Prof Zornitza Stark
Honorary Professorial Fellow
Department of Paediatrics
331 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
Monoallelic PSMB8 variants cause PRAAS with immunodeficiency through impaired immunoproteasome assembly
DOI: 10.1016/j.ajhg.2026.04.0152026
Journal article
Health economic evaluations of genomic newborn screening: Approaches by studies within the international consortium on newborn sequencing.
DOI: 10.1038/s41431-026-02136-42026
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
Scoping Review of Global Kidney Genetics Clinic Models and Outcomes
DOI: 10.1016/j.ekir.2026.106589
RECENT SCHOLARLY WORKS
2026
Journal article
Genomic Newborn Screening: Verdict From an Australian Citizens’ Jury
DOI: 10.5694/mja2.701842026
Journal article
Navigating ethical, legal and social implications in genomic newborn screening
DOI: 10.1038/s41576-026-00936-42026
Journal article
Diagnostic Yield of Comprehensive Reanalysis After Nondiagnostic Short-Read Genome Sequencing in Infants With Unexplained Epilepsy
DOI: 10.1212/WNL.0000000000214645