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| Issue Date | Title | Author(s) |
| 2019 | Familial glucocorticoid deficiency presenting with hyperpigmentation, gigantism, and motor development delay: a case report. | Uyangoda, K.; Kamalanathan, P.; Mettananda, S. |
| 2022 | Feeding practices of neonates admitted to the neonatal intensive care unit of colombo north teaching hospital, Sri Lanka | Suriapperuma, T.; Mettananda, S. |
| 2024 | GDF15 linked to maternal risk of nausea and vomiting during pregnancy | Fejzo, M.; Rocha, N.; Cimino, I.; Lockhart, S.M.; Petry, C.J.; Kay, R.G.; Burling, K.; Barker, P.; George, A.L.; Yasara, N.; Premawardhena, A.; Gong, S.; Cook, E.; Rimmington, D.; Rainbow, K.; Withers, D.J.; Cortessis, V.; Mullin, P.M.; MacGibbon, K.W.; Jin, E.; Kam, A.; Campbell, A.; Polasek, O.; Tzoneva, G.; Gribble, F.M.; Yeo, G.S.H.; Lam, B.Y.H.; Saudek, V.; Hughes, I.A.; Ong, K.K.; Perry, J.R.B.; Sutton, C.A.; Baumgarten, M.; Welsh, P.; Sattar, N.; Smith, G.C.S.; Charnock- Jones, D.S.; Coll, A.P.; Meek, C.L.; Mettananda, S.; Hayward, C.; Mancuso, N.; O'Rahilly, S. |
| 2024 | GDF15 molecule is responsible for low body mass index in children with thalassaemia | Mettananda, S. |
| 2021 | Genetic and epigenetic therapies for β-Thalassaemia by altering the expression of α-globin gene | Mettananda, S. |
| 2020 | Genetic modifiers of β-thalassemia and their therapeutic implications | Yasara, Y.W.N.; Mettananda, S. |
| 2019 | Genome editing of haemopoietic stem cells for treatment of thalassaemia | Badat, M.; Mettananda, S.; Hua, P.; Schwessinger, R.; Hughes, J.; Higgs, D.; Davies, J. |
| 2022 | Growth | Dissanayake, P.; Mettananda, S. |
| 2014 | Growth parameters of Sri Lankan children during infancy: A comparison with world health organization Multicentre growth reference study | Perera, P.J.; Fernanado, M.P.; Ranathunga, N.; Sampath, W.; Samaranayake, R.; Mettananda, S. |
| 2020 | A Guide to Paediatric Red Blood Cell Disorders | Mettananda, S.; Songdej, D.; Suriapperuma, T. |
| 2019 | Health related quality of life among children with transfusion dependent β-thalassaemia major and haemoglobin E β-thalassaemia in Sri Lanka: a case control study. | Mettananda, S.; Pathiraja, H.; Peiris, R.; Bandara, D.; de Silva, U.; Mettananda, C.; Premawardhena, A. |
| 2022 | Hematology | Mettananda, S.; Williams, S. |
| 2023 | Hemitruncus arteriosus: A rare congenital cardiac anomaly diagnosed and treated during the neonatal period | Pathiraja, H.; de Livera, R.; Wickramaratne, S.; Perera, S.; Mugunthan, M.S.; Mettananda, S. |
| 2023 | Hepatic and renal status of paediatric patients with thalassaemia | Wijenayake, W.; Pathiraja, H.; Thennakoon, R.; Fernando, M.; Bandara, D.; Mettananda, S. |
| 2021 | Hydroxyurea for transfusion dependent β-thalassaemia: A randomized double-blind placebo-controlled clinical trial | Yasara, N.; Wickramarathne, N.; Silva, I.; Hameed, N.; Attanayaka, A.M.K.R.; Jayasinghe, V.L.; Gunathilaka, P.A.C.K.; Wickramasinghe, N.; Rodrigo, R.; Perera, L; Perera, P.S.; Mettananda, K.C.D.; Manamperi, A.; Premawardhena, A.; Mettananda, S. |
| 2022 | Hydroxyurea reduces the blood transfusion burden in patients with thalassaemia. | Mettananda, S. |
| 2023 | Hypopharyngeal foreign body impaction presenting late as acute onset torticollis due to retropharyngeal abscess formation in a child | Sooreakumar, A.; Dissanayake, D.M.D.T.; Wijenayake, W.; Bandara, P.K.B.U.C.; Dayasiri, K.; Mettananda, S. |
| 2019 | Identifying haemoglobinopathy traits and iron deficiency in Sri Lanka using the dtchlorophenolindophenol (DCIP) and one- tube osmotic fragility (OF) tests and measurement of red cell zinc protoporphyrin (ZPP) | Perera, P. S.; Premawardhena, A.; Mettananda, S.; Rodrigo, R.; Perera, L.; Weatherall, D. J.; Allen, S.; Allen, A. |
| 2022 | Impact of covid-19 on the education and health of schooling children in Sri Lanka; A multi-provincial study | Dayasiri, K.; Thadchanamoorthy, V.; kankananarachchi, I.; Umasankar, N.; Dassanayake, S.; Gunasekara, S.; Mettananda, S. |
| 2020 | Improving standards of care for children with thalassaemia in Sri Lanka | Mettananda, S. |
