Mered Parnes

12PUBLICATIONS
39CO-AUTHORS
Aboriginal and Torres Strait Islander artefactsInfant and child healthGene expression (incl. microarray and other genome-wide approaches)Developmental genetics (incl. sex determination)Child and adolescent development
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Publications (12)

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

|Oct 28, 2023
Novel Genetic and Phenotypic Expansion in GOSR2-Related Progressive Myoclonus Epilepsy.

Lea Hentrich, Mered Parnes, Timothy Edward Lotze

|Apr 27, 2023
Botulinum Neurotoxin Injections in Children with Self-Injurious Behaviors.

Mariam Hull, Mered Parnes, Joseph Jankovic

|Jun 20, 2022
Highlighting the Dystonic Phenotype Related to GNAO1.

Thomas Wirth, Giacomo Garone, Manju A Kurian

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