The role of interneurons in autism and Tourette Syndrome

Diagnostic and Statistical Manual of Mental Disorders

Williams, J. B. W., & First, M. B. (2013) · Oxford University Press eBooks · doi:10.1093/acrefore/9780199975839.013.104 · Cited by 109,841 · see citing works

Diagnostic and Statistical Manual of Mental Disorders

(2012) · Springer eBooks · doi:10.1007/springerreference_121117 · Cited by 20,769 · see citing works

Prevalence of Autism Spectrum Disorder Among Children Aged 8 Years — Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2014

Baio, J., Wiggins, L., Christensen, D. L., Maenner, M. J., Daniels, J., Warren, Z., Kurzius-Spencer, M., Zahorodny, W., Robinson, C., Rosenberg, et al. (2018) · MMWR. Surveillance Summaries · doi:10.15585/mmwr.ss6706a1 · Cited by 6,078 · see citing works

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 · see citing works

Prevalence and Characteristics of Autism Spectrum Disorder Among Children Aged 8 Years — Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2012

Christensen, D. L., Baio, J., Braun, K. V. N., Bilder, D., Charles, J., Constantino, J. N., Daniels, J., Durkin, M. S., Fitzgerald, R. T., Kurzius-Spencer, M., et al. (2016) · MMWR. Surveillance Summaries · doi:10.15585/mmwr.ss6503a1 · Cited by 1,964 · see citing works

Shank3 mutant mice display autistic-like behaviours and striatal dysfunction

Peça, J., Feliciano, C., Ting, J. T., Wang, W., Wells, M. F., Venkatraman, T. N., Lascola, C. D., Fu, Z., & Feng, G. (2011) · Nature · doi:10.1038/nature09965 · Cited by 1,570 · see citing works

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 · see citing works

Prevalence of autism spectrum disorder among children aged 8 Years - Autism and developmental disabilities monitoring network, 11 Sites, United States, 2014

Naarden Braun, K. V., Lopez, M., White, T., et al. (2023) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/y3kk-5x30 · Cited by 1,381 · see citing works

Inhibition of inhibition in visual cortex: the logic of connections between molecularly distinct interneurons

Pfeffer, C. K., Xue, M., He, M., Huang, Z. J., & Scanziani, M. (2013) · Nature Neuroscience · doi:10.1038/nn.3446 · Cited by 1,353 · see citing works

Most genetic risk for autism resides with common variation

Gaugler, T., Klei, L., Sanders, S. J., Bodea, C. A., Goldberg, A. P., Lee, A. B., Mahajan, M., Manaa, D., Pawitan, Y., Reichert, J., et al. (2014) · Nature Genetics · doi:10.1038/ng.3039 · Cited by 1,239 · see citing works

Cortical interneurons that specialize in disinhibitory control

Pi, H.-J., Hangya, B., Kvitsiani, D., Sanders, J. I., Huang, Z. J., & Kepecs, A. (2013) · Nature · doi:10.1038/nature12676 · Cited by 1,136 · see citing works

Interneuron cell types are fit to function

Kepecs, A., & Fishell, G. (2014) · Nature · doi:10.1038/nature12983 · Cited by 1,110 · see citing works

Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits

Peñagarikano, O., Abrahams, B. S., Herman, E. I., Winden, K. D., Gdalyahu, A., Dong, H., Sonnenblick, L. I., Gruver, R., Almajano, J., Bragin, A., et al. (2011) · Cell · doi:10.1016/j.cell.2011.08.040 · Cited by 1,075 · see citing works

Excitatory/Inhibitory Balance and Circuit Homeostasis in Autism Spectrum Disorders

Nelson, S. B., & Valakh, V. (2015) · Neuron · doi:10.1016/j.neuron.2015.07.033 · Cited by 1,001 · see citing works

A Cortical Circuit for Gain Control by Behavioral State

Fu, Y., Tucciarone, J. M., Espinosa, J. S., Sheng, N., Darcy, D. P., Nicoll, R. A., Huang, Z. J., & Stryker, M. P. (2014) · Cell · doi:10.1016/j.cell.2014.01.050 · Cited by 937 · see citing works

Advancing the understanding of autism disease mechanisms through genetics

de la Torre-Ubieta, L., Won, H., Stein, J. L., & Geschwind, D. H. (2016) · Nature Medicine · doi:10.1038/nm.4071 · Cited by 827 · see citing works

Direct and indirect pathways of basal ganglia: a critical reappraisal

Calabresi, P., Picconi, B., Tozzi, A., Ghiglieri, V., & Filippo, M. D. (2014) · Nature Neuroscience · doi:10.1038/nn.3743 · Cited by 820 · see citing works

Neural Networks of the Mouse Neocortex

Zingg, B., Hintiryan, H., Gou, L., Song, M. Y., Bay, M., Bienkowski, M. S., Foster, N. N., Yamashita, S., Bowman, I., Toga, A. W., et al. (2014) · Cell · doi:10.1016/j.cell.2014.02.023 · Cited by 797 · see citing works

Patches of Disorganization in the Neocortex of Children with Autism

Stoner, R., Chow, M. L., Boyle, M. P., Sunkin, S. M., Mouton, P. R., Roy, S., Wynshaw-Boris, A., Colamarino, S. A., Lein, E. S., & Courchesne, E. (2014) · New England Journal of Medicine · doi:10.1056/nejmoa1307491 · Cited by 722 · see citing works

Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2

Strauss, K. A., Puffenberger, E. G., Huentelman, M. J., Gottlieb, S., Dobrin, S. E., Parod, J. M., Stephan, D. A., & Morton, D. H. (2006) · New England Journal of Medicine · doi:10.1056/nejmoa052773 · Cited by 630 · see citing works

Mice lacking Dlx1 show subtype-specific loss of interneurons, reduced inhibition and epilepsy

Cobos, I., Calcagnotto, M. E., Vilaythong, A. J., Thwin, M. T., Noebels, J. L., Baraban, S. C., & Rubenstein, J. L. R. (2005) · Nature Neuroscience · doi:10.1038/nn1499 · Cited by 502 · see citing works

Differential Innervation of Direct- and Indirect-Pathway Striatal Projection Neurons

Wall, N. R., De La Parra, M., Callaway, E. M., & Kreitzer, A. C. (2013) · Neuron · doi:10.1016/j.neuron.2013.05.014 · Cited by 489 · see citing works

Decreased number of parvalbumin and cholinergic interneurons in the striatum of individuals with Tourette syndrome

Kataoka, Y., Kalanithi, P. S. A., Grantz, H., Schwartz, M. L., Saper, C. B., Leckman, J. F., & Vaccarino, F. M. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22206 · Cited by 457 · see citing works

Complementary Contributions of Striatal Projection Pathways to Action Initiation and Execution

Tecuapetla, F., Jin, X., Lima, S. Q., & Costa, R. M. (2016) · Cell · doi:10.1016/j.cell.2016.06.032 · Cited by 396 · see citing works

Adult restoration of Shank3 expression rescues selective autistic-like phenotypes

Mei, Y., Monteiro, P., Zhou, Y., Kim, J.-A., Gao, X., Fu, Z., & Feng, G. (2016) · Nature · doi:10.1038/nature16971 · Cited by 392 · see citing works

Population prevalence of Tourette syndrome: A systematic review and meta‐analysis

Scharf, J. M., Miller, L. L., Gauvin, C. A., Alabiso, J., Mathews, C. A., & Ben‐Shlomo, Y. (2014) · Movement Disorders · doi:10.1002/mds.26089 · Cited by 375 · see citing works

Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

iPSYCH-SSI-Broad Autism Group, Robinson, E. B., St Pourcain, B., Anttila, V., Kosmicki, J. A., Bulik-Sullivan, B., Grove, J., Maller, J., Samocha, K. E., Sanders, S. J., et al. (2016) · Nature Genetics · doi:10.1038/ng.3529 · Cited by 367 · see citing works

Reduced GABAergic Action in the Autistic Brain

Robertson, C. E., Ratai, E.-M., & Kanwisher, N. (2016) · Current Biology · doi:10.1016/j.cub.2015.11.019 · Cited by 327 · see citing works

The Number of Parvalbumin-Expressing Interneurons Is Decreased in the Medial Prefrontal Cortex in Autism

Hashemi, E., Ariza, J., Rogers, H., Noctor, S. C., & Martínez-Cerdeño, V. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw021 · Cited by 322 · see citing works

Sensory Integration in Mouse Insular Cortex Reflects GABA Circuit Maturation

Gogolla, N., Takesian, A. E., Feng, G., Fagiolini, M., & Hensch, T. K. (2014) · Neuron · doi:10.1016/j.neuron.2014.06.033 · Cited by 310 · see citing works

Human-Induced Pluripotent Stem Cells form Functional Neurons and Improve Recovery After Grafting in Stroke-Damaged Brain

Oki, K., Tatarishvili, J., Wood, J. C., Koch, P., Wattananit, S., Mine, Y., Monni, E., Tornero, D., Ahlenius, H., Ladewig, J., et al. (2012) · Stem Cells · doi:10.1002/stem.1104 · Cited by 291 · see citing works

Autism-like Deficits in Shank3-Deficient Mice Are Rescued by Targeting Actin Regulators

Duffney, L. J., Zhong, P., Wei, J., Matas, E., Cheng, J., Qin, L., Ma, K., Dietz, D. M., Kajiwara, Y., Buxbaum, J. D., et al. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.04.064 · Cited by 281 · see citing works

Dynamic Balance of Excitation and Inhibition in Human and Monkey Neocortex

Dehghani, N., Peyrache, A., Teleńczuk, B., Quyen, M. L. V., Halgren, E., Cash, S. S., Hatsopoulos, N. G., & Alain Destexhe, A. (2016) · Scientific Reports · doi:10.1038/srep23176 · Cited by 270 · see citing works

Striatal Circuits as a Common Node for Autism Pathophysiology

Fuccillo, M. V. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00027 · Cited by 269 · see citing works

GABA estimation in the brains of children on the autism spectrum: measurement precision and regional cortical variation

Gaetz, W., Bloy, L., Wang, D. J., Port, R. G., Blaskey, L., Levy, S. E., & Roberts, T. P. L. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.068 · Cited by 267 · see citing works

Reduced GABA and altered somatosensory function in children with autism spectrum disorder

Puts, N. A. J., Wodka, E. L., Harris, A. D., Crocetti, D., Tommerdahl, M., Mostofsky, S. H., & Edden, R. A. E. (2016) · Autism Research · doi:10.1002/aur.1691 · Cited by 264 · see citing works

Lack of parvalbumin in mice leads to behavioral deficits relevant to all human autism core symptoms and related neural morphofunctional abnormalities

Wöhr, M., Orduz, D., Gregory, P., Moreno, H., Khan, U., Vörckel, K. J., Wolfer, D. P., Welzl, H., Gall, D., Schiffmann, S. N., et al. (2015) · Translational Psychiatry · doi:10.1038/tp.2015.19 · Cited by 258 · see citing works

Altered structural connectivity of cortico-striato-pallido-thalamic networks in Gilles de la Tourette syndrome

Worbe, Y., Marrakchi‐Kacem, L., Lecomte, S., Valabrègue, R., Poupon, F., Guevara, P., Tucholka, A., Mangin, J., Vidailhet, M., Lehéricy, S., et al. (2014) · Brain · doi:10.1093/brain/awu311 · Cited by 257 · see citing works

Changes in the Development of Striatum Are Involved in Repetitive Behavior in Autism

Langen, M., Bos, D., Noordermeer, S. D. S., Nederveen, H., van Engeland, H., & Durston, S. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.08.013 · Cited by 256 · see citing works

Comorbidities, Social Impact, and Quality of Life in Tourette Syndrome

Eapen, V., Cavanna, A. E., & Robertson, M. M. (2016) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2016.00097 · Cited by 250 · see citing works

Reduction in parvalbumin expression not loss of the parvalbumin-expressing GABA interneuron subpopulation in genetic parvalbumin and shank mouse models of autism

Filice, F., Vörckel, K. J., Sungur, A. Ö., Wöhr, M., & Schwaller, B. (2016) · Molecular Brain · doi:10.1186/s13041-016-0192-8 · Cited by 240 · see citing works

Synaptic Computation and Sensory Processing in Neocortical Layer 2/3

Petersen, C. C. H., & Crochet, S. (2013) · Neuron · doi:10.1016/j.neuron.2013.03.020 · Cited by 239 · see citing works

Striatal cholinergic interneuron regulation and circuit effects

Lim, S. A. O., Kang, U. J., & McGehee, D. S. (2014) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2014.00022 · Cited by 236 · see citing works

Enhancement of Inhibitory Neurotransmission by GABA A Receptors Having α 2,3 -Subunits Ameliorates Behavioral Deficits in a Mouse Model of Autism

Han, S., Tai, C., Jones, C. J., Scheuer, T., & Catterall, W. A. (2014) · Neuron · doi:10.1016/j.neuron.2014.01.016 · Cited by 231 · see citing works

Non-invasive evaluation of the GABAergic/glutamatergic system in autistic patients observed by MEGA-editing proton MR spectroscopy using a clinical 3 tesla instrument

Harada, M., Taki, M. M., Nose, A., Kubo, H., Mori, K., Nishitani, H., & Matsuda, T. (2011) · Journal of Autism and Developmental Disorders · doi:10.1007/s10803-010-1065-0 · Cited by 231 · see citing works

Transcriptome Analysis of the Human Striatum in Tourette Syndrome

Lennington, J. B., Coppola, G., Kataoka-Sasaki, Y., Fernandez, T. V., Palejev, D., Li, Y., Huttner, A., Pletikos, M., Sestan, N., Leckman, J. F., et al. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.07.018 · Cited by 211 · see citing works

Characterizing VIP neurons in the barrel cortex of VIPcre/tdTomato mice reveals layer-specific differences

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 · see citing works

Shaping action sequences in basal ganglia circuits

Jin, X., & Costa, R. M. (2015) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2015.06.011 · Cited by 194 · see citing works

Morphological alterations in the thalamus, striatum, and pallidum in autism spectrum disorder

Schuetze, M., Park, M. T. M., Cho, I. Y., MacMaster, F. P., Chakravarty, M. M., & Bray, S. L. (2016) · Neuropsychopharmacology · doi:10.1038/npp.2016.64 · Cited by 186 · see citing works

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 · see citing works

The Diversity of Cortical Inhibitory Synapses

Kubota, Y., Karube, F., Nomura, M., & Kawaguchi, Y. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00027 · Cited by 180 · see citing works

Widespread abnormality of the γ-aminobutyric acid-ergic system in Tourette syndrome

Lerner, A., Bagic, A. I., Simmons, J. M., Mari, Z. K., Bonne, O. B., Xu, B., Kazuba, D. M., Herscovitch, P., Carson, R. E., Murphy, D. L., et al. (2012) · Brain · doi:10.1093/brain/aws104 · Cited by 179 · see citing works

Learning robust cortico-cortical associations with the basal ganglia: An integrative review

Hélie, S., Ell, S. W., & Ashby, F. G. (2014) · Cortex · doi:10.1016/j.cortex.2014.10.011 · Cited by 172 · see citing works

Familial Risks of Tourette Syndrome and Chronic Tic Disorders

Mataix‐Cols, D., Isomura, K., Pérez-Vigil, A., Chang, Z., Rück, C., Larsson, K. J., Leckman, J. F., Serlachius, E., Larsson, H., & Lichtenstein, P. (2015) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2015.0627 · Cited by 171 · see citing works

Layer 6 Corticothalamic Neurons Activate a Cortical Output Layer, Layer 5a

Kim, J., Matney, C. J., Blankenship, A. G., Hestrin, S., & Brown, S. P. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1325-14.2014 · Cited by 169 · see citing works

Cholinergic interneurons in the dorsal and ventral striatum: anatomical and functional considerations in normal and diseased conditions

Gonzales, K. K., & Smith, Y. (2015) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12762 · Cited by 164 · see citing works

Cortical Control of Striatal Dopamine Transmission via Striatal Cholinergic Interneurons

Kosillo, P., Zhang, Y.-F., Threlfell, S., & Cragg, S. J. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw252 · Cited by 164 · see citing works

Targeted ablation of cholinergic interneurons in the dorsolateral striatum produces behavioral manifestations of Tourette syndrome

Xu, M., Kobets, A. J., Du, J., Lennington, J. B., Li, L., Banasr, M., Duman, R. S., Vaccarino, F. M., Dileone, R., & Pittenger, C. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1419533112 · Cited by 159 · see citing works

The Mouse Nervous System

(2012) · doi:10.1016/c2009-0-00185-8 · Cited by 152 · see citing works

Loss of MeCP2 in Parvalbumin-and Somatostatin-Expressing Neurons in Mice Leads to Distinct Rett Syndrome-like Phenotypes

Ito, A., Ure, K., Chen, H., Swann, J. W., & Zoghbi, H. Y. (2015) · Neuron · doi:10.1016/j.neuron.2015.10.029 · Cited by 152 · see citing works

Striatal D1 and D2 signaling differentially predict learning from positive and negative outcomes

Cox, S. M. L., Frank, M. J., Larcher, K. M.-H., Fellows, L. K., Clark, C. A., Leyton, M., & Dagher, A. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2014.12.070 · Cited by 144 · see citing works

Synaptic abnormalities and cytoplasmic glutamate receptor aggregates in contactin associated protein-like 2 /Caspr2 knockout neurons

Varea, O., Martin‐de‐Saavedra, M. D., Kopeikina, K. J., Schürmann, B., Fleming, H. J., Fawcett‐Patel, J. M., Bach, A. P., Jang, S., Peles, E., Kim, E., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1423205112 · Cited by 139 · see citing works

Inhibitory Circuits in Cortical Layer 5

Naka, A., & Adesnik, H. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00035 · Cited by 130 · see citing works

DISSECTING OCD CIRCUITS: FROM ANIMAL MODELS TO TARGETED TREATMENTS: Review: Dissecting OCD Circuits: Animals to Treatments

Ahmari, S. E., & Dougherty, D. D. (2015) · Depression and Anxiety · doi:10.1002/da.22367 · Cited by 128 · see citing works

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 126 · see citing works

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 123 · see citing works

The Number of Parvalbumin-Expressing Interneurons Is Decreased in the Prefrontal Cortex in Autism

Hashemi, E., Ariza, J., Rogers, H., Noctor, S. C., & Martínez-Cerdeño, V. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhx063 · Cited by 123 · see citing works

Novel Shank3 mutant exhibits behaviors with face validity for autism and altered striatal and hippocampal function

Jaramillo, T. C., Speed, H. E., Xuan, Z., Reimers, J. M., Escamilla, C. O., Weaver, T. P., Liu, S., Filonova, I., & Powell, C. M. (2017) · Autism Research · doi:10.1002/aur.1664 · Cited by 119 · see citing works

Principles of Synaptic Organization of GABAergic Interneurons in the Striatum

Straub, C., Saulnier, J. L., Bègue, A., Feng, D. D., Huang, K. W., & Sabatini, B. L. (2016) · Neuron · doi:10.1016/j.neuron.2016.09.007 · Cited by 116 · see citing works

Somatosensory–motor bodily representation cortical thinning in Tourette: Effects of tic severity, age and gender

Fahim, C., Yoon, U., Das, S., Lyttelton, O., Chen, J., Arnaoutelis, R., Rouleau, G., Sandor, P., Frey, K., Brandner, C., et al. (2010) · Cortex · doi:10.1016/j.cortex.2009.06.008 · Cited by 107 · see citing works

Are Striatal Tyrosine Hydroxylase Interneurons Dopaminergic?

Xenias, H. S., Ibáñez-Sandoval, O., Koós, T. Z., & Tepper, J. M. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0195-15.2015 · Cited by 101 · see citing works

The Number of Chandelier and Basket Cells Are Differentially Decreased in Prefrontal Cortex in Autism

Ariza, J., Rogers, H., Hashemi, E., Noctor, S. C., & Martínez-Cerdeño, V. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhw349 · Cited by 101 · see citing works

A systematic review of molecular imaging (PET and SPECT) in autism spectrum disorder: Current state and future research opportunities

Zürcher, N. R., Bhanot, A., McDougle, C. J., & Hooker, J. M. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.02.002 · Cited by 99 · see citing works

Exploring the relationship between cortical GABA concentrations, auditory gamma‐band responses and development in ASD: Evidence for an altered maturational trajectory in ASD

Port, R. G., Gaetz, W., Bloy, L., Wang, D., Blaskey, L., Kuschner, E. S., Levy, S. E., Brodkin, E. S., & Roberts, T. P. L. (2017) · Autism Research · doi:10.1002/aur.1686 · Cited by 94 · see citing works

Ablation of fast-spiking interneurons in the dorsal striatum, recapitulating abnormalities seen post-mortem in Tourette syndrome, produces anxiety and elevated grooming

Xu, M., Li, L., & Pittenger, C. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.02.074 · Cited by 91 · see citing works

Prenatal Valproate Exposure Differentially Affects Parvalbumin-Expressing Neurons and Related Circuits in the Cortex and Striatum of Mice

Lauber, E., Filice, F., & Schwaller, B. (2016) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2016.00150 · Cited by 90 · see citing works

Brain structure in pediatric Tourette syndrome

and The Tourette Association of America Neuroimaging Consortium, Greene, D. J., Williams III, A. C., Koller, J. M., Schlaggar, B. L., & Black, K. J. (2017) · Molecular Psychiatry · doi:10.1038/mp.2016.194 · Cited by 89 · see citing works

Targeted Interneuron Depletion in the Dorsal Striatum Produces Autism-like Behavioral Abnormalities in Male but Not Female Mice

Rapanelli, M., Frick, L. R., Xu, M., Groman, S. M., Jindachomthong, K., Tamamaki, N., Tanahira, C., Taylor, J. R., & Pittenger, C. (2017) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.01.020 · Cited by 86 · see citing works

Cortical plasticity induced by transplantation of embryonic somatostatin or parvalbumin interneurons

Tang, Y., Stryker, M. P., Álvarez-Buylla, A., & Espinosa, J. S. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1421844112 · Cited by 84 · see citing works

Selective Dysregulation of Hippocampal Inhibition in the Mouse Lacking Autism Candidate Gene CNTNAP2

Jürgensen, S., & Castillo, P. E. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.1666-15.2015 · Cited by 78 · see citing works

Tics are caused by alterations in prefrontal areas, thalamus and putamen, while changes in the cingulate gyrus reflect secondary compensatory mechanisms

Müller‐Vahl, K., Großkreutz, J., Prell, T., Kaufmann, J., Bodammer, N., & Peschel, T. (2014) · BMC Neuroscience · doi:10.1186/1471-2202-15-6 · Cited by 71 · see citing works

Neostriatal GABAergic Interneurons Mediate Cholinergic Inhibition of Spiny Projection Neurons

Faust, T. W., Assous, M., Tepper, J. M., & Koós, T. Z. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0466-16.2016 · Cited by 65 · see citing works

The disrupted basal ganglia and behavioural control: An integrative cross-domain perspective of spontaneous stereotypy

McBride, S. D., & Parker, M. O. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.05.057 · Cited by 63 · see citing works

Network over‐connectivity differentiates autism spectrum disorder from other developmental disorders in toddlers: A diffusion MRI study

Conti, E., Mitra, J., Calderoni, S., Pannek, K., Shen, K., Pagnozzi, A. M., Rose, S., Mazzotti, S., Scelfo, D., Tosetti, M., et al. (2017) · Human Brain Mapping · doi:10.1002/hbm.23520 · Cited by 62 · see citing works

The Genetic Etiology of Tourette Syndrome: Large-Scale Collaborative Efforts on the Precipice of Discovery

Georgitsi, M., Willsey, A. J., Mathews, C. A., State, M. W., Scharf, J. M., & Paschou, P. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00351 · Cited by 60 · see citing works

Optogenetic stimulation reveals distinct modulatory properties of thalamostriatal vs corticostriatal glutamatergic inputs to fast-spiking interneurons

Sciamanna, G., Ponterio, G., Mandolesi, G., Bonsi, P., & Pisani, A. (2015) · Scientific Reports · doi:10.1038/srep16742 · Cited by 51 · see citing works

A review of co-occurrence of autism spectrum disorder and Tourette syndrome

Kalyva, E., Kyriazi, M., Vargiami, E., & Zafeiriou, D. (2016) · Research in Autism · doi:10.1016/j.rasd.2016.01.007 · Cited by 49 · see citing works

Psychiatric Symptoms and Comorbidities in Autism Spectrum Disorder

Mazzone, L., & Vitiello, B. (2016) · Springer eBooks · doi:10.1007/978-3-319-29695-1 · Cited by 43 · see citing works

Transcription factor LIM homeobox 7 (Lhx7) maintains subtype identity of cholinergic interneurons in the mammalian striatum

Lopes, R., van Wijk, N. V., Neves, G., & Pachnis, V. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1109251109 · Cited by 42 · see citing works

Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general populationPreprint

Robinson, E., Pourcain, B. S., Anttila, V., Kosmicki, J. A., Bulik-Sullivan, B. K., Grove, J., Maller, J., Samocha, K. E., Sanders, S., Ripke, S., et al. (2015) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/027771 · Cited by 34 · see citing works

Pediatric Tourette syndrome: Insights from recent neuroimaging studies

Church, J. A., & Schlaggar, B. L. (2014) · Journal of Obsessive-Compulsive and Related Disorders · doi:10.1016/j.jocrd.2014.04.002 · Cited by 33 · see citing works

Cortical interneurons from human pluripotent stem cells: prospects for neurological and psychiatric disease

Arber, C., & Li, M. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00010 · Cited by 32 · see citing works

Social Deficits and Autism Spectrum Disorders in Tourette’s Syndrome

Hanks, C. E., Lewin, A. B., Mutch, P. J., Storch, E. A., & Murphy, T. K. (2015) · Current Developmental Disorders Reports · doi:10.1007/s40474-015-0060-8 · Cited by 25 · see citing works

Interneuron Progenitor Transplantation to Treat CNS Dysfunction

Chohan, M. O., & Moore, H. M. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00064 · Cited by 22 · see citing works

Neural Networks of the Mouse Neocortex

Zingg, B., Hintiryan, H., Gou, L., Song, M. Y., Bay, M., Bienkowski, M. S., Foster, N. N., Yamashita, S., Bowman, I., Toga, A. W., et al. (2015) · Annals of Neurosciences · doi:10.5214/ans.0972.7531.220409 · Cited by 8 · see citing works

Tics and Tourette Syndrome in Autism Spectrum Disorder

Capuano, A., & Valeri, G. (2016) · Springer eBooks · doi:10.1007/978-3-319-29695-1_7 · Cited by 2 · see citing works

Diversity of Interneurons in the Dorsal Striatum Revealed by Single-Cell RNA Sequencing and PatchSeq

Muñoz-Manchado, A. B., Bengtsson Gonzales, C., Zeisel, A., Munguba, H., Bekkouche, B., Skene, N. G., Lönnerberg, P., Ryge, J., Harris, K. D., Linnarsson, S., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.07.053 · Cited by 229 · see citing works

Linking mPFC circuit maturation to the developmental regulation of emotional memory and cognitive flexibility

Klune, C. B., Jin, B., & DeNardo, L. A. (2021) · eLife · doi:10.7554/elife.64567 · Cited by 171 · see citing works

Dopaminergic Disturbances in Tourette Syndrome: An Integrative Account

Maia, T. V., & Conceição, V. A. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2018.02.1172 · Cited by 138 · see citing works

Male and Female Mice Lacking Neuroligin-3 Modify the Behavior of Their Wild-Type Littermates

Kalbassi, S., Bachmann, S. O., Cross, E., Roberton, V. H., & Baudouin, S. J. (2017) · eNeuro · doi:10.1523/eneuro.0145-17.2017 · Cited by 136 · see citing works

Opportunities and limitations of genetically modified nonhuman primate models for neuroscience research

Feng, G., Jensen, F. E., Greely, H. T., Okano, H., Treue, S., Roberts, A., Fox, J. G., Caddick, S. J., Poo, M.-M., Newsome, W. T., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2006515117 · Cited by 118 · see citing works

Antibodies From Children With PANDAS Bind Specifically to Striatal Cholinergic Interneurons and Alter Their Activity

Xu, J., Liu, R.-J., Fahey, S., Frick, L. R., Leckman, J. F., Vaccarino, F. M., Duman, R. S., Williams, K. B., Swedo, S. E., & Pittenger, C. (2020) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2020.19070698 · Cited by 102 · see citing works

Joint Hypermobility Links Neurodivergence to Dysautonomia and Pain

Csecs, J. L. L., Iodice, V., Rae, C. L., Brooke, A., Simmons, R., Quadt, L., Savage, G. K., Dowell, N. G., Prowse, F., Themelis, K., et al. (2022) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2021.786916 · Cited by 98 · see citing works

A Bayesian Account of the Sensory-Motor Interactions Underlying Symptoms of Tourette Syndrome

Rae, C. L., Critchley, H., & Seth, A. K. (2019) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2019.00029 · Cited by 69 · see citing works

Sensory hypersensitivity in Tourette syndrome: A review

Isaacs, D. A., & Riordan, H. (2020) · Brain and Development · doi:10.1016/j.braindev.2020.06.003 · Cited by 71 · see citing works

Synaptic processes and immune-related pathways implicated in Tourette syndrome

Tsetsos, F., Yu, D., Sul, J. H., Huang, A. Y., Illmann, C., Osiecki, L., Darrow, S. M., Hirschtritt, M. E., Greenberg, E., Müller‐Vahl, K., et al. (2021) · Translational Psychiatry · doi:10.1038/s41398-020-01082-z · Cited by 63 · see citing works

Transcranial Magnetic Stimulation in Tourette Syndrome: A Historical Perspective, Its Current Use and the Influence of Comorbidities in Treatment Response

Grados, M. A., Huselid, R., & Duque, L. (2018) · Brain Sciences · doi:10.3390/brainsci8070129 · Cited by 49 · see citing works

Region and Cell Type Distribution of TCF4 in the Postnatal Mouse Brain

Kim, H., Berens, N., Ochandarena, N. E., & Philpot, B. D. (2020) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2020.00042 · Cited by 46 · see citing works

Evolutionarily conservative and non-conservative regulatory networks during primate interneuron development revealed by single-cell RNA and ATAC sequencing

Zhao, Z., Zhang, D., Yang, F., Xu, M., Zhao, S., Pan, T., Liu, C., Liu, Y., Wu, Q., Tu, Q., et al. (2022) · Cell Research · doi:10.1038/s41422-022-00635-9 · Cited by 43 · see citing works

Excitatory synaptic dysfunction cell-autonomously decreases inhibitory inputs and disrupts structural and functional plasticity

He, H., Shen, W., Zheng, L., Guo, X., & Cline, H. T. (2018) · Nature Communications · doi:10.1038/s41467-018-05125-4 · Cited by 42 · see citing works

Circulating miRNAs, Small but Promising Biomarkers for Autism Spectrum Disorder

Salloum‐Asfar, S., Satheesh, N. J., & Abdulla, S. A. (2019) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2019.00253 · Cited by 41 · see citing works

Language evolution: examining the link between cross-modality and aggression through the lens of disorders

Benítez‐Burraco, A., & Progovac, L. (2021) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2020.0188 · Cited by 32 · see citing works

Human pluripotent stem cell (hPSC) and organoid models of autism: opportunities and limitations

Kilpatrick, S., Irwin, C. L., & Singh, K. K. (2023) · Translational Psychiatry · doi:10.1038/s41398-023-02510-6 · Cited by 34 · see citing works

NMDA receptor hypofunction underlies deficits in parvalbumin interneurons and social behavior in neuroligin 3 R451C knockin mice

Cao, W., Li, J., Shen, L., Xia, Q.-Q., Du, Y.-L., Yang, Q., Ye, Y.-Z., Zeng, L., Li, X., Xu, J., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111771 · Cited by 31 · see citing works

Conditional Pten knockout in parvalbumin- or somatostatin-positive neurons sufficiently leads to autism-related behavioral phenotypes

Shin, S., Santi, A., & Huang, S. (2021) · Molecular Brain · doi:10.1186/s13041-021-00731-8 · Cited by 32 · see citing works

Optogenetic manipulation of astrocytes from synapses to neuronal networks: A potential therapeutic strategy for neurodegenerative diseases

Xie, Z., Yang, Q., Song, D. F., Quan, Z., & Qing, H. (2019) · Glia · doi:10.1002/glia.23693 · Cited by 29 · see citing works

Postinfectious Inflammation, Autoimmunity, and Obsessive-Compulsive Disorder: Sydenham Chorea, Pediatric Autoimmune Neuropsychiatric Disorder Associated with Streptococcal Infection, and Pediatric Acute-Onset Neuropsychiatric Disorder

Vreeland, A., Calaprice, D., Or‐Geva, N., Frye, R. E., Agalliu, D., Lachman, H. M., Pittenger, C., Pallanti, S., Williams, K., Ma, M., et al. (2023) · Developmental Neuroscience · doi:10.1159/000534261 · Cited by 28 · see citing works

Elevated antibody binding to striatal cholinergic interneurons in patients with pediatric acute-onset neuropsychiatric syndrome

Xu, J., Frankovich, J., Liu, R.-J., Thienemann, M., Silverman, M. A., Farhadian, B., Willett, T. A., Manko, C., Columbo, L. A., Leibold, C. M., et al. (2024) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2024.07.044 · Cited by 27 · see citing works

CellWalker integrates single-cell and bulk data to resolve regulatory elements across cell types in complex tissues

Przytycki, P. F., & Pollard, K. S. (2021) · Genome biology · doi:10.1186/s13059-021-02279-1 · Cited by 24 · see citing works

Impact of stress on inhibitory neuronal circuits, our tribute to Bruce McEwen

Pérez-Rando, M., Carceller, H., Castillo-Gómez, E., Bueno-Fernández, C., García-Mompó, C., Gilabert‐Juan, J., Guirado, R., Pesarico, A. P., & Nácher, J. (2022) · Neurobiology of Stress · doi:10.1016/j.ynstr.2022.100460 · Cited by 24 · see citing works

p140Cap Regulates GABAergic Synaptogenesis and Development of Hippocampal Inhibitory Circuits

Russo, I., Gavello, D., Menna, E., Vandael, D. H. F., Veglia, C., Morello, N., Corradini, I., Focchi, E., Alfieri, A., Angelini, C., et al. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx306 · Cited by 24 · see citing works

Developmental deficits of MGE-derived interneurons in the Cntnap2 knockout mouse model of autism spectrum disorder

Ahmed, N. Y., Knowles, R., Liu, L., Yan, Y., Li, X., Schümann, U., Wang, Y., Sontani, Y., Reynolds, N., Natoli, R., et al. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1112062 · Cited by 22 · see citing works

Human mutations in high-confidence Tourette disorder genes affect sensorimotor behavior, reward learning, and striatal dopamine in mice

Nasello, C., Poppi, L. A., Wu, J., Kowalski, T. F., Thackray, J. K., Wang, R., Persaud, A., Mahboob, M., Lin, S., Spaseska, R., et al. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2307156121 · Cited by 21 · see citing works

Gray matter abnormalities in Tourette Syndrome: a meta-analysis of voxel-based morphometry studies

Wan, X., Zhang, S., Wang, W., Su, X., Li, J., Yang, X., Tan, Q., Yue, Q., & Gong, Q. (2021) · Translational Psychiatry · doi:10.1038/s41398-021-01394-8 · Cited by 22 · see citing works

Lateralized Decrease of Parvalbumin+ Cells in the Somatosensory Cortex of ASD Models Is Correlated with Unilateral Tactile Hypersensitivity

Deemyad, T., Puig, S., Papale, A. E., Qi, H., LaRocca, G. M., Aravind, D., LaNoce, E., & Urban, N. N. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab233 · Cited by 20 · see citing works

Restoring prefrontal cortical excitation-inhibition balance with cannabidiol ameliorates neurobehavioral abnormalities in a mouse model of neurodevelopmental disorders

Zhang, L., Lin, C., Zhu, J., He, Y., Zhan, M., Xia, X., Yang, N., Yang, K., Wang, Y., Zhong, Z., et al. (2023) · Neuropharmacology · doi:10.1016/j.neuropharm.2023.109715 · Cited by 19 · see citing works

Vascular-derived SPARC and SerpinE1 regulate interneuron tangential migration and accelerate functional maturation of human stem cell-derived interneurons

Genestine, M., Ambriz, D., Crabtree, G. W., Dummer, P. D., Molotkova, A., Quintero, M., Mela, A., Biswas, S., Feng, H., Zhang, C., et al. (2021) · eLife · doi:10.7554/elife.56063 · Cited by 19 · see citing works

The role of neuroactive steroids in tic disorders

Branca, C., & Bortolato, M. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105637 · Cited by 20 · see citing works

Sex differences in the distribution and density of regulatory interneurons in the striatum

Zandt, M. A. V., Flanagan, D., & Pittenger, C. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1415015 · Cited by 17 · see citing works

Pediatric Acute-Onset Neuropsychiatric Syndrome (PANS) and Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal Infections (PANDAS): Immunological Features Underpinning Controversial Entities

Leonardi, L., Perna, C., Bernabei, I., Fiore, M., Ma, M., Frankovich, J., Tarani, L., & Spalice, A. (2024) · Children · doi:10.3390/children11091043 · Cited by 21 · see citing works

Gradient of Parvalbumin- and Somatostatin-Expressing Interneurons Across Cingulate Cortex Is Differentially Linked to Aggression and Sociability in BALB/cJ Mice

van Heukelum, S., Mogavero, F., van de Wal, M. A. E., Geers, F. E., França, A. S. C., Buitelaar, J. K., Beckmann, C. F., Glennon, J. C., & Havenith, M. N. (2019) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2019.00809 · Cited by 18 · see citing works

Disentangling Restrictive and Repetitive Behaviors and Social Impairments in Children and Adolescents with Gilles de la Tourette Syndrome and Autism Spectrum Disorder

Gulisano, M., Barone, R. M. E., Alaimo, S., Ferro, A., Pulvirenti, A., Cirnigliaro, L., di Silvestre, S., Martellino, S., Maugeri, N., Milana, M. C., et al. (2020) · Brain Sciences · doi:10.3390/brainsci10050308 · Cited by 18 · see citing works

Input-specific control of interneuron numbers in nascent striatal networks

Sreenivasan, V., Serafeimidou‐Pouliou, E., Exposito-Alonso, D., Bercsényi, K., Bernard, C., Bae, S., Oozeer, F., Hanusz-Godoy, A., Edwards, R. H., & Marín, Ó. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2118430119 · Cited by 16 · see citing works

A feasibility study for somatomotor cortical mapping in Tourette syndrome using neuronavigated transcranial magnetic stimulation

Sigurdsson, H. P., Jackson, S. R., Kim, S., Dyke, K., & Jackson, G. M. (2020) · Cortex · doi:10.1016/j.cortex.2020.04.014 · Cited by 14 · see citing works

Sensory phenomena in children with Tourette syndrome or autism spectrum disorder

Prato, A., Saia, F., Ferrigno, M., Finocchiaro, V., Barone, R. M. E., & Rizzo, R. (2024) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2024.1338234 · Cited by 12 · see citing works

Adult-specific Reelin expression alters striatal neuronal organization: implications for neuropsychiatric disorders

Pardo, M., Gregorio, S., Montalban, E., Pujadas, L., Elias-Tersa, A., Masachs, N., Vílchez-Acosta, A., Parent, A., Auladell, C., Girault, J., et al. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1143319 · Cited by 12 · see citing works

Incidence of Autism Spectrum Disorder in Youths Affected by Gilles de la Tourette Syndrome Based on Data from a Large Single Italian Clinical Cohort

Gulisano, M., Barone, R. M. E., Mosa, M. R., Milana, M. C., Saia, F., Scerbo, M., & Rizzo, R. (2020) · Brain Sciences · doi:10.3390/brainsci10110812 · Cited by 9 · see citing works

Targeted Tshz3 deletion in corticostriatal circuit components segregates core autistic behaviors

Caubit, X., Gubellini, P., Roubertoux, P. L., Carlier, M., Molitor, J., Chabbert, D., Metwaly, M., Salin, P., Fatmi, A., Belaïdouni, Y., et al. (2022) · Translational Psychiatry · doi:10.1038/s41398-022-01865-6 · Cited by 10 · see citing works

Cntnap2 loss drives striatal neuron hyperexcitability and behavioral inflexibility

Cording, K. R., Tu, E. M., Wang, H., Agopyan-Miu, A. H. C. W., & Bateup, H. S. (2025) · eLife · doi:10.1101/2024.05.09.593387 · Cited by 8 · see citing works

Identifying foetal forebrain interneurons as a target for monogenic autism risk factors and the polygenic 16p11.2 microdeletion

Yang, Y., Booker, S. A., Clegg, J. M., Urzainqui, I. Q., Sumera, A., Kozić, Z., Dando, O., Lorenzo, S. M., Hérault, Y., Kind, P. C., et al. (2023) · BMC Neuroscience · doi:10.1186/s12868-022-00771-3 · Cited by 7 · see citing works

Decreased density of cholinergic interneurons in striatal territories in Williams syndrome

Hanson, K. L., Lew, C. H., Hrvoj-Mihić, B., Cuevas, D., Greiner, D. M. Z., Groeniger, K. M., Edler, M. K., Halgren, E., Bellugi, U., Raghanti, M. A., et al. (2020) · Brain Structure and Function · doi:10.1007/s00429-020-02055-0 · Cited by 8 · see citing works

Striatal parvalbumin interneurons are activated in a mouse model of cerebellar dystonia

Matsuda, T., Morigaki, R., Hayasawa, H., Koyama, H., Oda, T., Miyake, K., & Takagi, Y. (2024) · Disease Models & Mechanisms · doi:10.1242/dmm.050338 · Cited by 7 · see citing works

Striatal Interneuron Imbalance in a Valproic Acid-Induced Model of Autism in Rodents Is Accompanied by Atypical Somatosensory Processing

Ibáñez-Sandoval, D. N., Hidalgo-Balbuena, A. E., Contreras, R. V., Saderi, N., Flores, G., Rueda‐Orozco, P. E., & Ibáñez-Sandoval, O. (2024) · eNeuro · doi:10.1523/eneuro.0326-24.2024 · Cited by 8 · see citing works

Syntax and the brain: language evolution as the missing link(ing theory)?

Benítez‐Burraco, A., & Progovac, L. (2024) · Frontiers in Psychology · doi:10.3389/fpsyg.2024.1445192 · Cited by 9 · see citing works

Planar cell polarity and the pathogenesis of Tourette Disorder: New hypotheses and perspectives

Wu, J., Poppi, L. A., & Tischfield, M. A. (2022) · Developmental Biology · doi:10.1016/j.ydbio.2022.05.017 · Cited by 6 · see citing works

GM1 Reduced the Symptoms of Autism Spectrum Disorder by Suppressing α-Syn Through Activating Autophagy

Yin, B.-Q., Li, H., Zhao, P., Zhao, Y.-H., Zheng, R., Feng, P., Xu, C., Li, E., & Li, L. (2023) · Journal of Molecular Neuroscience · doi:10.1007/s12031-023-02110-5 · Cited by 5 · see citing works

A Process-Oriented View of Procedural Memory Can Help Better Understand Tourette’s Syndrome

Farkas, B. C., Tóth-Fáber, E., Janacsek, K., & Németh, D. (2021) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2021.683885 · Cited by 5 · see citing works

CellWalker integrates single-cell and bulk data to resolve regulatory elements across cell types in complex tissuesPreprint

Przytycki, P. F., & Pollard, K. S. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/847657 · Cited by 5 · see citing works

Non-monotonic effects of GABAergic synaptic inputs on neuronal firing

Zadeh, A. A., Turner, B. D., Calakos, N., & Brunel, N. (2022) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1010226 · Cited by 4 · see citing works

Elevated expression of endogenous glial cell line‐derived neurotrophic factor impairs spatial memory performance and raises inhibitory tone in the hippocampus

Marshall, P., Garton, D. R., Taira, T., Võikar, V., Vilenius, C., Kulesskaya, N., Rivera, C., & Andressoo, J. (2021) · European Journal of Neuroscience · doi:10.1111/ejn.15126 · Cited by 4 · see citing works

Syntax and the brain: Language evolution is the missing link(ing theory)Preprint

Benítez‐Burraco, A., & Progovac, L. (2022) · doi:10.31234/osf.io/nfqvs · Cited by 4 · see citing works

Cntnap2 loss drives striatal neuron hyperexcitability and behavioral inflexibilityPreprint

Cording, K. R., Tu, E. M., Wang, H., Agopyan-Miu, A. H. C. W., & Bateup, H. S. (2024) · eLife · doi:10.7554/elife.100162 · Cited by 4 · see citing works

Maternal immunoglobulins are distributed in the offspring’s brain to support the maintenance of cortical interneurons in the postnatal period

Morimoto, K., Takahashi, R., Takahashi, G., Miyajima, M., & Nakajima, K. (2024) · Inflammation and Regeneration · doi:10.1186/s41232-024-00336-3 · Cited by 4 · see citing works

Tourette Syndrome: An Update

Ghosh, D., & Ghosh, D. (2024) · Journal of Modern Medicine · doi:10.4103/jomm.jomm_10_24 · Cited by 3 · see citing works

Neuropsychiatric symptoms in siblings of children with Tourette syndrome in the EMTICS study

Sidiropoulou, O., Glaus, J., Hagstrøm, J., Ranjbar, S., Rizzo, R., EMTICS collaborative group, Hoekstra, P. J., Dietrich, A., & Plessen, K. J. (2024) · JCPP Advances · doi:10.1002/jcv2.12277 · Cited by 2 · see citing works

Rigidity in Autism Spectrum Disorder (ASD): A Unified (Evolutionary) Account of Salient Linguistic and Non-Linguistic Characteristics

Progovac, L., & Benítez‐Burraco, A. (2025) · Autism & Developmental Language Impairments · doi:10.1177/23969415251379995 · Cited by 4 · see citing works

Reduced axon caliber in the associative striatum of the Sapap3 knockout mousePreprint

Lousada, E. L. R. D. S., Boudreau, M., Cohen‐Adad, J., Nait‐Oumesmar, B., Burguière, E., & Schreiweis, C. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.01.12.426339 · Cited by 2 · see citing works

Altered striosome-matrix distribution and activity of striatal cholinergic interneurons in a model of autism-linked repetitive behaviors

Molitor, J., Graniou, J., Salin, P., Castets, F., Fatmi, A., Goff, L. K., Fasano, L., Caubit, X., & Gubellini, P. (2025) · Molecular Psychiatry · doi:10.1038/s41380-025-03208-5 · Cited by 1 · see citing works

Neuromodulation for Tourette syndrome: current techniques and future perspectives

Haslam, S., Johnson, K. A., Anderson, D., Mahant, N., & Anderson, C. J. (2025) · Journal of Neural Engineering · doi:10.1088/1741-2552/ae1257 · Cited by 1 · see citing works

A Celsr3 Mutation Linked to Tourette Disorder Disrupts Cortical Dendritic Patterning and Striatal Cholinergic Interneuron Excitability

Nasello, C., Yilmaz, G. D., Poppi, L. A., Kowalski, T. F., Ho-Nguyen, K.-T., Wu, J., Matrongolo, M. J., Thackray, J. K., Shi, A., Carayannopoulos, N. L., et al. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262110307 · Cited by 1 · see citing works

A cadherin mutation in Celsr3 linked to Tourette Disorder affects dendritic patterning and excitability of cholinergic interneuronsPreprint

Poppi, L. A., Ho-Nguyen, K.-T., Wu, J., Matrongolo, M. J., Thackray, J. K., Nasello, C., Shi, A., Ricci, M. R., Carayannopoulos, N. L., Cheedalla, N., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.03.06.483205 · Cited by 1 · see citing works

Rigidity in autism spectrum disorder (ASD): A unified (evolutionary) account of linguistic and non-linguistic symptomsPreprint

Benítez‐Burraco, A., & Progovac, L. (2023) · doi:10.31234/osf.io/euq5k · Cited by 1 · see citing works

Cntnap2 loss drives striatal neuron hyperexcitability and behavioral inflexibilityPreprint

Cording, K. R., Tu, E. M., Wang, H., Agopyan-Miu, A. H. C. W., & Bateup, H. S. (2025) · eLife · doi:10.7554/elife.100162.2 · Cited by 1 · see citing works

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 · see citing works

Identifying developing interneurons as a potential target for multiple genetic autism risk factors in human and rodent forebrainPreprint

Yang, Y., Booker, S. A., Clegg, J. M., Urzainqui, I. Q., Sumera, A., Kozić, Z., Dando, O., Lorenzo, S. M., Hérault, Y., Kind, P. C., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.06.03.446920

Therapeutic Proposal of the Oral Manifestations of the Tourette Syndrome. A Case Report

Lorduy, M. C. C., Marrugo, S. P., & Tobón, T. R. (2022) · Salud Uninorte · doi:10.14482/sun.37.1.616.83

Other Psychiatric Comorbidities in Tourette Syndrome

Cath, D. C., Müller‐Vahl, K., & Mathews, C. A. (2022) · Oxford University Press eBooks · doi:10.1093/med/9780197543214.003.0005

Gilles de la Tourette Syndrome

Ghosh, D., & Ghosh, D. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-95702-1.00145-7

A Refined Approach to Isolate Interneurons for High-Validity Epigenetic Studies in Human Brain Tissue

Cariaga-Martínez, A. E., Gutiérrez, K. J., Regidor, I., del Álamo, M., Sáiz-Ruiz, J., & Alelú‐Paz, R. (2025) · Methods and Protocols · doi:10.3390/mps8030061

Additional file 1 of Identifying foetal forebrain interneurons as a target for monogenic autism risk factors and the polygenic 16p11.2 microdeletion

Yang, Y., Booker, S. A., Clegg, J. M., Urzainqui, I. Q., Sumera, A., Kozić, Z., Dando, O., Lorenzo, S. M., Hérault, Y., Kind, P. C., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26562655

Additional file 3 of Maternal immunoglobulins are distributed in the offspring’s brain to support the maintenance of cortical interneurons in the postnatal period

Morimoto, K., Takahashi, R., Takahashi, G., Miyajima, M., & Nakajima, K. (2024) · Figshare · doi:10.6084/m9.figshare.26721066

Additional file 4 of Maternal immunoglobulins are distributed in the offspring’s brain to support the maintenance of cortical interneurons in the postnatal period

Morimoto, K., Takahashi, R., Takahashi, G., Miyajima, M., & Nakajima, K. (2024) · Figshare · doi:10.6084/m9.figshare.26721069

Additional file 1 of CellWalker integrates single-cell and bulk data to resolve regulatory elements across cell types in complex tissues

Przytycki, P. F., & Pollard, K. S. (2021) · Figshare · doi:10.6084/m9.figshare.14033650

Additional file 1 of Conditional Pten knockout in parvalbumin- or somatostatin-positive neurons sufficiently leads to autism-related behavioral phenotypes

Shin, S., Santi, A., & Huang, S. (2021) · Figshare · doi:10.6084/m9.figshare.13655281

Additional file 3 of CellWalker integrates single-cell and bulk data to resolve regulatory elements across cell types in complex tissues

Przytycki, P. F., & Pollard, K. S. (2021) · Figshare · doi:10.6084/m9.figshare.14033656

Additional file 2 of Maternal immunoglobulins are distributed in the offspring’s brain to support the maintenance of cortical interneurons in the postnatal period

Morimoto, K., Takahashi, R., Takahashi, G., Miyajima, M., & Nakajima, K. (2024) · Figshare · doi:10.6084/m9.figshare.26721063

Additional file 5 of Maternal immunoglobulins are distributed in the offspring’s brain to support the maintenance of cortical interneurons in the postnatal period

Morimoto, K., Takahashi, R., Takahashi, G., Miyajima, M., & Nakajima, K. (2024) · Figshare · doi:10.6084/m9.figshare.26721072

Additional file 1 of Maternal immunoglobulins are distributed in the offspring’s brain to support the maintenance of cortical interneurons in the postnatal period

Morimoto, K., Takahashi, R., Takahashi, G., Miyajima, M., & Nakajima, K. (2024) · Figshare · doi:10.6084/m9.figshare.26721060

Conséquences de la délétion conditionnelle du gène Tshz3 dans la circuiterie cortico-striée : implications dans les troubles du spectre autistique

Chabbert, D. (2017) · theses.fr (ABES) · doi:10.70675/6ac224e2z22c7z4bd4zb6dazc3f301e5b758

Combining a real-time closed-loop system with neuromodulation : an integrative approach to prevent pathological repetitive behaviors

Mondragón-González, S. L. (2019) · doi:10.70675/e78705daz18a9z4695zac41zadeb07ee7c37

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

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

Etude de la contribution de l'hormone adipocytaire leptine dans la pathogenèse du syndrome de Rett

Belaïdouni, Y. (2022) · theses.fr (ABES) · doi:10.70675/f69d2875zfa9fz4465z917eza8e7b93935c6

Dysfonctionnement des interneurones cholinergiques du striatum comme substrat neuronal dans les troubles du spectre autistique en lien avec la délétion du gène Tshz3

Molitor, J. (2022) · doi:10.70675/ab255e16z655ez4821za484z23598ff51ed1

Therapeutic approaches in Tourette syndrome: From behavioral therapy to deep brain stimulation

Gündüz, H., & Erbaş, O. (2024) · Demiroglu Science University Florence Nightingale Journal of Medicine · doi:10.5606/fng.btd.2024.164

Identification of Potential Biomarkers in Autism: PRELID2, MYO1B, LRCH2, LIFR, and RERG May Serve as Regulators in Synaptic Membrane-Integrating Interneurons

Zhang, W., Wang, C., Zhao, X. X., Pang, S., Zhao, Z., Zhang, G., & Chen, J. (1970) · Current Gene Therapy · doi:10.2174/0115665232499854260512155018

16p11.2 microdeletion enhances gene expression variability between human IPSC-derived forebrain interneuron progenitor cells in culture

Yang, Y., Urzainqui, I. Q., & Pratt, T. (2026) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2026.1872405

Neurophytopharmacology in Depression: Emerging Antidepressant Potential of Medicinal Plants from Experimental Animal Models

Khutwad, D. D., Otari, K. V., & Kale, A. Y. (2026) · Biosciences Biotechnology Research Asia · doi:10.13005/bbra/3519

Tutorial: interrogating biology using organoid technologies

Bugter, J. M., Schafer, S. T., & Rad, R. (2026) · Nature Protocols · doi:10.1038/s41596-026-01447-6

Tourette syndrome

Eapen, V., Singer, H. S., Mathews, C. A., Martino, D., Vermilion, J. A., Cavanna, A. E., & Paschou, P. (2026) · Nature Reviews Disease Primers · doi:10.1038/s41572-026-00742-6

Cortical interneurons in autism

Contractor, A., Ethell, I. M., & Portera‐Cailliau, C. (2021) · Nature Neuroscience · doi:10.1038/s41593-021-00967-6 · Cited by 180 · see citing works

Cortical interneuron function in autism spectrum condition

Lunden, J. W., Durens, M., Phillips, A. W., & Nestor, M. W. (2018) · Pediatric Research · doi:10.1038/s41390-018-0214-6 · Cited by 52 · see citing works

Interneuron Dysfunction in Syndromic Autism: Recent Advances

Takano, T. (2015) · Developmental Neuroscience · doi:10.1159/000434638 · Cited by 38 · see citing works

Interneuron dysfunction in psychiatric disorders

Marín, O. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3155 · Cited by 1,190 · see citing works

Interneuron development and dysfunction

Yang, J., Yang, X. W., & Tang, K. (2021) · FEBS Journal · doi:10.1111/febs.15872 · Cited by 52 · see citing works