John Millichap

34PUBLICATIONS
16CO-AUTHORS
Neurology and neuromuscular diseasesInfant and child healthCentral nervous systemEpigenetics (incl. genome methylation and epigenomics)Fairness, accountability, transparency, trust and ethics of computer systems
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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 <i>KCNQ2</i>-DEE.

John J Millichap, Cynthia L Harden, Dennis J Dlugos

|Jan 11, 2021
<i>Pediatric Neurology Briefs</i>: 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
<i>Pediatric Neurology Briefs</i>: Year in Review.

John J Millichap

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Frequent Collaborators

11 joint publications

J Gordon Millichap

2 joint publications

Alfred L George

2 joint publications

Swaroop Aradhya

1 joint publications

Nuria Lacuey