-
Soraru, J, Jahan, S, Quinlan, C, Simons, C, Wardrop, L, O’Shea, R, Wood, A, Mallawaarachchi, A, Patel, C, Stark, Z, et al.
The HIDDEN Protocol: An Australian Prospective Cohort Study to Determine the Utility of Whole Genome Sequencing in Kidney Failure of Unknown Aetiology.
Frontiers in Medicine
9:
891223
2024
view publication
-
O’Shea, R, Wood, A, Patel, C, McCarthy, HJ, Mallawaarachchi, A, Quinlan, C, Simons, C, Stark, Z, Mallett, AJ.
Participant Choice towards Receiving Potential Additional Findings in an Australian Nephrology Research Genomics Study.
Genes
13(10)
:
1804
2024
view publication
-
Morgan, KJ, Doggett, K, Geng, F, Mieruszynski, S, Whitehead, L, Smith, KA, Hogan, BM, Simons, C, Baillie, GJ, Molania, R, et al.
ahctf1 and kras mutations combine to amplify oncogenic stress and restrict liver overgrowth in a zebrafish model of hepatocellular carcinoma.
eLife
12:
e73407
2024
view publication
-
Van Haute, L, O’Connor, E, Díaz-Maldonado, H, Munro, B, Polavarapu, K, Hock, DH, Arunachal, G, Athanasiou-Fragkouli, A, Bardhan, M, Barth, M, et al.
TEFM variants impair mitochondrial transcription causing childhood-onset neurological disease.
Nature Communications
14(1)
:
1009
2024
view publication
-
Mallawaarachchi, A, Hort, Y, Sullivan, P, Wedd, L, Fowles, L, Stevanonvski, I, Deveson, I, Simons, C, Mallett, A, Patel, C, et al.
Short and long-read whole genome sequencing explains most undiagnosed Autosomal Dominant Polycystic Kidney Disease.
2024
view publication