Tbr1 Regulates Differentiation of the Preplate and Layer 6

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Reelin Binds α3β1 Integrin and Inhibits Neuronal Migration

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

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The Earliest Thalamocortical Interactions

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Human-specific enrichment of schizophrenia risk-genes in callosal neurons of the developing neocortexPreprint

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A spatial transcriptomic atlas of autism-associated genes identifies convergence in the developing human thalamusPreprint

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Revealing the Impact of Mitochondrial Fitness During Early Neural Development Using Human Brain Organoids

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Loss of Zmiz1 in Mice Leads to Impaired Cortical Development and Autistic-Like Behaviors

Rajan, K. C., Patel, N., Thurmon, A. N., Kantor, B. L., Lorino, M. G., Tiemroth, A. S., Morrison, V. E., Akumuo, M., Shenoy, A., Blanco-Fernandez, X., et al. (2026) · Biological Psychiatry · doi:10.1016/j.biopsych.2026.01.014 · Cited by 5

A subpopulation of cortical neurons altered by mutations in the autism risk gene DDX3X

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Hyperoxygenation During Mid-Neurogenesis Accelerates Cortical Development in the Fetal Mouse Brain

Markert, F., & Storch, A. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.732682 · Cited by 5

Activation of Sonic Hedgehog Signaling Promotes Differentiation of Cortical Layer 4 Neurons via Regulation of Their Cell Positioning

Oishi, K., Nakajima, K., & Motoyama, J. (2022) · Journal of Developmental Biology · doi:10.3390/jdb10040050 · Cited by 5

Transcriptional regulation in the development and dysfunction of neocortical projection neurons

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Long-Term Functional and Cytoarchitectonic Effects of the Systemic Administration of the Histamine H1 Receptor Antagonist/Inverse Agonist Chlorpheniramine During Gestation in the Rat Offspring Primary Motor Cortex

Valle-Bautista, R., Márquez‐Valadez, B., Herrera‐López, G., Griego, E., Galván, E. J., Díaz, N. F., Arias‐Montaño, J., & Molina‐Hernández, A. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.740282 · Cited by 6

Frontotemporal dementia patient-derived iPSC neurons show cell pathological hallmarks and evidence for synaptic dysfunction and DNA damage

Huber, N., Hietanen, T., Heikkinen, S., Shakirzyanova, A., Hoffmann, D. B., Rostalski, H., Dhingra, A., Rodrı́guez-Nieto, S., Kärkkäinen, S., Koskuvi, M., et al. (2025) · Molecular Psychiatry · doi:10.1038/s41380-025-03272-x · Cited by 5

DNA replication fork speed acts as a pacer in cortical neurogenesis

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Neurotrophin-3 influences the number and the laminar fate of cortical progenitors in the developing cerebral cortex of mice through the MEK/ERK1/2 signaling pathway

Ohtsuka, M., Soumiya, H., Hanai, M., Furukawa, S., & Fukumitsu, H. (2013) · Biomedical Research · doi:10.2220/biomedres.34.231 · Cited by 4

A selective defect in the glial wedge as part of the neuroepithelium disruption in hydrocephalus development in the mouse hyh model is associated with complete corpus callosum dysgenesis

Rodríguez‐Pérez, L., Sebastian, J. L., de Diego, I., Smith‐Fernández, A., Roales‐Buján, R., Jimenez, A. J., & Páez, P. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1330412 · Cited by 4

Initial regional cytoarchitectonic differences in dorsal and orbitobasal human developing frontal cortex revealed by spatial transcriptomics

Kopić, J., Haldipur, P., Millen, K. J., Kostović, I., Krasić, J., & Krsnik, Ž. (2024) · Brain Structure and Function · doi:10.1007/s00429-024-02865-6 · Cited by 4

CellWalker2: Multi-omic discovery using hierarchical cell type relationships

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Effects of Atypical Neurotoxins on the Developing Fetal Brain

Tseng, C. (2019) · IntechOpen eBooks · doi:10.5772/intechopen.89755 · Cited by 4

Morphological Diversity of Calretinin Interneurons Generated From Adult Mouse Olfactory Bulb Core Neural Stem Cells

Acosta, F. J. F., Luque-Molina, I., Vecino, R., Díaz‐Guerra, E., Defteralı, Ç., Pignatelli, J., & Vicario‐Abejón, C. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.932297 · Cited by 5

Influence of the Postmortem/Storage Time of Human Corneas on the Properties of Cultured Limbal Epithelial Cells

Le‐Bel, G., Desjardins, P., Gross, C., Ghio, S. C., Couture, C., Germain, L., & Guérin, S. L. (2022) · Cells · doi:10.3390/cells11172716 · Cited by 4

Expression Profiles of MicroRNAs in Stem Cells Differentiation

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Origin and Migration of Olfactory Cajal-Retzius Cells

Frade-Pérez, M. D., Miquelajáuregui, A., & Varela‐Echavarría, A. (2017) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2017.00097 · Cited by 4

Subcortical and Neocortical Guidance of Area-specific Thalamic Innervation

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An aiHumanoid Simulation of Gram-Negative Sepsis: A Comprehensive Multi-Organoid Platform for Advanced Disease Modeling, Drug Discovery, and Personalized MedicinePreprint

Danter, W. R. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.07.18.549304 · Cited by 4

Single-Cell Atlas of Transcription and Chromatin States Reveals Regulatory Programs in the Human BrainPreprint

Xie, Y., Chang, L., Zhong, G., Rink, J. A., Baez-Becerra, T., Armand, E. J., Ding, W., Li, K., Bonne, É., Lie, A., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.02.703166 · Cited by 4

Shared and divergent alteration of whole-brain connectivity and sensory deficits in multiple autism mouse models

Hsu, T.-T., Chen, C.-P., Lin, M.-H., Hung, T.-E., Huang, T., Wang, C.-Y., & Hsueh, Y. (2025) · Molecular Psychiatry · doi:10.1038/s41380-025-03340-2 · Cited by 3

Promoting astrocyte-neuron triiodothyronine shuttling attenuates brain damage in neonatal hypoxic-ischemic encephalopathy

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DLG2–DLG4 Expression Is Associated with Improved Survival and a Synaptic Gene Signature in Lower-Grade Glioma

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FANS Unfixed: Isolation and Proteomic Analysis of Mouse Cell Type-Specific Brain Nuclei

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Cathepsin B deficiency disrupts cortical development via PEG3, leading to depression-like behavior

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Three puncture sites used for in utero electroporation show no significantly different negative impacts during gene transfer into the embryonic mouse brain

Zhang, P., Yan, Z., Wu, C., Niu, L., Liu, N., & Xu, R. (2014) · Neuroscience Letters · doi:10.1016/j.neulet.2014.06.049 · Cited by 3

Spatiotemporal Gradient of Cortical Neuron Death Contributes to Microcephaly in Knock-In Mouse Model of Ligase 4 Syndrome

Lun, M. P., Shannon, M. L., Keleş, S., Reisli, İ., Luche, N. M., Ryan, D., Capuder, K., Notarangelo, L. D., & Lehtinen, M. K. (2019) · American Journal Of Pathology · doi:10.1016/j.ajpath.2019.08.010 · Cited by 3

Positive Modulation of SK Channel Impedes Neuron-Specific Cytoskeletal Organization and Maturation

Shrestha, A., Sultana, R., Adeniyi, P. A., Lee, C. C., & Ogundele, O. M. (2020) · Developmental Neuroscience · doi:10.1159/000507989 · Cited by 3

Expression of Maf family proteins in glutamatergic neurons of the mouse olfactory bulb

Ito, A., & Imamura, F. (2021) · Developmental Neurobiology · doi:10.1002/dneu.22859 · Cited by 3

Cell Type–Specific Nuclei Markers: The Need for Human Brain Research to Go Nuclear

Wiseman, J. A., Dragunow, M., & Park, T. (2021) · The Neuroscientist · doi:10.1177/10738584211037351 · Cited by 5

Directly reprogrammed fragile X syndrome dorsal forebrain precursor cells generate cortical neurons exhibiting impaired neuronal maturation

Edwards, N., Combrinck, C., McCaughey‐Chapman, A., & Connor, B. J. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1254412 · Cited by 3

Suppression of BMP signaling restores mitral cell development impaired by FGF signaling deficits in mouse olfactory bulb

Ito, A., Miller, C., & Imamura, F. (2023) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2023.103913 · Cited by 3

Detailed phenotyping of Tbr1‐2A‐CreER knock‐in mice demonstrates significant impacts on TBR1 protein levels and axon development

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Distinct calcium signals in developing cortical interneurons persist despite disorganization of cortex by Tbr1 KO

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Fused dorsal-ventral cerebral organoids model human cortical interneuron migrationPreprint

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Maternal Poly (I:C)-Induced Placental Inflammation and Endocrine Dysfunction Are Associated with Disrupted Corticogenesis in Mouse Offspring

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Thalamic NRXN1-mediated input to human cortical progenitors drives excitatory neurogenesis

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Developmental Neurobiology of Autism Spectrum Disorders

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Enhanced Differentiation of Human Neural Stem Cells into Cortical Neurons Using 3D Chitosan Scaffolds

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Development and Developmental Disorders of the Cerebral Cortex

ten Donkelaar, H. J., Vasung, L., Molnár, Z., Aronica, E., Lammens, M. M. Y., van Bokhoven, H., Ulzen, K. K.-V., & Hori, A. (2023) · Springer eBooks · doi:10.1007/978-3-031-26098-8_10 · Cited by 3

Sex-Dependent Effects of Angiotensin Type 2 Receptor–Expressing Medial Prefrontal Cortex Interneurons in Fear Extinction Learning

Smith, H. C., Yu, Z., Iyer, L., & Marvar, P. J. (2024) · Biological Psychiatry Global Open Science · doi:10.1016/j.bpsgos.2024.100340 · Cited by 2

Prenatal diagnosis by whole exome sequencing in a family with a novel TBR1 mutation causing intellectual disability

Jin, C., Qian, H., Xu, T., Chen, J., Li, X., & Gu, Z. (2021) · Taiwanese Journal of Obstetrics and Gynecology · doi:10.1016/j.tjog.2021.09.023 · Cited by 2

Microcephaly-causative ASPM mutations disrupt mitotic spindle orientation and timely specification of human outer radial glia cells

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The microcephaly gene Donson is essential for progenitors of cortical glutamatergic and GABAergic neurons

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Reelin and Cajal-Retzius Cells

Mienville, J. (2008) · Springer eBooks · doi:10.1007/978-0-387-76761-1_18 · Cited by 2

Roles of bHLH Transcription Factors Neurod1, Neurod2 and Neurod6 in Cerebral Cortex Development and Commissure Formation.

Bormuth, I. (2016) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-5600 · Cited by 2

Complete loss of CASK causes severe ataxia through cerebellar degeneration in human and mousePreprint

Patel, P. A., Hegert, J. V., Cristian, I., Kerr, A., LaConte, L. E. W., Fox, M. A., Srivastava, S., & Mukherjee, K. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.03.22.436280 · Cited by 2

Persistent postnatal migration of interneurons into the human entorhinal cortexPreprint

Nascimento, M. A., Biagiotti, S. W., Herranz‐Pérez, V., Bueno, R., Ye, C., Abel, T. J., Rubio-Moll, J. S., García‐Verdugo, J. M., Huang, E. J., Álvarez-Buylla, A., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.03.19.484996 · Cited by 3

Mammalian Cortical Regional Specification

Ypsilanti, A. R., & Rubenstein, J. L. R. (2023) · Wiley eBooks · doi:10.1002/9781119860914.ch21 · Cited by 2

Lamin B1 physically regulates neuronal migration by modulating nuclear deformability in the developing cortexPreprint

Shin, M., Ishida, S., Yu, J., Iwashita, M., Jang, G.-U., Cortelli, P., Giorgio, E., Cani, I., Ramazzotti, G., Ratti, S., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.22.683830 · Cited by 2

Novel TBR1 c.1303C>T Variant Led to Diagnosis of Intellectual Developmental Disorder with Autism and Speech Delay: Application of Comprehensive Family-Based Whole-Genome Analysis

Ćuk, M., Unal, B., Bagarić, M., Krakar, G., Walker, M., Hayes, C. P., Gašpić, B., Skular, G., & Ghazani, A. A. (2025) · Genes · doi:10.3390/genes16020120 · Cited by 1

Developmental changes of Reelin-expressing cell populations in the marginal zone of the neocortex of the European wild boar, Sus scrofa

Sobierajski, E., González‐Gómez, M., González‐Arnay, E., Wahle, P., & Meyer, G. (2025) · Brain Structure and Function · doi:10.1007/s00429-025-02958-w · Cited by 1

Distinct contributions of calmodulin-encoding genes to the migration and development of neocortical layer 4 neurons

Ohte, N., Furusho, Y., Hou, P.-S., Sugita, Y., Nohara, A., Yoshizawa, S., Kobayashi, H., & Hanashima, C. (2025) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2025.153130 · Cited by 1

No indication of histological changes in embryonic somatosensory cortex development upon maternal aspartame consumption in mice

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In vivo transition in chromatin accessibility during differentiation of deep-layer excitatory neurons in the neocortex

Sakai, S., Maeda, Y., Saeki, M., Konno, D., Kawaji, K., Matsuzaki, F., Suzuki, Y., Gotoh, Y., & Kishi, Y. (2025) · Development · doi:10.1242/dev.204564 · Cited by 1

A historical and technological perspective on the evolution of the human brain transcriptome

Risgaard, R. D., Doll, H. M., & Sousa, A. M. M. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-27380-3.00053-1 · Cited by 1

Comparative analysis of 105 datasets across species and tissues reveals differential transcriptomic responses to cannabinoids THC and CBD

Liu, R., Kowal, T., Chow, C., Olson, T., Nguyen, E., Yang, S., Lee, J., Cai, H. “., Yang, X., & Blencowe, M. (2025) · Journal of Cannabis Research · doi:10.1186/s42238-025-00361-0 · Cited by 1

miR155, triplicated in Down syndrome, regulates the development of neural stem cells and GABAergic interneurons in Alzheimer's disease mouse and human iPSC models

Zhu, X., Haure‐Mirande, J., Bicak, M., Dong, P., Kruglikov, I., Li, A., Al‐subaie, A., Fossati, V., Noggle, S., Gandy, S., et al. (2026) · Alzheimer s & Dementia · doi:10.1002/alz.71684 · Cited by 1

CCNB1IP1 regulatory evolution underlies gradual increases in cortical size and folding in primates

Hu, T., Ma, P., Kong, Y., Tan, Y., Sun, X., Wang, J., Xiang, K., Mao, B., Wu, Q., Yi, S. V., et al. (2026) · Nature Genetics · doi:10.1038/s41588-026-02773-x · Cited by 2

Genetic Control of Cajal–Retzius Cell Development

Miquelajáuregui, A., & Varela‐Echavarría, A. (2008) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195369007.003.0003 · Cited by 1

Transcriptional and posttranscriptional mechanisms of neuronal migration

Krsnik, Ž., Popovitchenko, T., & Rašin, M. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814407-7.00022-5 · Cited by 2

Development and Developmental Disorders of the Forebrain

ten Donkelaar, H. J., Lammens, M. M. Y., Cruysberg, J. R. M., Ulzen, K. K.-V., Hori, A., Shiota, K., Itoh, K., & Willemsen, M. A. A. P. (2023) · Springer eBooks · doi:10.1007/978-3-031-26098-8_9 · Cited by 2

Die Funktion von Geminin beim Übergang von Neuro- zu Gliogenese in der Maus

Uerlings, Y. (2008) · doi:10.53846/goediss-302 · Cited by 1

Investigation of Sip1 gene interactions in the development of the mammalian telencephalon

Nityanandam, A. (2010) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3228 · Cited by 1

An interdisciplinary approach to brain evolution: A long due debate

Aboitiz, F., Morales, D., & Montiel, J. F. (2003) · Behavioral and Brain Sciences · doi:10.1017/s0140525x03420128 · Cited by 1

Complete Loss of CASK Causes Severe Ataxia Through Cerebellar DegenerationPreprint

Patel, P. A., Hegert, J. V., Cristian, I., Kerr, A., LaConte, L. E. W., Fox, M. A., Srivast, S., & Mukherjee, K. (2021) · Research Square · doi:10.21203/rs.3.rs-456061/v2 · Cited by 1

Inferring and perturbing cell fate regulomes in human cerebral organoids

Fleck, J. S., Jansen, S. M. J., Wollny, D., Seimiya, M., Zenk, F. L., Santel, M., He, Z., Camp, J. G., & Treutlein, B. (2021) · Zenodo (CERN European Organization for Nuclear Research) · doi:10.5281/zenodo.5242912 · Cited by 1

TNF⍺-driven Aβ aggregation, synaptic dysfunction and hypermetabolism in human iPSC-derived cortical neuronsPreprint

Díaz, A. G., Belli, E., Mannini, B., Urrutia, G. A., & Vendruscolo, M. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.30.610594 · Cited by 1

Loss of the autism associated gene Tbr1 disrupts prediction and encoding by prefrontal ensembles during socioemotional behaviorsPreprint

Turner, M., Schwartz, S. R., Darbandi, S. F., Rubenstein, J. L. R., & Sohal, V. S. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.01.21.633988 · Cited by 1

Shared Alteration of Whole-Brain Connectivity and Olfactory Deficits in Multiple Autism Mouse ModelsPreprint

Hsu, T., Chen, C.-P., Lin, M.-H., Huang, T., Wang, C.-Y., Lee, C.-M., Chen, B., Wang, C.-Y., & Hsueh, Y. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.02.02.636175 · Cited by 1

Neurod2/6 transcription factors control basal progenitor differentiation and sequential production of neocortical cell subtypesPreprint

Yan, K., Newman, A. G., Tutukova, S., Gavrish, M. S., Bormuth, I., Bormuth, O., & Tarabykin, V. S. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.02.12.637921 · Cited by 2

PEhub resolves the hierarchical regulatory architecture of multi-way enhancer hubs in the human brainPreprint

Tan, J., & Sun, Y. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.09.704931 · Cited by 1

Regulation of Cortical Circuit Formation

Rodríguez-Tornos, F. M., Cubelos, B., & Nieto, M. (2013) · Springer eBooks · doi:10.1007/978-4-431-54496-8_6

Dissecting human CNS gene expression

Francescatto, M. (2015) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) · doi:10.34626/jffj-3355

The Role of Neonatal Carnitine Palmitoyl Transferase Deficiency Type II on Proliferation of Neuronal Progenitor Cells and Layering of the Cerebral Cortex in the Developing Brain

Chang, H., & Faust, P. L. (2020) · Columbia Undergraduate Science Journal · doi:10.7916/cusj.v2i0.5624

Functional Characterization of Neurexophilins in the Central Nervous system

Benglopoulos, V. (2002) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-96

The role of TSC2 and deptor in fetal cortical development

Tsai, V. (2012) · ScholarlyCommons (University of Pennsylvania)

The Amyloidogenic Pathway Meets the Reelin Signaling Cascade: A Cytoskeleton Bridge Between Neurodevelopment and Neurodegeneration

Daniel, A., Palacios-García, I., & González-Billault, C. E. (2013) · InTech eBooks · doi:10.5772/54038 · Cited by 1

Functional analysis of transcription factor mScrt2 in cortical neurogenesis

Paul, V. (2010) · doi:10.53846/goediss-397

Neurogenesis from Neural Stem Cells, Ependymal Cells and Fibroblasts

Devaraju, K. (2014) · Lund University Publications (Lund University)

CASK: a scaffold protein involved in X‐linked brain malformation phenotypes

Sanders, S. (2009) · Clinical Genetics · doi:10.1111/j.1399-0004.2009.01171_2.x

Functional characterization of m Satb1 and Satb2 in the developing neocortex

del Camino, M. (2008) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-1338

Direct Reprogramming of Somatic Cells into Induced Neuronal Cells: Where We Are and Where We Want to Go

Masserdotti, G., & Berninger, B. (2014) · Stem cell biology and regenerative medicine · doi:10.1007/978-1-4939-1908-6_10

Comparison of Vertebrate Model Systems

Mueller, T., & Wullimann, M. F. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-418669-9.00004-0

Quantitative Expression Analysis of Functional Genes in Four Dog Breeds

Gim, J., Kim, S. H., Lee, H.-E., Jeong, H., Nam, G.-H., Kim, M. K., Huh, J., Choi, B., & Kim, H. (2015) · Journal of Life Science · doi:10.5352/jls.2015.25.8.861

Identification and characterization of neural progenitor cells in the central nervous system using the transcription factor SOX2

Hutton, S. R. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/871b-ky64

The Role Of Fibroblast Growth Factors In Cortical Regeneration After Perinatal Hypoxia: A Model For Neurological Recovery In Premature Children

Fagel, D. M. (2013)

How Can Studies of Animals Help to Uncover the Roles of Genes Implicated in Human Speech and Language Disorders?

Fisher, S. E. (2006) · Contemporary clinical neuroscience · doi:10.1007/978-1-59745-058-4_7

Haploinsufficiency of the T-box transcription factor Tbr1

Ago, Y. (2014) · Folia Pharmacologica Japonica · doi:10.1254/fpj.144.146

Understanding Cellular Differentiation

Vitalis, T. (2010) · Royal Society of Chemistry eBooks · doi:10.1039/9781849732284-00036

UNIVERSIDADE FEDERAL DO RIO GRANDE DO NORTE INSTITUTO DO CÉREBRO PÓS-GRADUAÇÃO EM NEUROCIÊNCIAS EFEITOS DA ELIMINAÇÃO DE NEURÔNIOS INFRAGRANULARES SOBRE A ESPECIFICAÇÃO DE NEURÔNIOS SUPRAGRANULARES DO CÓRTEX CEREBRAL

Landeira, B. S. (2012)

The regulatory role and environmental sensitivity of DNA methylation in neurodevelopment

Resendiz, M. (2017) · IUScholarWorks (Indiana University) · doi:10.7912/c2/2069

From inside-out to outside-in: cortical lamination development in the Reelin-deficient neocortex

Mingo-Moreno, N. (2019) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-7335

The role of α3β1 integrin in cortical development

Stanco, A. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/5jc4-rs44

Autism human neural precursor cells exhibit common defects in neurite outgrowth, cell migration, and mTOR signaling

Prem, S. (2018) · doi:10.7282/t3-2ktw-qt73

Synaptic protein DLG2 controls neurogenic transcriptional programs disrupted in schizophrenia and related disorders

Sanders, B., D’Andrea, D., Collins, M. O., Rees, E., Steward, T. G. J., Zhu, Y., Chapman, G., Legge, S. E., Pardiñas, A. F., Harwood, A. J., et al. (2020) · White Rose Research Online (University of Leeds, The University of Sheffield, University of York)

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