The outer subventricular zone and primate-specific cortical complexification
Open accessAbstract
Evolutionary expansion and complexification of the primate cerebral cortex are largely linked to the emergence of the outer subventricular zone (OSVZ), a uniquely structured germinal zone that generates the expanded primate supragranular layers. The primate OSVZ departs from rodent germinal zones in that it includes a higher diversity of precursor types, inter-related in bidirectional non-hierarchical lineages. In addition, primate-specific regulatory mechanisms are operating in primate cortical precursors via the occurrence of novel miRNAs. Here, we propose that the origin and evolutionary importance of the OSVZ is related to genetic changes in multiple regulatory loops and that cell-cycle regulation is a favored target for evolutionary adaptation of the cortex.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The developing human CNS has derived features including expanded proliferative zones and diverse neural stem/progenitor cell subtypes with enhanced proliferative capacity that facilitate brain expansion, especially neocortical expansion.
“the developing human CNS possesses certain divergent and highly derived features, such as expanded proliferative zones and diverse subtypes of neural stem and progenitor cells with enhanced proliferative capacities that facilitate brain expansion, especially of the neocortex (Bae et al., 2015; Bystron et al., 2006; Dehay et al., 2015; Gulden and Sestan, 2014; Howard et al., 2008; Lui et al., 2011;”
From The Cellular and Molecular Landscapes of the Developing Human Central Nervous System (2016) · cites this paper as Dehay et al., 2015
Cites
Specification of Cerebral Cortical Areas
Rakic, P. (1988) · Science · doi:10.1126/science.3291116 · Cited by 3,127 · see citing works
A mesoscale connectome of the mouse brain
Oh, S. W., Harris, J. A., Ng, L., Winslow, B., Cain, N., Mihalas, S., Wang, Q., Lau, C., Kuan, L., Henry, A. M., et al. (2014) · Nature · doi:10.1038/nature13186 · Cited by 2,612 · see citing works
The complete genome sequence of a Neanderthal from the Altai Mountains
Prüfer, K., Racimo, F., Patterson, N., Jay, F., Sankararaman, S., Sawyer, S., Heinze, A., Renaud, G., Sudmant, P. H., de Filippo, C., et al. (2014) · Nature · doi:10.1038/nature12886 · Cited by 2,254 · see citing works
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
Integrins αvβ3 and αvβ5 promote adenovirus internalization but not virus attachment
Wickham, T. J., Mathias, P., Cheresh, D. A., & Nemerow, G. R. (1993) · Cell · doi:10.1016/0092-8674(93)90231-e · Cited by 2,199 · 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
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
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
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
Transcriptional landscape of the prenatal human brain
Miller, J. A., Ding, S.-L., Sunkin, S. M., Smith, K. A., Ng, L., Szafer, A., Ebbert, A., Riley, Z. L., Royall, J. J., Aiona, K., et al. (2014) · Nature · doi:10.1038/nature13185 · Cited by 1,325 · see citing works
The Placental Mammal Ancestor and the Post–K-Pg Radiation of Placentals
O’Leary, M. A., Bloch, J. I., Flynn, J. J., Gaudin, T. J., Giallombardo, A., Giannini, N. P., Goldberg, S. L., Kraatz, B., Luo, Z., Meng, J., et al. (2013) · Science · doi:10.1126/science.1229237 · Cited by 1,194 · see citing works
MicroRNA-145 Regulates OCT4, SOX2, and KLF4 and Represses Pluripotency in Human Embryonic Stem Cells
Xu, N., Papagiannakopoulos, T. Y., Pan, G., Thomson, J. A., & Kosik, K. S. (2009) · Cell · doi:10.1016/j.cell.2009.02.038 · Cited by 1,128 · see citing works
Self-citationAn RNA gene expressed during cortical development evolved rapidly in humans
Pollard, K. S., Salama, S. R., Lambert, N., Lambot, M.-A., Coppens, S., Pedersen, J. S., Katzman, S., King, B., Onodera, C., Siepel, A., et al. (2006) · Nature · doi:10.1038/nature05113 · Cited by 1,005 · see citing works
Self-citationPollen, A. A., Nowakowski, T. J., Shuga, J., Wang, X., Leyrat, A. A., Lui, J. H., Li, N., Szpankowski, L., Fowler, B., Chen, P., et al. (2014) · Nature Biotechnology · doi:10.1038/nbt.2967 · Cited by 920 · see citing works
The evolution of distributed association networks in the human brain
Buckner, R. L., & Krienen, F. M. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.09.017 · Cited by 836 · cited 1× · see citing works
“The differential expression of primate-specific miRNAs enriched in distinct germinal compartments of the primate cortex imposes a finegrained, spatiotemporally tuned layer of regulation over cell-cycle progression, which constitutes a prerequisite for the generation of appropriate cell fates during corticogenesis, inc…”
Modeling transformations of neurodevelopmental sequences across mammalian species
Workman, A. D., Charvet, C. J., Clancy, B., Darlington, R. B., & Finlay, B. L. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.5746-12.2013 · Cited by 833 · see citing works
OSVZ progenitors of human and ferret neocortex are epithelial-like and expand by integrin signaling
Fietz, S. A., Kelava, I., Vogt, J., Wilsch-Bräuninger, M., Stenzel, D., Fish, J. L., Corbeil, D., Riehn, A., Distler, W., Nitsch, R., et al. (2010) · Nature Neuroscience · doi:10.1038/nn.2553 · Cited by 830 · see citing works
The frailty of adaptive hypotheses for the origins of organismal complexity
Lynch, M. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0702207104 · Cited by 804 · see citing works
Neural Networks of the Mouse Neocortex
Zingg, B., Hintiryan, H., Gou, L., Song, M. Y., Bay, M., Bienkowski, M. S., Foster, N. N., Yamashita, S., Bowman, I., Toga, A. W., et al. (2014) · Cell · doi:10.1016/j.cell.2014.02.023 · Cited by 797 · 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
Origin of GABAergic neurons in the human neocortex
Letinić, K., Zoncu, R., & RAKIC, P. T. (2002) · Nature · doi:10.1038/nature00779 · Cited by 718 · see citing works
Levitt, P., & Rakic, P. (1980) · Journal of Comparative Neurology · doi:10.1002/cne.901930316 · Cited by 704 · see citing works
Smart, I. H. M. (2002) · Cerebral Cortex · doi:10.1093/cercor/12.1.37 · Cited by 687 · see citing works
The cell cycle of the pseudostratified ventricular epithelium of the embryonic murine cerebral wall
Takahashi, T., Nowakowski, R. S., & Caviness, V. S. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-09-06046.1995 · Cited by 673 · see citing works
Cell-cycle control and cortical development
Dehay, C., & Kennedy, H. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2097 · Cited by 655 · see citing works
Self-citationA Role for Intermediate Radial Glia in the Tangential Expansion of the Mammalian Cerebral Cortex
Reillo, I., Romero, C. D. J., García‐Cabezas, M. Á., & Borrell, V. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhq238 · Cited by 631 · see citing works
The timing of cortical neurogenesis is encoded within lineages of individual progenitor cells
Shen, Q., Wang, Y., Dimos, J. T., Fasano, C. A., Phoenix, T. N., Lemischka, I. R., Ivanova, N. B., Stifani, S., Morrisey, E. E., & Temple, S. (2006) · Nature Neuroscience · doi:10.1038/nn1694 · Cited by 625 · see citing works
Neural progenitors, neurogenesis and the evolution of the neocortex
Florio, M., & Huttner, W. Β. (2014) · Development · doi:10.1242/dev.090571 · Cited by 625 · see citing works
Cortical high-density counterstream architectures
Markov, N. T., Ercsey-Ravasz, M., Van Essen, D. C., Knoblauch, K., Toroczkai, Z., & Kennedy, H. (2013) · Science · doi:10.1126/science.1238406 · Cited by 616 · see citing works
Self-citationLange, C. M., Huttner, W. Β., & Calegari, F. (2009) · Cell stem cell · doi:10.1016/j.stem.2009.05.026 · Cited by 565 · see citing works
Voigt, T. B. (1989) · The Journal of Comparative Neurology · doi:10.1002/cne.902890106 · Cited by 549 · see citing works
Human-specific loss of regulatory DNA and the evolution of human-specific traits
McLean, C. Y., Reno, P. L., Pollen, A. A., Bassan, A. I., Capellini, T. D., Guenther, C., Indjeian, V. B., Lim, X., Menke, D. B., Schaar, B. T., et al. (2011) · Nature · doi:10.1038/nature09774 · Cited by 535 · see citing works
Cortical Evolution: Judge the Brain by Its Cover
Geschwind, D. H., & Rakic, P. (2013) · Neuron · doi:10.1016/j.neuron.2013.10.045 · Cited by 519 · see citing works
A new subtype of progenitor cell in the mouse embryonic neocortex
Wang, X., Tsai, J.-W., LaMonica, B., & Kriegstein, A. R. (2011) · Nature Neuroscience · doi:10.1038/nn.2807 · Cited by 507 · see citing works
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
Self-citationShitamukai, A., Konno, D., & Matsuzaki, F. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4773-10.2011 · Cited by 450 · see citing works
Cellular scaling rules for primate brains.
Herculano-Houzel, S., Collins, C. E., Wong, P., & Kaas, J. H. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0611396104 · Cited by 422 · see citing works
Extracellular matrix, integrins, and growth factors as tailors of the stem cell niche
Brizzi, M. F., Tarone, G., & Defilippi, P. (2012) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2012.07.001 · Cited by 412 · see citing works
MicroRNAs and the advent of vertebrate morphological complexity
Heimberg, A. M., Sempere, L. F., Moy, V. N., Donoghue, P. C. J., & Peterson, K. J. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0712259105 · Cited by 406 · see citing works
Chromatin remodelling factor Mll1 is essential for neurogenesis from postnatal neural stem cells
Lim, D., Huang, Y.-C., Swigut, T., Mirick, A. L., García-Verdugo, J., Wysocka, J., Ernst, P., & Álvarez-Buylla, A. (2009) · Nature · doi:10.1038/nature07726 · Cited by 400 · see citing works
Calegari, F., Haubensak, W., Haffner, C., & Huttner, W. B. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.0778-05.2005 · Cited by 396 · see citing works
Levitt, P. R., Cooper, M., & RAKIC, P. T. (1981) · Journal of Neuroscience · doi:10.1523/jneurosci.01-01-00027.1981 · Cited by 395 · see citing works
Calegari, F., & Huttner, W. Β. (2003) · Journal of Cell Science · doi:10.1242/jcs.00825 · Cited by 367 · see citing works
Neural stem and progenitor cells shorten S-phase on commitment to neuron production
Arai, Y., Pulvers, J. N., Haffner, C., Schilling, B., Nüsslein, I., Calegari, F., & Huttner, W. Β. (2011) · Nature Communications · doi:10.1038/ncomms1155 · Cited by 366 · see citing works
Neuron densities vary across and within cortical areas in primates
Collins, C. E., Airey, D. C., Young, N. A., Leitch, D. B., & Kaas, J. H. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1010356107 · Cited by 361 · see citing works
Developmental and Evolutionary Adaptations of Cortical Radial Glia
RAKIC, P. T. (2003) · Cerebral Cortex · doi:10.1093/cercor/13.6.541 · Cited by 346 · see citing works
Gal, J. S., Morozov, Y. M., Ayoub, A. E., Chatterjee, M., RAKIC, P. T., & Haydar, T. F. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.4499-05.2006 · Cited by 343 · see citing works
Fietz, S. A., Lachmann, R., Brandl, H., Kircher, M., Samusik, N., Schröder, R., Lakshmanaperumal, N., Henry, I., Vogt, J., Riehn, A., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1209647109 · Cited by 337 · see citing works
MicroRNAs Potentiate Neural Development
Fineberg, S. K., Kosik, K. S., & Davidson, B. L. (2009) · Neuron · doi:10.1016/j.neuron.2009.10.020 · Cited by 330 · see citing works
Self-citationNon-epithelial stem cells and cortical interneuron production in the human ganglionic eminences
Hansen, D. V., Lui, J. H., Flandin, P., Yoshikawa, K., Rubenstein, J. L., Alvarez-Buylla, A., & Kriegstein, A. R. (2013) · Nature Neuroscience · doi:10.1038/nn.3541 · Cited by 328 · see citing works
Subcortical origins of human and monkey neocortical interneurons
Ma, T., Wang, C., Wang, L., Zhou, X., Tian, M., Zhang, Q., Zhang, Y., Li, J., Liu, Z., Cai, Y., et al. (2013) · Nature Neuroscience · doi:10.1038/nn.3536 · Cited by 322 · see citing works
G1 Phase Regulation, Area-Specific Cell Cycle Control, and Cytoarchitectonics in the Primate Cortex
Lukaszewicz, A., Savatier, P., Cortay, V., Giroud, P., Huissoud, C., Berland, M., Kennedy, H., & Dehay, C. (2005) · Neuron · doi:10.1016/j.neuron.2005.06.032 · Cited by 315 · see citing works
Self-citationHuttner, W. Β., & Kosodo, Y. (2005) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2005.10.005 · Cited by 295 · see citing works
The evolution of brains from early mammals to humans
Kaas, J. H. (2012) · Wiley Interdisciplinary Reviews Cognitive Science · doi:10.1002/wcs.1206 · Cited by 288 · see citing works
Choi, B. H., & Lapham, L. W. (1978) · Brain Research · doi:10.1016/0006-8993(78)90721-7 · Cited by 277 · see citing works
Making bigger brains–the evolution of neural-progenitor-cell division
Fish, J. L., Dehay, C., Kennedy, H., & Huttner, W. B. (2008) · Journal of Cell Science · doi:10.1242/jcs.023465 · Cited by 274 · see citing works
Self-citationCell polarity and cancer – cell and tissue polarity as a non-canonical tumor suppressor
Lee, M., & Vasioukhin, V. I. (2008) · Journal of Cell Science · doi:10.1242/jcs.016634 · Cited by 271 · see citing works
Contributions of cortical subventricular zone to the development of the human cerebral cortex
Zecevic, N., Chen, Y., & Filipovic, R. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20714 · Cited by 269 · see citing works
Stahl, R., Walcher, T., Romero, C. D. J., Pilz, G.-A., Cappello, S., Irmler, M., Sanz-Aquela, J. M., Beckers, J., Blum, R., Borrell, V., et al. (2013) · Cell · doi:10.1016/j.cell.2013.03.027 · Cited by 267 · see citing works
Comparative aspects of cerebral cortical development
Molnár, Z., Métin, C., Stoykova, A., Tarabykin, V. S., Price, D. J., Francis, F., Meyer, G., Dehay, C., & Kennedy, H. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04611.x · Cited by 266 · see citing works
Self-citationMobile DNA elements in the generation of diversity and complexity in the brain
Erwin, J. A., Marchetto, M. C., & Gage, F. H. (2014) · Nature reviews. Neuroscience · doi:10.1038/nrn3730 · Cited by 264 · see citing works
Neurogenesis and the Cell Cycle
Ohnuma, S., & Harris, W. A. (2003) · Neuron · doi:10.1016/s0896-6273(03)00632-9 · Cited by 259 · see citing works
Pilaz, L., Patti, D., Marcy, G., Ollier, É., Pfister, S., Douglas, R. J., Betizeau, M., Gautier, E., Cortay, V., Doerflinger, N., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0909894106 · Cited by 244 · see citing works
Self-citationMitotic spindle orientation predicts outer radial glial cell generation in human neocortex
Ostrem, B. E. L., Lui, J. H., Hansen, D. V., & Kriegstein, A. R. (2013) · Nature Communications · doi:10.1038/ncomms2647 · Cited by 233 · see citing works
Kornack, D. R., & RAKIC, P. T. (1995) · Neuron · doi:10.1016/0896-6273(95)90036-5 · Cited by 221 · see citing works
Regulation of cerebral cortex size and folding by expansion of basal progenitors
Nonaka‐Kinoshita, M., Reillo, I., Artegiani, B., Ángeles Martínez‐Martínez, M., Nelson, M., Borrell, V., & Calegari, F. (2013) · The EMBO Journal · doi:10.1038/emboj.2013.96 · Cited by 221 · see citing works
Seuntjens, E., Nityanandam, A., Miquelajáuregui, A., Debruyn, J., Stryjewska, A., Goebbels, S., Nave, K., Huylebroeck, D., & Tarabykin, V. S. (2009) · Nature Neuroscience · doi:10.1038/nn.2409 · Cited by 217 · see citing works
Stochastic Pulse Regulation in Bacterial Stress Response
Locke, J. C. W., Young, J. W., Fontes, M. E., Jiménez, M. J. H., & Elowitz, M. B. (2011) · Science · doi:10.1126/science.1208144 · Cited by 213 · see citing works
Kelava, I., Reillo, I., Murayama, A. Y., Kalinka, A. T., Stenzel, D., Tomančák, P., Matsuzaki, F., Lebrand, C., Sasaki, E., Schwamborn, J. C., et al. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhr301 · Cited by 212 · see citing works
Amplification of progenitors in the mammalian telencephalon includes a new radial glial cell type
Pilz, G.-A., Shitamukai, A., Reillo, I., Pacary, E., Schwausch, J., Stahl, R., Ninkovic, J., Snippert, H. J. G., Clevers, H. C., Godinho, L., et al. (2013) · Nature Communications · doi:10.1038/ncomms3125 · Cited by 210 · see citing works
Martínez-Cerdeño, V., Cunningham, C. L., Camacho, J., Antczak, J. L., Prakash, A. N., Cziep, M. E., Walker, A. I., & Noctor, S. C. (2012) · PLoS ONE · doi:10.1371/journal.pone.0030178 · Cited by 203 · see citing works
Yoon, K., Koo, B., Im, S.-K., Jeong, H., Ghim, J., Kwon, M.-C., Moon, J.-S., Miyata, T., & Kong, Y. (2008) · Neuron · doi:10.1016/j.neuron.2008.03.018 · Cited by 198 · see citing works
Wu, S.-X., Goebbels, S., Nakamura, K., Nakamura, K., Kometani, K., Minato, N., Kaneko, T., Nave, K.-A., & Tamamaki, N. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0508560102 · Cited by 198 · see citing works
Emerging roles of neural stem cells in cerebral cortex development and evolution
Borrell, V., & Reillo, I. (2012) · Developmental Neurobiology · doi:10.1002/dneu.22013 · Cited by 185 · see citing works
Cell-Cycle Kinetics of Neocortical Precursors Are Influenced by Embryonic Thalamic Axons
Dehay, C., Savatier, P., Cortay, V., & Kennedy, H. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-01-00201.2001 · Cited by 180 · see citing works
Self-citationChromatin Regulation by BAF170 Controls Cerebral Cortical Size and Thickness
Tuoc, T. C., Boretius, S., Sansom, S. N., Pitulescu, M.-E., Frahm, J., Livesey, F. J., & Stoykova, A. (2013) · Developmental Cell · doi:10.1016/j.devcel.2013.04.005 · Cited by 177 · see citing works
Proteolysis of MLL family proteins is essential for Taspase1-orchestrated cell cycle progressionPreprint
Takeda, S., Chen, D. Y., Westergard, T. D., Fisher, J. K., Rubens, J. A., Sasagawa, S., Kan, J. T., Korsmeyer, S. J., Cheng, E. H. Y., & Hsieh, J. J.-D. (2006) · Genes & Development · doi:10.1101/gad.1449406 · Cited by 171 · see citing works
Radial glia require PDGFD-PDGFRβ signalling in human but not mouse neocortex
Lui, J. H., Nowakowski, T. J., Pollen, A. A., Javaherian, A., Kriegstein, A. R., & Oldham, M. C. (2014) · Nature · doi:10.1038/nature13973 · Cited by 166 · see citing works
Bian, S., Hong, J., Li, Q., Schebelle, L., Pollock, A., Knauss, J. L., Garg, V., & Sun, T. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.03.037 · Cited by 161 · see citing works
Modulation of the cell cycle contributes to the parcellation of the primate visual cortex
Dehay, C., Giroud, P., Berland, M., Smart, I. H. M., & Kennedy, H. (1993) · Nature · doi:10.1038/366464a0 · Cited by 156 · see citing works
Self-citationAdhesion molecules in the stem cell niche – more than just staying in shape?
Marthiens, V., Kazanis, I., Moss, L., Long, K. R., & ffrench‐Constant, C. (2010) · Journal of Cell Science · doi:10.1242/jcs.054312 · Cited by 155 · see citing works
RAKIC, P. T. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0807271105 · Cited by 154 · see citing works
García‐Moreno, F., Vasistha, N. A., Trévia, N., Bourne, J. A., & Molnár, Z. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhr312 · Cited by 154 · see citing works
Interneurons in the developing human neocortex
Zečević, N., Hu, F., & Jakovčevski, I. (2010) · Developmental Neurobiology · doi:10.1002/dneu.20812 · Cited by 153 · see citing works
Predicting stem cell fate changes by differential cell cycle progression patterns
Roccio, M., Schmitter, D., Knobloch, M., Okawa, Y., Sage, D., & Lütolf, M. P. (2012) · Development · doi:10.1242/dev.086215 · Cited by 152 · see citing works
Asymmetric cell division of stem and progenitor cells during homeostasis and cancer
Gómez‐López, S., Lerner, R. G., & Petritsch, C. K. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1386-1 · Cited by 151 · see citing works
Lukaszewicz, A. I., Savatier, P., Cortay, V., Kennedy, H., & Dehay, C. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-15-06610.2002 · Cited by 148 · see citing works
Self-citationComparative aspects of cortical neurogenesis in vertebrates
Cheung, A. F. P., Pollen, A. A., Tavare, A. N., DeProto, J., & Molnár, Z. (2007) · Journal of Anatomy · doi:10.1111/j.1469-7580.2007.00769.x · Cited by 137 · see citing works
OSVZ progenitors in the human cortex: an updated perspective on neurodevelopmental disease
Ostrem, B. E. L., Lui, J. H., Wang, X., & Kriegstein, A. R. (2012) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2012.03.006 · Cited by 131 · see citing works
Origins of Cortical GABAergic Neurons in the Cynomolgus Monkey
Petanjek, Z., Berger, B., & Esclapez, M. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhn078 · Cited by 130 · see citing works
Cell cycle and cell fate in the nervous system
Ohnuma, S., Philpott, A., & Harris, W. A. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00175-6 · Cited by 127 · see citing works
MicroRNAs and Cellular Phenotypy
Kosik, K. S. (2010) · Cell · doi:10.1016/j.cell.2010.09.008 · Cited by 123 · see citing works
Self-citationIntegrin αvβ3 and thyroid hormones promote expansion of progenitors in embryonic neocortex
Stenzel, D., Wilsch‐Bräuninger, M., Wong, F. K., Heuer, H., & Huttner, W. Β. (2014) · Development · doi:10.1242/dev.101907 · Cited by 115 · see citing works
Early Specification of the Hierarchical Organization of Visual Cortical Areas in the Macaque Monkey
Batardière, A. (2002) · Cerebral Cortex · doi:10.1093/cercor/12.5.453 · Cited by 113 · see citing works
Control of Outer Radial Glial Stem Cell Mitosis in the Human Brain
Ostrem, B. E. L., Lui, J. H., Gertz, C. C., & Kriegstein, A. R. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.06.058 · Cited by 112 · see citing works
Liu, H., Cheng, E. H. Y., & Hsieh, J. J.-D. (2007) · Genes & Development · doi:10.1101/gad.1574507 · Cited by 112 · see citing works
Cortical Specification of Mice and Men
Kennedy, H., & Dehay, C. (1993) · Cerebral Cortex · doi:10.1093/cercor/3.3.171 · Cited by 109 · see citing works
Self-citationCytokinesis of neuroepithelial cells can divide their basal process before anaphase
Kosodo, Y., Toida, K., Dubreuil, V., Alexandre, P., Schenk, J., Kiyokage, E., Attardo, A., Mora‐Bermúdez, F., Arii, T., Clarke, J. D. W., et al. (2008) · The EMBO Journal · doi:10.1038/emboj.2008.227 · Cited by 108 · see citing works
Fertuzinhos, S., Krsnik, Ž., Kawasawa, Y. I., Rašin, M.-R., Kwan, K. Y., Chen, J.-G., Judaš, M., Hayashi, M., & Šestan, N. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp009 · Cited by 106 · see citing works
A morphological study of the mouse subependymal layer from embryonic life to old age.
Sturrock, R. R., & Smart, I. H. M. (1980) · PubMed · Cited by 104 · see citing works
Nelson, B. R., Hodge, R. D., Bedogni, F., & Hevner, R. F. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0791-13.2013 · Cited by 103 · see citing works
Intergenic lncRNAs and the evolution of gene expression
Marques, A. C., & Ponting, C. P. (2014) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2014.03.009 · Cited by 102 · see citing works
Smart, I. H. (1972) · PubMed · Cited by 95 · see citing works
MicroRNA-92b regulates the development of intermediate cortical progenitors in embryonic mouse brain
Nowakowski, T. J., Fotaki, V., Pollock, A., Sun, T., Pratt, T., & Price, D. J. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1219385110 · Cited by 95 · see citing works
Polleux, F., Dehay, C., Moraillon, B., & Kennedy, H. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-20-07763.1997 · Cited by 95 · see citing works
Self-citationMattick, J. S. (2009) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2009.04991.x · Cited by 94 · see citing works
Mairet‐Coello, G., Tury, A., Buskirk, E. K. V., Robinson, K. R., Genestine, M., & DiCicco-Bloom, E. M. (2012) · Development · doi:10.1242/dev.067314 · Cited by 93 · see citing works
The secondary loss of gyrencephaly as an example of evolutionary phenotypical reversal
Kelava, I., Lewitus, É., & Huttner, W. Β. (2013) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2013.00016 · Cited by 89 · see citing works
Park, B. O., Ahrends, R., & Teruel, M. N. (2012) · Cell Reports · doi:10.1016/j.celrep.2012.08.038 · Cited by 86 · see citing works
Segregation of feedforward and feedback projections in mouse visual cortex
Berezovskii, V. K., Nassi, J. J., & Born, R. T. (2011) · Journal of Comparative Neurology · doi:10.1002/cne.22675 · Cited by 84 · see citing works
Tyler, W. A., & Haydar, T. F. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.5380-12.2013 · Cited by 81 · see citing works
Neuronal scaling rules for primate brains
Herculano‐Houzel, S. (2012) · Progress in brain research · doi:10.1016/b978-0-444-53860-4.00015-5 · Cited by 80 · see citing works
Arcila, M. L., Betizeau, M., Cambronne, X. A., Guzman, E., Doerflinger, N., Bouhallier, F., Zhou, H., Wu, B., Rani, N., Bassett, D. S., et al. (2014) · Neuron · doi:10.1016/j.neuron.2014.01.017 · Cited by 80 · see citing works
Self-citationIs Pax6 Critical for Neurogenesis in the Human Fetal Brain?
Mo, Z., & Zečević, N. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhm181 · Cited by 80 · see citing works
Yu, X., & Zečević, N. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.5249-10.2011 · Cited by 79 · see citing works
Spatio-temporal extension in site of origin for cortical calretinin neurons in primates
Hladnik, A., Džaja, D., Darmopil, S., Jovanov-MiloÅ¡ević, N., & Petanjek, Z. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00050 · Cited by 72 · see citing works
On the Evolution of Eyes: Would You Like It Simple or Compound?
Zuker, C. S. (1994) · Science · doi:10.1126/science.8047881 · Cited by 72 · see citing works
Kawasaki, H., Toda, T., & Tanno, K. (2012) · Biology Open · doi:10.1242/bio.20123160 · Cited by 65 · see citing works
Goodfellow, M., Phillips, N. E., Manning, C. S., Galla, T., & Papalopulu, N. (2014) · Nature Communications · doi:10.1038/ncomms4399 · Cited by 62 · see citing works
Tapias, A., Zhou, Z., Shi, Y. X., Chong, Z., Wang, P., Groth, M., Platzer, M., Huttner, W. Β., Herceg, Z., Yang, Y., et al. (2014) · Cell stem cell · doi:10.1016/j.stem.2014.04.001 · Cited by 60 · see citing works
Polleux, F. (2001) · Cerebral Cortex · doi:10.1093/cercor/11.11.1027 · Cited by 52 · see citing works
MicroRNAs tell an evo–devo story
Kosik, K. S. (2009) · Nature reviews. Neuroscience · doi:10.1038/nrn2713 · Cited by 51 · see citing works
Self-citationGhosh, T., Aprea, J., Nardelli, J., Engel, H., Selinger, C., Mombereau, C., Lemonnier, T., Moutkine, I., Schwendimann, L., Dori, M., et al. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.05.029 · Cited by 47 · see citing works
Human fetal radial glia cells generate oligodendrocytes in vitro
Mo, Z., & Zečević, N. (2008) · Glia · doi:10.1002/glia.20775 · Cited by 45 · see citing works
Fei, J., Haffner, C., & Huttner, W. Β. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.03.033 · Cited by 42 · see citing works
A Novel Class of Mammalian-Specific Tailless RetropseudogenesPreprint
Schmitz, J., Churakov, G., Zischler, H., & Brosius, J. (2004) · Genome Research · doi:10.1101/gr.2720104 · Cited by 42 · see citing works
Price, D. J., & Lotto, R. B. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-10-03247.1996 · Cited by 31 · see citing works
Genetic Mechanisms Specifying Cortical Connectivity
Polleux, F. (2005) · Neuron · doi:10.1016/j.neuron.2005.04.017 · Cited by 29 · see citing works
Self-organization and interareal networks in the primate cortex
Kennedy, H., & Dehay, C. (2012) · Progress in brain research · doi:10.1016/b978-0-444-53860-4.00016-7 · Cited by 22 · see citing works
Self-citationtrnp: A Conserved Mammalian Gene Encoding a Nuclear Protein That Accelerates Cell-Cycle Progression
Volpe, M., Shpungin, S., Barbi, C., Abrham, G., Malovani, H., Wides, R., & Nir, U. (2006) · DNA and Cell Biology · doi:10.1089/dna.2006.25.331 · Cited by 19 · see citing works
Flagged first, then by citations
1 of the 133 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Human cerebral organoids recapitulate gene expression programs of fetal neocortex development
Camp, J. G., Badsha, F., Florio, M., Kanton, S., Gerber, T., Wilsch-Bräuninger, M., Lewitus, E., Sykes, A., Hevers, W., Lancaster, M., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1520760112 · Cited by 1,130 · see citing works
The Cellular and Molecular Landscapes of the Developing Human Central Nervous System
Silbereis, J. C., Pochareddy, S., Zhu, Y., Li, M., & Sestan, N. (2016) · Neuron · doi:10.1016/j.neuron.2015.12.008 · Cited by 818 · see citing works
Evolution of the Human Nervous System Function, Structure, and Development
Sousa, A. M. M., Meyer, K. A., Santpere, G., Gulden, F. O., & Sestan, N. (2017) · Cell · doi:10.1016/j.cell.2017.06.036 · Cited by 517 · see citing works
Cerebral cortex expansion and folding: what have we learned?
Fernández, V., Llinares-Benadero, C., & Borrell, V. (2016) · The EMBO Journal · doi:10.15252/embj.201593701 · Cited by 357 · see citing works
Otani, T., Marchetto, M. C., Gage, F. H., Simons, B. D., & Livesey, F. J. (2016) · Cell Stem Cell · doi:10.1016/j.stem.2016.03.003 · Cited by 353 · see citing works
Neural elements for predictive coding
Shipp, S. (2016) · Frontiers in Psychology · doi:10.3389/fpsyg.2016.01792 · Cited by 340 · see citing works
Definitions and classification of malformations of cortical development: practical guidelines
Severino, M., Geraldo, A. F., Utz, N., Tortora, D., Pogledić, I., Klonowski, W., Triulzi, F. M., Arrigoni, F., Mankad, K., Leventer, R. J., et al. (2020) · Brain · doi:10.1093/brain/awaa174 · Cited by 312 · see citing works
Mora‐Bermúdez, F., Badsha, F., Kanton, S., Camp, J. G., Vernot, B., Köhler, K., Voigt, B., Okita, K., Maričić, T., He, Z., et al. (2016) · eLife · doi:10.7554/elife.18683 · Cited by 289 · see citing works
An early cell shape transition drives evolutionary expansion of the human forebrain
Benito-Kwiecinski, S. K., Giandomenico, S. L., Sutcliffe, M. A., Riis, E. S., Freire-Pritchett, P., Kelava, I., Wunderlich, S., Martin, U., Wray, G. A., McDole, K., et al. (2021) · Cell · doi:10.1016/j.cell.2021.02.050 · Cited by 263 · see citing works
MicroRNAs in neural development: from master regulators to fine-tuners
Rajman, M., & Schratt, G. M. (2017) · Development · doi:10.1242/dev.144337 · Cited by 258 · see citing works
Neural histology and neurogenesis of the human fetal and infant brain
Kostović, I., Sedmak, G., & Judáš, M. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.12.043 · Cited by 259 · see citing works
Deconstructing cortical folding: genetic, cellular and mechanical determinants
Llinares-Benadero, C., & Borrell, V. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-018-0112-2 · Cited by 243 · see citing works
García‐Cabezas, M. Á., Zikopoulos, B., & Barbas, H. (2019) · Brain Structure and Function · doi:10.1007/s00429-019-01841-9 · Cited by 237 · see citing works
Fixed single-cell transcriptomic characterization of human radial glial diversity
Thomsen, E. R., Mich, J. K., Yao, Z., Hodge, R. D., Doyle, A. M., Jang, S., Shehata, S. I., Nelson, A. M., Shapovalova, N. V., Levi, B. P., et al. (2015) · Nature Methods · doi:10.1038/nmeth.3629 · Cited by 227 · see citing works
Rewiring of human neurodevelopmental gene regulatory programs by human accelerated regions
Girskis, K. M., Stergachis, A. B., DeGennaro, E. M., Doan, R. N., Qian, X., Johnson, M. B., Wang, P. P., Sejourne, G. M., Nagy, M. A., Pollina, E. A., et al. (2021) · Neuron · doi:10.1016/j.neuron.2021.08.005 · Cited by 193 · see citing works
Neural stem cell therapies and hypoxic-ischemic brain injury
Huang, L., & Zhang, L. (2018) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2018.05.004 · Cited by 208 · see citing works
Linaro, D., Vermaercke, B., Iwata, R., Ramaswamy, A., Davis, B. A., Boubakar, L., Libé-Philippot, B., Bilheu, A., Bruyne, L. D., Gall, D., et al. (2019) · doi:10.1101/626218 · Cited by 210 · see citing works
“The brain and cerebral neocortex in particular increased rapidly in size and complexity during human evolution (Dehay et al., 2015; Geschwind and Rakic, 2013; Gotz and Huttner, 2005; Lui et al., 2011).”
BackgroundFlorio, M., Heide, M., Pinson, A., Brandl, H., Albert, M., Winkler, S., Wimberger, P., Huttner, W. Β., & Hiller, M. (2018) · eLife · doi:10.7554/elife.32332 · Cited by 196 · see citing works
Cellular and molecular introduction to brain development
Jiang, X., & Nardelli, J. (2015) · Neurobiology of Disease · doi:10.1016/j.nbd.2015.07.007 · Cited by 199 · see citing works
Long, K. R., Newland, B., Florio, M., Kalebic, N., Langen, B., Kolterer, A., Wimberger, P., & Huttner, W. B. (2018) · Neuron · doi:10.1016/j.neuron.2018.07.013 · Cited by 196 · see citing works
Hedgehog signaling promotes basal progenitor expansion and the growth and folding of the neocortex
Wang, L., Hou, S., & Han, Y.-G. (2016) · Nature Neuroscience · doi:10.1038/nn.4307 · Cited by 190 · see citing works
Human Models Are Needed for Studying Human Neurodevelopmental Disorders
Zhao, X., & Bhattacharyya, A. (2018) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2018.10.009 · Cited by 192 · see citing works
Human-specific ARHGAP11B increases size and folding of primate neocortex in the fetal marmoset
Heide, M., Haffner, C., Murayama, A. Y., Kurotaki, Y., Shinohara, H., Okano, H., Sasaki, E., & Huttner, W. Β. (2020) · Science · doi:10.1126/science.abb2401 · Cited by 187 · see citing works
Developmental mechanisms underlying the evolution of human cortical circuits
Vanderhaeghen, P., & Polleux, F. (2023) · Nature Reviews Neuroscience · doi:10.1038/s41583-023-00675-z · Cited by 173 · see citing works
Kalebic, N., Gilardi, C., Stepien, B. K., Wilsch‐Bräuninger, M., Long, K. R., Namba, T., Florio, M., Langen, B., Lombardot, B., Shevchenko, A., et al. (2019) · Cell stem cell · doi:10.1016/j.stem.2019.02.017 · Cited by 152 · see citing works
Human-Specific ARHGAP11B Acts in Mitochondria to Expand Neocortical Progenitors by Glutaminolysis
Namba, T., Dóczi, J., Pinson, A., Xing, L., Kalebic, N., Wilsch‐Bräuninger, M., Long, K. R., Vaid, S., Lauer, J. L., Bogdanova, A. I., et al. (2019) · Neuron · doi:10.1016/j.neuron.2019.11.027 · Cited by 157 · see citing works
A Primate lncRNA Mediates Notch Signaling during Neuronal Development by Sequestering miRNA
Rani, N., Nowakowski, T. J., Zhou, H., Godshalk, S. E., Lisi, V., Kriegstein, A. R., & Kosik, K. S. (2016) · Neuron · doi:10.1016/j.neuron.2016.05.005 · Cited by 153 · see citing works
Self-citationLiu, J., Liu, W., Yang, L., Wu, Q., Zhang, H., Fang, A., Li, L., Xu, X., Sun, L., Zhang, J., et al. (2017) · Cell stem cell · doi:10.1016/j.stem.2017.08.013 · Cited by 138 · see citing works
A Laminar Organization for Selective Cortico-Cortical Communication
D’Souza, R. D., & Burkhalter, A. (2017) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2017.00071 · Cited by 138 · see citing works
How Cells Fold the Cerebral Cortex
Borrell, V. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1106-17.2017 · Cited by 139 · see citing works
Buchsbaum, I. Y., & Cappello, S. (2019) · Development · doi:10.1242/dev.163766 · Cited by 128 · see citing works
Vezoli, J., Magrou, L., Goebel, R., Wang, X., Knoblauch, K., Vinck, M. A., & Kennedy, H. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117479 · Cited by 125 · see citing works
Self-citationHuman-specific ARHGAP11B induces hallmarks of neocortical expansion in developing ferret neocortex
Kalebic, N., Gilardi, C., Albert, M., Namba, T., Long, K. R., Kostic, M., Langen, B., & Huttner, W. Β. (2018) · eLife · doi:10.7554/elife.41241 · Cited by 129 · see citing works
Namba, T., & Huttner, W. Β. (2016) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.256 · Cited by 115 · see citing works
Neuronal migration disorders: Focus on the cytoskeleton and epilepsy
Stouffer, M. A., Golden, J. A., & Francis, F. (2015) · Neurobiology of Disease · doi:10.1016/j.nbd.2015.08.003 · Cited by 114 · see citing works
Is this a brain which I see before me? Modeling human neural development with pluripotent stem cells
Suzuki, I. K., & Vanderhaeghen, P. (2015) · Development · doi:10.1242/dev.120568 · Cited by 110 · see citing works
Effects of antenatal glucocorticoids on the developing brain
Carson, R. A., Monaghan, A. P., DeFranco, D. B., & Rudine, A. C. (2016) · Steroids · doi:10.1016/j.steroids.2016.05.012 · Cited by 106 · see citing works
RNA-binding proteins balance brain function in health and disease
Schieweck, R., Ninkovic, J., & Kiebler, M. A. (2020) · Physiological Reviews · doi:10.1152/physrev.00047.2019 · Cited by 104 · see citing works
Emerging Roles of Long Non-Coding RNAs as Drivers of Brain Evolution
Zimmer‐Bensch, G. (2019) · Cells · doi:10.3390/cells8111399 · Cited by 98 · see citing works
Kostović, I. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101883 · Cited by 102 · see citing works
A single splice site mutation in human-specific ARHGAP11B causes basal progenitor amplification
Florio, M., Namba, T., Pääbo, S., Hiller, M., & Huttner, W. Β. (2016) · Science Advances · doi:10.1126/sciadv.1601941 · Cited by 99 · see citing works
Epigenetics and epitranscriptomics in temporal patterning of cortical neural progenitor competence
Yoon, K., Vissers, C. B., Ming, G., & Song, H. (2018) · The Journal of Cell Biology · doi:10.1083/jcb.201802117 · Cited by 96 · see citing works
A novel population of Hopx-dependent basal radial glial cells in the developing mouse neocortex
Vaid, S., Camp, J. G., Hersemann, L., Oegema, C. E., Heninger, A., Winkler, S., Brandl, H., Sarov, M., Treutlein, B., Huttner, W. Β., et al. (2018) · Development · doi:10.1242/dev.169276 · Cited by 96 · see citing works
Human-specific genomic signatures of neocortical expansion
Florio, M., Borrell, V., & Huttner, W. Β. (2016) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2016.11.004 · Cited by 96 · see citing works
Effect of polyvinylidene fluoride electrospun fiber orientation on neural stem cell differentiation
Lins, L. C., Wianny, F., Livi, S., Dehay, C., Duchet‐Rumeau, J., & Gérard, J. (2016) · Journal of Biomedical Materials Research Part B Applied Biomaterials · doi:10.1002/jbm.b.33778 · Cited by 91 · see citing works
Self-citationShaping the brain: The emergence of cortical structure and folding
Akula, S. K., Exposito-Alonso, D., & Walsh, C. A. (2023) · Developmental Cell · doi:10.1016/j.devcel.2023.11.004 · Cited by 97 · see citing works
Brain structure and dynamics across scales: in search of rules
Wang, X., & Kennedy, H. (2016) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2015.12.010 · Cited by 91 · see citing works
Self-citationKostović, I., Radoš, M., Srzentić, M. K., & Krsnik, Ž. (2021) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nlab024 · Cited by 90 · see citing works
Basal Progenitor Morphology and Neocortex Evolution
Kalebic, N., & Huttner, W. Β. (2020) · Trends in Neurosciences · doi:10.1016/j.tins.2020.07.009 · Cited by 82 · see citing works
Dwyer, N. D., Chen, B., Chou, S., Hippenmeyer, S., Nguyen, L., & Ghashghaei, H. T. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.2359-16.2016 · Cited by 79 · see citing works
From sauropsids to mammals and back: New approaches to comparative cortical development
Montiel, J. F., Vasistha, N. A., García‐Moreno, F., & Molnár, Z. (2015) · The Journal of Comparative Neurology · doi:10.1002/cne.23871 · Cited by 74 · see citing works
Gyrification of the cerebral cortex requires FGF signaling in the mammalian brain
Matsumoto, N., Shinmyo, Y., Ichikawa, Y., & Kawasaki, H. (2017) · eLife · doi:10.7554/elife.29285 · Cited by 76 · see citing works
Brain organoids as models to study human neocortex development and evolution
Heide, M., Huttner, W. Β., & Mora‐Bermúdez, F. (2018) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2018.06.006 · Cited by 73 · see citing works
Modeling neuropsychiatric disorders using human induced pluripotent stem cells
Wang, M., Zhang, L., & Gage, F. H. (2019) · Protein & Cell · doi:10.1007/s13238-019-0638-8 · Cited by 75 · see citing works
Folding brains: from development to disease modeling
Del-Valle-Anton, L., & Borrell, V. (2021) · Physiological Reviews · doi:10.1152/physrev.00016.2021 · Cited by 78 · see citing works
Neocortex expansion in development and evolution — from cell biology to single genes
Wilsch‐Bräuninger, M., Florio, M., & Huttner, W. Β. (2016) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2016.05.004 · Cited by 73 · see citing works
Doobin, D. J., Kemal, S., Dantas, T. J., & Vallee, R. B. (2016) · Nature Communications · doi:10.1038/ncomms12551 · Cited by 72 · see citing works
Matsumoto, N., Tanaka, S., Hamabe‐Horiike, T., Shinmyo, Y., & Kawasaki, H. (2020) · eLife · doi:10.7554/elife.54873 · Cited by 70 · see citing works
Developmental Origins of Human Cortical Oligodendrocytes and Astrocytes
Yang, L., Li, Z., Liu, G., Li, X., & Yang, Z. (2021) · Neuroscience Bulletin · doi:10.1007/s12264-021-00759-9 · Cited by 73 · see citing works
Kostović, I., Išasegi, I. Ž., & Krsnik, Ž. (2018) · Journal of Anatomy · doi:10.1111/joa.12920 · Cited by 67 · see citing works
Kostic, M., Paridaen, J. T. M. L., Long, K. R., Kalebic, N., Langen, B., Grübling, N., Wimberger, P., Kawasaki, H., Namba, T., & Huttner, W. Β. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.03.091 · Cited by 68 · see citing works
Behavior and lineage progression of neural progenitors in the mammalian cortex
Lin, Y., Yang, J., Shen, Z., Ma, J., Simons, B. D., & Shi, S. (2020) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2020.10.017 · Cited by 62 · see citing works
Human brain evolution: Emerging roles for regulatory DNA and RNA
Liu, J., Mosti, F., & Silver, D. L. (2021) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2021.11.005 · Cited by 63 · see citing works
Radial glia in the ventral telencephalon
Turrero García, M., & Harwell, C. C. (2017) · FEBS Letters · doi:10.1002/1873-3468.12829 · Cited by 62 · see citing works
The Ferret as a Model System for Neocortex Development and Evolution
Gilardi, C., & Kalebic, N. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.661759 · Cited by 57 · see citing works
ATP-Dependent Chromatin Remodeling During Cortical Neurogenesis
Sokpor, G., Castro-Hernández, R., Rosenbusch, J., Staiger, J. F., & Tuoc, T. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00226 · Cited by 60 · see citing works
The Extracellular Matrix in the Evolution of Cortical Development and Folding
Amin, S., & Borrell, V. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.604448 · Cited by 58 · see citing works
Xing, L., Kubik‐Zahorodna, A., Namba, T., Pinson, A., Florio, M., Procházka, J., Sarov, M., Sedláček, R., & Huttner, W. Β. (2021) · The EMBO Journal · doi:10.15252/embj.2020107093 · Cited by 55 · see citing works
Building brains in a dish: Prospects for growing cerebral organoids from stem cells
Mason, J. O., & Price, D. J. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.07.048 · Cited by 54 · see citing works
Fujimura, K., Mitsuhashi, T., Shibata, S., Shimozato, S., & Takahashi, T. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0229-16.2016 · Cited by 57 · see citing works
The Molecular Basis of Human Brain Evolution
Enard, W. (2016) · Current Biology · doi:10.1016/j.cub.2016.09.030 · Cited by 55 · see citing works
Thyroid hormone regulation of neural stem cell fate: From development to ageing
Gothié, J. M., Vancamp, P., DEMENEIX, B. A., & Remaud, S. (2019) · Acta Physiologica · doi:10.1111/apha.13316 · Cited by 51 · see citing works
Human‐specific ARHGAP11B ensures human‐like basal progenitor levels in hominid cerebral organoids
Fischer, J., Ortuño, E. F., Marsoner, F., Artioli, A., Peters, J., Namba, T., Oegema, C. E., Huttner, W. Β., Ladewig, J., & Heide, M. (2022) · EMBO Reports · doi:10.15252/embr.202254728 · Cited by 52 · see citing works
Unraveling mechanisms of human brain evolution
Lancaster, M. A. (2024) · Cell · doi:10.1016/j.cell.2024.08.052 · Cited by 54 · see citing works
The evolution of basal progenitors in the developing non-mammalian brain
Nomura, T., Ohtaka‐Maruyama, C., Yamashita, W., Wakamatsu, Y., Murakami, Y., Calegari, F., Suzuki, K., Gotoh, H., & Ono, K. (2016) · Development · doi:10.1242/dev.127100 · Cited by 52 · see citing works
Neuronal Polarity in the Embryonic Mammalian Cerebral Cortex
Kon, E., Cossard, A., & Jossin, Y. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00163 · Cited by 52 · see citing works
Daviaud, N., Chevalier, C., Friedel, R. H., & Zou, H. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00336 · Cited by 51 · see citing works
Mercury Toxicity and Neurogenesis in the Mammalian Brain
Abbott, L. C., & Nigussie, F. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22147520 · Cited by 49 · see citing works
Stepien, B. K., Naumann, R., Holtz, A. N., Helppi, J., Huttner, W. Β., & Vaid, S. (2020) · Current Biology · doi:10.1016/j.cub.2020.08.046 · Cited by 47 · see citing works
Coquand, L., Avalos, C. B., Macé, A., Farcy, S., Di-Cicco, A., Lampič, M., Wimmer, R., Bessières, B., Attié‐Bitach, T., Fraisier, V., et al. (2024) · Nature Cell Biology · doi:10.1038/s41556-024-01393-z · Cited by 48 · see citing works
The Combinatorial Creature: Cortical Phenotypes within and across Lifetimes
Krubitzer, L. A., & Prescott, T. J. (2018) · Trends in Neurosciences · doi:10.1016/j.tins.2018.08.002 · Cited by 47 · see citing works
Oproescu, A.-M., Han, S., & Schuurmans, C. J. (2021) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.642016 · Cited by 51 · see citing works
Advancing preclinical models of psychiatric disorders with human brain organoid cultures
Dixon, T. A., & Muotri, A. R. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01708-2 · Cited by 48 · see citing works
Lineage divergence of activity-driven transcription and evolution of cognitive ability
Hardingham, G. E., Pruunsild, P., Greenberg, M. E., & Bading, H. (2017) · Nature reviews. Neuroscience · doi:10.1038/nrn.2017.138 · Cited by 47 · see citing works
Güven, A., Kalebic, N., Long, K. R., Florio, M., Vaid, S., Brandl, H., Stenzel, D., & Huttner, W. Β. (2020) · eLife · doi:10.7554/elife.49808 · Cited by 44 · see citing works
Cell Metabolic Alterations due to Mcph1 Mutation in Microcephaly
Journiac, N., Gilabert‐Juan, J., Cipriani, S., Bénit, P., Liu, X., Jacquier, S., Faivre, V., Delahaye‐Duriez, A., Csaba, Z., Hourcade, T., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.03.070 · Cited by 47 · see citing works
Localized astrogenesis regulates gyrification of the cerebral cortex
Shinmyo, Y., Saito, K., Hamabe‐Horiike, T., Kameya, N., Ando, A., Kawasaki, K., Duong, T. A. D., Sakashita, M., Roboon, J., Hattori, T., et al. (2022) · Science Advances · doi:10.1126/sciadv.abi5209 · Cited by 47 · see citing works
Krefft, O., Jabali, A., Iefremova, V., Koch, P., & Ladewig, J. (2018) · Journal of Visualized Experiments · doi:10.3791/56768 · Cited by 50 · see citing works
Interactive histogenesis of axonal strata and proliferative zones in the human fetal cerebral wall
Išasegi, I. Ž., Radoš, M., Krsnik, Ž., Radoš, M., Benjak, V., & Kostović, I. (2018) · Brain Structure and Function · doi:10.1007/s00429-018-1721-2 · Cited by 46 · see citing works
Brain Organoids—A Bottom-Up Approach for Studying Human Neurodevelopment
Karzbrun, E., & Reiner, O. (2019) · Bioengineering · doi:10.3390/bioengineering6010009 · Cited by 45 · see citing works
Human-Specific Genes, Cortical Progenitor Cells, and Microcephaly
Heide, M., & Huttner, W. Β. (2021) · Cells · doi:10.3390/cells10051209 · Cited by 45 · see citing works
Guerra, M., Blázquez, J., & Rodríguez, E. M. (2017) · Fluids and Barriers of the CNS · doi:10.1186/s12987-017-0067-0 · Cited by 46 · see citing works
The Molecular Pathway Regulating Bergmann Glia and Folia Generation in the Cerebellum
Leung, A. W., & Li, J. Y. H. (2017) · The Cerebellum · doi:10.1007/s12311-017-0904-3 · Cited by 46 · see citing works
Cannabinoid Actions on Neural Stem Cells: Implications for Pathophysiology
Rodrigues, R. S., Lourenço, D. M., Paulo, S. L., Mateus, J. M., Ferreira, M. F., Mouro, F. M., Moreira, J. B., Ribeiro, F. F., Sebastião, A. M., & Xapelli, S. (2019) · Molecules · doi:10.3390/molecules24071350 · Cited by 45 · see citing works
Zhao, Z., Zhang, D., Yang, F., Xu, M., Zhao, S., Pan, T., Liu, C., Liu, Y., Wu, Q., Tu, Q., et al. (2022) · Cell Research · doi:10.1038/s41422-022-00635-9 · Cited by 43 · see citing works
Chromatin Remodeling BAF155 Subunit Regulates the Genesis of Basal Progenitors in Developing Cortex
Narayanan, R., Pham, L., Kerimoglu, C., Watanabe, T., Castro-Hernández, R., Sokpor, G., Ulmke, P. A., Kiszka, K. A., Tonchev, A. B., Rosenbusch, J., et al. (2018) · iScience · doi:10.1016/j.isci.2018.05.014 · Cited by 44 · see citing works
Using brain organoids to study human neurodevelopment, evolution and disease
Kyrousi, C., & Cappello, S. (2019) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.347 · Cited by 40 · see citing works
Recent advances in understanding neocortical development
Borrell, V. (2019) · F1000Research · doi:10.12688/f1000research.20332.1 · Cited by 42 · see citing works
Rosa, F., Dhingra, A., Uysal, B., Mendis, G. D. C., Loeffler, H., Elsen, G. E., Mueller, S., Schwarz, N., Castillo-Lizardo, M., Cuddy, C., et al. (2020) · Stem Cell Reports · doi:10.1016/j.stemcr.2020.05.015 · Cited by 42 · see citing works
Xing, L., Kalebic, N., Namba, T., Vaid, S., Wimberger, P., & Huttner, W. Β. (2020) · Neuron · doi:10.1016/j.neuron.2020.09.034 · Cited by 42 · see citing works
- Authors
- Dehay, C., Kennedy, H., & Kosik, K. S.
- Affiliations
- Lyon 1 Université (FR)
- University of California, Santa Barbara (US)
- Corresponding author
- Dehay, Colette
- Kennedy, Henry
- Kosik, Kenneth S.
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2015-02
- Volume
- 85
- Issue
- 4
- Pages
- 683-694
- ISSN
- 0896-6273 (ISSN-L)
- OpenAlex
- W1980117419
- Cited by
- 314
- References
- 133
- Citations by year
- 2026: 16 · 2025: 21 · 2024: 26 · 2023: 22 · 2022: 33 · 2021: 39 · 2020: 35 · 2019: 25 · 2018: 29 · 2017: 24 · 2016: 32 · 2015: 11
- FWCI
- 4.03
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- Agence Nationale de la Recherche (ANR-11-IDEX-0007, ANR-14-CE13-0036, ANR-11-LABX-0042, ANR-10-IBHU-0003)
- LabEx DEvweCAN
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Congenital heart defects research
- Keywords
- outer subventricular zone, germinal zone, microRNA, cell cycle regulation, supragranular layers, neurogenesis
- MeSH terms
- Animals, Cell Cycle, Cerebral Cortex, Biological Evolution, Humans, Primates, Lateral Ventricles
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