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Scientific Reports|August 14, 2019
Synergistic silencing of α-globin and induction of γ-globin by histone deacetylase inhibitor, vorinostat as a potential therapy for β-thalassaemiaSachith Mettananda, Nirmani Yasara, Christopher A Fisher, et al.Hemoglobin|February 2, 2010
Identification of three novel mutations [-41 (A>C), codon 24 (-G), and IVS-I-109 (-T)], in a study of beta-thalassemia alleles in the Isfahan region of IranRasoul Salehi, Christopher A Fisher, Patricia A Bignell, et al.Blood Cells, Molecules & Diseases|February 8, 2018
Haemoglobin variants, iron status and anaemia in Sri Lankan adolescents with low red cell indices: A cross sectional surveyRexan Rodrigo, Angela Allen, Aresha Manampreri, et al.Blood|June 11, 2005
A novel molecular basis for beta thalassemia intermedia poses new questions about its pathophysiologyAnuja Premawardhena, Christopher A Fisher, Nancy F Olivieri, et al.European Journal of Haematology|February 17, 2006
A novel mutation in the last exon of ATRX in a patient with alpha-thalassemia myelodysplastic syndromeDaniel B Costa, Christopher A Fisher, Kenneth B Miller, et al.British Journal of Haematology|May 20, 2003
The molecular basis for the thalassaemias in Sri LankaChristopher A Fisher, Anuja Premawardhena, Shanthimala de Silva, et al.Hemoglobin|January 10, 2015
Rare hemoglobin variants: Hb G-Szuhu (HBB: c.243C>G), Hb G-Coushatta (HBB: c.68A>C) and Hb Mizuho (HBB: c.206T>C) in Sri Lankan familiesP Shiromi Perera, Ishari Silva, Menaka Hapugoda, et al.Nature Communications|February 13, 2026
ATRX loss couples genome instability at a G-rich repeat to dysregulation of human alpha-globin expressionYuqi Shen, Kinam Gupta, Sue Mei Tan-Wong, et al.Human Mutation|April 15, 2008
Mutations in the chromatin-associated protein ATRXRichard J Gibbons, Takahito Wada, Christopher A Fisher, et al.Frontiers in Molecular Biosciences|August 27, 2019
A "One-Stop" Screening Protocol for Haemoglobinopathy Traits and Iron Deficiency in Sri LankaAngela Allen, Shiromi Perera, Luxman Perera, et al.Pageof 2