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Stark, Z, Boughtwood, T, Haas, M, Braithwaite, J, Gaff, CL, Goranitis, I, Spurdle, AB, Hansen, DP, Hofmann, O, Laing, N, et al.
Australian Genomics: Outcomes of a 5-year national program to accelerate the integration of genomics in healthcare..
Am J Hum Genet
110(3)
:
419 -426
2023
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Vos, N, Reilly, J, Elting, MW, Campeau, PM, Coman, D, Stark, Z, Tan, TY, Amor, DJ, Kaur, S, StJohn, M, et al.
DNA methylation episignatures are sensitive and specific biomarkers for detection of patients with KAT6A/KAT6B variants..
Epigenomics
15(6)
:
351 -367
2023
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Balasubramaniam, S, Li, K, Ma, A, Lunke, S, Trivedi, A, Gill, D, Curtin, J, Stark, Z.
Ultra-rapid genomic testing, a game changer in facilitating disease modifying treatment in a critically ill newborn.
Pathology
55:
s16
2023
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Snijders Blok, L, Verseput, J, Rots, D, Venselaar, H, Innes, AM, Stumpel, C, Õunap, K, Reinson, K, Seaby, EG, McKee, S, et al.
A clustering of heterozygous missense variants in the crucial chromatin modifier WDR5 defines a new neurodevelopmental disorder..
HGG Adv
4(1)
:
100157
2023
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Robertson, AJ, Tran, K, Patel, C, Sullivan, C, Stark, Z, Waddell, N.
Evolution of virtual gene panels over time and implications for genomic data re-analysis.
Genetics in Medicine Open
1(1)
:
100820
2023
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