Katja E. Boysen
Melbourne, VIC 3001, Australia
Last Updated: 09/26/2026
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Found 9 publications
Diversity and phylogenetic relationships of haemosporidian and hemogregarine parasites in Australian lizards.
Journal: Molecular phylogenetics and evolution
Published: May 13, 2021
BRAT1 encephalopathy: a recessive cause of epilepsy of infancy with migrating focal seizures.
Journal: Developmental medicine and child neurology
Published: November 04, 2019
Neuronal ceroid lipofuscinosis type 2: an Australian case series.
Journal: Journal of paediatrics and child health
Published: October 15, 2019
The Genetic Landscape of Epilepsy of Infancy with Migrating Focal Seizures.
Journal: Annals of neurology
Published: June 03, 2019
De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias.
Journal: American journal of human genetics
Published: March 09, 2019
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders.
Journal: Nature communications
Published: July 30, 2018
De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias.
Journal: American journal of human genetics
Published: July 20, 2018
Identifying hybridization and admixture using SNPs: application of the DArTseq platform in phylogeographic research on vertebrates.
Journal: Royal Society open science
Published: December 19, 2016
Showing 1-9 of 9
Last Updated: 09/26/2026