Tbr1 Regulates Differentiation of the Preplate and Layer 6

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

Reeler/Disabled-like Disruption of Neuronal Migration in Knockout Mice Lacking the VLDL Receptor and ApoE Receptor 2

Trommsdorff, M., Gotthardt, M., Hiesberger, T., Shelton, J., Stockinger, W., Nimpf, J., Hammer, R. E., Richardson, J. A., & Herz, J. (1999) · Cell · doi:10.1016/s0092-8674(00)80782-5 · Cited by 1,261

Commissural connections of the hippocampal region in the rat, with special reference to their mode of termination

Blackstad, T. W. (1956) · The Journal of Comparative Neurology · doi:10.1002/cne.901050305 · Cited by 964

The medial ganglionic eminence gives rise to a population of early neurons in the developing cerebral cortex

Lavdas, A. A., Grigoriou, M., Pachnis, V., & Parnavelas, J. G. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-18-07881.1999 · Cited by 765

The Subplate, A Transient Neocortical Structure: Its Role in the Development of Connections between Thalamus and Cortex

Allendoerfer, K. L., & Shatz, C. J. (1994) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.17.030194.001153 · Cited by 653

Subplate Neurons Pioneer the First Axon Pathway from the Cerebral Cortex

McConnell, S. K., Ghosh, A., & Shatz, C. J. (1989) · Science · doi:10.1126/science.2475909 · Cited by 647

Neocortical histogenesis in normal and reeler mice: A developmental study based upon [3H]thymidine autoradiography

Caviness, V. S. (1982) · Developmental Brain Research · doi:10.1016/0165-3806(82)90141-9 · Cited by 639

Reelin Binds α3β1 Integrin and Inhibits Neuronal Migration

Dulabon, L., Olson, E. C., Taglienti, M. G., Eisenhuth, S., McGrath, B., Walsh, C. A., Kreidberg, J. A., & Anton, E. S. (2000) · Neuron · doi:10.1016/s0896-6273(00)00007-6 · Cited by 577

Regional and Cellular Patterns of reelin mRNA Expression in the Forebrain of the Developing and Adult Mouse

Alcántara, S., Ruiz, M., D’Arcangelo, G., Ezan, F., de Lecea, L., Curran, T., Sotelo, C., & Soriano, E. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-19-07779.1998 · Cited by 568

Requirement for subplate neurons in the formation of thalamocortical connections

Ghosh, A., Antonini, A., McConnell, S. K., & Shatz, C. J. (1990) · Nature · doi:10.1038/347179a0 · Cited by 563

Cerebral organoids model human brain development and microcephaly

Lancaster, M. A., Renner, M., Martin, C.-A., Wenzel, D., Bicknell, L. S., Hurles, M. E., Homfray, T., Penninger, J. M., Jackson, A. P., & Knoblich, J. A. (2013) · Nature · doi:10.1038/nature12517 · Cited by 5,372

Spatio-temporal transcriptome of the human brain

Kang, H. J., Kawasawa, Y. I., Cheng, F., Zhu, Y., Xu, X., Li, M., Sousa, A. M. M., Pletikos, M., Meyer, K. A., Sedmak, G., et al. (2011) · Nature · doi:10.1038/nature10523 · Cited by 2,084

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 1,704

Reconstruction and Simulation of Neocortical Microcircuitry

Markram, H., Muller, E., Ramaswamy, S., Reimann, M. W., Abdellah, M., Sanchez, C. A., Ailamaki, A., Alonso-Nanclares, L., Antille, N., Arsever, S., et al. (2015) · Cell · doi:10.1016/j.cell.2015.09.029 · Cited by 1,557

Endothelial Cells Stimulate Self-Renewal and Expand Neurogenesis of Neural Stem Cells

Shen, Q., Goderie, S. K., Jin, L., Karanth, N., Sun, Y., Abramova, N. E., Vincent, P. A., Pumiglia, K. M., & Temple, S. (2004) · Science · doi:10.1126/science.1095505 · Cited by 1,574

Self-Organized Formation of Polarized Cortical Tissues from ESCs and Its Active Manipulation by Extrinsic Signals

Eiraku, M., Watanabe, K., Matsuo-Takasaki, M., Kawada, M., Yonemura, S., Matsumura, M., Wataya, T., Nishiyama, A., Muguruma, K., & Sasai, Y. (2008) · Cell Stem Cell · doi:10.1016/j.stem.2008.09.002 · Cited by 1,522

Pax6, Tbr2, and Tbr1 Are Expressed Sequentially by Radial Glia, Intermediate Progenitor Cells, and Postmitotic Neurons in Developing Neocortex

Englund, C., Fink, A., Lau, C., Pham, D., Daza, R. A. M., Bulfone, A., Kowalczyk, T., & Hevner, R. F. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.2899-04.2005 · Cited by 1,261

Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders

O’Roak, B. J., Vives, L., Fu, W., Egertson, J. D., Stanaway, I. B., Phelps, I. G., Carvill, G., Kumar, A., Lee, C., Ankenman, K., et al. (2012) · Science · doi:10.1126/science.1227764 · Cited by 1,240

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 1,077

Dissecting the genomic complexity underlying medulloblastoma

Jones, D. T. W., Jäger, N., Kool, M., Zichner, T., Hutter, B., Sultan, M., Cho, Y.-J., Pugh, T. J., Hovestadt, V., Stütz, A. M., et al. (2012) · Nature · doi:10.1038/nature11284 · Cited by 839

Advancing the understanding of autism disease mechanisms through genetics

de la Torre-Ubieta, L., Won, H., Stein, J. L., & Geschwind, D. H. (2016) · Nature Medicine · doi:10.1038/nm.4071 · Cited by 827

Fused cerebral organoids model interactions between brain regions

Bagley, J. A., Reumann, D., Bian, S., Lévi-Strauss, J., & Knoblich, J. A. (2017) · Nature Methods · doi:10.1038/nmeth.4304 · Cited by 790

A developmental and genetic classification for malformations of cortical development

Barkovich, A. J., Kuzniecky, R., Jackson, G. D., Guerrini, R., & Dobyns, W. B. (2005) · Neurology · doi:10.1212/01.wnl.0000183747.05269.2d · Cited by 730

Satb2 Is a Postmitotic Determinant for Upper-Layer Neuron Specification in the Neocortex

Britanova, O., de Juan Romero, C., Cheung, A., Kwan, K. Y., Schwark, M., Gyorgy, A., Vogel, T., Akopov, S., Mitkovski, M., Agoston, D., et al. (2008) · Neuron · doi:10.1016/j.neuron.2007.12.028 · Cited by 674

Satb2 Regulates Callosal Projection Neuron Identity in the Developing Cerebral Cortex

Alcamo, E. A., Chirivella, L., Dautzenberg, M., Dobreva, G., Fariñas, I., Grosschedl, R., & McConnell, S. K. (2008) · Neuron · doi:10.1016/j.neuron.2007.12.012 · Cited by 658

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

Expression of Cux‐1 and Cux‐2 in the subventricular zone and upper layers II–IV of the cerebral cortex

Nieto, M., Monuki, E. S., Tang, H., Imitola, J., Haubst, N., Khoury, S. J., Cunningham, J., Götz, M., & Walsh, C. A. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20322 · Cited by 569

Multipolar Migration: The Third Mode of Radial Neuronal Migration in the Developing Cerebral Cortex

Tabata, H., & Nakajima, K. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-31-09996.2003 · Cited by 556

Autism spectrum disorder: neuropathology and animal models

Varghese, M., Keshav, N., Jacot-Descombes, S., Warda, T., Wicinski, B., Dickstein, D. L., Harony-Nicolas, H., De Rubeis, S., Drapeau, E., Buxbaum, J. D., et al. (2017) · Acta Neuropathologica · doi:10.1007/s00401-017-1736-4 · Cited by 536

Architectonic Mapping of the Human Brain beyond Brodmann

Amunts, K., & Zilles, K. (2015) · Neuron · doi:10.1016/j.neuron.2015.12.001 · Cited by 559

Modeling human cortical development in vitro using induced pluripotent stem cells

Mariani, J., Simonini, M. V., Palejev, D., Tomasini, L., Coppola, G., Szekely, A. M., Horvath, T. L., & Vaccarino, F. M. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1202944109 · Cited by 526

G Protein-Coupled Receptor-Dependent Development of Human Frontal Cortex

Piao, X., Hill, R. S., Bodell, A., Chang, B. S., Basel-Vanagaite, L., Straussberg, R., Dobyns, W. B., Qasrawi, B., Winter, R. M., Innes, A. M., et al. (2004) · Science · doi:10.1126/science.1092780 · Cited by 517

Teleostean and mammalian forebrains contrasted: Evidence from genes to behavior

Wullimann, M. F., & Mueller, T. (2004) · Journal of Comparative Neurology · doi:10.1002/cne.20183 · Cited by 491

Molecular characterization of selectively vulnerable neurons in Alzheimer’s disease

Leng, K., Li, E., Eser, R., Piergies, A., Sit, R., Tan, M., Neff, N., Li, S. H., Rodriguez, R. D., Suemoto, C. K., et al. (2021) · Nature Neuroscience · doi:10.1038/s41593-020-00764-7 · Cited by 485

Fezl Is Required for the Birth and Specification of Corticospinal Motor Neurons

Molyneaux, B. J., Arlotta, P., Hirata, T., Hibi, M., & Macklis, J. D. (2005) · Neuron · doi:10.1016/j.neuron.2005.08.030 · Cited by 491

Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain

Ferland, R. J., Cherry, T. J., Preware, P. O., Morrisey, E. E., & Walsh, C. A. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10654 · Cited by 486

Multiple origins of Cajal-Retzius cells at the borders of the developing pallium

Bielle, F., Griveau, A., Narboux‐Nême, N., Vigneau, S., Sigrist, M., Arber, S., Wassef, M., & Pierani, A. (2005) · Nature Neuroscience · doi:10.1038/nn1511 · Cited by 478

Ezh2, the histone methyltransferase of PRC2, regulates the balance between self-renewal and differentiation in the cerebral cortex

Pereira, J. D., Sansom, S. N., Smith, J. C., Dobenecker, M., Tarakhovsky, A., & Livesey, F. J. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1002530107 · Cited by 465

Transcription factors in glutamatergic neurogenesis: conserved programs in neocortex, cerebellum, and adult hippocampus

Hevner, R. F., Hodge, R. D., Daza, R. A. M., & Englund, C. (2006) · Neuroscience Research · doi:10.1016/j.neures.2006.03.004 · Cited by 410

T-Box Genes in Vertebrate Development

Naiche, L. A., Harrelson, Z., Kelly, R. G., & Papaioannou, V. E. (2005) · Annual Review of Genetics · doi:10.1146/annurev.genet.39.073003.105925 · Cited by 437

Intermediate Neuronal Progenitors (Basal Progenitors) Produce Pyramidal–Projection Neurons for All Layers of Cerebral Cortex

Kowalczyk, T., Pontious, A., Englund, C., Daza, R. A. M., Bedogni, F., Hodge, R. D., Attardo, A., Bell, C., Huttner, W. Β., & Hevner, R. F. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhn260 · Cited by 438

LKB1 and SAD Kinases Define a Pathway Required for the Polarization of Cortical Neurons

Barnes, A. P., Lilley, B. N., Pan, Y. A., Plummer, L. J., Powell, A. W., Raines, A. N., Sanes, J. R., & Polleux, F. (2007) · Cell · doi:10.1016/j.cell.2007.03.025 · Cited by 418

Transcriptional co-regulation of neuronal migration and laminar identity in the neocortex

Kwan, K. Y., Šestan, N., & Anton, E. S. (2012) · Development · doi:10.1242/dev.069963 · Cited by 414

The determination of projection neuron identity in the developing cerebral cortex

Leone, D. P., Srinivasan, K., Chen, B., Alcamo, E., & McConnell, S. K. (2008) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2008.05.006 · Cited by 382

Tbr2 Directs Conversion of Radial Glia into Basal Precursors and Guides Neuronal Amplification by Indirect Neurogenesis in the Developing Neocortex

Sessa, A., Mao, C., Hadjantonakis, A., Klein, W. H., & Broccoli, V. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.028 · Cited by 389

Adult generation of glutamatergic olfactory bulb interneurons

Brill, M. S., Ninkovic, J., Winpenny, E. M., Hodge, R. D., Ozen, I., Yang, R., Lepier, A., Gascón, S., Erdélyi, F., Szabó, G., et al. (2009) · Nature Neuroscience · doi:10.1038/nn.2416 · Cited by 364

Dose-dependent functions of Fgf8 in regulating telencephalic patterning centers

Storm, E. E., Garel, S., Borello, U., Hébert, J. M., Martı́nez, S., McConnell, S. K., Martin, G. R., & Rubenstein, J. L. R. (2006) · Development · doi:10.1242/dev.02324 · Cited by 361

Fezl regulates the differentiation and axon targeting of layer 5 subcortical projection neurons in cerebral cortex

Chen, B., Schaevitz, L. R., & McConnell, S. K. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0508732102 · Cited by 353

Mitotic Spindle Regulation by Nde1 Controls Cerebral Cortical Size

Feng, Y., & Walsh, C. A. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.023 · Cited by 368

miRNAs are essential for survival and differentiation of newborn neurons but not for expansion of neural progenitors during early neurogenesis in the mouse embryonic neocortex

De Pietri Tonelli, D., Pulvers, J. N., Haffner, C., Murchison, E. P., Hannon, G. J., & Huttner, W. B. (2008) · Development · doi:10.1242/dev.025080 · Cited by 343

The CSF-1 receptor ligands IL-34 and CSF-1 exhibit distinct developmental brain expression patterns and regulate neural progenitor cell maintenance and maturation

Nandi, S., Gökhan, Ş., Dai, X.-M., Wei, S., Enikolopov, G., Lin, H., Mehler, M. F., & Stanley, E. R. (2012) · Developmental Biology · doi:10.1016/j.ydbio.2012.03.026 · Cited by 356

Molecular mechanisms underlying cell fate specification in the developing telencephalon

Schuurmans, C. J., & Guillemot, F. (2002) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(02)00286-6 · Cited by 339

The Fezf2–Ctip2 genetic pathway regulates the fate choice of subcortical projection neurons in the developing cerebral cortex

Chen, B., Wang, S. S., Hattox, A. M., Rayburn, H., Nelson, S. B., & McConnell, S. K. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804918105 · Cited by 351

The T-box transcription factor Eomes/Tbr2 regulates neurogenesis in the cortical subventricular zonePreprint

Arnold, S. J., Huang, G., Cheung, A. F. P., Era, T., Nishikawa, S. I., Bikoff, E. K., Molnár, Z., Robertson, E. J., & Groszer, M. (2008) · Genes & Development · doi:10.1101/gad.475408 · Cited by 340

Tbr1 regulates regional and laminar identity of postmitotic neurons in developing neocortex

Bedogni, F., Hodge, R. D., Elsen, G. E., Nelson, B. R., Daza, R. A. M., Beyer, R. P., Bammler, T. K., Rubenstein, J. L. R., & Hevner, R. F. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1002285107 · Cited by 322

Inferring and perturbing cell fate regulomes in human brain organoids

Fleck, J. S., Jansen, S. M. J., Wollny, D., Zenk, F., Seimiya, M., Jain, A., Okamoto, R., Santel, M., He, Z., Camp, J. G., et al. (2023) · Nature · doi:10.1038/s41586-022-05279-8 · Cited by 315

Development of the Deep Cerebellar Nuclei: Transcription Factors and Cell Migration from the Rhombic Lip

Fink, A. J. P., Englund, C., Daza, R. A. M., Pham, D., Lau, C., Nivison, M. P., Kowalczyk, T., & Hevner, R. F. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.5203-05.2006 · Cited by 314

SOX5 Controls the Sequential Generation of Distinct Corticofugal Neuron Subtypes

Lai, T. S., Jabaudon, D., Molyneaux, B. J., Azim, E., Arlotta, P., Menezes, J. R. L., & Macklis, J. D. (2008) · Neuron · doi:10.1016/j.neuron.2007.12.023 · Cited by 307

N-cadherin mediates cortical organization in the mouse brain

Kadowaki, M., Nakamura, S., Machoň, O., Krauss, S. J. K., Radice, G. L., & Takeichi, M. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.12.014 · Cited by 298

The T-box gene family: emerging roles in development, stem cells and cancer

Papaioannou, V. E. (2014) · Development · doi:10.1242/dev.104471 · Cited by 293

Four-Dimensional Migratory Coordinates of GABAergic Interneurons in the Developing Mouse Cortex

Ang, E. S. B. C., Haydar, T. F., Gluncic, V., & Rakic, P. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-13-05805.2003 · Cited by 282

Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum

Najm, J., Horn, D., Wimplinger, I., Golden, J. A., Chizhikov, V. V., Sudi, J., Christian, S. L., Ullmann, R., Kuechler, A., Haas, C. A., et al. (2008) · Nature Genetics · doi:10.1038/ng.194 · Cited by 278

The Genetics of Primary Microcephaly

Jayaraman, D., Bae, B.-I., & Walsh, C. A. (2018) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev-genom-083117-021441 · Cited by 285

On the epigenetic regulation of the human reelin promoter

Chen, Y. (2002) · Nucleic Acids Research · doi:10.1093/nar/gkf401 · Cited by 276

Fundamental Elements in Autism: From Neurogenesis and Neurite Growth to Synaptic Plasticity

Gilbert, J. P., & Man, H. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00359 · Cited by 286

A comparative strategy for single-nucleus and single-cell transcriptomes confirms accuracy in predicted cell-type expression from nuclear RNA

Lake, B. B., Codeluppi, S., Yung, Y. C., Gao, D., Chun, J., Kharchenko, P. V., Linnarsson, S., & Zhang, K. (2017) · Scientific Reports · doi:10.1038/s41598-017-04426-w · Cited by 271

SOX5 postmitotically regulates migration, postmigratory differentiation, and projections of subplate and deep-layer neocortical neurons

Kwan, K. Y., Lam, M. M. S., Krsnik, Ž., Kawasawa, Y. I., Lefebvre, V., & Šestan, N. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0806791105 · Cited by 271

Role of Sox2 in the development of the mouse neocortex

Bani‐Yaghoub, M., Tremblay, R. G., Lei, J. X., Zhang, D., Zurakowski, B., Sandhu, J. K., Smith, B., Ribecco‐Lutkiewicz, M., Kennedy, J. A., Walker, P. R., et al. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.03.007 · Cited by 271

Molecular Biomarkers for Embryonic and Adult Neural Stem Cell and Neurogenesis

Zhang, J., & Jiao, J. (2015) · BioMed Research International · doi:10.1155/2015/727542 · Cited by 294

Cdk5rap2 regulates centrosome function and chromosome segregation in neuronal progenitors

Lizarraga, S. B., Margossian, S. P., Harris, M. H., Campagna, D. R., Han, A., Blevins, S., Mudbhary, R., Barker, J. E., Walsh, C. A., & Fleming, M. D. (2010) · Development · doi:10.1242/dev.040410 · Cited by 281

Development, evolution and pathology of neocortical subplate neurons

Hoerder‐Suabedissen, A., & Molnár, Z. (2015) · Nature reviews. Neuroscience · doi:10.1038/nrn3915 · Cited by 278

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

Neocortical layer 6, a review

Thomson (2010) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2010.00013 · Cited by 293

Getting to the cores of autism

Iakoucheva, L. M., Muotri, A. R., & Sebat, J. (2019) · Cell · doi:10.1016/j.cell.2019.07.037 · Cited by 260

doublecortin-like kinase Functions with doublecortin to Mediate Fiber Tract Decussation and Neuronal Migration

Koizumi, H., Tanaka, T., & Gleeson, J. G. (2006) · Neuron · doi:10.1016/j.neuron.2005.10.040 · Cited by 263

Ectopic expression of the Dlx genes induces glutamic acid decarboxylase and Dlx expression

Stühmer, T., Anderson, S. A., Ekker, M., & Rubenstein, J. L. R. (2002) · Development · doi:10.1242/dev.129.1.245 · Cited by 257

The Magnificent Compromise: Cortical Field Evolution in Mammals

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

Tbr1 and Fezf2 Regulate Alternate Corticofugal Neuronal Identities during Neocortical Development

McKenna, W. L., Betancourt, J., Larkin, K. A., Abrams, B., Guo, C., Rubenstein, J. L. R., & Chen, B. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.4131-10.2011 · Cited by 252

Zfp312 is required for subcortical axonal projections and dendritic morphology of deep-layer pyramidal neurons of the cerebral cortex

Chen, J.-G., Rašin, M.-R., Kwan, K. Y., & Šestan, N. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0509032102 · Cited by 246

Beyond Laminar Fate: Toward a Molecular Classification of Cortical Projection/Pyramidal Neurons

Hevner, R. F., Daza, R. A. M., Rubenstein, J. L. R., Stunnenberg, H. G., Olavarría, J. F., & Englund, C. (2003) · Developmental Neuroscience · doi:10.1159/000072263 · Cited by 250

Cell fate specification in the mammalian telencephalon

Guillemot, F. (2007) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2007.02.009 · Cited by 248

Dynamics of Cux2 Expression Suggests that an Early Pool of SVZ Precursors is Fated to Become Upper Cortical Layer Neurons

Zimmer, C. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh102 · Cited by 250

Expression ofDbx1,Neurogenin 2,Semaphorin 5A,Cadherin 8, andEmx1distinguish ventral and lateral pallial histogenetic divisions in the developing mouse claustroamygdaloid complex

Medina, L. M., Legáz, I., González, G. G., Castro, F. D., Rubenstein, J. L. R., & Puelles, L. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20141 · Cited by 244

The Cells of Cajal-Retzius: Still a Mystery One Century After

Soriano, E., & del Rı́o, J. A. (2005) · Neuron · doi:10.1016/j.neuron.2005.04.019 · Cited by 243

Novel transcription factor Satb2 interacts with matrix attachment region DNA elements in a tissue‐specific manner and demonstrates cell‐type‐dependent expression in the developing mouse CNS

Britanova, O. V., Akopov, S. B., Lukyanov, S., Gruß, P., & Tarabykin, V. S. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.03897.x · Cited by 233

Ciliary transition zone activation of phosphorylated Tctex-1 controls ciliary resorption, S-phase entry and fate of neural progenitors

Li, A., Saito, M., Chuang, J.-Z., Tseng, Y. Y., Dedesma, C., Tomizawa, K., Kaitsuka, T., & Sung, C.-H. (2011) · Nature Cell Biology · doi:10.1038/ncb2218 · Cited by 231

Three hypotheses for developmental defects that may underlie some forms of autism spectrum disorder

Rubenstein, J. L. (2010) · Current Opinion in Neurology · doi:10.1097/wco.0b013e328336eb13 · Cited by 230

A Molecular Neuroanatomical Study of the Developing Human Neocortex from 8 to 17 Postconceptional Weeks Revealing the Early Differentiation of the Subplate and Subventricular Zone

Bayatti, N., Moss, J. A., Sun, L. Y., Ambrose, P. M., Ward, J. F. H., Lindsay, S., & Clowry, G. J. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhm184 · Cited by 232

Neural development of the neuregulin receptor ErbB4 in the cerebral cortex and the hippocampus: preferential expression by interneurons tangentially migrating from the ganglionic eminences

Yau, H.-J. (2003) · Cerebral Cortex · doi:10.1093/cercor/13.3.252 · Cited by 225

Candidate genes, pathways and mechanisms for bipolar (manic-depressive) and related disorders: an expanded convergent functional genomics approach

Ogden, C. A., Rich, M. E., Schork, N. J., Paulus, M. P., Geyer, M. A., Lohr, J. B., Kuczenski, R., & Niculescu, A. B. (2004) · Molecular Psychiatry · doi:10.1038/sj.mp.4001547 · Cited by 221

The development of cortical connections

Price, D. J., Kennedy, H., Dehay, C., Zhou, L., Mercier, M., Jossin, Y., Goffinet, A. M., Tissir, F., Blakey, D., & Molnár, Z. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04620.x · Cited by 223

The Cell-Intrinsic Requirement of Sox6 for Cortical Interneuron Development

Batista-Brito, R., Rossignol, E., Hjerling-Leffler, J., Denaxa, M., Wegner, M., Lefebvre, V., Pachnis, V., & Fishell, G. (2009) · Neuron · doi:10.1016/j.neuron.2009.08.005 · Cited by 214

Abnormal Development of Forebrain Midline Glia and Commissural Projections inNfiaKnock-Out Mice

Shu, T., Butz, K. G., Plachez, C., Gronostajski, R. M., & Richards, L. J. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-01-00203.2003 · Cited by 218

Role of β-catenin in the developing cortical and hippocampal neuroepithelium

Machoň, O., van den Bout, C. J., Backman, M., Kemler, R., & Krauss, S. J. K. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00519-0 · Cited by 221

Ena/VASP Is Required for Neuritogenesis in the Developing Cortex

Kwiatkowski, A. V., Rubinson, D. A., Dent, E. W., van Veen, J. E., Leslie, J. D., Zhang, J., Mebane, L. M., Philippar, U., Pinheiro, E. M., Burds, A. A., et al. (2007) · Neuron · doi:10.1016/j.neuron.2007.09.008 · Cited by 222

Genetics and genomics of autism spectrum disorder: embracing complexity

De Rubeis, S., & Buxbaum, J. D. (2015) · Human Molecular Genetics · doi:10.1093/hmg/ddv273 · Cited by 208

CORTECON: A Temporal Transcriptome Analysis of In Vitro Human Cerebral Cortex Development from Human Embryonic Stem Cells

van de Leemput, J., Boles, N. C., Kiehl, T. R., Corneo, B., Lederman, P. L., Menon, V., Lee, C., Martinez, R. A., Levi, B. P., Thompson, C. L., et al. (2014) · Neuron · doi:10.1016/j.neuron.2014.05.013 · Cited by 210

Semaphorin 3F Is Critical for Development of Limbic System Circuitry and Is Required in Neurons for Selective CNS Axon Guidance Events

Sahay, A., Molliver, M. E., Ginty, D. D., & Kolodkin, A. L. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-17-06671.2003 · Cited by 217

TBR1 directly represses Fezf2 to control the laminar origin and development of the corticospinal tract

Han, W., Kwan, K. Y., Shim, S., Lam, M. M. S., Shin, Y., Xu, X., Zhu, Y., Li, M., & Šestan, N. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1016723108 · Cited by 206

Fgf10 Regulates Transition Period of Cortical Stem Cell Differentiation to Radial Glia Controlling Generation of Neurons and Basal Progenitors

Sahara, S., & O’Leary, D. D. M. (2009) · Neuron · doi:10.1016/j.neuron.2009.06.006 · Cited by 206

Expression of p73 and Reelin in the Developing Human Cortex

Meyer, G., Pérez‐García, C. G., Ábrahám, H., & Caput, D. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-12-04973.2002 · Cited by 209

Cortical and thalamic axon pathfinding defects in Tbr1 , Gbx2 , and Pax6 mutant mice: Evidence that cortical and thalamic axons interact and guide each other

Hevner, R. F., Miyashita‐Lin, E., & Rubenstein, J. L. R. (2002) · Journal of Comparative Neurology · doi:10.1002/cne.10219 · Cited by 202

Absence of Fyn and Src Causes a Reeler-Like Phenotype

Kuo, G., Arnaud, L., Kronstad-O'Brien, P., & Cooper, J. A. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.1656-05.2005 · Cited by 205

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 204

Zika virus infection disrupts neurovascular development and results in postnatal microcephaly with brain damage

Shao, Q., Herrlinger, S. A., Yang, S., Lai, F., Moore, J. M., Brindley, M. A., & Chen, J.-F. (2016) · Development · doi:10.1242/dev.143768 · Cited by 203

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

Cajal–Retzius cells in the mouse: transcription factors, neurotransmitters, and birthdays suggest a pallial origin

Hevner, R. F., Neogi, T., Englund, C., Daza, R. A. M., & Fink, A. (2003) · Developmental Brain Research · doi:10.1016/s0165-3806(02)00641-7 · Cited by 202

Histogenetic compartments of the mouse centromedial and extended amygdala based on gene expression patterns during development

García‐López, M., Abellán, A., Legáz, I., Rubenstein, J. L. R., Puelles, L., & Medina, L. M. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21524 · Cited by 197

Developmental Emergence of Adult Neural Stem Cells as Revealed by Single-Cell Transcriptional Profiling

Yuzwa, S. A., Borrett, M. J., Innes, B. T., Voronova, A., Ketela, T., Kaplan, D. R., Bader, G. D., & Miller, F. D. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.12.017 · Cited by 205

Specialized Subpopulations of Deep-Layer Pyramidal Neurons in the Neocortex: Bridging Cellular Properties to Functional Consequences

Baker, A. L., Kalmbach, B. E., Morishima, M., Kim, J., Juavinett, A., Li, N., & Dembrow, N. C. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.0150-18.2018 · Cited by 205

Tbr1 and Fezf2 Regulate Alternate Corticofugal Neuronal Identities during Neocortical Development

McKenna, W. L., Betancourt, J., Larkin, K. A., Abrams, B., Guo, C., Rubenstein, J. L. R., & Chen, B. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.4131-10.2011 · Cited by 252

Tbr1 regulates regional and laminar identity of postmitotic neurons in developing neocortex

Bedogni, F., Hodge, R. D., Elsen, G. E., Nelson, B. R., Daza, R. A. M., Beyer, R. P., Bammler, T. K., Rubenstein, J. L. R., & Hevner, R. F. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1002285107 · Cited by 322

Tbr1 Conducts the Orchestration of Early Cortical Development

Dwyer, N. D., & O’Leary, D. D. M. (2001) · Neuron · doi:10.1016/s0896-6273(01)00202-1 · Cited by 20

Tbr1 Misexpression Alters Neuronal Development in the Cerebral Cortex

Crespo, I., Pignatelli, J., Kinare, V., Méndez‐Gómez, H. R., Esgleas, M., Román, M. J., Canals, J. M., Tole, S., & Vicario‐Abejón, C. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-02936-x · Cited by 32

A unique subpopulation of Tbr1-expressing deep layer neurons in the developing cerebral cortex

Kolk, S. M., Whitman, M. C., Yun, M. E., Shete, P. B., & Donoghue, M. J. (2005) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2005.08.017 · Cited by 43