photo of Sumudu Amarasekera

Sumudu Amarasekera

Sumudu Amarasekera

Details

Role PhD student (submitted)
Research area Genomic Medicine

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Top Publications

  • Abeyratne, SAE, Amarasekera, SSC, Ranaweera, LT, Salpadoru, TB, Thilakarathne, SMNK, Knowles, NJ, Wadsworth, J, Puvanendiran, S, Kothalawala, H, Jayathilake, BK, et al. Correction: The phylogenetic analysis of VP1 genomic region in foot-and-mouth disease virus serotype O isolates in Sri Lanka reveals the existence of 'Srl-97', a newly named endemic lineage. PLOS ONE 13(4) : e0196491 2024
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  • Abeyratne, SAE, Amarasekera, SSC, Ranaweera, LT, Salpadoru, TB, Thilakarathne, SMNK, Knowles, NJ, Wadsworth, J, Puvanendiran, S, Kothalawala, H, Jayathilake, BK, et al. The phylogenetic analysis of VP1 genomic region in foot-and-mouth disease virus serotype O isolates in Sri Lanka reveals the existence of 'Srl-97', a newly named endemic lineage. PLOS ONE 13(3) : e0194077 2024
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  • Amarasekera, SSC, Hock, DH, Lake, NJ, Calvo, SE, Grønborg, SW, Krzesinski, EI, Amor, DJ, Fahey, MC, Simons, C, Wibrand, F, et al. Multi-omics identifies large mitoribosomal subunit instability caused by pathogenic MRPL39 variants as a cause of pediatric onset mitochondrial disease. Human Molecular Genetics 32(15) : 2441 -2454 2023
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  • Bakhshalizadeh, S, Hock, DH, Siddall, NA, Kline, BL, Sreenivasan, R, Bell, KM, Casagranda, F, Kamalanathan, S, Sahoo, J, Narayanan, N, et al. Deficiency of the mitochondrial ribosomal subunit, MRPL50, causes autosomal recessive syndromic premature ovarian insufficiency. Human Genetics 142(7) : 879 -907 2023
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  • Akesson, LS, Rius, R, Brown, NJ, Rosenbaum, J, Donoghue, S, Stormon, M, Chai, C, Bordador, E, Guo, Y, Hakonarson, H, et al. Distinct diagnostic trajectories in NBAS‐associated acute liver failure highlights the need for timely functional studies. 63(3) : 240 -249 2022
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