John Millichap

34PUBLICATIONS
16CO-AUTHORS
Neurology and neuromuscular diseasesInfant and child healthCentral nervous systemEpigenetics (incl. genome methylation and epigenomics)Systems physiology
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Publications (34)

|Aug 14, 2023
Epilepsy-associated SCN2A (NaV1.2) variants exhibit diverse and complex functional properties.

Christopher H Thompson, Franck Potet, Tatiana V Abramova

|Apr 27, 2022
Value of genetic testing for pediatric epilepsy: Driving earlier diagnosis of ceroid lipofuscinosis type 2 Batten disease.

Fernanda Leal-Pardinas, Rebecca Truty, Dianalee A McKnight

|Mar 08, 2021
Capturing seizures in clinical trials of antiseizure medications for KCNQ2-DEE.

John J Millichap, Cynthia L Harden, Dennis J Dlugos

|Jan 11, 2021
Pediatric Neurology Briefs: Year in Review.

John J Millichap

|Aug 05, 2020
Functional and pharmacological evaluation of a novel SCN2A variant linked to early-onset epilepsy.

Scott K Adney, John J Millichap, Jean-Marc DeKeyser

|Feb 29, 2020
Pediatric Neurology Briefs: Year in Review.

John J Millichap

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