Prof Zornitza Stark
Honorary Professorial Fellow
Department of Paediatrics
335 Scholarly works
0 Projects
HIGHLIGHTS
2026
Journal article
Supporting decisions about genomic newborn screening at scale in the digital age: the BabyScreen study
DOI: 10.1038/s41525-026-00551-62026
Journal article
Genomics workforce views on automating genomic reanalysis: trust, equity and governance
DOI: 10.1007/s00439-026-02824-72026
Journal article
Scoping Review of Global Kidney Genetics Clinic Models and Outcomes.
DOI: 10.1016/j.ekir.2026.1065892026
Journal article
Pathological disruption of CELF2 shuttling causes neuronal hyperactivity, learning deficits, and seizures.
DOI: 10.1172/JCI1996982026
Journal article
Precision Antisense Oligonucleotide Therapy Amenability for Infantile Genetic Epilepsies
DOI: 10.1001/jamaneurol.2026.10212026
Journal article
Monoallelic PSMB8 variants cause PRAAS with immunodeficiency through impaired immunoproteasome assembly
DOI: 10.1016/j.ajhg.2026.04.0152026
Journal article
KCNQ2 neonatal epilepsy: Impact of prompt diagnosis and treatment, and early predictors of outcome severity
DOI: 10.1002/epi4.70266
RECENT SCHOLARLY WORKS
2026
Journal article
Automating genomic reanalysis: perspectives of people living with, or impacted by, a genetic, rare or undiagnosed condition.
DOI: 10.1186/s12910-026-01493-52026
Journal article
Mainstreaming genomic testing for mitochondrial disease in Australia
DOI: 10.1038/s41431-026-02053-62026
Journal article
Childhood motor speech disorders: who to prioritise for genetic testing
DOI: 10.1038/s41431-025-01993-9