Physiologically Distinct Temporal Cohorts of Cortical Interneurons Arise from Telencephalic Olig2 -Expressing Precursors

The Mouse Brain in Stereotaxic Coordinates

Paxinos, G. (2001) · Cited by 12,859

Generalized lacZ expression with the ROSA26 Cre reporter strain

Soriano, P. (1999) · Nature Genetics · doi:10.1038/5007 · Cited by 5,237

Interneurons of the neocortical inhibitory system

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

Proneural genes and the specification of neural cell types

Bertrand, N., Castro, D. S., & Guillemot, F. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn874 · Cited by 1,572

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

Interneuron Migration from Basal Forebrain to Neocortex: Dependence on Dlx 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

GABAergic cell subtypes and their synaptic connections in rat frontal cortex

Kawaguchi, Y. (1997) · Cerebral Cortex · doi:10.1093/cercor/7.6.476 · Cited by 1,416

Efficient Recombination in Diverse Tissues by a Tamoxifen-Inducible Form of Cre: A Tool for Temporally Regulated Gene Activation/Inactivation in the Mouse

Hayashi, S., & McMahon, A. P. (2002) · Developmental Biology · doi:10.1006/dbio.2002.0597 · Cited by 1,351

Competing waves of oligodendrocytes in the forebrain and postnatal elimination of an embryonic lineage

Kessaris, N., Fogarty, M., Iannarelli, P., Grist, M., Wegner, M., & Richardson, W. D. (2006) · Nature Neuroscience · doi:10.1038/nn1620 · Cited by 1,195

Neurons in Rhesus Monkey Visual Cortex: Systematic Relation between Time of Origin and Eventual Disposition

Rakic, P. (1974) · Science · doi:10.1126/science.183.4123.425 · Cited by 1,161

Genes Associated with Disturbed Cerebral Neurogenesis in the Embryonic Brain of Mouse Models of Down Syndrome

Ishihara, K. (2021) · Genes · doi:10.3390/genes12101598 · Cited by 8

Inferred developmental origins of brain tumors from single-cell RNA-sequencing data

Wang, S., Curry, R., McDonald, M. F., Koh, H. Y., Erickson, A. W., Kleinman, C. L., Taylor, M. D., Rao, G., Deneen, B., Harmanci, A., et al. (2025) · Neuro-Oncology Advances · doi:10.1093/noajnl/vdaf016 · Cited by 4

The Generation of Cortical Interneurons

Batista‐Brito, R., & Fishell, G. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397265-1.00071-x · Cited by 9

Dab1 expression level controls Reelin-induced PI3K-Akt activation in early GABAergic neurons

Sajukumar, K., Yadav, P., & Lee, G. H. (2025) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2025.151444 · Cited by 7

Cell-Type-Specific Gene Inactivation and In Situ Restoration via Recombinase-Based Flipping of Targeted Genomic Region

Liu, X., Ma, L., Liu, H., Gan, J., Xu, Y., Zhang, T., Mu, P., Wu, J., Shi, Y., Zhang, Y., et al. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1044-20.2020 · Cited by 7

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

Suzuki, T., & Sato, M. (2017) · Developmental Biology · doi:10.1016/j.ydbio.2017.09.029 · Cited by 8

Developmental characterization of Zswim5 expression in the progenitor domains and tangential migration pathways of cortical interneurons in the mouse forebrain

Chang, C.-C., Kuo, H., Chen, S., Lu, K.-M., Fong, W. L., Wu, H.-L., Saito, T., & Liu, F.-C. (2020) · The Journal of Comparative Neurology · doi:10.1002/cne.24900 · Cited by 7

Neurogenesis in the basal ganglia

Rubenstein, J. L. R., & Campbell, K. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814405-3.00018-7 · Cited by 7

Contributions of Single-Cell Approaches for Probing Heterogeneity and Dynamics of Neural Progenitors Throughout Life: Concise Review

Marcy, G., & Raineteau, O. (2019) · Stem Cells · doi:10.1002/stem.3071 · Cited by 7

GABAB receptors in maintenance of neocortical circuit function

Sebe, J. Y., Looke-Stewart, E., & Baraban, S. C. (2014) · Experimental Neurology · doi:10.1016/j.expneurol.2014.05.018 · Cited by 6

Islet1 Precursors Contribute to Mature Interneuron Subtypes in Mouse Neocortex

Siddiqi, F., Trakimas, A. L., Joseph, D. J., Lippincott, M. L., Marsh, E. D., & Wolfe, J. H. N. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab152 · Cited by 5

The generation of cortical interneurons

Batista‐Brito, R., Ward, C., & Fishell, G. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814405-3.00020-5 · Cited by 6

Characterization of heterotopic cell clusters in the hippocampus of the rat after prenatal treatment of methylazoxymethanol acetate

Imai, H., Yamamoto, T., Terashima, T., & Sugioka, K. (2012) · Congenital Anomalies · doi:10.1111/j.1741-4520.2012.00358.x · Cited by 4

Cell-type specific transcriptomic signatures of neocortical circuit organization and their relevance to autism

Moussa, A. J., & Wester, J. C. (2022) · Frontiers in Neural Circuits · doi:10.3389/fncir.2022.982721 · Cited by 6

OLIG2 is an in vivo bookmarking transcription factor in the developing neural tube in mouse

Hayashi, S., Oe, S., Koike, T., Seki, R., Nakano, Y., Hirahara, Y., Tanaka, S., Ito, T., Yasukochi, Y., Higasa, K., et al. (2022) · Journal of Neurochemistry · doi:10.1111/jnc.15746 · Cited by 4

Cell type specification and diversity in subpallial organoids

Pavon, N., Sun, Y., & Pak, C. (2024) · Frontiers in Genetics · doi:10.3389/fgene.2024.1440583 · Cited by 4

Dendrite-Targeting Inhibitory Interneurons Form Biased Circuits with Deep and Superficial Pyramidal Cells in Hippocampal CA1

Johantges, A. C., Hanson, M. A., Marshall, A. H., Safa, A., Payne, E. K., Hariths, N. R., Bibi, N., & Wester, J. C. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.1102-25.2025 · Cited by 6

Emerging Concepts in Neuro-Oncology

Sciuscio, D., & Hegi, M. E. (2012) · Springer eBooks · doi:10.1007/978-0-85729-458-6 · Cited by 5

Functional maturation of neocortical inhibitory interneurons

Larimer, P., & Hasenstaub, A. R. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-823672-7.00019-3 · Cited by 5

The origins of interneuron diversity

Whalley, K. (2007) · Nature reviews. Neuroscience · doi:10.1038/nrn2225 · Cited by 4

Temporally‐ and spatially regulated generation of distinct descendants by sonic hedgehog‐expressing progenitors in the forebrain

Wada, Y., Yamauchi, K., Murakami, F., & Tanabe, Y. (2012) · Developmental Neurobiology · doi:10.1002/dneu.20861 · Cited by 5

Maternal inflammation has a profound effect on cortical interneuron development in a stage and subtype-specific mannerPreprint

Vasistha, N. A., Pardo-Navarro, M., Gasthaus, J., Weijers, D., Müller, M. K., García-González, D., Malwade, S., Korshunova, I., Pfisterer, U., von Engelhardt, J., et al. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/412981 · Cited by 4

PAX6 LIMITS THE COMPETENCE OF DEVELOPING CEREBRAL CORTICAL CELLSPreprint

Manuel, M. N., Tan, K. B., Kozić, Z., Molinek, M., Marcos, T. S., Razak, F. M. A., Dobolyi, D., Dobie, R., Henderson, B. E. P., Henderson, N. C., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.02.03.478927 · Cited by 4

Human Stem Cell-Derived GABAergic Interneuron Development Reveals Early Emergence of Subtype Diversity Followed by Gradual Electrochemical MaturationPreprint

Bershteyn, M., Zhou, H., Fuentealba, L. C., Chen, C., Subramanyam, G., Cherkowsky, D., Salvatierra, J., Sezan, M., Maury, Y., Havlicek, S., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.03.626662 · Cited by 4

Somatic mosaicism and interneuron involvement in mTORopathies

Jerow, L. G., Krueger, D. A., Groß, C., & Danzer, S. C. (2025) · Trends in Neurosciences · doi:10.1016/j.tins.2025.02.009 · Cited by 5

ASCL1 and OLIG2 Expression Dynamics Control Glial Cell Fate and Regional Diversity in the Dorsal Forebrain

Paez-Beltran, L. E., Chen, H., Villicana, E., Liyanapathirana, M., Myers, B. L., Duan, J., Fletcher, D. E., Esparza, A. L., Riega, A., & Vue, T. Y. (2026) · Journal of Neuroscience · doi:10.1523/jneurosci.0240-26.2026 · Cited by 2

Selective dopamine D2 receptor deletion from Nkx6.2 expressing cells causes impaired cognitive, motivation and anxiety phenotypes in mice

Bechelli, L., Tomasella, E., Cardoso, S. L., Belmonte, M., & Gelman, D. M. (2023) · Scientific Reports · doi:10.1038/s41598-023-46954-8 · Cited by 3

Migration in the Hippocampus

Li, G., & Pleasure, S. J. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397266-8.00029-6 · Cited by 6

Structural changes in the neocortex as correlates of variations in EEG spectra and seizure susceptibility in rat brains with different degrees of dysplasia

Setkowicz, Z., Gzieło, K., Kiełbiński, M., & Janeczko, K. J. (2021) · The Journal of Comparative Neurology · doi:10.1002/cne.25282 · Cited by 3

Interneuron Diversity: How Form Becomes FunctionPreprint

García, N. V. D. M., & Fishell, G. (2024) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a041513 · Cited by 3

Hippocampal circuit-specific enhancement of GABA-inhibition caused by discrete gene regions in a Down syndrome modelPreprint

Hannan, S., Lana-Elola, E., Watson-Scales, S., Fisher, E. M. C., Tybulewicz, V. L. J., & Smart, T. G. (2025) · bioRxiv · doi:10.1101/2025.07.21.665861 · Cited by 3

Functional KCC2 expression marks an evolutionarily conserved population of early-maturing interneurons in the perinatal cortex

Szrinivasan, R., Trontti, K., Mathieu, R., Draia-Nicolau, T., Chazal, G., Loukasmäki, S., Bodington-Celma, S., Achim, K., Uvarov, P., Khirug, S., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-67270-x · Cited by 3

Targeting notch signaling to restore neural development and behavior in mouse models of ASD

Hanno, Y., Nakanishi, M., Takase, A., Nomura, J., Tanaka, M., Iida, Y., Tanaka, M., Hosokawa, H., Ito, M., Mikami, K., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-70321-6 · Cited by 2

The transcription regulator Lmo3 is required for the development of medial ganglionic eminence derived neurons in the external globus pallidus

Biswas, S., Chan, C. S., Rubenstein, J. L. R., & Gan, L. (2023) · Developmental Biology · doi:10.1016/j.ydbio.2023.07.007 · Cited by 4

Single-cell RNA sequencing of adult primate neocortex reveals the regulatory dynamics of neural plasticity

Zhang, C. (2025) · American Journal of Translational Research · doi:10.62347/zeor5569 · Cited by 2

Transcriptional Profiling Defines Unique Subtypes of Transit Amplifying Neural Progenitors Within the Neonatal Mouse Subventricular Zone

Zaritsky, R., Kumari, E., Velloso, F. J., Lemenze, A. D., Husain, S., & Levison, S. W. (2025) · Biomolecules · doi:10.3390/biom15101438 · Cited by 2

Neural progenitor diversity and their therapeutic potential for spinal cord repair

Li, H.-D., & Shi, W. (2010) · Frontiers in Biology · doi:10.1007/s11515-010-0830-y · Cited by 2

Superior performance of decloaking chamber-based heat-induced epitope retrieval method improves the quantification of Olig2 cells in paraffin-embedded section of embryonic mouse brain

Magalhães, A. C., & Rivera, C. (2014) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2014.06.032 · Cited by 2

Characterization and Stage-Dependent Lineage Analysis of Intermediate Progenitors of Cortical GABAergic Interneurons

Esumi, S., Nasu, M., Kawauchi, T., Miike, K., Morooka, K., Yanagawa, Y., Seki, T., Sakimura, K., Fukuda, T., & Tamamaki, N. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.607908 · Cited by 2

The Origins and Specification of Cortical Interneurons

Maroof, A. M., & Anderson, S. A. (2009) · Springer eBooks · doi:10.1007/978-1-4419-1243-5_2 · Cited by 2

Mechanisms of tangential migration of interneurons in the developing forebrain

Lepiemme, F., Silva, C. G., & Nguyen, L. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814407-7.00016-x · Cited by 2

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

Venkataramanappa, S., Schütz, D., Saaber, F., Kumar, P. A., Abe, P., Schulz, S., & Stumm, R. K. (2021) · PLoS Genetics · doi:10.1371/journal.pgen.1009441 · Cited by 2

Multifunctional requirements for ERK1/2 signaling in the development of ganglionic eminence derived glia and cortical inhibitory neuronsPreprint

Knowles, S. J., Holter, M. C., Li, G., Bjorklund, G. R., Rees, K. P., Martinez-Fuentes, J. S., Nishimura, K. J., Afshari, A. E., Fry, N., Stafford, A. M., et al. (2023) · doi:10.7554/elife.88313.1 · Cited by 2

Disruption of the anterior commissure in Olig2 deficient mice

Gotoh, H., Maruyama, K., Yoshii, K., Yamauchi, N., Nomura, T., Ohtsuka, S., Shirasaki, R., Takebayashi, H., & Ono, K. (2022) · European Journal of Neuroscience · doi:10.1111/ejn.15861

Ablation of the D1 Dopamine Receptor Alters the Migration and the Cortical Distribution of MGE‐Derived Inhibitory Interneurons by a Preponderant Non–Cell‐Autonomous Effect

Toutain, A., Scotto‐Lomassese, S., Muzerelle, A., Puech, J., Fayad, A., Roumier, A., Hervé, D., & Métin, C. (2026) · European Journal of Neuroscience · doi:10.1111/ejn.70385 · Cited by 1

Aberrant medial ganglionic eminence (MGE) GABAergic neurogenesis contributes to Huntington's disease pathogenesis

Molero, A. E., Devakanmalai, G. S., Altun, Y., Jover‐Mengual, T., Zhang, J., Khan, N., & Mehler, M. F. (2026) · Neurobiology of Disease · doi:10.1016/j.nbd.2026.107297 · Cited by 1

The Many Faces of Inhibitory Plasticity: Adding Flexibility to Cortical Circuits Throughout Development

Wang, L., & Maffei, A. (2010) · Springer eBooks · doi:10.1007/978-1-4419-6978-1_1 · Cited by 1

Mapping Lineage Using BAC‐Cre Reporter Lines

Xu, Q., & Anderson, S. A. (2010) · Current Protocols in Neuroscience · doi:10.1002/0471142301.ns0119s50 · Cited by 1

The Maturation of Firing Properties of Forebrain GABAergic Interneurons

Okaty, B. W., & Nelson, S. B. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397266-8.00154-x · Cited by 1

Neocortical Neurogenesis and Circuit Assembly

Gao, P., Sultan, K. T., Zhang, X., & Shi, S. (2013) · Springer eBooks · doi:10.1007/978-4-431-54496-8_7 · Cited by 1

Epigenetic function in neurodevelopment and cognitive impairment

Jakovcevski, M., & Zimmer‐Bensch, G. (2021) · e-Neuroforum · doi:10.1515/nf-2021-0028 · 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

Astrocyte Differentiation from Oligodendrocyte Precursors

Nishiyama, A. (2012) · Springer eBooks · doi:10.1007/978-0-85729-458-6_3 · Cited by 1

Dlx Gene Regulation of Zebrafish GABAergic Interneuron Development

Ma, W. (2011) · uO Research (University of Ottawa) · doi:10.20381/ruor-4584 · Cited by 1

Control of neuronal survival, migration and outgrowth by GDNF and its receptors

Perrinjaquet, M. (2010) · Figshare · Cited by 1

The Diversity of Cortical Interneurons

Nakajima, M. (2025) · Digital Commons - RU (Rockefeller University) · doi:10.48496/pz2y-7v84 · Cited by 1

Investigating the Roles of Parvalbumin and Cholecystokinin Interneurons of the Ventral Hippocampus and Medial Prefrontal Cortex in Schizophrenia-Related Behaviours

Nguyen, R. (2018) · TSpace (University of Toronto) · Cited by 1

Multifunctional requirements for ERK1/2 signaling in the development of ganglionic eminence derived glia and cortical inhibitory neuronsPreprint

Knowles, S. J., Holter, M. C., Li, G., Bjorklund, G. R., Rees, K. P., Martinez-Fuentes, J. S., Nishimura, K. J., Afshari, A. E., Fry, N., Stafford, A. M., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.08.02.502073 · Cited by 1

Multifunctional requirements for ERK1/2 signaling in the development of ganglionic eminence derived glia and cortical inhibitory neuronsPreprint

Knowles, S. J., Holter, M. C., Li, G., Bjorklund, G. R., Rees, K. P., Martinez-Fuentes, J. S., Nishimura, K. J., Afshari, A. E., Fry, N., Stafford, A. M., et al. (2023) · doi:10.7554/elife.88313 · Cited by 2

Autism-associated oxysterol regulates GABAergic neurogenesis and subtype fatesPreprint

Cruz-Santos, M., Kidd, E., Li, Z., de la Fuente, D. C., Davies, S., Vinh, N., Fjodorova, M., & Li, M. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.07.01.662540 · Cited by 1

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

Biochemical analysis of the basic helix-loop-helix transcription factor Olig2

Meijer, D. H. (2014) · Utrecht University Repository (Utrecht University)

Molecular development and laminar distribution of GABAergic interneurons of the cerebral cortex

Lodato, S. (2011) · Università degli Studi di Napoli Federico II · doi:10.6092/unina/fedoa/8450

The integrity of basal forebrain neurons depends on permanent expression of Nkx2-1: potential for understanding haploinsufficiency in humans

Magno, L. (2010) · Universitätsbibliothek der FU Berlin Hochschulschriftenstelle u. Dokumentenserver · doi:10.17169/refubium-17965

The serotonin 5-HT 3 receptor: a novel neurodevelopmental

Smidt, M. P., & van Hooft, J. A. (2013)

Developmental programming of cortical interneurons

Welagen, J. (2011)

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

Non-Canonical Wnt-Signaling through Ryk Regulates the Generation of Somatostatin- and Parvalbumin-Expressing Cortical InterneuronsPreprint

McKenzie, M. G., Cobbs, L., Petros, T. J., Halford, M. M., Stacker, S. A., Zou, Y., Fishell, G., & Au, E. (2018) · SSRN Electronic Journal · doi:10.2139/ssrn.3155597

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

Gallerani, N. (2021) · doi:10.7916/d8-nbyk-3y33

Tissue-Specific Actions of Pax6 on the Balance of Proliferation and Differentiation in Developing Forebrain are Foxg1-DependentPreprint

Urzainqui, I. Q., Kozić, Z., Mitra, S., Tian, T., Manuel, M. N., Mason, J. O., & Price, D. J. (2018) · SSRN Electronic Journal · doi:10.2139/ssrn.3249469

The construction of 3D cognitive networks from iPSCs through precise spatiotemporal specification

Miu, K.-K., Cao, D., Wang, Z., Hao, S., & Chan, W. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-823809-7.00012-8

Migration in the hippocampus

Noguchi, H., Li, G., & Pleasure, S. J. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814407-7.00017-1

The transcription regulator Lmo3 is required for cell fate specification in the external globus pallidusPreprint

Biswas, S., Chan, C. S., Rubenstein, J. L. R., & Gan, L. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.05.24.493171

Imbalance in glutamatergic and GABAergic transmission in Down syndrome and therapeutic targets

Ganguly, B. B. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-90456-8.00007-7 · Cited by 1

Reviewer #2 (Public Review): Multifunctional requirements for ERK1/2 signaling in the development of ganglionic eminence derived glia and cortical inhibitory neurons

Knowles, S. J., Holter, M. C., Li, G., et al. (2023) · doi:10.7554/elife.88313.1.sa0

NFIB influences progenitor competence in maturation of GABAergic neurons in micePreprint

Bright, A. R., Kotlyarenko, Y., Neuhaus, F., Rodrigues, D., Feng, C., Peters, C., Vitali, I., Dönmez, E., Myoga, M. H., Dvoretskova, E., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.03.18.585524

Multidimensional analysis of cortical interneuron synaptic features reveals underlying synaptic heterogeneityPreprint

Dummer, P. D., Lee, D. I., Hossain, S., Wang, R., Evard, A., Newman, G., Ho, C., Schneider-Mizell, C. M., Menon, V., & Au, E. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.03.22.586340

The Development of Neocortical Inhibitory Neurons and Neurodevelopmental Disorders

Miyoshi, G. (2024) · The Kitakanto Medical Journal · doi:10.2974/kmj.74.175

Adolescent Alcohol Exposure Dysregulates Developing Cortical GABA Circuits

Sicher, A. R., & Crowley, N. A. (2025) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-81908-7_8 · Cited by 1

CCN1 forms a complex with GPC4 and heparin to fine-tune signaling activities for cortical neural stem cell maintenancePreprint

Zheng, J., Qi, S.-J., Wu, H., Wu, J., Chen, G., Wang, H. J., Pan, H., Li, J., Cheng, C., Tang, K., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.05.16.654402

Mature interneuron subtypes arise from distinct spatial and temporal subdomains within the caudal ganglionic eminencePreprint

Garg, V., Beyene, S., Tanzillo, A. F., Tucker, A., Johantges, A. C., Abebe, D. T., Zhang, Y., & Petros, T. J. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.07.28.667082 · Cited by 1

Neural stem cell-specific deficiency of (pro)renin receptor causes brain malformation and perinatal lethality in mice

Hashimoto, M., Hibi, M., Matsukubo, K., Kimura, H., Hiraoka, K., Biswas, S. P., Suzuki-Nakagawa, C., Kizuka, Y., Kim, J., Fukamizu, A., et al. (2025) · The Journal of Biochemistry · doi:10.1093/jb/mvaf047

Subtype- and Layer-Specific Developmental Gradients of Postnatal GABAergic Neurons in the Rodent Barrel Cortex

Kallo, H., Sitdikova, V., Логашкин, А. Е., Loukasmäki, S., Ludwig, A., Minlebaev, M., & Rivera, C. (2025) · Developmental Neuroscience · doi:10.1159/000549093

Additional file 2 of PDK1 regulates the survival of the developing cortical interneurons

Wei, Y., Han, X., & Zhao, C. (2020) · Figshare · doi:10.6084/m9.figshare.12246773

Selective Lis1 inactivation disrupts migration and positioning of cortical somatostatin interneurons

Pombero, A., García-López, R., Geijo‐Barrientos, E., & Martı́nez, S. (2026) · Scientific Reports · doi:10.1038/s41598-026-38316-x

Origine embryonnaire et propriétés morpho-physiologiques des neurones hubs de l'hippocampe en développement

Picardo, M. A. (2012) · theses.fr (ABES) · doi:10.70675/81e53597z7620z496cz9277za78f0afbad20

Structure-fonction des patrons d'activité séquentiels des réseaux corticaux au cours du développement postnatal chez le rongeur

Allène, C. (2010) · theses.fr (ABES) · doi:10.70675/a4f94b86z8e1az478ez8c57zaa5916d1da0a

The inhibitory microcircuit in mouse presubiculum : from interneuron properties to input-output connectivity

Nassar, M. (2016) · theses.fr (ABES) · doi:10.70675/7b264280z8d4dz4837z96a9z431ee487047b

Propriétés morpho-fonctionnelles des neurones GABAergiques générés tôt dans la région CA1 de l'hippocampe adulte et en développement

Gouny, C. (2018) · theses.fr (ABES) · doi:10.70675/7499b452z29afz407bzab43z29f842fcca01

Une approche tout optique pour l'étude de schémas remarquables de connectivité fonctionnelle

Tressard, T. (2019) · theses.fr (ABES) · doi:10.70675/8a629ef0zb182z4315zbf9az0c3f999e9868

Direct Reprogramming of glial cell into functional GABAergic neurons : a new avenue to epileptic seizure relief

Lentini, C. (2019) · theses.fr (ABES) · doi:10.70675/6816666az3fdfz41c0zb106zc7d30c1931eb

Probing transcriptional specificities and fate potential of postnatal neural progenitors in the mouse forebrain

Marcy, G. (2018) · theses.fr (ABES) · doi:10.70675/a03ff1d9z4c28z4a0fz94ffz95ea582c393f

Etude du rôle de la kinésine KIF21B au cours du développement cortical

Asselin, L. (2019) · theses.fr (ABES) · doi:10.70675/bd543948zdb0fz4298zae3fzf4fc50923d78

Effets de l'alcoolisation prénatale sur le développement du système GABAergique et de la myélinisation chez l'humain

Marguet, F. (2020) · theses.fr (ABES) · doi:10.70675/7590e822z0aa7z4868z972bz90e8061311fb

Altérations de la connectivité corticale au cours de périodes critiques du développement

Druart, M. (2020) · theses.fr (ABES) · doi:10.70675/b4f48d73za850z42b2z8dadzfad47d4f0a69

Cajal-Retzius cells and Reelin in mouse cortical development and human pathologies

Riva, M. (2021) · theses.fr (ABES) · doi:10.70675/b321eca5ze455z480bzb6d4z43505d8c9faf

Impact of PV interneuron - OPC synapse disruption on cognitive functioning

Vidal, M. (2021) · theses.fr (ABES) · doi:10.70675/66c1e527zbd3ez49f6z8736ze9817c27856d

Etude du développement cortical à travers la caractérisation d'un modèle murin d'autisme et l'inférence des interactions cellulaires par séquençage en cellules uniques

Mathieu, R. (2022) · theses.fr (ABES) · doi:10.70675/252edc66z623ez48e8zad07z2fe84bfc77fe

Cortical excitability : Prefrontal conditional bistability for parametric working memory in physiological and Alzheimer's Disease conditions & Somatosensory epileptic network activity following neurodevelopmental interneuron mutations

Leroux, M. (2023) · theses.fr (ABES) · doi:10.70675/d51b586bz96daz4ecbzbac2zc54c3576aef2

SST interneuron maturation extends beyond the second postnatal week and is driven by coordinated transcriptional and functional remodeling

Christodoulou, O., Diskos, K., Velli, A., Moulos, P., Sidiropoulou, K., & Denaxa, M. (2026) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2026.1892850

The temporal and spatial origins of cortical interneurons predict their physiological subtype

Butt, S. J. B., Fuccillo, M., Nery, S., Noctor, S., Kriegstein, A., Corbin, J. G., & Fishell, G. (2005) · Neuron · doi:10.1016/j.neuron.2005.09.034 · Cited by 587

The origins of interneuron diversity

Whalley, K. (2007) · Nature reviews. Neuroscience · doi:10.1038/nrn2225 · Cited by 4

Development/Plasticity/Repair Genetic Fate Mapping Reveals That the Caudal Ganglionic Eminence Produces a Large and Diverse Population of Superficial Cortical Interneurons

Miyoshi, G., Hjerling‐Leffler, J., Karayannis, T., Sousa, V. H., Butt, S. J. B., Battiste, J. D., Johnson, J. E., Machold, R. P., & Fishell, G. (2013)

Cortical interneuron specification: the juncture of genes, time and geometry

Bandler, R. C., Mayer, C., & Fishell, G. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2016.10.003 · Cited by 125

Genetic Fate Mapping Reveals That the Caudal Ganglionic Eminence Produces a Large and Diverse Population of Superficial Cortical Interneurons

Miyoshi, G., Hjerling-Leffler, J., Karayannis, T., Sousa, V. H., Butt, S. J. B., Battiste, J., Johnson, J. E., Machold, R. P., & Fishell, G. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4515-09.2010 · Cited by 559