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Australian Genomics: Outcomes of a 5-year national program to accelerate the integration of genomics in healthcare.

Authors :
Stark Z
Boughtwood T
Haas M
Braithwaite J
Gaff CL
Goranitis I
Spurdle AB
Hansen DP
Hofmann O
Laing N
Metcalfe S
Newson AJ
Scott HS
Thorne N
Ward RL
Dinger ME
Best S
Long JC
Grimmond SM
Pearson J
Waddell N
Barnett CP
Cook M
Field M
Fielding D
Fox SB
Gecz J
Jaffe A
Leventer RJ
Lockhart PJ
Lunke S
Mallett AJ
McGaughran J
Mileshkin L
Nones K
Roscioli T
Scheffer IE
Semsarian C
Simons C
Thomas DM
Thorburn DR
Tothill R
White D
Dunwoodie S
Simpson PT
Phillips P
Brion MJ
Finlay K
Quinn MC
Mattiske T
Tudini E
Boggs K
Murray S
Wells K
Cannings J
Sinclair AH
Christodoulou J
North KN
Source :
American journal of human genetics [Am J Hum Genet] 2023 Mar 02; Vol. 110 (3), pp. 419-426.
Publication Year :
2023

Abstract

Australian Genomics is a national collaborative partnership of more than 100 organizations piloting a whole-of-system approach to integrating genomics into healthcare, based on federation principles. In the first five years of operation, Australian Genomics has evaluated the outcomes of genomic testing in more than 5,200 individuals across 19 rare disease and cancer flagship studies. Comprehensive analyses of the health economic, policy, ethical, legal, implementation and workforce implications of incorporating genomics in the Australian context have informed evidence-based change in policy and practice, resulting in national government funding and equity of access for a range of genomic tests. Simultaneously, Australian Genomics has built national skills, infrastructure, policy, and data resources to enable effective data sharing to drive discovery research and support improvements in clinical genomic delivery.<br />Competing Interests: Declaration of interests R.L.W. is the Chair of the Medical Services Advisory Committee; the views in this paper are not representing those of the Commonwealth of Australia. I.E.S. has served on scientific advisory boards for BioMarin, Chiesi, Eisai, Encoded Therapeutics, GlaxoSmithKline, Knopp Biosciences, Nutricia, Rogcon, Takeda Pharmaceuticals, UCB, and Xenon Pharmaceuticals; has received speaker honoraria from GlaxoSmithKline, UCB, BioMarin, Biocodex, Chiesi, Liva Nova, Nutricia, Zuellig Pharma, and Eisai; has received funding for travel from UCB, Biocodex, GlaxoSmithKline, Biomarin, and Eisai; has served as an investigator for Anavex Life Sciences, Cerecin Inc, Cerevel Therapeutics, Eisai, Encoded Therapeutics, EpiMinder Inc, Epygenyx, ES-Therapeutics, GW Pharma, Marinus, Neurocrine BioSciences, Ovid Therapeutics, Takeda Pharmaceuticals, UCB, Ultragenyx, Xenon Pharmaceuticals, Zogenix, and Zynerba; and has consulted for Care Beyond Diagnosis, Epilepsy Consortium, Atheneum Partners, Ovid Therapeutics, UCB, Zynerba Pharmaceuticals, BioMarin, Encoded Therapeutics, and Biohaven Pharmaceuticals; and is a Non-Executive Director of Bellberry Ltd and a Director of the Australian Academy of Health and Medical Sciences and the Australian Council of Learned Academies Limited. She may accrue future revenue on pending patent WO61/010,176 (filed: 2008): Therapeutic Compound; has a patent for SCN1A testing held by Bionomics Inc and licensed to various diagnostic companies; and has a patent molecular diagnostic/theranostic target for benign familial infantile epilepsy (BFIE) (PRRT2) 2,011,904,493 & 2,012,900,190 and PCT/AU2012/001,321 (TECH ID:2012-009).<br /> (Copyright © 2023 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1537-6605
Volume :
110
Issue :
3
Database :
MEDLINE
Journal :
American journal of human genetics
Publication Type :
Academic Journal
Accession number :
36868206
Full Text :
https://doi.org/10.1016/j.ajhg.2023.01.018