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Internal Medicine Journal
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April 5, 2024
Implementation of reimbursement for genomic testing in Australia: early successes and the pathway ahead
Andrew J Mallett, Jodie Ingles, Ilias Goranitis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 7, 2020
The personal utility and uptake of genomic sequencing in pediatric and adult conditions: eliciting societal preferences with three discrete choice experiments
Ilias Goranitis, Stephanie Best, John Christodoulou, et al.
American Journal of Medical Genetics. Part A
|
January 11, 2016
Novel missense mutations in a conserved loop between ERCC6 (CSB) helicase motifs V and VI: Insights into Cockayne syndrome
Brian T Wilson, Anneline Lochan, Zornitza Stark, et al.
Human Genetics
|
March 5, 2026
Genomics workforce views on automating genomic reanalysis: trust, equity and governance
Emily A King, Fiona Lynch, Zornitza Stark, et al.
Ophthalmic Genetics
|
April 10, 2026
Novel heterozygous UCHL1 variant causing severe optic atrophy and vision loss
Natalie S Lee, Clare L Fraser, Zornitza Stark, et al.
Neuro-Ophthalmology (Aeolus Press)
|
June 30, 2026
UCHL1-Related Dominant Optic Atrophy: Report of Two New Families
Natalie S Lee, John R Grigg, Zornitza Stark, et al.
European Journal of Human Genetics : EJHG
|
April 3, 2021
Preferences and values for rapid genomic testing in critically ill infants and children: a discrete choice experiment
Ilias Goranitis, Stephanie Best, John Christodoulou, et al.
Value in Health : the Journal of the International Society for Pharmacoeconomics and Outcomes Research
|
October 17, 2025
Genomic Testing in Australia: A Budget Impact Analysis Using Diffusion Modeling From a Healthcare System Perspective
Dylan A Mordaunt, Zornitza Stark, Adam G Elshaug, et al.
Pediatrics
|
November 28, 2022
Rapid Genome Sequencing: Consent for New Technologies in the Neonatal Intensive Care Context
Fiona Lynch, Trisha Prentice, Lynn Gillam, et al.
Human Genomics
|
August 16, 2023
Determining the utility of diagnostic genomics: a conceptual framework
Andrew Mallett, Zornitza Stark, Zoe Fehlberg, et al.
Page
of 27
Search research articles
Search
Showing results (21-30 of 270) with videos related to
Sort By:
Page
of 27
Internal Medicine Journal
|
April 5, 2024
Implementation of reimbursement for genomic testing in Australia: early successes and the pathway ahead
Andrew J Mallett, Jodie Ingles, Ilias Goranitis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 7, 2020
The personal utility and uptake of genomic sequencing in pediatric and adult conditions: eliciting societal preferences with three discrete choice experiments
Ilias Goranitis, Stephanie Best, John Christodoulou, et al.
American Journal of Medical Genetics. Part A
|
January 11, 2016
Novel missense mutations in a conserved loop between ERCC6 (CSB) helicase motifs V and VI: Insights into Cockayne syndrome
Brian T Wilson, Anneline Lochan, Zornitza Stark, et al.
Human Genetics
|
March 5, 2026
Genomics workforce views on automating genomic reanalysis: trust, equity and governance
Emily A King, Fiona Lynch, Zornitza Stark, et al.
Ophthalmic Genetics
|
April 10, 2026
Novel heterozygous UCHL1 variant causing severe optic atrophy and vision loss
Natalie S Lee, Clare L Fraser, Zornitza Stark, et al.
Neuro-Ophthalmology (Aeolus Press)
|
June 30, 2026
UCHL1-Related Dominant Optic Atrophy: Report of Two New Families
Natalie S Lee, John R Grigg, Zornitza Stark, et al.
European Journal of Human Genetics : EJHG
|
April 3, 2021
Preferences and values for rapid genomic testing in critically ill infants and children: a discrete choice experiment
Ilias Goranitis, Stephanie Best, John Christodoulou, et al.
Value in Health : the Journal of the International Society for Pharmacoeconomics and Outcomes Research
|
October 17, 2025
Genomic Testing in Australia: A Budget Impact Analysis Using Diffusion Modeling From a Healthcare System Perspective
Dylan A Mordaunt, Zornitza Stark, Adam G Elshaug, et al.
Pediatrics
|
November 28, 2022
Rapid Genome Sequencing: Consent for New Technologies in the Neonatal Intensive Care Context
Fiona Lynch, Trisha Prentice, Lynn Gillam, et al.
Human Genomics
|
August 16, 2023
Determining the utility of diagnostic genomics: a conceptual framework
Andrew Mallett, Zornitza Stark, Zoe Fehlberg, et al.
Page
of 27