Researchclopedia

Research Researchers Institutions Topics Submit About

Command Palette

Search for a command to run...

Researchclopedia

Research Researchers Institutions About

© 2026 Researchclopedia. Powered by OpenAlex under CC0 license.

Zornitza Stark | Researchclopedia

Back to researchers

Zornitza Stark

The University of Melbourne ORCID

332

Works

11,081

Citations

52

h-index

176

i10-index

Research Topics

Genomics and Rare Diseases Genomic variations and chromosomal abnormalities Genetics and Neurodevelopmental Disorders

Affiliations

Boston Children's Hospital2024–2024

Royal Children's Hospital2004–2023

Royal Women's Hospital2013–2014

University of Wisconsin–Madison2024–2024

The University of Melbourne2010–2025

Top Works

Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseases

Michelle M. Clark,Zornitza Stark,et al.

2018623 citations

BRCA gene mutations in cancer

Prenatal Screening and Diagnostics

Zornitza Stark,Ravi Savarirayan

2009446 citations

A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders

Zornitza Stark,Tiong Yang Tan,et al.

2016405 citations

Integrating Genomics into Healthcare: A Global Responsibility

Zornitza Stark,Lena Dolman,et al.

2019382 citations

Diagnostic Impact and Cost-effectiveness of Whole-Exome Sequencing for Ambulant Children With Suspected Monogenic Conditions

Tiong Yang Tan,Oliver James Dillon,et al.

2017322 citations

Prospective comparison of the cost-effectiveness of clinical whole-exome sequencing with that of usual care overwhelmingly supports early use and reimbursement

Zornitza Stark,Deborah Schofield,et al.

2017238 citations

Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System

Australian Genomics Health Alliance Acute Care Flagship,Sebastian Lunke,et al.

2020231 citations

Mutation update for the <i>CSB</i> / <i>ERCC6</i> and <i>CSA</i> / <i>ERCC8</i> genes involved in Cockayne syndrome

Vincent Laugel,C Dalloz,et al.

2009226 citations

Genomic newborn screening for rare diseases

Zornitza Stark,Richard H. Scott

2023191 citations