Dr Sebastian Lunke
Dr Sebastian Lunke
Details
Role
EGM- VCGS Genetics & Genomics Innovation
Group
VCGS Lab Management
Top Publications
- Nisselle, A, Liddicoat, D, Cliffe, C, Gallacher, L, Martyn, M, Hodgson, J, Baker, NL, Beshay, V, Fanjul-Fernandez, M, Fellowes, AP, et al. Variant interpretation training for the genomics era: Learning outcomes to inform professional competencies and education.. Am J Hum Genet 113(3) : 428 -436 2026 view publication
- Lundie, B, Chai, SY, Byrne, AB, Azmanov, D, Christodoulou, J, Haas, MA, Kassahn, KS, Lunke, S, Stott, A, Thompson, BA, et al. Piloting an Interpretive External Quality Assurance Model for Genomic Testing for Childhood Syndromes and Intellectual Disability.. J Mol Diagn 28(3) : 227 -237 2026 view publication
- Ball, M, Baker, N, Lim, SC, Casauria, S, Lunke, S, Compton, AG, Thorburn, DR, Christodoulou, J, Stark, Z. Mainstreaming genomic testing for mitochondrial disease in Australia.. Eur J Hum Genet 2026 view publication
- Tutty, E, Kanga-Parabia, A, Kugenthiran, N, Caruana, J, Downie, L, Gaff, C, Lang, N, Lunke, S, Scarff, K, Stark, Z, et al. Parental experiences of receiving genomic newborn screening results: findings from the BabyScreen+ study.. Eur J Hum Genet 2026 view publication
- Downie, L, Caruana, J, Kugenthiran, N, Kanga-Parabia, A, Tutty, E, Bombard, Y, Clausen, M, Bouffler, S, Gaff, C, Archibald, AD, et al. Supporting decisions about genomic newborn screening at scale in the digital age: the BabyScreen+ study.. NPJ Genom Med 2026 view publication
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