Rapid Genomic Testing in Intensive Care: Health Professionals’ Perspectives on Ethical Challenges

by Katie Arkell, Christopher Gyngell, Zornitza Stark, Danya F. Vears
Published 2023-05-01

It Is in Our DNA: Bringing Electronic Health Records and Genomic Data Together for Precision Medicine

by Alan J Robertson, Andrew J Mallett, Zornitza Stark, Clair Sullivan
Published 2024-06-01

Determining the utility of diagnostic genomics: a conceptual framework

by Andrew Mallett, Zornitza Stark, Zoe Fehlberg, Stephanie Best, Ilias Goranitis
Published 2023-08-01

Development of a microcosting protocol to determine the economic cost of diagnostic genomic testing for rare diseases in Australia

by Kim Dalziel, Zornitza Stark, Ilias Goranitis, Dylan A Mordaunt, Francisco Santos Gonzalez
Published 2023-11-01

The application of long-read sequencing in clinical settings

by Josephine B. Oehler, Helen Wright, Zornitza Stark, Andrew J. Mallett, Ulf Schmitz
Published 2023-08-01

Evolution of virtual gene panels over time and implications for genomic data re-analysis

by Alan J. Robertson, Khoa Tran, Chirag Patel, Clair Sullivan, Zornitza Stark, Nicola Waddell
Published 2023-01-01

Intensive Care Clinicians’ Perspectives on Ethical Challenges Raised by Rapid Genomic Testing in Critically Ill Infants

by Sachini Poogoda, Fiona Lynch, Zornitza Stark, Dominic Wilkinson, Julian Savulescu, Danya Vears, Christopher Gyngell
Published 2023-05-01

Clinically significant changes in genes and variants associated with epilepsy over time: implications for re-analysis

by Alan J. Robertson, Khoa A. Tran, Carmen Bennett, Clair Sullivan, Zornitza Stark, Lata Vadlamudi, Nicola Waddell
Published 2024-04-01

Eliciting parental preferences and values for the return of additional findings from genomic sequencing

by Ilias Goranitis, Yan Meng, Melissa Martyn, Stephanie Best, Sophie Bouffler, Yvonne Bombard, Clara Gaff, Zornitza Stark
Published 2024-02-01

The HIDDEN Protocol: An Australian Prospective Cohort Study to Determine the Utility of Whole Genome Sequencing in Kidney Failure of Unknown Aetiology

by Jacqueline Soraru, Sadia Jahan, Sadia Jahan, Catherine Quinlan, Catherine Quinlan, Catherine Quinlan, Catherine Quinlan, Cas Simons, Cas Simons, Louise Wardrop, Louise Wardrop, Rosie O’Shea, Rosie O’Shea, Alasdair Wood, Alasdair Wood, Amali Mallawaarachchi, Amali Mallawaarachchi, Amali Mallawaarachchi, Chirag Patel, Chirag Patel, Zornitza Stark, Zornitza Stark, Zornitza Stark, Andrew John Mallett, Andrew John Mallett, Andrew John Mallett, Andrew John Mallett, Andrew John Mallett
Published 2022-05-01

Theory Designed Strategies to Support Implementation of Genomics in Nephrology

by Arushi Kansal, Catherine Quinlan, Zornitza Stark, Peter G. Kerr, Andrew J. Mallett, Chandni Lakshmanan, Stephanie Best, Kushani Jayasinghe
Published 2022-10-01

Clinical and Molecular Differences between 4-Year-Old Monozygous Male Twins Mosaic for Normal, Premutation and Fragile X Full Mutation Alleles

by Alison Pandelache, Emma K Baker, Solange M. Aliaga, Marta Arpone, Robin Forbes, Zornitza Stark, David Francis, David E. Godler
Published 2019-04-01

Meeting report of the 2017 KidGen Renal Genetics Symposium

by Kushani Jayasinghe, Cathy Quinlan, Zornitza Stark, Chirag Patel, Matthew G. Sampson, Moin Saleem, Andrew J. Mallett, on behalf of the KidGen Collaborative
Published 2018-01-01

Co-design, implementation, and evaluation of plain language genomic test reports

by Gemma R. Brett, Aisha Ward, Sophie E. Bouffler, Elizabeth E. Palmer, Kirsten Boggs, Fiona Lynch, Amanda Springer, Amy Nisselle, Zornitza Stark
Published 2022-10-01

Isolated proteinuria due to CUBN homozygous mutation – challenging the investigative paradigm

by Kushani Jayasinghe, Susan M. White, Peter G. Kerr, Duncan MacGregor, Zornitza Stark, Ella Wilkins, Cas Simons, Andrew Mallett, Catherine Quinlan
Published 2019-08-01

Participant Choice towards Receiving Potential Additional Findings in an Australian Nephrology Research Genomics Study

by Rosie O’Shea, Alasdair Wood, Chirag Patel, Hugh J. McCarthy, Amali Mallawaarachchi, Catherine Quinlan, Cas Simons, Zornitza Stark, Andrew J. Mallett
Published 2022-10-01

Australian Public Perspectives on Genomic Newborn Screening: Risks, Benefits, and Preferences for Implementation

by Fiona Lynch, Stephanie Best, Clara Gaff, Lilian Downie, Alison D. Archibald, Christopher Gyngell, Ilias Goranitis, Riccarda Peters, Julian Savulescu, Sebastian Lunke, Zornitza Stark, Danya F. Vears
Published 2024-01-01

Australian public perspectives on genomic newborn screening: which conditions should be included?

by Fiona Lynch, Stephanie Best, Clara Gaff, Lilian Downie, Alison D. Archibald, Christopher Gyngell, Ilias Goranitis, Riccarda Peters, Julian Savulescu, Sebastian Lunke, Zornitza Stark, Danya F. Vears
Published 2024-05-01

Learning from scaling up ultra-rapid genomic testing for critically ill children to a national level

by Stephanie Best, Helen Brown, Sebastian Lunke, Chirag Patel, Jason Pinner, Christopher P. Barnett, Meredith Wilson, Sarah A. Sandaradura, Belinda McClaren, Gemma R. Brett, Jeffrey Braithwaite, Zornitza Stark
Published 2021-01-01

Comprehensive evaluation of a prospective Australian patient cohort with suspected genetic kidney disease undergoing clinical genomic testing: a study protocol

by Stephanie Best, Melissa Martyn, Kushani Jayasinghe, Zornitza Stark, Hugh McCarthy, Randall Faull, Madhivanan Sundaram, Peter Kerr, You Wu, Louise Wardrop, Ilias Goranitis, Catherine Quinlan, Andrew J Mallett
Published 2019-08-01