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https://doi.org/10.1186/s12885-020-6573-5
De Silva S, Tennekoon KH , Karunanayake EH. Overview of the genetic basis towards early detection of breast cancer. Breast Cancer: Targets and Therapy, 2019
Manoharan V, Karunanayake EH, Tennekoon KH, De Silva S, De Silva K, Angunawela P, Lunec J. Nucleotide variants and protein expression of TP53 in a Sri Lankan cohort of head and neck cancer patients. Molecular Medicine Reports, 2019
Sundralingam T, Tennekoon KH, de Silva S, De Silva S, Hewage AS, Ranasinghe R. Novel gross deletion at the GHRHR gene locus possibly mediated by Alu specific microhomology identified in a Sri Lankan patient with isolated growth hormone deficiency. Growth Hormone & IGF Research, 2018; 42–43:94-101. Doi: https://doi.org/10.1016/j.ghir.2018.10.005
Sundralingam T, Tennekoon KH, De Silva KSH, De Silva S, Hewage AS. Pathogenic and likely pathogenic genetic alterations and polymorphisms in growth hormone gene (GH1) and growth hormone releasing hormone receptor gene (GHRHR) in a cohort of isolated growth hormone deficient (IGHD) children in Sri Lanka. Growth Hormone & IGF Research, 2017; 36: 22–29. Doi: http://dx.doi.org/10.1016/j.ghir.2017.08.006
De Silva, S, Tennekoon, KH, Dissanayake, A, De Silva K, Jayasekera L. Novel and reported pathogenic variants in exon 11 of BRCA2 gene in a cohort of Sri Lankan young breast cancer patients. Familial Cancer. 2017; 16(3): 329–338. Doi: 10.1007/s10689-016-9962-9
Jayathilaka D K, Tennekoon K H, de Silva KSH, De Silva S. A pilot study on CYP21 gene deletions among a cohort of Sri Lankan children with congenital adrenal hyperplasia, Ceylon Medical Journal, 2017; 62(2); 112–113. Doi: http://doi.org/10.4038/cmj.v62i2.8479
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De Silva S, Tennekoon KH, Karunanayake EH., Amarasinghe I and Angunawela P. Analysis of BRCA1and BRCA2 large genomic rearrangements in Sri Lankan familial breast cancer patients and at risk individuals. BMC Research Notes. 2014;7:344. Doi:10.1186/1756-0500-7-344
De Silva S, Tennekoon KH, Karunanayake EH., De Silva W, Amarasinghe I and Angunawela P. Novel sequence variants and common recurrent polymorphisms of BRCA2 in Sri Lankan breast cancer patients and a family with BRCA1 mutations. Experimental and Therapeutic Medicine. 2011; 2: 1163-1170. Doi: 10.3892/etm.2011.337