Prof Zornitza Stark
Honorary Professorial Fellow
Department of Paediatrics
323 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
Novel heterozygous UCHL1 variant causing severe optic atrophy and vision loss.
DOI: 10.1080/13816810.2026.26558872026
Journal article
Navigating ethical, legal and social implications in genomic newborn screening
DOI: 10.1038/s41576-026-00936-42026
Journal article
Genomic Newborn Screening: Verdict From an Australian Citizens’ Jury
DOI: 10.5694/mja2.701842026
Journal article
Diagnostic Yield of Comprehensive Reanalysis After Nondiagnostic Short-Read Genome Sequencing in Infants With Unexplained Epilepsy
DOI: 10.1212/WNL.00000000002146452026
Journal article
Variant interpretation training for the genomics era: Learning outcomes to inform professional competencies and education
DOI: 10.1016/j.ajhg.2026.01.009
RECENT SCHOLARLY WORKS
2026
Journal article
Genomic Testing in Australia: A Budget Impact Analysis Using Diffusion Modeling From a Healthcare System Perspective
DOI: 10.1016/j.jval.2025.09.30672026
Journal article
De novo variants in KDM2A cause a syndromic neurodevelopmental disorder
DOI: 10.1016/j.ajhg.2025.12.0042026
Journal article
P483: A framework for reporting genomic newborn screening Results: Illustrative cases from ten international genomic newborn screening programs*
DOI: 10.1016/j.gimo.2026.103975