Decision making during interneuron migration in the developing cerebral cortex

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Cxcr7 controls neuronal migration by regulating chemokine responsiveness

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Postmitotic Nkx2-1 controls the migration of telencephalic interneurons by direct repression of guidance receptors

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Embryonic depletion of serotonin affects cortical development

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Arx is a direct target of Dlx2 and thereby contributes to the tangential migration of GABAergic interneurons

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Biased selection of leading process branches mediates chemotaxis during tangential neuronal migration

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Both Doublecortin and Doublecortin-Like Kinase Play a Role in Cortical Interneuron Migration

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Nishimura, Y., Nabeshima, Y., & Kawauchi, T. (2017) · Brain Sciences · doi:10.3390/brainsci7070087 · Cited by 15 · see citing works

Cadherin 8 regulates proliferation of cortical interneuron progenitors

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The polymicrogyria-associated GPR56 promoter preferentially drives gene expression in developing GABAergic neurons in common marmosets

Murayama, A. Y., Kuwako, K.-I., Okahara, J., Bae, B.-I., Okuno, M., Mashiko, H., Shimogori, T., Walsh, C. A., Sasaki, E., & Okano, H. (2020) · Scientific Reports · doi:10.1038/s41598-020-78608-4 · Cited by 14 · see citing works

Ascl1 promotes tangential migration and confines migratory routes by induction of Ephb2 in the telencephalon

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Altered inhibition and excitation in neocortical circuits in congenital microcephaly

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Human brain organoids for understanding substance use disorders

Li, K., Gu, L., Cai, H., Lu, H., Mackie, K., & Guo, F. (2024) · Drug Metabolism and Pharmacokinetics · doi:10.1016/j.dmpk.2024.101036 · Cited by 12 · see citing works

Deletion of BDNF in Pax2 Lineage-Derived Interneuron Precursors in the Hindbrain Hampers the Proportion of Excitation/Inhibition, Learning, and Behavior

Eckert, P., Marchetta, P., Manthey, M., Walter, M. H., Jovanović, S., Savitska, D., Singer, W., Jacob, M. H., Rüttiger, L., Schimmang, T., et al. (2021) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.642679 · Cited by 12 · see citing works

Fast-spiking parvalbumin-positive interneurons: new perspectives of treatment and future challenges in dementia

Zhang, X., Wu, M., Cheng, L., Cao, W., Liu, Z., Yang, S., & Kim, M. S. (2024) · Molecular Psychiatry · doi:10.1038/s41380-024-02756-6 · Cited by 11 · see citing works

d-serine availability modulates prefrontal cortex inhibitory interneuron development and circuit maturation

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ARX regulates cortical interneuron differentiation and migrationPreprint

Lim, Y., Akula, S. K., Myers, A. K., Chen, C., Rafael, K. A., Walsh, C. A., Golden, J. A., & Cho, G. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.31.578282 · Cited by 10 · see citing works

Identification of a Protein Network Driving Neuritogenesis of MGE-Derived GABAergic Interneurons

Franchi, S. A., Astro, V., Macco, R., Tonoli, D., Barnier, J., Botta, M., & de Curtis, I. (2016) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2016.00289 · Cited by 9 · see citing works

Cell‐autonomous impact of polysialic acid‐producing enzyme ST8SIA2 on developmental migration and distribution of cortical interneurons

Schuster, U. E., Rossdam, C., Röckle, I., Schiff, M., & Hildebrandt, H. (2019) · Journal of Neurochemistry · doi:10.1111/jnc.14896 · Cited by 9 · see citing works

The neuronal Golgi in neural circuit formation and reorganization

Nakagawa, N. (2024) · Frontiers in Neural Circuits · doi:10.3389/fncir.2024.1504422 · Cited by 7 · see citing works

Temporal Differences in Interneuron Invasion of Neocortex and Piriform Cortex during Mouse Cortical Development

Hsing, H.-W., Zhuang, Z.-H., Niou, Z., & Chou, S. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz291 · Cited by 7 · see citing works

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

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Loss of ARHGAP15 affects the directional control of migrating interneurons in the embryonic cortex and increases susceptibility to epilepsy

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Dysfunction of specific auditory fibers impacts cortical oscillations, driving an autism phenotype despite near‐normal hearing

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Transcriptional Regulation of Cortical Interneuron Development

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How Cell-Autonomous Is Neuronal Migration in the Forebrain? Molecular Cross-Talk at the Cell Membrane

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Fused dorsal-ventral cerebral organoids model human cortical interneuron migrationPreprint

Bagley, J. A., Reumann, D., Bian, S., & Knoblich, J. A. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/131250 · Cited by 3 · see citing works

Publisher's note

Li, K., Gu, L., Cai, H., Lu, H., Mackie, K., & Guo, F. (2024) · Drug Metabolism and Pharmacokinetics · doi:10.1016/j.dmpk.2024.101031 · Cited by 3 · see citing works

Interneuron migration impairment and brain region-specific DNA damage response following irradiation during early neurogenesis in mice

Berden, L., Rajan, N., Mfossa, A. C. M., Bie, I. D., Etlioglu, E., Benotmane, M. A., Verslegers, M., Aourz, N., Smolders, I. J., Rigo, J., et al. (2025) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-025-05643-7 · Cited by 3 · see citing works

Onecut factors and Pou2f2 regulate the distribution of V2 interneurons in the mouse developing spinal cord

Harris, A., Masgutova, G., Collin, A., Toch, M., Hidalgo-Figueroa, M., Jacob, B., Corcoran, L. M., Francius, C., & Clotman, F. (2018) · doi:10.1101/413054 · Cited by 2 · see citing works

Cat‐Ear‐Line : A Sonographic Sign of Cortical Development?

Matsuzawa, N., Poon, L. C., Machida, M., Nakamura, T. K., Uenishi, K., Wah, Y. M. I., Moungmaithong, S., Itakura, A., Chiyo, H., & Pooh, R. K. (2022) · Journal of Ultrasound in Medicine · doi:10.1002/jum.16153 · Cited by 2 · see citing works

Cell Migration in the Mammalian Cortex

Kim, J. Y., Pleasure, S. J., & Paredes, M. F. (2022) · Springer eBooks · doi:10.1007/978-3-030-88832-9_191 · Cited by 2 · see citing works

Organizers in a dish: Modeling human CNS morphogenesis

Miller, G., Sanchez, D. J. L.-D., Martínez, J. G., Justin, A. W., Lancaster, M. A., & Guglielmi, L. (2026) · Developmental Cell · doi:10.1016/j.devcel.2026.01.003 · Cited by 2 · see citing works

Epigenetic function in neurodevelopment and cognitive impairment

Jakovcevski, M., & Zimmer‐Bensch, G. (2021) · e-Neuroforum · doi:10.1515/nf-2021-0028 · Cited by 1 · see citing works

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 1 · see citing works

Polypyrimidine Tract Binding Protein blocks microRNA-124 biogenesis to enforce its neuronal specific expressionPreprint

Yeom, K., Mitchell, S. A., Linares, A. J., Zheng, S., Lin, C.-H., Wang, X., Hoffmann, A., & Black, D. L. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/297515 · Cited by 1 · see citing works

Extrinsic regulation of interneuron specification and migrationPreprint

Pipicelli, F., Baumann, N., Giaimo, R. D., Kyrousi, C., Bonrath, R., Jabaudon, D., & Cappello, S. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.05.03.490384 · Cited by 1 · see citing works

Mechanisms of Synapse Formation and Synaptic Plasticity

Luk, C. (2015) · Libraries and Cultural Resources (University of Calgary) · doi:10.11575/prism/26867

Characterisation of the gene PTPRS in the development of the cerebral cortex

Sherlock, W. T. (2017) · UCL Discovery (University College London)

Repurposing Clinic-Tested Drugs to Treat Rare Neurogenetic Diseases by Transcriptional Modulation

Hadwen, J. (2018) · uO Research (University of Ottawa) · doi:10.20381/ruor-21849

Single-cell transcriptomic analysis identifies neocortical developmental differences between human and mousePreprint

Zhou, Z., Wang, S., Zhang, D., Jiang, X., Li, J., Gu, Y., & Sun, H. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.04.23.056390

Coordination of different modes of neuronal migration and functional organization of the cerebral cortex

Higginbotham, H. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814407-7.00024-9

Semaphorin 3C attracts MGE-derived cortical interneurons in the deep migratory stream guiding them into the developing neocortexPreprint

Aiello-Holden, K., & Bolz, J. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.03.18.435991

The spatial distribution of cortical interneurons: the role of clustered protocadherins

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Neurodevelopmental Mechanisms of Pediatric Psychiatric Disorders

Rubeis, S. D., Roeder, K., & Devlin, B. (2017) · Oxford University Press eBooks · doi:10.1093/med/9780190681425.003.0062

Cell Migration in the Mammalian Cortex

Kim, J. Y., Pleasure, S. J., & Paredes, M. F. (2022) · Springer eBooks · doi:10.1007/978-1-4614-6434-1_191-1

The indirect pathway hypothesis of schizophrenia: insights from perinatal asphyxia

Vázquez-Borsetti, P. (2026) · Frontiers in Physiology · doi:10.3389/fphys.2026.1759386

Deletion of Alg13 disrupts postnatal development and migration of GABAergic cortical interneurons

Liu, H., Qian, X., Ma, H., Liu, A. J., Li, S., Wang, X., Zhang, J., & Gao, P. (2026) · Frontiers in Neurology · doi:10.3389/fneur.2026.1757800

Mise en place des interneurones GABAergiques de la couche moléculaire du cervelet au cours du développement

Cadilhac, C. (2015) · doi:10.70675/1866648cza7e8z4ba9za992z3d86a8f13ad3

Régulation de la migration radiale et de l’intégration synaptique dans le cerveau antérieur postnatal : liens avec l’activité neuronale

Bugeon, S. (2017) · doi:10.70675/75120f88z213cz43f0z9a09z26fbe5825a27

Physiopathologie moléculaire et cellulaire des anomalies du développement du cortex cérébral : le syndrome d'Aicardi

Cavallin, M. (2019) · theses.fr (ABES) · doi:10.70675/e19605c3z0e27z4653zbad3zebf3f0cb6da5

Identification de nouveaux régulateurs de la synaptogénèse GABAergique à la jonction neuromusculaire du nématode Caenorhabditis elegans

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Caractérisation fonctionnelle et exploration du spectre phénotypique de gènes responsables de malformations cérébrales

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Cellular and molecular mechanisms controlling the migration of neocortical interneurons

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[SY1.1]: Cellular and molecular mechanisms controlling the migration of cortical gabaergic interneurons

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Interneuron odyssey: molecular mechanisms of tangential migration

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Migratory pathways of GABAergic interneurons when they enter the neocortex

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