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Australian Mitochondrial Disease Foundation

Homepage: mito.org.au
Alternate names: Australian Mitochondrial Disease Foundation Ltd., Mito Foundation
ROR: 04efqw959
OpenAlex ID: I4405269525
Australian Genomics: Outcomes of a 5-year national program to accelerate the integration of genomics in healthcare
2023 · Zornitza Stark, Tiffany Boughtwood, et al. · The American Journal of Human Genetics · 85
The long and winding road: perspectives of people and parents of children with mitochondrial conditions negotiating management after diagnosis
2021 · Janet C. Long, Stephanie Best, et al. · Orphanet Journal of Rare Diseases · 22
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Patient care standards for primary mitochondrial disease in Australia: an Australian adaptation of the Mitochondrial Medicine Society recommendations
2021 · Carolyn M. Sue, Shanti Balasubramaniam, et al. · Internal Medicine Journal · 19
Public attitudes towards novel reproductive technologies: a citizens’ jury on mitochondrial donation
2019 · A J Newson, S de Lacey, et al. · Human Reproduction · 15
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The Australian Genomics Mitochondrial Flagship: A national program delivering mitochondrial diagnoses
2024 · Rocio Rius, Alison G. Compton, et al. · Genetics in Medicine · 13
“I just don’t know enough”: Australian perspectives on community involvement in health and medical research
2024 · Fiona Russo, Isabella Sherburn, et al. · Research Involvement and Engagement · 6
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Pregnancy in women with mitochondrial disease—A literature review and suggested guidance for preconception and pregnancy care
2024 · Lisa Hui, Pema Hayman, et al. · Australian and New Zealand Journal of Obstetrics and Gynaecology · 5
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Interoperability of Leigh Syndrome Patient Registry Data with Regulatory Submission Standards
2023 · Parag Shiralkar, Pallavi Bakare, et al. · Journal of the Society for Clinical Data Management · 5
2000–2025: Emerging therapies in primary mitochondrial disease: A structured review, horizon scan, and roadmap for the future
2026 · Amel Karaa, Maria Isabel G. Lopez Sanchez, et al. · Therapeutic Advances in Rare Disease · 1
Transforming a Leigh Syndrome Patient Registry to the OMOP Common Data Model
2026 · Sushma Ghanta, Parag Shiralkar, et al. · Research Square · 1
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Content validity, face validity and comprehensiveness of generic quality-of-life measures in adults and children with rare genetic conditions and their carers: a think aloud qualitative study
2026 · Mackenzie Bourke, Xuemin Zhu, et al. · Quality of Life Research
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Works count: 11
Citation count: 196
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