The DOI matches its Crossref record; 80 of the 81 references it cites were found in a registry or an index.
Genetic Fate Mapping Reveals That the Caudal Ganglionic Eminence Produces a Large and Diverse Population of Superficial Cortical Interneurons
Open accessAbstract
By combining an inducible genetic fate mapping strategy with electrophysiological analysis, we have systematically characterized the populations of cortical GABAergic interneurons that originate from the caudal ganglionic eminence (CGE). Interestingly, compared with medial ganglionic eminence (MGE)-derived cortical interneuron populations, the initiation [embryonic day 12.5 (E12.5)] and peak production (E16.5) of interneurons from this embryonic structure occurs 3 d later in development. Moreover, unlike either pyramidal cells or MGE-derived cortical interneurons, CGE-derived interneurons do not integrate into the cortex in an inside-out manner but preferentially (75%) occupy superficial cortical layers independent of birthdate. In contrast to previous estimates, CGE-derived interneurons are both considerably greater in number (approximately 30% of all cortical interneurons) and diversity (comprised by at least nine distinct subtypes). Furthermore, we found that a large proportion of CGE-derived interneurons, including the neurogliaform subtype, express the glycoprotein Reelin. In fact, most CGE-derived cortical interneurons express either Reelin or vasoactive intestinal polypeptide. Thus, in conjunction with previous studies, we have now determined the spatial and temporal origins of the vast majority of cortical interneuron subtypes.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source doesn’t support the claim as written.
In the citing paper
“Close inspection of the electrophysiological properties of these cells, however, highlight few features that are distinct to one or few cell types, with only minor exceptions, and all nine identified cell types largely exhibit a continuum of intrinsic parameters.”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [796]
Checked by a reasoning model — may be wrong.
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Molecular markers associated with NGFCs include NPY, reelin, neuronal nitric oxide synthase (nNOS), α-actinin 2, and COUP transcription factor 2 (COUPTF2) (48, 367, 549, 796, 858, 926, 1137).”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [796]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In both neocortex and hippocampus, CR- and VIP-expressing ISIs represent subsets of 5-HT3AR-expressing interneurons and have singular origin in the CGE (combined ISIs represent 30% of CGE-derived interneurons based on assumptions outlined above) (102, 203, 651, 796, 1138, 1179).”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [796]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In the neocortex NGFCs (reelin-expressing, SST negative), ISIs (VIP- and CR-expressing), and CCK-expressing interneurons (e.g., CCKBCs) are derived from CGE progenitors”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [796]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“In contrast, neocortical NGFCs have singular origins within the CGE (651, 796, 1179).”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [796]
The cited source says what the claim attributes to it.
In the citing paper
“Complementing the spatial control of interneuron specification within the GEs is a temporal dynamic that has significant impact on mature interneuron fate”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [796]
In the citing paper
“Two additional types of interneuron express 5HT3aR: NPY+ multipolar cells and Meis2+ interstitial GABAergic neurons. NPY+ multipolar interneurons exhibit irregular spiking properties and are particularly abundant at the boundary between layers 1 and 2”
From Development and Functional Diversification of Cortical Interneurons (2018) · cites this paper as Miyoshi et al., 2010
In the citing paper
“a temporal sequence has also been described for the generation of neuronal diversity in the CGE”
From Development and Functional Diversification of Cortical Interneurons (2018) · cites this paper as Miyoshi et al., 2010
In the citing paper
“We manually dissected the embryonic day (E)13.5 MGE or E14.5 CGE and LGE from wild type mouse embryos, timepoints corresponding to peak neurogenesis in these structures7,8”
From Developmental diversification of cortical inhibitory interneurons (2018) · cites this paper as [8]
In the citing paper
“Reelin is frequently coexpressed with SST in O-LM and Martinotti cells, but is not selective for or necessarily comprehensively expressed by these interneurons (203, 367, 651, 796, 899).”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [796]
In the citing paper
“CGE interneuronogenesis was demonstrated to lag that of the MGE both for initial (E12.5 for CGE vs. E9.5 for MGE) and peak (E16.5 for CGE vs. E13.5 for MGE) generation”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [796]
In the citing paper
“The CGE produces ~30% of neocortical and hippocampal interneurons”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [796]
In the citing paper
“in contrast to the MGE, the subtypes of neocortical interneurons generated within the CGE do not change significantly over time with similar proportions of reelin-expressing NGFCs and VIP/CR-expressing ISIs generated across CGE neurogenesis”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [796]
In the citing paper
“In cortex, MGE- and CGE-derived cells are biased towards the deep and superficial layers, respectively”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [796]
In the citing paper
“CGE-derived interneurons lack any such correlation with birth order; rather, their attraction to the superficial layers is dominant regardless of birthdate”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [796]
In the citing paper
“The majority of CGE-derived interneurons that did not express reelin expressed VIP.”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [796]
In the citing paper
“They observed that this divergent population of CGE-derived cells parsed into nine distinct subtypes based on morphology, cell layer positioning, firing patterns, and other intrinsic properties.”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [796]
In the citing paper
“because CGE-derived interneurons preferentially occupy the expanded upper neocortical layers49”
From Innovations present in the primate interneuron repertoire (2020) · cites this paper as [49]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Shrestha, S., & Offer, S. M. (2016) · Medical Epigenetics · doi:10.1159/000444713 · Cited by 8,951
Generalized lacZ expression with the ROSA26 Cre reporter strain
Soriano, P. (1999) · Nature Genetics · doi:10.1038/5007 · Cited by 5,237
Efficient selection for high-expression transfectants with a novel eukaryotic vector
Niwa, H., Yamamura, K., & Miyazaki, J. (1991) · Gene · doi:10.1016/0378-1119(91)90434-d · Cited by 5,149
Cre reporter strains produced by targeted insertion of EYFP and ECFP into the ROSA26 locus
Srinivas, S., Watanabe, T., Lin, C.-S., William, C. M., Tanabe, Y., Jessell, T. M., & Costantini, F. (2001) · BMC Developmental Biology · doi:10.1186/1471-213x-1-4 · Cited by 3,121
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
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
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
Petilla terminology: nomenclature of features of GABAergic interneurons of the cerebral cortex
The Petilla Interneuron Nomenclature Group (PING) (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2402 · Cited by 1,491
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
Cited by
Sorted by citations
A resource of Cre driver lines for genetic targeting of GABAergic neurons in cerebral cortex
Taniguchi, H., He, M., Wu, P., Kim, S., Paik, R., Sugino, K., Kvitsani, D., Fu, Y., Lu, J., Lin, Y., et al. (2011) · Neuron · doi:10.1016/j.neuron.2011.07.026 · Cited by 1,828
Self-citationGABAergic Interneurons in the Neocortex: From Cellular Properties to Circuits
Tremblay, R., Lee, S., & Rudy, B. (2016) · Neuron · doi:10.1016/j.neuron.2016.06.033 · Cited by 2,033
Conserved cell types with divergent features in human versus mouse cortex
Hodge, R. D., Bakken, T. E., Miller, J. A., Smith, K. A., Barkan, E. R., Graybuck, L. T., Close, J. L., Long, B., Johansen, N., Penn, O., et al. (2019) · Nature · doi:10.1038/s41586-019-1506-7 · Cited by 1,775
Three groups of interneurons account for nearly 100% of neocortical GABAergic neurons
Rudy, B., Fishell, G., Lee, S., & Hjerling‐Leffler, J. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20853 · Cited by 1,420
Self-citationInterneuron cell types are fit to function
Kepecs, A., & Fishell, G. (2014) · Nature · doi:10.1038/nature12983 · Cited by 1,110
Self-citationA developmental and genetic classification for malformations of cortical development: update 2012
Barkovich, A. J., Guerrini, R., Kuzniecky, R., Jackson, G. D., & Dobyns, W. B. (2012) · Brain · doi:10.1093/brain/aws019 · Cited by 1,146
Hippocampal GABAergic Inhibitory Interneurons
Pelkey, K. A., Chittajallu, R., Craig, M. T., Tricoire, L., Wester, J. C., & McBain, C. J. (2017) · Physiological Reviews · doi:10.1152/physrev.00007.2017 · Cited by 889
A disinhibitory circuit mediates motor integration in the somatosensory cortex
Lee, S., Kruglikov, I., Huang, Z. J., Fishell, G., & Rudy, B. (2013) · Nature Neuroscience · doi:10.1038/nn.3544 · Cited by 758
Self-citationDevelopment and Functional Diversification of Cortical Interneurons
Lim, L., Mi, D., Llorca, A., & Marín, O. (2018) · Neuron · doi:10.1016/j.neuron.2018.10.009 · Cited by 714
Lee, S., Hjerling-Leffler, J., Zagha, E., Fishell, G., & Rudy, B. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.1869-10.2010 · Cited by 600
Self-citationIdentification of Spinal Circuits Transmitting and Gating Mechanical Pain
Duan, B., Cheng, L., Bourane, S., Britz, O., Padilla, C., Garcia-Campmany, L., Krashes, M., Knowlton, W., Velasquez, T., Ren, X., et al. (2014) · Cell · doi:10.1016/j.cell.2014.11.003 · Cited by 582
Electrophysiological, transcriptomic and morphologic profiling of single neurons using Patch-seq
Cadwell, C. R., Palasantza, A., Jiang, X., Berens, P., Deng, Q., Yilmaz, M., Reimer, J., Shen, S., Bethge, M., Tolias, K. F., et al. (2016) · Nature Biotechnology · doi:10.1038/nbt.3445 · Cited by 581
A viral strategy for targeting and manipulating interneurons across vertebrate species
Dimidschstein, J., Chen, Q., Tremblay, R., Rogers, S. L., Saldi, G.-A., Guo, L., Xu, Q., Liu, R., Lu, C., Chu, J., et al. (2016) · Nature Neuroscience · doi:10.1038/nn.4430 · Cited by 541
Self-citationDevelopmental diversification of cortical inhibitory interneurons
Mayer, C., Hafemeister, C., Bandler, R. C., Machold, R., Batista Brito, R., Jaglin, X., Allaway, K., Butler, A., Fishell, G., & Satija, R. (2018) · Nature · doi:10.1038/nature25999 · Cited by 492
Self-citationGABAergic Interneurons Shape the Functional Maturation of the Cortex
Le Magueresse, C., & Monyer, H. (2013) · Neuron · doi:10.1016/j.neuron.2013.01.011 · Cited by 425
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
Wu, B., Zhang, Z., Lui, W., Chen, X., Wang, Y., Chamberlain, A. A., Moreno‐Rodriguez, R. A., Markwald, R. R., O'Rourke, B. P., Sharp, D. J., et al. (2012) · Cell · doi:10.1016/j.cell.2012.10.023 · Cited by 402
Generating Neuronal Diversity in the Mammalian Cerebral Cortex
Lodato, S., & Arlotta, P. (2015) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-100814-125353 · Cited by 389
Innovations present in the primate interneuron repertoire
Krienen, F. M., Goldman, M., Zhang, Q., C. H. del Rosario, R., Florio, M., Machold, R., Saunders, A., Levandowski, K., Zaniewski, H., Schuman, B., et al. (2020) · Nature · doi:10.1038/s41586-020-2781-z · Cited by 381
Self-citationInnovations in Primate Interneuron Repertoire
Krienen, F. M., Goldman, M., Zhang, Q., del Rosario, R., Florio, M., Machold, R., Saunders, A., Levandowski, K., Zaniewski, H., Schuman, B., et al. (2019) · doi:10.1101/709501 · Cited by 372
Self-citationFung, S. J., Webster, M. J., Sivagnanasundaram, S., Duncan, C., Elashoff, M., & Weickert, C. S. (2010) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2010.09060784 · Cited by 366
Non-epithelial stem cells and cortical interneuron production in the human ganglionic eminences
Hansen, D. V., Lui, J. H., Flandin, P., Yoshikawa, K., Rubenstein, J. L., Alvarez-Buylla, A., & Kriegstein, A. R. (2013) · Nature Neuroscience · doi:10.1038/nn.3541 · Cited by 328
Strategies and Tools for Combinatorial Targeting of GABAergic Neurons in Mouse Cerebral Cortex
He, M., Tucciarone, J., Lee, S., Nigro, M. J., Kim, Y., Levine, J. M., Kelly, S. M., Krugikov, I., Wu, P., Chen, Y., et al. (2016) · Neuron · doi:10.1016/j.neuron.2016.08.021 · Cited by 339
Subcortical origins of human and monkey neocortical interneurons
Ma, T., Wang, C., Wang, L., Zhou, X., Tian, M., Zhang, Q., Zhang, Y., Li, J., Liu, Z., Cai, Y., et al. (2013) · Nature Neuroscience · doi:10.1038/nn.3536 · Cited by 322
Histone H3.3 Mutations Drive Pediatric Glioblastoma through Upregulation of MYCN
Bjerke, L. M., Mackay, A. G., Nandhabalan, M., Burford, A., Jury, A., Popov, S., Bax, D. A., Carvalho, D. M., Taylor, K. R., Vinci, M., et al. (2013) · Cancer Discovery · doi:10.1158/2159-8290.cd-12-0426 · Cited by 333
Evolutionary changes in promoter and enhancer activity during human corticogenesis
Reilly, S. K., Yin, J., Ayoub, A. E., Emera, D., Leng, J., Cotney, J., Sarro, R., Rakic, P., & Noonan, J. P. (2015) · Science · doi:10.1126/science.1260943 · Cited by 297
Neuronal activity is required for the development of specific cortical interneuron subtypes
De Marco García, N. V., Karayannis, T., & Fishell, G. (2011) · Nature · doi:10.1038/nature09865 · Cited by 294
Self-citationA Blueprint for the Spatiotemporal Origins of Mouse Hippocampal Interneuron Diversity
Tricoire, L., Pelkey, K. A., Erkkila, B. E., Jeffries, B. W., Yuan, X., & McBain, C. J. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.0323-11.2011 · Cited by 292
bHLH Factors in Self-Renewal, Multipotency, and Fate Choice of Neural Progenitor Cells
Imayoshi, I., & Kageyama, R. (2014) · Neuron · doi:10.1016/j.neuron.2014.03.018 · Cited by 279
Gating of hippocampal activity, plasticity, and memory by entorhinal cortex long-range inhibition
Basu, J., Zaremba, J. D., Cheung, S. K., Hitti, F. L., Zemelman, B. V., Losonczy, A., & Siegelbaum, S. A. (2016) · Science · doi:10.1126/science.aaa5694 · Cited by 274
Miyoshi, G., & Fishell, G. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhq155 · Cited by 230
Self-citationLodato, S., Rouaux, C., Quast, K. B., Jantrachotechatchawan, C., Studer, M., Hensch, T. K., & Arlotta, P. (2011) · Neuron · doi:10.1016/j.neuron.2011.01.015 · Cited by 244
Herring, C. A., Simmons, R. K., Freytag, S., Poppe, D., Moffet, J. J. D., Pflueger, J., Buckberry, S., Vargas-Landín, D. B., Clément, O., Goñi, E., et al. (2022) · Cell · doi:10.1016/j.cell.2022.09.039 · Cited by 242
Mechanisms of Inhibition within the Telencephalon: “Where the Wild Things Are”
Fishell, G., & Rudy, B. (2011) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-061010-113717 · Cited by 233
Self-citationAlpha oscillations and traveling waves: Signatures of predictive coding?
Alamia, A., & VanRullen, R. (2019) · PLoS Biology · doi:10.1371/journal.pbio.3000487 · Cited by 213
A spatially resolved brain region- and cell type-specific isoform atlas of the postnatal mouse brain
Joglekar, A., Prjibelski, A., Mahfouz, A., Collier, P., Lin, S., Schlusche, A. K., Marrocco, J., Williams, S. R., Haase, B., Hayes, A., et al. (2021) · Nature Communications · doi:10.1038/s41467-020-20343-5 · Cited by 229
Shaping Our Minds: Stem and Progenitor Cell Diversity in the Mammalian Neocortex
Franco, S. J., & Müller, U. (2013) · Neuron · doi:10.1016/j.neuron.2012.12.022 · Cited by 240
Cortical interneuron development: a tale of time and space
Hu, J. S., Vogt, D., Sandberg, M., & Rubenstein, J. L. (2017) · Development · doi:10.1242/dev.132852 · Cited by 189
Cellular and molecular mechanisms controlling the migration of neocortical interneurons
Marín, Ó. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12225 · Cited by 224
Prönneke, A., Scheuer, B., Wagener, R. J., Möck, M., Witte, M., & Staiger, J. F. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv202 · Cited by 204
Genetic Approaches to Neural Circuits in the Mouse
Josh Huang, Z., & Zeng, H. (2013) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062012-170307 · Cited by 200
Interneuron Types as Attractors and Controllers
Fishell, G., & Kepecs, Á. (2019) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-070918-050421 · Cited by 212
Self-citationGeneration of interneuron diversity in the mouse cerebral cortex
Gelman, D. M., & Marín, O. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07267.x · Cited by 188
Genetics and Function of Neocortical GABAergic Interneurons in Neurodevelopmental Disorders
Rossignol, E. (2011) · Neural Plasticity · doi:10.1155/2011/649325 · Cited by 192
Reelin and neuropsychiatric disorders
Ishii, K., Kubo, K.-I., & Nakajima, K. (2016) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2016.00229 · Cited by 185
Integration of GABAergic interneurons into cortical cell assemblies: lessons from embryos and adults
Bartolini, G., Ciceri, G., & Marín, O. (2013) · Neuron · doi:10.1016/j.neuron.2013.08.014 · Cited by 185
Four Unique Interneuron Populations Reside in Neocortical Layer 1
Schuman, B., Machold, R. P., Hashikawa, Y., Fuzik, J., Fishell, G. J., & Rudy, B. (2019) · The Journal of Neuroscience · doi:10.1523/jneurosci.1613-18.2018 · Cited by 184
“03 for the NDNF/nonNPY and 7 populations respectively; for statistics, see Table 3), resembling the “fast-adapting” VIP INs previously described in layers 1–3 (Lee et al., 2010; Miyoshi et al., 2010; Prönneke et al., 2015).”
MethodInfluentialSelf-citationCntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission
Karayannis, T., Au, E., Patel, J. C., Kruglikov, I., Markx, S., Delorme, R., Héron, D., Salomon, D., Glessner, J., Restituito, S., et al. (2014) · Nature · doi:10.1038/nature13248 · Cited by 183
Self-citationA wide diversity of cortical GABAergic interneurons derives from the embryonic preoptic area
Gelman, D., Griveau, A., Dehorter, N., Teissier, A., Varela, C., Pla, R., Pierani, A., & Marín, O. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.4068-11.2011 · Cited by 179
Fenno, L. E., Ramakrishnan, C., Kim, Y. S., Evans, K. E., Lo, M., Vesuna, S. S., Inoue, M., Cheung, K. Y. M., Yuen, E., Pichamoorthy, N., et al. (2020) · Neuron · doi:10.1016/j.neuron.2020.06.003 · Cited by 180
Brain-Wide Maps of Synaptic Input to Cortical Interneurons
Wall, N. R., Parra, M. D. L., Sorokin, J. M., Taniguchi, H., Huang, Z. J., & Callaway, E. M. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.3967-15.2016 · Cited by 186
Development and specification of GABAergic cortical interneurons
Kelsom, C., & Lu, W. (2013) · Cell & Bioscience · doi:10.1186/2045-3701-3-19 · Cited by 193
Common Origins of Hippocampal Ivy and Nitric Oxide Synthase Expressing Neurogliaform Cells
Tricoire, L., Pelkey, K. A., Daw, M. I., Sousa, V. H., Miyoshi, G., Jeffries, B., Cauli, B., Fishell, G., & McBain, C. J. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.5123-09.2010 · Cited by 171
Self-citationEpilepsy as a Neurodevelopmental Disorder
Bozzi, Y., Casarosa, S., & Caleo, M. (2012) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2012.00019 · Cited by 184
Dodson, P. D., Larvin, J. T., Duffell, J. M., Garas, F. N., Doig, N. M., Kessaris, N., Duguid, I., Bogacz, R., Butt, S. J. B., & Magill, P. J. (2015) · Neuron · doi:10.1016/j.neuron.2015.03.007 · Cited by 167
Self-citationPioneer GABA Cells Comprise a Subpopulation of Hub Neurons in the Developing Hippocampus
Picardo, M. A., Guigue, P., Bonifazi, P., Batista-Brito, R., Allene, C., Ribas, A., Fishell, G., Baude, A., & Cossart, R. (2011) · Neuron · doi:10.1016/j.neuron.2011.06.018 · Cited by 167
Self-citationThe MAP kinase phosphatase MKP-1 regulates BDNF-induced axon branching
Jeanneteau, F. D., Deinhardt, K., Miyoshi, G., Bennett, A. M., & Chao, M. V. (2010) · Nature Neuroscience · doi:10.1038/nn.2655 · Cited by 168
Self-citationInan, M., Welagen, J., & Anderson, S. A. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr148 · Cited by 161
Miyoshi, G., & Fishell, G. (2012) · Neuron · doi:10.1016/j.neuron.2012.04.025 · Cited by 159
Self-citationRegulation of cerebral cortical neurogenesis by the Pax6 transcription factor
Manuel, M. N., Mi, D., Mason, J. O., & Price, D. J. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00070 · Cited by 153
Bidirectional perisomatic inhibitory plasticity of a Fos neuronal network
Yap, E.-L., Pettit, N. L., Davis, C. P., Nagy, M. A., Harmin, D. A., Golden, E., Dağliyan, O., Lin, C., Rudolph, S., Sharma, N., et al. (2020) · Nature · doi:10.1038/s41586-020-3031-0 · Cited by 154
Neurogliaform cells in cortical circuits
Overstreet-Wadiche, L., & McBain, C. J. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn3969 · Cited by 152
Clonal production and organization of inhibitory interneurons in the neocortex
Brown, K. N., Chen, S., Han, Z., Lu, C.-H., Tan, X., Zhang, X.-J., Ding, L., Lopez-Cruz, A., Saur, D., Anderson, S. A., et al. (2011) · Science · doi:10.1126/science.1208884 · Cited by 152
Close, J., Xu, H., De Marco García, N., Batista-Brito, R., Rossignol, E., Rudy, B., & Fishell, G. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.3583-12.2012 · Cited by 141
Self-citationCharacterization of dopamine D1 and D2 receptor‐expressing neurons in the mouse hippocampus
Gangarossa, G., Longueville, S., Bundel, D. D., Perroy, J., Hervé, D., Girault, J., & Valjent, E. (2012) · Hippocampus · doi:10.1002/hipo.22044 · Cited by 142
Song, Y.-H., Yoon, J., & Lee, S. (2021) · Experimental & Molecular Medicine · doi:10.1038/s12276-021-00580-4 · Cited by 154
Integrative Mechanisms of Oriented Neuronal Migration in the Developing Brain
Evsyukova, I. Y., Plestant, C., & Anton, E. S. (2013) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-101512-122400 · Cited by 151
Activity regulates cell death within cortical interneurons through a Calcineurin-dependent mechanism
Priya, R., Paredes, M. F., Karayannis, T., Yusuf, N., Liu, X., Jaglin, X., Graef, I., Alvarez-Buylla, A., & Fishell, G. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.01.007 · Cited by 127
Self-citationInhibitory Interneurons and their Circuit Motifs in the Many Layers of the Barrel Cortex
Feldmeyer, D., Qi, G., Emmenegger, V., & Staiger, J. F. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.05.027 · Cited by 140
Dedic, N., Kühne, C., Jakovcevski, M., Hartmann, J., Genewsky, A. J., Gomes, K. S., Anderzhanova, E. A., Pöhlmann, M. L., Chang, S., Kolarz, A., et al. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0151-z · Cited by 135
Lozovaya, N., Eftekhari, S., Cloarec, R., Gouty‐Colomer, L., Dufour, A., Riffault, B., Billon-Grand, M., Pons-Bennaceur, A., Oumar, N., Burnashev, N., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-03802-y · Cited by 143
Miyoshi, G., Young, A., Petros, T., Karayannis, T., McKenzie Chang, M., Lavado, A., Iwano, T., Nakajima, M., Taniguchi, H., Huang, Z. J., et al. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.1164-15.2015 · Cited by 135
Self-citationPOm Thalamocortical Input Drives Layer-Specific Microcircuits in Somatosensory Cortex
Audette, N. J., Urban‐Ciećko, J., Matsushita, M. T., & Barth, A. L. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx044 · Cited by 143
Developmental Cell Death in the Cerebral Cortex
Wong, F. K., & Marín, Ó. (2019) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-100818-125204 · Cited by 139
The Parvalbumin/Somatostatin Ratio Is Increased in Pten Mutant Mice and by Human PTEN ASD Alleles
Vogt, D. L., Cho, K. K. A., Lee, A. T., Sohal, V. S., & Rubenstein, J. L. R. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.04.019 · Cited by 135
Sakamoto, M., Ieki, N., Miyoshi, G., Mochimaru, D., Miyachi, H., Imura, T., Yamaguchi, M., Fishell, G., Mori, K., Kageyama, R., et al. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.0674-14.2014 · Cited by 131
Self-citationLhx6 directly regulates Arx and CXCR7 to determine cortical interneuron fate and laminar position
Vogt, D., Hunt, R. F., Mandal, S., Sandberg, M., Silberberg, S. N., Nagasawa, T., Yang, Z., Baraban, S. C., & Rubenstein, J. L. R. (2014) · Neuron · doi:10.1016/j.neuron.2014.02.030 · Cited by 129
Sürmeli, G., Marcu, D.-C., McClure, C., Garden, D. L. F., Pastoll, H., & Nolan, M. F. (2015) · Neuron · doi:10.1016/j.neuron.2015.10.041 · Cited by 133
Neuronal nitric oxide synthase expressing neurons: a journey from birth to neuronal circuits
Tricoire, L., & Vitalis, T. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00082 · Cited by 133
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
Self-citationLineage-specific laminar organization of cortical GABAergic interneurons
Ciceri, G., Dehorter, N., Sols, I., Huang, Z. J., Maravall, M., & Marín, O. (2013) · Nature Neuroscience · doi:10.1038/nn.3485 · Cited by 124
Regulation of neuronal migration, an emerging topic in autism spectrum disorders
Reiner, O., Karzbrun, E., Kshirsagar, A., & Kaibuchi, K. (2015) · Journal of Neurochemistry · doi:10.1111/jnc.13403 · Cited by 129
Gangarossa, G., Espallergues, J., d’Exaerde, A. D. K., Mestikawy, S. E., Gerfen, C. R., Hervé, D., Girault, J., & Valjent, E. (2013) · Frontiers in Neural Circuits · doi:10.3389/fncir.2013.00022 · Cited by 122
Basu, J., Srinivas, K. V., Cheung, S. K., Taniguchi, H., Huang, Z. J., & Siegelbaum, S. A. (2013) · Neuron · doi:10.1016/j.neuron.2013.07.001 · Cited by 122
Directed migration of cortical interneurons depends on the cell-autonomous action of Sip1
van den Berghe, V., Stappers, E., Vandesande, B., Dimidschstein, J., Kroes, R., Francis, A., Conidi, A., Lesage, F., Dries, R., Cazzola, S., et al. (2013) · Neuron · doi:10.1016/j.neuron.2012.11.009 · Cited by 120
Self-citationGangarossa, G., Espallergues, J., Mailly, P., Bundel, D. D., d’Exaerde, A. D. K., Hervé, D., Girault, J., Valjent, E., & Krieger, P. (2013) · Frontiers in Neural Circuits · doi:10.3389/fncir.2013.00124 · Cited by 117
Dual origins of functionally distinct O-LM interneurons revealed by differential 5-HT3AR expression
Chittajallu, R., Craig, M. T., McFarland, A., Yuan, X., Gerfen, S., Tricoire, L., Erkkila, B., Barron, S. C., Lopez, C. M., Liang, B. J., et al. (2013) · Nature Neuroscience · doi:10.1038/nn.3538 · Cited by 119
Comparative density of CCK- and PV-GABA cells within the cortex and hippocampus
Whissell, P. D., Cajanding, J. D., Fogel, N., & Kim, J. C. (2015) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2015.00124 · Cited by 118
Expanding the power of recombinase-based labeling to uncover cellular diversity
Plummer, N. W., Evsyukova, I. Y., Robertson, S. D., de Marchena, J., Tucker, C. J., & Jensen, P. (2015) · Development · doi:10.1242/dev.129981 · Cited by 112
Lodato, S., Tomassy, G. S., De Leonibus, E., Uzcategui, Y. G., Andolfi, G., Armentano, M., Touzot, A., Gaztelu, J. M., Arlotta, P., Menendez de la Prida, L., et al. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.6580-10.2011 · Cited by 112
The development and evolution of inhibitory neurons in primate cerebrum
Schmitz, M. T., Sandoval, K., Chen, C. P., Mostajo-Radji, M. A., Seeley, W. W., Nowakowski, T. J., Ye, C. J., Paredes, M. F., & Pollen, A. A. (2022) · Nature · doi:10.1038/s41586-022-04510-w · Cited by 111
Maturation-Promoting Activity of SATB1 in MGE-Derived Cortical Interneurons
Denaxa, M., Kalaitzidou, M., Garefalaki, A., Achimastou, A., Lasrado, R., Maes, T., & Pachnis, V. (2012) · Cell Reports · doi:10.1016/j.celrep.2012.10.003 · Cited by 108
Inhibitory interneurons in visual cortical plasticity
van Versendaal, D., & Levelt, C. N. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2264-4 · Cited by 113
Anastasiades, P. G., Boada, C. M., & Carter, A. G. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy299 · Cited by 117
Genetic dissection of GABAergic neural circuits in mouse neocortex
Taniguchi, H. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00008 · Cited by 106
Sonic hedgehog functions through dynamic changes in temporal competence in the developing forebrain
Sousa, V. H., & Fishell, G. (2010) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2010.04.008 · Cited by 106
“In agreement with this, spatial biases have been found in the generation of individual neuron types in the MGE and LGE [40,45,46 ,47–49] However, a causal link between the function of these spatially restricted transcription factors and individual neuronal types has yet to be established.”
InfluentialSelf-citationMapping cell fate and function using recombinase-based intersectional strategies
Dymecki, S. M., Ray, R. S., & Kim, J. C. (2010) · Methods in Enzymology · doi:10.1016/s0076-6879(10)77011-7 · Cited by 104
Prenatal stress delays inhibitory neuron progenitor migration in the developing neocortex
Stevens, H. E., Su, T., Yanagawa, Y., & Vaccarino, F. M. (2012) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2012.07.011 · Cited by 105
Involvement of cortical fast-spiking parvalbumin-positive basket cells in epilepsy
Jiang, X., Lachance, M., & Rossignol, E. (2016) · Progress in brain research · doi:10.1016/bs.pbr.2016.04.012 · Cited by 101
Rbfox1 Mediates Cell-type-Specific Splicing in Cortical Interneurons
Wamsley, B., Jaglin, X. H., Favuzzi, E., Quattrocolo, G., Nigro, M. J., Yusuf, N., Khodadadi‐Jamayran, A., Rudy, B., & Fishell, G. (2018) · Neuron · doi:10.1016/j.neuron.2018.09.026 · Cited by 101
Self-citation
Metadata
- Authors
- Miyoshi, G., Hjerling-Leffler, J., Karayannis, T., Sousa, V. H., Butt, S. J. B., Battiste, J., Johnson, J. E., Machold, R. P., & Fishell, G.
- Affiliations
- New York University (US)
- Imperial College London (GB)
- The University of Texas Southwestern Medical Center (US)
- NYU Langone Health (US)
- ORCID
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2010-02-03
- Volume
- 30
- Issue
- 5
- Pages
- 1582-1594
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC2826846
- OpenAlex
- W1975767398
- Cited by
- 559
- References
- 81
- Citations by year
- 2026: 14 · 2025: 20 · 2024: 23 · 2023: 26 · 2022: 25 · 2021: 34 · 2020: 54 · 2019: 42 · 2018: 30 · 2017: 37 · 2016: 37 · 2015: 40 · 2014: 38 · 2013: 53 · 2012: 38
- FWCI
- 13.98
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Simons Foundation
- New York State Stem Cell Science
- National Institutes of Health (GAD67)
- Japan Society for the Promotion of Science
- National Institute of Mental Health (R01MH071679, R37MH071679)
- National Institute of Neurological Disorders and Stroke (R01NS039007)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- caudal ganglionic eminence, cortical interneurons, GABAergic interneurons, interneuron subtypes, reelin, vasoactive intestinal peptide, medial ganglionic eminence, cortical development
- MeSH terms
- Reelin Protein, Animals, Cell Differentiation, Cerebral Cortex, Genetic Markers, Genetic Techniques, Interneurons, Male, Nerve Tissue Proteins, Serine Endopeptidases, Cell Adhesion Molecules, Neuronal, Extracellular Matrix Proteins, Prosencephalon, Patch-Clamp Techniques, Cell Lineage, Body Patterning, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
