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

Journal Paper
Sundralingam T, Tennekoon KH, De Silva S, De Silva S, Hewage AS
Publication year: 2018

Sundralingam T, Tennekoon KH, De Silva S, De Silva S, Hewage AS. 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 Oct – Dec;42-43:94-101

YP2D6 polymorphisms may predict occurrence of adverse effects to tamoxifen: a preliminary retrospective study

Journal Paper
Wickramage I,  Tennekoon KH, Ariyaratne MAY,  Hewage AS, and Sundralingam T
Publication year: 2017

Wickramage I,  Tennekoon KH, Ariyaratne MAY,  Hewage AS, and Sundralingam T. CYP2D6 polymorphisms may predict occurrence of adverse effects to tamoxifen: a preliminary retrospective study. Breast cancer- Targets and therapy, 2017; 9: 111–120.

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

Journal Paper
Sundralingam T, Tennekoon KH, De Silva S, De Silva S, Hewage AS
Publication year: 2017

Sundralingam T, Tennekoon KH, De Silva S, 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

Growth hormone releasing hormone receptor codon 72 mutation in a cohort of Sri Lankan patients with growth hormone deficiency

Journal Paper
De Silva KS, Tennekoon KH, Sundralingam T, Navarathne B, Hewage AS, de Silva WS, Ganihigama D, Jayasinghe HD, Muhandiram ME
Publication year: 2016

De Silva KS, Tennekoon KH, Sundralingam T, Navarathne B, Hewage AS, de Silva WS, Ganihigama D, Jayasinghe HD, Muhandiram ME. Growth hormone releasing hormone receptor codon 72 mutation in a cohort of Sri Lankan patients with growth hormone deficiency. Ceylon Medical Journal, 2016 Mar; 61(1):18-21

H19 rs217727 genotype and IGF-1/intron -2 dinucleotide CT repeat polymorphism are independently associated with birth weight

Journal Paper
A.S.Hewage, P.Jayanthiny, K.H.Tennekoon, J.M.Kumarasiri, A.P.De.S.Wijesundere, E.H.Karunanayake
Publication year: 2015

A.S.Hewage, P.Jayanthiny, K.H.Tennekoon, J.M.Kumarasiri, A.P.De.S.Wijesundere, E.H.Karunanayake. H19 rs217727 genotype and IGF-1/intron -2 dinucleotide CT repeat polymorphism are independently associated with birth weight. Endocrine. 2015