Christopher H Thompson

Publication Activity (10 Years)

Years Active: 2023-2024
Publications (10 Years): 5

Top Topics

Randomized Controlled Trial

Autism Spectrum Disorder

Top Venues

Brain : a journal of neurology

The Journal of general physiology

bioRxiv : the preprint server for biology

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

Publications

Anne T Berg, Christopher H Thompson, Leah Schust Myers, Erica Anderson, Lindsey Evans, Ariela J E Kaiser, Katherine Paltell, Amanda N Nili, Jean-Marc L DeKeyser, Tatiana V Abramova, Gerry Nesbitt, Shawn M Egan, Carlos G Vanoye, Alfred L George
Expanded clinical phenotype spectrum correlates with variant function in SCN2A-related disorders. Brain : a journal of neurology 147 (8) (2024)
Anne T Berg, Christopher H Thompson, Leah Schust Myers, Erica Anderson, Lindsey Evans, Ariela J E Kaiser, Katherine Paltell, Amanda N Nili, Jean-Marc L DeKeyser, Tatiana V Abramova, Gerry Nesbitt, Shawn M Egan, Carlos G Vanoye, Alfred L George
Expanded clinical phenotype spectrum correlates with variant function in SCN2A-related disorders. Brain : a journal of neurology 147 (8) (2024)
Anne T Berg, Christopher H Thompson, Leah Schust Myers, Erica Anderson, Lindsey Evans, Ariela J E Kaiser, Katherine Paltell, Amanda N Nili, Jean-Marc L DeKeyser, Tatiana V Abramova, Gerry Nesbitt, Shawn M Egan, Carlos G Vanoye, Alfred L George
Expanded clinical phenotype spectrum correlates with variant function in SCN2A-related disorders. Brain : a journal of neurology 147 (8) (2024)
Christopher H Thompson, Franck Potet, Tatiana V Abramova, Jean-Marc DeKeyser, Nora F Ghabra, Carlos G Vanoye, John J Millichap, Alfred L George
Epilepsy-associated SCN2A (NaV1.2) variants exhibit diverse and complex functional properties. The Journal of general physiology 155 (10) (2023)
Carlos G Vanoye, Tatiana V Abramova, Jean-Marc DeKeyser, Nora F Ghabra, Madeleine J Oudin, Christopher B Burge, Ingo Helbig, Christopher H Thompson, Alfred L George
Molecular and Cellular Context Influences SCN8A Variant Function. bioRxiv : the preprint server for biology (2023)