Zornitza Stark
University of Melbourne(AU)The University of Melbourne(AU)Victorian Clinical Genetics Services(AU)Zoos Victoria(AU)Melbourne Clinic(AU)Murdoch Children's Research Institute(AU)Murdoch Children's Research Institute(AU)Melbourne Genomics Health Alliance(AU)
Publications by Year
Research Areas
Genomics and Rare Diseases, Genomic variations and chromosomal abnormalities, Genetics and Neurodevelopmental Disorders, BRCA gene mutations in cancer, Prenatal Screening and Diagnostics
Most-Cited Works
- → Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseases(2018)622 cited
- → Osteopetrosis(2009)446 cited
- → A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders(2016)405 cited
- → Integrating Genomics into Healthcare: A Global Responsibility(2019)382 cited
- → Diagnostic Impact and Cost-effectiveness of Whole-Exome Sequencing for Ambulant Children With Suspected Monogenic Conditions(2017)322 cited
- → Prospective comparison of the cost-effectiveness of clinical whole-exome sequencing with that of usual care overwhelmingly supports early use and reimbursement(2017)238 cited