Ilias Goranitis

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 26

Top Topics

Urinary Incontinence

Decision Making

Top Venues

European journal of human genetics : EJHG

NPJ genomic medicine

Genetics in medicine : official journal of the American College of Medical Genetics

PharmacoEconomics

This page only lists publications with an associated author ORCID identifier.

Publications

Yan Meng, Stephanie Best, David J Amor, Ruth Braden, Angela T Morgan, Ilias Goranitis
The value of genomic testing in severe childhood speech disorders. European journal of human genetics : EJHG 32 (4) (2024)
Jemimah Ride, Ilias Goranitis, Yan Meng, Christine LaBond, Emily Lancsar
A Reporting Checklist for Discrete Choice Experiments in Health: The DIRECT Checklist. PharmacoEconomics (2024)
Yan Meng, Stephanie Best, David J Amor, Ruth Braden, Angela T Morgan, Ilias Goranitis
The value of genomic testing in severe childhood speech disorders. European journal of human genetics : EJHG (2024)
Deborah A Marshall, Nicolle Hua, James Buchanan, Kurt D Christensen, Geert W J Frederix, Ilias Goranitis, Maarten J IJzerman, Jeroen P Jansen, Tara A Lavelle, Deirdre Weymann, Hadley Stevens Smith, Wendy J Ungar, Deirdre Weymann, Sarah Wordsworth, Kathryn A Phillips
Paving the path for implementation of clinical genomic sequencing globally: Are we ready? Health affairs scholar 2 (5) (2024)
Yan Meng, Stephanie Best, David J Amor, Ruth Braden, Angela T Morgan, Ilias Goranitis
The value of genomic testing in severe childhood speech disorders. European journal of human genetics : EJHG 32 (4) (2024)
Yan Meng, Stephanie Best, David J Amor, Ruth Braden, Angela T Morgan, Ilias Goranitis
The value of genomic testing in severe childhood speech disorders. European journal of human genetics : EJHG 32 (4) (2024)
Ilias Goranitis, Yan Meng, Melissa Martyn, Stephanie Best, Sophie E Bouffler, Yvonne Bombard, Clara L Gaff, Zornitza Stark
Eliciting parental preferences and values for the return of additional findings from genomic sequencing. NPJ genomic medicine 9 (1) (2024)
Stephanie Best, Zoe Fehlberg, Christopher Richards, Michael C J Quinn, Sebastian Lunke, Amanda B Spurdle, Karin S Kassahn, Chirag Patel, Danya F Vears, Ilias Goranitis, Fiona Lynch, Alan Robertson, Emma Tudini, John Chrisodoulou, Hamish S Scott, Julie McGaughran, Zornitza Stark
Reanalysis of genomic data in rare disease: current practice and attitudes among Australian clinical and laboratory genetics services. European journal of human genetics : EJHG (2024)
Deborah A Marshall, Nicolle Hua, James Buchanan, Kurt D Christensen, Geert W J Frederix, Ilias Goranitis, Maarten J IJzerman, Jeroen P Jansen, Tara A Lavelle, Deirdre Weymann, Hadley Stevens Smith, Wendy J Ungar, Deirdre Weymann, Sarah Wordsworth, Kathryn A Phillips
Paving the path for implementation of clinical genomic sequencing globally: Are we ready? Health affairs scholar 2 (5) (2024)
Ilias Goranitis, Yan Meng, Melissa Martyn, Stephanie Best, Sophie E Bouffler, Yvonne Bombard, Clara L Gaff, Zornitza Stark
Eliciting parental preferences and values for the return of additional findings from genomic sequencing. NPJ genomic medicine 9 (1) (2024)
Ilias Goranitis, Yan Meng, Melissa Martyn, Stephanie Best, Sophie E Bouffler, Yvonne Bombard, Clara L Gaff, Zornitza Stark
Eliciting parental preferences and values for the return of additional findings from genomic sequencing. NPJ genomic medicine 9 (1) (2024)
Navdeep Kaur, Catherine Lewis, Sandra E Staffieri, Jonathan B Ruddle, Ilias Goranitis, Jay A Stiles, Gabriel Dabscheck
Cost Analysis of Orthoptist-Led Neurofibromatosis Type 1 Screening Clinics. The British and Irish orthoptic journal 19 (1) (2023)
Fiona Lynch, Yan Meng, Stephanie Best, Ilias Goranitis, Julian Savulescu, Christopher Gyngell, Danya F Vears
Australian public perspectives on genomic data governance: responsibility, regulation, and logistical considerations. European journal of human genetics : EJHG (2023)
Eden G Robertson, Lauren Kelada, Stephanie Best, Ilias Goranitis, Kristine Pierce, null null, Annie Bye, Emma Elizabeth Palmer
Quality of life in caregivers of a child with a developmental and epileptic encephalopathy. Developmental medicine and child neurology (2023)
Dylan A Mordaunt, Kim Dalziel, Ilias Goranitis, Zornitza Stark
Uptake of funded genomic testing for syndromic and non-syndromic intellectual disability in Australia. European journal of human genetics : EJHG (2023)
Tianxin Pan, You Wu, James Buchanan, Ilias Goranitis
QALYs and rare diseases: exploring the responsiveness of SF-6D, EQ-5D-5L and AQoL-8D following genomic testing for childhood and adult-onset rare genetic conditions in Australia. Health and quality of life outcomes 21 (1) (2023)
Yan Meng, Philip M Clarke, Ilias Goranitis
The Value of Genomic Testing: A Contingent Valuation Across Six Child- and Adult-Onset Genetic Conditions. PharmacoEconomics (2021)
You Wu, Shanti Balasubramaniam, Rocio Rius, David R Thorburn, John Chrisodoulou, Ilias Goranitis
Genomic sequencing for the diagnosis of childhood mitochondrial disorders: a health economic evaluation. European journal of human genetics : EJHG (2021)
Arri Coomarasamy, Hoda M Harb, Adam J Devall, Versha Cheed, Tracy E Roberts, Ilias Goranitis, Chidubem Okeke Ogwulu, Helen Marie Williams, Ioannis D Gallos, Abey Eapen, Jane P Daniels, Amna Ahmed, Ruth Bender Atik, Kalsang Bhatia, Cecilia Bottomley, Jane Brewin, Meenakshi Choudhary, Fiona Crosfill, Shilpa Deb, William Colin Duncan, Andrew K Ewer, Kim Hinshaw, Thomas Holland, Feras Izzat, Jemma Johns, Mary-Ann Lumsden, Padma Manda, Jane E Norman, Natalie Nunes, Caroline E Overton, Kathiuska Kriedt, Siobhan Quenby, Sandhya Rao, Jackie A Ross, Anupama Shahid, Martyn Underwood, Nirmala Vaithilingham, Linda Watkins, Catherine Wykes, Andrew W Horne, Davor Jurkovic, Lee J Middleton
Progesterone to prevent miscarriage in women with early pregnancy bleeding: the PRISM RCT. Health technology assessment (Winchester, England) 24 (33) (2021)
Ilias Goranitis, Stephanie Best, John Chrisodoulou, Tiffany F Boughtwood, Zornitza Stark
Preferences and values for rapid genomic testing in critically ill infants and children: a discrete choice experiment. European journal of human genetics : EJHG 29 (11) (2021)
Ilias Goranitis, Stephanie Best, John Christodoulou, Zornitza Stark, Tiffany Boughtwood
The personal utility and uptake of genomic sequencing in pediatric and adult conditions: eliciting societal preferences with three discrete choice experiments. Genetics in medicine : official journal of the American College of Medical Genetics 22 (8) (2020)
Lilian Downie, David J Amor, Jane Halliday, Sharon Lewis, Melissa Martyn, Ilias Goranitis
Exome Sequencing for Isolated Congenital Hearing Loss: A Cost-Effectiveness Analysis. The Laryngoscope 131 (7) (2020)
Stephanie Best, Zornitza Stark, Peta Phillips, You Wu, Janet C Long, Natalie Taylor, Jeffrey Braithwaite, John Chrisodoulou, Ilias Goranitis
Clinical genomic testing: what matters to key stakeholders? European journal of human genetics : EJHG 28 (7) (2020)
Max Catchpool, Jay Ramchand, David L Hare, Melissa Martyn, Ilias Goranitis
Mapping the Minnesota Living with Heart Failure Questionnaire (MLHFQ) onto the Assessment of Quality of Life 8D (AQoL-8D) utility scores. Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation 29 (10) (2020)
Ilias Goranitis, Stephanie Best, Zornitza Stark, Tiffany Boughtwood, John Christodoulou
The value of genomic sequencing in complex pediatric neurological disorders: a discrete choice experiment. Genetics in medicine : official journal of the American College of Medical Genetics 23 (1) (2020)
Ilias Goranitis, Pelham Barton, Lee J Middleton, Jonathan J Deeks, Jane P Daniels, Pallavi Latthe, Arri Coomarasamy, Suneetha Rachaneni, Shanteela McCooty, Tina S Verghese, Tracy E Roberts
Testing and Treating Women after Unsuccessful Conservative Treatments for Overactive Bladder or Mixed Urinary Incontinence: A Model-Based Economic Evaluation Based on the BUS Study. PloS one 11 (8) (2016)