Goldberg, Ethan M.
Children's Hospital of Philadelphia
10 papers on CoChatORCID 0000-0002-7404-735X
Most cited papers
- Verified
Mechanisms of epileptogenesis: a convergence on neural circuit dysfunction
Goldberg, E. M., & Coulter, D. A. (2013) · Nature Reviews Neuroscience
Epilepsy research and treatmentNeuroscience and Neuropharmacology Research
Cited by 542
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Sliced Human Cortical Organoids for Modeling Distinct Cortical Layer Formation
Qian, X., Su, Y., Adam, C. D., Deutschmann, A. U., Pather, S. R., Goldberg, E. M., Su, K., Li, S., Lu, L., Jacob, F., et al. (2020) · Cell Stem Cell
Neurogenesis and neuroplasticity mechanismsPluripotent Stem Cells Research
Cited by 479
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K+ Channels at the Axon Initial Segment Dampen Near-Threshold Excitability of Neocortical Fast-Spiking GABAergic Interneurons
Goldberg, E. M., Clark, B. D., Zagha, E., Nahmani, M., Erisir, A., & Rudy, B. (2008) · Neuron
Ion channel regulation and functionNeuroscience and Neuropharmacology Research
Cited by 271
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A Transient Developmental Window of Fast-Spiking Interneuron Dysfunction in a Mouse Model of Dravet Syndrome
Favero, M., Sotuyo, N. P., Lopez, E., Kearney, J. A., & Goldberg, E. M. (2018) · The Journal of Neuroscience
Epilepsy research and treatmentIon channel regulation and function
Cited by 163
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Genotype-phenotype correlations in SCN8A -related disorders reveal prognostic and therapeutic implications
Johannesen, K. M., Liu, Y., Koko, M., Gjerulfsen, C. E., Sonnenberg, L., Schubert, J., Fenger, C. D., Eltokhi, A., Rannap, M., Koch, N. A., et al. (2022) · Brain
Epilepsy research and treatmentIon channel regulation and function
Cited by 147
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Mutations in SCN3A cause early infantile epileptic encephalopathy
Zaman, T., Helbig, I., Božović, I. B., DeBrosse, S. D., Bergqvist, A. C., Wallis, K., Medne, L., Maver, A., Peterlin, B., Helbig, K. L., et al. (2018) · Annals of Neurology
Epilepsy research and treatmentIon channel regulation and function
Cited by 102
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SCN3A‐Related Neurodevelopmental Disorder: A Spectrum of Epilepsy and Brain Malformation
Zaman, T., Helbig, K. L., Clatot, J., Thompson, C. H., Kang, S. K., Stouffs, K., Jansen, A. E., Verstraete, L., Jacquinet, A., Parrini, E., et al. (2020) · Annals of Neurology
Epilepsy research and treatmentIon channel regulation and function
Cited by 94
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Vasoactive intestinal peptide-expressing interneurons are impaired in a mouse model of Dravet syndrome
Goff, K. M., & Goldberg, E. M. (2019) · eLife
Epilepsy research and treatmentIon channel regulation and function
Cited by 93
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Developmentally regulated impairment of parvalbumin interneuron synaptic transmission in an experimental model of Dravet syndrome
Kaneko, K., Currin, C. B., Goff, K. M., Wengert, E. R., Somarowthu, A., Vogels, T. P., & Goldberg, E. M. (2022) · Cell Reports
Epilepsy research and treatmentIon channel regulation and function
Cited by 72
- Verified
Variants in GNAI1 cause a syndrome associated with variable features including developmental delay, seizures, and hypotonia
Muir, A. M., Gardner, J. F., van Jaarsveld, R. H., de Lange, I. M., van der Smagt, J. J., Wilson, G. N., Dubbs, H., Goldberg, E. M., Zitano, L., Bupp, C., et al. (2021) · Genetics in Medicine
Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases
Cited by 35
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