Ethan M. Goldberg, M.D., Ph.D.

faculty photo
Assistant Professor of Neurology
Department: Neurology
Graduate Group Affiliations

Contact information
The Children's Hospital of Philadelphia
Division of Neurology
Abramson Research Center, Room 516G
3615 Civic Center Boulevard
Philadelphia, PA 19104
Office: 215-590-6894
Fax: 215-590-1771
Lab: 215-590-5671
Education:
B.A. (Neurobiology)
Harvard University, 1999.
Ph.D. (Physiology & Neuroscience)
New York University School of Medicine, 2006.
M.D.
New York University School of Medicine, 2008.
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Description of Clinical Expertise

Pediatric Neurology; Neurology; Epilepsy; Neurogenetics; Epiepsy Neurogenetics; Developmental Delay and Autism.

Description of Research Expertise

Epilepsy; Neurobiology of Disease; Physiology; Ion channels; Two-photon imaging.

Selected Publications

Platzer Konrad, Yuan Hongjie, Schütz Hannah, Winschel Alexander, Chen Wenjuan, Hu Chun, Kusumoto Hirofumi, Heyne Henrike O, Helbig Katherine L, Tang Sha, Willing Marcia C, Tinkle Brad T, Adams Darius J, Depienne Christel, Keren Boris, Mignot Cyril, Frengen Eirik, Strømme Petter, Biskup Saskia, Döcker Dennis, Strom Tim M, Mefford Heather C, Myers Candace T, Muir Alison M, LaCroix Amy, Sadleir Lynette, Scheffer Ingrid E, Brilstra Eva, van Haelst Mieke M, van der Smagt Jasper J, Bok Levinus A, Møller Rikke S, Jensen Uffe B, Millichap John J, Berg Anne T, Goldberg Ethan M, De Bie Isabelle, Fox Stephanie, Major Philippe, Jones Julie R, Zackai Elaine H, Abou Jamra Rami, Rolfs Arndt, Leventer Richard J, Lawson John A, Roscioli Tony, Jansen Floor E, Ranza Emmanuelle, Korff Christian M, Lehesjoki Anna-Elina, Courage Carolina, Linnankivi Tarja, Smith Douglas R, Stanley Christine, Mintz Mark, McKnight Dianalee, Decker Amy, Tan Wen-Hann, Tarnopolsky Mark A, Brady Lauren I, Wolff Markus, Dondit Lutz, Pedro Helio F, Parisotto Sarah E, Jones Kelly L, Patel Anup D, Franz David N, Vanzo Rena, Marco Elysa, Ranells Judith D, Di Donato Nataliya, Dobyns William B, Laube Bodo, Traynelis Stephen F, Lemke Johannes R: GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects. Journal of medical genetics 54(7): 460-470, Jul 2017.

Shen Dingding, Hernandez Ciria C, Shen Wangzhen, Hu Ningning, Poduri Annapurna, Shiedley Beth, Rotenberg Alex, Datta Alexandre N, Leiz Steffen, Patzer Steffi, Boor Rainer, Ramsey Kerri, Goldberg Ethan, Helbig Ingo, Ortiz-Gonzalez Xilma R, Lemke Johannes R, Marsh Eric D, Macdonald Robert L: De novo GABRG2 mutations associated with epileptic encephalopathies. Brain : a journal of neurology 140(Pt 1): 49-67, Jan 2017.

Tian Guoling, Cristancho Ana G, Dubbs Holly A, Liu Grant T, Cowan Nicholas J, Goldberg Ethan M: A patient with lissencephaly, developmental delay, and infantile spasms, due to de novo heterozygous mutation of KIF2A. Molecular genetics & genomic medicine 4(6): 599-603, Nov 2016.

Natan, R.G., Briguglio, J.J., Mwilambwe-Tshilobo, L., Jones, S., Aizenberg, M., Goldberg, E.M., Geffen, M.N.: Complementary control of sensory adaptation by two types of cortical interneurons. eLife 4: e09868, November 2015.

Tyson Jennifer A, Goldberg Ethan M, Maroof Asif M, Xu Qing, Petros Timothy J, Anderson Stewart A: Duration of culture and sonic hedgehog signaling differentially specify PV versus SST cortical interneuron fates from embryonic stem cells. Development (Cambridge, England) 142(7): 1267-78, Apr 2015.

Goldberg E.M., Zhou J., Yue C., Wang P.J., Coulter D.A.: A novel mouse model of chromosome Xq22.1 deletion syndrome displays epilepsy and cortical circuit dysfunction. Platform Session C.06 at American Epilepsy Society 68th Annual Meeting in Seattle, WA. December 2014.

Goldberg Ethan M, Coulter Douglas A: Seizing the opportunity: stem cells take on epilepsy. Cell stem cell 15(5): 527-8, Nov 2014.

Bearden David, Strong Alanna, Ehnot Jessica, DiGiovine Marissa, Dlugos Dennis, Goldberg Ethan M: Targeted treatment of migrating partial seizures of infancy with quinidine. Annals of neurology 76(3): 457-61, Sep 2014.

Zhou Jian, Goldberg EM, Leu NA, Zhou L, Coulter DA, Wang PJ.: Respiratory failure, cleft palate and epilepsy in the mouse model of human Xq22.1 deletion syndrome. Hum Mol Genet 23(14): 3823-29, July 2014.

Lang Shih-Shan, Goldberg Ethan, Zarnow Deborah, Johnson Mark P, Storm Phillip B, Heuer Gregory G: Prenatal diagnosis of hemimegalencephaly. World neurosurgery 82(1-2): 241.e5-8, Jul-Aug 2014.

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Last updated: 07/03/2017
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