dynamics and information flow in a data-driven model of the primary motor cortex microcircuitPreprint

Durá-Bernal, S., Neymotin, S. A., Suter, B. A., Shepherd, G. M., & Lytton, W. W. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/201707 · Cited by 11 · see citing works

Visual Attention to Features and Space in Mice Using Reverse Correlation

Lehnert, J., Cha, K., Halperin, J., Yang, K., Zheng, D. F., Khadra, A., Cook, E. P., & Krishnaswamy, A. (2022) · Current Biology · doi:10.1016/j.cub.2023.07.060 · Cited by 11 · see citing works

Pinpointing Morphology and Projection of Excitatory Neurons in Mouse Visual Cortex

Zhang, Y., Jiang, S., Xu, Z., Gong, H., Li, A., Luo, Q., Ren, M., Li, X., Wu, H., Yuan, J., et al. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00912 · Cited by 10 · see citing works

Multipotent radial glia sequentially deploy fate-restricted intermediate progenitors to diversify cortical interneuronsPreprint

Kelly, S. M., Raudales, R., Moissidis, M., & Huang, Z. J. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/735019 · Cited by 9 · see citing works

Dissection of the long-range circuit of the mouse intermediate retrosplenial cortex

Li, Y., Ren, M., Liu, B., Jiang, T., Jia, X., Zhang, H., Gong, H., & Wang, X. (2025) · Communications Biology · doi:10.1038/s42003-025-07463-8 · Cited by 9 · see citing works

GABAergic Retinal Ganglion Cells Projecting to the Superior Colliculus Mediate the Looming-Evoked Flight Response

Yuan, M., Tan, G., Cai, D., Luo, X. G., Shen, K., Deng, Q., Lei, X., Zeng, W., Luo, M., Huang, L., et al. (2024) · Neuroscience Bulletin · doi:10.1007/s12264-024-01295-y · Cited by 8 · see citing works

Differential regulation of pruritic sensation and emotion by cannabinoid type 1 receptors on mPFC glutamatergic and GABAergic neurons

Zhanmu, O., Yang, Y., Feng, B., Wang, H., Li, H., Zhou, H., Ge, W., Wan, K.-X., Wang, S.-X., Zhang, K. J., et al. (2024) · Acta Pharmacologica Sinica · doi:10.1038/s41401-024-01426-1 · Cited by 8 · see citing works

A mouse organoid platform for modeling cerebral cortex development and cis-regulatory evolution in vitro

Medina-Cano, D., Islam, M. T., Petrova, V., Dixit, S., Balic, Z., Yang, M. G., Stadtfeld, M., Wong, E. S. W., & Vierbuchen, T. (2025) · Developmental Cell · doi:10.1016/j.devcel.2025.08.001 · Cited by 9 · see citing works

Assessing the replicability of spatial gene expression using atlas data from the adult mouse brain

Lu, S., Ortiz, C., Fürth, D., Fischer, S., Meletis, K., Zador, A. M., & Gillis, J. (2021) · PLoS Biology · doi:10.1371/journal.pbio.3001341 · Cited by 7 · see citing works

Inter-progenitor pool wiring: An evolutionarily conserved strategy that expands neural circuit diversity

Suzuki, T., & Sato, M. (2017) · Developmental Biology · doi:10.1016/j.ydbio.2017.09.029 · Cited by 7 · see citing works

Cre-assisted fine-mapping of neural circuits using orthogonal split inteins

Luan, H., Kuzin, A., Odenwald, W. F., & White, B. H. (2020) · eLife · doi:10.7554/elife.53041 · Cited by 7 · see citing works

Diminished activation of excitatory neurons in the prelimbic cortex leads to impaired working memory capacity in mice

Jiang, L.-X., Huang, G.-D., Tian, Y., Cong, R., Meng, X. W., Wang, H., Zhang, C., & Yu, X. (2023) · BMC Biology · doi:10.1186/s12915-023-01674-3 · Cited by 6 · see citing works

Single-cell chromatin accessibility landscape profiling reveals the diversity of epigenetic regulation in the rat nervous system

Ma, P., Duan, S., Ma, W., Deng, Q., Yu, Y., Gao, P., Yuan, Y., & Liu, C. (2025) · Scientific Data · doi:10.1038/s41597-025-04432-y · Cited by 6 · see citing works

An AAV capsid proposed as microglia-targeting directs genetic expression in forebrain excitatory neurons

Cao, W., Tan, Z., Berackey, B. T., Nguyen, J. K., Brown, S. R., Du, S., Lin, B., Ye, Q., Seiler, M. J., Holmes, T. C., et al. (2025) · Cell Reports Methods · doi:10.1016/j.crmeth.2025.101054 · Cited by 5 · see citing works

Lineage-dependent circuit assembly in the neocortex

Gao, P., Sultan, K. T., Zhang, X., & Shi, S. (2013) · Development · doi:10.1242/dev.087668 · Cited by 64 · see citing works

Molecular logic of cellular diversification in the mouse cerebral cortex

Di Bella, D. J., Habibi, E., Stickels, R. R., Scalia, G., Brown, J., Yadollahpour, P., Yang, S. M., Abbate, C., Biancalani, T., Macosko, E. Z., et al. (2021) · Nature · doi:10.1038/s41586-021-03670-5 · Cited by 464 · see citing works

Genetic Approaches to Neural Circuits in the Mouse

Josh Huang, Z., & Zeng, H. (2013) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062012-170307 · Cited by 200 · see citing works

Molecular Logic of Cellular Diversification in the Mammalian Cerebral Cortex

Di Bella, D. J., Habibi, E., Yang, S.-M., Stickels, R. R., Brown, J., Yadollahpour, P., Chen, F., Macosko, E. Z., Regev, A., & Arlotta, P. (2020) · doi:10.1101/2020.07.02.185439 · Cited by 20 · see citing works

Patterning the cerebral cortex into distinct functional domains during development

Appan, D., Hsu, S.-M., Hsu, W.-H., & Chou, S. (2023) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2023.102698 · Cited by 14 · see citing works