Laina Lusk Stripe

4PUBLICATIONS
52CO-AUTHORS
Aboriginal and Torres Strait Islander artefactsEpigenetics (incl. genome methylation and epigenomics)Infant and child healthAdolescent health
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Publications (4)

|Sep 18, 2026
SLC7A6OS Founder Mutation: A Rare Cause of Progressive Myoclonus Epilepsy Dated to 1100 Years Ago.

|Mar 08, 2026
Genetic testing for familial epilepsies: Diagnostic yield and genetic findings.

Colin A Ellis, Juliette Copeland, Isabella Velez

|Jul 01, 2024
A Longitudinal Exploration of CACNA1A -related Hemiplegic Migraine in Children.

Donna Schaare, Laina Lusk, Alexis Karlin

|Oct 20, 2017
Multisite Semiautomated Clinical Data Repository for Duplication 15q Syndrome: Study Protocol and Early Uses.

Oluwaseun Jessica Ajayi, Ebony Jeannae Smith, Teeradache Viangteeravat

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Frequent Collaborators

2 joint publications

Pamela Pojomovsky McDonnell

2 joint publications

Karen L Oliver

2 joint publications

Colin A Ellis

2 joint publications

Ingo Helbig