Noor FA, Sultana N, Bhuyan GS, Islam MT, Hossain M, Sarker SK et al. Nationwide carrier detection and molecular characterization of β-thalassemia and hemoglobin E variants in Bangladeshi population. Orphanet Journal of Rare Diseases. 2020; doi.org/10.1186/s13023-020-1294-z
Hossain M, Noor FA, Bhuyan GS, Qadri SS, Mannoor K1. Role of XmnI Polymorphism in HbF Induction in HbE/β and β-Thalassaemia Patients. Bangladesh Med Res Counc Bull. 2019 ; 45:133-142 DOI: https://doi.org/10.3329/bmrcb.v45i3.44642
Sarker SK, Islam MT, Hasib SH, Sultana N, Hossain SR, Biswas A et al. A novel missense mutation of Isovaleryl-CoA dehydrogenase gene associated with chronic intermittent Isovaleric acidemia in a Bangladeshi patient. Meta Gene. 2019; doi.org/10.1016/j.mgene.2019.100557
Begum MN, Islam MT, Hossain SR, Bhuyan GS, Halim MA, Shahriar I et al. Mutation Spectrum in TPO Gene of Bangladeshi Patients with Thyroid Dyshormonogenesis and Analysis of the Effects of Different Mutations on the Structural Features and Functions of TPO Protein through In Silico Approach. BioMed Research International. 2019; 10.1155/2019/9218903
Sarker SK, Islam MT, Biswas A, Bhuyan GS, Sultana R, Sultana N et al. Age-Specific Cut-off Values of Amino Acids and Acylcarnitines for Diagnosis of Inborn Errors of Metabolism Using Liquid Chromatography Tandem Mass Spectrometry. BioMed Research International. 2019; 10.1155/2019/3460902
Islam MT, Sarker SK, Shithi ST, Bhuyan GS, Rahat A, Islam NN et al. High resolution melting curve analysis enables rapid and reliable detection of G6PD variants in heterozygous females. BMC Genetics. 2018;19(1).
Sarker SK, Islam MT, Bhuyan GS, Sultana N, Begum MN, Al Mahmud-Un-Nabi M et al. Impaired acylcarnitine profile in transfusion-dependent beta-thalassemia major patients in Bangladesh. J. Adv. Res. 2018;12:55-66.
Islam MT, Sarkar SK, Sultana N, Begum MN, Bhuyan GS, Shithi ST et al. High resolution melting curve analysis targeting the HBB gene mutational hot-spot offers a reliable screening approach for all common as well as most of the rare beta-globin gene mutations in Bangladesh. BMC Genetics. 2018;19(1).
Sarker SK, Islam MT, Eckhoff GM, Hossain MA, Qadri SK, Muraduzzaman A et al. Molecular Analysis of Glucose-6-Phosphate Dehydrogenase Gene Mutations in Bangladeshi Individuals. PLOS ONE. 2016;11(11):e0166977.
Al-Mamun MM, Sarker SK, Qadri SK, Shirin T, Mohammad QD, LaRocque R et al. Examination of Huntington's disease with atypical clinical features in a Bangladeshi family tree. Clinical Case Reports. 2016;4(12):1191-1194.