Dr Sebastian Lunke
Dr Sebastian Lunke
Details
Role
EGM- VCGS Genetics & Genomics Innovation
Group
VCGS Lab Management
Top Publications
- Lynch, F, Best, S, Gaff, C, Downie, L, Archibald, AD, Gyngell, C, Goranitis, I, Peters, R, Savulescu, J, Lunke, S, et al. Australian public perspectives on genomic newborn screening: which conditions should be included?. Hum Genomics 18(1) : 45 2024 view publication
- Dias, K-R, Shrestha, R, Schofield, D, Evans, C-A, O'Heir, E, Zhu, Y, Zhang, F, Standen, K, Weisburd, B, Stenton, SL, et al. Narrowing the diagnostic gap: Genomes, episignatures, long-read sequencing, and health economic analyses in an exome-negative intellectual disability cohort.. Genet Med 26(5) : 101076 2024 view publication
- Downie, L, Bouffler, SE, Amor, DJ, Christodoulou, J, Yeung, A, Horton, AE, Macciocca, I, Archibald, AD, Wall, M, Caruana, J, et al. Gene selection for genomic newborn screening: Moving toward consensus?. Genet Med 26(5) : 101077 2024 view publication
- Lunke, S, Bouffler, SE, Downie, L, Caruana, J, Amor, DJ, Archibald, A, Bombard, Y, Christodoulou, J, Clausen, M, De Fazio, P, et al. Prospective cohort study of genomic newborn screening: BabyScreen+ pilot study protocol.. BMJ Open 14(4) : e081426 2024 view publication
- Mordaunt, DA, Gonzalez, FS, Lunke, S, Eggers, S, Sadedin, S, Chong, B, Dalziel, K, Stark, Z, Goranitis, I. The cost of proband and trio exome and genome analysis in rare disease: A micro-costing study.. Genet Med 26(4) : 101058 2024 view publication
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