Prof Zornitza Stark
Honorary Professorial Fellow
Department of Paediatrics
339 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
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
Challenges and approaches to genetic variants of uncertain significance in clinical practice and research
DOI: 10.1186/s13073-026-01740-92026
Journal article
Automated reanalysis of genomic data for rare disease diagnostics at scale
DOI: 10.1038/s41591-026-04477-52026
Journal article
Scoping Review of Global Kidney Genetics Clinic Models and Outcomes.
DOI: 10.1016/j.ekir.2026.1065892026
Journal article
Gene–disease relationships for glomerular phenotypes: expert recommendations from ClinGen
DOI: 10.1038/s41581-026-01087-9
RECENT SCHOLARLY WORKS
2026
Journal article
A Clinical-Grade Patch Clamp Assay for the Functional Assessment of SCN5A GOF Variants Associated With Long QT Syndrome
DOI: 10.1016/j.hlc.2026.07.0032026
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.2026.1021