Impaired TrkB Receptor Signaling Underlies Corticostriatal Dysfunction in Huntington’s Disease von Plotkin, Joshua L., Day, Michelle, Peterson, Jayms D., Xie, Zhong, Kress, Geraldine J., Rafalovich, Igor, Kondapalli, Jyothisri, Gertler, Tracy S., Flajolet, Marc, Greengard, Paul, Stavarache, Mihaela, Kaplitt, Michael G., Rosinski, Jim, Chan, C. Savio, Surmeier, D. James

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Dichotomous Anatomical Properties of Adult Striatal Medium Spiny Neurons von Gertler, Tracy S, Chan, C. Savio, Surmeier, D. James

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Cell type-specific plasticity of striatal projection neurons in parkinsonism and L-DOPA-induced dyskinesia von Fieblinger, Tim, Graves, Steven M., Sebel, Luke E., Alcacer, Cristina, Plotkin, Joshua L., Gertler, Tracy S., Chan, C. Savio, Heiman, Myriam, Greengard, Paul, Cenci, M. Angela, Surmeier, D. James

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KNa1.1 gain-of-function preferentially dampens excitability of murine parvalbumin-positive interneurons von Gertler, Tracy S., Cherian, Suraj, DeKeyser, Jean-Marc, Kearney, Jennifer A., George, Alfred L.

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Control of Cognition and Adaptive Behavior by the GLP/G9a Epigenetic Suppressor Complex von Schaefer, Anne, Sampath, Srihari C., Intrator, Adam, Min, Alice, Gertler, Tracy S., Surmeier, D. James, Tarakhovsky, Alexander, Greengard, Paul

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Bringing nutritional ketosis to the table as an option for healing the pediatric brain von Gertler, Tracy S, Blackford, Robyn

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HCN channelopathy in external globus pallidus neurons in models of Parkinson's disease von Surmeier, D James, Chan, C Savio, Glajch, Kelly E, Gertler, Tracy S, Guzman, Jaime N, Mercer, Jeff N, Lewis, Alan S, Goldberg, Alan B, Tkatch, Tatiana, Shigemoto, Ryuichi, Fleming, Sheila M, Chetkovich, Dane M, Osten, Pavel, Kita, Hitoshi

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Screening of conventional anticonvulsants in a genetic mouse model of epilepsy von Hawkins, Nicole A., Anderson, Lyndsey L., Gertler, Tracy S., Laux, Linda, George, Alfred L., Kearney, Jennifer A.

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A single-center, retrospective analysis of genotype-phenotype correlations in children with Dravet syndrome von Gertler, Tracy S., Calhoun, Jeffrey, Laux, Linda

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Functional consequences of a KCNT1 variant associated with status dystonicus and early‐onset infantile encephalopathy von Gertler, Tracy S., Thompson, Christopher H., Vanoye, Carlos G., Millichap, John J., George, Alfred L.

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Corrigendum to “A single-center, retrospective analysis of genotype–phenotype correlations in children with Dravet syndrome” [Seizure: Eur. J. Epilepsy 75 (2020) 1–6] von Gertler, Tracy S., Calhoun, Jeffrey, Laux, Linda

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Calcium homeostasis, selective vulnerability and Parkinson's disease von Chan, C. Savio, Gertler, Tracy S, Surmeier, D. James

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Treatment Responsiveness in KCNT1-Related Epilepsy von Fitzgerald, Mark P., Fiannacca, Martina, Smith, Douglas M., Gertler, Tracy S., Gunning, Boudewijn, Syrbe, Steffen, Verbeek, Nienke, Stamberger, Hannah, Weckhuysen, Sarah, Ceulemans, Berten, Schoonjans, An-Sofie, Rossi, Massimiliano, Demarquay, Geneviève, Lesca, Gaetan, Olofsson, Kern, Koolen, D. A., Hornemann, Frauke, Baulac, Stephanie, Rubboli, Guido, Minks, Kelly Q., Lee, Bohoon, Helbig, Ingo, Dlugos, Dennis, Møller, Rikke S., Bearden, David

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Loss-of-function variants in TIAM1 are associated with developmental delay, intellectual disability, and seizures von Lu, Shenzhao, Hernan, Rebecca, Marcogliese, Paul C., Huang, Yan, Gertler, Tracy S., Akcaboy, Meltem, Liu, Shiyong, Chung, Hyung-lok, Pan, Xueyang, Sun, Xiaoqin, Oguz, Melahat Melek, Oztoprak, Ulkühan, de Baaij, Jeroen H.F., Ivanisevic, Jelena, McGinnis, Erin, Guillen Sacoto, Maria J., Chung, Wendy K., Bellen, Hugo J.

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Pearls & Oy-sters: When Genetic Generalized Epilepsy Becomes Progressive von Purushothaman, Priya, McGinnis, Erin M., Aldulescu, Monica, Stack, Cynthia V., Gertler, Tracy S.

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Visual Processing in Infants with Tuberous Sclerosis Complex von Gertler, Tracy S, Nangia, Srishti

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Imaging of Glutamate Concentration in Sturge-Weber Syndrome von Gertler, Tracy S, Stack, Cynthia V

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Excitatory Dysfunction Drives Network and Calcium Handling Deficits in 16p11.2 Duplication Schizophrenia Induced Pluripotent Stem Cell–Derived Neurons von Parnell, Euan, Culotta, Lorenza, Forrest, Marc P., Jalloul, Hiba A., Eckman, Blair L., Loizzo, Daniel D., Horan, Katherine K.E., Dos Santos, Marc, Piguel, Nicolas H., Tai, Derek J.C., Zhang, Hanwen, Gertler, Tracy S., Simkin, Dina, Sanders, Alan R., Talkowski, Michael E., Gejman, Pablo V., Kiskinis, Evangelos, Duan, Jubao, Penzes, Peter

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A molecular basis for the increased vulnerability of substantia nigra dopamine neurons in aging and Parkinson's disease von Chan, C. Savio, Gertler, Tracy S., Surmeier, D. James

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Monoallelic and biallelic mutations in RELN underlie a graded series of neurodevelopmental disorders von Di Donato, Nataliya, Guerrini, Renzo, Billington, Charles J, Barkovich, A James, Dinkel, Philine, Freri, Elena, Heide, Michael, Gershon, Elliot S, Gertler, Tracy S, Hopkin, Robert J, Jacob, Suma, Keedy, Sarah K, Kooshavar, Daniz, Lockhart, Paul J, Lohmann, Dietmar R, Mahmoud, Iman G, Parrini, Elena, Schrock, Evelin, Severi, Giulia, Timms, Andrew E, Webster, Richard I, Willis, Mary J H, Zaki, Maha S, Gleeson, Joseph G, Leventer, Richard J, Dobyns, William B

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