Stacey R Cohen

3PUBLICATIONS
11CO-AUTHORS
Neurology and neuromuscular diseasesDevelopmental genetics (incl. sex determination)Major global burdens of disease
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Publications (3)

|Oct 27, 2022
SCN1B Genetic Variants: A Review of the Spectrum of Clinical Phenotypes and a Report of Early Myoclonic Encephalopathy.

Zahra Zhu, Elizabeth Bolt, Kyra Newmaster

|Oct 26, 2022
SCN1A gain-of-function mutation causing an early onset epileptic encephalopathy.

Jérôme Clatot, Shridhar Parthasarathy, Stacey Cohen

|Mar 01, 2022
Caregiver assessment of quality of life in individuals with genetic developmental and epileptic encephalopathies.

Stacey R Cohen, Ingo Helbig, Michael C Kaufman

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