The Requirement of Nkx2-1 in the Temporal Specification of Cortical Interneuron Subtypes

Interneurons of the neocortical inhibitory system

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Neuronal specification in the spinal cord: inductive signals and transcriptional codes

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GABAergic cell subtypes and their synaptic connections in rat frontal cortex

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The T/ebp null mouse: thyroid-specific enhancer-binding protein is essential for the organogenesis of the thyroid, lung, ventral forebrain, and pituitary.Preprint

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Regulation of Cre Recombinase Activity by Mutated Estrogen Receptor Ligand-Binding Domains

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Cell fate determination in the vertebrate retina.

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Salient features of synaptic organisation in the cerebral cortex1Published on the World Wide Web on 3 March 1998.1

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Loss of Nkx2.1 homeobox gene function results in a ventral to dorsal molecular respecification within the basal telencephalon: evidence for a transformation of the pallidum into the striatum

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Nkx-2.5: a novel murine homeobox gene expressed in early heart progenitor cells and their myogenic descendants

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Cell-based therapies for the treatment of schizophrenia

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Progressive divisions of multipotent neural progenitors generate late-born chandelier cells in the neocortex

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Sticking out of the crowd: the molecular identity and development of cholecystokinin‐containing basket cells

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Both GEF domains of the autism and developmental epileptic encephalopathy-associated Trio protein are required for proper tangential migration of GABAergic interneurons

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Modelling monogenic autism spectrum disorder using mouse cortical organoids

Hali, S., Kim, J., Kwak, T. H., Lee, H., Shin, C. Y., & Han, D. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.10.097 · Cited by 18

Benign hereditary chorea

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MicroRNA-934 is a novel primate-specific small non-coding RNA with neurogenic function during early development

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NMDARs Drive the Expression of Neuropsychiatric Disorder Risk Genes Within GABAergic Interneuron Subtypes in the Juvenile Brain

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The proximal chromosome 14q microdeletion syndrome: Delineation of the phenotype using high resolution SNP oligonucleotide microarray analysis (SOMA) and review of the literature

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Thyroid transcription factor-1 expression in colorectal adenocarcinomas

Dettmer, M. S., Kim, T. E., Jung, C. K., Jung, E. S., Lee, K. Y., & Kang, C. S. (2011) · Pathology - Research and Practice · doi:10.1016/j.prp.2011.08.009 · Cited by 16

Maintenance of Positional Identity of Neural Progenitors in the Embryonic and Postnatal Telencephalon

Delgado, R. N., & Lim, D. A. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00373 · Cited by 18

Understanding and modeling regional specification of the human ganglionic eminence

Hunt, C. J., Moriarty, N., Deursen, C. V., Gantner, C. W., Thompson, L. H., & Parish, C. L. (2023) · Stem Cell Reports · doi:10.1016/j.stemcr.2023.01.010 · Cited by 14

microRNA-dependent regulation of gene expression in GABAergic interneurons

Kołosowska, K., Schratt, G. M., & Winterer, J. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1188574 · Cited by 16

Neurogenesis in the Basal Ganglia

Rubenstein, J. L. R., & Campbell, K. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397265-1.00097-6 · Cited by 14

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. (2014) · Springer eBooks · doi:10.1007/978-3-642-54687-7_9 · Cited by 16

Hypoperfusion in caudate nuclei in patients with brain–lung–thyroid syndrome

Uematsu, M., Haginoya, K., Kikuchi, A., Nakayama, T., Kakisaka, Y., Numata, Y., Kobayashi, T., Hino‐Fukuyo, N., Fujiwara, I., & Kure, S. (2011) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2011.11.025 · Cited by 16

Brain-Lung-Thyroid Disease

Ferrara, J. M., Adam, O. R., Kirwin, S. M., Houghton, D. J., Shepherd, C., Vinette, K. M. B., & Litvan, I. (2011) · Journal of Child Neurology · doi:10.1177/0883073811413584 · Cited by 15

BRAIN–LUNG–THYROID SYNDROME

Александровна, Б. М., & Ovsyannikov, D. Y. (2014) · Педиатрическая фармакология · doi:10.15690/pf.v11i6.1216 · Cited by 14

Impaired synaptic plasticity in the prefrontal cortex of mice with developmentally decreased number of interneurons

Konstantoudaki, X., Chalkiadaki, K., Tivodar, S., Karagogeos, D., & Sidiropoulou, K. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.02.048 · Cited by 14

Specification of GABAergic Neocortical Interneurons

Miyoshi, G., Machold, R. P., & Fishell, G. (2013) · Springer eBooks · doi:10.1007/978-4-431-54496-8_5 · Cited by 16

Transcriptional maintenance of cortical somatostatin interneuron subtype identity during migration

Munguba, H., Nikouei, K., Hochgerner, H., Oberst, P., Kouznetsova, A., Ryge, J., Muñoz‐Manchado, A. B., Close, J., Batista‐Brito, R., Linnarsson, S., et al. (2023) · Neuron · doi:10.1016/j.neuron.2023.07.018 · Cited by 20

Distinct hyperactive RAS/MAPK alleles converge on common GABAergic interneuron core programs

Knowles, S. J., Stafford, A. M., Zaman, T., Angara, K., Williams, M. R., Newbern, J. M., & Vogt, D. L. (2023) · Development · doi:10.1242/dev.201371 · Cited by 14

Cell cycle regulation and interneuron production

Ross, M. E. (2010) · Developmental Neurobiology · doi:10.1002/dneu.20823 · Cited by 13

Transcription factors in microcephaly

Lim, Y. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1302033 · Cited by 13

Multiple Origins of Secretagogin Expressing Cortical GABAergic Neuron Precursors in the Early Human Fetal Telencephalon

Alzu’bi, A., & Clowry, G. J. (2020) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2020.00061 · Cited by 12

Clonal origins of neocortical interneurons

Sultan, K. T., Shi, W., & Shi, S. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.01.010 · Cited by 13

Analysis of Islet‐1, Nkx2.1 , Pax6 , and Orthopedia in the forebrain of the sturgeon Acipenser ruthenus identifies conserved prosomeric characteristics

López, J. M., Jiménez, S., Morona, R., Lozano, D. D., & Moreno, N. (2021) · The Journal of Comparative Neurology · doi:10.1002/cne.25249 · Cited by 11

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

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Cortical arealization of interneurons defines shared and distinct molecular programs in developing human and macaque brains

Feng, X., Gao, Y., Chu, F., Shan, Y., Liu, M., Wang, Y.-Y., Zhu, Y., Lu, Q. R., & Li, M. (2025) · Nature Communications · doi:10.1038/s41467-025-56058-8 · Cited by 10

Cell Type-Specific Role of RNA Nuclease SMG6 in Neurogenesis

Guerra, G. M., May, D., Kroll, T. C., Koch, P., Groth, M., Wang, Z., Li, T., & Grigaravičius, P. (2021) · Cells · doi:10.3390/cells10123365 · Cited by 10

Neuronal Transplantation for Alzheimer’s Disease and Prospects for Generating Exogenic Neurons as a Source of Cells for Implantation

Strell, P., Johnson, S. T., Carchi, C., & Low, W. C. (2023) · Cell Transplantation · doi:10.1177/09636897231164712 · Cited by 10

Neuronal tangential migration from Nkx2.1-positive hypothalamus

Murcia‐Ramón, R., Juárez-Leal, I., Andreu‐Cervera, A., Almagro‐García, F., Martı́nez, S., Echevarrı́a, D., & Puelles, E. (2020) · Brain Structure and Function · doi:10.1007/s00429-020-02163-x · Cited by 9

Striatal cholinergic interneurons in isolated generalized dystonia—rationale and perspectives for stem cell-derived cellular models

Capetian, P., Pauly, M. G., Azmitia, L. M., & Klein, C. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00205 · Cited by 9

Transcriptional maintenance of cortical somatostatin interneuron subtype identity during migrationPreprint

Munguba, H., Nikouei, K., Hochgerner, H., Oberst, P., Kouznetsova, A., Ryge, J., Batista‐Brito, R., Muñoz‐Manchado, A. B., Close, J., Linnarsson, S., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/593285 · Cited by 9

Cortical interneurons: fit for function and fit to function? Evidence from development and evolution

Keijser, J., & Sprekeler, H. (2023) · Frontiers in Neural Circuits · doi:10.3389/fncir.2023.1172464 · Cited by 9

Transcriptome and in Vitro Differentiation Profile of Human Embryonic Stem Cell Derived NKX2.1-Positive Neural Progenitors

Chen, C. Y., Plocik, A. M., Anderson, N. C., Moakley, D. F., Boyi, T., Dundes, C. E., Lassiter, C. M., Graveley, B. R., & Grabel, L. B. (2016) · Stem Cell Reviews and Reports · doi:10.1007/s12015-016-9676-2 · Cited by 8

Functional Implications of Dynamic DNA Methylation for the Developing, Aging and Diseased Brain

Zimmer‐Bensch, G. (2019) · RNA technologies · doi:10.1007/978-3-030-14792-1_6 · Cited by 8

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

A Sip of GABA for the Cerebral Cortex

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ALK4 coordinates extracellular and intrinsic signals to regulate development of cortical somatostatin interneurons

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Mechanisms of Development

ten Donkelaar, H. J. (2014) · Springer eBooks · doi:10.1007/978-3-642-54687-7_2 · Cited by 8

Gestational iron deficiency affects the ratio between interneuron subtypes in the postnatal cerebral cortex in mice

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Symptomatic epilepsy

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

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Developmental abnormalities in cortical GABAergic system in mice lacking mGlu3 metabotropic glutamate receptors

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Neurogenesis in the basal ganglia

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Telencephalon patterning

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Commentary: The Prospect of Cell-Based Therapy for Epilepsy

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Differential diagnosis of Huntington’s disease− neurological aspects of NKX2-1-related disorders

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Perinatal serotonin signalling dynamically influences the development of cortical GABAergic circuits with consequences for lifelong sensory encoding

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Polyglutamine-expanded ataxin3 alter specific gene expressions through changing DNA methylation status in SCA3/MJD

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Interneuron dysfunction in epilepsy: An experimental approach using immature brain insults to induce neuronal migration disorders

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Telencephalon Patterning

Tole, S., & Hébert, J. M. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397265-1.00018-6 · Cited by 6

Homologs of genes expressed in Caenorhabditis elegans GABAergic neurons are also found in the developing mouse forebrain

Hammock, E. A. D., Eagleson, K. L., Barlow, S. J., Earls, L. R., Miller, D. M., & Levitt, P. R. (2010) · Neural Development · doi:10.1186/1749-8104-5-32 · Cited by 6

Altered pituitary morphology as a sign of benign hereditary chorea caused by TITF1/NKX2.1 mutations

Thust, S. C., Veneziano, L., Parkinson, M. H., Bhatia, K. P., Mantuano, E., Gonzalez‐Robles, C., Davagnanam, I., & Giunti, P. (2022) · Neurogenetics · doi:10.1007/s10048-021-00680-3 · Cited by 5

Caspase 9-induced apoptosis enables efficient fetal cell ablation and disease modeling

Matsui, K., Watanabe, M., Yamamoto, S., Kawagoe, S., Ikeda, T., Ohashi, H., Kuroda, T., Koda, N., Morimoto, K., Kinoshita, Y., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-57795-6 · Cited by 5

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

Transcriptional Regulation of Cortical Interneuron Development

Pai, E. L.-L., Vogt, D. L., Hu, J. S., & Rubenstein, J. L. R. (2024) · Oxford University Press eBooks · doi:10.1093/med/9780197549469.003.0047 · Cited by 6

Levodopa-responsive chorea: A review

Gupta, H., & Farrenburg, M. (2019) · Annals of Indian Academy of Neurology · doi:10.4103/aian.aian_221_19 · Cited by 5

Telencephalic Neurogenesis Versus Telencephalic Differentiation of Pluripotent Stem Cells

Nat, R., Apostolova, G., & Dechant, G. (2013) · InTech eBooks · doi:10.5772/54251 · Cited by 7

Examining the role of the surfactant family member SFTA3 in interneuron specification

Chen, C. Y., Anderson, N. C., Becker, S., Schicht, M., Stoddard, C. E., Bräuer, L., Paulsen, F. P., & Grabel, L. B. (2018) · PLoS ONE · doi:10.1371/journal.pone.0198703 · Cited by 4

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

Temporal Lobe Epilepsy: What do we understand about protein alterations?

Perveen, N., Ashraf, W., Alqahtani, F., Rasool, M. F., Samad, N., & Imran, I. (2021) · Chemical Biology & Drug Design · doi:10.1111/cbdd.13858 · Cited by 4

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

NMDAR-mediated transcriptional control of gene expression during the development of medial ganglionic eminence-derived interneuronsPreprint

Mahadevan, V., Mitra, A., Zhang, Y., Yuan, X. Q., Peltekian, A., Chittajallu, R., Esnault, C., Maric, D., Rhodes, C. T., Pelkey, K. A., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.06.10.144295 · 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

Dual effects of ARX poly-alanine mutations in human cortical and interneuron developmentPreprint

Nieto‐Estévez, V., Varma, P., Mirsadeghi, S., Caballero, J., Gamero-Alameda, S., Hosseini, A., Silvosa, M. J., Thodeson, D. M., Lybrand, Z. R., Giugliano, M., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.25.577271 · Cited by 4

The molecular and cellular choreography of early mammalian lung development

Yang, X., Chen, Y., Yang, Y., Li, S., Mi, P., & Jing, N. (2024) · Medical Review · doi:10.1515/mr-2023-0064 · Cited by 3

Behavioral and Neuroanatomical Consequences of Cell-Type Specific Loss of Dopamine D2 Receptors in the Mouse Cerebral Cortex

Lee, G. S., Graham, D. L., Noble, B. L., Trammell, T. S., McCarthy, D. M., Anderson, L., Rubinstein, M., Bhide, P. G., & Stanwood, G. D. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.815713 · Cited by 4

Ex Utero Electroporation and Organotypic Slice Cultures of Embryonic Mouse Brains for Live-Imaging of Migrating GABAergic Interneurons

Eid, L., Lachance, M., Hickson, G. R. X., & Rossignol, E. (2018) · Journal of Visualized Experiments · doi:10.3791/57526 · Cited by 4

Manipulation of Signal Gradient and Transcription Factors Recapitulates: Multiple Hypothalamic Identities

Yamamoto, M., Ong, A. L. C., Shinozuka, T., Shirai, M., & Sasai, N. (2023) · Stem Cells · doi:10.1093/stmcls/sxad018 · Cited by 3

Distinct oligodendrocyte populations have spatial preference and injury-specific responsesPreprint

Floriddia, E. M., Zhang, S., van Bruggen, D., dos Santos, J. P. G., Altinkök, M., Llorens-Bobadilla, E., Frisén, J., & Castelo‐Branco, G. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/580985 · Cited by 3

Cortical interneurons: fit for function and fit to function? Evidence from development and evolutionPreprint

Keijser, J., & Sprekeler, H. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.02.23.529671 · Cited by 3

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

Prenatal-induced psychopathologies: All roads lead to microglia

Lebow, M., Kuperman, Y., & Chen, A. (2023) · Elsevier eBooks · doi:10.1016/b978-0-12-817558-3.00016-0 · Cited by 2

Transcriptional Regulation of Tangential Neuronal Migration in the Vertebrate Hindbrain

Meglio, T. D., & Rijli, F. M. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397266-8.00033-8 · 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

Hedgehog Promotes Production of Inhibitory Interneurons in Vivo and in Vitro from Pluripotent Stem Cells

Anderson, N. C., Chen, C. Y., & Grabel, L. B. (2016) · Journal of Developmental Biology · doi:10.3390/jdb4030026 · Cited by 3

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

Foxe1 orchestrates thyroid and lung cell lineage divergence in mouse stem cell-derived organoidsPreprint

Fonseca, B. F., Barbée, C., Romitti, M., Eski, S. E., Gillotay, P., Monteyne, D., Pérez-Morga, D. L., Refetoff, S., Singh, S. P., & Costagliola, S. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.05.16.492074 · Cited by 2

Gene regulatory networks controlling neuronal development

Lambert, J. T., Haigh, J. L., & Nord, A. S. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814405-3.00027-8 · Cited by 1

Dual developmental effects of ARX poly-alanine mutations on human cortical excitatory and inhibitory neurons

Nieto‐Estévez, V., Varma, P., Mirsadeghi, S., Caballero, J., Gamero-Alameda, S., Hosseini, A., Silvosa, M. J., Thodeson, D. M., Goswami, S., Lybrand, Z. R., et al. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116746 · Cited by 6

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Foxe1 deficiency impairs thyroid fate while supporting lung differentiation

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Development and Developmental Disorders of the Forebrain

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Both GEF domains of the autism and epilepsy-associated Trio protein are required for proper tangential migration of GABAergic interneuronsPreprint

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

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Neuron Article The Requirement of Nkx2-1 in the Temporal Specification of Cortical Interneuron Subtypes

Butt, S. J. B., Sousa, V. H., Fuccillo, M. V., Hjerling‐Leffler, J., Miyoshi, G., & Kimura, S. (2013)

The many faces of NKX2-1

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doi:10.1093/cercor/bhp038 Advance Access publication April 10, 2009 Characterization of Nkx6-2-Derived

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