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Hansen, D.P., Dinger, M.E., Hofmann, O., Thorne, N., & Boughtwood, T.F. (2019). Preparing Australia for genomic medicine: data, computing and digital health. Med J Aust, 210 Suppl 6, S30-s32.
Ayres, S., Gallacher, L., Stark, Z., & Brett, G.R. (2019). Genetic counseling in pediatric acute care: Reflections on ultra-rapid genomic diagnoses in neonates. J Genet Couns, 28(2), 273-282.
Nisselle, A., Macciocca, I., McKenzie, F., Vuong, H., Dunlop, K., McClaren, B., et al. (2019). Readiness of clinical genetic healthcare professionals to provide genomic medicine: An Australian census. J Genet Couns, 28(2), 367-377.
Taylor, N., Best, S., Martyn, M., Long, J.C., North, K.N., Braithwaite, J., et al. (2019). A transformative translational change programme to introduce genomics into healthcare: a complexity and implementation science study protocol. BMJ Open, 9(3), e024681.
Jayasinghe, K., Quinlan, C., Stark, Z., Patel, C., Mallawaarachchi, A., Wardrop, L., et al. (2019). Renal genetics in Australia: Kidney medicine in the genomic age. Nephrology (Carlton), 24(3), 279-286.
Long JC, Pomare C, Best S, Boughtwood T, North K, Ellis LA, Churruca K, Braithwaite J. Building a learning community of Australian clinical genomics: a social network study of the Australian Genomic Health Alliance. BMC Medicine. 2019. 17 (1) : 44.
Gyngell, C., Newson, A.J., Wilkinson, D., Stark, Z., & Savulescu, J. (2019). Rapid Challenges: Ethics and Genomic Neonatal Intensive Care. Pediatrics, 143(Suppl 1), S14-s21.
Stark, Z., Dolman, L., Manolio, T.A., Ozenberger, B., Hill, S.L., Caulfied, M.J., et al. (2019). Integrating Genomics into Healthcare: A Global Responsibility. Am J Hum Genet, 104(1), 13-20.
Dillon OJ, Lunke S, Stark Z, Yeung A, Thorne N, Melbourne Genomics Health Alliance, et al. Exome sequencing has higher diagnostic yield compared to simulated disease-specific panels in children with suspected monogenic disorders. European Journal of Human Genetics. 2018. [Epub ahead of print]