Ethan M Goldberg (Evan C Rosenberg, Ethan Goldberg)

Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 37

Top Venues

Epilepsy currents

Proceedings of the National Academy of Sciences of the United States of America

The Journal of neuroscience : the official journal of the Society for Neuroscience

Annals of neurology

University of Pennsylvania Perelman School of Medicine

NYU Langone Medical Center (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of Pennsylvania Perelman School of Medicine Jul 01 2015

United States

Assistant Professor :: Neurology

Education History

NYU Langone Medical Center

United States

PHD :: Physiology & Neuroscience

Publications

Jérôme Clatot, Ethan M Goldberg
No Pain, No Gain of Function: Epilepsy-Associated Variants in SCN2A Defy Classification. Epilepsy currents 24 (2) (2024)
Jerome Clatot, Christopher B Currin, Qiansheng Liang, Tanadet Pipatpolkai, Shavonne L Massey, Ingo Helbig, Lucie Delemotte, Tim P Vogels, Manuel Covarrubias, Ethan M Goldberg
A structurally precise mechanism links an epilepsy-associated KCNC2 potassium channel mutation to interneuron dysfunction. Proceedings of the National Academy of Sciences of the United States of America 121 (3) (2024)
Sophie R Liebergall, Ethan M Goldberg
Ndnf Interneuron Excitability Is Spared in a Mouse Model of Dravet Syndrome. The Journal of neuroscience : the official journal of the Society for Neuroscience 44 (17) (2024)
Jerome Clatot, Christopher B Currin, Qiansheng Liang, Tanadet Pipatpolkai, Shavonne L Massey, Ingo Helbig, Lucie Delemotte, Tim P Vogels, Manuel Covarrubias, Ethan M Goldberg
A structurally precise mechanism links an epilepsy-associated KCNC2 potassium channel mutation to interneuron dysfunction. Proceedings of the National Academy of Sciences of the United States of America 121 (3) (2024)
Ania K Dabrowski, Ethan M Goldberg
A Human Touch: Hominid-Specific LRRC37B Regulates Axon Initial Segment Excitability. Epilepsy currents 24 (4) (2024)
Jerome Clatot, Christopher B Currin, Qiansheng Liang, Tanadet Pipatpolkai, Shavonne L Massey, Ingo Helbig, Lucie Delemotte, Tim P Vogels, Manuel Covarrubias, Ethan M Goldberg
A structurally precise mechanism links an epilepsy-associated KCNC2 potassium channel mutation to interneuron dysfunction. Proceedings of the National Academy of Sciences of the United States of America 121 (3) (2024)
Jerome Clatot, Christopher B Currin, Qiansheng Liang, Tanadet Pipatpolkai, Shavonne L Massey, Ingo Helbig, Lucie Delemotte, Tim P Vogels, Manuel Covarrubias, Ethan M Goldberg
A structurally precise mechanism links an epilepsy-associated KCNC2 potassium channel mutation to interneuron dysfunction. Proceedings of the National Academy of Sciences of the United States of America 121 (3) (2024)
Sophie R Liebergall, Ethan M Goldberg
Ndnf Interneuron Excitability Is Spared in a Mouse Model of Dravet Syndrome. The Journal of neuroscience : the official journal of the Society for Neuroscience 44 (17) (2024)
Jerome Clatot, Christopher B Currin, Qiansheng Liang, Tanadet Pipatpolkai, Shavonne L Massey, Ingo Helbig, Lucie Delemotte, Tim P Vogels, Manuel Covarrubias, Ethan M Goldberg
A structurally precise mechanism links an epilepsy-associated KCNC2 potassium channel mutation to interneuron dysfunction. Proceedings of the National Academy of Sciences of the United States of America 121 (3) (2024)
Jerome Clatot, Christopher B Currin, Qiansheng Liang, Tanadet Pipatpolkai, Shavonne L Massey, Ingo Helbig, Lucie Delemotte, Tim P Vogels, Manuel Covarrubias, Ethan M Goldberg
A structurally precise mechanism links an epilepsy-associated KCNC2 potassium channel mutation to interneuron dysfunction. Proceedings of the National Academy of Sciences of the United States of America 121 (3) (2024)
Jerome Clatot, Christopher B Currin, Qiansheng Liang, Tanadet Pipatpolkai, Shavonne L Massey, Ingo Helbig, Lucie Delemotte, Tim P Vogels, Manuel Covarrubias, Ethan M Goldberg
A structurally precise mechanism links an epilepsy-associated KCNC2 potassium channel mutation to interneuron dysfunction. Proceedings of the National Academy of Sciences of the United States of America 121 (3) (2024)
Sophie R Liebergall, Ethan M Goldberg
Ndnf Interneuron Excitability Is Spared in a Mouse Model of Dravet Syndrome. The Journal of neuroscience : the official journal of the Society for Neuroscience 44 (17) (2024)
Guojie Qu, Julie P Merchant, Jérôme Clatot, Leah M DeFlitch, Danny J Frederick, Sheng Tang, Madeleine Salvatore, Xiaohong Zhang, Jianping Li, Stewart A Anderson, Ethan M Goldberg
Targeted blockade of aberrant sodium current in a stem cell-derived neuron model of SCN3A encephalopathy. Brain : a journal of neurology (2023)
Ethan M Goldberg, Ethan M Goldberg
Don't Give Me Lip: A Role for Lipid-Accumulated Reactive Astrocytes in Temporal Lobe Epilepsy. Epilepsy currents 23 (5) (2023)
Jérôme Clatot, Natalie Ginn, Gregory Costain, Ethan M Goldberg
A KCNC1-related neurological disorder due to gain of Kv3.1 function. Annals of clinical and translational neurology (2022)
Jérôme Clatot, Shridhar Parthasarathy, Stacey R Cohen, Jillian L McKee, Shavonne Massey, Ala Somarowthu, Ethan M Goldberg, Ingo Helbig
SCN1A gain-of-function mutation causing an early onset epileptic encephalopathy. Epilepsia (2022)
Juliet K Knowles, Ingo Helbig, Cameron S Metcalf, Laura S Lubbers, Lori L Isom, Scott T Demarest, Ethan M Goldberg, Alfred L George, Holger Lerche, Sarah Weckhuysen, Vicky Whittemore, Samuel Frank Berkovic, Daniel H Lowenstein
Precision medicine for genetic epilepsy on the horizon: Recent advances, present challenges, and suggestions for continued progress. Epilepsia 63 (10) (2022)
Patrick N Lawlor, Ethan M Goldberg
Dynamic Fluorescence Imaging in Experimental Epilepsy. Epilepsy currents 22 (6) (2022)
Joanna Mattis, Ala Somarowthu, Kevin M Goff, Evan Jiang, Jina Yom, Nathaniel Sotuyo, Laura M Mcgarry, Huijie Feng, Keisuke Kaneko, Ethan M Goldberg
Corticohippocampal circuit dysfunction in a mouse model of Dravet syndrome. eLife 11 (2022)
Ethan M Goldberg
Rational Small Molecule Treatment for Genetic Epilepsies. Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics 18 (3) (2021)
Laura M McGarry, Ethan M Goldberg
The Course of Inhibition Never Did Run Smooth: Parvalbumin Interneuron Dysfunction in a Mouse Model of Lissencephaly. Epilepsy currents 21 (4) (2021)
Mark P Fitzgerald, Michael C Kaufman, Shavonne L Massey, Sara Fridinger, Marisa Prelack, Colin Ellis, Xilma Ortiz-Gonzalez, Lawrence E Fried, Marissa P DiGiovine, null null, Susan Melamed, Marissa Malcolm, Brenda Banwell, Donna Stephenson, Stephanie M Witzman, Alexander Gonzalez, Dennis Dlugos, Sudha Kilaru Kessler, Ethan M Goldberg, Nicholas S Abend, Ingo Helbig
Assessing seizure burden in pediatric epilepsy using an electronic medical record-based tool through a common data element approach. Epilepsia 62 (7) (2021)
Vishnu Anand Cuddapah, Ethan M Goldberg
REVing up the Brain: A Mechanism Driving Seizure Timing. Epilepsy currents 22 (1) (2021)
Ingo Helbig, Ethan M Goldberg
The dose makes the poison-Novel insights into Dravet syndrome and SCN1A regulation through nonproductive splicing. PLoS genetics 17 (1) (2021)
Ethan M Goldberg
Getting a Foot IN the Door: GABAergic INterneuron-Specific Enhancers. Epilepsy currents 21 (2) (2021)
Conny H Tran, Michael Vaiana, Johan Nakuci, Ala Somarowthu, Kevin M Goff, Nitsan Goldstein, Priya Murthy, Sarah F Muldoon, Ethan M Goldberg
Interneuron Desynchronization Precedes Seizures in a Mouse Model of Dravet Syndrome. The Journal of neuroscience : the official journal of the Society for Neuroscience 40 (13) (2020)
Ala Somarowthu, Ethan M Goldberg
2P or not 2P: The Question of Seizure Initiation. Epilepsy currents (2020)
Tariq Zaman, Katherine L Helbig, Jérôme Clatot, Christopher H Thompson, Seok Kyu Kang, Katrien Stouffs, Anna E Jansen, Lieve Verstraete, Adeline Jacquinet, Elena Parrini, Renzo Guerrini, Yuh Fujiwara, Satoko Miyatake, Bruria Ben-Zeev, Haim Bassan, Orit Reish, Daphna Marom, Natalie Hauser, Thuy-Anh Vu, Sally Ackermann, Careni E Spencer, Natalie Lippa, Shraddha Srinivasan, Agnieszka Charzewska, Dorota Hoffman-Zacharska, David Fitzpatrick, Victoria Harrison, Pradeep Vasudevan, Shelagh Joss, Daniela T Pilz, Katherine A Fawcett, Ingo Helbig, Naomichi Matsumoto, Jennifer A Kearney, Andrew E Fry, Ethan M Goldberg
SCN3A-Related Neurodevelopmental Disorder: A Spectrum of Epilepsy and Brain Malformation. Annals of neurology 88 (2) (2020)
Ethan M Goldberg
Gene Therapy in Models of Severe Epilepsy due to Sodium Channelopathy. Epilepsy currents 20 (4) (2020)
Tariq Zaman, Ahmad Abou Tayoun, Ethan M Goldberg
A single-center SCN8A-related epilepsy cohort: clinical, genetic, and physiologic characterization. Annals of clinical and translational neurology 6 (8) (2019)
Seok Kyu Kang, Carlos G Vanoye, Sunita N Misra, Dennis M Echevarria, Jeffrey D Calhoun, John B O'Connor, Katarina L Fabre, Dianalee McKnight, Laurie Demmer, Paula Goldenberg, Lauren E Grote, Isabelle Thiffault, Carol Saunders, Kevin A Strauss, Ali Torkamani, Jasper van der Smagt, Koen van Gassen, Robert P Carson, Jullianne Diaz, Eyby Leon, Joseph E Jacher, Mark C Hannibal, Jessica Litwin, Neil R Friedman, Allison Schreiber, Bryan Lynch, Annapurna Poduri, Eric D Marsh, Ethan M Goldberg, John J Millichap, Alfred L George, Jennifer A Kearney
Spectrum of KV 2.1 Dysfunction in KCNB1-Associated Neurodevelopmental Disorders. Annals of neurology 86 (6) (2019)
Kevin M Goff, Ethan M Goldberg
Vasoactive intestinal peptide-expressing interneurons are impaired in a mouse model of Dravet syndrome. eLife 8 (2019)
Jianping Li, Sean K Ryan, Erik Deboer, Kieona Cook, Shane Fitzgerald, Herbert M Lachman, Douglas C Wallace, Ethan M Goldberg, Stewart A Anderson
Mitochondrial deficits in human iPSC-derived neurons from patients with 22q11.2 deletion syndrome and schizophrenia. Translational psychiatry 9 (1) (2019)
Morgana Favero, Nathaniel P Sotuyo, Emily Lopez, Jennifer A Kearney, Ethan M Goldberg
A Transient Developmental Window of Fast-Spiking Interneuron Dysfunction in a Mouse Model of Dravet Syndrome. The Journal of neuroscience : the official journal of the Society for Neuroscience 38 (36) (2018)
Tariq Zaman, Ingo Helbig, Ivana Babić Božović, Suzanne D DeBrosse, A Christina Bergqvist, Kimberly Wallis, Livija Medne, Aleš Maver, Borut Peterlin, Katherine L Helbig, Xiaohong Zhang, Ethan M Goldberg
Mutations in SCN3A cause early infantile epileptic encephalopathy. Annals of neurology 83 (4) (2018)
Ethan M Goldberg, Ingo Helbig
Reply to "Recurrent SCN3A p.Ile875Thr variant in patients with polymicrogyria". Annals of neurology 84 (1) (2018)
Guoling Tian, Ana G Cristancho, Holly A Dubbs, Grant T Liu, Nicholas J Cowan, Ethan M Goldberg
A patient with lissencephaly, developmental delay, and infantile spasms, due to de novo heterozygous mutation of KIF2A. Molecular genetics & genomic medicine 4 (6) (2016)

Ethan M Goldberg.css-eqlu8i{font-size:small;padding-left:4px;} (Evan C Rosenberg, Ethan Goldberg)

Publication Activity (10 Years)

Top Topics

Top Venues

Ethan M Goldberg (Evan C Rosenberg, Ethan Goldberg)